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1.
A large-scale transcriptome-wide association study (TWAS) of 10 blood cell phenotypes reveals complexities of TWAS fine-mapping.
Genet Epidemiol
; 46(1): 3-16, 2022 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-34779012
2.
Assessing efficiency of fine-mapping obesity-associated variants through leveraging ancestry architecture and functional annotation using PAGE and UKBB cohorts.
Hum Genet
; 142(10): 1477-1489, 2023 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-37658231
3.
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations.
PLoS Genet
; 15(12): e1008500, 2019 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-31869403
4.
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
5.
Alternative genomic diagnoses for individuals with a clinical diagnosis of Dubowitz syndrome.
Am J Med Genet A
; 185(1): 119-133, 2021 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-33098347
6.
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
7.
Generalization and fine mapping of red blood cell trait genetic associations to multi-ethnic populations: The PAGE Study.
Am J Hematol
; 2018 Jun 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-29905378
8.
Correction to: 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): 656, 2021 Sep 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-34517814
9.
Phenome-wide association study (PheWAS) for detection of pleiotropy within the Population Architecture using Genomics and Epidemiology (PAGE) Network.
PLoS Genet
; 9(1): e1003087, 2013.
Artículo
en Inglés
| MEDLINE | ID: mdl-23382687
10.
A systematic mapping approach of 16q12.2/FTO and BMI in more than 20,000 African Americans narrows in on the underlying functional variation: results from the Population Architecture using Genomics and Epidemiology (PAGE) study.
PLoS Genet
; 9(1): e1003171, 2013.
Artículo
en Inglés
| MEDLINE | ID: mdl-23341774
11.
Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-differential effects via GAUDI.
Nat Commun
; 15(1): 1016, 2024 Feb 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-38310129
12.
Causal effects on complex traits are similar for common variants across segments of different continental ancestries within admixed individuals.
Nat Genet
; 55(4): 549-558, 2023 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-36941441
13.
Transcriptome-Wide Association Study of Blood Cell Traits in African Ancestry and Hispanic/Latino Populations.
Genes (Basel)
; 12(7)2021 07 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-34356065
14.
Multi-Ethnic Genome-Wide Association Study of Decomposed Cardioelectric Phenotypes Illustrates Strategies to Identify and Characterize Evidence of Shared Genetic Effects for Complex Traits.
Circ Genom Precis Med
; 13(4): e002680, 2020 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-32602732
15.
Social (Pragmatic) Communication Disorder: Another name for the Broad Autism Phenotype?
Autism
; 23(8): 1982-1992, 2019 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-30931583
16.
Pilot Study for Implementing an Osteoporosis Education and Exercise Program in an Assisted Living Facility and Senior Community.
J Appl Gerontol
; 37(6): 745-762, 2018 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-27733660
17.
HLA DR and DQ alleles and haplotypes associated with clinical response to glatiramer acetate in multiple sclerosis.
Mult Scler Relat Disord
; 2(4): 340-8, 2013 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-25877844
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