Advances in the genetics of inflammatory bowel disease by Cho, Judy H

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Fine-mapping inflammatory bowel disease loci to single-variant resolution by Huang, Hailiang, Fang, Ming, Jostins, Luke, Umićević Mirkov, Maša, Boucher, Gabrielle, Anderson, Carl A., Andersen, Vibeke, Cleynen, Isabelle, Cortes, Adrian, Crins, François, D’Amato, Mauro, Deffontaine, Valérie, Dmitrieva, Julia, Docampo, Elisa, Elansary, Mahmoud, Farh, Kyle Kai-How, Franke, Andre, Gori, Ann-Stephan, Goyette, Philippe, Halfvarson, Jonas, Haritunians, Talin, Knight, Jo, Lawrance, Ian C., Lees, Charlie W., Louis, Edouard, Mariman, Rob, Meuwissen, Theo, Mni, Myriam, Momozawa, Yukihide, Parkes, Miles, Spain, Sarah L., Théâtre, Emilie, Trynka, Gosia, Satsangi, Jack, van Sommeren, Suzanne, Vermeire, Severine, Xavier, Ramnik J., Weersma, Rinse K., Duerr, Richard H., Mathew, Christopher G., Rioux, John D., McGovern, Dermot P. B., Cho, Judy H., Georges, Michel, Daly, Mark J., Barrett, Jeffrey C.

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Very Early Onset Inflammatory Bowel Disease: A Clinical Approach With a Focus on the Role of Genetics and Underlying Immune Deficiencies by Ouahed, Jodie, Spencer, Elizabeth, Kotlarz, Daniel, Shouval, Dror S, Kowalik, Matthew, Peng, Kaiyue, Field, Michael, Grushkin-Lerner, Leslie, Pai, Sung-Yun, Bousvaros, Athos, Cho, Judy, Argmann, Carmen, Schadt, Eric, Mcgovern, Dermot P B, Mokry, Michal, Nieuwenhuis, Edward, Clevers, Hans, Powrie, Fiona, Uhlig, Holm, Klein, Christoph, Muise, Aleixo, Dubinsky, Marla, Snapper, Scott B

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Transcript expression-aware annotation improves rare variant interpretation by Cummings, Beryl B., Karczewski, Konrad J., Kosmicki, Jack A., Seaby, Eleanor G., Watts, Nicholas A., Singer-Berk, Moriel, Mudge, Jonathan M., Karjalainen, Juha, Satterstrom, F. Kyle, O’Donnell-Luria, Anne H., Poterba, Timothy, Seed, Cotton, Solomonson, Matthew, Alföldi, Jessica, Daly, Mark J., MacArthur, Daniel G.

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THE ROLE OF GROUP 3 INNATE LYMPHOID CELLS (ILC3) IN GM-CSF/CSF2RB-DEPENDENT INTESTINAL HOMEOSTASIS IN CROHN’S DISEASE by Chuang, Ling-shiang, Morrison, Joshua, Chai, Zhi, Korie, Ujunwa, Mortha, Arthur, Gnjatic, Sacha, Cho, Judy

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Evaluating drug targets through human loss-of-function genetic variation by Minikel, Eric Vallabh, Karczewski, Konrad J., Martin, Hilary C., Cummings, Beryl B., Whiffin, Nicola, Rhodes, Daniel, Alföldi, Jessica, Trembath, Richard C., van Heel, David A., Daly, Mark J., Schreiber, Stuart L., MacArthur, Daniel G.

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REPOGRAMING OF THE INTESTINAL IMMUNE CELL COMPARTMENT DEFINES THE RESPONSE TO AUTOLOGOUS STEM CELL TRANSPLANTATION IN CROHNS DISEASE by Guisado, Daniela, Talware, Sayali, Singh, Shishir, Gold, Stephanie, Mansi, Moutasem, Fozilov, Elbek, Etra, Aaron, Cho, Judy, Cohen, Louis

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Coronary Risk Estimation Based on Clinical Data in Electronic Health Records by Petrazzini, Ben O., Chaudhary, Kumardeep, Márquez-Luna, Carla, Forrest, Iain S., Rocheleau, Ghislain, Cho, Judy, Narula, Jagat, Nadkarni, Girish, Do, Ron

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Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes by Wang, Qingbo, Pierce-Hoffman, Emma, Cummings, Beryl B., Alföldi, Jessica, Francioli, Laurent C., Gauthier, Laura D., Hill, Andrew J., O’Donnell-Luria, Anne H., Karczewski, Konrad J., MacArthur, Daniel G.

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Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals by Whiffin, Nicola, Karczewski, Konrad J., Zhang, Xiaolei, Chothani, Sonia, Smith, Miriam J., Evans, D. Gareth, Roberts, Angharad M., Quaife, Nicholas M., Schafer, Sebastian, Rackham, Owen, Alföldi, Jessica, O’Donnell-Luria, Anne H., Francioli, Laurent C., Cook, Stuart A., Barton, Paul J. R., MacArthur, Daniel G., Ware, James S.

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A genome scan in 260 inflammatory bowel disease‐affected relative pairs by Barmada, M. Michael, Brant, Steven R., Nicolae, Dan L., Achkar, Jean‐Paul, Panhuysen, Carolien I., Bayless, Theodore M., Cho, Judy H., Duerr, Richard H.

