Detalles de la búsqueda
1.
Mapping and characterization of structural variation in 17,795 human genomes.
Nature;
583(7814): 83-89, 2020 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-32460305
2.
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
3.
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
4.
Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study.
Diabetologia;
65(3): 477-489, 2022 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-34951656
5.
The Future of Genomic Studies Must Be Globally Representative: Perspectives from PAGE.
Annu Rev Genomics Hum Genet;
20: 181-200, 2019 08 31.
Artículo
en Inglés
| MEDLINE | ID: mdl-30978304
6.
Centers for Mendelian Genomics: A decade of facilitating gene discovery.
Genet Med;
24(4): 784-797, 2022 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-35148959
7.
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
8.
Insights into genetics, human biology and disease gleaned from family based genomic studies.
Genet Med;
21(4): 798-812, 2019 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-30655598
9.
Correction to: Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium.
Diabetologia;
60(12): 2542-2543, 2017 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-29038867
10.
Transethnic insight into the genetics of glycaemic traits: fine-mapping results from the Population Architecture using Genomics and Epidemiology (PAGE) consortium.
Diabetologia;
60(12): 2384-2398, 2017 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-28905132
11.
The orphan GPCR, Gpr161, regulates the retinoic acid and canonical Wnt pathways during neurulation.
Dev Biol;
402(1): 17-31, 2015 Jun 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-25753732
12.
Fine Mapping and Identification of BMI Loci in African Americans.
Am J Hum Genet;
93(4): 661-71, 2013 Oct 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-24094743
13.
Generalization and dilution of association results from European GWAS in populations of non-European ancestry: the PAGE study.
PLoS Biol;
11(9): e1001661, 2013 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-24068893
14.
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
15.
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
16.
Imputation of coding variants in African Americans: better performance using data from the exome sequencing project.
Bioinformatics;
29(21): 2744-9, 2013 Nov 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-23956302
17.
A novel method for analyzing genetic association with longitudinal phenotypes.
Stat Appl Genet Mol Biol;
12(2): 241-61, 2013 Mar 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-23502345
18.
Association of functional polymorphism rs2231142 (Q141K) in the ABCG2 gene with serum uric acid and gout in 4 US populations: the PAGE Study.
Am J Epidemiol;
177(9): 923-32, 2013 May 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-23552988
19.
Effects of smoking on the genetic risk of obesity: the population architecture using genomics and epidemiology study.
BMC Med Genet;
14: 6, 2013 Jan 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-23311614
20.
Single-variant and multi-variant trend tests for genetic association with next-generation sequencing that are robust to sequencing error.
Hum Hered;
74(3-4): 172-83, 2012.
Artículo
en Inglés
| MEDLINE | ID: mdl-23594495