Detalhe da pesquisa
1.
Predicted gene expression in ancestrally diverse populations leads to discovery of susceptibility loci for lifestyle and cardiometabolic traits.
Am J Hum Genet
; 109(4): 669-679, 2022 04 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35263625
2.
Prioritizing diversity in human genomics research.
Nat Rev Genet
; 19(3): 175-185, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29151588
3.
Clinical Genetics Lacks Standard Definitions and Protocols for the Collection and Use of Diversity Measures.
Am J Hum Genet
; 107(1): 72-82, 2020 07 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32504544
4.
Conducting clinical genomics research during the COVID-19 pandemic: Lessons learned from the CSER consortium experience.
Am J Med Genet A
; 191(2): 391-399, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36341765
5.
Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study.
PLoS Genet
; 16(3): e1008684, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32226016
6.
The Genomic Medicine Integrative Research Framework: A Conceptual Framework for Conducting Genomic Medicine Research.
Am J Hum Genet
; 104(6): 1088-1096, 2019 06 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31104772
7.
US private payers' perspectives on insurance coverage for genome sequencing versus exome sequencing: A study by the Clinical Sequencing Evidence-Generating Research Consortium (CSER).
Genet Med
; 24(1): 238-244, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34906461
8.
Cost-effectiveness frameworks for comparing genome and exome sequencing versus conventional diagnostic pathways: A scoping review and recommended methods.
Genet Med
; 24(10): 2014-2027, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35833928
9.
Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.
BMC Genomics
; 22(1): 432, 2021 Jun 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34107879
10.
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
11.
The NHGRI-EBI GWAS Catalog of published genome-wide association studies, targeted arrays and summary statistics 2019.
Nucleic Acids Res
; 47(D1): D1005-D1012, 2019 01 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30445434
12.
Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.
BMC Genomics
; 21(1): 228, 2020 Mar 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-32171239
13.
Discovery, fine-mapping, and conditional analyses of genetic variants associated with C-reactive protein in multiethnic populations using the Metabochip in the Population Architecture using Genomics and Epidemiology (PAGE) study.
Hum Mol Genet
; 27(16): 2940-2953, 2018 08 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29878111
14.
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.
Am J Hum Genet
; 98(6): 1051-1066, 2016 06 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27181682
15.
Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.
Genet Med
; 21(5): 1100-1110, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30287922
16.
Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.
Genet Med
; 21(5): 1261-1262, 2019 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-30670880
17.
The clinical imperative for inclusivity: Race, ethnicity, and ancestry (REA) in genomics.
Hum Mutat
; 39(11): 1713-1720, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30311373
18.
Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans.
Hum Mol Genet
; 25(19): 4350-4368, 2016 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27577874
19.
Anticipated responses of early adopter genetic specialists and nongenetic specialists to unsolicited genomic secondary findings.
Genet Med
; 20(10): 1186-1195, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-29388940
20.
Characterizing reduced coverage regions through comparison of exome and genome sequencing data across 10 centers.
Genet Med
; 20(8): 855-866, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29144510