Michael Arthur Hauser | Scholars@Duke

Michael Arthur Hauser
Professor in Medicine

Dr. Hauser has a strong interest in ocular genetics. Genomic studies at the Center for Human Genetics have identified multiple linkage peaks and susceptibility genes in primary open angle glaucoma (POAG) and age related macular degeneration (AMD). Dr. Hauser has recently accepted a 20% appointment at the Singapore Eye Research INstitute and the Duke/National University of Singapore. In collaboration with multiple collaborators in Singapore, and Dr. Rand Allingham at the Duke Eye Center, Dr. Hauser is currently conducting a genome wide association study for glaucoma in individuals of African ancestry. These investigations include large datasets collected in Ghana, Nigeria, and South Africa.

Dr. Hauser is also involved in collaborative investigations into the genetics of post-tramatic stress disorder in US veterans from Iraq and Afghanistan. Major collaborators include Dr. Allison Ashley Koch, Dr. Jean Beckham, Dr. Christine Marx and the MIRECC Collaborative group at the Durham Veteran's Administration. We have published a genome wide association study, as well as numerous investigations into candidate genes. Epigenomic DNA methylation analysis and gene expression analysis of 3500 individuals is currently ongoing.

Current Appointments & Affiliations

Professor in Medicine, Medicine, Medical Genetics, Medicine 2021
Associate Research Professor in Molecular Genetics and Microbiology, Molecular Genetics and Microbiology, Basic Science Departments 2008
Member of Duke Molecular Physiology Institute, Duke Molecular Physiology Institute, Duke Molecular Physiology Institute 2013

Contact Information

2016 Genome Science Research Bldg I, Durham, NC 27710
Duke Box 104775, Durham, NC 27710
mike.hauser@duke.edu (919) 684-3508

Background
Education, Training, & Certifications
- Ph.D., Johns Hopkins University 1990
Previous Appointments & Affiliations
- Professor in Medicine, Medicine, Medical Genetics, Medicine 2013 - 2020
- Professor in Biostatistics and Bioinformatics, Biostatistics & Bioinformatics, Basic Science Departments 2013 - 2015
- Professor in Ophthalmology, Medicine, Endocrinology, Metabolism, and Nutrition, Medicine 2014 - 2015
- Associate Research Professor of Biostatistics and Bioinformatics, Biostatistics & Bioinformatics, Basic Science Departments 2004 - 2014
- Associate Professor in Ophthalmology, Medicine, Endocrinology, Metabolism, and Nutrition, Medicine 2011 - 2014
- Associate Professor in Medicine, Duke Molecular Physiology Institute, Duke Molecular Physiology Institute 2006 - 2013
- Associate Professor in Ophthalmology, Ophthalmology, Clinical Science Departments 2010 - 2011
- Associate Professor in Ophthalmology, Ophthalmology, Clinical Science Departments 2006 - 2008
- Associate Research Professor in Molecular Genetics and Microbiology, Molecular Genetics and Microbiology, Basic Science Departments 2006 - 2007
- Associate Research Professor in Medicine, Duke Molecular Physiology Institute, Duke Molecular Physiology Institute 2004 - 2006
- Assistant Research Professor in Ophthalmology, Ophthalmology, Clinical Science Departments 2000 - 2006
- Assistant Research Professor in Medicine, Duke Molecular Physiology Institute, Duke Molecular Physiology Institute 1999 - 2004
- Assistant Research Professor in Medicine, Neurology, Clinical Science Departments 1998 - 1999
Recognition
In the News
- JAN 13, 2014
  
  Global Research, Domestic Benefits
Expertise
Global Scholarship
- Research
Research
Selected Grants
- Genetic and Genomics Training Grant awarded by National Institutes of Health 2020 - 2025
- Molecular Mechanisms of Exfoliation Glaucoma awarded by National Institutes of Health 2019 - 2024
- Case Western sub to Duke Hauser awarded by Case Western Reserve University 2022 - 2023
- Longevity and Stress in African American Families awarded by University of Nevada - Las Vegas 2020 - 2023
- Single nuclear RNAseq to characterize glaucoma risk genes awarded by BrightFocus Foundation 2021 - 2023
- Eyes of Africa: The Genetics of Blindness awarded by University of Ibadan 2017 - 2022
- IPA MIRECC - Michelle Dennis awarded by Durham Veterans Affairs Medical Center 2020 - 2022
- Abnormal Extracellular Matrix Homeostasis of Trabecular Meshwork Cells in Pseudoexfoliation Syndrome and Glaucoma awarded by The Glaucoma Foundation 2020 - 2022
- IPA MIRECC - Michael Hauser awarded by Durham Veterans Affairs Medical Center 2019 - 2021
- IPA MVP - Michael Hauser awarded by Durham Veterans Affairs Medical Center 2019 - 2021
- IPA - Michael Hauser awarded by Durham Veterans Affairs Medical Center 2019 - 2021
- MVP IPA - Xue Jun Qin awarded by Durham Veterans Affairs Medical Center 2019 - 2021
- Genetics Training Grant awarded by National Institutes of Health 1979 - 2020
- Longevity and Stress in African American Families awarded by Wayne State University 2016 - 2020
- MVP IPA - Allison Ashley-Koch awarded by Durham Veterans Affairs Medical Center 2019 - 2020
- IPA--Allison Ashley-Koch awarded by Durham Veterans Affairs Medical Center 2018 - 2020
- IPA--Melanie Garrett awarded by Durham Veterans Affairs Medical Center 2018 - 2020
- NEIGHBORHOOD Consortium for POAG Genomics awarded by Harvard University 2015 - 2019
- IPA - Allison Ashley-Koch awarded by Durham Veterans Affairs Medical Center 2016 - 2018
- Functional Analysis of Rare Protective Coding Variants in LOXL 1 awarded by The Glaucoma Foundation 2016 - 2017
- Mexican American Glaucoma Genetic Study (MAGGS) awarded by University of Illinois at Chicago 2015 - 2017
- Gene Discovery in Primary Congenital Glaucoma awarded by National Institutes of Health 2013 - 2017
- Longevity and Stress in African American Families awarded by National Institutes of Health 2016
- PTSD GWAS awarded by Cohen Veterans Bioscience 2016
- Miami Sub for Sample Collection awarded by National Institutes of Health 2015 - 2016
- VA Contract awarded by Durham Veterans Affairs Medical Center 2014 - 2015
- Roles of Regulatory Variants for LOXL1 in Pseudoexfoliation Glaucoma: Year 2 awarded by The Glaucoma Foundation 2010 - 2015
- Biorepository Core Lab for the PTSD-TBI Clinical Consortium awarded by University of California - San Diego 2009 - 2015
- IPA - Allison Ashley-Koch awarded by Durham Veterans Affairs Medical Center 2012 - 2014
- IPA - Melanie Garrett awarded by Durham Veterans Affairs Medical Center 2012 - 2014
- IPA - Yutao Liu awarded by Durham Veterans Affairs Medical Center 2012 - 2014
- Admixture Mapping of Glaucoma Genes in African Americans awarded by National Institutes of Health 2008 - 2013
- IPA - Jason Gibson awarded by Durham Veterans Affairs Medical Center 2011 - 2013
- Whole Genome Genotyping and Association Analysis Services for the VAMC awarded by Durham Veterans Affairs Medical Center 2012 - 2013
- CTSA UL awarded by National Institutes of Health 2006 - 2012
- IPA - MIRECC Jacqueline Rimmler awarded by Veterans Administration Medical Center 2011 - 2012
- Characterizing Alcohol's Effects on Repair of Liver Injury awarded by National Institutes of Health 2009 - 2012
- Candidate Genes for Primary Open Angle Glaucoma awarded by National Institutes of Health 2007 - 2012
- IPA Yutao Liu awarded by Durham Veterans Affairs Medical Center 2011 - 2012
- IPA- Lydia Kwee awarded by Veterans Administration Medical Center 2008 - 2011
- Genetic Epidemiology of ALS in Veterans awarded by Department of Veterans Affairs 2010 - 2011
- IPA Michael Hauser awarded by Veterans Administration Medical Center 2010 - 2011
- Genetic Epidemiology of ALS in Veterans awarded by Department of Veterans Affairs 2009 - 2011
- IPA- Heidi Munger awarded by Veterans Administration Medical Center 2011
- IPA - Jacqueline Rimmler awarded by Veterans Administration Medical Center 2009 - 2011
- IPA- Heidi Munger awarded by Veterans Administration Medical Center 2009 - 2011
- Genomic Convergence in Primary Open Angle Glaucoma awarded by National Institutes of Health 2004 - 2010
- Genetic Epidemiology of ALS in Veterans awarded by National Institutes of Health 2004 - 2010
- IPA - Michael Hauser awarded by Veterans Administration Medical Center 2008 - 2010
- VISN 6 MIRECC RNA Extraction and Purification awarded by Veterans Administration Medical Center 2008 - 2009
- Genetic Studies of POAG in Ghana, West Africa awarded by National Institutes of Health 2003 - 2007
- Patho-Gen Explorarations of Myotilin, the LGMD1A Gene awarded by National Institutes of Health 2004 - 2007
- The Pathophysiology of CMT2A in Cell and Animal Models awarded by National Institutes of Health 2006 - 2007
- Candidate genes for primary open angle glaucoma awarded by National Institutes of Health 2001 - 2007
- Unifying Genetics Epidemiology of Macular Degeneration awarded by National Institutes of Health 2000 - 2007
- Hereditary benign intraepithelial dyskeratosis awarded by National Institutes of Health 1997 - 2006
- Hereditary benign intraepithelial dyskeratosis awarded by National Institutes of Health 2003 - 2005
External Relationships
- ROYALTY;ADVANCED LIQUID LOGIC AGR#1455
Publications & Artistic Works
Selected Publications
- Academic Articles
  - Adebamowo, Clement A., Adebowale Adeyemo, Adeyinka Ashaye, Onoja M. Akpa, Tinashe Chikowore, Ananyo Choudhury, Yasmina J. Fakim, et al. “Polygenic risk scores for CARDINAL study.” Nat Genet 54, no. 5 (May 2022): 527–30. https://doi.org/10.1038/s41588-022-01074-3.
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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.
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  - Maihofer, Adam X., Karmel W. Choi, Jonathan R. I. Coleman, Nikolaos P. Daskalakis, Christy A. Denckla, Elizabeth Ketema, Rajendra A. Morey, et al. “Enhancing Discovery of Genetic Variants for Posttraumatic Stress Disorder Through Integration of Quantitative Phenotypes and Trauma Exposure Information.” Biol Psychiatry 91, no. 7 (April 1, 2022): 626–36. https://doi.org/10.1016/j.biopsych.2021.09.020.
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  - Youngblood, Hannah A., Emily Parker, Jingwen Cai, Kristin Perkumas, Hongfang Yu, Jason Sun, Sylvia B. Smith, et al. “Identification of Estrogen Signaling in a Prioritization Study of Intraocular Pressure-Associated Genes.” Int J Mol Sci 22, no. 19 (September 24, 2021). https://doi.org/10.3390/ijms221910288.
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  - Gharahkhani, Puya, Eric Jorgenson, Pirro Hysi, Anthony P. Khawaja, Sarah Pendergrass, Xikun Han, Jue Sheng Ong, et al. “Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries.” Nat Commun 12, no. 1 (February 24, 2021): 1258. https://doi.org/10.1038/s41467-020-20851-4.
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  - Genetics of Exfoliation Syndrome Partnership, Chiea Chuen, Zheng Li, Zhenxun Wang, Mei Chin Lee, Matthias Zenkel, Esther Peh, Mineo Ozaki, et al. “Association of Rare CYP39A1 Variants With Exfoliation Syndrome Involving the Anterior Chamber of the Eye.” Jama 325, no. 8 (February 23, 2021): 753–64. https://doi.org/10.1001/jama.2021.0507.
