Imputing amino acid polymorphisms in human leukocyte antigens von Jia, Xiaoming, Han, Buhm, Onengut-Gumuscu, Suna, Chen, Wei-Min, Concannon, Patrick J, Rich, Stephen S, Raychaudhuri, Soumya, de Bakker, Paul I W

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Robust relationship inference in genome-wide association studies von Manichaikul, Ani, Mychaleckyj, Josyf C., Rich, Stephen S., Daly, Kathy, Sale, Michèle, Chen, Wei-Min

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Precision Medicine in Diabetes: A Consensus Report From the American Diabetes Association (ADA) and the European Association for the Study of Diabetes (EASD) von Chung, Wendy K, Erion, Karel, Florez, Jose C, Hattersley, Andrew T, Hivert, Marie-France, Lee, Christine G, McCarthy, Mark I, Nolan, John J, Norris, Jill M, Pearson, Ewan R, Philipson, Louis, McElvaine, Allison T, Cefalu, William T, Rich, Stephen S, Franks, Paul W

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Development and Standardization of an Improved Type 1 Diabetes Genetic Risk Score for Use in Newborn Screening and Incident Diagnosis von Sharp, Seth A, Rich, Stephen S, Wood, Andrew R, Jones, Samuel E, Beaumont, Robin N, Harrison, James W, Schneider, Darius A, Locke, Jonathan M, Tyrrell, Jess, Weedon, Michael N, Hagopian, William A, Oram, Richard A

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Gut Microbiomes of Malawian Twin Pairs Discordant for Kwashiorkor von Smith, Michelle I., Yatsunenko, Tanya, Manary, Mark J., Trehan, Indi, Mkakosya, Rajhab, Cheng, Jiye, Kau, Andrew L., Rich, Stephen S., Concannon, Patrick, Mychaleckyj, Josyf C., Liu, Jie, Houpt, Eric, Li, Jia V., Holmes, Elaine, Nicholson, Jeremy, Knights, Dan, Ursell, Luke K., Knight, Rob, Gordon, Jeffrey I.

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Additive and interaction effects at three amino acid positions in HLA-DQ and HLA-DR molecules drive type 1 diabetes risk von Hu, Xinli, Deutsch, Aaron J, Lenz, Tobias L, Onengut-Gumuscu, Suna, Han, Buhm, Chen, Wei-Min, Howson, Joanna M M, Todd, John A, de Bakker, Paul I W, Rich, Stephen S, Raychaudhuri, Soumya

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Monogenic Diabetes: From Genetic Insights to Population-Based Precision in Care. Reflections From a Diabetes Care Editors' Expert Forum von Riddle, Matthew C, Philipson, Louis H, Rich, Stephen S, Carlsson, Annelie, Franks, Paul W, Greeley, Siri Atma W, Nolan, John J, Pearson, Ewan R, Zeitler, Philip S, Hattersley, Andrew T

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Fine-mapping and functional studies highlight potential causal variants for rheumatoid arthritis and type 1 diabetes von Westra, Harm-Jan, Martínez-Bonet, Marta, Onengut-Gumuscu, Suna, Lee, Annette, Luo, Yang, Teslovich, Nikola, Worthington, Jane, Martin, Javier, Huizinga, Tom, Klareskog, Lars, Rantapaa-Dahlqvist, Solbritt, Chen, Wei-Min, Quinlan, Aaron, Todd, John A., Eyre, Steve, Nigrovic, Peter A., Gregersen, Peter K., Rich, Stephen S., Raychaudhuri, Soumya

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Genetics and its potential to improve type 1 diabetes care von Rich, Stephen S

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Sexually Dimorphic Crosstalk at the Maternal-Fetal Interface von Sun, Tianyanxin, Gonzalez, Tania L, Deng, Nan, DiPentino, Rosemarie, Clark, Ekaterina L, Lee, Bora, Tang, Jie, Wang, Yizhou, Stripp, Barry R, Yao, Changfu, Tseng, Hsian-Rong, Karumanchi, S Ananth, Koeppel, Alexander F, Turner, Stephen D, Farber, Charles R, Rich, Stephen S, Wang, Erica T, Williams, John, Pisarska, Margareta D

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Functional IL6R 358Ala allele impairs classical IL-6 receptor signaling and influences risk of diverse inflammatory diseases von Ferreira, Ricardo C, Freitag, Daniel F, Cutler, Antony J, Howson, Joanna M M, Rainbow, Daniel B, Smyth, Deborah J, Kaptoge, Stephen, Clarke, Pamela, Boreham, Charlotte, Coulson, Richard M, Pekalski, Marcin L, Chen, Wei-Min, Onengut-Gumuscu, Suna, Rich, Stephen S, Butterworth, Adam S, Malarstig, Anders, Danesh, John, Todd, John A

