Detalhe da pesquisa
1.
Genetic variants regulating immune cell levels in health and disease.
Cell
; 155(1): 242-56, 2013 Sep 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-24074872
2.
Common and rare variant associations with clonal haematopoiesis phenotypes.
Nature
; 612(7939): 301-309, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36450978
3.
Whole-genome sequencing reveals host factors underlying critical COVID-19.
Nature
; 607(7917): 97-103, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35255492
4.
Exome sequencing and analysis of 454,787 UK Biobank participants.
Nature
; 599(7886): 628-634, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34662886
5.
Whole genome sequencing of 4,787 individuals identifies gene-based rare variants in age-related macular degeneration.
Hum Mol Genet
; 33(4): 374-385, 2024 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37934784
6.
Exome sequencing and characterization of 49,960 individuals in the UK Biobank.
Nature
; 586(7831): 749-756, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33087929
7.
Germline Mutations in CIDEB and Protection against Liver Disease.
N Engl J Med
; 387(4): 332-344, 2022 07 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35939579
8.
A fast linkage method for population GWAS cohorts with related individuals.
Genet Epidemiol
; 47(3): 231-248, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36739617
9.
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
10.
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
11.
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
12.
Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes.
Nature
; 615(7950): E3, 2023 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-36807635
13.
Ancestry-agnostic estimation of DNA sample contamination from sequence reads.
Genome Res
; 30(2): 185-194, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31980570
14.
LabWAS: Novel findings and study design recommendations from a meta-analysis of clinical labs in two independent biobanks.
PLoS Genet
; 16(11): e1009077, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33175840
15.
Age-of-onset information helps identify 76 genetic variants associated with allergic disease.
PLoS Genet
; 16(6): e1008725, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32603359
16.
Family-based exome sequencing identifies rare coding variants in age-related macular degeneration.
Hum Mol Genet
; 29(12): 2022-2034, 2020 07 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-32246154
17.
Genes for Good: Engaging the Public in Genetics Research via Social Media.
Am J Hum Genet
; 105(1): 65-77, 2019 07 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31204010
18.
Identifying Novel Susceptibility Genes for Colorectal Cancer Risk From a Transcriptome-Wide Association Study of 125,478 Subjects.
Gastroenterology
; 160(4): 1164-1178.e6, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33058866
19.
LocusZoom.js: interactive and embeddable visualization of genetic association study results.
Bioinformatics
; 37(18): 3017-3018, 2021 09 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-33734315
20.
Exploring various polygenic risk scores for skin cancer in the phenomes of the Michigan genomics initiative and the UK Biobank with a visual catalog: PRSWeb.
PLoS Genet
; 15(6): e1008202, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31194742