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  - Schmitt, Heather M., William M. Johnson, Inas F. Aboobakar, Shelby Strickland, María Gomez-Caraballo, Megan Parker, Laura Finnegan, et al. “Identification and activity of the functional complex between hnRNPL and the pseudoexfoliation syndrome-associated lncRNA, LOXL1-AS1.” Hum Mol Genet 29, no. 12 (July 29, 2020): 1986–95. https://doi.org/10.1093/hmg/ddaa021.
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  - Grasby, Katrina L., Neda Jahanshad, Jodie N. Painter, Lucía Colodro-Conde, Janita Bralten, Derrek P. Hibar, Penelope A. Lind, et al. “The genetic architecture of the human cerebral cortex.” Science 367, no. 6484 (March 20, 2020). https://doi.org/10.1126/science.aay6690.
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  - Genetics of Glaucoma in People of African Descent (GGLAD) Consortium, Chiea Chuen, Michael A. Hauser, R Rand Allingham, Tin Aung, Carly J. Van Der Heide, Kent D. Taylor, Jerome I. Rotter, et al. “Association of Genetic Variants With Primary Open-Angle Glaucoma Among Individuals With African Ancestry.” Jama 322, no. 17 (November 5, 2019): 1682–91. https://doi.org/10.1001/jama.2019.16161.
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  - Youngblood, Hannah, Michael A. Hauser, and Yutao Liu. “Update on the genetics of primary open-angle glaucoma.” Exp Eye Res 188 (November 2019): 107795. https://doi.org/10.1016/j.exer.2019.107795.
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  - Nievergelt, Caroline M., Adam X. Maihofer, Torsten Klengel, Elizabeth G. Atkinson, Chia-Yen Chen, Karmel W. Choi, Jonathan R. I. Coleman, et al. “International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci.” Nat Commun 10, no. 1 (October 8, 2019): 4558. https://doi.org/10.1038/s41467-019-12576-w.
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  - Fan, Bao Jian, Jessica Cooke Bailey, Rob P. Igo, Jae H. Kang, Tahani Boumenna, Murray H. Brilliant, Donald L. Budenz, et al. “Association of a Primary Open-Angle Glaucoma Genetic Risk Score With Earlier Age at Diagnosis.” Jama Ophthalmol 137, no. 10 (October 1, 2019): 1190–94. https://doi.org/10.1001/jamaophthalmol.2019.3109.
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  - Laville, Vincent, Jae H. Kang, Clara C. Cousins, Adriana I. Iglesias, Réka Nagy, Jessica N. Cooke Bailey, Robert P. Igo, et al. “Genetic Correlations Between Diabetes and Glaucoma: An Analysis of Continuous and Dichotomous Phenotypes.” Am J Ophthalmol 206 (October 2019): 245–55. https://doi.org/10.1016/j.ajo.2019.05.015.
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  - Bonnemaijer, Pieter W. M., Elisabeth M van Leeuwen, Adriana I. Iglesias, Puya Gharahkhani, Veronique Vitart, Anthony P. Khawaja, Mark Simcoe, et al. “Multi-trait genome-wide association study identifies new loci associated with optic disc parameters.” Commun Biol 2 (2019): 435. https://doi.org/10.1038/s42003-019-0634-9.
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  - Kimbrel, Nathan A., Melanie E. Garrett, Michelle F. Dennis, Michelle F. VA Mid-Atlantic Mental Illness Research, Education, and Clinical Center Workgroup, Michael A. Hauser, Allison E. Ashley-Koch, and Jean C. Beckham. “A genome-wide association study of suicide attempts and suicidal ideation in U.S. military veterans.” Psychiatry Res 269 (November 2018): 64–69. https://doi.org/10.1016/j.psychres.2018.07.017.
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  - Khawaja, Anthony P., Michelle P. Y. Chan, Jennifer L. Y. Yip, David C. Broadway, David F. Garway-Heath, Ananth C. Viswanathan, Robert Luben, et al. “A Common Glaucoma-risk Variant of SIX6 Alters Retinal Nerve Fiber Layer and Optic Disc Measures in a European Population: The EPIC-Norfolk Eye Study.” J Glaucoma 27, no. 9 (September 2018): 743–49. https://doi.org/10.1097/IJG.0000000000001026.
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  - Wolf, Erika J., Hannah Maniates, Nicole Nugent, Adam X. Maihofer, Don Armstrong, Andrew Ratanatharathorn, Allison E. Ashley-Koch, et al. “Traumatic stress and accelerated DNA methylation age: A meta-analysis.” Psychoneuroendocrinology 92 (June 2018): 123–34. https://doi.org/10.1016/j.psyneuen.2017.12.007.
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  - Khaled, Mariam Lofty, Yelena Bykhovskaya, Sarah E. R. Yablonski, Hanzhou Li, Michelle D. Drewry, Inas F. Aboobakar, Amy Estes, et al. “Differential Expression of Coding and Long Noncoding RNAs in Keratoconus-Affected Corneas.” Invest Ophthalmol Vis Sci 59, no. 7 (June 1, 2018): 2717–28. https://doi.org/10.1167/iovs.18-24267.
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  - Nievergelt, Caroline M., Allison E. Ashley-Koch, Shareefa Dalvie, Michael A. Hauser, Rajendra A. Morey, Alicia K. Smith, and Monica Uddin. “Genomic Approaches to Posttraumatic Stress Disorder: The Psychiatric Genomic Consortium Initiative.” Biol Psychiatry 83, no. 10 (May 15, 2018): 831–39. https://doi.org/10.1016/j.biopsych.2018.01.020.
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  - Iglesias, Adriana I., Aniket Mishra, Veronique Vitart, Yelena Bykhovskaya, René Höhn, Henriët Springelkamp, Gabriel Cuellar-Partida, et al. “Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases.” Nat Commun 9, no. 1 (May 14, 2018): 1864. https://doi.org/10.1038/s41467-018-03646-6.
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  - Shiga, Yukihiro, Masato Akiyama, Koji M. Nishiguchi, Kota Sato, Nobuhiro Shimozawa, Atsushi Takahashi, Yukihide Momozawa, et al. “Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma.” Hum Mol Genet 27, no. 8 (April 15, 2018): 1486–96. https://doi.org/10.1093/hmg/ddy053.
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  - Johnson, William M., Laura K. Finnegan, Michael A. Hauser, and W Daniel Stamer. “lncRNAs, DNA Methylation, and the Pathobiology of Exfoliation Glaucoma.” J Glaucoma 27, no. 3 (March 2018): 202–9. https://doi.org/10.1097/IJG.0000000000000711.
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  - Duncan, L. E., A. Ratanatharathorn, A. E. Aiello, L. M. Almli, A. B. Amstadter, A. E. Ashley-Koch, D. G. Baker, et al. “Largest GWAS of PTSD (N=20 070) yields genetic overlap with schizophrenia and sex differences in heritability.” Mol Psychiatry 23, no. 3 (March 2018): 666–73. https://doi.org/10.1038/mp.2017.77.
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  - Gharahkhani, Puya, Kathryn P. Burdon, Jessica N. Cooke Bailey, Alex W. Hewitt, Matthew H. Law, Louis R. Pasquale, Jae H. Kang, et al. “Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma.” Sci Rep 8, no. 1 (February 15, 2018): 3124. https://doi.org/10.1038/s41598-018-20435-9.
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  - Bailey, Jessica N Cooke, Puya Gharahkhani, Jae H. Kang, Mariusz Butkiewicz, David A. Sullivan, Robert N. Weinreb, Hugues Aschard, et al. “Testosterone Pathway Genetic Polymorphisms in Relation to Primary Open-Angle Glaucoma: An Analysis in Two Large Datasets.” Invest Ophthalmol Vis Sci 59, no. 2 (February 1, 2018): 629–36. https://doi.org/10.1167/iovs.17-22708.
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  - Carnes, Megan Ulmer, R Rand Allingham, Allison Ashley-Koch, and Michael A. Hauser. “Transcriptome analysis of adult and fetal trabecular meshwork, cornea, and ciliary body tissues by RNA sequencing.” Exp Eye Res 167 (February 2018): 91–99. https://doi.org/10.1016/j.exer.2016.11.021.
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  - King, Rebecca, Felix L. Struebing, Ying Li, Jiaxing Wang, Allison Ashley Koch, Jessica N. Cooke Bailey, Puya Gharahkhani, et al. “Genomic locus modulating corneal thickness in the mouse identifies POU6F2 as a potential risk of developing glaucoma.” Plos Genet 14, no. 1 (January 2018): e1007145. https://doi.org/10.1371/journal.pgen.1007145.
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  - Morey, Rajendra A., Sarah L. Davis, Melanie E. Garrett, Courtney C. Haswell, Courtney C. Mid-Atlantic MIRECC Workgroup, Christine E. Marx, Jean C. Beckham, Gregory McCarthy, Michael A. Hauser, and Allison E. Ashley-Koch. “Genome-wide association study of subcortical brain volume in PTSD cases and trauma-exposed controls.” Transl Psychiatry 7, no. 11 (November 30, 2017): 1265. https://doi.org/10.1038/s41398-017-0021-6.
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  - Polimanti, Renato, Ananda B. Amstadter, Murray B. Stein, Lynn M. Almli, Dewleen G. Baker, Laura J. Bierut, Bekh Bradley, et al. “A putative causal relationship between genetically determined female body shape and posttraumatic stress disorder.” Genome Med 9, no. 1 (November 27, 2017): 99. https://doi.org/10.1186/s13073-017-0491-4.
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  - Chintalapudi, Sumana R., Doaa Maria, Xiang Di Wang, Jessica N Cooke Bailey, Jessica N Cooke NEIGHBORHOOD consortium, Jessica N Cooke International Glaucoma Genetics consortium, Pirro G. Hysi, Janey L. Wiggs, Robert W. Williams, and Monica M. Jablonski. “Systems genetics identifies a role for Cacna2d1 regulation in elevated intraocular pressure and glaucoma susceptibility.” Nat Commun 8, no. 1 (November 24, 2017): 1755. https://doi.org/10.1038/s41467-017-00837-5.
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  - Aschard, Hugues, Jae H. Kang, Adriana I. Iglesias, Pirro Hysi, Jessica N. Cooke Bailey, Anthony P. Khawaja, R Rand Allingham, et al. “Genetic correlations between intraocular pressure, blood pressure and primary open-angle glaucoma: a multi-cohort analysis.” Eur J Hum Genet 25, no. 11 (November 2017): 1261–67. https://doi.org/10.1038/ejhg.2017.136.
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  - Teotia, Pooja, Matthew J. Van Hook, Christopher S. Wichman, R Rand Allingham, Michael A. Hauser, and Iqbal Ahmad. “Modeling Glaucoma: Retinal Ganglion Cells Generated from Induced Pluripotent Stem Cells of Patients with SIX6 Risk Allele Show Developmental Abnormalities.” Stem Cells 35, no. 11 (November 2017): 2239–52. https://doi.org/10.1002/stem.2675.
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  - Ratanatharathorn, Andrew, Marco P. Boks, Adam X. Maihofer, Allison E. Aiello, Ananda B. Amstadter, Allison E. Ashley-Koch, Dewleen G. Baker, et al. “Epigenome-wide association of PTSD from heterogeneous cohorts with a common multi-site analysis pipeline.” Am J Med Genet B Neuropsychiatr Genet 174, no. 6 (September 2017): 619–30. https://doi.org/10.1002/ajmg.b.32568.
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  - Aung, Tin, Mineo Ozaki, Mei Chin Lee, Ursula Schlötzer-Schrehardt, Gudmar Thorleifsson, Takanori Mizoguchi, Robert P. Igo, et al. “Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.” Nat Genet 49, no. 7 (July 2017): 993–1004. https://doi.org/10.1038/ng.3875.
