Detalhe da pesquisa
1.
Extreme Phenotype Approach Suggests Taste Transduction Pathway for Carotid Plaque in a Multi-Ethnic Cohort.
Stroke
; 51(9): 2761-2769, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32811377
2.
Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities.
Stroke
; 51(7): 2111-2121, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32517579
3.
Sickle Cell Trait and Renal Function in Hispanics in the United States: The Northern Manhattan Study.
Ethn Dis
; 27(1): 11-14, 2017 01 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-28115816
4.
Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas.
Cell Genom
; 4(1): 100468, 2024 Jan 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-38190104
5.
Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease.
Nat Med
; 29(4): 950-962, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-37069360
6.
Rare variants in previously identified linkage regions associated with carotid plaque in Dominican Republic families.
PLoS One
; 17(1): e0250799, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35020748
7.
Genetic determinants of intracranial large artery stenosis in the northern Manhattan study.
J Neurol Sci
; 436: 120218, 2022 05 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-35259553
8.
Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention.
Nat Genet
; 54(9): 1332-1344, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-36071172
9.
Family History of Eating Disorder and the Broad Autism Phenotype in Autism.
Autism Res
; 13(9): 1573-1581, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32888262
10.
Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies.
Nat Commun
; 10(1): 29, 2019 01 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30604766
11.
Sequencing of Linkage Region on Chromosome 12p11 Identifies PKP2 as a Candidate Gene for Left Ventricular Mass in Dominican Families.
G3 (Bethesda)
; 8(2): 659-668, 2018 02 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29288195
12.
Rare Variants in NOD1 Associated with Carotid Bifurcation Intima-Media Thickness in Dominican Republic Families.
PLoS One
; 11(12): e0167202, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27936005
13.
Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants.
Mol Autism
; 6: 43, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26185613
14.
Analysis of genetic linkage data for Mendelian traits.
Curr Protoc Hum Genet
; 83: 1.4.1-31, 2014 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25271837
15.
Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders.
Mol Autism
; 5(1): 1, 2014 Jan 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-24410847