Elizabeth Rebecca Hauser
Professor of Biostatistics & Bioinformatics
My research interests are focused on developing and applying statistical methods to search for genes causing common human diseases. Recent work has been in the development of statistical methods for genetic studies and in identifying optimal study designs for genetic studies of complex traits. As application of these methods to specific diseases has progressed it has become apparent that etiologic and genetic heterogeneity is a major stumbling block in identification of genes for common diseases. I am interested in developing methods to detect and account for genetic heterogeneity as one type of complex genetic model. I am also interested in the extent to which environmental exposures interact with genetic variants to modify risks of complex diseases. Both genetic heterogeneity and gene-environment interactions must be taken into account to achieve the goals of personalized medicine.
Collaborative studies under way at Duke University, the Durham VA and elsewhere provide the opportunity to apply new methods to ongoing studies. My main area of application is in identifying genes for cardiovascular conditions using a variety of study designs. One such study is the GENECARD study to identify genes for early onset coronary artery disease in families. Another study is the AGENDA study based on the CATHGEN cohort of patients from the Duke Cardiac Catheterization Lab. These two studies have been used to successfully identify a number of novel genes for coronary artery disease. I also work on studies of genetic effects in aging, kidney disease and colon cancer.
In turn these Collaborative studies continue to raise methodological research questions such as the effect of model misspecification on the results of linkage studies, the interpretation of confirmation studies to replicate linkage results, and the utility of a method for including additional phenotypic information when assessing linkage results.
Keywords: linkage analysis, genetic association, gene mapping, genetic epidemiology, statistical genetics, biostatistics, cardiovascular disease, computational biology, diabetes, aging, colon cancer, colon polyps, kidney disease
Collaborative studies under way at Duke University, the Durham VA and elsewhere provide the opportunity to apply new methods to ongoing studies. My main area of application is in identifying genes for cardiovascular conditions using a variety of study designs. One such study is the GENECARD study to identify genes for early onset coronary artery disease in families. Another study is the AGENDA study based on the CATHGEN cohort of patients from the Duke Cardiac Catheterization Lab. These two studies have been used to successfully identify a number of novel genes for coronary artery disease. I also work on studies of genetic effects in aging, kidney disease and colon cancer.
In turn these Collaborative studies continue to raise methodological research questions such as the effect of model misspecification on the results of linkage studies, the interpretation of confirmation studies to replicate linkage results, and the utility of a method for including additional phenotypic information when assessing linkage results.
Keywords: linkage analysis, genetic association, gene mapping, genetic epidemiology, statistical genetics, biostatistics, cardiovascular disease, computational biology, diabetes, aging, colon cancer, colon polyps, kidney disease
Current Appointments & Affiliations
- Professor of Biostatistics & Bioinformatics, Biostatistics & Bioinformatics, Basic Science Departments 2021
- Member of Duke Molecular Physiology Institute, Duke Molecular Physiology Institute, Duke Molecular Physiology Institute 2013
Contact Information
- 300 N Duke St, Rm 47-121 Carmichael Bldg, Durham, NC 27701
- Duke Box 104775, Durham, NC 27708
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elizabeth.hauser@duke.edu
(919) 684-0603
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Computational Biology, Duke Molecular Physiology Institute
- Background
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Education, Training, & Certifications
- Ph.D., University of Michigan, Ann Arbor 1998
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Previous Appointments & Affiliations
- Professor of Biostatistics and Bioinformatics, Biostatistics & Bioinformatics, Basic Science Departments 2010 - 2020
- Research Professor in the Department of Statistical Science, Statistical Science, Trinity College of Arts & Sciences 2012 - 2015
- Chief, Division of Medical Genetics, Duke Molecular Physiology Institute, Duke Molecular Physiology Institute 2008 - 2014
- Professor in Medicine, Medicine, Medical Genetics, Medicine 2013 - 2014
- Professor in Medicine, Duke Molecular Physiology Institute, Duke Molecular Physiology Institute 2010 - 2013
- Research Professor in the School of Nursing, School of Nursing, Duke University 2010 - 2013
- Associate Research Professor of Statistical Science, Statistical Science, Trinity College of Arts & Sciences 2008 - 2011
- Associate Research Professor of Biostatistics and Bioinformatics, Biostatistics & Bioinformatics, Basic Science Departments 2004 - 2010
- Associate Professor in Medicine, Duke Molecular Physiology Institute, Duke Molecular Physiology Institute 2006 - 2010
- Associate Research Professor in the School of Nursing, School of Nursing, Duke University 2007 - 2010
- Associate Research Professor in Medicine, Duke Molecular Physiology Institute, Duke Molecular Physiology Institute 2004 - 2006
- Assistant Research Professor in Medicine, Duke Molecular Physiology Institute, Duke Molecular Physiology Institute 1999 - 2004
- Assistant Research Professor of Biostatistics and Bioinformatics, Biostatistics & Bioinformatics, Basic Science Departments 2001 - 2004
- Assistant Research Professor in Medicine, Neurology, Clinical Science Departments 1998 - 1999
- Instructor, Temporary in the Department of Medicine, Neurology, Clinical Science Departments 1998
- Recognition
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In the News
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OCT 2, 2014 Duke Today -
OCT 2, 2014 -
OCT 2, 2014 U.S. News & World Report -
OCT 2, 2014 U.S. News & World Report, HealthDay News
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- Research
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Selected Grants
- Early Life Adversity and the Developmental Programming of Early Childhood Telomere Biology: A Longitudinal Study of Developmental Context and Behavioral Mediators awarded by National Institutes of Health 2021 - 2026
- Skeletal Muscle Molecular Drug Targets for Exercise-induced Cardiometabolic Health awarded by National Institutes of Health 2021 - 2025
- Duke Creating ADRD Researchers for the Next Generation - Stimulating Access to Research in Residency Program (CARiNG-StARR)" awarded by National Institutes of Health 2020 - 2024
- Duke University Program in Environmental Health awarded by National Institutes of Health 2019 - 2024
- Preparing Genetic Counselors for Genomic Medicine Research awarded by National Institutes of Health 2017 - 2023
- Duke Training Grant in Nephrology awarded by National Institutes of Health 1995 - 2023
- Postdoctoral Training in Genomic Medicine Research awarded by National Institutes of Health 2017 - 2023
- Duke CTSA (TL1) Year 5 awarded by National Institutes of Health 2018 - 2023
- Characterizing the (epi)genetics of oxytocin response in clinical and animal models awarded by National Institutes of Health 2017 - 2023
- IPA--Rodney Jones awarded by Durham Veterans Affairs Medical Center 2020 - 2022
- Bioinformatics and Computational Biology Training Program awarded by National Institutes of Health 2005 - 2021
- AN ATLAS OF SHARED GENETIC ARCHITECTURE CONNECTING CELL BIOLOGY AND HUMAN DISEASE awarded by National Institutes of Health 2018 - 2021
- IPA - Xue J Qin awarded by Durham Veterans Affairs Medical Center 2018 - 2020
- Duke University Program in Environmental Health awarded by National Institute of Environmental Health Sciences 2013 - 2019
- Duke-UNC Clinical Hematology and Transfusion Research Career Development Program awarded by National Institutes of Health 2006 - 2019
- Air Quality by Genomics Interactions in a Cardiovascular Disease Cohort awarded by Health Effects Institute 2014 - 2017
- Identifying Regulatory Variants Associated with Maternal Hyperglycemia awarded by National Institutes of Health 2015 - 2016
- Metabolomic Quantitative Trait Locus (mQTL) Genetic Mapping in Human CVD awarded by National Institutes of Health 2009 - 2016
- Engaging, Inspiring, and Preparing the Next Generation of Biostatisticians awarded by North Carolina State University 2009 - 2016
- Behavior And Physiology In Aging awarded by National Institutes of Health 1999 - 2015
- Gene-Environment Interplay, Development, and Emotional Disorders awarded by National Institutes of Health 2008 - 2014
- Understanding the Response to Fesoterodine through Genetic Evaluation in the Elderly (URGE) awarded by National Institutes of Health 2012 - 2013
- Translational Research in Pelvic Floor Disorders awarded by National Institutes of Health 2011 - 2013
- Genetic Mediators of Metabolic Cardiovascular Disease Risk awarded by National Institutes of Health 2009 - 2012
- Candidate Genes and Longitudinal Disability Phenotypes awarded by National Institutes of Health 2006 - 2012
- Recovery Act Funds for Administrative Supplements for Conte Center grant programs awarded by National Institutes of Health 2010 - 2011
- Survival and Age Biases in Gene Associations with Coronary Disease awarded by National Institutes of Health 2009 - 2011
- Genetic Epidemiology of Pelvic Organ Prolapse awarded by National Institutes of Health 2009 - 2011
- Software for Integrated Linkage and Association Analysis awarded by National Institutes of Health 2000 - 2010
- IPA Silke Schmidt awarded by Veterans Administration Medical Center 2009 - 2010
- Advanced Haplotype Analyses in Coronary Artery Disease awarded by National Institutes of Health 2004 - 2010
- IPA - Silke Schmidt awarded by Veterans Administration Medical Center 2005 - 2009
- Molecular Dissection of Cardiovascular Disease: From Genes to Models to Function awarded by National Institutes of Health 2007 - 2009
- GENECARD: Gene identification in Early-Onset CAD awarded by National Institutes of Health 2003 - 2009
- IPA - Jacqueline Rimmler awarded by Veterans Administration Medical Center 2005 - 2009
- IPA- Heidi Munger awarded by Veterans Administration Medical Center 2007 - 2009
- Genetic Analysis Methods for Medical Researchers awarded by National Institutes of Health 1994 - 2007
- Modifier Genes in Heart Failure awarded by National Institutes of Health 2001 - 2007
- Genetic studies of successful aging in the Amish awarded by National Institutes of Health 2003 - 2007
- Statistical Models for Genetic Studies of AMD awarded by National Institutes of Health 2004 - 2006
- Genetic analysis methods for medical researchers awarded by National Institutes of Health 1994 - 2004
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External Relationships
- MeTree&You
- Publications & Artistic Works
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Selected Publications
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Academic Articles
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Collins, Katherine A., William E. Kraus, Renee J. Rogers, Elizabeth R. Hauser, Wei Lang, Rong Jiang, Erik B. Schelbert, Kim M. Huffman, and John M. Jakicic. “Effect of behavioral weight-loss program on biomarkers of cardiometabolic disease risk: Heart Health Study randomized trial.” Obesity (Silver Spring) 31, no. 2 (February 2023): 338–49. https://doi.org/10.1002/oby.23618.Full Text Link to Item
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Su, Yu-Ru, Lori C. Sakoda, Jihyoun Jeon, Minta Thomas, Yi Lin, Jennifer L. Schneider, Natalia Udaltsova, et al. “Validation of a genetic-enhanced risk prediction model for colorectal cancer in a large community-based cohort.” Cancer Epidemiol Biomarkers Prev, January 9, 2023. https://doi.org/10.1158/1055-9965.EPI-22-0817.Full Text Link to Item
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Siecinski, Stephen K., Stephanie N. Giamberardino, Marina Spanos, Annalise C. Hauser, Jason R. Gibson, Tara Chandrasekhar, Maria Del Pilar Trelles, et al. “Genetic and epigenetic signatures associated with plasma oxytocin levels in children and adolescents with autism spectrum disorder.” Autism Res, January 7, 2023. https://doi.org/10.1002/aur.2884.Full Text Open Access Copy Link to Item
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Duong, Linh M., Alice B. S. Nono Djotsa, Jacqueline Vahey, Lea Steele, Rachel Quaden, Kelly M. Harrington, Sarah T. Ahmed, et al. “Association of Gulf War Illness with Characteristics in Deployed vs. Non-Deployed Gulf War Era Veterans in the Cooperative Studies Program 2006/Million Veteran Program 029 Cohort: A Cross-Sectional Analysis.” Int J Environ Res Public Health 20, no. 1 (December 24, 2022). https://doi.org/10.3390/ijerph20010258.Full Text Link to Item
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Kimbrel, Nathan A., Allison E. Ashley-Koch, Xue J. Qin, Jennifer H. Lindquist, Melanie E. Garrett, Michelle F. Dennis, Lauren P. Hair, et al. “Identification of Novel, Replicable Genetic Risk Loci for Suicidal Thoughts and Behaviors Among US Military Veterans.” Jama Psychiatry, December 14, 2022. https://doi.org/10.1001/jamapsychiatry.2022.3896.Full Text Link to Item
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Jiang, Rong, Elizabeth R. Hauser, Lydia Coulter Kwee, Svati H. Shah, Jessica A. Regan, Janet L. Huebner, Virginia B. Kraus, William E. Kraus, and Cavin K. Ward-Caviness. “The association of accelerated epigenetic age with all-cause mortality in cardiac catheterization patients as mediated by vascular and cardiometabolic outcomes.” Clin Epigenetics 14, no. 1 (December 3, 2022): 165. https://doi.org/10.1186/s13148-022-01380-x.Full Text Link to Item
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Katz, Alexander E., Min-Lee Yang, Michael G. Levin, Catherine Tcheandjieu, Michael Mathis, Kristina Hunker, Susan Blackburn, et al. “Fibromuscular Dysplasia and Abdominal Aortic Aneurysms Are Dimorphic Sex-Specific Diseases With Shared Complex Genetic Architecture.” Circ Genom Precis Med 15, no. 6 (December 2022): e003496. https://doi.org/10.1161/CIRCGEN.121.003496.Full Text Link to Item
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Slosky, Lauren M., Andrea Pires, Yushi Bai, Nicholas B. Clark, Elizabeth R. Hauser, Joshua D. Gross, Fiona Porkka, et al. “Establishment of multi-stage intravenous self-administration paradigms in mice.” Scientific Reports 12, no. 1 (December 2022): 21422. https://doi.org/10.1038/s41598-022-24740-2.Full Text
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Mirowsky, Jaime E., Martha Sue Carraway, Radhika Dhingra, Haiyan Tong, Lucas Neas, David Diaz-Sanchez, Wayne E. Cascio, et al. “Exposures to low-levels of fine particulate matter are associated with acute changes in heart rate variability, cardiac repolarization, and circulating blood lipids in coronary artery disease patients.” Environ Res 214, no. Pt 1 (November 2022): 113768. https://doi.org/10.1016/j.envres.2022.113768.Full Text Link to Item
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Waksmunski, Andrea R., Tyler G. Kinzy, Lauren A. Cruz, Cari L. Nealon, Christopher W. Halladay, Piana Simpson, Rachael L. Canania, et al. “Glaucoma Genetic Risk Scores in the Million Veteran Program.” Ophthalmology 129, no. 11 (November 2022): 1263–74. https://doi.org/10.1016/j.ophtha.2022.06.012.Full Text Link to Item
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Voils, Corrine I., Cynthia J. Coffman, R Ryanne Wu, Janet M. Grubber, Deborah A. Fisher, Elizabeth M. Strawbridge, Nina Sperber, et al. “A Cluster Randomized Trial of a Family Health History Platform to Identify and Manage Patients at Increased Risk for Colorectal Cancer.” J Gen Intern Med, October 28, 2022. https://doi.org/10.1007/s11606-022-07787-9.Full Text Link to Item
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Kobe, Elizabeth A., Brian A. Sullivan, Xuejun Qin, Thomas S. Redding, Elizabeth R. Hauser, Ashton N. Madison, Cameron Miller, et al. “Longitudinal assessment of colonoscopy adverse events in the prospective Cooperative Studies Program no. 380 colorectal cancer screening and surveillance cohort.” Gastrointest Endosc 96, no. 3 (September 2022): 553-562.e3. https://doi.org/10.1016/j.gie.2022.04.1343.Full Text Link to Item
