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Genetic association analysis identifies variants associated with disease progression in primary sclerosing cholangitis

Title: Genetic association analysis identifies variants associated with disease progression in primary sclerosing cholangitis
Authors: Alberts, Rudi; De Vries, Elisabeth M. G; Goode, Elizabeth C; Jiang, Xiaojun; Sampaziotis, Fotis; Rombouts, Krista; Böttcher, Katrin; Folseraas, Trine; Weismüller, Tobias J; Mason, Andrew L; Wang, Weiwei; Alexander, Graeme; ALVARO, Domenico; Bergquist, Annika; Björkström, Niklas K; Beuers, Ulrich; Björnsson, Einar; Boberg, Kirsten Muri; Bowlus, Christopher L; BRAGAZZI, MARIA CONSIGLIA; Carbone, Marco; Chazouillères, Olivier; Cheung, Angela; Dalekos, Georgios; Eaton, John; Eksteen, Bertus; Ellinghaus, David; Färkkilä, Martti; Festen, Eleonora A. M; Floreani, Annarosa; Franceschet, Irene; Gotthardt, Daniel Nils; Hirschfield, Gideon M; Hoek, Bart Van; Holm, Kristian; Hohenester, Simon; Hov, Johannes Roksund; Imhann, Floris; Invernizzi, Pietro; Juran, Brian D; Lenzen, Henrike; Lieb, Wolfgang; Liu, Jimmy Z; Marschall, Hanns ulrich; Marzioni, Marco; Melum, Espen; Milkiewicz, Piotr; Müller, Tobias; Pares, Albert; Rupp, Christian; Rust, Christian; Sandford, Richard N; Schramm, Christoph; Schreiber, Stefan; Schrumpf, Erik; Silverberg, Mark S; Srivastava, Brijesh; Sterneck, Martina; Teufel, Andreas; Vallier, Ludovic; Verheij, Joanne; Vila, Arnau Vich; Vries, Boudewijn De; Zachou, Kalliopi; Chapman, Roger W; Manns, Michael P; Pinzani, Massimo; Rushbrook, Simon M; Lazaridis, Konstantinos N; Franke, Andre; Anderson, Carl A; Karlsen, Tom H; Ponsioen, Cyriel Y; Weersma, Rinse K.
Contributors: Alberts, Rudi; De Vries, Elisabeth M. G; Goode, Elizabeth C; Jiang, Xiaojun; Sampaziotis, Foti; Rombouts, Krista; Böttcher, Katrin; Folseraas, Trine; Weismüller, Tobias J; Mason, Andrew L; Wang, Weiwei; Alexander, Graeme; Alvaro, Domenico; Bergquist, Annika; Björkström, Niklas K; Beuers, Ulrich; Björnsson, Einar; Boberg, Kirsten Muri; Bowlus, Christopher L; Bragazzi, Maria Consiglia; Carbone, Marco; Chazouillères, Olivier; Cheung, Angela; Dalekos, Georgio; Eaton, John; Eksteen, Bertu; Ellinghaus, David; Färkkilä, Martti; Festen, Eleonora A. M; Floreani, Annarosa; Franceschet, Irene; Gotthardt, Daniel Nil; Hirschfield, Gideon M; Hoek, Bart Van; Holm, Kristian; Hohenester, Simon; Hov, Johannes Roksund; Imhann, Flori; Invernizzi, Pietro; Juran, Brian D; Lenzen, Henrike; Lieb, Wolfgang; Liu, Jimmy Z; Marschall, Hanns Ulrich; Marzioni, Marco; Melum, Espen; Milkiewicz, Piotr; Müller, Tobia; Pares, Albert; Rupp, Christian; Rust, Christian; Sandford, Richard N; Schramm, Christoph; Schreiber, Stefan; Schrumpf, Erik; Silverberg, Mark S; Srivastava, Brijesh; Sterneck, Martina; Teufel, Andrea; Vallier, Ludovic; Verheij, Joanne; Vila, Arnau Vich; Vries, Boudewijn De; Zachou, Kalliopi; Chapman, Roger W; Manns, Michael P; Pinzani, Massimo; Rushbrook, Simon M; Lazaridis, Konstantinos N; Franke, Andre; Anderson, Carl A; Karlsen, Tom H; Ponsioen, Cyriel Y; Weersma, Rinse K.
Publication Year: 2017
Collection: Sapienza Università di Roma: CINECA IRIS
Subject Terms: Primary sclerosing cholangiti; genetic; liver transplantation
Description: Primary sclerosing cholangitis (PSC) is a genetically complex, inflammatory bile duct disease of largely unknown aetiology often leading to liver transplantation or death. Little is known about the genetic contribution to the severity and progression of PSC. The aim of this study is to identify genetic variants associated with PSC disease progression and development of complications.
Document Type: article in journal/newspaper
Language: English
Relation: info:eu-repo/semantics/altIdentifier/pmid/28779025; info:eu-repo/semantics/altIdentifier/wos/WOS:000442465300018; journal:EGUT; https://hdl.handle.net/11573/1011696
DOI: 10.1136/gutjnl-2016-313598
Availability: https://hdl.handle.net/11573/1011696; https://doi.org/10.1136/gutjnl-2016-313598
Rights: info:eu-repo/semantics/openAccess ; license:Tutti i diritti riservati (All rights reserved)
Accession Number: edsbas.7B7CEF3B
Database: BASE