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A genome scan in 260 inflammatory bowel disease‐affected relative pairs by Barmada, M. Michael, Brant, Steven R., Nicolae, Dan L., Achkar, Jean‐Paul, Panhuysen, Carolien I., Bayless, Theodore M., Cho, Judy H., Duerr, Richard H.

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The IBD international genetics consortium provides further evidence for linkage to IBD4 and shows gene‐environment interaction by Pierik, Marie, Yang, Huiying, Barmada, Michael M., Cavanaugh, Juleen A., Annese, Vito, Brant, Steven R., Cho, Judy H., Duerr, Richard H., Hugot, Jean‐Pierre, McGovern, Dermot P., Paavola‐Sakki, Paulina, Radford‐Smith, Graham L., Pavli, P., Silverberg, Mark S., Schreiber, Stephan, Taylor, Kent D., Vlietinck, Robert

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Predictors of Hospital Readmissions for Ulcerative Colitis in the United States: A National Database Study by Poojary, Priti, Saha, Aparna, Chauhan, Kinsuk, Simoes, Priya, Sands, Bruce E, Cho, Judy, Ullman, Thomas, Nadkarni, Girish, Ungaro, Ryan

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Earlier Anti-Tumor Necrosis Factor Therapy of Crohn’s Disease Correlates with Slower Progression of Bowel Damage by Panchal, Hinaben, Wagner, Mathilde, Chatterji, Manjil, Taouli, Bachir, McBride, Russell, Patterson, Jeromy R., Ungaro, Ryan, Dubinsky, Marla, Cho, Judy, Sachar, David B.

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Linkage and linkage disequilibrium in chromosome band 1p36 in American Chaldeans with inflammatory bowel disease by Cho, J H, Nicolae, D L, Ramos, R, Fields, C T, Rabenau, K, Corradino, S, Brant, S R, Espinosa, R, LeBeau, M, Hanauer, S B, Bodzin, J, Bonen, D K

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Guilt by rewiring: gene prioritization through network rewiring in Genome Wide Association Studies by Hou, Lin, Chen, Min, Zhang, Clarence K., Cho, Judy, Zhao, Hongyu

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Comparisons of multi-marker association methods to detect association between a candidate region and disease by Ballard, David H., Cho, Judy, Zhao, Hongyu

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Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease by Zhou, Wei, Tsuo, Kristin, Hirbo, Jibril B., Wang, Ying, Bhattacharya, Arjun, Zhao, Huiling, Surakka, Ida, Wolford, Brooke N., Lo Faro, Valeria, Lopera-Maya, Esteban A., Läll, Kristi, Favé, Marie-Julie, Chapman, Sinéad B., Karjalainen, Juha, Maasha, Mutaamba, Chavan, Sameer, Daya, Michelle, Ding, Yi, Feng, Yen-Chen A., Guare, Lindsay A., Gignoux, Christopher R., Graham, Sarah E., Ingold, Nathan, Ismail, Said I., Laisk, Triin, Lin, Kuang, Millwood, Iona Y., Moreno-Grau, Sonia, Nam, Kisung, Palta, Priit, Saad, Chadi, Setia-Verma, Shefali, Thorsteinsdottir, Unnur, Verma, Anurag, Zawistowski, Matthew, Afifi, Nahla, Al-Dabhani, Kawthar M., Campbell, Archie, Crooks, Kristy, Fritsche, Lars G., Fthenou, Eleni, Guo, Yu, Hunt, Karen A., Ioannidis, Alexander, Jansonius, Nomdo M., Konuma, Takahiro, Lee, Ming Ta Michael, Lopez-Pineda, Arturo, Matsuda, Yuta, Marioni, Riccardo E., Numakura, Kensuke, Patil, Snehal, Richmond, Anne, Rojas-Muñoz, Agustin, Shortt, Jonathan A., Tao, Ran, Vanderwerff, Brett, Vernekar, Manvi, Veturi, Yogasudha, Barnes, Kathleen C., Chen, Zhengming, Smith, George Davey, Finucane, Hilary K., Gamazon, Eric R., Gaunt, Tom R., Ge, Tian, Katsanis, Nicholas, Koskela, Jukka T., Law, Matthew H., Li, Liming, Loos, Ruth J.F., Matsuda, Koichi, Olsen, Catherine M., Shavit, Jordan A., Snieder, Harold, Takano, Tomohiro, Vonk, Judith M., Wicks, Stephen J., Wijmenga, Cisca, Wright, John, Zhou, Xiang, Awadalla, Philip, Boehnke, Michael, Bustamante, Carlos D., Fatumo, Segun, Hayward, Caroline, Hveem, Kristian, Kenny, Eimear E., Lee, Seunggeun, Mbarek, Hamdi, Mägi, Reedik, Martin, Hilary C., Medland, Sarah E., Palotie, Aarno V., Pasaniuc, Bogdan, Rader, Daniel J., Ritchie, Marylyn D., Smoller, Jordan W., Stefansson, Kari, Martin, Alicia R.

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A common variant in PNPLA3 is associated with age at diagnosis of NAFLD in patients from a multi-ethnic biobank by Walker, Ryan W., Belbin, Gillian M., Sorokin, Elena P., Van Vleck, Tielman, Wojcik, Genevieve L., Moscati, Arden, Gignoux, Christopher R., Cho, Judy, Abul-Husn, Noura S., Nadkarni, Girish, Kenny, Eimear E., Loos, Ruth J.F.

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