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Tcheandjieu, Catherine, Xiang Zhu, Austin T. Hilliard, Shoa L. Clarke, Valerio Napolioni, Shining Ma, Kyung Min Lee, et al. “Large-scale genome-wide association study of coronary artery disease in genetically diverse populations.” Nat Med 28, no. 8 (August 2022): 1679–92. https://doi.org/10.1038/s41591-022-01891-3.Full Text Link to Item
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Kim, Minsu, Jennifer E. Huffman, Amy Justice, Ian Goethert, Greeshma Agasthya, Greeshma VA Million Veteran Program, and Ioana Danciu. “Identifying intragenic functional modules of genomic variations associated with cancer phenotypes by learning representation of association networks.” Bmc Med Genomics 15, no. 1 (July 6, 2022): 151. https://doi.org/10.1186/s12920-022-01298-6.Full Text Link to Item
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Raghavan, Sridharan, Jie Huang, Catherine Tcheandjieu, Jennifer E. Huffman, Elizabeth Litkowski, Chang Liu, Yuk-Lam A. Ho, et al. “A multi-population phenome-wide association study of genetically-predicted height in the Million Veteran Program.” Plos Genet 18, no. 6 (June 2022): e1010193. https://doi.org/10.1371/journal.pgen.1010193.Full Text Link to Item
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Sullivan, Brian A., Thomas S. Redding, Xuejun Qin, Ziad F. Gellad, Elizabeth R. Hauser, Meghan C. O’Leary, Christina D. Williams, et al. “Ten or More Cumulative Lifetime Adenomas Are Associated with Increased Risk for Advanced Neoplasia and Colorectal Cancer.” Dig Dis Sci 67, no. 6 (June 2022): 2526–34. https://doi.org/10.1007/s10620-021-07069-0.Full Text Link to Item
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Andonian, Brian J., Alec Koss, Timothy R. Koves, Elizabeth R. Hauser, Monica J. Hubal, David M. Pober, Janet M. Lord, et al. “Rheumatoid arthritis T cell and muscle oxidative metabolism associate with exercise-induced changes in cardiorespiratory fitness.” Sci Rep 12, no. 1 (May 6, 2022): 7450. https://doi.org/10.1038/s41598-022-11458-4.Full Text Link to Item
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Dungan, Jennifer R., Xue Qin, Simon G. Gregory, Rhonda Cooper-Dehoff, Julio D. Duarte, Huaizhen Qin, Martha Gulati, et al. “Sex-dimorphic gene effects on survival outcomes in people with coronary artery disease.” Am Heart J Plus 17 (May 2022). https://doi.org/10.1016/j.ahjo.2022.100152.Full Text Link to Item
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Gifford, Elizabeth J., Stephen H. Boyle, Jacqueline Vahey, Kellie J. Sims, Jimmy T. Efird, Blair Chesnut, Crystal Stafford, et al. “Health-Related Quality of Life by Gulf War Illness Case Status.” Int J Environ Res Public Health 19, no. 8 (April 7, 2022). https://doi.org/10.3390/ijerph19084425.Full Text Link to Item
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Hung, Adriana M., Shailja C. Shah, Alexander G. Bick, Zhihong Yu, Hua-Chang Chen, Christine M. Hunt, Frank Wendt, et al. “APOL1 Risk Variants, Acute Kidney Injury, and Death in Participants With African Ancestry Hospitalized With COVID-19 From the Million Veteran Program.” Jama Intern Med 182, no. 4 (April 1, 2022): 386–95. https://doi.org/10.1001/jamainternmed.2021.8538.Full Text Link to Item
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Kimbrel, Nathan A., Allison E. Ashley-Koch, Xue J. Qin, Jennifer H. Lindquist, Melanie E. Garrett, Michelle F. Dennis, Lauren P. Hair, et al. “A genome-wide association study of suicide attempts in the million veterans program identifies evidence of pan-ancestry and ancestry-specific risk loci.” Mol Psychiatry 27, no. 4 (April 2022): 2264–72. https://doi.org/10.1038/s41380-022-01472-3.Full Text Link to Item
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Sullivan, Brian A., Xuejun Qin, Cameron Miller, Elizabeth R. Hauser, Thomas S. Redding, Ziad F. Gellad, Ashton N. Madison, et al. “Screening Colonoscopy Findings Are Associated With Noncolorectal Cancer Mortality.” Clin Transl Gastroenterol 13, no. 4 (April 1, 2022): e00479. https://doi.org/10.14309/ctg.0000000000000479.Full Text Link to Item
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Ahmed, Sarah T., Lea Steele, Peter Richardson, Shree Nadkarni, Sandhya Bandi, Mazhgan Rowneki, Kellie J. Sims, et al. “Association of Gulf War Illness-Related Symptoms with Military Exposures among 1990-1991 Gulf War Veterans Evaluated at the War-Related Illness and Injury Study Center (WRIISC).” Brain Sci 12, no. 3 (February 27, 2022). https://doi.org/10.3390/brainsci12030321.Full Text Link to Item
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Wu, Jiao-Hui, Lisheng Zhang, Igor Nepliouev, Leigh Brian, Taiqin Huang, Kamie P. Snow, Brandon M. Schickling, et al. “Drebrin attenuates atherosclerosis by limiting smooth muscle cell transdifferentiation.” Cardiovasc Res 118, no. 3 (February 21, 2022): 772–84. https://doi.org/10.1093/cvr/cvab156.Full Text Open Access Copy Link to Item
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Mullins, Niamh, JooEun Kang, Adrian I. Campos, Jonathan R. I. Coleman, Alexis C. Edwards, Hanga Galfalvy, Daniel F. Levey, et al. “Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors.” Biol Psychiatry 91, no. 3 (February 1, 2022): 313–27. https://doi.org/10.1016/j.biopsych.2021.05.029.Full Text Link to Item
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Collins, Katherine A., Kim M. Huffman, Ruth Q. Wolever, Patrick J. Smith, Ilene C. Siegler, Leanna M. Ross, Elizabeth R. Hauser, et al. “Determinants of Dropout from and Variation in Adherence to an Exercise Intervention: The STRRIDE Randomized Trials.” Transl J Am Coll Sports Med 7, no. 1 (2022). https://doi.org/10.1249/tjx.0000000000000190.Full Text Link to Item
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Weaver, Anne M., Laura A. McGuinn, Lucas Neas, Robert B. Devlin, Radhika Dhingra, Cavin K. Ward-Caviness, Wayne E. Cascio, William E. Kraus, Elizabeth R. Hauser, and David Diaz-Sanchez. “Associations between neighborhood socioeconomic cluster and hypertension, diabetes, myocardial infarction, and coronary artery disease within a cohort of cardiac catheterization patients.” Am Heart J 243 (January 2022): 201–9. https://doi.org/10.1016/j.ahj.2021.09.013.Full Text Link to Item
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Vahey, Jacqueline, Elizabeth R. Hauser, Kellie J. Sims, Drew A. Helmer, Dawn Provenzale, and Elizabeth J. Gifford. “Research tool for classifying Gulf War illness using survey responses: Lessons for writing replicable algorithms for symptom-based conditions.” Life Sci 282 (October 1, 2021): 119808. https://doi.org/10.1016/j.lfs.2021.119808.Full Text Link to Item
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Gifford, Elizabeth J., Jacqueline Vahey, Elizabeth R. Hauser, Kellie J. Sims, Jimmy T. Efird, Erin K. Dursa, Lea Steele, Drew A. Helmer, and Dawn Provenzale. “Gulf War illness in the Gulf War Era Cohort and Biorepository: The Kansas and Centers for Disease Control definitions.” Life Sci 278 (August 1, 2021): 119454. https://doi.org/10.1016/j.lfs.2021.119454.Full Text Link to Item
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Radhakrishnan, Krishnan, Elizabeth R. Hauser, Renato Polimanti, Drew A. Helmer, Dawn Provenzale, Rebecca B. McNeil, Alysia Maffucci, et al. “Genomics of Gulf War Illness in U.S. Veterans Who Served during the 1990-1991 Persian Gulf War: Methods and Rationale for Veterans Affairs Cooperative Study #2006.” Brain Sci 11, no. 7 (June 25, 2021). https://doi.org/10.3390/brainsci11070845.Full Text Link to Item
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Slawsky, Erik, Cavin K. Ward-Caviness, Lucas Neas, Robert B. Devlin, Wayne E. Cascio, Armistead G. Russell, Ran Huang, et al. “Evaluation of PM2.5 air pollution sources and cardiovascular health.” Environ Epidemiol 5, no. 3 (June 2021): e157. https://doi.org/10.1097/EE9.0000000000000157.Full Text Link to Item
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Wang, Liuyang, Thomas J. Balmat, Alejandro L. Antonia, Florica J. Constantine, Ricardo Henao, Thomas W. Burke, Andy Ingham, et al. “An atlas connecting shared genetic architecture of human diseases and molecular phenotypes provides insight into COVID-19 susceptibility.” Genome Med 13, no. 1 (May 17, 2021): 83. https://doi.org/10.1186/s13073-021-00904-z.Full Text Link to Item
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Pazoki, Raha, Marijana Vujkovic, Joshua Elliott, Evangelos Evangelou, Dipender Gill, Mohsen Ghanbari, Peter J. van der Most, et al. “Genetic analysis in European ancestry individuals identifies 517 loci associated with liver enzymes.” Nat Commun 12, no. 1 (May 10, 2021): 2579. https://doi.org/10.1038/s41467-021-22338-2.Full Text Link to Item
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Breeze, Charles E., Anna Batorsky, Mi Kyeong Lee, Mindy D. Szeto, Xiaoguang Xu, Daniel L. McCartney, Rong Jiang, et al. “Epigenome-wide association study of kidney function identifies trans-ethnic and ethnic-specific loci.” Genome Med 13, no. 1 (April 30, 2021): 74. https://doi.org/10.1186/s13073-021-00877-z.Full Text Open Access Copy Link to Item
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Zhang, Siqi, Susanne Breitner, Wayne E. Cascio, Robert B. Devlin, Lucas M. Neas, Cavin Ward-Caviness, David Diaz-Sanchez, et al. “Association between short-term exposure to ambient fine particulate matter and myocardial injury in the CATHGEN cohort.” Environ Pollut 275 (April 15, 2021): 116663. https://doi.org/10.1016/j.envpol.2021.116663.Full Text Link to Item
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Hong, Julian C., Elizabeth R. Hauser, Thomas S. Redding, Kellie J. Sims, Ziad F. Gellad, Meghan C. O’Leary, Terry Hyslop, et al. “Characterizing chronological accumulation of comorbidities in healthy veterans: a computational approach.” Sci Rep 11, no. 1 (April 14, 2021): 8104. https://doi.org/10.1038/s41598-021-85546-2.Full Text Open Access Copy Link to Item
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Hartiala, Jaana A., Yi Han, Qiong Jia, James R. Hilser, Pin Huang, Janet Gukasyan, William S. Schwartzman, et al. “Genome-wide analysis identifies novel susceptibility loci for myocardial infarction.” Eur Heart J 42, no. 9 (March 1, 2021): 919–33. https://doi.org/10.1093/eurheartj/ehaa1040.Full Text Link to Item
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Bone, William P., Katherine M. Siewert, Anupama Jha, Derek Klarin, Scott M. Damrauer, Scott M. VA Million Veteran Program, Kyong-Mi Chang, et al. “Multi-trait association studies discover pleiotropic loci between Alzheimer's disease and cardiometabolic traits.” Alzheimers Res Ther 13, no. 1 (February 4, 2021): 34. https://doi.org/10.1186/s13195-021-00773-z.Full Text Link to Item
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Dungan, Jennifer R., Xue Qin, Melissa Hurdle, Carol S. Haynes, Elizabeth R. Hauser, and William E. Kraus. “Genome-Wide Variants Associated With Longitudinal Survival Outcomes Among Individuals With Coronary Artery Disease.” Frontiers in Genetics 12 (January 2021): 661497. https://doi.org/10.3389/fgene.2021.661497.Full Text
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Dungan, Jennifer R., Xue Qin, Melissa Hurdle, Carol S. Haynes, Elizabeth R. Hauser, and William E. Kraus. “Corrigendum: Genome-Wide Variants Associated With Longitudinal Survival Outcomes Among Individuals With Coronary Artery Disease.” Front Genet 12 (2021): 726466. https://doi.org/10.3389/fgene.2021.726466.Full Text Link to Item
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Vahey, Jacqueline, Elizabeth J. Gifford, Kellie J. Sims, Blair Chesnut, Stephen H. Boyle, Crystal Stafford, Julie Upchurch, et al. “Gene–Toxicant Interactions in Gulf War Illness: Differential Effects of the PON1 Genotype.” Brain Sciences 11, no. 12 (2021): 1558–1558. https://doi.org/10.3390/brainsci11121558.Full Text
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Wang, Liuyang, Thomas J. Balmat, Alejandro L. Antonia, Florica J. Constantine, Ricardo Henao, Thomas W. Burke, Andy Ingham, et al. “An atlas connecting shared genetic architecture of human diseases and molecular phenotypes provides insight into COVID-19 susceptibility.” Medrxiv, December 22, 2020. https://doi.org/10.1101/2020.12.20.20248572.Full Text Link to Item
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Ward-Caviness, Cavin K., Armistead G. Russell, Anne M. Weaver, Erik Slawsky, Radhika Dhingra, Lydia Coulter Kwee, Rong Jiang, et al. “Accelerated epigenetic age as a biomarker of cardiovascular sensitivity to traffic-related air pollution.” Aging (Albany Ny) 12, no. 23 (December 7, 2020): 24141–55. https://doi.org/10.18632/aging.202341.Full Text Link to Item
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Chen, Zhanghua, Tingyu Yang, Douglas I. Walker, Duncan C. Thomas, Chenyu Qiu, Leda Chatzi, Tanya L. Alderete, et al. “Dysregulated lipid and fatty acid metabolism link perfluoroalkyl substances exposure and impaired glucose metabolism in young adults.” Environ Int 145 (December 2020): 106091. https://doi.org/10.1016/j.envint.2020.106091.Full Text Link to Item
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Slosky, Lauren M., Andrea Pires, Yushi Bai, Nicholas Clark, Elizabeth R. Hauser, Joshua D. Gross, Fiona Porkka, et al. “Establishment of Multi-stage Intravenous Self-administration Paradigms in Mice,” November 27, 2020. https://doi.org/10.1101/2020.11.25.398503.Full Text
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Singh, Abanish, Michael A. Babyak, Mario Sims, Solomon K. Musani, Beverly H. Brummett, Rong Jiang, William E. Kraus, et al. “Evaluating the precision of EBF1 SNP x stress interaction association: sex, race, and age differences in a big harmonized data set of 28,026 participants.” Transl Psychiatry 10, no. 1 (October 20, 2020): 351. https://doi.org/10.1038/s41398-020-01028-5.Full Text Open Access Copy Link to Item
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Sullivan, Brian A., Thomas S. Redding, Elizabeth R. Hauser, Ziad F. Gellad, Xuejun Qin, Samir Gupta, Douglas J. Robertson, et al. “High-Risk Adenomas at Screening Colonoscopy Remain Predictive of Future High-Risk Adenomas Despite an Intervening Negative Colonoscopy.” Am J Gastroenterol 115, no. 8 (August 2020): 1275–82. https://doi.org/10.14309/ajg.0000000000000677.Full Text Link to Item
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Vujkovic, Marijana, Jacob M. Keaton, Julie A. Lynch, Donald R. Miller, Jin Zhou, Catherine Tcheandjieu, Jennifer E. Huffman, et al. “Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis.” Nat Genet 52, no. 7 (July 2020): 680–91. https://doi.org/10.1038/s41588-020-0637-y.Full Text Link to Item
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Hunter-Zinck, Haley, Yunling Shi, Man Li, Bryan R. Gorman, Sun-Gou Ji, Ning Sun, Teresa Webster, et al. “Genotyping Array Design and Data Quality Control in the Million Veteran Program.” Am J Hum Genet 106, no. 4 (April 2, 2020): 535–48. https://doi.org/10.1016/j.ajhg.2020.03.004.Full Text Link to Item
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Lieberman, David, Brian A. Sullivan, Elizabeth R. Hauser, Xuejun Qin, Laura W. Musselwhite, Meghan C. O’Leary, Thomas S. Redding, et al. “Baseline Colonoscopy Findings Associated With 10-Year Outcomes in a Screening Cohort Undergoing Colonoscopy Surveillance.” Gastroenterology 158, no. 4 (March 2020): 862-874.e8. https://doi.org/10.1053/j.gastro.2019.07.052.Full Text Link to Item
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Brummett, Beverly H., Michael A. Babyak, Rong Jiang, Kim M. Huffman, William E. Kraus, Abanish Singh, Elizabeth R. Hauser, Ilene C. Siegler, and Redford B. Williams. “Systolic Blood Pressure and Socioeconomic Status in a large multi-study population.” Ssm Popul Health 9 (December 2019): 100498. https://doi.org/10.1016/j.ssmph.2019.100498.Full Text Open Access Copy Link to Item
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Musselwhite, Laura W., Thomas S. Redding, Kellie J. Sims, Meghan C. O’Leary, Elizabeth R. Hauser, Terry Hyslop, Ziad F. Gellad, Brian A. Sullivan, David Lieberman, and Dawn Provenzale. “Advanced neoplasia in Veterans at screening colonoscopy using the National Cancer Institute Risk Assessment Tool.” Bmc Cancer 19, no. 1 (November 12, 2019): 1097. https://doi.org/10.1186/s12885-019-6204-1.Full Text Link to Item
-
Goldstein, Karen M., Deborah A. Fisher, R Ryanne Wu, Lori A. Orlando, Cynthia J. Coffman, Janet M. Grubber, Tejinder Rakhra-Burris, et al. “An electronic family health history tool to identify and manage patients at increased risk for colorectal cancer: protocol for a randomized controlled trial.” Trials 20, no. 1 (October 7, 2019): 576. https://doi.org/10.1186/s13063-019-3659-y.Full Text Link to Item
-