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  - Grassmann, Felix, Christina Kiel, Martina E. Zimmermann, Mathias Gorski, Veronika Grassmann, Klaus Stark, Klaus International AMD Genomics Consortium (IAMDGC), Iris M. Heid, and Bernhard H. F. Weber. “Genetic pleiotropy between age-related macular degeneration and 16 complex diseases and traits.” Genome Med 9, no. 1 (March 27, 2017): 29. https://doi.org/10.1186/s13073-017-0418-0.
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  - Grassmann, Felix, Iris M. Heid, Bernhard H. F. Weber, and Bernhard H. F. International AMD Genomics Consortium (IAMDGC). “Recombinant Haplotypes Narrow the ARMS2/HTRA1 Association Signal for Age-Related Macular Degeneration.” Genetics 205, no. 2 (February 2017): 919–24. https://doi.org/10.1534/genetics.116.195966.
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  - Pasquale, Louis R., Hugues Aschard, Jae H. Kang, Jessica N Cooke Bailey, Sara Lindström, Daniel I. Chasman, William G. Christen, et al. “Age at natural menopause genetic risk score in relation to age at natural menopause and primary open-angle glaucoma in a US-based sample.” Menopause 24, no. 2 (February 2017): 150–56. https://doi.org/10.1097/GME.0000000000000741.
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  - Hauser, Michael A., Melanie E. Garrett, Yutao Liu, Michelle F. Dennis, Nathan A. Kimbrel, Nathan A. Veterans Affairs Mid-Atlantic Mental Illness Research Education And Clinical Center Workgroup, Jean C. Beckham, and Allison E. Ashley-Koch. “Further evidence for a role of the ADRB2 gene in risk for posttraumatic stress disorder.” J Psychiatr Res 84 (January 2017): 59–61. https://doi.org/10.1016/j.jpsychires.2016.09.013.
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  - Aboobakar, Inas F., William M. Johnson, W Daniel Stamer, Michael A. Hauser, and R Rand Allingham. “Major review: Exfoliation syndrome; advances in disease genetics, molecular biology, and epidemiology.” Exp Eye Res 154 (January 2017): 88–103. https://doi.org/10.1016/j.exer.2016.11.011.
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  - Verma, Shefali Setia, Jessica N. Cooke Bailey, Anastasia Lucas, Yuki Bradford, James G. Linneman, Michael A. Hauser, Louis R. Pasquale, et al. “Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium.” Plos Genet 12, no. 9 (September 2016): e1006186. https://doi.org/10.1371/journal.pgen.1006186.
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  - Khawaja, Anthony P., Jessica N. Cooke Bailey, Jae Hee Kang, R Rand Allingham, Michael A. Hauser, Murray Brilliant, Donald L. Budenz, et al. “Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses.” Invest Ophthalmol Vis Sci 57, no. 11 (September 1, 2016): 5046–52. https://doi.org/10.1167/iovs.16-20017.
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  - Liu, Yutao, Jessica Cooke Bailey, Inas Helwa, W Michael Dismuke, Jingwen Cai, Michelle Drewry, Murray H. Brilliant, et al. “A Common Variant in MIR182 Is Associated With Primary Open-Angle Glaucoma in the NEIGHBORHOOD Consortium.” Invest Ophthalmol Vis Sci 57, no. 10 (August 1, 2016): 4528–35. https://doi.org/10.1167/iovs.16-19688.
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  - Drewry, Michelle, Inas Helwa, R Rand Allingham, Michael A. Hauser, and Yutao Liu. “miRNA Profile in Three Different Normal Human Ocular Tissues by miRNA-Seq.” Invest Ophthalmol Vis Sci 57, no. 8 (July 1, 2016): 3731–39. https://doi.org/10.1167/iovs.16-19155.
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  - Roach, Allana N., Tasanee Braithwaite, Christine Carrington, Elysse Marcellin, Subash Sharma, Aroon Hingorani, Juan P. Casas, et al. “Addressing ethical challenges in the Genetics Substudy of the National Eye Survey of Trinidad and Tobago (GSNESTT).” Appl Transl Genom 9 (June 2016): 6–14. https://doi.org/10.1016/j.atg.2016.05.001.
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  - Khor, Chiea Chuen, Tan Do, Hongyan Jia, Masakazu Nakano, Ronnie George, Khaled Abu-Amero, Roopam Duvesh, et al. “Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma.” Nat Genet 48, no. 5 (May 2016): 556–62. https://doi.org/10.1038/ng.3540.
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  - Bailey, Jessica N Cooke, Stephanie J. Loomis, Jae H. Kang, R Rand Allingham, Puya Gharahkhani, Chiea Chuen Khor, Kathryn P. Burdon, et al. “Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma.” Nat Genet 48, no. 2 (February 2016): 189–94. https://doi.org/10.1038/ng.3482.
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  - Fritsche, Lars G., Wilmar Igl, Jessica N Cooke Bailey, Felix Grassmann, Sebanti Sengupta, Jennifer L. Bragg-Gresham, Kathryn P. Burdon, et al. “A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants.” Nat Genet 48, no. 2 (February 2016): 134–43. https://doi.org/10.1038/ng.3448.
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  - Liu, Yutao, Jessica Cooke Bailey, Inas Helwa, W Michael Dismuke, Jingwen Cai, Michelle Drewry, Murray H. Brilliant, et al. “A Common Variant in MIR182 Is Associated With Primary Open-Angle Glaucoma in the NEIGHBORHOOD Consortium.” Investigative Ophthalmology & Visual Science 57, no. 10 (2016): 4528–35. https://doi.org/10.1167/iovs.16-19688.
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  - Hauser, Michael A., Inas F. Aboobakar, Yutao Liu, Shiroh Miura, Benjamin T. Whigham, Pratap Challa, Joshua Wheeler, et al. “Genetic variants and cellular stressors associated with exfoliation syndrome modulate promoter activity of a lncRNA within the LOXL1 locus.” Hum Mol Genet 24, no. 22 (November 15, 2015): 6552–63. https://doi.org/10.1093/hmg/ddv347.
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  - Cai, Jingwen, Kristin M. Perkumas, Xuejun Qin, Michael A. Hauser, W Daniel Stamer, and Yutao Liu. “Expression Profiling of Human Schlemm's Canal Endothelial Cells From Eyes With and Without Glaucoma.” Invest Ophthalmol Vis Sci 56, no. 11 (October 2015): 6747–53. https://doi.org/10.1167/iovs.15-17720.
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  - Kimbrel, Nathan A., Melanie E. Garrett, Michelle F. Dennis, Yutao Liu, Ilyas Patanam, Va Mid-Atlantic Mirecc Workgroup, Allison E. Ashley-Koch, Michael A. Hauser, and Jean C. Beckham. “Effect of genetic variation in the nicotinic receptor genes on risk for posttraumatic stress disorder.” Psychiatry Res 229, no. 1–2 (September 30, 2015): 326–31. https://doi.org/10.1016/j.psychres.2015.07.002.
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  - Abu-Amero, Khaled K., Inas Helwa, Abdulrahman Al-Muammar, Shelby Strickland, Michael A. Hauser, R Rand Allingham, and Yutao Liu. “Screening of the Seed Region of MIR184 in Keratoconus Patients from Saudi Arabia.” Biomed Res Int 2015 (2015): 604508. https://doi.org/10.1155/2015/604508.
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  - Cheng, Ching-Yu, R Rand Allingham, Tin Aung, Yih-Chung Tham, Michael A. Hauser, Eranga N. Vithana, Chiea Chuen Khor, and Tien Yin Wong. “Association of common SIX6 polymorphisms with peripapillary retinal nerve fiber layer thickness: the Singapore Chinese Eye Study.” Invest Ophthalmol Vis Sci 56, no. 1 (December 23, 2014): 478–83. https://doi.org/10.1167/iovs.14-15863.
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  - Roses, Allen D., Michael W. Lutz, Ann M. Saunders, Dmitry Goldgaber, Robert Saul, Scott S. Sundseth, P Anthony Akkari, et al. “African-American TOMM40'523-APOE haplotypes are admixture of West African and Caucasian alleles.” Alzheimers Dement 10, no. 6 (November 2014): 592-601.e2. https://doi.org/10.1016/j.jalz.2014.06.009.
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  - Guffanti, G., A. E. Ashley-Koch, A. L. Roberts, M. E. Garrett, N. Solovieff, A. Ratanatharathorn, I. De Vivo, et al. “No association between RORA polymorphisms and PTSD in two independent samples.” Mol Psychiatry 19, no. 10 (October 2014): 1056–57. https://doi.org/10.1038/mp.2014.19.
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  - Li, Yi-Ju, Mollie A. Minear, Xuejun Qin, Jacqueline Rimmler, Michael A. Hauser, R Rand Allingham, Robert P. Igo, et al. “Mitochondrial polymorphism A10398G and Haplogroup I are associated with Fuchs' endothelial corneal dystrophy.” Invest Ophthalmol Vis Sci 55, no. 7 (June 10, 2014): 4577–84. https://doi.org/10.1167/iovs.13-13517.
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  - Liu, Jian, Lindsay M. Wallace, Sara E. Garwick-Coppens, Darcée D. Sloboda, Carol S. Davis, Chady H. Hakim, Michael A. Hauser, Susan V. Brooks, Jerry R. Mendell, and Scott Q. Harper. “RNAi-mediated Gene Silencing of Mutant Myotilin Improves Myopathy in LGMD1A Mice.” Mol Ther Nucleic Acids 3, no. 4 (April 29, 2014): e160. https://doi.org/10.1038/mtna.2014.13.
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  - Maselli, R. A., J. Arredondo, J. Nguyen, M. Lara, F. Ng, M. Ngo, J. M. Pham, et al. “Exome sequencing detection of two untranslated GFPT1 mutations in a family with limb-girdle myasthenia.” Clin Genet 85, no. 2 (February 2014): 166–71. https://doi.org/10.1111/cge.12118.
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  - Moylan, Cynthia A., Herbert Pang, Andrew Dellinger, Ayako Suzuki, Melanie E. Garrett, Cynthia D. Guy, Susan K. Murphy, et al. “Hepatic gene expression profiles differentiate presymptomatic patients with mild versus severe nonalcoholic fatty liver disease.” Hepatology 59, no. 2 (February 2014): 471–82. https://doi.org/10.1002/hep.26661.
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  - Carnes, M. U. L. “Discovery and functional annotation of SIX6 variants in primary open-angle glaucoma.” Plos Genetics 10, no. 5 (January 1, 2014): e1004372. https://doi.org/10.1371/journal.pgen.1004372.
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  - Dietz, Joel A., Margaret E. Maes, Shuang Huang, Brian S. Yandell, Cassandra L. Schlamp, Angela D. Montgomery, R Rand Allingham, Michael A. Hauser, and Robert W. Nickells. “Spink2 modulates apoptotic susceptibility and is a candidate gene in the Rgcs1 QTL that affects retinal ganglion cell death after optic nerve damage.” Plos One 9, no. 4 (2014): e93564. https://doi.org/10.1371/journal.pone.0093564.
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  - Sun, Wen, Yan Sheng, Yu Weng, Chun-Xiao Xu, Susan E. I. Williams, Yu-Tao Liu, Michael A. Hauser, R Rand Allingham, Ming-Juan Jin, and Guang-Di Chen. “Lack of association between lysyl oxidase-like 1 polymorphisms and primary open angle glaucoma: a meta-analysis.” Int J Ophthalmol 7, no. 3 (2014): 550–56. https://doi.org/10.3980/j.issn.2222-3959.2014.03.29.
