Detalhe da pesquisa
1.
Autoimmune alleles at the major histocompatibility locus modify melanoma susceptibility.
Am J Hum Genet
; 110(7): 1138-1161, 2023 07 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37339630
2.
Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells.
Nature
; 586(7831): 769-775, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33057200
3.
Correlates of suicidal behaviors and genetic risk among United States veterans with schizophrenia or bipolar I disorder.
Mol Psychiatry
; 2024 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38491344
4.
A multi-population phenome-wide association study of genetically-predicted height in the Million Veteran Program.
PLoS Genet
; 18(6): e1010193, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35653334
5.
A Phenome-Wide Association Study of genes associated with COVID-19 severity reveals shared genetics with complex diseases in the Million Veteran Program.
PLoS Genet
; 18(4): e1010113, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35482673
6.
Regulatory variants in TCF7L2 are associated with thoracic aortic aneurysm.
Am J Hum Genet
; 108(9): 1578-1589, 2021 09 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34265237
7.
Design and Pilot Results from Million Veteran Program Return Of Actionable Genetic Results (MVP-ROAR) Study.
Am Heart J
; 2024 May 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-38762090
8.
Modeling the longitudinal changes of ancestry diversity in the Million Veteran Program.
Hum Genomics
; 17(1): 46, 2023 06 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37268996
9.
Genotyping Array Design and Data Quality Control in the Million Veteran Program.
Am J Hum Genet
; 106(4): 535-548, 2020 04 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32243820
10.
A MUC5B Gene Polymorphism, rs35705950-T, Confers Protective Effects Against COVID-19 Hospitalization but Not Severe Disease or Mortality.
Am J Respir Crit Care Med
; 206(10): 1220-1229, 2022 11 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35771531
11.
Harmonizing Genetic Ancestry and Self-identified Race/Ethnicity in Genome-wide Association Studies.
Am J Hum Genet
; 105(4): 763-772, 2019 10 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31564439
12.
Effectiveness of Smallpox Vaccination to Prevent Mpox in Military Personnel.
N Engl J Med
; 389(12): 1147-1148, 2023 Sep 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-37733313
13.
Genome-wide association study of cognitive performance in U.S. veterans with schizophrenia or bipolar disorder.
Am J Med Genet B Neuropsychiatr Genet
; 183(3): 181-194, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31872970
14.
Impact of genotyping errors on statistical power of association tests in genomic analyses: A case study.
Genet Epidemiol
; 41(2): 152-162, 2017 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-28019059
15.
With equal access, African American patients have superior survival compared to white patients with multiple myeloma: a VA study.
Blood
; 133(24): 2615-2618, 2019 06 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-31003998
16.
Neighborhood Deprivation, Race and Ethnicity, and Prostate Cancer Outcomes Across California Health Care Systems.
JAMA Netw Open
; 7(3): e242852, 2024 Mar 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38502125
17.
A multi-ancestry GWAS of Fuchs corneal dystrophy highlights the contributions of laminins, collagen, and endothelial cell regulation.
Commun Biol
; 7(1): 418, 2024 Apr 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-38582945
18.
Development and utility of a clinical research informatics application for participant recruitment and workflow management for a return of results pilot trial in familial hypercholesterolemia in the Million Veteran Program.
JAMIA Open
; 7(1): ooae020, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38464744
19.
Rare genetic variation in VE-PTP is associated with central serous chorioretinopathy, venous dysfunction and glaucoma.
medRxiv
; 2024 May 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-38766240
20.
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis.
Nat Genet
; 56(5): 827-837, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38632349