Detalhe da pesquisa
1.
2023 lifetime achievement award: "If you want to go fast, go alone; if you want to go far, go together".
Am J Hum Genet;
111(3): 412-423, 2024 Mar 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38458162
2.
A brief history of human disease genetics.
Nature;
577(7789): 179-189, 2020 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31915397
3.
Analysis of putative cis-regulatory elements regulating blood pressure variation.
Hum Mol Genet;
29(11): 1922-1932, 2020 07 21.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32436959
4.
The difficulties of broad data sharing in genomic medicine: Empirical evidence from diverse participants in prenatal and pediatric clinical genomics research.
Genet Med;
24(2): 410-418, 2022 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34906477
5.
Modest effect of statins on fasting glucose in a longitudinal electronic health record based cohort.
Cardiovasc Diabetol;
21(1): 132, 2022 07 14.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35836181
6.
Torsade de pointes: A nested case-control study in an integrated healthcare delivery system.
Ann Noninvasive Electrocardiol;
27(1): e12888, 2022 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34547155
7.
The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations.
Am J Hum Genet;
103(3): 319-327, 2018 09 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30193136
8.
Challenges in providing residual risks in carrier testing.
Prenat Diagn;
41(9): 1049-1056, 2021 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34057205
9.
Genetic ancestry does not explain increased atopic dermatitis susceptibility or worse disease control among African American subjects in 2 large US cohorts.
J Allergy Clin Immunol;
145(1): 192-198.e11, 2020 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31369801
10.
A novel truncating variant in ring finger protein 113A (RNF113A) confirms the association of this gene with X-linked trichothiodystrophy.
Am J Med Genet A;
182(3): 513-520, 2020 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31880405
11.
Structured mating: Patterns and implications.
PLoS Genet;
13(4): e1006655, 2017 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28384154
12.
Assessing the clinical impact of CYP2C9 pharmacogenetic variation on phenytoin prescribing practice and patient response in an integrated health system.
Pharmacogenet Genomics;
29(8): 192-199, 2019 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31461080
13.
The Inclusion of Race in Prenatal Screening Algorithms.
Clin Chem;
2024 Jun 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38842043
14.
A Large Genome-Wide Association Study of Age-Related Hearing Impairment Using Electronic Health Records.
PLoS Genet;
12(10): e1006371, 2016 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27764096
15.
Imputation of the rare HOXB13 G84E mutation and cancer risk in a large population-based cohort.
PLoS Genet;
11(1): e1004930, 2015 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25629170
16.
Estimating genotype error rates from high-coverage next-generation sequence data.
Genome Res;
24(11): 1734-9, 2014 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25304867
17.
Genome-wide association and admixture analysis of glaucoma in the Women's Health Initiative.
Hum Mol Genet;
23(24): 6634-43, 2014 Dec 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25027321
18.
Newton E. Morton (1929-2018).
Am J Hum Genet;
102(6): 1011-1017, 2018 Jun 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33220219
19.
Genome-wide characterization of shared and distinct genetic components that influence blood lipid levels in ethnically diverse human populations.
Am J Hum Genet;
92(6): 904-16, 2013 Jun 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23726366
20.
The Association of Refractive Error with Glaucoma in a Multiethnic Population.
Ophthalmology;
123(1): 92-101, 2016 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26260281