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  - Ozel, A Bilge, Sayoko E. Moroi, David M. Reed, Melisa Nika, Caroline M. Schmidt, Sara Akbari, Kathleen Scott, et al. “Genome-wide association study and meta-analysis of intraocular pressure.” Hum Genet 133, no. 1 (January 2014): 41–57. https://doi.org/10.1007/s00439-013-1349-5.
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  - Wallace, Dana J., Felix Y. Chau, Cecilia Santiago-Turla, Michael Hauser, Pratap Challa, Paul P. Lee, Leon W. Herndon, and R Rand Allingham. “Osteogenesis imperfecta and primary open angle glaucoma: genotypic analysis of a new phenotypic association.” Mol Vis 20 (2014): 1174–81.
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  - Murphy, Susan K., Hyuna Yang, Cynthia A. Moylan, Herbert Pang, Andrew Dellinger, Manal F. Abdelmalek, Melanie E. Garrett, et al. “Relationship between methylome and transcriptome in patients with nonalcoholic fatty liver disease.” Gastroenterology 145, no. 5 (November 2013): 1076–87. https://doi.org/10.1053/j.gastro.2013.07.047.
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  - Liu, Yutao, R Rand Allingham, Xuejun Qin, David Layfield, Andrew E. Dellinger, Jason Gibson, Joshua Wheeler, Allison E. Ashley-Koch, W Daniel Stamer, and Michael A. Hauser. “Gene expression profile in human trabecular meshwork from patients with primary open-angle glaucoma.” Invest Ophthalmol Vis Sci 54, no. 9 (September 27, 2013): 6382–89. https://doi.org/10.1167/iovs.13-12128.
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  - Liu, Yutao, Michael A. Hauser, Stephen K. Akafo, Xuejun Qin, Shiroh Miura, Jason R. Gibson, Joshua Wheeler, et al. “Investigation of known genetic risk factors for primary open angle glaucoma in two populations of African ancestry.” Invest Ophthalmol Vis Sci 54, no. 9 (September 17, 2013): 6248–54. https://doi.org/10.1167/iovs.13-12779.
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  - Wiggs, Janey L., Michael A. Hauser, Wael Abdrabou, Robert Rand Allingham, Donald L. Budenz, Elizabeth Delbono, David S. Friedman, et al. “The NEIGHBOR consortium primary open-angle glaucoma genome-wide association study: rationale, study design, and clinical variables.” J Glaucoma 22, no. 7 (September 2013): 517–25. https://doi.org/10.1097/IJG.0b013e31824d4fd8.
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  - Liu, Yutao, Jacqueline Rimmler, Michelle F. Dennis, Allison E. Ashley-Koch, Michael A. Hauser, Michael A. Mid-Atlantic Mental Illness Research Education and Clinical Center Workgroup, and Jean C. Beckham. “Association of Variant rs4790904 in Protein Kinase C Alpha with Posttraumatic Stress Disorder in a U.S. Caucasian and African-American Veteran Sample.” J Depress Anxiety 2, no. 1 (June 1, 2013): S4001. https://doi.org/10.4172/2167-1044.s4-001.
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  - Garrett, Melanie E., Manal F. Abdelmalek, Allison Ashley-Koch, Michael A. Hauser, Cynthia A. Moylan, Herbert Pang, Anna Mae Diehl, and Hans L. Tillmann. “IL28B rs12979860 is not associated with histologic features of NAFLD in a cohort of Caucasian North American patients.” J Hepatol 58, no. 2 (February 2013): 402–3. https://doi.org/10.1016/j.jhep.2012.09.035.
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  - Bhattacharya, Sanjoy K., Richard K. Lee, Franz H. Grus, and Franz H. Seventh ARVO/Pfizer Ophthalmics Research Institute Conference Working Group. “Molecular biomarkers in glaucoma.” Invest Ophthalmol Vis Sci 54, no. 1 (January 7, 2013): 121–31. https://doi.org/10.1167/iovs.12-11067.
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  - Abu-Amero, Khaled K., Essam A. Osman, Mohammad T. Azad, R Rand Allingham, Michael A. Hauser, and Saleh A. Al-Obeidan. “Lack of association between LOXL1 gene polymorphisms and primary open angle glaucoma in the Saudi Arabian population.” Ophthalmic Genet 33, no. 3 (September 2012): 130–33. https://doi.org/10.3109/13816810.2011.575430.
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  - Dedert, Eric A., Eric B. Elbogen, Michael A. Hauser, Jeff S. Hertzberg, Sarah M. Wilson, Michelle F. Dennis, Patrick S. Calhoun, Angela C. Kirby, and Jean C. Beckham. “Consumer perspectives on genetic testing for psychiatric disorders: the attitudes of veterans with posttraumatic stress disorder and their families.” Genet Test Mol Biomarkers 16, no. 9 (September 2012): 1122–29. https://doi.org/10.1089/gtmb.2012.0048.
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  - Wheeler, Joshua, Michael A. Hauser, Natalie A. Afshari, R Rand Allingham, and Yutao Liu. “The Genetics of Keratoconus: A Review.” Reprod Syst Sex Disord, no. Suppl 6 (June 3, 2012). https://doi.org/10.4172/2161-038X.S6-001.
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  - Sarparanta, Jaakko, Per Harald Jonson, Christelle Golzio, Satu Sandell, Helena Luque, Mark Screen, Kristin McDonald, et al. “Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophy.” Nat Genet 44, no. 4 (February 26, 2012): 450-S2. https://doi.org/10.1038/ng.1103.
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  - Abu-Amero, Khaled K., Michael A. Hauser, Gamal Mohamed, Yutao Liu, Jason Gibson, Ana M. Gonzalez, Stephen Akafo, and R Rand Allingham. “Mitochondrial genetic background in Ghanaian patients with primary open-angle glaucoma.” Mol Vis 18 (2012): 1955–59.
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  - Linnertz, Colton, Ann M. Saunders, Michael W. Lutz, Donna M. Crenshaw, Iris Grossman, Daniel K. Burns, Keith E. Whitfield, et al. “Characterization of the poly-T variant in the TOMM40 gene in diverse populations.” Plos One 7, no. 2 (2012): e30994. https://doi.org/10.1371/journal.pone.0030994.
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  - Liu, Wenjing, Yutao Liu, Pratap Challa, Leon W. Herndon, Janey L. Wiggs, Christopher A. Girkin, R Rand Allingham, and Michael A. Hauser. “Low prevalence of myocilin mutations in an African American population with primary open-angle glaucoma.” Mol Vis 18 (2012): 2241–46.
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  - Morey, Rajendra A., Ahmad R. Hariri, Andrea L. Gold, Michael A. Hauser, Heidi J. Munger, Florin Dolcos, and Gregory McCarthy. “Serotonin transporter gene polymorphisms and brain function during emotional distraction from cognitive processing in posttraumatic stress disorder.” Bmc Psychiatry 11 (May 5, 2011): 76. https://doi.org/10.1186/1471-244X-11-76.
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  - Whigham, Benjamin T., Susan E. I. Williams, Yutao Liu, Robyn M. Rautenbach, Trevor R. Carmichael, Joshua Wheeler, Ari Ziskind, et al. “Myocilin mutations in black South Africans with POAG.” Mol Vis 17 (April 27, 2011): 1064–69.
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  - Liu, Yutao, Drew Munro, David Layfield, Andrew Dellinger, Jeffrey Walter, Katherine Peterson, Catherine Bowes Rickman, R Rand Allingham, and Michael A. Hauser. “Serial analysis of gene expression (SAGE) in normal human trabecular meshwork.” Mol Vis 17 (April 8, 2011): 885–93.
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  - McDonald, Kristin K., Karen Abramson, Marco A. Beltran, Maria G. Ramirez, Miguel Alvarez, Alice Ventura, Cecilia Santiago-Turla, Silke Schmidt, Michael A. Hauser, and R Rand Allingham. “Myocilin and optineurin coding variants in Hispanics of Mexican descent with POAG.” J Hum Genet 55, no. 10 (October 2010): 697–700. https://doi.org/10.1038/jhg.2010.91.
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  - Williams, Susan E. I., Benjamin T. Whigham, Yutao Liu, Trevor R. Carmichael, Xuejun Qin, Silke Schmidt, Michele Ramsay, Michael A. Hauser, and R Rand Allingham. “Major LOXL1 risk allele is reversed in exfoliation glaucoma in a black South African population.” Mol Vis 16 (April 21, 2010): 705–12.
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  - Anderson, Don H., Monte J. Radeke, Natasha B. Gallo, Ethan A. Chapin, Patrick T. Johnson, Christy R. Curletti, Lisa S. Hancox, et al. “The pivotal role of the complement system in aging and age-related macular degeneration: hypothesis re-visited.” Prog Retin Eye Res 29, no. 2 (March 2010): 95–112. https://doi.org/10.1016/j.preteyeres.2009.11.003.
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  - Liu, Wenjing, Yutao Liu, Xue-Jun Qin, Silke Schmidt, Michael A. Hauser, and R Rand Allingham. “AQP1 and SLC4A10 as candidate genes for primary open-angle glaucoma.” Mol Vis 16 (January 20, 2010): 93–97.
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  - Weis, J., M. Krieger, M. Elbracht, V. Guergueltcheva, I. Tournev, A. Urtizberea, S. M. Garvey, et al. “Muscle biopsy findings in a new hereditary distal vacuolar myopathy associated with mutation of the nuclear matrix protein, matrin 3.” Acta Neuropathologica 118, no. 3 (September 1, 2009): 464–464.
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  - Senderek, J., S. M. Garvey, M. Krieger, I. Tournev, M. Elbracht, A. Roos, C. Stendel, et al. “G.O.5 A new autosomal dominant distal vacuolar myopathy associated with mutation of the nuclear matrix protein, matrin 3.” Neuromuscular Disorders 19, no. 8–9 (September 2009): 599–599. https://doi.org/10.1016/j.nmd.2009.06.177.
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  - Kelly, Una, Catherine Bowes Rickman, Eric A. Postel, Michael A. Hauser, Gregory S. Hageman, Vadim Y. Arshavsky, and Nikolai P. Skiba. “Rapid and sensitive method for detection of Y402, H402, I62, and V62 variants of complement factor H in human plasma samples using mass spectrometry.” Invest Ophthalmol Vis Sci 50, no. 4 (April 2009): 1540–45. https://doi.org/10.1167/iovs.08-2782.
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  - Senderek, Jan, Sean M. Garvey, Michael Krieger, Velina Guergueltcheva, Andoni Urtizberea, Andreas Roos, Miriam Elbracht, et al. “Autosomal-dominant distal myopathy associated with a recurrent missense mutation in the gene encoding the nuclear matrix protein, matrin 3.” Am J Hum Genet 84, no. 4 (April 2009): 511–18. https://doi.org/10.1016/j.ajhg.2009.03.006.
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  - Liu, Yutao, Silke Schmidt, Xuejun Qin, Jason Gibson, Kristen Hutchins, Cecile Santiago-Turla, Janey L. Wiggs, et al. “Lack of association between LOXL1 variants and primary open-angle glaucoma in three different populations.” Invest Ophthalmol Vis Sci 49, no. 8 (August 2008): 3465–68. https://doi.org/10.1167/iovs.08-1850.
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  - Wistow, Graeme, Katherine Peterson, James Gao, Patee Buchoff, Cynthia Jaworski, Catherine Bowes-Rickman, Jessica N. Ebright, Michael A. Hauser, and David Hoover. “NEIBank: genomics and bioinformatics resources for vision research.” Mol Vis 14 (July 18, 2008): 1327–37.
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  - Canter, Jeffrey A., Lana M. Olson, Kylee Spencer, Nathalie Schnetz-Boutaud, Brent Anderson, Michael A. Hauser, Silke Schmidt, et al. “Mitochondrial DNA polymorphism A4917G is independently associated with age-related macular degeneration.” Plos One 3, no. 5 (May 7, 2008): e2091. https://doi.org/10.1371/journal.pone.0002091.