Fang, Huaying, Qin Hui, Julie Lynch, Jacqueline Honerlaw, Themistocles L. Assimes, Jie Huang, Marijana Vujkovic, et al. “Harmonizing Genetic Ancestry and Self-identified Race/Ethnicity in Genome-wide Association Studies.” Am J Hum Genet 105, no. 4 (October 3, 2019): 763–72. https://doi.org/10.1016/j.ajhg.2019.08.012.Full Text Link to Item
-
Chen, Zhanghua, Christopher B. Newgard, Jeniffer S. Kim, Olga IIkayeva, Tanya L. Alderete, Duncan C. Thomas, Kiros Berhane, et al. “Near-roadway air pollution exposure and altered fatty acid oxidation among adolescents and young adults - The interplay with obesity.” Environ Int 130 (September 2019): 104935. https://doi.org/10.1016/j.envint.2019.104935.Full Text Link to Item
-
Harrington, Kelly M., Xuan-Mai T. Nguyen, Rebecca J. Song, Keri Hannagan, Rachel Quaden, David R. Gagnon, Kelly Cho, et al. “Gender Differences in Demographic and Health Characteristics of the Million Veteran Program Cohort.” Womens Health Issues 29 Suppl 1, no. Suppl 1 (June 25, 2019): S56–66. https://doi.org/10.1016/j.whi.2019.04.012.Full Text Link to Item
-
Weaver, Anne M., Laura McGuinn, Lucas Neas, Jaime Mirowsky, Robert B. Devlin, Radhika Dhingra, Cavin Ward-Caviness, et al. “Neighborhood sociodemographic effects on the associations between long-term PM2.5 exposure and cardiovascular outcomes and diabetes.” Environ Epidemiol 3, no. 1 (February 2019). https://doi.org/10.1097/EE9.0000000000000038.Full Text Link to Item
-
Dhingra, Radhika, Lydia Coulter Kwee, David Diaz-Sanchez, Robert B. Devlin, Wayne Cascio, Elizabeth R. Hauser, Simon Gregory, et al. “Evaluating DNA methylation age on the Illumina MethylationEPIC Bead Chip.” Plos One 14, no. 4 (2019): e0207834. https://doi.org/10.1371/journal.pone.0207834.Full Text Link to Item
-
McGuinn, Laura A., Alexandra Schneider, Robert W. McGarrah, Cavin Ward-Caviness, Lucas M. Neas, Qian Di, Joel Schwartz, et al. “Association of long-term PM2.5 exposure with traditional and novel lipid measures related to cardiovascular disease risk.” Environ Int 122 (January 2019): 193–200. https://doi.org/10.1016/j.envint.2018.11.001.Full Text Link to Item
-
Khalil, Lara, Rebecca B. McNeil, Kellie J. Sims, Kristina A. Felder, Elizabeth R. Hauser, Karen M. Goldstein, Corrine I. Voils, et al. “The Gulf War Era Cohort and Biorepository: A Longitudinal Research Resource of Veterans of the 1990-1991 Gulf War Era.” Am J Epidemiol 187, no. 11 (November 1, 2018): 2279–91. https://doi.org/10.1093/aje/kwy147.Full Text Link to Item
-
Zhang, Siqi, Susanne Breitner, Wayne E. Cascio, Robert B. Devlin, Lucas M. Neas, David Diaz-Sanchez, William E. Kraus, et al. “Short-term effects of fine particulate matter and ozone on the cardiac conduction system in patients undergoing cardiac catheterization.” Part Fibre Toxicol 15, no. 1 (October 11, 2018): 38. https://doi.org/10.1186/s12989-018-0275-z.Full Text Link to Item
-
Cai, Tianxi, Yichi Zhang, Yuk-Lam Ho, Nicholas Link, Jiehuan Sun, Jie Huang, Tianrun A. Cai, et al. “Association of Interleukin 6 Receptor Variant With Cardiovascular Disease Effects of Interleukin 6 Receptor Blocking Therapy: A Phenome-Wide Association Study.” Jama Cardiol 3, no. 9 (September 1, 2018): 849–57. https://doi.org/10.1001/jamacardio.2018.2287.Full Text Link to Item
-
Zeng, Yi, Chao Nie, Junxia Min, Huashuai Chen, Xiaomin Liu, Rui Ye, Zhihua Chen, et al. “Sex Differences in Genetic Associations With Longevity.” Jama Netw Open 1, no. 4 (August 2018): e181670. https://doi.org/10.1001/jamanetworkopen.2018.1670.Full Text Link to Item
-
Singh, Abanish, Michael A. Babyak, Beverly H. Brummett, William E. Kraus, Ilene C. Siegler, Elizabeth R. Hauser, and Redford B. Williams. “Developing a synthetic psychosocial stress measure and harmonizing CVD-risk data: a way forward to GxE meta- and mega-analyses.” Bmc Res Notes 11, no. 1 (July 24, 2018): 504. https://doi.org/10.1186/s13104-018-3595-z.Full Text Link to Item
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Brummett, Beverly H., Michael A. Babyak, Abanish Singh, Elizabeth R. Hauser, Rong Jiang, Kim M. Huffman, William E. Kraus, Svati H. Shah, Ilene C. Siegler, and Redford B. Williams. “Lack of Association of a Functional Polymorphism in the Serotonin Receptor Gene With Body Mass Index and Depressive Symptoms in a Large Meta-Analysis of Population Based Studies.” Front Genet 9 (2018): 423. https://doi.org/10.3389/fgene.2018.00423.Full Text Link to Item
-
Chatterjee, Ranee, Clemontina A. Davenport, Laura M. Raffield, Nisa Maruthur, Leslie Lange, Elizabeth Selvin, Kenneth Butler, et al. “KCNJ11 variants and their effect on the association between serum potassium and diabetes risk in the Atherosclerosis Risk in Communities (ARIC) Study and Jackson Heart Study (JHS) cohorts.” Plos One 13, no. 8 (2018): e0203213. https://doi.org/10.1371/journal.pone.0203213.Full Text Link to Item
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Lewis, Lauren S., Kim M. Huffman, Ira J. Smith, Mark P. Donahue, Cris A. Slentz, Joseph A. Houmard, Monica J. Hubal, et al. “Genetic Variation in Acid Ceramidase Predicts Non-completion of an Exercise Intervention.” Front Physiol 9 (2018): 781. https://doi.org/10.3389/fphys.2018.00781.Full Text Link to Item
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Ward-Caviness, Cavin K., William E. Kraus, Colette Blach, Carol S. Haynes, Elaine Dowdy, Marie Lynn Miranda, Robert Devlin, et al. “Associations Between Residential Proximity to Traffic and Vascular Disease in a Cardiac Catheterization Cohort.” Arterioscler Thromb Vasc Biol 38, no. 1 (January 2018): 275–82. https://doi.org/10.1161/ATVBAHA.117.310003.Full Text Link to Item
-
Mirowsky, Jaime E., Martha Sue Carraway, Radhika Dhingra, Haiyan Tong, Lucas Neas, David Diaz-Sanchez, Wayne Cascio, et al. “Ozone exposure is associated with acute changes in inflammation, fibrinolysis, and endothelial cell function in coronary artery disease patients.” Environ Health 16, no. 1 (November 21, 2017): 126. https://doi.org/10.1186/s12940-017-0335-0.Full Text Link to Item
-
McGuinn, Laura A., Cavin Ward-Caviness, Lucas M. Neas, Alexandra Schneider, Qian Di, Alexandra Chudnovsky, Joel Schwartz, et al. “Fine particulate matter and cardiovascular disease: Comparison of assessment methods for long-term exposure.” Environ Res 159 (November 2017): 16–23. https://doi.org/10.1016/j.envres.2017.07.041.Full Text Link to Item
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Zhang, Lisheng, Jiao-Hui Wu, James C. Otto, Susan B. Gurley, Elizabeth R. Hauser, Sudha K. Shenoy, Karim Nagi, et al. “Interleukin-9 mediates chronic kidney disease-dependent vein graft disease: a role for mast cells.” Cardiovasc Res 113, no. 13 (November 1, 2017): 1551–59. https://doi.org/10.1093/cvr/cvx177.Full Text Open Access Copy Link to Item
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Wang, Hanghang, Michael J. Muehlbauer, Sara K. O’Neal, Christopher B. Newgard, Elizabeth R. Hauser, James R. Bain, and Svati H. Shah. “Recommendations for Improving Identification and Quantification in Non-Targeted, GC-MS-Based Metabolomic Profiling of Human Plasma.” Metabolites 7, no. 3 (August 25, 2017). https://doi.org/10.3390/metabo7030045.Full Text Link to Item
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Jiang, Rong, Michael A. Babyak, Beverly H. Brummett, Elizabeth R. Hauser, Svati H. Shah, Richard C. Becker, Ilene C. Siegler, et al. “Brain-derived neurotrophic factor rs6265 (Val66Met) polymorphism is associated with disease severity and incidence of cardiovascular events in a patient cohort.” Am Heart J 190 (August 2017): 40–45. https://doi.org/10.1016/j.ahj.2017.05.002.Full Text Link to Item
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Guimarães, Patrícia O., Jie-Lena Sun, Kristian Kragholm, Svati H. Shah, Karen S. Pieper, William E. Kraus, Elizabeth R. Hauser, Christopher B. Granger, L. Kristin Newby, and L. MURDOCK Horizon 1 Cardiovascular Study Investigators Durham, NC. “Corrigendum to 'Association of Standard Clinical and Laboratory Variables with Red Blood Cell Distribution Width (RDW)'[Am. Heart J. (2016) 22-28].” Am Heart J 188 (June 2017): 196. https://doi.org/10.1016/j.ahj.2017.05.011.Full Text Link to Item
-
Mirowsky, Jaime E., Robert B. Devlin, David Diaz-Sanchez, Wayne Cascio, Shannon C. Grabich, Carol Haynes, Colette Blach, et al. “A novel approach for measuring residential socioeconomic factors associated with cardiovascular and metabolic health.” J Expo Sci Environ Epidemiol 27, no. 3 (May 2017): 281–89. https://doi.org/10.1038/jes.2016.53.Full Text Link to Item
-
Wang, Hanghang, Patrick H. Pun, Lydia Kwee, Damian Craig, Carol Haynes, Megan Chryst-Ladd, Laura P. Svetkey, et al. “Apolipoprotein L1 Genetic Variants Are Associated with Chronic Kidney Disease but Not with Cardiovascular Disease in a Population Referred for Cardiac Catheterization.” Cardiorenal Med 7, no. 2 (February 2017): 96–103. https://doi.org/10.1159/000453458.Full Text Link to Item
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Wu, R Ryanne, Rachel A. Myers, Elizabeth R. Hauser, Allison Vorderstrasse, Alex Cho, Geoffrey S. Ginsburg, and Lori A. Orlando. “Impact of Genetic Testing and Family Health History Based Risk Counseling on Behavior Change and Cognitive Precursors for Type 2 Diabetes.” J Genet Couns 26, no. 1 (February 2017): 133–40. https://doi.org/10.1007/s10897-016-9988-z.Full Text Open Access Copy Link to Item
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Hall, Gentzon, Brandon Lane, Megan Chryst-Ladd, Guanghong Wu, Jen-Jar Lin, XueJun Qin, Elizabeth R. Hauser, and Rasheed Gbadegesin. “Dysregulation of WTI (-KTS) is Associated with the Kidney-Specific Effects of the LMX1B R246Q Mutation.” Sci Rep 7 (January 6, 2017): 39933. https://doi.org/10.1038/srep39933.Full Text Link to Item
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Stanifer, John W., Francis Karia, Venance Maro, Kajiru Kilonzo, Xuejun Qin, Uptal D. Patel, and Elizabeth R. Hauser. “APOL1 risk alleles among individuals with CKD in Northern Tanzania: A pilot study.” Plos One 12, no. 7 (2017): e0181811. https://doi.org/10.1371/journal.pone.0181811.Full Text Link to Item
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Ward-Caviness, Cavin K., Lucas M. Neas, Colette Blach, Carol S. Haynes, Karen LaRocque-Abramson, Elizabeth Grass, Z Elaine Dowdy, et al. “A genome-wide trans-ethnic interaction study links the PIGR-FCAMR locus to coronary atherosclerosis via interactions between genetic variants and residential exposure to traffic.” Plos One 12, no. 3 (2017): e0173880. https://doi.org/10.1371/journal.pone.0173880.Full Text Link to Item
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Breitner, Susanne, Alexandra Schneider, Robert B. Devlin, Cavin K. Ward-Caviness, David Diaz-Sanchez, Lucas M. Neas, Wayne E. Cascio, et al. “Associations among plasma metabolite levels and short-term exposure to PM2.5 and ozone in a cardiac catheterization cohort.” Environ Int 97 (December 2016): 76–84. https://doi.org/10.1016/j.envint.2016.10.012.Full Text Link to Item
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Hampel, Regina, Susanne Breitner, William E. Kraus, Elizabeth Hauser, Svati Shah, Cavin K. Ward-Caviness, Robert Devlin, et al. “Short-term effects of air temperature on plasma metabolite concentrations in patients undergoing cardiac catheterization.” Environ Res 151 (November 2016): 224–32. https://doi.org/10.1016/j.envres.2016.07.010.Full Text Link to Item
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Orlando, Lori A., R Ryanne Wu, Rachel A. Myers, Adam H. Buchanan, Vincent C. Henrich, Elizabeth R. Hauser, and Geoffrey S. Ginsburg. “Clinical utility of a Web-enabled risk-assessment and clinical decision support program.” Genet Med 18, no. 10 (October 2016): 1020–28. https://doi.org/10.1038/gim.2015.210.Full Text Open Access Copy Link to Item
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Zeng, Yi, Huashuai Chen, Ting Ni, Rongping Ruan, Chao Nie, Xiaomin Liu, Lei Feng, et al. “Interaction Between the FOXO1A-209 Genotype and Tea Drinking Is Significantly Associated with Reduced Mortality at Advanced Ages.” Rejuvenation Res 19, no. 3 (June 2016): 195–203. https://doi.org/10.1089/rej.2015.1737.Full Text Open Access Copy Link to Item
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Guimarães, Patrícia O., Jie-Lena Sun, Kristian Kragholm, Svati H. Shah, Karen S. Pieper, William E. Kraus, Elizabeth R. Hauser, Christopher B. Granger, L Kristin Newby, and L Kristin MURDOCK Horizon 1 Cardiovascular Study Investigators. “Association of standard clinical and laboratory variables with red blood cell distribution width.” Am Heart J 174 (April 2016): 22–28. https://doi.org/10.1016/j.ahj.2016.01.001.Full Text Link to Item
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Zeng, Yi, Chao Nie, Junxia Min, Xiaomin Liu, Mengmeng Li, Huashuai Chen, Hanshi Xu, et al. “Novel loci and pathways significantly associated with longevity.” Sci Rep 6 (February 25, 2016): 21243. https://doi.org/10.1038/srep21243.Full Text Open Access Copy Link to Item
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McGuinn, Laura A., Cavin K. Ward-Caviness, Lucas M. Neas, Alexandra Schneider, David Diaz-Sanchez, Wayne E. Cascio, William E. Kraus, et al. “Association between satellite-based estimates of long-term PM2.5 exposure and coronary artery disease.” Environ Res 145 (February 2016): 9–17. https://doi.org/10.1016/j.envres.2015.10.026.Full Text Link to Item
-
Dungan, Jennifer R., Xuejun Qin, Benjamin D. Horne, John F. Carlquist, Abanish Singh, Melissa Hurdle, Elizabeth Grass, et al. “Case-Only Survival Analysis Reveals Unique Effects of Genotype, Sex, and Coronary Disease Severity on Survivorship.” Plos One 11, no. 5 (2016): e0154856. https://doi.org/10.1371/journal.pone.0154856.Full Text Link to Item
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Ward-Caviness, Cavin K., Lucas M. Neas, Colette Blach, Carol S. Haynes, Karen LaRocque-Abramson, Elizabeth Grass, Elaine Dowdy, et al. “Genetic Variants in the Bone Morphogenic Protein Gene Family Modify the Association between Residential Exposure to Traffic and Peripheral Arterial Disease.” Plos One 11, no. 4 (2016): e0152670. https://doi.org/10.1371/journal.pone.0152670.Full Text Link to Item
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Kraus, William E., Christopher B. Granger, Michael H. Sketch, Mark P. Donahue, Geoffrey S. Ginsburg, Elizabeth R. Hauser, Carol Haynes, et al. “A Guide for a Cardiovascular Genomics Biorepository: the CATHGEN Experience.” J Cardiovasc Transl Res 8, no. 8 (November 2015): 449–57. https://doi.org/10.1007/s12265-015-9648-y.Full Text Link to Item
-
Kraus, William E., Deborah M. Muoio, Robert Stevens, Damian Craig, James R. Bain, Elizabeth Grass, Carol Haynes, et al. “Metabolomic Quantitative Trait Loci (mQTL) Mapping Implicates the Ubiquitin Proteasome System in Cardiovascular Disease Pathogenesis.” Plos Genet 11, no. 11 (November 2015): e1005553. https://doi.org/10.1371/journal.pgen.1005553.Full Text Open Access Copy Link to Item
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Stafford-Smith, Mark, Yi-Ju Li, Joseph P. Mathew, Yen-Wei Li, Yunqi Ji, Barbara G. Phillips-Bute, Carmelo A. Milano, et al. “Genome-wide association study of acute kidney injury after coronary bypass graft surgery identifies susceptibility loci.” Kidney Int 88, no. 4 (October 2015): 823–32. https://doi.org/10.1038/ki.2015.161.Full Text Open Access Copy Link to Item
-
Ward-Caviness, Cavin K., William E. Kraus, Colette Blach, Carol S. Haynes, Elaine Dowdy, Marie Lynn Miranda, Robert B. Devlin, et al. “Association of Roadway Proximity with Fasting Plasma Glucose and Metabolic Risk Factors for Cardiovascular Disease in a Cross-Sectional Study of Cardiac Catheterization Patients.” Environ Health Perspect 123, no. 10 (October 2015): 1007–14. https://doi.org/10.1289/ehp.1306980.Full Text Link to Item
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Singh, Abanish, Michael A. Babyak, Beverly H. Brummett, Rong Jiang, Lana L. Watkins, John C. Barefoot, William E. Kraus, et al. “Computing a Synthetic Chronic Psychosocial Stress Measurement in Multiple Datasets and its Application in the Replication of G × E Interactions of the EBF1 Gene.” Genet Epidemiol 39, no. 6 (September 2015): 489–97. https://doi.org/10.1002/gepi.21910.Full Text Link to Item
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Shah, Asad A., Simon G. Gregory, Deidre Krupp, Sheng Feng, Allison Dorogi, Carol Haynes, Elizabeth Grass, et al. “Epigenetic profiling identifies novel genes for ascending aortic aneurysm formation with bicuspid aortic valves.” Heart Surg Forum 18, no. 4 (August 30, 2015): E134–39. https://doi.org/10.1532/hsf.1247.Full Text Link to Item
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Singh, Abanish, Michael A. Babyak, Daniel K. Nolan, Beverly H. Brummett, Rong Jiang, Ilene C. Siegler, William E. Kraus, Svati H. Shah, Redford B. Williams, and Elizabeth R. Hauser. “Gene by stress genome-wide interaction analysis and path analysis identify EBF1 as a cardiovascular and metabolic risk gene.” Eur J Hum Genet 23, no. 6 (June 2015): 854–62. https://doi.org/10.1038/ejhg.2014.189.Full Text Link to Item
