Detalhe da pesquisa
1.
Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa.
Cell
; 179(4): 984-1002.e36, 2019 10 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-31675503
2.
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program.
Nature
; 590(7845): 290-299, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33568819
3.
Whole genome sequencing based analysis of inflammation biomarkers in the Trans-Omics for Precision Medicine (TOPMed) consortium.
Hum Mol Genet
; 2024 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38747556
4.
TOP-LD: A tool to explore linkage disequilibrium with TOPMed whole-genome sequence data.
Am J Hum Genet
; 109(6): 1175-1181, 2022 06 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35504290
5.
A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies.
Nat Methods
; 19(12): 1599-1611, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36303018
6.
Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors.
Hum Mol Genet
; 31(18): 3120-3132, 2022 09 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35552711
7.
Donor germ-line variants associate with outcomes of allogeneic hematopoietic stem cell transplantation in patients with myelodysplastic syndromes.
Am J Hematol
; 99(4): 770-773, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38339773
8.
Comparison of multiple imputation and other methods for the analysis of imputed genotypes.
BMC Genomics
; 24(1): 303, 2023 Jun 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37277705
9.
A genome-wide gene-environment interaction study of breast cancer risk for women of European ancestry.
Breast Cancer Res
; 25(1): 93, 2023 08 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37559094
10.
Allelic Heterogeneity at the CRP Locus Identified by Whole-Genome Sequencing in Multi-ancestry Cohorts.
Am J Hum Genet
; 106(1): 112-120, 2020 01 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31883642
11.
Individualized multi-omic pathway deviation scores using multiple factor analysis.
Biostatistics
; 23(2): 362-379, 2022 04 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-32766691
12.
On asymptotic distributions of several test statistics for familial relatedness in linear mixed models.
Stat Med
; 42(17): 2962-2981, 2023 07 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-37345498
13.
Association analysis identifies 65 new breast cancer risk loci.
Nature
; 551(7678): 92-94, 2017 11 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29059683
14.
Rare and low-frequency coding variants alter human adult height.
Nature
; 542(7640): 186-190, 2017 02 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28146470
15.
Mendelian randomization analysis with survival outcomes.
Genet Epidemiol
; 45(1): 16-23, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32918779
16.
A unified linear mixed model for familial relatedness and population structure in genetic association studies.
Genet Epidemiol
; 45(3): 305-315, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33175443
17.
Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project.
Stroke
; 53(3): 875-885, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34727735
18.
Common variants in breast cancer risk loci predispose to distinct tumor subtypes.
Breast Cancer Res
; 24(1): 2, 2022 01 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34983606
19.
Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes.
Am J Hum Genet
; 104(1): 21-34, 2019 01 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30554720
20.
Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology.
Am J Hum Genet
; 105(1): 15-28, 2019 07 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31178129