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  - Garvey, Sean M., Yutao Liu, Sara E. Miller, and Michael A. Hauser. “Myotilin overexpression enhances myopathology in the LGMD1A mouse model.” Muscle Nerve 37, no. 5 (May 2008): 663–67. https://doi.org/10.1002/mus.20994.
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  - Spencer, Kylee L., Michael A. Hauser, Lana M. Olson, Silke Schmidt, William K. Scott, Paul Gallins, Anita Agarwal, Eric A. Postel, Margaret A. Pericak-Vance, and Jonathan L. Haines. “Deletion of CFHR3 and CFHR1 genes in age-related macular degeneration.” Hum Mol Genet 17, no. 7 (April 1, 2008): 971–77. https://doi.org/10.1093/hmg/ddm369.
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  - Shuler, R Keith, Silke Schmidt, Paul Gallins, Michael A. Hauser, William K. Scott, Jennifer Caldwell, Anita Agarwal, Jonathan L. Haines, Margaret A. Pericak-Vance, and Eric A. Postel. “Peripheral reticular pigmentary change is associated with complement factor H polymorphism (Y402H) in age-related macular degeneration.” Ophthalmology 115, no. 3 (March 2008): 520–24. https://doi.org/10.1016/j.ophtha.2007.06.021.
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  - Shuler, R Keith, Silke Schmidt, Paul Gallins, Michael A. Hauser, William K. Scott, Jennifer Caldwell, Anita Agarwal, Jonathan L. Haines, Margaret A. Pericak-Vance, and Eric A. Postel. “Phenotype analysis of patients with the risk variant LOC387715 (A69S) in age-related macular degeneration.” Am J Ophthalmol 145, no. 2 (February 2008): 303–7. https://doi.org/10.1016/j.ajo.2007.09.027.
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  - Challa, Pratap, Silke Schmidt, Yutao Liu, Xuejun Qin, Robin R. Vann, Pedro Gonzalez, R Rand Allingham, and Michael A. Hauser. “Analysis of LOXL1 polymorphisms in a United States population with pseudoexfoliation glaucoma.” Mol Vis 14 (January 29, 2008): 146–49.
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  - Liu, Yutao, Stephen Akafo, Cecile Santiago-Turla, Claudia S. Cohen, Karen R. Larocque-Abramson, Xuejun Qin, Leon W. Herndon, et al. “Optineurin coding variants in Ghanaian patients with primary open-angle glaucoma.” Mol Vis 14 (2008): 2367–72.
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  - Liu, Yutao, Silke Schmidt, Xuejun Qin, Jason Gibson, Drew Munro, Janey L. Wiggs, Michael A. Hauser, and R Rand Allingham. “No association between OPA1 polymorphisms and primary open-angle glaucoma in three different populations.” Mol Vis 13 (November 26, 2007): 2137–41.
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  - Xu, Pu-Ting, Yi-Ju Li, Xue-Jun Qin, Charles Kroner, Anya Green-Odlum, Hong Xu, Tian-Yuan Wang, et al. “A SAGE study of apolipoprotein E3/3, E3/4 and E4/4 allele-specific gene expression in hippocampus in Alzheimer disease.” Mol Cell Neurosci 36, no. 3 (November 2007): 313–31. https://doi.org/10.1016/j.mcn.2007.06.009.
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  - Spencer, Kylee L., Michael A. Hauser, Lana M. Olson, Nathalie Schnetz-Boutaud, William K. Scott, Silke Schmidt, Paul Gallins, et al. “Haplotypes spanning the complement factor H gene are protective against age-related macular degeneration.” Invest Ophthalmol Vis Sci 48, no. 9 (September 2007): 4277–83. https://doi.org/10.1167/iovs.06-1427.
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  - Spencer, Kylee L., Michael A. Hauser, Lana M. Olson, Silke Schmidt, William K. Scott, Paul Gallins, Anita Agarwal, Eric A. Postel, Margaret A. Pericak-Vance, and Jonathan L. Haines. “Protective effect of complement factor B and complement component 2 variants in age-related macular degeneration.” Hum Mol Genet 16, no. 16 (August 15, 2007): 1986–92. https://doi.org/10.1093/hmg/ddm146.
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  - Scott, William K., Silke Schmidt, Michael A. Hauser, Paul Gallins, Nathalie Schnetz-Boutaud, Kylee L. Spencer, John R. Gilbert, et al. “Independent effects of complement factor H Y402H polymorphism and cigarette smoking on risk of age-related macular degeneration.” Ophthalmology 114, no. 6 (June 2007): 1151–56. https://doi.org/10.1016/j.ophtha.2006.08.054.
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  - Liu, Y., and M. Hauser. “Distinct and predictive chromatin signatures of transcriptional promoters and enhancers in the human genome.” Chemtracts 20, no. 4 (April 1, 2007): 156–57.
  - Scherzer, Clemens R., Aron C. Eklund, Lee J. Morse, Zhixiang Liao, Joseph J. Locascio, Daniel Fefer, Michael A. Schwarzschild, et al. “Molecular markers of early Parkinson's disease based on gene expression in blood.” Proc Natl Acad Sci U S A 104, no. 3 (January 16, 2007): 955–60. https://doi.org/10.1073/pnas.0610204104.
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  - Pillai, S. G., M. N. Chiano, N. J. White, M. Speer, K. C. Barnes, K. Carlsen, J. Gerritsen, et al. “Erratum: A genome-wide search for linkage to asthma phenotypes in the genetics of asthma international network families: Evidence for a major susceptibility locus on chromosome 2p (European Journal of Human Genetics (2006) vol. 14 (307-3167) 10.1038/sj.ejhg.5201532).” European Journal of Human Genetics 15, no. 6 (January 1, 2007): 714. https://doi.org/10.1038/sj.ejhg.5201840.
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  - Shuler, R Keith, Michael A. Hauser, Jennifer Caldwell, Paul Gallins, Silke Schmidt, William K. Scott, Anita Agarwal, Jonathan L. Haines, Margaret A. Pericak-Vance, and Eric A. Postel. “Neovascular age-related macular degeneration and its association with LOC387715 and complement factor H polymorphism.” Arch Ophthalmol 125, no. 1 (January 2007): 63–67. https://doi.org/10.1001/archopht.125.1.63.
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  - Kang, Sun J., William K. Scott, Yi-Ju Li, Michael A. Hauser, Joelle M. van der Walt, Kenichiro Fujiwara, Gregory M. Mayhew, Sandra G. West, Jeffery M. Vance, and Eden R. Martin. “Family-based case-control study of MAOA and MAOB polymorphisms in Parkinson disease.” Mov Disord 21, no. 12 (December 2006): 2175–80. https://doi.org/10.1002/mds.21151.
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  - Hauser, Michael A., Dayse Figueiredo Sena, Jason Flor, Jeff Walter, Josette Auguste, Karen Larocque-Abramson, Felicia Graham, et al. “Distribution of optineurin sequence variations in an ethnically diverse population of low-tension glaucoma patients from the United States.” J Glaucoma 15, no. 5 (October 2006): 358–63. https://doi.org/10.1097/01.ijg.0000212255.17950.42.
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  - Postel, Eric A., Anita Agarwal, Jennifer Caldwell, Paul Gallins, Cynthia Toth, Silke Schmidt, William K. Scott, Michael A. Hauser, Jonathan L. Haines, and Margaret A. Pericak-Vance. “Complement factor H increases risk for atrophic age-related macular degeneration.” Ophthalmology 113, no. 9 (September 2006): 1504–7. https://doi.org/10.1016/j.ophtha.2006.02.049.
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  - Hancock, Dana B., Eden R. Martin, Kenichiro Fujiwara, Mark A. Stacy, Burton L. Scott, Jeffrey M. Stajich, Rita Jewett, et al. “NOS2A and the modulating effect of cigarette smoking in Parkinson's disease.” Ann Neurol 60, no. 3 (September 2006): 366–73. https://doi.org/10.1002/ana.20915.
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  - Challa, Pratap, Michael Arthur Hauser, Coralia Catalina Luna, Sharon Fridovich Freedman, Margaret Pericak-Vance, Jun Yang, Marie Theresa McDonald, and R Rand Allingham. “Juvenile bilateral lens dislocation and glaucoma associated with a novel mutation in the fibrillin 1 gene.” Mol Vis 12 (August 28, 2006): 1009–15.
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  - Garvey, Sean M., Sara E. Miller, Dennis R. Claflin, John A. Faulkner, and Michael A. Hauser. “Transgenic mice expressing the myotilin T57I mutation unite the pathology associated with LGMD1A and MFM.” Hum Mol Genet 15, no. 15 (August 1, 2006): 2348–62. https://doi.org/10.1093/hmg/ddl160.
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  - Bowes Rickman, Catherine, Jessica N. Ebright, Zachary J. Zavodni, Ling Yu, Tianyuan Wang, Stephen P. Daiger, Graeme Wistow, Kathy Boon, and Michael A. Hauser. “Defining the human macula transcriptome and candidate retinal disease genes using EyeSAGE.” Invest Ophthalmol Vis Sci 47, no. 6 (June 2006): 2305–16. https://doi.org/10.1167/iovs.05-1437.
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  - Hauser, Michael A., R Rand Allingham, Kevin Linkroum, Jun Wang, Karen LaRocque-Abramson, Dayse Figueiredo, Cecilia Santiago-Turla, et al. “Distribution of WDR36 DNA sequence variants in patients with primary open-angle glaucoma.” Invest Ophthalmol Vis Sci 47, no. 6 (June 2006): 2542–46. https://doi.org/10.1167/iovs.05-1476.
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  - Schmidt, Silke, Michael A. Hauser, William K. Scott, Eric A. Postel, Anita Agarwal, Paul Gallins, Frank Wong, et al. “Cigarette smoking strongly modifies the association of LOC387715 and age-related macular degeneration.” Am J Hum Genet 78, no. 5 (May 2006): 852–64. https://doi.org/10.1086/503822.
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  - Garvey, Sean M., Jan Senderek, Jacques S. Beckmann, Eric Seboun, Charles E. Jackson, and Michael A. Hauser. “Myotilin is not the causative gene for vocal cord and pharyngeal weakness with distal myopathy (VCPDM).” Annals of Human Genetics 70, no. Pt 3 (May 2006): 414–16. https://doi.org/10.1111/j.1529-8817.2005.00252.x.
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  - Pillai, Sreekumar G., Mathias N. Chiano, Nicola J. White, Marcy Speer, Kathleen C. Barnes, Karin Carlsen, Jorrit Gerritsen, et al. “A genome-wide search for linkage to asthma phenotypes in the genetics of asthma international network families: evidence for a major susceptibility locus on chromosome 2p.” Eur J Hum Genet 14, no. 3 (March 2006): 307–16. https://doi.org/10.1038/sj.ejhg.5201532.
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  - Haines, Jonathan L., Nathalie Schnetz-Boutaud, Silke Schmidt, William K. Scott, Anita Agarwal, Eric A. Postel, Lana Olson, et al. “Functional candidate genes in age-related macular degeneration: significant association with VEGF, VLDLR, and LRP6.” Invest Ophthalmol Vis Sci 47, no. 1 (January 2006): 329–35. https://doi.org/10.1167/iovs.05-0116.
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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.
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  - Lin, S., and M. Hauser. “Data Analysis Issues in Expression Profiling,” October 7, 2005, 193–217. https://doi.org/10.1002/9780471781141.ch7.
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  - Noureddine, Maher A., Yi-Ju Li, Joelle M. van der Walt, Robert Walters, Rita M. Jewett, Hong Xu, Tianyuan Wang, et al. “Genomic convergence to identify candidate genes for Parkinson disease: SAGE analysis of the substantia nigra.” Mov Disord 20, no. 10 (October 2005): 1299–1309. https://doi.org/10.1002/mds.20573.