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Human airway branch variation and chronic obstructive pulmonary disease von Smith, Benjamin M., Traboulsi, Hussein, Austin, John H. M., Manichaikul, Ani, Hoffman, Eric A., Bleecker, Eugene R., Cardoso, Wellington V., Cooper, Christopher, Couper, David J., Dashnaw, Stephen M., Guo, Jia, Han, MeiLan K., Hansel, Nadia N., Hughes, Emlyn W., Jacobs, David R., Kanner, Richard E., Kaufman, Joel D., Kleerup, Eric, Lin, Ching-Long, Liu, Kiang, Cascio, Christian M. Lo, Martinez, Fernando J., Nguyen, Jennifer N., Prince, Martin R., Rennard, Stephen, Rich, Stephen S., Simon, Leora, Sun, Yanping, Watson, Karol E., Woodruff, Prescott G., Baglole, Carolyn J., Barr, R. Graham

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Genome-wide discovery for diabetes-dependent triglycerides-associated loci von Selvaraj, Margaret Sunitha, Paruchuri, Kaavya, Haidermota, Sara, Bernardo, Rachel, Rich, Stephen S, Peloso, Gina M, Natarajan, Pradeep

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Leveraging type 1 diabetes human genetic and genomic data in the T1D knowledge portal von Kudtarkar, Parul, Costanzo, Maria C, Sun, Ying, Jang, Dongkeun, Koesterer, Ryan, Mychaleckyj, Josyf C, Nayak, Uma, Onengut-Gumuscu, Suna, Rich, Stephen S, Flannick, Jason A, Gaulton, Kyle J, Burtt, Noël P

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Role of Type 1 Diabetes-Associated SNPs on Risk of Autoantibody Positivity in the TEDDY Study von Törn, Carina, Hadley, David, Lee, Hye-Seung, Hagopian, William, Lernmark, Åke, Simell, Olli, Rewers, Marian, Ziegler, Anette, Schatz, Desmond, Akolkar, Beena, Onengut-Gumuscu, Suna, Chen, Wei-Min, Toppari, Jorma, Mykkänen, Juha, Ilonen, Jorma, Rich, Stephen S, She, Jin-Xiong, Steck, Andrea K, Krischer, Jeffrey

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Genetic modification of inflammation- and clonal hematopoiesis-associated cardiovascular risk von Yu, Zhi, Fidler, Trevor P, Ruan, Yunfeng, Vlasschaert, Caitlyn, Nakao, Tetsushi, Uddin, Md Mesbah, Mack, Taralynn, Niroula, Abhishek, Heimlich, J Brett, Zekavat, Seyedeh M, Gibson, Christopher J, Griffin, Gabriel K, Wang, Yuxuan, Peloso, Gina M, Heard-Costa, Nancy, Levy, Daniel, Vasan, Ramachandran S, Aguet, François, Ardlie, Kristin G, Taylor, Kent D, Rich, Stephen S, Rotter, Jerome I, Libby, Peter, Jaiswal, Siddhartha, Ebert, Benjamin L, Bick, Alexander G, Tall, Alan R, Natarajan, Pradeep

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Guidelines for Large-Scale Sequence-Based Complex Trait Association Studies: Lessons Learned from the NHLBI Exome Sequencing Project von Auer, Paul L., Reiner, Alex P., Wang, Gao, Kang, Hyun Min, Abecasis, Goncalo R., Altshuler, David, Bamshad, Michael J., Nickerson, Deborah A., Tracy, Russell P., Rich, Stephen S., Leal, Suzanne M.

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Neurocognitive trajectory and proteomic signature of inherited risk for Alzheimer's disease von Paranjpe, Manish D, Chaffin, Mark, Zahid, Sohail, Ritchie, Scott, Rotter, Jerome I, Rich, Stephen S, Gerszten, Robert, Guo, Xiuqing, Heckbert, Susan, Tracy, Russ, Danesh, John, Lander, Eric S, Inouye, Michael, Kathiresan, Sekar, Butterworth, Adam S, Khera, Amit V

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The impact of Mendelian sleep and circadian genetic variants in a population setting von Weedon, Michael N, Jones, Samuel E, Lane, Jacqueline M, Lee, Jiwon, Ollila, Hanna M, Dawes, Amy, Tyrrell, Jess, Beaumont, Robin N, Partonen, Timo, Merikanto, Ilona, Rich, Stephen S, Rotter, Jerome I, Frayling, Timothy M, Rutter, Martin K, Redline, Susan, Sofer, Tamar, Saxena, Richa, Wood, Andrew R

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Identification of breast cancer associated variants that modulate transcription factor binding von Liu, Yunxian, Walavalkar, Ninad M, Dozmorov, Mikhail G, Rich, Stephen S, Civelek, Mete, Guertin, Michael J

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