Detalhe da pesquisa
1.
A deep catalogue of protein-coding variation in 983,578 individuals.
Nature
; 2024 May 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-38768635
2.
Genotyping, sequencing and analysis of 140,000 adults from Mexico City.
Nature
; 622(7984): 784-793, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37821707
3.
Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program.
Am J Hum Genet
; 109(5): 857-870, 2022 05 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35385699
4.
Author Correction: Genotyping, sequencing and analysis of 140,000 adults from Mexico City.
Nature
; 626(8001): E18, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38332034
5.
Genome-wide association study in the Taiwan Biobank identifies four novel genes for human height: NABP2, RASA2, RNF41 and SLC39A5.
Hum Mol Genet
; 30(23): 2362-2369, 2021 11 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-34270706
6.
X-Chromosome Association Study in Latin American Cohorts Identifies New Loci in Parkinson's Disease.
Mov Disord
; 38(9): 1625-1635, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37469269
7.
On the cross-population generalizability of gene expression prediction models.
PLoS Genet
; 16(8): e1008927, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32797036
8.
Genome-Wide Admixture Mapping of Estimated Glomerular Filtration Rate and Chronic Kidney Disease Identifies European and African Ancestry-of-Origin Loci in Hispanic and Latino Individuals in the United States.
J Am Soc Nephrol
; 33(1): 77-87, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34670813
9.
Association of African Ancestry-Specific APOE Missense Variant R145C With Risk of Alzheimer Disease.
JAMA
; 329(7): 551-560, 2023 02 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-36809323
10.
REHE: Fast variance components estimation for linear mixed models.
Genet Epidemiol
; 45(8): 891-905, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34658056
11.
Genome-wide Significance Thresholds for Admixture Mapping Studies.
Am J Hum Genet
; 104(3): 454-465, 2019 03 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30773276
12.
Characterizing the Genetic Architecture of Parkinson's Disease in Latinos.
Ann Neurol
; 90(3): 353-365, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34227697
13.
Soluble CD14 Levels in the Jackson Heart Study: Associations With Cardiovascular Disease Risk and Genetic Variants.
Arterioscler Thromb Vasc Biol
; 41(6): e369-e378, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33910371
14.
Associating sleep problems with advanced cancer diagnosis, and immune checkpoint treatment outcomes: a pilot study.
Support Care Cancer
; 30(5): 3829-3838, 2022 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-35034197
15.
Associations of variants In the hexokinase 1 and interleukin 18 receptor regions with oxyhemoglobin saturation during sleep.
PLoS Genet
; 15(4): e1007739, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30990817
16.
Admixture mapping identifies novel loci for obstructive sleep apnea in Hispanic/Latino Americans.
Hum Mol Genet
; 28(4): 675-687, 2019 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30403821
17.
In Vivo Functional Effects of CYP2C9 M1L, a Novel and Common Variant in the Yup'ik Alaska Native Population.
Drug Metab Dispos
; 49(5): 345-352, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33632714
18.
Genome-Wide Analysis of Copy Number Variation in Latin American Parkinson's Disease Patients.
Mov Disord
; 36(2): 434-441, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33150996
19.
Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease.
PLoS Genet
; 14(3): e1007293, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29590102
20.
Non-coding variants in MYH11, FZD3, and SORCS3 are associated with dementia in women.
Alzheimers Dement
; 17(2): 215-225, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32966694