Human intelectin-1 (ITLN1) genetic variation and intestinal expression.
Scientific Reports
Nonnecke, Eric B EB; Castillo, Patricia A PA; Dugan, Amanda E AE; Almalki, Faisal F; Underwood, Mark A MA; De La Motte, Carol A CA; Yuan, Weirong W; Lu, Wuyuan W; Shen, Bo B; Johansson, Malin E V MEV; Kiessling, Laura L LL; Hollox, Edward J EJ; Lönnerdal, Bo B; Bevins, Charles L CL
Exome-wide study of ankylosing spondylitis demonstrates additional shared genetic background with inflammatory bowel disease.
Npj Genomic Medicine
Robinson, Philip C PC; Leo, Paul J PJ; Pointon, Jennifer J JJ; Harris, Jessica J; Cremin, Katie K; Bradbury, Linda A LA; Stebbings, Simon S; Harrison, Andrew A AA; , ; , ; , ; , ; , ; , ; Duncan, Emma L EL; Evans, David M DM; Wordsworth, Paul B PB; Brown, Matthew A MA
Clinical Implementation of Pharmacogenetic Testing in a Hospital of the Spanish National Health System: Strategy and Experience Over 3 Years.
Clinical And Translational Science
Borobia, Alberto M AM; Dapia, Irene I; Tong, Hoi Y HY; Arias, Pedro P; Muñoz, Mario M; Tenorio, Jair J; Hernández, Rafael R; García García, Irene I; Gordo, Gema G; Ramírez, Elena E; Frías, Jesús J; Lapunzina, Pablo P; Carcas, Antonio J AJ
Exome-wide association study reveals novel psoriasis susceptibility locus at TNFSF15 and rare protective alleles in genes contributing to type I IFN signalling.
Human Molecular Genetics
Dand, Nick N; Mucha, Sören S; Tsoi, Lam C LC; Mahil, Satveer K SK; Stuart, Philip E PE; Arnold, Andreas A; Baurecht, Hansjörg H; Burden, A David AD; Callis Duffin, Kristina K; Chandran, Vinod V; Curtis, Charles J CJ; Das, Sayantan S; Ellinghaus, David D; Ellinghaus, Eva E; Enerback, Charlotta C; Esko, Tõnu T; Gladman, Dafna D DD; Griffiths, Christopher E M CEM; Gudjonsson, Johann E JE; Hoffman, Per P; Homuth, Georg G; Hüffmeier, Ulrike U; Krueger, Gerald G GG; Laudes, Matthias M; Lee, Sang Hyuck SH; Lieb, Wolfgang W; Lim, Henry W HW; Löhr, Sabine S; Mrowietz, Ulrich U; Müller-Nurayid, Martina M; Nöthen, Markus M; Peters, Annette A; Rahman, Proton P; Reis, André A; Reynolds, Nick J NJ; Rodriguez, Elke E; Schmidt, Carsten O CO; Spain, Sarah L SL; Strauch, Konstantin K; Tejasvi, Trilokraj T; Voorhees, John J JJ; Warren, Richard B RB; Weichenthal, Michael M; Weidinger, Stephan S; Zawistowski, Matthew M; Nair, Rajan P RP; Capon, Francesca F; Smith, Catherine H CH; Trembath, Richard C RC; Abecasis, Goncalo R GR; Elder, James T JT; Franke, Andre A; Simpson, Michael A MA; Barker, Jonathan N JN
Results of the Fifth Scientific Workshop of the ECCO (II): Pathophysiology of Perianal Fistulizing Disease.
Journal Of Crohn'S & Colitis
Siegmund, Britta B; Feakins, Roger M RM; Barmias, Giorgos G; Ludvig, Juliano Coelho JC; Teixeira, Fabio Vieira FV; Rogler, Gerhard G; Scharl, Michael M
Intestinal DMBT1 expression is modulated by Crohn's disease-associated IL23R variants and by a DMBT1 variant which influences binding of the transcription factors CREB1 and ATF-2.
Plos One
Diegelmann, Julia J; Czamara, Darina D; Le Bras, Emmanuelle E; Zimmermann, Eva E; Olszak, Torsten T; Bedynek, Andrea A; Göke, Burkhard B; Franke, Andre A; Glas, Jürgen J; Brand, Stephan S
An efficient algorithm to perform multiple testing in epistasis screening.
Bmc Bioinformatics
Van Lishout, François F; Mahachie John, Jestinah M JM; Gusareva, Elena S ES; Urrea, Victor V; Cleynen, Isabelle I; Théâtre, Emilie E; Charloteaux, Benoît B; Calle, Malu Luz ML; Wehenkel, Louis L; Van Steen, Kristel K
IRGM variants and susceptibility to inflammatory bowel disease in the German population.
Plos One
Glas, Jürgen J; Seiderer, Julia J; Bues, Stephanie S; Stallhofer, Johannes J; Fries, Christoph C; Olszak, Torsten T; Tsekeri, Eleni E; Wetzke, Martin M; Beigel, Florian F; Steib, Christian C; Friedrich, Matthias M; Göke, Burkhard B; Diegelmann, Julia J; Czamara, Darina D; Brand, Stephan S
PTGER4 expression-modulating polymorphisms in the 5p13.1 region predispose to Crohn's disease and affect NF-κB and XBP1 binding sites.
Plos One
Glas, Jürgen J; Seiderer, Julia J; Czamara, Darina D; Pasciuto, Giulia G; Diegelmann, Julia J; Wetzke, Martin M; Olszak, Torsten T; Wolf, Christiane C; Müller-Myhsok, Bertram B; Balschun, Tobias T; Achkar, Jean-Paul JP; Kamboh, M Ilyas MI; Franke, Andre A; Duerr, Richard H RH; Brand, Stephan S
Suggestive association between PLA2G12A single nucleotide polymorphism rs2285714 and response to anti-vascular endothelial growth factor therapy in patients with exudative age-related macular degeneration.
Molecular Vision
Wang, Vinson M VM; Rosen, Richard B RB; Meyerle, Catherine B CB; Kurup, Shree K SK; Ardeljan, Daniel D; Agron, Elvira E; Tai, Katy K; Pomykala, Matthew M; Chew, Emily Y EY; Chan, Chi-Chao CC; Tuo, Jingsheng J
Investigation of genetic risk factors for chronic adult diseases for association with preterm birth.
Human Genetics
Falah, Nadia N; McElroy, Jude J; Snegovskikh, Victoria V; Lockwood, Charles J CJ; Norwitz, Errol E; Murray, Jeffey C JC; Kuczynski, Edward E; Menon, Ramkumar R; Teramo, Kari K; Muglia, Louis J LJ; Morgan, Thomas T