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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.

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.

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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.

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.

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 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.

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.

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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.

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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.

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.

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.

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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.

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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.

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.

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.

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.

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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 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.

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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.

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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.

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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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

Orlando, Lori A., Vincent C. Henrich, Elizabeth R. Hauser, Charles Wilson, Geoffrey S. Ginsburg, and 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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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).

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).

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.

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.

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.

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.

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.

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).

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

Shah, Svati Hasmukh, Jie-Lena Sun, Karen Pieper, Carol Haynes, Michael Muehlbauer, James R. Bain, Elizabeth R. Hauser, et al. “INSULIN-LIKE GROWTH FACTOR BINDING PROTEIN (IGFBP) 2: A NOVEL METABOLIC BIOMARKER STRONGLY PREDICTIVE OF FUTURE CARDIOVASCULAR EVENTS.” In JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, Vol. 55, 2010.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

Hauser, E. R., J. Haines, and D. E. Goldgar. “Nonparametric Linkage Analysis,” October 7, 2005, 283–328. https://doi.org/10.1002/9780471781141.ch11.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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).

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

Hauser, M. A. “Genomic convergence: identifying candidate genes for Parkinson's disease by combining serial analysis of gene expression and genetic linkage.” Human Molecular Genetics 12, no. 6 (March 15, 2003): 671–77. https://doi.org/10.1093/hmg/12.6.671.

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.

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.

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.

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.

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.

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.” American Heart Journal 144, no. 5 (November 2002): 747–49. https://doi.org/10.1016/s0002-8703(02)80003-5.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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).

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.

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.

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.

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.

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.

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.

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.

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.

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.

Tuchman, M. “Allopurinol-induced orotidinuria.” N Engl J Med 323, no. 19 (November 8, 1990): 1352–53.

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.

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.

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.

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.

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.

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.