Detalhe da pesquisa
1.
Predicting genes from phenotypes using human phenotype ontology (HPO) terms.
Hum Genet
; 141(11): 1749-1760, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-35357580
2.
Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder.
Mol Psychiatry
; 26(9): 5239-5250, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33483695
3.
Whole exome and whole genome sequencing with dried blood spot DNA without whole genome amplification.
Hum Mutat
; 39(1): 167-171, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29067733
4.
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
5.
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
6.
Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder.
Mol Psychiatry
; 26(9): 5251, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-33674754
7.
Genetic ancestry and diagnostic yield of exome sequencing in a diverse population.
NPJ Genom Med
; 9(1): 1, 2024 Jan 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38172272
8.
SLCO1B1 functional variants and statin-induced myopathy in people with recent genealogical ancestors from Africa: a population-based real-world study.
medRxiv
; 2023 Dec 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38076949
9.
Diagnostic Yield of Exome Sequencing in a Diverse Pediatric and Prenatal Population is not Associated with Genetic Ancestry.
medRxiv
; 2023 May 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-37293051
10.
Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population.
NPJ Genom Med
; 8(1): 10, 2023 May 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-37236975
11.
Design and coverage of high throughput genotyping arrays optimized for individuals of East Asian, African American, and Latino race/ethnicity using imputation and a novel hybrid SNP selection algorithm.
Genomics
; 98(6): 422-30, 2011 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-21903159
12.
Next generation genome-wide association tool: design and coverage of a high-throughput European-optimized SNP array.
Genomics
; 98(2): 79-89, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21565264
13.
Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experience.
HGG Adv
; 3(3): 100120, 2022 Jul 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-35707062
14.
A Large-Scale Association Study Detects Novel Rare Variants, Risk Genes, Functional Elements, and Polygenic Architecture of Prostate Cancer Susceptibility.
Cancer Res
; 81(7): 1695-1703, 2021 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33293427
15.
VALID: visualization of association study results and linkage disequilibrium.
Genet Epidemiol
; 33(7): 599-603, 2009 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-19197947
16.
Segmentation and estimation for SNP microarrays: a Bayesian multiple change-point approach.
Biometrics
; 66(3): 675-83, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-19764955
17.
Genetic ancestry, skin pigmentation, and the risk of cutaneous squamous cell carcinoma in Hispanic/Latino and non-Hispanic white populations.
Commun Biol
; 3(1): 765, 2020 12 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-33318654
18.
A multiethnic genome-wide analysis of 44,039 individuals identifies 41 new loci associated with central corneal thickness.
Commun Biol
; 3(1): 301, 2020 06 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32528159
19.
The role of exome sequencing in newborn screening for inborn errors of metabolism.
Nat Med
; 26(9): 1392-1397, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32778825
20.
Telomere length and socioeconomic status at neighborhood and individual levels among 80,000 adults in the Genetic Epidemiology Research on Adult Health and Aging cohort.
Environ Epidemiol
; 3(3): e049, 2019 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-33778338