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Zeng, Yi, Huashuai Chen, Ting Ni, Rongping Ruan, Lei Feng, Chao Nie, Lingguo Cheng, et al. “GxE interactions between FOXO genotypes and drinking tea are significantly associated with prevention of cognitive decline in advanced age in China.” J Gerontol a Biol Sci Med Sci 70, no. 4 (April 2015): 426–33. https://doi.org/10.1093/gerona/glu060.Full Text Open Access Copy Link to Item
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Shah, Asad A., Carol Haynes, Damian M. Craig, Jacqueline Sebek, Elizabeth Grass, Karen Abramson, Elizabeth Hauser, et al. “Genetic variants associated with vein graft stenosis after coronary artery bypass grafting.” Heart Surg Forum 18, no. 1 (February 27, 2015): E1–5. https://doi.org/10.1532/hsf.1214.Full Text Link to Item
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Halim, Sharif A., Megan L. Neely, Karen S. Pieper, Svati H. Shah, William E. Kraus, Elizabeth R. Hauser, Robert M. Califf, Christopher B. Granger, and L Kristin Newby. “Simultaneous consideration of multiple candidate protein biomarkers for long-term risk for cardiovascular events.” Circ Cardiovasc Genet 8, no. 1 (February 2015): 168–77. https://doi.org/10.1161/CIRCGENETICS.113.000490.Full Text Link to Item
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Chen, Huann-Sheng, Carolyn M. Hutter, Leah E. Mechanic, Christopher I. Amos, Vineet Bafna, Elizabeth R. Hauser, Ryan D. Hernandez, et al. “Genetic simulation tools for post-genome wide association studies of complex diseases.” Genet Epidemiol 39, no. 1 (January 2015): 11–19. https://doi.org/10.1002/gepi.21870.Full Text Link to Item
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Chung, Ren-Hua, Wei-Yun Tsai, Chang-Hsun Hsieh, Kuan-Yi Hung, Chao A. Hsiung, and Elizabeth R. Hauser. “SeqSIMLA2: simulating correlated quantitative traits accounting for shared environmental effects in user-specified pedigree structure.” Genet Epidemiol 39, no. 1 (January 2015): 20–24. https://doi.org/10.1002/gepi.21850.Full Text Link to Item
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Phillips, Susan L., Scott J. Richter, Sandra L. Teglas, Ishan S. Bhatt, Robin C. Morehouse, Elizabeth R. Hauser, and Vincent C. Henrich. “Feasibility of a bilateral 4000-6000 Hz notch as a phenotype for genetic association analysis.” Int J Audiol 54, no. 10 (2015): 645–52. https://doi.org/10.3109/14992027.2015.1030512.Full Text Link to Item
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Beadles, Chris A., R. Ryanne Wu, Tiffany Himmel, Adam H. Buchanan, Karen P. Powell, Elizabeth Hauser, Vincent C. Henrich, Geoffrey S. Ginsburg, and Lori A. Orlando. “Providing patient education: impact on quantity and quality of family health history collection.” Fam Cancer 13, no. 2 (June 2014): 325–32. https://doi.org/10.1007/s10689-014-9701-z.Full Text Link to Item
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Orlando, Lori A., R Ryanne Wu, Chris Beadles, Tiffany Himmel, Adam H. Buchanan, Karen P. Powell, Elizabeth R. Hauser, Vincent C. Henrich, and Geoffrey S. Ginsburg. “Implementing family health history risk stratification in primary care: impact of guideline criteria on populations and resource demand.” Am J Med Genet C Semin Med Genet 166C, no. 1 (March 2014): 24–33. https://doi.org/10.1002/ajmg.c.31388.Full Text Link to Item
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Wu, R Ryanne, Tiffany L. Himmel, Adam H. Buchanan, Karen P. Powell, Elizabeth R. Hauser, Geoffrey S. Ginsburg, Vincent C. Henrich, and Lori A. Orlando. “Quality of family history collection with use of a patient facing family history assessment tool.” Bmc Fam Pract 15 (February 13, 2014): 31. https://doi.org/10.1186/1471-2296-15-31.Full Text Link to Item
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Wu, R. R., T. L. Himmel, A. H. Buchanan, K. P. Powell, E. R. Hauser, G. S. Ginsburg, V. C. Henrich, and L. A. Orlando. “Quality of family history collection with use of a patient facing family history assessment tool.” Bmc Family Practice 15, no. 1 (2014). https://doi.org/10.1186/1471-2296-15-31.Full Text
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Bhattacharya, Sayanti, Christopher B. Granger, Damian Craig, Carol Haynes, James Bain, Robert D. Stevens, Elizabeth R. Hauser, et al. “Validation of the association between a branched chain amino acid metabolite profile and extremes of coronary artery disease in patients referred for cardiac catheterization.” Atherosclerosis 232, no. 1 (January 2014): 191–96. https://doi.org/10.1016/j.atherosclerosis.2013.10.036.Full Text Link to Item
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Connelly, Jessica J., Olga A. Cherepanova, Jennifer F. Doss, Themistoclis Karaoli, Travis S. Lillard, Christina A. Markunas, Sarah Nelson, et al. “Epigenetic regulation of COL15A1 in smooth muscle cell replicative aging and atherosclerosis.” Hum Mol Genet 22, no. 25 (December 20, 2013): 5107–20. https://doi.org/10.1093/hmg/ddt365.Full Text Link to Item
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Ward-Caviness, Cavin, Carol Haynes, Colette Blach, Elaine Dowdy, Simon G. Gregory, Svati H. Shah, Benjamin D. Horne, William E. Kraus, and Elizabeth R. Hauser. “Gene-smoking interactions in multiple Rho-GTPase pathway genes in an early-onset coronary artery disease cohort.” Hum Genet 132, no. 12 (December 2013): 1371–82. https://doi.org/10.1007/s00439-013-1339-7.Full Text Link to Item
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Garman, Katherine S., Kouros Owzar, Elizabeth R. Hauser, Kristen Westfall, Blair R. Anderson, Rhonda F. Souza, Anna Mae Diehl, Dawn Provenzale, and Nicholas J. Shaheen. “MicroRNA expression differentiates squamous epithelium from Barrett's esophagus and esophageal cancer.” Dig Dis Sci 58, no. 11 (November 2013): 3178–88. https://doi.org/10.1007/s10620-013-2806-7.Full Text Link to Item
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Zeng, Yi, Lingguo Cheng, Ling Zhao, Qihua Tan, Qiushi Feng, Huashuai Chen, Ke Shen, et al. “Interactions between social/ behavioral factors and ADRB2 genotypes may be associated with health at advanced ages in China.” Bmc Geriatr 13 (September 9, 2013): 91. https://doi.org/10.1186/1471-2318-13-91.Full Text Open Access Copy Link to Item
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Wu, R Ryanne, Lori A. Orlando, Tiffany L. Himmel, Adam H. Buchanan, Karen P. Powell, Elizabeth R. Hauser, Astrid B. Agbaje, Vincent C. Henrich, and Geoffrey S. Ginsburg. “Patient and primary care provider experience using a family health history collection, risk stratification, and clinical decision support tool: a type 2 hybrid controlled implementation-effectiveness trial.” Bmc Fam Pract 14 (August 6, 2013): 111. https://doi.org/10.1186/1471-2296-14-111.Full Text Link to Item
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Orlando, Lori A., Vincent C. Henrich, Elizabeth R. Hauser, Charles Wilson, Geoffrey S. Ginsburg, and Geoffrey S. Genomedical Connection. “The genomic medicine model: an integrated approach to implementation of family health history in primary care.” Per Med 10, no. 3 (May 2013): 295–306. https://doi.org/10.2217/pme.13.20.Full Text Link to Item
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Wu, Jennifer M., Renée M. Ward, Kristina L. Allen-Brady, Todd L. Edwards, Peggy A. Norton, Katherine E. Hartmann, Elizabeth R. Hauser, and Digna R. Velez Edwards. “Phenotyping clinical disorders: lessons learned from pelvic organ prolapse.” Am J Obstet Gynecol 208, no. 5 (May 2013): 360–65. https://doi.org/10.1016/j.ajog.2012.11.030.Full Text Link to Item
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Xiong, Q., N. Ancona, E. R. Hauser, S. Mukherjee, and T. S. Furey. “Erratum: Integrating genetic and gene expression evidence into genome-wide association analysis of gene sets (Genome Research (2012) 22 (386-397)).” Genome Research 23, no. 5 (May 1, 2013): 905.
-
Jiang, Rong, Beverly H. Brummett, Elizabeth R. Hauser, Michael A. Babyak, Ilene C. Siegler, Abanish Singh, Arne Astrup, et al. “Chronic family stress moderates the association between a TOMM40 variant and triglyceride levels in two independent Caucasian samples.” Biol Psychol 93, no. 1 (April 2013): 184–89. https://doi.org/10.1016/j.biopsycho.2013.02.006.Full Text Link to Item
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Chan, Kenneth, Riyaz S. Patel, Paul Newcombe, Christopher P. Nelson, Atif Qasim, Stephen E. Epstein, Susan Burnett, et al. “Association between the chromosome 9p21 locus and angiographic coronary artery disease burden: a collaborative meta-analysis.” J Am Coll Cardiol 61, no. 9 (March 5, 2013): 957–70. https://doi.org/10.1016/j.jacc.2012.10.051.Full Text Link to Item
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Taylor, Warren D., Zheen Zhao, Allison Ashley-Koch, Martha E. Payne, David C. Steffens, Ranga R. Krishnan, Elizabeth Hauser, and James R. MacFall. “Fiber tract-specific white matter lesion severity Findings in late-life depression and by AGTR1 A1166C genotype.” Hum Brain Mapp 34, no. 2 (February 2013): 295–303. https://doi.org/10.1002/hbm.21445.Full Text Link to Item
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McNeil, Rebecca B., Catherine M. Thomas, Steven S. Coughlin, Elizabeth Hauser, Grant D. Huang, Karen M. Goldstein, Marcus R. Johnson, Tyra Dunn-Thomas, and Dawn T. Provenzale. “An assessment of survey measures used across key epidemiologic studies of United States Gulf War I Era veterans.” Environ Health 12 (January 9, 2013): 4. https://doi.org/10.1186/1476-069X-12-4.Full Text Link to Item
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Brummett, Beverly H., Michael A. Babyak, Rong Jiang, Svati H. Shah, Richard C. Becker, Carol Haynes, Megan Chryst-Ladd, et al. “A functional polymorphism in the 5HTR2C gene associated with stress responses also predicts incident cardiovascular events.” Plos One 8, no. 12 (2013): e82781. https://doi.org/10.1371/journal.pone.0082781.Full Text Open Access Copy Link to Item
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Dungan, Jennifer R., Elizabeth R. Hauser, Xuejun Qin, and William E. Kraus. “The genetic basis for survivorship in coronary artery disease.” Front Genet 4 (2013): 191. https://doi.org/10.3389/fgene.2013.00191.Full Text Link to Item
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Nolan, Daniel, William E. Kraus, Elizabeth Hauser, Yi-Ju Li, Dana K. Thompson, Jessica Johnson, Hsiang-Cheng Chen, et al. “Genome-wide linkage analysis of cardiovascular disease biomarkers in a large, multigenerational family.” Plos One 8, no. 8 (2013): e71779. https://doi.org/10.1371/journal.pone.0071779.Full Text Open Access Copy Link to Item
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Powell, Karen P., Carol A. Christianson, Susan E. Hahn, Gaurav Dave, Leslie R. Evans, Susan H. Blanton, Elizabeth Hauser, et al. “Collection of family health history for assessment of chronic disease risk in primary care.” N C Med J 74, no. 4 (2013): 279–86.Link to Item
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Shah, Svati H., Sheng Feng, Elizabeth Grass, Carol Haynes, Megan Chryst-Ladd, Damian Craig, Elizabeth R. Hauser, Christopher B. Newgard, William E. Kraus, and Simon G. Gregory. “Integration of Whole Genome Methylation with Metabolomics Identifies Novel Cardiovascular Disease Genes.” Circulation 126, no. 21 (November 20, 2012).Link to Item
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Ward-Caviness, Cavin, Lucas Neas, Carol Haynes, Colette Blach, Elizabeth Burns, Karen LaRocque-Abramson, Elaine Dowdy, et al. “Genetic Variants in the Bone Morphogenic Protein (BMP) Family of Genes Interact with Mobile Source Air Pollution to Increase Risk of Peripheral Arterial Disease.” Circulation 126, no. 21 (November 20, 2012).Link to Item
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Shah, Svati H., Jie-Lena Sun, Robert D. Stevens, James R. Bain, Michael J. Muehlbauer, Karen S. Pieper, Carol Haynes, et al. “Baseline metabolomic profiles predict cardiovascular events in patients at risk for coronary artery disease.” Am Heart J 163, no. 5 (May 2012): 844-850.e1. https://doi.org/10.1016/j.ahj.2012.02.005.Full Text Link to Item
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Shah, Asad A., Damian M. Craig, Jacqueline K. Sebek, Carol Haynes, Robert C. Stevens, Michael J. Muehlbauer, Christopher B. Granger, et al. “Metabolic profiles predict adverse events after coronary artery bypass grafting.” J Thorac Cardiovasc Surg 143, no. 4 (April 2012): 873–78. https://doi.org/10.1016/j.jtcvs.2011.09.070.Full Text Link to Item
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Nolan, Daniel K., Beth Sutton, Carol Haynes, Jessica Johnson, Jacqueline Sebek, Elaine Dowdy, David Crosslin, et al. “Fine mapping of a linkage peak with integration of lipid traits identifies novel coronary artery disease genes on chromosome 5.” Bmc Genet 13 (February 27, 2012): 12. https://doi.org/10.1186/1471-2156-13-12.Full Text Link to Item
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Xiong, Qing, Nicola Ancona, Elizabeth R. Hauser, Sayan Mukherjee, and Terrence S. Furey. “Integrating genetic and gene expression evidence into genome-wide association analysis of gene sets.” Genome Res 22, no. 2 (February 2012): 386–97. https://doi.org/10.1101/gr.124370.111.Full Text Link to Item
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Bhattacharya, Sayanti, Damian Craig, Carol Haynes, Christopher B. Granger, Robert D. Stevens, Elizabeth R. Hauser, William E. Kraus, Christopher B. Newgard, L. K. Newby, and Svati H. Shah. “Peripheral Metabolite Profiles Discriminate Coronary Artery Disease in a Sequential Cohort of Cardiac Catheterization Patients.” Circulation 124, no. 21 (November 22, 2011).Link to Item
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Orlando, Lori A., Elizabeth R. Hauser, Carol Christianson, Karen P. Powell, Adam H. Buchanan, Blair Chesnut, Astrid B. Agbaje, Vincent C. Henrich, and Geoffrey Ginsburg. “Protocol for implementation of family health history collection and decision support into primary care using a computerized family health history system.” Bmc Health Serv Res 11 (October 11, 2011): 264. https://doi.org/10.1186/1472-6963-11-264.Full Text Open Access Copy Link to Item
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Rudock, M. E., A. J. Cox, J. T. Ziegler, A. B. Lehtinen, J. J. Connelly, B. I. Freedman, J. J. Carr, et al. “Cigarette smoking status has a modifying effect on the association between polymorphisms in KALRN and measures of cardiovascular risk in the diabetes heart study.” Genes and Genomics 33, no. 5 (October 1, 2011): 483–90. https://doi.org/10.1007/s13258-011-0069-2.Full Text
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Minear, Mollie A., David R. Crosslin, Beth S. Sutton, Jessica J. Connelly, Sarah C. Nelson, Shera Gadson-Watson, Tianyuan Wang, et al. “Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease.” Hum Genet 129, no. 6 (June 2011): 641–54. https://doi.org/10.1007/s00439-011-0959-z.Full Text Link to Item
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Orlando, Lori A., Elizabeth R. Hauser, Carol Christianson, Karen P. Powell, Adam H. Buchanan, Astrid B. Agbaje, Vincent C. Henrich, and Geoffrey Ginsburg. “WHAT'S THE IMPACT? CLINICAL VALIDITY AND UTILITY OF METREE, AN ELECTRONIC FAMILY HISTORY COLLECTION AND DECISION SUPPORT TOOL FOR PRIMARY CARE.” Journal of General Internal Medicine 26 (May 1, 2011): S35–36.Link to Item
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Kral, Brian G., Rasika A. Mathias, Bhoom Suktitipat, Ingo Ruczinski, Dhananjay Vaidya, Lisa R. Yanek, Arshed A. Quyyumi, et al. “A common variant in the CDKN2B gene on chromosome 9p21 protects against coronary artery disease in Americans of African ancestry.” J Hum Genet 56, no. 3 (March 2011): 224–29. https://doi.org/10.1038/jhg.2010.171.Full Text Link to Item
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Zeng, Yi, Lingguo Cheng, Huashuai Chen, Huiqing Cao, Elizabeth R. Hauser, Yuzhi Liu, Zhenyu Xiao, Qihua Tan, Xiao-Li Tian, and James W. Vaupel. “Effects of FOXO genotypes on longevity: a biodemographic analysis.” J Gerontol a Biol Sci Med Sci 65, no. 12 (December 2010): 1285–99. https://doi.org/10.1093/gerona/glq156.Full Text Open Access Copy Link to Item