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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.
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  - Hauser, Michael A., Yi-Ju Li, Hong Xu, Maher A. Noureddine, Yujun S. Shao, Steven R. Gullans, Clemens R. Scherzer, et al. “Expression profiling of substantia nigra in Parkinson disease, progressive supranuclear palsy, and frontotemporal dementia with parkinsonism.” Arch Neurol 62, no. 6 (June 2005): 917–21. https://doi.org/10.1001/archneur.62.6.917.
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  - Noureddine, Maher A., Xue-Jun Qin, Sofia A. Oliveira, Tara J. Skelly, Joelle van der Walt, Michael A. Hauser, Margaret A. Pericak-Vance, Jeffery M. Vance, and Yi-Ju Li. “Association between the neuron-specific RNA-binding protein ELAVL4 and Parkinson disease.” Hum Genet 117, no. 1 (June 2005): 27–33. https://doi.org/10.1007/s00439-005-1259-2.
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  - Haines, Jonathan L., Michael A. Hauser, Silke Schmidt, William K. Scott, Lana M. Olson, Paul Gallins, Kylee L. Spencer, et al. “Complement factor H variant increases the risk of age-related macular degeneration.” Science 308, no. 5720 (April 15, 2005): 419–21. https://doi.org/10.1126/science.1110359.
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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.
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  - Oliveira, Sofia A., William K. Scott, Fengyu Zhang, Jeffrey M. Stajich, Kenichiro Fujiwara, Michael Hauser, Burton L. Scott, Margaret A. Pericak-Vance, Jeffery M. Vance, and Eden R. Martin. “Linkage disequilibrium and haplotype tagging polymorphisms in the Tau H1 haplotype.” Neurogenetics 5, no. 3 (September 2004): 147–55. https://doi.org/10.1007/s10048-004-0180-5.
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  - Li, Y. J., M. A. Hauser, W. K. Scott, E. R. Martin, M. W. Booze, X. J. Qin, J. W. Walter, et al. “Apolipoprotein E controls the risk and age at onset of Parkinson disease.” Neurology 62, no. 11 (June 8, 2004): 2005–9. https://doi.org/10.1212/01.wnl.0000128089.53030.ac.
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  - Walt, Joelle M. van der, Maher A. Noureddine, Raja Kittappa, Michael A. Hauser, William K. Scott, Ron McKay, Fengyu Zhang, et al. “Fibroblast growth factor 20 polymorphisms and haplotypes strongly influence risk of Parkinson disease.” Am J Hum Genet 74, no. 6 (June 2004): 1121–27. https://doi.org/10.1086/421052.
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  - Li, Y. L., S. A. Oliveira, P. Xu, E. R. Martin, J. E. Stenger, C. Hulette, C. R. Scherzer, et al. “Erratum: Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease (Human Molecular Genetics (2003) vol. 12 (3259-3267)).” Human Molecular Genetics 13, no. 5 (March 1, 2004): 573. https://doi.org/10.1093/hmg/ddh059.
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  - Li, Yi-Ju, Sofia A. Oliveira, Puting Xu, Eden R. Martin, Judith E. Stenger, Clemens R. Scherzer, Michael A. Hauser, et al. “Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease.” Hum Mol Genet 12, no. 24 (December 15, 2003): 3259–67. https://doi.org/10.1093/hmg/ddg357.
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  - Speer, Marcy C., David S. Enterline, Lorraine Mehltretter, Preston Hammock, Judith Joseph, Margaret Dickerson, Richard G. Ellenbogen, Thomas H. Milhorat, Michael A. Hauser, and Timothy M. George. “Review Article: Chiari Type I Malformation with or Without Syringomyelia: Prevalence and Genetics.” J Genet Couns 12, no. 4 (August 2003): 297–311. https://doi.org/10.1023/A:1023948921381.
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  - Wiggs, Janey L., Josette Auguste, R Rand Allingham, Jason D. Flor, Margaret A. Pericak-Vance, Kathryn Rogers, Karen R. LaRocque, et al. “Lack of association of mutations in optineurin with disease in patients with adult-onset primary open-angle glaucoma.” Arch Ophthalmol 121, no. 8 (August 2003): 1181–83. https://doi.org/10.1001/archopht.121.8.1181.
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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.
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  - Hauser, Michael A., Cecilia B. Conde, Valeria Kowaljow, Guillermo Zeppa, Ana L. Taratuto, Udana M. Torian, Jeffery Vance, Margaret A. Pericak-Vance, Marcy C. Speer, and Alberto L. Rosa. “myotilin Mutation found in second pedigree with LGMD1A.” Am J Hum Genet 71, no. 6 (December 2002): 1428–32. https://doi.org/10.1086/344532.
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  - Challa, P., L. W. Herndon, M. A. Hauser, B. W. Broomer, M. A. Pericak-Vance, Ben Ababio-Danso, and R. R. Allingham. “Prevalence of myocilin mutations in adults with primary open-angle glaucoma in Ghana, West Africa.” J Glaucoma 11, no. 5 (October 2002): 416–20. https://doi.org/10.1097/00061198-200210000-00008.
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  - Harper, Scott Q., Michael A. Hauser, Christiana DelloRusso, Dongsheng Duan, Robert W. Crawford, Stephanie F. Phelps, Hollie A. Harper, et al. “Modular flexibility of dystrophin: implications for gene therapy of Duchenne muscular dystrophy.” Nat Med 8, no. 3 (March 2002): 253–61. https://doi.org/10.1038/nm0302-253.
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  - Bauer, Kim A., Timothy M. George, David S. Enterline, Rolf W. Stottmann, Elizabeth C. Melvin, Deborah Siegel, Surekha Samal, et al. “A novel mutation in the gene encoding noggin is not causative in human neural tube defects.” J Neurogenet 16, no. 1 (2002): 65–71.
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  - Martin, E. R., W. K. Scott, M. A. Nance, R. L. Watts, J. P. Hubble, W. C. Koller, K. Lyons, et al. “Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson disease.” Jama 286, no. 18 (November 14, 2001): 2245–50. https://doi.org/10.1001/jama.286.18.2245.
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  - Allingham, R. R., J. L. Wiggs, K. R. LaRocque, M. A. Hauser, F. L. Graham, B. Broomer, E. A. del Bono, R. Bailey, J. L. Haines, and M. A. Pericak-Vance. “Phenotype stratification of linkage analysis in primary open-angle glaucoma (POAG): Evidence for age of onset heterogeneity.” American Journal of Human Genetics 69, no. 4 (October 1, 2001): 516–516.
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  - Dancel, R. D., J. M. Stajich, J. M. Vance, M. A. Pricak-Vance, P. C. Gaskell, J. M. Gilchrist, R. W. Tim, M. C. Speer, and M. A. Hauser. “Mutation screening of caveolin-3 and myotilin in autosomal dominant limb girdle muscular dystrophy and other dominant myopathies.” American Journal of Human Genetics 69, no. 4 (October 1, 2001): 625–625.
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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.
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  - Oliveira, S. A., E. R. Martin, W. K. Scott, M. A. Nance, R. L. Watts, J. P. Hubble, W. C. Koller, et al. “Association of tau with late-onset Parkinson disease.” American Journal of Human Genetics 69, no. 4 (October 1, 2001): 511–511.
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  - Allingham, R. R., J. L. Wiggs, K. R. LaRoque, B. Broomer, F. L. Graham, M. A. Hauser, E. A. del Bono, R. Bailey, J. L. Haines, and M. A. Pericak-Vance. “Phenotype stratification of linkage analysis in POAG: Evidence for age of onset heterogeneity.” Investigative Ophthalmology & Visual Science 42, no. 4 (March 15, 2001): S531–S531.
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  - Hauser, M. A., P. Salmikangas, U. M. Torian, R. Dancel, L. V. B. Anderson, U. Taivainen, J. M. Stajich, et al. “Molecular analysis of myotilin, the gene responsible for LGMD1A.” American Journal of Human Genetics 67, no. 4 (October 1, 2000): 390–390.
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  - Hauser, M. A., S. K. Horrigan, P. Salmikangas, U. M. Torian, K. D. Viles, R. Dancel, R. W. Tim, et al. “Myotilin is mutated in limb girdle muscular dystrophy 1A.” Hum Mol Genet 9, no. 14 (September 1, 2000): 2141–47. https://doi.org/10.1093/hmg/9.14.2141.
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  - Hauser, M. A., A. Robinson, D. Hartigan-O’Connor, D. A. Williams-Gregory, J. N. Buskin, S. Apone, C. J. Kirk, S. Hardy, S. D. Hauschka, and J. S. Chamberlain. “Analysis of muscle creatine kinase regulatory elements in recombinant adenoviral vectors.” Mol Ther 2, no. 1 (July 2000): 16–25. https://doi.org/10.1006/mthe.2000.0089.
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  - Wiggs, J. L., R. R. Allingham, A. Hossain, J. Kern, J. Auguste, E. A. DelBono, B. Broomer, et al. “Genome-wide scan for adult onset primary open angle glaucoma.” Hum Mol Genet 9, no. 7 (April 12, 2000): 1109–17. https://doi.org/10.1093/hmg/9.7.1109.
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  - Hauser, M. A., P. Salmikangas, S. K. Horrigan, K. D. Viles, U. M. Torian, U. Taivainen, L. Bartoloni, et al. “Positional cloning of the gene responsible for Limb Girdle Muscular Dystrophy 1A.” American Journal of Human Genetics 65, no. 4 (October 1, 1999): A109–A109.
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  - Lumeng, C. N., M. Hauser, V. Brown, and J. S. Chamberlain. “Expression of the 71 kDa dystrophin isoform (Dp71) evaluated by gene targeting.” Brain Res 830, no. 1 (May 29, 1999): 174–78. https://doi.org/10.1016/s0006-8993(99)01201-9.
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  - Amalfitano, A., M. A. Hauser, H. Hu, D. Serra, C. R. Begy, and J. S. Chamberlain. “Production and characterization of improved adenovirus vectors with the E1, E2b, and E3 genes deleted.” J Virol 72, no. 2 (February 1998): 926–33. https://doi.org/10.1128/JVI.72.2.926-933.1998.
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  - Hauser, M. A., A. Amalfitano, R. Kumar-Singh, S. D. Hauschka, and J. S. Chamberlain. “Improved adenoviral vectors for gene therapy of Duchenne muscular dystrophy.” Neuromuscul Disord 7, no. 5 (July 1997): 277–83. https://doi.org/10.1016/s0960-8966(97)00052-7.
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  - Chamberlain, J. S., K. Corrado, J. A. Rafael, G. A. Cox, M. Hauser, and C. Lumeng. “Interactions between dystrophin and the sarcolemma membrane.” Soc Gen Physiol Ser 52 (1997): 19–29.
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  - Chamberlain, J. S., K. Corrado, J. A. Rafael, G. A. Cox, M. Hauser, and C. Lumeng. “Interactions between dystrophin and the sarcolemma membrane.” Journal of General Physiology, no. 50TH ANN. SYMP. (January 1, 1997): 19–29.
  - Hauser, M. A., and J. S. Chamberlain. “Progress towards gene therapy for Duchenne muscular dystrophy.” J Endocrinol 149, no. 3 (June 1996): 373–78. https://doi.org/10.1677/joe.0.1490373.
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  - Phelps, S. F., M. A. Hauser, N. M. Cole, J. A. Rafael, R. T. Hinkle, J. A. Faulkner, and J. S. Chamberlain. “Expression of full-length and truncated dystrophin mini-genes in transgenic mdx mice.” Hum Mol Genet 4, no. 8 (August 1995): 1251–58. https://doi.org/10.1093/hmg/4.8.1251.
