Andrew J Schork
The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions.
Rahmioglu N, Mortlock S, Ghiasi M, Møller P, Stefansdottir L, Galarneau G, Turman C, Danning R, Law M, Sapkota Y, Christofidou P, Skarp S, Giri A, Banasik K, Krassowski M, Lepamets M, Marciniak B, Nõukas M, Perro D, Sliz E, Sobalska-Kwapis M, Thorleifsson G, Topbas-Selcuki N, Vitonis A, Westergaard D, Arnadottir R, Burgdorf K, Campbell A, Cheuk C, Clementi C, Cook J, De Vivo I, DiVasta A, Dorien O, Donoghue J, Edwards T, Fontanillas P, Fung J, Geirsson R, Girling J, Harkki P, Harris H, Healey M, Heikinheimo O, Holdsworth-Carson S, Hostettler I, Houlden H, Houshdaran S, Irwin J, Jarvelin M, Kamatani Y, Kennedy S, Kepka E, Kettunen J, Kubo M, Kulig B, Kurra V, Laivuori H, Laufer M, Lindgren C, MacGregor S, Mangino M, Martin N, Matalliotaki C, Matalliotakis M, Murray A, Ndungu A, Nezhat C, Olsen C, Opoku-Anane J, Padmanabhan S, Paranjpe M, Peters M, Polak G, Porteous D, Rabban J, Rexrode K, Romanowicz H, Saare M, Saavalainen L, Schork A, Sen S, Shafrir A, Siewierska-Górska A, Słomka M, Smith B, Smolarz B, Szaflik T, Szyłło K, Takahashi A, Terry K, Tomassetti C, Treloar S, Vanhie A, Vincent K, Vo K, Werring D, Zeggini E, Zervou M, DBDS Genomic Consortium, FinnGen Study, FinnGen Endometriosis Taskforce, Celmatix Research Team, 23andMe Research Team, Adachi S, Buring J, Ridker P, D'Hooghe T, Goulielmos G, Hapangama D, Hayward C, Horne A, Low S, Martikainen H, Chasman D, Rogers P, Saunders P, Sirota M, Spector T, Strapagiel D, Tung J, Whiteman D, Giudice L, Velez Edwards D, Uimari O, Kraft P, Salumets A, Nyholt D, Mägi R, Stefansson K, Becker C, Yurttas-Beim P, Steinthorsdottir V, Nyegaard M, Missmer S, Montgomery G, Morris A, Zondervan K. The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions. Nat Genet 2023; 55:423-436.
13.03.2023The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions.
13.03.2023Nat Genet 2023; 55:423-436
Rahmioglu Nilufer, Mortlock Sally, Ghiasi Marzieh, Møller Peter L, Stefansdottir Lilja, Galarneau Geneviève, Turman Constance, Danning Rebecca, Law Matthew H, Sapkota Yadav, Christofidou Paraskevi, Skarp Sini, Giri Ayush, Banasik Karina, Krassowski Michal, Lepamets Maarja, Marciniak Błażej, Nõukas Margit, Perro Danielle, Sliz Eeva, Sobalska-Kwapis Marta, Thorleifsson Gudmar, Topbas-Selcuki Nura F, Vitonis Allison, Westergaard David, Arnadottir Ragnheidur, Burgdorf Kristoffer S, Campbell Archie, Cheuk Cecilia S K, Clementi Caterina, Cook James P, De Vivo Immaculata, DiVasta Amy, Dorien O, Donoghue Jacqueline F, Edwards Todd L, Fontanillas Pierre, Fung Jenny N, Geirsson Reynir T, Girling Jane E, Harkki Paivi, Harris Holly R, Healey Martin, Heikinheimo Oskari, Holdsworth-Carson Sarah, Hostettler Isabel, Houlden Henry, Houshdaran Sahar, Irwin Juan C, Jarvelin Marjo-Riitta, Kamatani Yoichiro, Kennedy Stephen H, Kepka Ewa, Kettunen Johannes, Kubo Michiaki, Kulig Bartosz, Kurra Venla, Laivuori Hannele, Laufer Marc R, Lindgren Cecilia M, MacGregor Stuart, Mangino Massimo, Martin Nicholas G, Matalliotaki Charoula, Matalliotakis Michail, Murray Alison D, Ndungu Anne, Nezhat Camran, Olsen Catherine M, Opoku-Anane Jessica, Padmanabhan Sandosh, Paranjpe Manish, Peters Maire, Polak Grzegorz, Porteous David J, Rabban Joseph, Rexrode KathyM, Romanowicz Hanna, Saare Merli, Saavalainen Liisu, Schork Andrew J, Sen Sushmita, Shafrir Amy L, Siewierska-Górska Anna, Słomka Marcin, Smith Blair H, Smolarz Beata, Szaflik Tomasz, Szyłło Krzysztof, Takahashi