Detalhe da pesquisa
1.
The power of genetic diversity in genome-wide association studies of lipids.
Nature
; 600(7890): 675-679, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34887591
2.
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids.
Am J Hum Genet
; 109(8): 1366-1387, 2022 08 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35931049
3.
Author Correction: The power of genetic diversity in genome-wide association studies of lipids.
Nature
; 618(7965): E19-E20, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-37237109
4.
Genome-wide Modeling of Polygenic Risk Score in Colorectal Cancer Risk.
Am J Hum Genet
; 107(3): 432-444, 2020 09 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32758450
5.
Loci identified by a genome-wide association study of carotid artery stenosis in the eMERGE network.
Genet Epidemiol
; 45(1): 4-15, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32964493
6.
Rates of Actionable Genetic Findings in Individuals with Colorectal Cancer or Polyps Ascertained from a Community Medical Setting.
Am J Hum Genet
; 105(3): 526-533, 2019 09 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31422818
7.
The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotype.
Genet Epidemiol
; 43(1): 63-81, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30298529
8.
Association of Genetic Risk of Obesity with Postoperative Complications Using Mendelian Randomization.
World J Surg
; 44(1): 84-94, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31605180
9.
Unfolding of hidden white blood cell count phenotypes for gene discovery using latent class mixed modeling.
Genes Immun
; 20(7): 555-565, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30459343
10.
Response to Li and Hopper.
Am J Hum Genet
; 108(3): 527-529, 2021 03 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33667396
11.
Rare loss of function variants in candidate genes and risk of colorectal cancer.
Hum Genet
; 137(10): 795-806, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-30267214
12.
Actionable exomic incidental findings in 6503 participants: challenges of variant classification.
Genome Res
; 25(3): 305-15, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25637381
13.
Association Between Absolute Neutrophil Count and Variation at TCIRG1: The NHLBI Exome Sequencing Project.
Genet Epidemiol
; 40(6): 470-4, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27229898
14.
Joint linkage and association analysis with exome sequence data implicates SLC25A40 in hypertriglyceridemia.
Am J Hum Genet
; 93(6): 1035-45, 2013 Dec 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-24268658
15.
Actionable, pathogenic incidental findings in 1,000 participants' exomes.
Am J Hum Genet
; 93(4): 631-40, 2013 Oct 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-24055113
16.
Family Studies for Classification of Variants of Uncertain Classification: Current Laboratory Clinical Practice and a New Web-Based Educational Tool.
J Genet Couns
; 25(6): 1146-1156, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27422780
17.
PLTP activity inversely correlates with CAAD: effects of PON1 enzyme activity and genetic variants on PLTP activity.
J Lipid Res
; 56(7): 1351-62, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-26009633
18.
TCIRG1-associated congenital neutropenia.
Hum Mutat
; 35(7): 824-7, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24753205
19.
Comparing ancestry calibration approaches for a trans-ancestry colorectal cancer polygenic risk score.
medRxiv
; 2024 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37961088
20.
Clinical associations with a polygenic predisposition to benign lower white blood cell counts.
Nat Commun
; 15(1): 3384, 2024 Apr 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38649760