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  - Hanzlik, A. J., M. M. Osemlak-Hanzlik, M. A. Hauser, and D. M. Kurnit. “A recombination-based assay demonstrates that the fragile X sequence is transcribed widely during development.” Nat Genet 3, no. 1 (January 1993): 44–48. https://doi.org/10.1038/ng0193-44.
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  - Hauser, M. A., and J. J. Scocca. “Site-specific integration of the Haemophilus influenzae bacteriophage HP1: location of the boundaries of the phage attachment site.” J Bacteriol 174, no. 20 (October 1992): 6674–77. https://doi.org/10.1128/jb.174.20.6674-6677.1992.
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  - Hauser, M. A., and J. J. Scocca. “Site-specific integration of the Haemophilus influenzae bacteriophage HP1. Identification of the points of recombinational strand exchange and the limits of the host attachment site.” J Biol Chem 267, no. 10 (April 5, 1992): 6859–64.
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  - Stewart, G. D., M. A. Hauser, H. Kang, D. P. McCann, M. M. Osemlak, D. M. Kurnit, and A. J. Hanzlik. “Plasmids for recombination-based screening.” Gene 106, no. 1 (September 30, 1991): 97–101. https://doi.org/10.1016/0378-1119(91)90571-r.
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  - Hauser, M. A., and J. J. Scocca. “Location of the host attachment site for phage HPl within a cluster of Haemophilus influenzae tRNA genes.” Nucleic Acids Res 18, no. 17 (September 11, 1990): 5305. https://doi.org/10.1093/nar/18.17.5305.
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  - Hauser, M. A., M. D. Koob, and J. A. Roth. “Variation of neutrophil function with age in calves.” American Journal of Veterinary Research 47, no. 1 (January 1986): 152–53.
  - Yamazaki, R. K., R. D. Sax, and M. A. Hauser. “Glucagon stimulation of mitochondrial ATPase and potassium ion transport.” Febs Lett 75, no. 1 (March 15, 1977): 295–99. https://doi.org/10.1016/0014-5793(77)80106-3.
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  - Hauser, M. A. “Initiation into peer review.” The American Journal of Nursing 75, no. 12 (December 1975): 2204–7.
- Other Articles
  - Aung, Tin, Mineo Ozaki, Takanori Mizoguchi, R Rand Allingham, Zheng Li, Aravind Haripriya, Satoko Nakano, et al. “Corrigendum: a common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome.” Nat Genet, June 2015. https://doi.org/10.1038/ng0615-689c.
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  - Liu, Yutao, Xuejun Qin, Silke Schmidt, R Rand Allingham, and Michael A. Hauser. “Association between chromosome 2p16.3 variants and glaucoma in populations of African descent.” Proc Natl Acad Sci U S A, April 13, 2010. https://doi.org/10.1073/pnas.0913838107.
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  - Liu, Yutao, Wenjing Liu, Kristy Crooks, Silke Schmidt, R Rand Allingham, and Michael A. Hauser. “No evidence of association of heterozygous NTF4 mutations in patients with primary open-angle glaucoma.” Am J Hum Genet, March 12, 2010. https://doi.org/10.1016/j.ajhg.2009.11.018.
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- Conference Papers
  - Bonnemaijer, Pieter W. M., Adriana I. Iglesias, Girish N. Nadkarni, Anna J. Sanyiwa, Hassan G. Hassan, Colin Cook, Colin GIGA Study Group, et al. “Genome-wide association study of primary open-angle glaucoma in continental and admixed African populations.” In Hum Genet, 137:847–62, 2018. https://doi.org/10.1007/s00439-018-1943-7.
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  - Aboobakar, Inas F., Xue Qin, W Daniel Starner, R Rand Allingham, and Michael A. Hauser. “A lncRNA in the LOXL1 locus modulates expression of genes relevant to exfoliation glaucoma pathobiology.” In Investigative Ophthalmology & Visual Science, Vol. 57. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2016.
    Link to Item
  - Bailey, Jessica Cooke, Mariusz Butkiewicz, Louis R. Pasquale, Jae H. Kang, Michael A. Hauser, Rand R. Allingham, Janey L. Wiggs, and Jonathan L. Haines. “Genome-Wide Pathway Approach to Dissecting Primary Open-Angle Glaucoma.” In Investigative Ophthalmology & Visual Science, Vol. 57. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2016.
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  - Cai, Jingwen, Michelle Dianne Drewry, Kristin Perkumas, Michael Dismuke, Iris Navarro, Michael A. Hauser, W Daniel Starner, and Yutao Liu. “DNA methylation in Human SC Cells with Glaucoma.” In Investigative Ophthalmology & Visual Science, Vol. 57. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2016.
    Link to Item
  - Drewry, Michelle Dianne, Inas Helwa, R Rand Allingham, Michael A. Hauser, and Yutao Liu. “miRNA-Seq in four different normal human ocular tissues.” In Investigative Ophthalmology & Visual Science, Vol. 57. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2016.
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  - Gao, Xiaoyi Raymond, Drew Nannini, Kristen Goulee, Inas F. Aboobakar, R Rand Allingham, Michael A. Hauser, and Yutao Liu. “Differential gene expression and pathway enrichment in the human cornea and retina.” In Investigative Ophthalmology & Visual Science, Vol. 57. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2016.
    Link to Item
  - Igo, Robert P., Jessica Cooke Bailey, William Scott, Rebecca J. Sardell, Margaret A. Pericak-Vance, Louis R. Pasquale, Michael A. Hauser, Terry Gaasterland, Janey L. Wiggs, and Jonathan Haines. “Genetic Association and Linkage at Putative Risk Loci for Primary Open-angle Glaucoma.” In Investigative Ophthalmology & Visual Science, Vol. 57. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2016.
    Link to Item
  - Liu, Yutao, Jessica Cooke Bailey, Inas Helwa, W Daniel Starner, Rachel W. Kuchtey, R Rand Allingham, Michael A. Hauser, Louis R. Pasquale, Jonathan L. Haines, and Laney L. Wiggs. “Association of miR-182 with High Tension Glaucoma.” In Investigative Ophthalmology & Visual Science, Vol. 57. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2016.
    Link to Item
  - Ozaki, Mineo, Francesca Pasutto, Takanori Mizoguchi, Michael A. Hauser, Fotis Topouzis, Michael Dubina, Deepak P. Edward, Ningli Wang, Tin Aung, and Chiea Chuen Khor. “Genome-wide association study comparing patients with exfoliation syndrome and exfoliation glaucoma.” In Investigative Ophthalmology & Visual Science, Vol. 57. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2016.
    Link to Item
  - Pasquale, Louis R., Jessica Cooke Bailey, Jae H. Kang, Hugo Aschard, Michael A. Hauser, R Rand Allingham, David A. Sullivan, Jonathan L. Haines, and Janey L. Wiggs. “Testosterone pathway polymorphisms in relation to primary open angle glaucoma: an analysis stratified by sex.” In Investigative Ophthalmology & Visual Science, Vol. 57. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2016.
    Link to Item
  - Aboobakar, Inas F., Jin Liang, Michael A. Hauser, R Rand Allingham, and W Daniel Stamer. “Cyclic mechanical stress alters LOXL1 gene expression in trabecular meshwork and Schlemm's canal cells.” In Investigative Ophthalmology & Visual Science, Vol. 56. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2015.
    Link to Item
  - Geisert, Eldon E., Felix L. Struebing, Rebecca King, Louis R. Pasquale, Allison E. Ashley-Koch, Michael A. Hauser, R Rand Allingham, and Janey L. Wiggs. “GENOMIC LOCI MODULATING GANGLION CELL DEATH FOLLOWING ELEVATED IOP IN THE MOUSE.” In Investigative Ophthalmology & Visual Science, Vol. 56. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2015.
    Link to Item
  - Hauser, Michael A., Ching-Yu Cheng, R Rand Allingham, Tin Aung, Yih-Chung Tham, Eranga Nishanthie Vithana, Chiea Chuen Khor, and Tien Yin Wong. “A common, protein-coding variant of SIX6 is associated with reduced retinal nerve fiber layer thickness.” In Investigative Ophthalmology & Visual Science, Vol. 56. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2015.
    Link to Item
  - Helwa, Inas, Khaled Abu-Amero, Abdulrahman Al-Muammar, Shelby Strickland, Michael A. Hauser, R Rand Allingham Allingham, and Yutao Liu. “Association between CCT-associated variants and keratoconus in a Saudi Arabian population.” In Investigative Ophthalmology & Visual Science, Vol. 56. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2015.
    Link to Item
  - Kang, Jae H., Hugues Aschard, Michael A. Hauser, Jonathan L. Haines, William Gerard Christen, Peter Kraft, Daniel Ian Chasman, Jessica Cooke Bailey, Janey L. Wiggs, and Louis R. Pasquale. “Age at menopause genetic risk score in relation to primary open-angle glaucoma in the Augmented GLAUGEN study.” In Investigative Ophthalmology & Visual Science, Vol. 56. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2015.
    Link to Item
  - King, Rebecca, Michael A. Hauser, Louis R. Pasquale, Janey L. Wiggs, Allison E. Ashley-Koch, R Rand Allingham, and Eldon E. Geisert. “Mouse Genomic Loci Modulating Corneal Thickness.” In Investigative Ophthalmology & Visual Science, Vol. 56. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2015.
    Link to Item
  - Liu, Yutao, Khaled Abu-Amero, Yelena Bykhovskaya, Arthur Zimmerman, Abdulrahman Al-Muammar, Xiaohui Li, Jerome I. Rotter, R Rand Allingham, Michael A. Hauser, and Yaron S. Rabinowitz. “The Role of Rare Coding Variants in Keratoconus-associated Candidate Genes using Exome Sequencing.” In Investigative Ophthalmology & Visual Science, Vol. 56. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2015.
    Link to Item
  - Ozaki, Mineo, Tin Aung, Takanori Mizoguchi, R Rand Allingham, Robert Ritch, Michael A. Hauser, and Chiea Chuen Khor. “Identification of a novel locus for Exfoliation Syndrome.” In Investigative Ophthalmology & Visual Science, Vol. 56. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2015.
    Link to Item
  - Reddy, Varun, Sharon Freedman, Shelby Strickland, Yu Chen-Hsin, Rachel W. Kuchtey, John Kuchtey, R Rand Allingham, and Michael A. Hauser. “In search of novel CYP1B1 mutations that cause primary congenital glaucoma.” In Investigative Ophthalmology & Visual Science, Vol. 56. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2015.
    Link to Item
  - Struebing, Felix L., Rebecca King, Allison Ashley-Koch, Michael A. Hauser, R Rand Allingham, and Eldon E. Geisert. “Interval mapping reveals a quantitative trait locus controlling retinal ganglion cell number in mice.” In Investigative Ophthalmology & Visual Science, Vol. 56. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2015.
    Link to Item
  - Moylan, Cynthia A., Hyuna Yang, Herbert Pang, Andrew Dellinger, Ayako Suzuki, Hans L. Tillmann, Cynthia D. Guy, et al. “Epigenetic Regulation of Gene Expression in NAFLD.” In Gastroenterology, 142:S929–S929. W B SAUNDERS CO-ELSEVIER INC, 2012.
    Link to Item
  - Moylan, Cynthia A., Andrew Dellinger, Herbert Pang, Ayako Suzuki, Hans L. Tillmann, Daniel Hampton, Yuping Chen, et al. “Modest Alcohol Consumption Attenuates Expression of Fibrosis-Associated Genes in Patients With Non-Alcoholic Fatty Liver Disease (NAFLD).” In Gastroenterology, 140:S914–15. W B SAUNDERS CO-ELSEVIER INC, 2011.
