Search details
1.
Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.
Nature
; 616(7958): 755-763, 2023 04.
Article
in English
| MEDLINE | ID: mdl-37046083
2.
Genetic diversity fuels gene discovery for tobacco and alcohol use.
Nature
; 612(7941): 720-724, 2022 12.
Article
in English
| MEDLINE | ID: mdl-36477530
3.
A saturated map of common genetic variants associated with human height.
Nature
; 610(7933): 704-712, 2022 10.
Article
in English
| MEDLINE | ID: mdl-36224396
4.
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program.
Nature
; 590(7845): 290-299, 2021 02.
Article
in English
| MEDLINE | ID: mdl-33568819
5.
Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.
Am J Hum Genet
; 110(10): 1704-1717, 2023 10 05.
Article
in English
| MEDLINE | ID: mdl-37802043
6.
Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program.
Am J Hum Genet
; 109(5): 857-870, 2022 05 05.
Article
in English
| MEDLINE | ID: mdl-35385699
7.
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.
Article
in English
| MEDLINE | ID: mdl-34932938
8.
A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies.
Nat Methods
; 19(12): 1599-1611, 2022 12.
Article
in English
| MEDLINE | ID: mdl-36303018
9.
Leveraging pleiotropy to discover and interpret GWAS results for sleep-associated traits.
PLoS Genet
; 18(12): e1010557, 2022 12.
Article
in English
| MEDLINE | ID: mdl-36574455
10.
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry.
Am J Hum Genet
; 108(4): 564-582, 2021 04 01.
Article
in English
| MEDLINE | ID: mdl-33713608
11.
Association of clonal hematopoiesis with chronic obstructive pulmonary disease.
Blood
; 139(3): 357-368, 2022 01 20.
Article
in English
| MEDLINE | ID: mdl-34855941
12.
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.
Article
in English
| MEDLINE | ID: mdl-31883642
13.
Targeted Genome Sequencing Identifies Multiple Rare Variants in Caveolin-1 Associated with Obstructive Sleep Apnea.
Am J Respir Crit Care Med
; 206(10): 1271-1280, 2022 11 15.
Article
in English
| MEDLINE | ID: mdl-35822943
14.
De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population.
Proc Natl Acad Sci U S A
; 117(5): 2560-2569, 2020 02 04.
Article
in English
| MEDLINE | ID: mdl-31964835
15.
Rare coding variants in RCN3 are associated with blood pressure.
BMC Genomics
; 23(1): 148, 2022 Feb 19.
Article
in English
| MEDLINE | ID: mdl-35183128
16.
Sequencing Analysis at 8p23 Identifies Multiple Rare Variants in DLC1 Associated with Sleep-Related Oxyhemoglobin Saturation Level.
Am J Hum Genet
; 105(5): 1057-1068, 2019 11 07.
Article
in English
| MEDLINE | ID: mdl-31668705
17.
Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing Studies.
Am J Hum Genet
; 104(2): 260-274, 2019 02 07.
Article
in English
| MEDLINE | ID: mdl-30639324
18.
Interaction of obesity polygenic score with lifestyle risk factors in an electronic health record biobank.
BMC Med
; 20(1): 5, 2022 01 12.
Article
in English
| MEDLINE | ID: mdl-35016652
19.
Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure.
Mol Psychiatry
; 26(11): 6293-6304, 2021 11.
Article
in English
| MEDLINE | ID: mdl-33859359
20.
Associations of sleep duration and sleep-wake rhythm with lung parenchymal abnormalities on computed tomography: The MESA study.
J Sleep Res
; 31(2): e13475, 2022 04.
Article
in English
| MEDLINE | ID: mdl-34498326