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Shah, Svati H., Christopher B. Granger, Elizabeth R. Hauser, William E. Kraus, Jie-Lena Sun, Karen Pieper, Charlotte L. Nelson, et al. “Reclassification of cardiovascular risk using integrated clinical and molecular biosignatures: Design of and rationale for the Measurement to Understand the Reclassification of Disease of Cabarrus and Kannapolis (MURDOCK) Horizon 1 Cardiovascular Disease Study.” Am Heart J 160, no. 3 (September 2010): 371-379.e2. https://doi.org/10.1016/j.ahj.2010.06.051.Full Text Link to Item
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Gbadegesin, Rasheed, Peter Lavin, Louis Janssens, Bartlomiej Bartkowiak, Alison Homstad, Guanghong Wu, Brandy Bowling, et al. “A new locus for familial FSGS on chromosome 2p.” J Am Soc Nephrol 21, no. 8 (August 2010): 1390–97. https://doi.org/10.1681/ASN.2009101046.Full Text Link to Item
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Zhang, Lisheng, Jessica J. Connelly, Karsten Peppel, Leigh Brian, Svati H. Shah, Sarah Nelson, David R. Crosslin, et al. “Aging-related atherosclerosis is exacerbated by arterial expression of tumor necrosis factor receptor-1: evidence from mouse models and human association studies.” Hum Mol Genet 19, no. 14 (July 15, 2010): 2754–66. https://doi.org/10.1093/hmg/ddq172.Full Text Link to Item
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Qin, Xuejun, Elizabeth R. Hauser, and Silke Schmidt. “Ordered subset analysis for case-control studies.” Genet Epidemiol 34, no. 5 (July 2010): 407–17. https://doi.org/10.1002/gepi.20489.Full Text Link to Item
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Shah, Svati H., James R. Bain, Michael J. Muehlbauer, Robert D. Stevens, David R. Crosslin, Carol Haynes, Jennifer Dungan, et al. “Association of a peripheral blood metabolic profile with coronary artery disease and risk of subsequent cardiovascular events.” Circ Cardiovasc Genet 3, no. 2 (April 2010): 207–14. https://doi.org/10.1161/CIRCGENETICS.109.852814.Full Text Open Access Copy Link to Item
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Chen, Hsiang-Cheng, Virginia Byers Kraus, Yi-Ju Li, Sarah Nelson, Carol Haynes, Jessica Johnson, Thomas Stabler, et al. “Genome-wide linkage analysis of quantitative biomarker traits of osteoarthritis in a large, multigenerational extended family.” Arthritis Rheum 62, no. 3 (March 2010): 781–90. https://doi.org/10.1002/art.27288.Full Text Link to Item
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Crosslin, David R., Xuejun Qin, and Elizabeth R. Hauser. “Assessment of LD matrix measures for the analysis of biological pathway association.” Stat Appl Genet Mol Biol 9, no. 1 (2010): Article35. https://doi.org/10.2202/1544-6115.1561.Full Text Open Access Copy Link to Item
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Cupples, L Adrienne, Joseph Beyene, Heike Bickeböller, E Warwick Daw, M Daniele Fallin, W James Gauderman, Saurabh Ghosh, et al. “Genetic Analysis Workshop 16: Strategies for genome-wide association study analyses.” Bmc Proc 3 Suppl 7, no. Suppl 7 (December 15, 2009): S1. https://doi.org/10.1186/1753-6561-3-s7-s1.Full Text Link to Item
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Horne, Benjamin D., Elizabeth R. Hauser, Liyong Wang, Joseph B. Muhlestein, Jeffrey L. Anderson, John F. Carlquist, Svati H. Shah, and William E. Kraus. “Validation study of genetic associations with coronary artery disease on chromosome 3q13-21 and potential effect modification by smoking.” Ann Hum Genet 73, no. Pt 6 (November 2009): 551–58. https://doi.org/10.1111/j.1469-1809.2009.00540.x.Full Text Link to Item
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Wang, Tianyuan, Terrence S. Furey, Jessica J. Connelly, Shihao Ji, Sarah Nelson, Steffen Heber, Simon G. Gregory, and Elizabeth R. Hauser. “A general integrative genomic feature transcription factor binding site prediction method applied to analysis of USF1 binding in cardiovascular disease.” Hum Genomics 3, no. 3 (April 2009): 221–35. https://doi.org/10.1186/1479-7364-3-3-221.Full Text Link to Item
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Crosslin, David R., Svati H. Shah, Sarah C. Nelson, Carol S. Haynes, Jessica J. Connelly, Shera Gadson, Pascal J. Goldschmidt-Clermont, et al. “Genetic effects in the leukotriene biosynthesis pathway and association with atherosclerosis.” Hum Genet 125, no. 2 (March 2009): 217–29. https://doi.org/10.1007/s00439-008-0619-0.Full Text Link to Item
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Hauser, Elizabeth, Nadine Cremer, Rebecca Hein, and Harshal Deshmukh. “Haplotype-based analysis: a summary of GAW16 Group 4 analysis.” Genet Epidemiol 33 Suppl 1, no. Suppl 1 (2009): S24–28. https://doi.org/10.1002/gepi.20468.Full Text Link to Item
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Shah, Svati H., Elizabeth R. Hauser, James R. Bain, Michael J. Muehlbauer, Carol Haynes, Robert D. Stevens, Brett R. Wenner, et al. “High heritability of metabolomic profiles in families burdened with premature cardiovascular disease.” Mol Syst Biol 5 (2009): 258. https://doi.org/10.1038/msb.2009.11.Full Text Link to Item
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Shah, Svati H., Neil J. Freedman, Lisheng Zhang, David R. Crosslin, David H. Stone, Carol Haynes, Jessica Johnson, et al. “Neuropeptide Y gene polymorphisms confer risk of early-onset atherosclerosis.” Plos Genet 5, no. 1 (January 2009): e1000318. https://doi.org/10.1371/journal.pgen.1000318.Full Text Open Access Copy Link to Item
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Chung, Ren-Hua, Silke Schmidt, Eden R. Martin, and Elizabeth R. Hauser. “Ordered-subset analysis (OSA) for family-based association mapping of complex traits.” Genet Epidemiol 32, no. 7 (November 2008): 627–37. https://doi.org/10.1002/gepi.20340.Full Text Link to Item
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Shah, Svati H., Elizabeth R. Hauser, David Crosslin, Liyong Wang, Carol Haynes, Jessica Connelly, Sarah Nelson, et al. “ALOX5AP variants are associated with in-stent restenosis after percutaneous coronary intervention.” Atherosclerosis 201, no. 1 (November 2008): 148–54. https://doi.org/10.1016/j.atherosclerosis.2008.01.011.Full Text Link to Item
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Goswami, Robi, Beth S. Sutton, Cynthia Rouf, Sarah Nelson, Carol Haynes, Jessica Johnson, Pascal Goldschmidt-Clermont, et al. “Biliverdin Reductase Genetic Polymorphisms are Associated with Early-Onset Coronary Artery Disease In Two Datasets.” Circulation 118, no. 18 (October 28, 2008): S389–90.Link to Item
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Wang, L., E. R. Hauser, S. H. Shah, D. Seo, P. Sivashanmugam, S. T. Exum, S. G. Gregory, et al. “Polymorphisms of the tumor suppressor gene LSAMP are associated with left main coronary artery disease.” Ann Hum Genet 72, no. Pt 4 (July 2008): 443–53. https://doi.org/10.1111/j.1469-1809.2008.00433.x.Full Text Link to Item
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Sutton, Beth S., David R. Crosslin, Svati H. Shah, Sarah C. Nelson, Anthony Bassil, A Brent Hale, Carol Haynes, et al. “Comprehensive genetic analysis of the platelet activating factor acetylhydrolase (PLA2G7) gene and cardiovascular disease in case-control and family datasets.” Hum Mol Genet 17, no. 9 (May 1, 2008): 1318–28. https://doi.org/10.1093/hmg/ddn020.Full Text Link to Item
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Connelly, Jessica J., Svati H. Shah, Jennifer F. Doss, Shera Gadson, Sarah Nelson, David R. Crosslin, A Brent Hale, et al. “Genetic and functional association of FAM5C with myocardial infarction.” Bmc Med Genet 9 (April 22, 2008): 33. https://doi.org/10.1186/1471-2350-9-33.Full Text Link to Item
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Schmidt, Silke, Michael A. Schmidt, Xuejun Qin, Eden R. Martin, and Elizabeth R. Hauser. “Increased efficiency of case-control association analysis by using allele-sharing and covariate information.” Hum Hered 65, no. 3 (2008): 154–65. https://doi.org/10.1159/000109732.Full Text Link to Item
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Schmidt, Silke, Xuejun Qin, Michael A. Schmidt, Eden R. Martin, and Elizabeth R. Hauser. “Interpreting analyses of continuous covariates in affected sibling pair linkage studies.” Genet Epidemiol 31, no. 6 (September 2007): 541–52. https://doi.org/10.1002/gepi.20227.Full Text Link to Item
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Wang, Liyong, Elizabeth R. Hauser, Svati H. Shah, Margaret A. Pericak-Vance, Carol Haynes, David Crosslin, Marco Harris, et al. “Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease.” Am J Hum Genet 80, no. 4 (April 2007): 650–63. https://doi.org/10.1086/512981.Full Text Link to Item
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Chung, Ren-Hua, Elizabeth R. Hauser, and Eden R. Martin. “Interpretation of simultaneous linkage and family-based association tests in genome screens.” Genet Epidemiol 31, no. 2 (February 2007): 134–42. https://doi.org/10.1002/gepi.20196.Full Text Link to Item
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Murtha, Amy P., Tammy Sinclair, Elizabeth R. Hauser, Geeta K. Swamy, William N. P. Herbert, and R Phillips Heine. “Maternal serum cytokines in preterm premature rupture of membranes.” Obstet Gynecol 109, no. 1 (January 2007): 121–27. https://doi.org/10.1097/01.AOG.0000250474.35369.12.Full Text Link to Item
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Cordell, Heather J., Mariza de Andrade, Marie-Claude Babron, Christopher W. Bartlett, Joseph Beyene, Heike Bickeböller, Robert Culverhouse, et al. “Genetic Analysis Workshop 15: gene expression analysis and approaches to detecting multiple functional loci.” Bmc Proc 1 Suppl 1, no. Suppl 1 (2007): S1. https://doi.org/10.1186/1753-6561-1-s1-s1.Full Text Link to Item
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Dubé, Marie-Pierre, Silke Schmidt, Elizabeth Hauser, Hatef Darabi, Jing Li, Amina Barhdadi, Xuexia Wang, et al. “Multistage designs in the genomic era: providing balance in complex disease studies.” Genet Epidemiol 31 Suppl 1, no. Suppl 1 (2007): S118–23. https://doi.org/10.1002/gepi.20288.Full Text Link to Item
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Lou, Xuemei, Silke Schmidt, and Elizabeth R. Hauser. “Comparison of GIST and LAMP on the GAW15 simulated data.” Bmc Proc 1 Suppl 1, no. Suppl 1 (2007): S41. https://doi.org/10.1186/1753-6561-1-s1-s41.Full Text Link to Item
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Qin, Xuejun, Silke Schmidt, Eden Martin, and Elizabeth R. Hauser. “Visualizing genotype x phenotype relationships in the GAW15 simulated data.” Bmc Proc 1 Suppl 1, no. Suppl 1 (2007): S132. https://doi.org/10.1186/1753-6561-1-s1-s132.Full Text Link to Item
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Schmidt, Mike, Xuejun Qin, Eden R. Martin, Elizabeth R. Hauser, and Silke Schmidt. “Two-stage study designs for analyzing disease-associated covariates: linkage thresholds and case-selection strategies.” Bmc Proc 1 Suppl 1, no. Suppl 1 (2007): S138. https://doi.org/10.1186/1753-6561-1-s1-s138.Full Text Link to Item
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Murtha, Amy P., Angel Nieves, Elizabeth R. Hauser, Geeta K. Swamy, Bryan A. Yonish, Tammy R. Sinclair, and R Phillips Heine. “Association of maternal IL-1 receptor antagonist intron 2 gene polymorphism and preterm birth.” Am J Obstet Gynecol 195, no. 5 (November 2006): 1249–53. https://doi.org/10.1016/j.ajog.2006.09.002.Full Text Link to Item
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Shah, S. H., W. E. Kraus, D. C. Crossman, C. B. Granger, J. L. Haines, C. J. H. Jones, V. Mooser, et al. “Serum lipids in the GENECARD study of coronary artery disease identify quantitative trait loci and phenotypic subsets on chromosomes 3q and 5q.” Ann Hum Genet 70, no. Pt 6 (November 2006): 738–48. https://doi.org/10.1111/j.1469-1809.2006.00288.x.Full Text Link to Item
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Connelly, J. J., T. Wang, J. E. Cox, C. Haynes, L. Wang, S. H. Shah, D. R. Crosslin, et al. “GATA2 is associated with familial early-onset coronary artery disease.” Plos Genetics 2, no. 8 (August 25, 2006). https://doi.org/10.1371/journal.pgen.0020139.Full Text
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Connelly, Jessica J., Tianyuan Wang, Julie E. Cox, Carol Haynes, Liyong Wang, Svati H. Shah, David R. Crosslin, et al. “GATA2 is associated with familial early-onset coronary artery disease.” Plos Genet 2, no. 8 (August 25, 2006): e139. https://doi.org/10.1371/journal.pgen.0020139.Full Text Link to Item
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Schmidt, Silke, Michael A. Schmidt, Xuejun Qin, Eden R. Martin, and Elizabeth R. Hauser. “Linkage analysis with gene-environment interaction: model illustration and performance of ordered subset analysis.” Genet Epidemiol 30, no. 5 (July 2006): 409–22. https://doi.org/10.1002/gepi.20152.Full Text Link to Item
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Chung, Ren-Hua, Elizabeth R. Hauser, and Eden R. Martin. “The APL test: extension to general nuclear families and haplotypes and examination of its robustness.” Hum Hered 61, no. 4 (2006): 189–99. https://doi.org/10.1159/000094774.Full Text Link to Item
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Shah, Svati H., Michael A. Schmidt, Hao Mei, William K. Scott, Elizabeth R. Hauser, and Silke Schmidt. “Searching for epistatic interactions in nuclear families using conditional linkage analysis.” Bmc Genet 6 Suppl 1, no. Suppl 1 (December 30, 2005): S148. https://doi.org/10.1186/1471-2156-6-S1-S148.Full Text Link to Item
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Rampersaud, E., W. K. Scott, E. R. Hauser, and M. C. Speer. “Potential for expanded power in linkage studies using the ALLEGRO and MERLIN software programs.” J Med Genet 42, no. 12 (December 2005): e68. https://doi.org/10.1136/jmg.2005.032029.Full Text Link to Item
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Xu, Hong, Simon G. Gregory, Elizabeth R. Hauser, Judith E. Stenger, Margaret A. Pericak-Vance, Jeffery M. Vance, Stephan Züchner, and Michael A. Hauser. “SNPselector: a web tool for selecting SNPs for genetic association studies.” Bioinformatics 21, no. 22 (November 15, 2005): 4181–86. https://doi.org/10.1093/bioinformatics/bti682.Full Text Link to Item
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Hauser, E. R., J. Haines, and D. E. Goldgar. “Nonparametric Linkage Analysis,” October 7, 2005, 283–328. https://doi.org/10.1002/9780471781141.ch11.Full Text
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Allingham, R Rand, Janey L. Wiggs, Elizabeth R. Hauser, Karen R. Larocque-Abramson, Cecilia Santiago-Turla, Bob Broomer, Elizabeth A. Del Bono, et al. “Early adult-onset POAG linked to 15q11-13 using ordered subset analysis.” Invest Ophthalmol Vis Sci 46, no. 6 (June 2005): 2002–5. https://doi.org/10.1167/iovs.04-1477.Full Text Link to Item
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Stenger, Judith E., Hong Xu, Carol Haynes, Elizabeth R. Hauser, Margaret Pericak-Vance, Pascal J. Goldschmidt-Clermont, and Jeffery M. Vance. “Statistical Viewer: a tool to upload and integrate linkage and association data as plots displayed within the Ensembl genome browser.” Bmc Bioinformatics 6 (April 12, 2005): 95. https://doi.org/10.1186/1471-2105-6-95.Full Text Link to Item
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Stafford-Smith, Mark, Mihai Podgoreanu, Madhav Swaminathan, Barbara Phillips-Bute, Joseph P. Mathew, Elizabeth H. Hauser, Michelle P. Winn, et al. “Association of genetic polymorphisms with risk of renal injury after coronary bypass graft surgery.” Am J Kidney Dis 45, no. 3 (March 2005): 519–30. https://doi.org/10.1053/j.ajkd.2004.11.021.Full Text Link to Item
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Boyles, Abee L., William K. Scott, Eden R. Martin, Silke Schmidt, Yi-Ju Li, Allison Ashley-Koch, Meredyth P. Bass, et al. “Linkage disequilibrium inflates type I error rates in multipoint linkage analysis when parental genotypes are missing.” Hum Hered 59, no. 4 (2005): 220–27. https://doi.org/10.1159/000087122.Full Text Link to Item
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Schmidt, Mike, Elizabeth R. Hauser, Eden R. Martin, and Silke Schmidt. “Extension of the SIMLA package for generating pedigrees with complex inheritance patterns: environmental covariates, gene-gene and gene-environment interaction.” Stat Appl Genet Mol Biol 4 (2005): Article15. https://doi.org/10.2202/1544-6115.1133.Full Text Link to Item
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Schmidt, M., E. R. Martin, E. R. Hauser, and S. Schmidt. “Extension of the SIMLA package for generating pedigrees with complex inheritance patterns: Environmental covariates, gene-gene and gene-environment interaction.” Statistical Applications in Genetics and Molecular Biology 4, no. 1 (2005): i–19.