Atsushi, Terry Kathryn L, Tomassetti Carla, Treloar Susan A, Vanhie Arne, Vincent Katy, Vo Kim C, Werring David J, Zeggini Eleftheria, Zervou Maria I, DBDS Genomic Consortium, FinnGen Study, FinnGen Endometriosis Taskforce, Celmatix Research Team, 23andMe Research Team, Adachi Sosuke, Buring Julie E, Ridker Paul M, D'Hooghe Thomas, Goulielmos George N, Hapangama Dharani K, Hayward Caroline, Horne Andrew W, Low Siew-Kee, Martikainen Hannu, Chasman Daniel I, Rogers Peter A W, Saunders Philippa T, Sirota Marina, Spector Timothy D, Strapagiel Dominik, Tung Joyce Y, Whiteman David C, Giudice Linda C, Velez Edwards Digna R, Uimari Outi, Kraft Peter, Salumets Andres, Nyholt Dale R, Mägi Reedik, Stefansson Kari, Becker Christian M, Yurttas-Beim Piraye, Steinthorsdottir Valgerdur, Nyegaard Mette, Missmer Stacey A, Montgomery Grant W, Morris Andrew P, Zondervan Krina T
Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis
Thomsen I, Vatn M, Silverberg M, Duerr R, Padyukov L, Brand S, Sans M, Annese V, Achkar J, Melum E, Durie P, Sandford R, Mayr G, König I, Hveem K, Cleynen I, Gutierrez-Achury J, Ricaño-Ponce I, van Heel D, Björnsson E, Boberg K, Marschall H, Schreiber S, Manns M, Färkkilä M, Dale A, Chapman R, Lazaridis K, Franke A, Anderson C, Cho J, Bergquist A, Alexander G, Chazouillères O, Bowlus C, Wijmenga C, Schrumpf E, Vermeire S, Albrecht M, Rioux J, Karlsen T, Næss S, Liu J, Gotthardt D, Pares A, Ellinghaus D, Shah T, Juran B, Milkiewicz P, Rust C, Schramm C, Hirschfield G, Invernizzi P, Eksteen B, Hov J, Folseraas T, Ellinghaus E, Rushbrook S, Doncheva N, Andreassen O, Weersma R, Weismüller T, Müller T, Srivastava B, Saarela J, Leppa V, Dorfman R, Alvaro D, Floreani A, Onengut-Gumuscu S, Rich S, Thompson W, Mason A, Teufel A, Sterneck M, Dalekos G, Nöthen M, Herms S, Winkelmann J, Mitrovic M, Braun F, Ponsioen C, Croucher P, Schork A. Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis. Nat Genet 2013; 45:670-5.
21.04.2013Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis
21.04.2013Nat Genet 2013; 45:670-5
Thomsen Ingo, Vatn Morten H, Silverberg Mark S, Duerr Richard H, Padyukov Leonid, Brand Stephan, Sans Miquel, Annese Vito, Achkar Jean-Paul, Melum Espen, Durie Peter R, Sandford Richard N, Mayr Gabriele, König Inke R, Hveem Kristian, Cleynen Isabelle, Gutierrez-Achury Javier, Ricaño-Ponce Isis, van Heel David, Björnsson Einar, Boberg Kirsten Muri, Marschall Hanns-Ulrich, Schreiber Stefan, Manns Michael P, Färkkilä Martti, Dale Anders M, Chapman Roger W, Lazaridis Konstantinos N, Franke Andre, Anderson Carl A, Cho Judy, Bergquist Annika, Alexander Graeme, Chazouillères Olivier, Bowlus Christopher L, Wijmenga Cisca, Schrumpf Erik, Vermeire Severine, Albrecht Mario, Rioux John D, Karlsen Tom H, Næss Sigrid, Liu Jimmy Z, Gotthardt Daniel Nils, Pares Albert, Ellinghaus David, Shah Tejas, Juran Brian D, Milkiewicz Piotr, Rust Christian, Schramm Christoph, Hirschfield Gideon M, Invernizzi Pietro, Eksteen Bertus, Hov Johannes Roksund, Folseraas Trine, Ellinghaus Eva, Rushbrook Simon M, Doncheva Nadezhda T, Andreassen Ole A, Weersma Rinse K, Weismüller Tobias J, Müller Tobias, Srivastava Brijesh, Saarela Janna, Leppa Virpi, Dorfman Ruslan, Alvaro Domenico, Floreani Annarosa, Onengut-Gumuscu Suna, Rich Stephen S, Thompson Wesley K, Mason Andrew L, Teufel Andreas, Sterneck Martina, Dalekos Georgios, Nöthen Markus M, Herms Stefan, Winkelmann Juliane, Mitrovic Mitja, Braun Felix, Ponsioen Cyriel Y, Croucher Peter J P, Schork Andrew J