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Okada, Yukinori, Kwangwoo Kim, Buhm Han, Nisha Pillai, Rick Ong, Woei-Yuh Saw, Ma Luo, et al. 2014. “Risk for ACPA-Positive Rheumatoid Arthritis Is Driven by Shared HLA Amino Acid Polymorphisms in Asian and European Populations”. Hum Mol Genet 23 (25): 6916-26.

Trynka, Gosia, and Soumya Raychaudhuri. 2013. “Using Chromatin Marks to Interpret and Localize Genetic Associations to Complex Human Traits and Diseases”. Curr Opin Genet Dev 23 (6): 635-41.

Trynka, Gosia, Cynthia Sandor, Buhm Han, Han Xu, Barbara Stranger, Shirley Liu, and Soumya Raychaudhuri. 2013. “Chromatin Marks Identify Critical Cell Types for Fine Mapping Complex Trait Variants”. Nat Genet 45 (2): 124-30.

Li, Gang, Dorothee Diogo, Di Wu, Jim Spoonamore, Vlado Dancik, Lude Franke, Fina Kurreeman, et al. 2013. “Human Genetics in Rheumatoid Arthritis Guides a High-Throughput Drug Screen of the CD40 Signaling Pathway”. PLoS Genet 9 (5): e1003487.

Diogo, Dorothee, Fina Kurreeman, Eli Stahl, Katherine Liao, Namrata Gupta, Jeffrey Greenberg, Manuel Rivas, et al. 2013. “Rare, Low-Frequency, and Common Variants in the Protein-Coding Sequence of Biological Candidate Genes from GWASs Contribute to Risk of Rheumatoid Arthritis”. Am J Hum Genet 92 (1): 15-27.

Raychaudhuri, Soumya, Cynthia Sandor, Eli Stahl, Jan Freudenberg, Hye-Soon Lee, Xiaoming Jia, Lars Alfredsson, et al. 2012. “Five Amino Acids in Three HLA Proteins Explain Most of the Association Between MHC and Seropositive Rheumatoid Arthritis”. Nat Genet 44 (3): 291-6.

Chen, Stahl, Kurreeman, Gregersen, Siminovitch, Worthington, Padyukov, Raychaudhuri, and Plenge. 2011. “Fine Mapping the TAGAP Risk Locus in Rheumatoid Arthritis”. Genes Immun 12 (4): 314-8.

Raychaudhuri, Soumya, Brian Thomson, Elaine Remmers, Stephen Eyre, Anne Hinks, Candace Guiducci, Joseph Catanese, et al. 2009. “Genetic Variants at CD28, PRDM1 and CD2/CD58 Are Associated With Rheumatoid Arthritis Risk”. Nat Genet 41 (12): 1313-8.

De Jager, Philip, Xiaoming Jia, Joanne Wang, Paul Bakker, Linda Ottoboni, Neelum Aggarwal, Laura Piccio, et al. 2009. “Meta-Analysis of Genome Scans and Replication Identify CD6, IRF8 and TNFRSF1A As New Multiple Sclerosis Susceptibility Loci”. Nat Genet 41 (7): 776-82.

Bitar, Maya, Cailing Liu, Alireza Ziaei, Yuming Chen, Thore Schmedt, and Ula Jurkunas. 2012. “Decline in DJ-1 and Decreased Nuclear Translocation of Nrf2 in Fuchs Endothelial Corneal Dystrophy”. Invest Ophthalmol Vis Sci 53 (9): 5806-13.