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
Inglês
| MEDLINE | ID: mdl-31675503
2.
MagicalRsq-X: A cross-cohort transferable genotype imputation quality metric.
Am J Hum Genet
; 111(5): 990-995, 2024 May 02.
Artigo
Inglês
| MEDLINE | ID: mdl-38636510
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
Inglês
| MEDLINE | ID: mdl-38747556
4.
Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney disease.
Hum Mol Genet
; 32(6): 1048-1060, 2023 03 06.
Artigo
Inglês
| MEDLINE | ID: mdl-36444934
5.
Integration of rare expression outlier-associated variants improves polygenic risk prediction.
Am J Hum Genet
; 109(6): 1055-1064, 2022 06 02.
Artigo
Inglês
| MEDLINE | ID: mdl-35588732
6.
Age at Menopause, Leukocyte Telomere Length, and Coronary Artery Disease in Postmenopausal Women.
Circ Res
; 133(5): 376-386, 2023 08 18.
Artigo
Inglês
| MEDLINE | ID: mdl-37489536
7.
Super interactive promoters provide insight into cell type-specific regulatory networks in blood lineage cell types.
PLoS Genet
; 18(1): e1009984, 2022 01.
Artigo
Inglês
| MEDLINE | ID: mdl-35100265
8.
An empirical Bayes approach to improving population-specific genetic association estimation by leveraging cross-population data.
Genet Epidemiol
; 47(1): 45-60, 2023 02.
Artigo
Inglês
| MEDLINE | ID: mdl-36116031
9.
Transcriptome-wide association study in UK Biobank Europeans identifies associations with blood cell traits.
Hum Mol Genet
; 31(14): 2333-2347, 2022 07 21.
Artigo
Inglês
| MEDLINE | ID: mdl-35138379
10.
A large-scale transcriptome-wide association study (TWAS) of 10 blood cell phenotypes reveals complexities of TWAS fine-mapping.
Genet Epidemiol
; 46(1): 3-16, 2022 02.
Artigo
Inglês
| MEDLINE | ID: mdl-34779012
11.
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
Inglês
| MEDLINE | ID: mdl-31883642
12.
Genetic examination of hematological parameters in SARS-CoV-2 infection and COVID-19.
Blood Cells Mol Dis
; 103: 102782, 2023 11.
Artigo
Inglês
| MEDLINE | ID: mdl-37558590
13.
Premature Menopause, Clonal Hematopoiesis, and Coronary Artery Disease in Postmenopausal Women.
Circulation
; 143(5): 410-423, 2021 02 02.
Artigo
Inglês
| MEDLINE | ID: mdl-33161765
14.
Clonal Hematopoiesis Is Associated With Higher Risk of Stroke.
Stroke
; 53(3): 788-797, 2022 03.
Artigo
Inglês
| MEDLINE | ID: mdl-34743536
15.
Genome-wide Significance Thresholds for Admixture Mapping Studies.
Am J Hum Genet
; 104(3): 454-465, 2019 03 07.
Artigo
Inglês
| MEDLINE | ID: mdl-30773276
16.
Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program.
Am J Hum Genet
; 105(4): 706-718, 2019 10 03.
Artigo
Inglês
| MEDLINE | ID: mdl-31564435
17.
Longitudinal profiling of clonal hematopoiesis provides insight into clonal dynamics.
Immun Ageing
; 19(1): 23, 2022 May 24.
Artigo
Inglês
| MEDLINE | ID: mdl-35610705
18.
Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.
BMC Genomics
; 22(1): 432, 2021 Jun 09.
Artigo
Inglês
| MEDLINE | ID: mdl-34107879
19.
Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism.
Blood
; 134(19): 1645-1657, 2019 11 07.
Artigo
Inglês
| MEDLINE | ID: mdl-31420334
20.
Non-coding variants in MYH11, FZD3, and SORCS3 are associated with dementia in women.
Alzheimers Dement
; 17(2): 215-225, 2021 02.
Artigo
Inglês
| MEDLINE | ID: mdl-32966694