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Hauser, Elizabeth R., David C. Crossman, Christopher B. Granger, Jonathan L. Haines, Christopher J. H. Jones, Vincent Mooser, Brendan McAdam, et al. “A genomewide scan for early-onset coronary artery disease in 438 families: the GENECARD Study.” Am J Hum Genet 75, no. 3 (September 2004): 436–47. https://doi.org/10.1086/423900.Full Text Link to Item
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Schmidt, S., W. K. Scott, E. A. Postel, A. Agarwal, E. R. Hauser, M. A. De La Paz, J. R. Gilbert, et al. “Ordered subset linkage analysis supports a susceptibility locus for age-related macular degeneration on chromosome 16p12.” Bmc Genetics 5 (July 6, 2004).
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Schmidt, Silke, William K. Scott, Eric A. Postel, Anita Agarwal, Elizabeth R. Hauser, Monica A. De La Paz, John R. Gilbert, et al. “Ordered subset linkage analysis supports a susceptibility locus for age-related macular degeneration on chromosome 16p12.” Bmc Genet 5 (July 6, 2004): 18. https://doi.org/10.1186/1471-2156-5-18.Full Text Link to Item
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Hauser, Elizabeth R., Richard M. Watanabe, William L. Duren, Meredyth P. Bass, Carl D. Langefeld, and Michael Boehnke. “Ordered subset analysis in genetic linkage mapping of complex traits.” Genet Epidemiol 27, no. 1 (July 2004): 53–63. https://doi.org/10.1002/gepi.20000.Full Text Link to Item
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Silander, Kaisa, Laura J. Scott, Timo T. Valle, Karen L. Mohlke, Heather M. Stringham, Kerry R. Wiles, William L. Duren, et al. “A large set of Finnish affected sibling pair families with type 2 diabetes suggests susceptibility loci on chromosomes 6, 11, and 14.” Diabetes 53, no. 3 (March 2004): 821–29. https://doi.org/10.2337/diabetes.53.3.821.Full Text Link to Item
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Bass, M. P., E. R. Martin, and E. R. Hauser. “Pedigree generation for analysis of genetic linkage and association.” Pac Symp Biocomput, 2004, 93–103. https://doi.org/10.1142/9789812704856_0010.Full Text Link to Item
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Rampersaud, Evadnie, Andrew Allen, Yi-Ju Li, Yujun Shao, Meredyth Bass, Carol Haynes, Allison Ashley-Koch, Eden R. Martin, Silke Schmidt, and Elizabeth R. Hauser. “Adjusting for covariates on a slippery slope: linkage analysis of change over time.” Bmc Genet 4 Suppl 1, no. Suppl 1 (December 31, 2003): S50. https://doi.org/10.1186/1471-2156-4-S1-S50.Full Text Link to Item
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Hauser, Elizabeth R., and Andrew S. Allen. “Where the rubber meets the road in pharmacogenetics: assessment of gene-environment interactions.” Am Heart J 146, no. 6 (December 2003): 929–31. https://doi.org/10.1016/S0002-8703(03)00502-7.Full Text Link to Item
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Martin, E. R., M. P. Bass, J. R. Gilbert, M. A. Pericak-Vance, and E. R. Hauser. “Genotype-based association test for general pedigrees: the genotype-PDT.” Genet Epidemiol 25, no. 3 (November 2003): 203–13. https://doi.org/10.1002/gepi.10258.Full Text Link to Item
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Martin, Eden R., Meredyth P. Bass, Elizabeth R. Hauser, and Norman L. Kaplan. “Accounting for linkage in family-based tests of association with missing parental genotypes.” Am J Hum Genet 73, no. 5 (November 2003): 1016–26. https://doi.org/10.1086/378779.Full Text Link to Item
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Scott, William K., Elizabeth R. Hauser, Donald E. Schmechel, Kathleen A. Welsh-Bohmer, Gary W. Small, Allen D. Roses, Ann M. Saunders, et al. “Ordered-subsets linkage analysis detects novel Alzheimer disease loci on chromosomes 2q34 and 15q22.” Am J Hum Genet 73, no. 5 (November 2003): 1041–51. https://doi.org/10.1086/379083.Full Text Link to Item
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Markert, M Louise, Marcella Sarzotti, Daniel A. Ozaki, Gregory D. Sempowski, Maria E. Rhein, Laura P. Hale, Francoise Le Deist, et al. “Thymus transplantation in complete DiGeorge syndrome: immunologic and safety evaluations in 12 patients.” Blood 102, no. 3 (August 1, 2003): 1121–30. https://doi.org/10.1182/blood-2002-08-2545.Full Text Link to Item
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Hauser, Elizabeth R., Vincent Mooser, David C. Crossman, Jonathan L. Haines, Christopher H. Jones, Bernhard R. Winkelmann, Silke Schmidt, et al. “Design of the Genetics of Early Onset Cardiovascular Disease (GENECARD) study.” Am Heart J 145, no. 4 (April 2003): 602–13. https://doi.org/10.1067/mhj.2003.13.Full Text Link to Item
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Hauser, Michael A., Yi-Ju Li, Satoshi Takeuchi, Robert Walters, Maher Noureddine, Melinda Maready, Tiffany Darden, et al. “Genomic convergence: identifying candidate genes for Parkinson's disease by combining serial analysis of gene expression and genetic linkage.” Hum Mol Genet 12, no. 6 (March 15, 2003): 671–77.Link to Item
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Shao, Yujun, M. L. Cuccaro, E. R. Hauser, K. L. Raiford, M. M. Menold, C. M. Wolpert, S. A. Ravan, et al. “Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes.” Am J Hum Genet 72, no. 3 (March 2003): 539–48. https://doi.org/10.1086/367846.Full Text Link to Item
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Hauser, Elizabeth R., Fang-Chi Hsu, Denise Daley, Jane M. Olson, Evadnie Rampersaud, Jing-Ping Lin, Andrew D. Paterson, et al. “Effects of covariates: a summary of Group 5 contributions.” Genet Epidemiol 25 Suppl 1 (2003): S43–49. https://doi.org/10.1002/gepi.10283.Full Text Link to Item
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Kraus, William E., and Elizabeth R. Hauser. “Angiotensin-converting enzyme gene insertion/deletion polymorphism and cardiovascular disease: identifying the guideposts for navigating the genetics landscape.” Am Heart J 144, no. 5 (November 2002): 747–49. https://doi.org/10.1067/mhj.2002.125510.Full Text Link to Item
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Lebel-Hardenack, Sabine, Elizabeth Hauser, Teresa F. Law, Jurg Schmid, and Sarah R. Grant. “Mapping of sex determination loci on the white campion (Silene latifolia) Y chromosome using amplified fragment length polymorphism.” Genetics 160, no. 2 (February 2002): 717–25. https://doi.org/10.1093/genetics/160.2.717.Full Text Link to Item
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Bass, M. P., E. R. Martin, M. Boehnke, and E. R. Hauser. “Identification of gene locations from maximum likelihood ASP linkage analysis: What lessons can we learn from peak shape?” American Journal of Human Genetics 69, no. 4 (October 1, 2001): 508–508.Link to Item
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Hauser, E. R., M. P. Bass, E. R. Martin, R. M. Watanabe, W. L. Duren, and M. Boehnke. “Power of the ordered subset method for detection and localization of genes in linkage analysis of complex traits.” American Journal of Human Genetics 69, no. 4 (October 1, 2001): 529–529.Link to Item
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Hauser, M. A., M. Maready, S. Takeuchi, H. H. Dai, C. M. Hulette, J. E. Stajich, C. Rosenberg, et al. “Identification of candidate genes for Parkinson's Disease (PD) by profiling gene exoression in the substantia nigra.” American Journal of Human Genetics 69, no. 4 (October 1, 2001): 562–562.Link to Item
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Jones, R. V., B. L. Chesnut, C. P. Blach, C. W. Howe, C. S. Haynes, E. R. Hauser, and M. A. Pericak-Vance. “Clinical applications: An interactive clinical data management system for genetic studies.” American Journal of Human Genetics 69, no. 4 (October 1, 2001): 503–503.Link to Item
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Martin, E. R., M. P. Bass, and E. R. Hauser. “Correlation between linkage and association tests in families.” American Journal of Human Genetics 69, no. 4 (October 1, 2001): 511–511.Link to Item
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Stajich, J. E., E. R. Hauser, and J. M. Vance. “Using genetic, radiation hybrid, and sequence maps comparisons to analyze recombination and gene density.” American Journal of Human Genetics 69, no. 4 (October 1, 2001): 457–457.Link to Item
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Hauser, E. R., and D. E. Weeks. “Pedigree selection and information content.” Curr Protoc Hum Genet Chapter 1 (August 2001): Unit-1.2. https://doi.org/10.1002/0471142905.hg0102s29.Full Text Link to Item
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Schmidt, S., Y. Shao, E. R. Hauser, S. H. Slifer, E. R. Martin, W. K. Scott, M. C. Speer, and M. A. Pericak-Vance. “Life after the screen: making sense of many P-values.” Genet Epidemiol 21 Suppl 1 (2001): S546–51. https://doi.org/10.1002/gepi.2001.21.s1.s546.Full Text Link to Item
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Ghosh, S., R. M. Watanabe, T. T. Valle, E. R. Hauser, V. L. Magnuson, C. D. Langefeld, D. S. Ally, et al. “The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. I. An autosomal genome scan for genes that predispose to type 2 diabetes.” Am J Hum Genet 67, no. 5 (November 2000): 1174–85.Link to Item
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Watanabe, R. M., S. Ghosh, C. D. Langefeld, T. T. Valle, E. R. Hauser, V. L. Magnuson, K. L. Mohlke, et al. “The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. II. An autosomal genome scan for diabetes-related quantitative-trait loci.” Am J Hum Genet 67, no. 5 (November 2000): 1186–1200.Link to Item
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Hauser, E. R., V. Mooser, S. Schmidt, D. C. Crossman, J. L. Haines, C. Jones, B. Winkelmann, et al. “Concordance for cardiovascular risk factors in affected sib pairs (ASPs) with early-onset coronary artery disease (CAD).” American Journal of Human Genetics 67, no. 4 (October 1, 2000): 212–212.Link to Item
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Hauser, E. R., and M. A. Pericak-Vance. “Genetic analysis for common complex disease.” Am Heart J 140, no. 4 (October 2000): S36–44. https://doi.org/10.1067/mhj.2000.108946.Full Text Link to Item
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Bass, M. P., M. M. Menold, C. M. Wolpert, S. L. Donnelly, S. A. Ravan, E. R. Hauser, L. O. Maddox, et al. “Genetic studies in autistic disorder and chromosome 15.” Neurogenetics 2, no. 4 (March 2000): 219–26. https://doi.org/10.1007/s100489900081.Full Text Link to Item
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Jacksch, R., T. M. Schiele, W. Knobloch, R. Niehues, E. R. Hauser, and K. Massalha. “[Carotid stenting with the new slotted tube stent--prospective multicenter study. Essen experiences]].” Z Kardiol 89 Suppl 8 (2000): 40–46.Link to Item
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Hauser, E. R., A. Ashley-Koch, M. A. Pericak-Vance, and M. Boehnke. “Affected sibpair analysis: Exploring the efficiency of fine mapping in the presence of genotyping error.” American Journal of Human Genetics 65, no. 4 (October 1, 1999): A99–A99.Link to Item
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Haynes, C., E. Crew, C. Blach, E. R. Hauser, J. E. Stajich, B. D. Slotterbeck, J. B. Rimmler, et al. “Use of optical scanning capabilities to ensure accurate and efficient data entry in a multicenter genetic study.” American Journal of Human Genetics 65, no. 4 (October 1, 1999): A253–A253.Link to Item
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Rimmler, J. B., C. S. Haynes, J. G. McDowell, J. E. Stajich, C. S. Adams, B. D. Slotterbeck, A. R. Rogala, et al. “DataTracker: Comprehensive software for data quality control protocols in complex disease studies.” American Journal of Human Genetics 65, no. 4 (October 1, 1999): A442–A442.Link to Item
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Bass, M. P., C. M. Wolpert, M. M. Menold, S. L. Donnelly, S. A. Ravan, E. R. Hauser, B. Slotterbeck, et al. “Genomic screen for Autistic Disorder.” Molecular Psychiatry 4 (September 1, 1999): S13–S13.Link to Item
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Watanabe, R. M., T. Valle, E. R. Hauser, S. Ghosh, J. Eriksson, K. Kohtamäki, C. Ehnholm, et al. “Familiality of quantitative metabolic traits in Finnish families with non-insulin-dependent diabetes mellitus. Finland-United States Investigation of NIDDM Genetics (FUSION) Study investigators.” Hum Hered 49, no. 3 (June 1999): 159–68. https://doi.org/10.1159/000022865.Full Text Link to Item
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Ghosh, S., R. M. Watanabe, E. R. Hauser, T. Valle, V. L. Magnuson, M. R. Erdos, C. D. Langefeld, et al. “Type 2 diabetes: evidence for linkage on chromosome 20 in 716 Finnish affected sib pairs.” Proc Natl Acad Sci U S A 96, no. 5 (March 2, 1999): 2198–2203. https://doi.org/10.1073/pnas.96.5.2198.Full Text Link to Item
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Ghosh, S., C. D. Langefeld, D. Ally, R. M. Watanabe, E. R. Hauser, V. L. Magnuson, S. J. Nylund, et al. “The W64R variant of the beta3-adrenergic receptor is not associated with type II diabetes or obesity in a large Finnish sample.” Diabetologia 42, no. 2 (February 1999): 238–44. https://doi.org/10.1007/s001250051144.Full Text Link to Item
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Anderson, J. L., E. R. Hauser, E. R. Martin, W. K. Scott, A. Ashley-Koch, K. J. Kim, S. A. Monks, C. S. Haynes, M. C. Speer, and M. A. Pericak-Vance. “Complete genomic screen for disease susceptibility loci in nuclear families.” Genet Epidemiol 17 Suppl 1 (1999): S473–78. https://doi.org/10.1002/gepi.1370170776.Full Text Link to Item
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Hauser, E. R., and M. Boehnke. “Genetic linkage analysis of complex genetic traits by using affected sibling pairs.” Biometrics 54, no. 4 (December 1998): 1238–46.Link to Item
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Ghosh, S., E. R. Hauser, V. L. Magnuson, T. Valle, D. S. Ally, Z. E. Karanjawala, J. B. Rayman, et al. “A large sample of finnish diabetic sib-pairs reveals no evidence for a non-insulin-dependent diabetes mellitus susceptibility locus at 2qter.” J Clin Invest 102, no. 4 (August 15, 1998): 704–9. https://doi.org/10.1172/JCI2512.Full Text Link to Item
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Valle, T., J. Tuomilehto, R. N. Bergman, S. Ghosh, E. R. Hauser, J. Eriksson, S. J. Nylund, et al. “Mapping genes for NIDDM. Design of the Finland-United States Investigation of NIDDM Genetics (FUSION) Study.” Diabetes Care 21, no. 6 (June 1998): 949–58. https://doi.org/10.2337/diacare.21.6.949.Full Text Link to Item
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Ghosh, S., Z. E. Karanjawala, E. R. Hauser, D. Ally, J. I. Knapp, J. B. Rayman, A. Musick, et al. “Methods for precise sizing, automated binning of alleles, and reduction of error rates in large-scale genotyping using fluorescently labeled dinucleotide markers. FUSION (Finland-U.S. Investigation of NIDDM Genetics) Study Group.” Genome Res 7, no. 2 (February 1997): 165–78. https://doi.org/10.1101/gr.7.2.165.Full Text Link to Item
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Richards, J. E., P. R. Lichter, S. Herman, E. R. Hauser, Y. C. Hou, A. T. Johnson, and M. Boehnke. “Probable exclusion of GLC1A as a candidate glaucoma gene in a family with middle-age-onset primary open-angle glaucoma.” Ophthalmology 103, no. 7 (July 1996): 1035–40. https://doi.org/10.1016/s0161-6420(96)30570-8.Full Text Link to Item
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Richards, J. E., P. R. Lichter, S. Herman, E. Hauser, Y. C. Hou, A. T. Johnson, and M. Boehnke. “Genetics of middle-age onset primary open angle glaucoma.” Investigative Ophthalmology and Visual Science 37, no. 3 (February 15, 1996).
