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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.
Artículo
en Inglés
| MEDLINE | ID: mdl-35263625
2.
The NHGRI-EBI GWAS Catalog: knowledgebase and deposition resource.
Nucleic Acids Res
; 51(D1): D977-D985, 2023 01 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-36350656
3.
Prioritizing diversity in human genomics research.
Nat Rev Genet
; 19(3): 175-185, 2018 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-29151588
4.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-32504544
5.
Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies.
Am J Hum Genet
; 107(5): 932-941, 2020 11 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-33108757
6.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-36341765
7.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-32226016
8.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-31104772
9.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-34906461
10.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-35833928
11.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-34107879
12.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-30193136
13.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-30445434
14.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-32171239
15.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-29878111
16.
Alaska Native genomic research: perspectives from Alaska Native leaders, federal staff, and biomedical researchers.
Genet Med
; 22(12): 1935-1943, 2020 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-32839571
17.
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.
Am J Hum Genet
; 98(6): 1051-1066, 2016 06 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-27181682
18.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-30287922
19.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-30670880
20.
The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog).
Nucleic Acids Res
; 45(D1): D896-D901, 2017 01 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-27899670