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Yarwood, Annie, Sebastien Viatte, Yukinori Okada, Robert Plenge, Kazuhiko Yamamoto, RACI BRAGGSS, Anne Barton, et al. 2016. “Loci Associated With N-Glycosylation of Human IgG Are Not Associated With Rheumatoid Arthritis: A Mendelian Randomisation Study”. Ann Rheum Dis 75 (1): 317-20.

Won, Hong-Hee, Pradeep Natarajan, Amanda Dobbyn, Daniel Jordan, Panos Roussos, Kasper Lage, Soumya Raychaudhuri, Eli Stahl, and Ron Do. 2015. “Disproportionate Contributions of Select Genomic Compartments and Cell Types to Genetic Risk for Coronary Artery Disease”. PLoS Genet 11 (10): e1005622.

Kim, Kwangwoo, Xia Jiang, Jing Cui, Bing Lu, Karen Costenbader, Jeffrey Sparks, So-Young Bang, et al. 2015. “Interactions Between Amino Acid-Defined Major Histocompatibility Complex Class II Variants and Smoking in Seropositive Rheumatoid Arthritis”. Arthritis Rheumatol 67 (10): 2611-23.

Hayes, James, Gosia Trynka, Joseph Vijai, Kenneth Offit, Soumya Raychaudhuri, and Robert Klein. 2015. “Tissue-Specific Enrichment of Lymphoma Risk Loci in Regulatory Elements”. PLoS One 10 (9): e0139360.

Scott, Ian, Frühling Rijsdijk, Jemma Walker, Jelmar Quist, Sarah Spain, Rachael Tan, Sophia Steer, et al. 2015. “Do Genetic Susceptibility Variants Associate With Disease Severity in Early Active Rheumatoid Arthritis?”. J Rheumatol 42 (7): 1131-40.

Gutierrez-Achury, Javier, Alexandra Zhernakova, Sara Pulit, Gosia Trynka, Karen Hunt, Jihane Romanos, Soumya Raychaudhuri, David Heel, Cisca Wijmenga, and Paul Bakker. 2015. “Fine Mapping in the MHC Region Accounts for 18% Additional Genetic Risk for Celiac Disease”. Nat Genet 47 (6): 577-8.

Kim, Kwangwoo, So-Young Bang, Hye-Soon Lee, Soo-Kyung Cho, Chan-Bum Choi, Yoon-Kyoung Sung, Tae-Hwan Kim, et al. 2015. “High-Density Genotyping of Immune Loci in Koreans and Europeans Identifies Eight New Rheumatoid Arthritis Risk Loci”. Ann Rheum Dis 74 (3): e13.

Roussos, Panos, Amanda Mitchell, Georgios Voloudakis, John Fullard, Venu Pothula, Jonathan Tsang, Eli Stahl, et al. 2014. “A Role for Noncoding Variation in Schizophrenia”. Cell Rep 9 (4): 1417-29.

Gusev, Alexander, Hong Lee, Gosia Trynka, Hilary Finucane, Bjarni Vilhjálmsson, Han Xu, Chongzhi Zang, et al. 2014. “Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases”. Am J Hum Genet 95 (5): 535-52.

Yu, Yi, Michael Triebwasser, Edwin Wong, Elizabeth Schramm, Brett Thomas, Robyn Reynolds, Elaine Mardis, et al. 2014. “Whole-Exome Sequencing Identifies Rare, Functional CFH Variants in Families With Macular Degeneration”. Hum Mol Genet 23 (19): 5283-93.