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Hauser, E. R., M. Boehnke, S. W. Guo, and N. Risch. “Affected-sib-pair interval mapping and exclusion for complex genetic traits: sampling considerations.” Genet Epidemiol 13, no. 2 (1996): 117–37. https://doi.org/10.1002/(SICI)1098-2272(1996)13:2<117::AID-GEPI1>3.0.CO;2-5.Full Text Link to Item
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Couch, F. J., J. Garber, S. Kiousis, K. Calzone, E. R. Hauser, S. D. Merajver, T. S. Frank, M. Boehnke, J. S. Chamberlain, and F. S. Collins. “Genetic analysis of eight breast-ovarian cancer families with suspected BRCA1 mutations.” J Natl Cancer Inst Monogr, no. 17 (1995): 9–14.Link to Item
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Richard, C. W., M. Boehnke, D. J. Berg, J. H. Lichy, T. C. Meeker, E. Hauser, R. M. Myers, and D. R. Cox. “A radiation hybrid map of the distal short arm of human chromosome 11, containing the Beckwith-Wiedemann and associated embryonal tumor disease loci.” Am J Hum Genet 52, no. 5 (May 1993): 915–21.Link to Item
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Chamberlain, J. S., M. Boehnke, T. S. Frank, S. Kiousis, J. Xu, S. W. Guo, E. R. Hauser, R. A. Norum, E. A. Helmbold, and D. S. Markel. “BRCA1 maps proximal to D17S579 on chromosome 17q21 by genetic analysis.” Am J Hum Genet 52, no. 4 (April 1993): 792–98.Link to Item
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Smith, C. C., E. Hauser, N. K. Renaud, A. Leff, S. Aksentijevich, G. P. Chrousos, R. L. Wilder, P. W. Gold, and E. M. Sternberg. “Increased hypothalamic [3H]flunitrazepam binding in hypothalamic-pituitary-adrenal axis hyporesponsive Lewis rats.” Brain Res 569, no. 2 (January 13, 1992): 295–99. https://doi.org/10.1016/0006-8993(92)90642-m.Full Text Link to Item
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Maestri, N. E., E. R. Hauser, D. Bartholomew, and S. W. Brusilow. “Prospective treatment of urea cycle disorders.” J Pediatr 119, no. 6 (December 1991): 923–28. https://doi.org/10.1016/s0022-3476(05)83044-6.Full Text Link to Item
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Hinshelwood, M. M., F. Kamel, D. J. Dierschke, and E. R. Hauser. “Effects of charcoal-extracted follicular fluid on reproductive function in postpartum cows.” Domest Anim Endocrinol 8, no. 1 (January 1991): 37–54. https://doi.org/10.1016/0739-7240(91)90038-l.Full Text Link to Item
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Finkelstein, J. E., E. R. Hauser, C. O. Leonard, and S. W. Brusilow. “Late-onset ornithine transcarbamylase deficiency in male patients.” J Pediatr 117, no. 6 (December 1990): 897–902. https://doi.org/10.1016/s0022-3476(05)80129-5.Full Text Link to Item
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Tuchman, M. “Allopurinol-induced orotidinuria.” N Engl J Med 323, no. 19 (November 8, 1990): 1352–53.Link to Item
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Carroll, D. J., M. J. Jerred, R. R. Grummer, D. K. Combs, R. A. Pierson, and E. R. Hauser. “Effects of fat supplementation and immature alfalfa to concentrate ratio on plasma progesterone, energy balance and reproductive traits of dairy cattle.” J Dairy Sci 73, no. 10 (October 1990): 2855–63. https://doi.org/10.3168/jds.S0022-0302(90)78973-4.Full Text Link to Item
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Arn, P. H., E. R. Hauser, G. H. Thomas, G. Herman, D. Hess, and S. W. Brusilow. “Hyperammonemia in women with a mutation at the ornithine carbamoyltransferase locus. A cause of postpartum coma.” N Engl J Med 322, no. 23 (June 7, 1990): 1652–55. https://doi.org/10.1056/NEJM199006073222307.Full Text Link to Item
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Hauser, E. R., J. E. Finkelstein, D. Valle, and S. W. Brusilow. “Allopurinol-induced orotidinuria. A test for mutations at the ornithine carbamoyltransferase locus in women.” N Engl J Med 322, no. 23 (June 7, 1990): 1641–45. https://doi.org/10.1056/NEJM199006073222305.Full Text Link to Item
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Hauser, E. R., J. E. Finkelstein, D. Valle, and S. W. Brusilow. “Allopurinol-induced orotidinuria (Reply).” New England Journal of Medicine 323, no. 19 (January 1, 1990): 1353.
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Brusilow, S. W., and E. Hauser. “Simple method of measurement of orotic acid and orotidine in urine.” J Chromatogr 493, no. 2 (September 1, 1989): 388–91. https://doi.org/10.1016/s0378-4347(00)82746-2.Full Text Link to Item
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Other Articles
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Kertai, Miklos D., Yen-Wei Li, Yi-Ju Li, Svati H. Shah, William E. Kraus, Manuel L. Fontes, Mark Stafford-Smith, et al. “G protein-coupled receptor kinase 5 gene polymorphisms are associated with postoperative atrial fibrillation after coronary artery bypass grafting in patients receiving β-blockers.” Circ Cardiovasc Genet, October 2014. https://doi.org/10.1161/CIRCGENETICS.113.000451.Full Text Link to Item
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Scholarly Editions
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Zeng, Yi, Huashuai Chen, Xiaomin Liu, Rui Ye, Enjun Xie, Zhihua Chen, Jiehua Lu, et al. “Sex differences in genetic associations with longevity in Han Chinese: sex-stratified genome-wide association study and polygenic risk score analysis,” n.d.
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Conference Papers
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Huang, Hsin-I, Mark L. Jewell, Nourhan Youssef, Min-Nung Huang, Elizabeth R. Hauser, Brian E. Fee, Nathan P. Rudemiller, et al. “Th17 Immunity in the Colon Is Controlled by Two Novel Subsets of Colon-Specific Mononuclear Phagocytes.” In Front Immunol, 12:661290, 2021. https://doi.org/10.3389/fimmu.2021.661290.Full Text Link to Item
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Jiang, Rong, Elizabeth R. Hauser, Lydia C. Kwee, Svati H. Shah, William E. Kraus, and Cavin K. Ward-Caviness. “The Association of Accelerated Epigenetic Age with Time-to-death Mediated by Subclinical and Clinical Vascular Outcomes.” In Genetic Epidemiology, 45:763–64, 2021.Link to Item
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Kobe, Elizabeth A., Brian Sullivan, Xuejun Qin, Thomas S. Redding, Elizabeth R. Hauser, Ashton Madison, Cameron Miller, et al. “PRIOR COMPLICATIONS DURING LONGITUDINAL COLORECTAL CANCER SCREENING AND SURVEILLANCE ARE ASSOCIATED WITH INCREASED COMPLICATION RISK AT FOLLOW-UP COLONOSCOPY.” In Gastroenterology, 160:S31–32, 2021.Link to Item
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Sullivan, Brian A., Xuejun Qin, Thomas S. Redding, Ziad F. Gellad, Anjanette Stone, David Weiss, Ashton N. Madison, et al. “Genetic Colorectal Cancer and Adenoma Risk Variants Are Associated with Increasing Cumulative Adenoma Counts.” In Cancer Epidemiol Biomarkers Prev, 29:2269–76, 2020. https://doi.org/10.1158/1055-9965.EPI-20-0465.Full Text Link to Item
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Jiang, Rong, Kim M. Huffman, Elizabeth R. Hauser, Janet L. Huebner, Monica J. Hubal, Redford B. Williams, Ilene C. Siegler, and William E. Kraus. “The role of brain-derived neurotropic factor (BDNF) genetic variants in exercise training.” In Genetic Epidemiology, 44:491–92, 2020.Link to Item
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Miller, Cameron, Xuejun Qin, Brian Sullivan, Elizabeth R. Hauser, Thomas S. Redding, Ziad F. Gellad, David Weiss, et al. “THE ASSOCIATION OF MODIFIABLE RISK FACTORS WITH A DIAGNOSIS OF ADVANCED NEOPLASIA AMONG AN ASYMPTOMATIC VETERAN POPULATION.” In Gastroenterology, 158:S757–S757, 2020.Link to Item
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Sullivan, Brian, Xuejun Qin, Cameron Miller, Elizabeth R. Hauser, Thomas S. Redding, David Weiss, Ashton Madison, et al. “SCREENING AND SURVEILLANCE COLONOSCOPY FINDINGS ARE ASSOCIATED WITH ALL-CAUSE MORTALITY.” In Gastroenterology, 158:S219–S219, 2020.Link to Item
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Hong, Julian C., Elizabeth R. Hauser, Thomas S. Redding, Kellie J. Sims, Ziad F. Gellad, Meghan O’Leary, Ashton Madison, et al. “Characterization of temporal relationships of comorbidities developed following cancer diagnoses in veterans.” In Journal of Clinical Oncology, 37:e18049–e18049. American Society of Clinical Oncology (ASCO), 2019. https://doi.org/10.1200/jco.2019.37.15_suppl.e18049.Full Text
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Musselwhite, Laura W., Thomas S. Redding, Elizabeth R. Hauser, David A. Lieberman, and Dawn T. Provenzale. “Validation of the NCI Colorectal Cancer Risk Assessment Tool for baseline advanced neoplasia in a veterans cohort.” In Journal of Clinical Oncology, 37:521–521. American Society of Clinical Oncology (ASCO), 2019. https://doi.org/10.1200/jco.2019.37.4_suppl.521.Full Text
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Jiang, Rong, Kim M. Huffman, Elizabeth R. Hauser, Monica J. Hubal, Cris A. Slentz, Johanna L. Johnson, Michael Babyak, Redford B. Williams, Ilene C. Siegler, and William E. Kraus. “Genome-wide Analysis of Non-completion of Controlled Exercise Trials in Sedentary Adults.” In Genetic Epidemiology, 43:885–86, 2019.Link to Item
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Jiang, Rong, Lydia Kwee, Svati H. Shah, Abanish Singh, Michael A. Babyak, Beverly H. Brummett, Ilene C. Siegler, Redford B. Williams, and Elizabeth R. Hauser. “Understanding of DNA methylation in the biological basis of stress related cardiovascular disease.” In Genetic Epidemiology, 42:708–708. WILEY, 2018.Link to Item
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Singh, Abanish, Michael A. Babyak, Beverly H. Brummett, William E. Kraus, Ilene C. Siegler, Elizabeth R. Hauser, and Redford B. Williams. “Harmonizing psychosocial stress and CVD-risk variables for developing robust estimates of GxE analyses.” In Genetic Epidemiology, 42:731–731. WILEY, 2018.Link to Item
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Qin, Xuejun, Elizabeth R. Hauser, Annjanette Stone, Weleetka C. Carter, Kellie Sims, R. L. Whitley, Ashton Madison, et al. “GENETIC ASSOCIATION ANALYSIS OF ADVANCED NEOPLASIA IN A COLON CANCER SCREENING COHORT.” In Gastroenterology, 154:S277–S277. W B SAUNDERS CO-ELSEVIER INC, 2018.Link to Item
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Sullivan, Brian, Thomas S. Redding, Elizabeth R. Hauser, Ziad F. Gellad, Xuejun Qin, Samir Gupta, Douglas J. Robertson, et al. “HIGH RISK ADENOMAS AT BASELINE COLONOSCOPY ASSOCIATED WITH FUTURE ADVANCED ADENOMA DESPITE AN INTERVENING NEGATIVE COLONOSCOPY.” In Gastroenterology, 154:S29–S29. W B SAUNDERS CO-ELSEVIER INC, 2018.Link to Item
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Jiang, Rong, Michael A. Babyak, Beverly H. Brummett, Elizabeth R. Hauser, Abanish Singh, Ilene C. Siegler, and Redford B. Williams. “The effect of Brain- Derived Neurotrophic Factor (BDNF) Val66Met Variants on the Path from Psychosocial Stress to Depression, Body Mass Index and Pre-Clinical Atherosclerosis.” In Genetic Epidemiology, 41:665–66. WILEY, 2017.Link to Item
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Jiang, Rong, Michael A. Babyak, Beverly H. Brummett, Elizabeth R. Hauser, Brett C. Haberstick, Andrew Smolen, Ilene C. Siegler, Kathleen Mullan Harris, and Redford B. Williams. “Gender Differences in Brain-Derived Neurotrophic Factor (BDNF) Val66Met Variants and Stressful Life Events on Psychological and Metabolic Phenotypes.” In Genetic Epidemiology, 41:665–665. WILEY, 2017.Link to Item
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Musselwhite, Laura W., Thomas S. Redding, Kellie J. Sims, Meghan O’Leary, Elizabeth R. Hauser, Terry Hyslop, David A. Lieberman, and Dawn T. Provenzale. “Validation of the NCI colorectal cancer risk assessment tool in the CSP 380 veterans cohort.” In Journal of Clinical Oncology, 35:e15135–e15135. American Society of Clinical Oncology (ASCO), 2017. https://doi.org/10.1200/jco.2017.35.15_suppl.e15135.Full Text
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Sullivan, Brian, Meghan C. O’Leary, Xuejun Qin, Kellie Sims, Jasmine Bullard, Elizabeth R. Hauser, Rebecca B. McNeil, et al. “Colorectal Cancer Risk Factors in Veterans with and Without Adenoma Multiplicity in a Screening Cohort.” In Gastroenterology, 152:S543–44. Elsevier BV, 2017. https://doi.org/10.1016/s0016-5085(17)31977-7.Full Text
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Jiang, Rong, Michael A. Babyak, Beverly H. Brummett, Elizabeth R. Hauser, Abanish Singh, Ilene C. Siegler, Svati H. Shah, Carol Haynes, Megan Chryst-Ladd, and Redford B. Williams. “Brain-Derived Neurotrophic Factor Val66Met Variants (RS6265) are Associated with Coronary Heart Disease (CHD) Outcomes in a Patient Sample.” In Genetic Epidemiology, 40:643–643. WILEY-BLACKWELL, 2016.Link to Item
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Singh, Abanish, Elizabeth R. Hauser, Johanna L. Johnson, Michael A. Babyak, Beverly H. Brummett, Rong Jiang, Cris A. Slentz, et al. “Follow-up of GxE Interactions: EBF1 GxE Association, Synthetic Chronic Psychosocial Stress, and Dropout from a Structured Exercise Program.” In Genetic Epidemiology, 40:662–63. WILEY-BLACKWELL, 2016.Link to Item
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Lieberman, David, David H. Abbott, Meghan C. O’Leary, Elizabeth R. Hauser, Christina Williams, Rebecca B. McNeil, Brian Sullivan, et al. “858 Clinical Risk Group at Baseline Is Associated With 10 Year Outcomes in a Screening Cohort-Longitudinal Analysis of the CSP 380 Cohort.” In Gastroenterology, 150:S184–S184. Elsevier BV, 2016. https://doi.org/10.1016/s0016-5085(16)30701-6.Full Text
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Sullivan, Brian, David H. Abbott, Meghan C. O’Leary, Elizabeth R. Hauser, Christina Williams, Rebecca B. McNeil, Laura Musselwhite, et al. “Mo1724 Risk Factors Associated With the Development of Adenoma Multiplicity in a Screening Cohort.” In Gastroenterology, 150:S763–S763. Elsevier BV, 2016. https://doi.org/10.1016/s0016-5085(16)32587-2.Full Text
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Musselwhite, Laura W., Catherine M. Thomas, David H. Abbott, Elizabeth R. Hauser, Laura K. Wagner, Sara F. Morris, David G. Weiss, David A. Lieberman, and Dawn T. Provenzale. “Risk factors for interval advanced colorectal neoplasia after screening colonoscopy.” In Journal of Clinical Oncology, 33:3539–3539. American Society of Clinical Oncology (ASCO), 2015. https://doi.org/10.1200/jco.2015.33.15_suppl.3539.Full Text
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Williams, R. B., A. Georgiades, B. H. Brummett, M. A. Babyak, R. Jiang, S. H. Shah, R. C. Becker, et al. “DRD2 SNP RS4586205, CHD METABOLIC RISK FACTORS IN NORMALS AND CLINICAL COURSE IN CHD PATIENTS.” In International Journal of Behavioral Medicine, 21:S52–S52. SPRINGER, 2014.Link to Item
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Shah, Svati H., Lydia Kwee, Nathan Stitziel, Elizabeth R. Hauser, Carol Haynes, Sekar Kathiresan, Simon G. Gregory, and William E. Kraus. “Rare Variants Identified With Whole Exome Chip Genotyping Are Associated With Insulin Resistance and Glycemic Control.” In Circulation, Vol. 128. LIPPINCOTT WILLIAMS & WILKINS, 2013.Link to Item
