Detalhe da pesquisa
1.
Gut Microbiota and Blood Metabolites Related to Fiber Intake and Type 2 Diabetes.
Circ Res
; 134(7): 842-854, 2024 Mar 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-38547246
2.
Polygenic Risk Score Associates With Atherosclerotic Plaque Characteristics at Autopsy.
Arterioscler Thromb Vasc Biol
; 44(1): 300-313, 2024 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37916415
3.
X-linked genetic associations in sporadic thoracic aortic dissection.
Am J Med Genet A
; : e63644, 2024 Apr 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38688863
4.
Factors associated with blood mercury concentrations and their interactions with three glutathione S-transferase genes (GSTT1, GSTM1, and GSTP1): an exposure assessment study of typically developing Jamaican children.
BMC Pediatr
; 24(1): 14, 2024 01 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38178055
5.
Epigenome-wide association study of mitochondrial genome copy number.
Hum Mol Genet
; 31(2): 309-319, 2021 12 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-34415308
6.
A Genome-wide Association Study Discovers 46 Loci of the Human Metabolome in the Hispanic Community Health Study/Study of Latinos.
Am J Hum Genet
; 107(5): 849-863, 2020 11 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33031748
7.
Host and gut microbial tryptophan metabolism and type 2 diabetes: an integrative analysis of host genetics, diet, gut microbiome and circulating metabolites in cohort studies.
Gut
; 71(6): 1095-1105, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34127525
8.
Analysis of putative cis-regulatory elements regulating blood pressure variation.
Hum Mol Genet
; 29(11): 1922-1932, 2020 07 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-32436959
9.
Multiple SCN5A variant enhancers modulate its cardiac gene expression and the QT interval.
Proc Natl Acad Sci U S A
; 116(22): 10636-10645, 2019 05 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-31068470
10.
Genetically determined NLRP3 inflammasome activation associates with systemic inflammation and cardiovascular mortality.
Eur Heart J
; 42(18): 1742-1756, 2021 05 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33748830
11.
A systematic analysis of protein-altering exonic variants in chronic obstructive pulmonary disease.
Am J Physiol Lung Cell Mol Physiol
; 321(1): L130-L143, 2021 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33909500
12.
A System for Phenotype Harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) Program.
Am J Epidemiol
; 190(10): 1977-1992, 2021 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33861317
13.
Functionally oriented analysis of cardiometabolic traits in a trans-ethnic sample.
Hum Mol Genet
; 28(7): 1212-1224, 2019 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30624610
14.
Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder.
Am J Hum Genet
; 102(3): 494-504, 2018 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29478781
15.
PPA2-associated sudden cardiac death: extending the clinical and allelic spectrum in 20 new families.
Genet Med
; 23(12): 2415-2425, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34400813
16.
GSTM1 Deletion Exaggerates Kidney Injury in Experimental Mouse Models and Confers the Protective Effect of Cruciferous Vegetables in Mice and Humans.
J Am Soc Nephrol
; 31(1): 102-116, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31727850
17.
Plasma amyloid ß levels are driven by genetic variants near APOE, BACE1, APP, PSEN2: A genome-wide association study in over 12,000 non-demented participants.
Alzheimers Dement
; 17(10): 1663-1674, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34002480
18.
Correlation between concentrations of four heavy metals in cord blood and childhood blood of Jamaican children.
J Environ Sci Health A Tox Hazard Subst Environ Eng
; 56(11): 1196-1205, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34542373
19.
Ultrarapid Nanopore Genome Sequencing in a Critical Care Setting.
N Engl J Med
; 386(7): 700-702, 2022 02 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-35020984
20.
Genetic Variants in LRP1 and ULK4 Are Associated with Acute Aortic Dissections.
Am J Hum Genet
; 99(3): 762-769, 2016 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27569546