Detalhe da pesquisa
1.
Transmission of human mtDNA heteroplasmy in the Genome of the Netherlands families: support for a variable-size bottleneck.
Genome Res
; 26(4): 417-26, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26916109
2.
A comprehensive evaluation of the genetic architecture of sudden cardiac arrest.
Eur Heart J
; 39(44): 3961-3969, 2018 11 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-30169657
3.
Resetting the bar: Statistical significance in whole-genome sequencing-based association studies of global populations.
Genet Epidemiol
; 41(2): 145-151, 2017 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-27990689
4.
A general framework for meta-analyzing dependent studies with overlapping subjects in association mapping.
Hum Mol Genet
; 25(9): 1857-66, 2016 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26908615
5.
Twenty-eight genetic loci associated with ST-T-wave amplitudes of the electrocardiogram.
Hum Mol Genet
; 25(10): 2093-2103, 2016 05 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26962151
6.
Genetically predicted longer telomere length is associated with increased risk of B-cell lymphoma subtypes.
Hum Mol Genet
; 25(8): 1663-76, 2016 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27008888
7.
Accurate and fast multiple-testing correction in eQTL studies.
Am J Hum Genet
; 96(6): 857-68, 2015 Jun 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-26027500
8.
Leveraging Distant Relatedness to Quantify Human Mutation and Gene-Conversion Rates.
Am J Hum Genet
; 97(6): 775-89, 2015 Dec 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-26581902
9.
Characteristics of de novo structural changes in the human genome.
Genome Res
; 25(6): 792-801, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25883321
10.
Genetic variation at 16q24.2 is associated with small vessel stroke.
Ann Neurol
; 81(3): 383-394, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-27997041
11.
Polymorphisms of large effect explain the majority of the host genetic contribution to variation of HIV-1 virus load.
Proc Natl Acad Sci U S A
; 112(47): 14658-63, 2015 Nov 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-26553974
12.
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
13.
Evaluating the Impact of Functional Genetic Variation on HIV-1 Control.
J Infect Dis
; 216(9): 1063-1069, 2017 11 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-28968755
14.
Fine mapping major histocompatibility complex associations in psoriasis and its clinical subtypes.
Am J Hum Genet
; 95(2): 162-72, 2014 Aug 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-25087609
15.
Fine mapping seronegative and seropositive rheumatoid arthritis to shared and distinct HLA alleles by adjusting for the effects of heterogeneity.
Am J Hum Genet
; 94(4): 522-32, 2014 Apr 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-24656864
16.
Causal effects of body mass index on cardiometabolic traits and events: a Mendelian randomization analysis.
Am J Hum Genet
; 94(2): 198-208, 2014 Feb 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-24462370
17.
Genome-wide association study identifies five susceptibility loci for follicular lymphoma outside the HLA region.
Am J Hum Genet
; 95(4): 462-71, 2014 Oct 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-25279986
18.
Annotation of loci from genome-wide association studies using tissue-specific quantitative interaction proteomics.
Nat Methods
; 11(8): 868-74, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24952909
19.
Behçet disease-associated MHC class I residues implicate antigen binding and regulation of cell-mediated cytotoxicity.
Proc Natl Acad Sci U S A
; 111(24): 8867-72, 2014 Jun 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-24821759
20.
A novel MMP12 locus is associated with large artery atherosclerotic stroke using a genome-wide age-at-onset informed approach.
PLoS Genet
; 10(7): e1004469, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25078452