Detalhe da pesquisa
1.
A Platform for Generation of Chamber-Specific Cardiac Tissues and Disease Modeling.
Cell
; 176(4): 913-927.e18, 2019 02 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30686581
2.
Thymic regulatory T cells arise via two distinct developmental programs.
Nat Immunol
; 20(2): 195-205, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30643267
3.
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry.
Am J Hum Genet
; 108(4): 564-582, 2021 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33713608
4.
Incorporating G6PD genotyping to identify patients with G6PD deficiency.
Pharmacogenet Genomics
; 32(3): 87-93, 2022 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34693927
5.
Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits.
Am J Hum Genet
; 104(1): 112-138, 2019 01 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30595373
6.
Donor-specific phenotypic variation in hiPSC cardiomyocyte-derived exosomes impacts endothelial cell function.
Am J Physiol Heart Circ Physiol
; 320(3): H954-H968, 2021 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33416449
7.
Human IL12RB1 expression is allele-biased and produces a novel IL12 response regulator.
Genes Immun
; 20(3): 181-197, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29599514
8.
Concordance between glucose-6-phosphate dehydrogenase (G6PD) genotype and phenotype and rasburicase use in patients with hematologic malignancies.
Pharmacogenomics J
; 19(3): 305-314, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30206300
9.
Preemptive clinical pharmacogenetics implementation: current programs in five US medical centers.
Annu Rev Pharmacol Toxicol
; 55: 89-106, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25292429
10.
Hepatic Abundance and Activity of Androgen- and Drug-Metabolizing Enzyme UGT2B17 Are Associated with Genotype, Age, and Sex.
Drug Metab Dispos
; 46(6): 888-896, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29602798
11.
The ENTPD1 promoter polymorphism -860 A > G (rs3814159) is associated with increased gene transcription, protein expression, CD39/NTPDase1 enzymatic activity, and thromboembolism risk.
FASEB J
; 31(7): 2771-2784, 2017 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28302652
12.
The introduction of RNA-DNA differences underlies interindividual variation in the human IL12RB1 mRNA repertoire.
Proc Natl Acad Sci U S A
; 112(50): 15414-9, 2015 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26621740
13.
Incorporating a Genetic Risk Score Into Coronary Heart Disease Risk Estimates: Effect on Low-Density Lipoprotein Cholesterol Levels (the MI-GENES Clinical Trial).
Circulation
; 133(12): 1181-8, 2016 Mar 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-26915630
14.
Genetic and Nongenetic Factors Associated with Protein Abundance of Flavin-Containing Monooxygenase 3 in Human Liver.
J Pharmacol Exp Ther
; 363(2): 265-274, 2017 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28819071
15.
Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations.
Am J Hum Genet
; 93(3): 545-54, 2013 Sep 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-23972371
16.
Comprehensive evaluation of AmpliSeq transcriptome, a novel targeted whole transcriptome RNA sequencing methodology for global gene expression analysis.
BMC Genomics
; 16: 1069, 2015 Dec 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-26673413
17.
Challenges in clinical implementation of CYP2D6 genotyping: choice of variants to test affects phenotype determination.
Genet Med
; 22(1): 232-233, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31341243
18.
Whole exome sequencing identifies a POLRID mutation segregating in a father and two daughters with findings of Klippel-Feil and Treacher Collins syndromes.
Am J Med Genet A
; 167A(1): 95-102, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25348728
19.
PG4KDS: a model for the clinical implementation of pre-emptive pharmacogenetics.
Am J Med Genet C Semin Med Genet
; 166C(1): 45-55, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24619595
20.
Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans.
Hum Mol Genet
; 21(24): 5385-94, 2012 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23001564