Detalhe da pesquisa
1.
Comparison and assessment of family- and population-based genotype imputation methods in large pedigrees.
Genome Res
; 29(1): 125-134, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30514702
2.
Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project.
Genomics
; 111(4): 808-818, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29857119
3.
Analysis of pedigree data in populations with multiple ancestries: Strategies for dealing with admixture in Caribbean Hispanic families from the ADSP.
Genet Epidemiol
; 42(6): 500-515, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29862559
4.
GIGI-Quick: a fast approach to impute missing genotypes in genome-wide association family data.
Bioinformatics
; 34(9): 1591-1593, 2018 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29267877
5.
Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project.
Dement Geriatr Cogn Disord
; 45(1-2): 1-17, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29486463
6.
The orphan GPCR, Gpr161, regulates the retinoic acid and canonical Wnt pathways during neurulation.
Dev Biol
; 402(1): 17-31, 2015 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25753732
7.
PBAP: a pipeline for file processing and quality control of pedigree data with dense genetic markers.
Bioinformatics
; 31(23): 3790-8, 2015 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26231429
8.
Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes.
Hum Genet
; 134(10): 1055-68, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26204995
9.
Post-genome-wide association study challenges for lipid traits: describing age as a modifier of gene-lipid associations in the Population Architecture using Genomics and Epidemiology (PAGE) study.
Ann Hum Genet
; 77(5): 416-25, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23808484
10.
No evidence of interaction between known lipid-associated genetic variants and smoking in the multi-ethnic PAGE population.
Hum Genet
; 132(12): 1427-31, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24100633
11.
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.
Artigo
em Inglês
| MEDLINE | ID: mdl-23594495
12.
Admixture mapping implicates 13q33.3 as ancestry-of-origin locus for Alzheimer disease in Hispanic and Latino populations.
HGG Adv
; 4(3): 100207, 2023 07 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-37333771
13.
Identity-by-descent estimation with population- and pedigree-based imputation in admixed family data.
BMC Proc
; 10(Suppl 7): 295-301, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27980652
14.
Estimating relationships between phenotypes and subjects drawn from admixed families.
BMC Proc
; 10(Suppl 7): 357-362, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27980662
15.
Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech.
PLoS One
; 11(4): e0153864, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27120335
16.
Mapping genes with longitudinal phenotypes via Bayesian posterior probabilities.
BMC Proc
; 8(Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo): S81, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25519410
17.
Lack of associations of ten candidate coronary heart disease risk genetic variants and subclinical atherosclerosis in four US populations: the Population Architecture using Genomics and Epidemiology (PAGE) study.
Atherosclerosis
; 228(2): 390-9, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23587283
18.
Divergent haplotypes and human history as revealed in a worldwide survey of X-linked DNA sequence variation.
Mol Biol Evol
; 24(3): 687-98, 2007 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-17175528