Detalhe da pesquisa
1.
Author Correction: Approaches and advances in the genetic causes of autoimmune disease and their implications.
Nat Immunol
; 21(6): 695, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32296167
2.
Publisher Correction: Approaches and advances in the genetic causes of autoimmune disease and their implications.
Nat Immunol
; 20(3): 375, 2019 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-30728494
3.
Lineage-Specific Genome Architecture Links Enhancers and Non-coding Disease Variants to Target Gene Promoters.
Cell
; 167(5): 1369-1384.e19, 2016 11 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-27863249
4.
Approaches and advances in the genetic causes of autoimmune disease and their implications.
Nat Immunol
; 19(7): 674-684, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29925982
5.
Rare variant associations with plasma protein levels in the UK Biobank.
Nature
; 622(7982): 339-347, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37794183
6.
Plasma proteomic associations with genetics and health in the UK Biobank.
Nature
; 622(7982): 329-338, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37794186
7.
Whole-genome sequencing of patients with rare diseases in a national health system.
Nature
; 583(7814): 96-102, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32581362
8.
Whole-genome sequencing of a sporadic primary immunodeficiency cohort.
Nature
; 583(7814): 90-95, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32499645
9.
Publisher Correction: Whole-genome sequencing of a sporadic primary immunodeficiency cohort.
Nature
; 584(7819): E2, 2020 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-32678341
10.
A minimal role for synonymous variation in human disease.
Am J Hum Genet
; 109(12): 2105-2109, 2022 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36459978
11.
The effects of pathogenic and likely pathogenic variants for inherited hemostasis disorders in 140 214 UK Biobank participants.
Blood
; 142(24): 2055-2068, 2023 12 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-37647632
12.
Prevalence of CFTR variants in primary immunodeficiency patients with bronchiectasis is an important modifying cofactor.
J Allergy Clin Immunol
; 152(1): 257-265, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36828084
13.
Fine mapping chromatin contacts in capture Hi-C data.
BMC Genomics
; 20(1): 77, 2019 Jan 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-30674271
14.
Dissection of a Complex Disease Susceptibility Region Using a Bayesian Stochastic Search Approach to Fine Mapping.
PLoS Genet
; 11(6): e1005272, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26106896
15.
Integration of disease association and eQTL data using a Bayesian colocalisation approach highlights six candidate causal genes in immune-mediated diseases.
Hum Mol Genet
; 24(12): 3305-13, 2015 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25743184
16.
Detection and correction of artefacts in estimation of rare copy number variants and analysis of rare deletions in type 1 diabetes.
Hum Mol Genet
; 24(6): 1774-90, 2015 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25424174
17.
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls.
Nature
; 464(7289): 713-20, 2010 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-20360734
18.
Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.
Nat Genet
; 39(7): 857-64, 2007 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-17554260
19.
A method for gene-based pathway analysis using genomewide association study summary statistics reveals nine new type 1 diabetes associations.
Genet Epidemiol
; 38(8): 661-70, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25371288
20.
VSEAMS: a pipeline for variant set enrichment analysis using summary GWAS data identifies IKZF3, BATF and ESRRA as key transcription factors in type 1 diabetes.
Bioinformatics
; 30(23): 3342-8, 2014 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25170024