    Link to Item
  - Tillmann, H., A. Suzuki, H. Pang, A. Dellinger, C. D. Guy, C. A. Moylan, D. Piercy, et al. “869 COFFEE CONSUMPTION INCREASES HEPATIC EXPRESSION OF CYTOCHROME P450S AND SIGNIFICANTLY REDUCES LIVER FIBROSIS IN PATIENTS WITH NONALCOHOLIC FATTY LIVER DISEASE (NAFLD).” In Journal of Hepatology, 54:S346–47. Elsevier BV, 2011. https://doi.org/10.1016/s0168-8278(11)60871-4.
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  - Tillmann, Hans L., Herbert Pang, Andrew Dellinger, Ayako Suzuki, Cynthia D. Guy, Cynthia A. Moylan, Dawn Piercy, et al. “Coffee's Beneficial Effect on Liver Disease Confirmed in NASH Cohort, but Only Partially Confirmation of In Vitro Pre-Described Differentially Expressed Genes in This Patient Cohort.” In Gastroenterology, 140:S987–S987, 2011.
    Link to Item
  - Abdelmalek, Manal F., Ayako Suzuki, Silke Schmidt, Jacqueline Rimmler, Aynur Unalp, Cynthia D. Guy, Richard Johnson, Michael A. Hauser, and Anna Mae Diehl. “FRUCTOKINASE POLYMORPHISMS IN PATIENTS WITH NONALCOHOLIC FATTY LIVER DISEASE ARE ASSOCIATED WITH DECREASED URIC ACID AND THE PRESENCE OF HEPATIC FIBROSIS.” In Hepatology, 52:644A-645A. WILEY-BLACKWELL, 2010.
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  - Moylan, Cynthia A., Manal F. Abdelmalek, Herbert Pang, Andrew Dellinger, Steve S. Choi, Alessia Omenetti, Yuping Chen, et al. “SIGNALS FROM THE FIBROTIC LIVER IN PATIENTS WITH NAFLD MAY PROMOTE DIABETES AND OBESITY.” In Hepatology, 52:1049A-1050A. WILEY-BLACKWELL, 2010.
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  - Moylan, Cynthia A., Steve S. Choi, Andrew Dellinger, Herbert Pang, Manal F. Abdelmalek, Daniel Hampton, Yuping Chen, et al. “CONSERVED GENE EXPRESSION PATTERNS IN MYOFIBROBLASTIC MURINE AND HUMAN HEPATIC STELLATE CELLS AND NAFLD PATIENTS WITH LIVER FIBROSIS COMPATIBLE WITH EPITHELIAL-TO-MESENCHYMAL LIKE TRANSITION.” In Hepatology, 52:1286A-1287A. WILEY-BLACKWELL, 2010.
    Link to Item
  - Kwee, Lydia C., Kelli D. Allen, Valerie T. Loiacono, Catherine L. Stanwyck, Heidi J. Munger, Michael A. Hauser, Eugene Z. Oddone, and Silke Schmidt. “Association of the H63D Polymorphism in HFE with ALS in a Population of US Veterans.” In Neurology, 72:A390–A390. LIPPINCOTT WILLIAMS & WILKINS, 2009.
    Link to Item
  - Ebright, J. N., K. Boon, M. A. Hauser, S. P. Daiger, and C. B. Rickman. “Using the human retina and RPE transcriptomes to identify candidate disease genes for retinal dystrophies.” In Investigative Ophthalmology & Visual Science, Vol. 46. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2005.
    Link to Item
  - Challa, P., N. Wagle, M. A. Hauser, S. H. Freedman, M. Pericak-Vance, M. M. McDonald, C. C. Luna, and R. R. Allingham. “Juvenile bilateral lens dislocation, corneal guttatae, and glaucoma associated with a novel mutation in the FBN1 gene.” In Investigative Ophthalmology & Visual Science, Vol. 46. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2005.
    Link to Item
  - Hauser, M. A., F. L. Graham, R. R. Allingham, K. LaRocgue-Abramson, C. M. Santiago, E. DelBono, L. Olson, J. L. Haines, J. L. Wiggs, and M. A. Pericak-Vance. “Evidence for linkage but not association to the GABRB3 region of chromosome 15 in a subset of primary open angle glaucoma (POAG) families.” In Investigative Ophthalmology & Visual Science, 45:U436–U436. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2004.
    Link to Item
  - Lambert, W. S., J. Clapp, D. J. Bolland, A. Jenkinson, J. E. Hewitt, M. Bembe, R. Allingham, J. Vance, and M. A. Hauser. “Expression of genes and ESTs within the HBID duplication region in human conjunctival cell lines and tissue.” In Investigative Ophthalmology & Visual Science, 45:U568–U568. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2004.
    Link to Item
  - Sena, D. R. F., L. R. Pasquale, R. R. Allinghan, M. A. Hauser, M. A. Pericak-Vance, E. A. DelBono, J. L. Haines, and J. L. Wiggs. “Evaluation of NOS3 polymorphisms in patients with primary open angle glaucoma.” In Investigative Ophthalmology & Visual Science, 45:U436–U436. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2004.
    Link to Item
  - Wiggs, J. L., R. R. Allingham, J. Auguste, L. Olsen, K. LaRocque-Abramson, M. A. Hauser, E. A. Del Bono, F. L. Graham, M. A. Pericak-Vance, and J. L. Haines. “Genomic screen for adult-onset primary open angle glaucoma: Follow-up studies suggest loci on 14q11 and 15q.” In Investigative Ophthalmology & Visual Science, 45:U436–U436. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2004.
    Link to Item
  - Hauser, M. A., M. Noureddine, C. M. Hulette, L. Yi-Ju, S. Clemens, and J. M. Vance. “Identification of candidate genes for Parkinson's disease using genetic linkage and gene expression in the substantia nigra.” In Movement Disorders, 19:S364–S364. WILEY-LISS, 2004.
    Link to Item
  - Abramson, K. R., M. A. Hauser, O. A. Marks, C. Santiago, F. L. Graham, E. A. del Bono, M. A. Pericak-Vance, J. L. Wiggs, J. L. Haines, and R. R. Allingham. “Investigating candidate genes and novel ESTS in primary open angle glaucoma.” In American Journal of Human Genetics, 73:542–542. UNIV CHICAGO PRESS, 2003.
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  - Hauser, M. A., M. Noureddine, J. W. Walter, R. W. Walters, C. M. Hulette, D. E. Schmechel, M. L. Bembe, et al. “Genomic convergence: Identification of candidate genes for Parkinson Disease (PD) using genetic linkage and gene expression in the substantia nigra.” In American Journal of Human Genetics, 73:507–507. UNIV CHICAGO PRESS, 2003.
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  - Noureddine, M. A., Y. J. Li, L. Zhang, X. J. Qin, R. W. Walters, M. W. Booze, K. Fujiwara, et al. “Significant association between single-nucleotide polymorphisms in the neuron-specific RNA-binding protein ELAVL4 and Parkinson disease.” In American Journal of Human Genetics, 73:469–469. UNIV CHICAGO PRESS, 2003.
    Link to Item
  - Walter, J. W., R. R. Allingham, J. D. Flor, K. R. Abramson, F. L. Graham, C. S. Cohen, C. Santiago, et al. “Optineurin sequence variants do not contribute to high-tension primary open-angle glaucoma.” In American Journal of Human Genetics, 73:506–506. UNIV CHICAGO PRESS, 2003.
    Link to Item
  - Vance, J. M., Y. Li, A. S. Oliveira, M. A. Hauser, E. R. Martin, W. K. Scott, J. E. Stenger, et al. “Glutathione S-transferase, omega-1 (GSTO1) modifies age at onset of Alzheimer disease and Parkinson disease.” In American Journal of Human Genetics, 73:182–182. UNIV CHICAGO PRESS, 2003.
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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
  - Hauser, M. A., K. R. Abramson, J. L. Wiggs, E. A. del Bono, F. L. Graham, M. A. Pericak-Vance, J. L. Haines, and R. R. Allingham. “Primary open-angle glaucoma (POAG) candidate gene analysis.” In Investigative Ophthalmology & Visual Science, 44:U301–U301. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2003.
    Link to Item
  - Walter, J. W., R. R. Allingham, J. D. Flor, K. R. Abramson, F. L. Graham, E. A. del Bono, J. L. Haines, M. A. Pericak-Vance, M. A. Hauser, and J. L. Wiggs. “Optineurin sequence variants do not predispose to primary open angle glaucoma.” In Investigative Ophthalmology & Visual Science, 44:U203–U203. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2003.
    Link to Item
  - 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
  - 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
  - Garvey, S. M., K. S. Christine, W. C. Wetsel, R. M. Rodriguiz, C. B. Conde, V. Kowaljow, J. M. Stajich, et al. “Transgenic models of LGMD1A: expression of altered human myotilin results in a dominant-negative phenotype.” In American Journal of Human Genetics, 71:195–195. UNIV CHICAGO PRESS, 2002.
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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
  - 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
  - Larocque, K. R., M. A. Hauser, J. L. Wiggs, B. Broomer, E. A. del Bono, F. L. Graham, M. A. Pericak-Vance, J. L. Haines, and R. R. Allingham. “Primary open-angle glaucoma (POAG) candidate gene analysis.” In American Journal of Human Genetics, 71:481–481. UNIV CHICAGO PRESS, 2002.
    Link to Item
  - Walter, J. W., R. R. Allingham, J. D. Flor, K. R. LaRocque, F. L. Graham, B. Broomer, E. A. del Bono, et al. “Optineurin sequence variants do not predispose to primary open angle glaucoma.” In American Journal of Human Genetics, 71:489–489. UNIV CHICAGO PRESS, 2002.
    Link to Item
  - Wiggs, J. L., J. D. Flor, R. R. Allingham, M. A. Pericak-Vance, J. Auguste, K. Rodgers, B. Broomer, E. A. DelBono, J. L. Haines, and M. A. Hauser. “DNA sequence variants in optineurin in patients with primary open angle glaucoma and low tension glaucoma.” In American Journal of Human Genetics, 71:485–485. UNIV CHICAGO PRESS, 2002.
    Link to Item
  - Allingham, R. R., J. L. Wiggs, M. A. Hauser, K. R. LaRocque, B. Broomer, F. L. Graham, E. A. del Bono, J. R. Shi, J. L. Haines, and M. A. Pericak-Vance. “Analysis of TJP1 (tight junction protein 1) as a candidate gene for POAG.” In Investigative Ophthalmology & Visual Science, 43:U959–U959. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2002.
    Link to Item
  - LaRocque, K. R., R. R. Allingham, M. A. Hauser, L. W. Herndon, B. W. Broomer, M. A. Pericak-Vance, and P. Challa. “Novel myocilin mutations in West African individuals with primary open angle glaucoma.” In American Journal of Human Genetics, 69:563–563. UNIV CHICAGO PRESS, 2001.
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  - Challa, P., M. A. Hauser, L. W. Herndon, B. W. Broomer, M. A. Pericak-Vance, and R. R. Allingham. “Novel myocilin mutations in individuals with POAG from West Africa.” In Investigative Ophthalmology & Visual Science, 42:S562–S562. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2001.
    Link to Item
  - Challa, P., M. A. Hauser, M. A. Pericak-Vance, and R. R. Allingham. “Genetic mapping of a syndrome of early-onset lens dislocation.” In Investigative Ophthalmology & Visual Science, 41:S32–S32. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2000.
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- Preprints
  - Docherty, Anna, Niamh Mullins, Allison Ashley-Koch, Xue Qin, Jonathan Coleman, Andrey Shabalin, Jooeun Kang, et al. “Genome-wide association study meta-analysis of suicide attempt in 43,871 cases identifies twelve genome-wide significant loci.” MedRxiv, 2022. https://doi.org/10.1101/2022.07.03.22277199.
    Full Text

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