Detalhe da pesquisa
1.
Complement genes contribute sex-biased vulnerability in diverse disorders.
Nature
; 582(7813): 577-581, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32499649
2.
Epigenetic and transcriptional dysregulation in CD4+ T cells in patients with atopic dermatitis.
PLoS Genet
; 18(5): e1009973, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35576187
3.
Shared and distinct interactions of type 1 and type 2 Epstein-Barr Nuclear Antigen 2 with the human genome.
BMC Genomics
; 25(1): 273, 2024 Mar 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-38475709
4.
Association between systemic lupus erythematosus and myasthenia gravis: A population-based National Study.
Clin Immunol
; 260: 109810, 2024 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37949200
5.
Positive thinking about negative studies.
Br J Psychiatry
; 224(3): 79-81, 2024 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38174364
6.
Protecting and promoting editorial independence.
Br J Psychiatry
; : 1-3, 2024 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38356355
7.
The integrity of the research record: a mess so big and so deep and so tall.
Br J Psychiatry
; 221(3): 580-581, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35611401
8.
A systematic review and meta-analysis of treatments for rapid cycling bipolar disorder.
Acta Psychiatr Scand
; 146(4): 290-311, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35778967
9.
Validation of low-coverage whole-genome sequencing for mitochondrial DNA variants suggests mitochondrial DNA as a genetic cause of preterm birth.
Hum Mutat
; 42(12): 1602-1614, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34467602
10.
Genetic fine mapping of systemic lupus erythematosus MHC associations in Europeans and African Americans.
Hum Mol Genet
; 27(21): 3813-3824, 2018 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30085094
11.
Identification of a Sjögren's syndrome susceptibility locus at OAS1 that influences isoform switching, protein expression, and responsiveness to type I interferons.
PLoS Genet
; 13(6): e1006820, 2017 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-28640813
12.
Genetic variants at the 16p13 locus confer risk for eosinophilic esophagitis.
Genes Immun
; 20(4): 281-292, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29904099
13.
Copb2 is essential for embryogenesis and hypomorphic mutations cause human microcephaly.
Hum Mol Genet
; 26(24): 4836-4848, 2017 12 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29036432
14.
Ensuring research integrity: setting standards for robust and ethical conduct and reporting of research.
Br J Psychiatry
; 215(1): 381-382, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31112115
15.
Genetic variants with gene regulatory effects are associated with diisocyanate-induced asthma.
J Allergy Clin Immunol
; 142(3): 959-969, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29969634
16.
Lupus Risk Variant Increases pSTAT1 Binding and Decreases ETS1 Expression.
Am J Hum Genet
; 96(5): 731-9, 2015 May 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-25865496
17.
HLA-DRB1*11 and variants of the MHC class II locus are strong risk factors for systemic juvenile idiopathic arthritis.
Proc Natl Acad Sci U S A
; 112(52): 15970-5, 2015 Dec 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-26598658
18.
Profound loss of esophageal tissue differentiation in patients with eosinophilic esophagitis.
J Allergy Clin Immunol
; 140(3): 738-749.e3, 2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-28104354
19.
Two functional lupus-associated BLK promoter variants control cell-type- and developmental-stage-specific transcription.
Am J Hum Genet
; 94(4): 586-98, 2014 Apr 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-24702955
20.
Genetic architecture distinguishes systemic juvenile idiopathic arthritis from other forms of juvenile idiopathic arthritis: clinical and therapeutic implications.
Ann Rheum Dis
; 76(5): 906-913, 2017 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-27927641