Detalhe da pesquisa
1.
Transethnic analysis of the human leukocyte antigen region for ulcerative colitis reveals not only shared but also ethnicity-specific disease associations.
Hum Mol Genet
; 30(5): 356-369, 2021 04 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-33555323
2.
A novel unconventional T cell population enriched in Crohn's disease.
Gut
; 71(11): 2194-2204, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35264446
3.
Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease.
Gut
; 2021 Apr 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-33888516
4.
Protein-coding variants contribute to the risk of atopic dermatitis and skin-specific gene expression.
J Allergy Clin Immunol
; 145(4): 1208-1218, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31707051
5.
Sucrase-isomaltase genotype and response to a starch-reduced and sucrose-reduced diet in IBS-D patients.
Gut
; 73(4): 706-708, 2024 Mar 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36878682
6.
A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1.
Nat Genet
; 39(2): 207-11, 2007 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-17200669
7.
XIAP variants in male Crohn's disease.
Gut
; 64(1): 66-76, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24572142
8.
Association between variants of PRDM1 and NDP52 and Crohn's disease, based on exome sequencing and functional studies.
Gastroenterology
; 145(2): 339-47, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23624108
9.
Intragenic allele pyramiding combines different specificities of wheat Pm3 resistance alleles.
Plant J
; 64(3): 433-45, 2010 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-20804457
10.
Variants in a novel epidermal collagen gene (COL29A1) are associated with atopic dermatitis.
PLoS Biol
; 5(9): e242, 2007 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-17850181
11.
Missense variants in NOX1 and p22phox in a case of very-early-onset inflammatory bowel disease are functionally linked to NOD2.
Cold Spring Harb Mol Case Stud
; 5(1)2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30709874
12.
Structure-function analysis of the NB-ARC domain of plant disease resistance proteins.
J Exp Bot
; 59(6): 1383-97, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18390848
13.
Compound heterozygous mutations in IL10RA combined with a complement factor properdin mutation in infantile-onset inflammatory bowel disease.
Eur J Gastroenterol Hepatol
; 30(12): 1491-1496, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30199474
14.
Comparative analysis of protein structure alignments.
BMC Struct Biol
; 7: 50, 2007 Jul 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-17672887
15.
Targeted Resequencing and Functional Testing Identifies Low-Frequency Missense Variants in the Gene Encoding GARP as Significant Contributors to Atopic Dermatitis Risk.
J Invest Dermatol
; 136(12): 2380-2386, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27448748
16.
Autophagy receptor CALCOCO2/NDP52 takes center stage in Crohn disease.
Autophagy
; 9(8): 1256-7, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23820297
17.
Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis.
Nat Genet
; 45(6): 670-5, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23603763
18.
Structure collisions between interacting proteins.
PLoS One
; 6(6): e19581, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21655095
19.
Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2.
Nat Genet
; 42(11): 991-5, 2010 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-20953188
20.
Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL).
Nat Genet
; 42(4): 292-4, 2010 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-20228798