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Transethnic analysis of the human leukocyte antigen region for ulcerative colitis reveals not only shared but also ethnicity-specific disease associations

Autor: Degenhardt, Frauke, Mayr, Gabriele, Wendorff, Mareike, Boucher, Gabrielle, Ellinghaus, Eva, Ellinghaus, David, ElAbd, Hesham, Rosati, Elisa, Hubenthal, Matthias, Juzenas, Simonas, Abedian, Shifteh, Vahedi, Homayoon, Thelma, B. K., Yang, Suk-Kyan, Duk Ye, Byong, Cheon, Jae Hee, Datta, Lisa Wu, Dariany, Naser Ebrahim, Ellul, Pierre, Esaki, Motohiro, Fuyuno, Yuta, McGovern, Dermot PB, Haritunians, Talin, Hong, Myhunghee, Juyal, Garima, Jung, Eun Suk, Kubo, Michiaki, Kugathasan, Subra, Lenz, Tobias L., Leslie, Stephen, Malekzadeh, Reza, Midha, Vandana, Motyer, Allan, Ng, Siew C, Okou, David T, Raychaudhuri, Soumya, Schembri, John, Schreiber, Stefan, Song, Kyuyoung, Sood, Ajit, Takahashi, Atsushi, Torres, Esther A., Umeno, Junji, Alizadeh, Behrooz Z., Weersma, Rinse K, Wong, Sunny H., Yamazaki, Keiko, Karlsen, Tom Hemming, Rioux, John D, Brant, Steven R, Franke, Andre

Publikováno v: Degenhardt, Frauke Mayr, Gabriele Wendorff, Mareike Boucher, Gabrielle Ellinghaus, Eva Ellinghaus, David ElAbd, Hesham Rosati, Elisa Hubenthal, Matthias Juzenas, Simonas Abedian, Shifteh Vahedi, Homayoon Thelma, B. K. Yang, Suk-Kyan Duk Ye, Byong Cheon, Jae Hee Datta, Lisa Wu Dariany, Naser Ebrahim Ellul, Pierre Esaki, Motohiro Fuyuno, Yuta McGovern, Dermot PB Haritunians, Talin Hong, Myhunghee Juyal, Garima Jung, Eun Suk Kubo, Michiaki Kugathasan, Subra Lenz, Tobias L. Leslie, Stephen Malekzadeh, Reza Midha, Vandana Motyer, Allan Ng, Siew C Okou, David T Raychaudhuri, Soumya Schembri, John Schreiber, Stefan Song, Kyuyoung Sood, Ajit Takahashi, Atsushi Torres, Esther A. Umeno, Junji Alizadeh, Behrooz Z. Weersma, Rinse K Wong, Sunny H. Yamazaki, Keiko Karlsen, Tom Hemming Rioux, John D Brant, Steven R Franke, Andre . Transethnic analysis of the human leukocyte antigen region for ulcerative colitis reveals not only shared but also ethnicity-specific disease associations. Human Molecular Genetics. 2021
Human Molecular Genetics

Externí odkaz: http://hdl.handle.net/10852/92296
https://www.duo.uio.no/bitstream/handle/10852/92296/1/ddab017.pdf

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Identification of PKD1L1 Gene Variants in Children with the Biliary Atresia Splenic Malformation Syndrome

Autor: Berauer, John-Paul, Mezina, Anya I., Okou, David T., Sabo, Aniko, Muzny, Donna M., Gibbs, Richard A., Hegde, Madhuri R., Chopra, Pankaj, Cutler, David J., Perlmutter, David H., Bull, Laura N., Thompson, Richard J., Loomes, Kathleen M., Spinner, Nancy B., Rajagopalan, Ramakrishnan, Guthery, Stephen L., Moore, Barry, Yandell, Mark, Harpavat, Sanjiv, Magee, John C., Kamath, Binita M., Molleston, Jean P., Bezerra, Jorge A., Murray, Karen F., Alonso, Estella M., Rosenthal, Philip, Squires, Robert H., Wang, Kasper S., Finegold, Milton J., Russo, Pierre, Sherker, Averell H., Sokol, Ronald J., Karpen, Saul J.

Publikováno v: Hepatology

Biliary atresia (BA) is the most common cause of end-stage liver disease in children and the primary indication for pediatric liver transplantation, yet underlying etiologies remain unknown. Approximately 10% of infants affected by BA exhibit various

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::3082d0302215e222eb01ab4a56e009aa
https://europepmc.org/articles/PMC6642859/