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Chan, K., R. S. Patel, P. Newcombe, C. P. Nelson, A. Qasim, S. E. Epstein, S. Burnett, et al. “126 CHROMOSOME 9P21 LOCUS AND ANGIOGRAPHIC CORONARY ARTERY DISEASE BURDEN: A COLLABORATIVE META-ANALYSIS.” In Heart, 99:A75.1-A75. BMJ, 2013. https://doi.org/10.1136/heartjnl-2013-304019.126.Full Text
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Kraus, William E., Sheng Feng, Elizabeth R. Hauser, Simon G. Gregory, Carol Haynes, Z. E. Dowdy, Damian M. Craig, and Svati H. Shah. “Association of Gene Expression Signatures with Small Molecule Metabolic Intermediates that Predict Cardiovascular Mortality in CATHGEN.” In Circulation, Vol. 127. LIPPINCOTT WILLIAMS & WILKINS, 2013.Link to Item
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Ward-Caviness, Cavin, Lucas Neas, Carol Haynes, Colette Blachi, Wayne Cascio, Robert Devlin, David Diaz-Sanchez, et al. “Mobile Source Air Pollution is Associated with the Plasma Concentration of Multiple Acylcarnitines in a Large Cardiovascular Cohort.” In Circulation, Vol. 127. LIPPINCOTT WILLIAMS & WILKINS, 2013.Link to Item
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McGarrah, Robert, Svati Shah, Elizabeth Hauser, Carol Haynes, Deborah Winegar, Ray Pourfarzib, and William Kraus. “NMR-BASED LIPOPROTEIN PARTICLE PROFILING IDENTIFIES NOVEL SIGNATURES FOR CARDIOVASCULAR DISEASE.” In Journal of the American College of Cardiology, 61:E1213–E1213. Elsevier BV, 2013. https://doi.org/10.1016/s0735-1097(13)61213-9.Full Text
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Halim, Sharif A., Megan Neely, Karen Pieper, Svati Shah, William Kraus, Elizabeth Hauser, Robert Califf, Christopher Granger, and L Kristin Newby. “SIMULTANEOUS ANALYSIS OF MULTIPLE PROTEIN BIOMARKERS IDENTIFIES INDEPENDENT MARKERS OF LONG-TERM RISK FOR DEATH OR MYOCARDIAL INFARCTION.” In Journal of the American College of Cardiology, 59:E1476–E1476. Elsevier BV, 2012. https://doi.org/10.1016/s0735-1097(12)61477-6.Full Text
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Shah, Asad A., Damian M. Craig, Carol Haynes, Jacqueline K. Sebek, Elizabeth Grass, Karen Abramson, Peter K. Smith, et al. “Genome-Wide Association Identifies Genetic Variants Associated With Vein Graft Stenosis After Coronary Artery Bypass Grafting.” In Circulation, Vol. 124. LIPPINCOTT WILLIAMS & WILKINS, 2011.Link to Item
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Newby, L. K., Svati H. Shah, Jie-Lena Sun, Karen Pieper, Elizabeth R. Hauser, William E. Kraus, and Christopher B. Granger. “Red Cell Distribution Width (RDW) is a Strong Predictor of Outcome and is Weakly Associated With Clinical Variables in Patients at Risk for Cardiovascular Events.” In Circulation, 120:S1174–S1174. LIPPINCOTT WILLIAMS & WILKINS, 2009.Link to Item
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Shah, Svati H., Jie-Lena Sun, Karen Pieper, David R. Crosslin, Carol Haynes, James R. Bain, Michael Muehlbauer, et al. “Plasma Metabolomic Profiles Predict Future Cardiovascular Events.” In Circulation, 120:S466–67. LIPPINCOTT WILLIAMS & WILKINS, 2009.Link to Item
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Shah, Svati H., James Bain, Michael J. Muehlbauer, Robert D. Stevens, Brett R. Wenner, Lauren C. Naliboff, Carol Haynes, et al. “Peripheral blood metabolic signatures are markers of coronary artery disease and myocardial infarction.” In Circulation, Vol. 117. LIPPINCOTT WILLIAMS & WILKINS, 2008.Link to Item
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Wang, Liyong, Elizabeth R. Hauser, David Crosslin, Sarah Nelson, A. B. Hale, Simon G. Gregory, Svati H. Shah, William E. Kraus, Pascal J. Goldschmidt-Clermont, and Jeffery M. Vance. “Genomic convergence identified CAPG and VAMP8 as candidate genes for CAD.” In Circulation, 116:807–807. LIPPINCOTT WILLIAMS & WILKINS, 2007.Link to Item
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Wang, Liyong, Elizabeth R. Hauser, David Crosslin, Sarah Nelson, A. B. Hale, Simon Gregory, Svati H. Shah, William E. Kraus, Pascal J. Goldschmidt-Clermont, and Jeffery M. Vance. “A multi-stage evaluation of genetic association with early-onset coronary artery disease in MYLK gene.” In Circulation, 116:806–806. LIPPINCOTT WILLIAMS & WILKINS, 2007.Link to Item
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Schmidt, Silke, Ren-Hua Chung, Xuejun Qin, Xuemei Lou, and Elizabeth R. Hauser. “Integration of SIMIA and SIMLAPLOT: A graphical user interface for complex disease simulation and analysis.” In Genetic Epidemiology, 31:643–643. WILEY-LISS, 2007.Link to Item
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Lou, X., L. Wang, W. E. Kraus, E. R. Hauser, and S. Shah. “Relationship between genotype variants in coronary artery disease (CAD) and HDL level.” In Genetic Epidemiology, 31:486–486. WILEY-LISS, 2007.Link to Item
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Schmidt, Qin S., M. A. Schmidt, E. Martin, and E. R. Hauser. “A visualization tool for genetic parameters in complex human traits.” In Genetic Epidemiology, 31:494–95. WILEY-LISS, 2007.Link to Item
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Frazier, Camille G., Svati Shah, Charlotte L. Nelson, David Seo, Elizabeth R. Hauser, David Crosslin, Simon Gregory, Pascal J. Goldschmidt-Clermont, Christopher B. Granger, and L Kristin Newby. “Variants in genes associated with inflammation and vascular cell function are associated with vulnerable plaque.” In Journal of the American College of Cardiology, 49:199A-199A. ELSEVIER SCIENCE INC, 2007.Link to Item
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Shah, Svati H., Charlotte Nelson, Judith A. Stafford, Christopher B. Granger, William E. Kraus, and Elizabeth R. Hauser. “Clinical predictors of presence of left main coronary artery disease on angiography in a large cohort.” In Journal of the American College of Cardiology, 49:218A-218A. ELSEVIER SCIENCE INC, 2007.Link to Item
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Shah, Svati H., Elizabeth R. Hauser, Charlotte Nelson, Simon Gregory, David Crosslin, Carol Haynes, Jessica Johnson, et al. “ALOX5AP genetic variants are associated with in-stent restenosis after percutaneous coronary intervention.” In Journal of the American College of Cardiology, 49:211A-211A. ELSEVIER SCIENCE INC, 2007.Link to Item
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Shah, Svati H., Christopher B. Newgard, James Bain, Robert Stevens, Brett Wenner, Michael Muehlbauer, Elaine Dowdy, et al. “High heritabilities of serum metabolites and differential metabolomic profiles in families burdened with early onset coronary artery disease.” In Circulation, 114:677–677. LIPPINCOTT WILLIAMS & WILKINS, 2006.Link to Item
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Wang, Liyong, Elizabeth R. Hauser, Svati H. Shah, Carol Haynes, Jason M. Rose, Marco Harris, Julie Rombaut, et al. “Identification of kalirin gene as a novel coronary artery disease gene through peak-wide association mapping on chromosome 3q13-21.” In Circulation, 114:887–887. LIPPINCOTT WILLIAMS & WILKINS, 2006.Link to Item
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Pedersen, B. R., K. Carlson, M. P. Donahue, W. E. Kraus, L. E. Wagoner, G. Dorn, D. A. Marchuk, E. R. Hauser, and H. A. Rockman. “Evidence for collagen type XXIV as a modifier of survival after heart failure.” In Circulation, 112:U472–U472. LIPPINCOTT WILLIAMS & WILKINS, 2005.Link to Item
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Shah, S. H., L. Y. Wang, J. Rose, D. C. Crossman, C. B. Granger, J. L. Haines, C. J. Jones, et al. “Neuropeptide Y gene variants are linked to and associated with premature coronary artery disease in two independent datasets.” In Circulation, 112:U850–U850. LIPPINCOTT WILLIAMS & WILKINS, 2005.Link to Item
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Wang, L. Y., E. R. Hauser, S. H. Shah, W. E. Kraus, D. Seo, L. L. Huang, J. M. Rose, et al. “Identification of a novel locus for left main coronary artery disease.” In Circulation, 112:U413–U413. LIPPINCOTT WILLIAMS & WILKINS, 2005.Link to Item
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Carlson, K. M., B. Pedersen, M. P. Donahue, E. R. Hauser, W. E. Kraus, H. A. Rockman, and D. A. Marchuk. “An association between COL24A1 and ejection fraction in a human heart failure population: Evidence supporting COL24A1 as a modifier gene in human heart failure.” In Circulation, 110:720–720. LIPPINCOTT WILLIAMS & WILKINS, 2004.Link to Item
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Donahue, M. P., M. J. Wofe, J. L. Jennings, B. Pedersen, E. R. Hauser, D. A. Marchuk, and W. E. Kraus. “PPAR17 polymorphism is associated with reduced cardiac function identifying it as a modifier of heart failure.” In Circulation, 110:555–555. LIPPINCOTT WILLIAMS & WILKINS, 2004.Link to Item
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Hauser, E. R., S. Gregory, D. Seo, A. Dobra, E. Iversen, R. Karra, C. Haynes, et al. “Convergence of genome-wide expression analysis and genome-wide linkage analysis identifies candidate genes for atherosclerosis.” In Circulation, 110:823–823. LIPPINCOTT WILLIAMS & WILKINS, 2004.Link to Item
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Pericak-Vance, M. A., S. Schmidt, W. K. Scott, E. R. Hauser, E. A. Postel, A. Agarwal, J. D. M. Gass, C. B. Rickman, J. R. Gilbert, and J. L. Haines. “Ordered subsets linkage analysis and expression profiling of chromosome 16p in age-related macular degeneration.” In Investigative Ophthalmology & Visual Science, 45:U992–U992. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2004.Link to Item
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Carlson, K. M., E. R. Hauser, M. P. Donahue, W. E. Kraus, H. A. Rockman, and D. A. Marchuk. “Identification of COL24A1 as a novel candidate gene for heart failure in mice and humans.” In American Journal of Human Genetics, 73:515–515. UNIV CHICAGO PRESS, 2003.Link to Item
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Hauser, E. R., M. Bass, and E. R. Martin. “Identification of gene locations from maximum likelihood ASP linkage analysis: Are there features of the lod score curve that distinguish regions with two loci?” In American Journal of Human Genetics, 73:615–615. UNIV CHICAGO PRESS, 2003.Link to Item
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Scott, W. K., P. C. Gaskell, C. E. Jackson, J. L. Haines, M. A. Pericak-Vance, and E. R. Hauser. “Combinatorial mismatch scan for Successful Aging Loci in the Amish.” In American Journal of Human Genetics, 73:186–186. UNIV CHICAGO PRESS, 2003.Link to Item
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Carlson, K. M., E. R. Hauser, M. P. Donahue, W. E. Kraus, H. A. Rockman, and D. A. Marchuk. “Collagen XXIV, alpha 1: A novel candidate gene for the modification of heart failure outcome in both mice and humans.” In Circulation, 108:120–120. LIPPINCOTT WILLIAMS & WILKINS, 2003.Link to Item
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Allingham, R. R., E. R. Hauser, J. L. Wiggs, M. A. Hauser, F. L. Graham, K. R. Abramson, E. A. del Bono, J. R. Shi, J. L. Haines, and M. A. Pericak-Vance. “Ordered subset analysis in primary open-angle glaucoma (POAG): Evidence for linkage to chromosomes 14 and 15.” In Investigative Ophthalmology & Visual Science, 44:U133–U133. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2003.Link to Item
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Hauser, E. R., D. C. Crossman, C. Granger, J. L. Haines, C. J. H. Jones, V. Mooser, M. A. Hauser, et al. “Results of a genome-wide scan in 438 families with early-onset coronary artery disease.” In Circulation, 106:745–745. LIPPINCOTT WILLIAMS & WILKINS, 2002.Link to Item
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Shao, Y., M. L. Cuccaro, E. R. Hauser, C. M. Wolpert, S. A. Ravan, R. K. Abramson, H. H. Wright, R. G. DeLong, J. R. Gilbert, and M. A. Pericak-Vance. “Linkage of autistic disorder to chromosome 15q11-q13 using phenotypic subtypes.” In American Journal of Medical Genetics, 114:787–787. WILEY-LISS, 2002.Link to Item
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Allinghaml, R. R., J. L. Wiggs, E. R. Hauser, M. A. Hauser, F. L. Graham, K. R. LaRocque, B. W. Broomer, et al. “Ordered subset analysis in primary open-angle glaucoma (POAG): Evidence for linkage to chromosomes 14 and 15.” In American Journal of Human Genetics, 71:453–453. UNIV CHICAGO PRESS, 2002.Link to Item
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Bass, M. P., E. R. Martin, and E. R. Hauser. “Software for simulation studies of complex traits: SIMLA.” In American Journal of Human Genetics, 71:569–569. UNIV CHICAGO PRESS, 2002.Link to Item
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Hauser, E. R., D. C. Crossman, C. Granger, J. L. Haines, C. J. H. Jones, V. Mooser, L. Middleton, et al. “A genome-wide scan in 433 families with early-onset coronary artery disease.” In American Journal of Human Genetics, 71:459–459. UNIV CHICAGO PRESS, 2002.Link to Item
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Hauser, M. A., J. W. Walter, R. W. Walters, M. Maready, S. Takeuchi, W. P. Segars, C. M. Hulette, et al. “Identification of candidate genes for Parkinson disease (PD)by the convergence of genetic linkage and association data with gene expression in the substantia nigra.” In American Journal of Human Genetics, 71:467–467. UNIV CHICAGO PRESS, 2002.Link to Item
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Martin, E. R., M. P. Bass, and E. R. Hauser. “A genotype-based association test for general pedigrees: The geno-PDT.” In American Journal of Human Genetics, 71:573–573. UNIV CHICAGO PRESS, 2002.Link to Item
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Scott, W. K., K. K. Nicodemus, P. C. Gaskell, D. J. Hedges, S. N. Walters, G. W. Small, P. M. Connealy, et al. “Ordered subsets analysis in Alzheimer disease: Refined linkage to 9p and novel linkage to 2q and 15q.” In American Journal of Human Genetics, 71:460–460. UNIV CHICAGO PRESS, 2002.Link to Item
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Shao, Y., M. E. Cuccaro, E. R. Hauser, K. L. Raiford, C. M. Wolpert, S. L. Donnelly, L. A. Elston, et al. “Linkage of autistic disorder to chromosome 15q11-q13 using phenotypic subtypes.” In American Journal of Human Genetics, 71:455–455. UNIV CHICAGO PRESS, 2002.Link to Item
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Richards, J. E., P. R. Lichter, S. Herman, E. Hauser, Y. C. Hou, A. T. Johnson, and M. Boehnke. “Genetics of middle-age onset primary open angle glaucoma.” In Investigative Ophthalmology & Visual Science, 37:155–155, 1996.Link to Item
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Datasets
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Stanton, Michael V., Charles Jonassaint, Gary Bennett, Elizabeth Hauser, Timothy Strauman, Richard Surwit, and Redford Williams. “Socioeconomic stress by dopamine receptor 2 gene interactions in the development of obesity,” 2013. https://doi.org/10.1037/e546872013-113.Data Access
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