Detalhe da pesquisa
1.
Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.
Nature
; 616(7958): 755-763, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-37046083
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.
Rare coding variants in 35 genes associate with circulating lipid levels-A multi-ancestry analysis of 170,000 exomes.
Am J Hum Genet
; 109(1): 81-96, 2022 01 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34932938
4.
Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative.
Hum Mol Genet
; 31(3): 347-361, 2022 02 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34553764
5.
Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program.
Am J Hum Genet
; 108(10): 1836-1851, 2021 10 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34582791
6.
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.
Am J Hum Genet
; 108(5): 874-893, 2021 05 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33887194
7.
Secondary analyses for genome-wide association studies using expression quantitative trait loci.
Genet Epidemiol
; 46(3-4): 170-181, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35312098
8.
Transcriptional profile of platelets and iPSC-derived megakaryocytes from whole-genome and RNA sequencing.
Blood
; 137(7): 959-968, 2021 02 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-33094331
9.
Rare coding variants in RCN3 are associated with blood pressure.
BMC Genomics
; 23(1): 148, 2022 Feb 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-35183128
10.
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations.
PLoS Genet
; 15(12): e1008500, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31869403
11.
Association of Coronary Artery Atherosclerosis With Brain White Matter Hyperintensity.
Stroke
; 52(8): 2594-2600, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34000829
12.
White Matter Injury Is Associated with Reduced Manual Dexterity and Elevated Serum Ceramides in Subjects with Cerebral Small Vessel Disease.
Cerebrovasc Dis
; 50(1): 100-107, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33279889
13.
Leveraging linkage evidence to identify low-frequency and rare variants on 16p13 associated with blood pressure using TOPMed whole genome sequencing data.
Hum Genet
; 138(2): 199-210, 2019 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-30671673
14.
Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals.
Am J Hum Genet
; 99(1): 40-55, 2016 Jul 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27346686
15.
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.
Am J Hum Genet
; 108(6): 1165, 2021 Jun 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34087167
16.
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis.
Am J Hum Genet
; 99(2): 481-8, 2016 08 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27486782
17.
Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits.
Am J Hum Genet
; 99(1): 8-21, 2016 Jul 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27346685
18.
Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases.
Am J Hum Genet
; 99(1): 22-39, 2016 Jul 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27346689
19.
Targeted deep sequencing of the PEAR1 locus for platelet aggregation in European and African American families.
Platelets
; 30(3): 380-386, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-29553866
20.
Exome-chip meta-analysis identifies association between variation in ANKRD26 and platelet aggregation.
Platelets
; 30(2): 164-173, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-29185836