Fuchs endothelial corneal dystrophy
Elhalis, Hussain, Behrooz Azizi, and Ula Jurkunas. 2010. “Fuchs Endothelial Corneal Dystrophy”. Ocul Surf 8 (4): 173-84.
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Unusual presentation of presumed posterior polymorphous dystrophy associated with iris heterochromia, band keratopathy, and keratoconus
Lam, Helene, Janey Wiggs, and Ula Jurkunas. 2010. “Unusual Presentation of Presumed Posterior Polymorphous Dystrophy Associated With Iris Heterochromia, Band Keratopathy, and Keratoconus”. Cornea 29 (10): 1180-5.
Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error
Cheng, Ching-Yu, Maria Schache, Kamran Ikram, Terri Young, Jeremy Guggenheim, Veronique Vitart, Stuart Macgregor, et al. 2013. “Nine Loci for Ocular Axial Length Identified through Genome-Wide Association Studies, Including Shared Loci With Refractive Error”. Am J Hum Genet 93 (2): 264-77.
52 Genetic Loci Influencing Myocardial Mass
Harst, Pim, Jessica Setten, Niek Verweij, Georg Vogler, Lude Franke, Matthew Maurano, Xinchen Wang, et al. 2016. “52 Genetic Loci Influencing Myocardial Mass”. J Am Coll Cardiol 68 (13): 1435-48.
Recent Advances in Defining the Genetic Basis of Rheumatoid Arthritis
Terao, Chikashi, Soumya Raychaudhuri, and Peter Gregersen. 2016. “Recent Advances in Defining the Genetic Basis of Rheumatoid Arthritis”. Annu Rev Genomics Hum Genet 17: 273-301.
Rheumatoid Factor Is Associated With the Distribution of Hand Joint Destruction in Rheumatoid Arthritis
Terao, Chikashi, Noriyuki Yamakawa, Koichiro Yano, Iris Markusse, Katsunori Ikari, Shinji Yoshida, Moritoshi Furu, et al. 2015. “Rheumatoid Factor Is Associated With the Distribution of Hand Joint Destruction in Rheumatoid Arthritis”. Arthritis Rheumatol 67 (12): 3113-23.
Partitioning heritability by functional annotation using genome-wide association summary statistics
Finucane, Hilary, Brendan Bulik-Sullivan, Alexander Gusev, Gosia Trynka, Yakir Reshef, Po-Ru Loh, Verneri Anttila, et al. 2015. “Partitioning Heritability by Functional Annotation Using Genome-Wide Association Summary Statistics”. Nat Genet 47 (11): 1228-35.
Rare genetic variants in the CFI gene are associated with advanced age-related macular degeneration and commonly result in reduced serum factor I levels
Kavanagh, David, Yi Yu, Elizabeth Schramm, Michael Triebwasser, Erin Wagner, Soumya Raychaudhuri, Mark Daly, John Atkinson, and Johanna Seddon. 2015. “Rare Genetic Variants in the CFI Gene Are Associated With Advanced Age-Related Macular Degeneration and Commonly Result in Reduced Serum Factor I Levels”. Hum Mol Genet 24 (13): 3861-70.
Accurate and fast multiple-testing correction in eQTL studies
Sul, Jae Hoon, Towfique Raj, Simone Jong, Paul Bakker, Soumya Raychaudhuri, Roel Ophoff, Barbara Stranger, Eleazar Eskin, and Buhm Han. 2015. “Accurate and Fast Multiple-Testing Correction in EQTL Studies”. Am J Hum Genet 96 (6): 857-68.
Biological interpretation of genome-wide association studies using predicted gene functions
Pers, Tune, Juha Karjalainen, Yingleong Chan, Harm-Jan Westra, Andrew Wood, Jian Yang, Julian Lui, et al. 2015. “Biological Interpretation of Genome-Wide Association Studies Using Predicted Gene Functions”. Nat Commun 6: 5890.