Detalhe da pesquisa
1.
Leveraging drug perturbation to reveal genetic regulators of hepatic gene expression in African Americans.
Am J Hum Genet
; 110(1): 58-70, 2023 01 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36608685
2.
Germline Mutations in CIDEB and Protection against Liver Disease.
N Engl J Med
; 387(4): 332-344, 2022 07 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35939579
3.
Discovery of novel hepatocyte eQTLs in African Americans.
PLoS Genet
; 16(4): e1008662, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32310939
4.
Cardiovascular Pharmacogenomics: Does It Matter If You're Black or White?
Annu Rev Pharmacol Toxicol
; 59: 577-603, 2019 01 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30296897
5.
Genetic association of primary nonresponse to anti-TNFα therapy in patients with inflammatory bowel disease.
Pharmacogenet Genomics
; 32(1): 1-9, 2022 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34380996
6.
Effect of temperature on lysosomal enzyme activity during preparation and storage of dried blood spots.
J Clin Lab Anal
; 32(1)2018 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-28345760
7.
Association of Genetic Variants With Warfarin-Associated Bleeding Among Patients of African Descent.
JAMA
; 320(16): 1670-1677, 2018 10 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-30357299
8.
LA-GEM: imputation of gene expression with incorporation of Local Ancestry.
Pac Symp Biocomput
; 29: 341-358, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38160291
9.
Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetes.
Nat Commun
; 13(1): 4844, 2022 08 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-35999217
10.
Postnatal variations in blood free and acylcarnitines.
J Clin Lab Anal
; 25(2): 126-9, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21438006
11.
Incorporation of DNA methylation into eQTL mapping in African Americans.
Pac Symp Biocomput
; 26: 244-255, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33691021
12.
Genetic and functional evidence links a missense variant in B4GALT1 to lower LDL and fibrinogen.
Science
; 374(6572): 1221-1227, 2021 Dec 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34855475
13.
The Advantages and Challenges of Diversity in Pharmacogenomics: Can Minority Populations Bring Us Closer to Implementation?
Clin Pharmacol Ther
; 106(2): 338-349, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31038731
14.
Age and gender-specific reference intervals for lysosomal enzymes in dried blood spot samples: A study in Indian population.
Clin Biochem
; 50(15): 858-863, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28396248
15.
Protein Z G79A polymorphism and puerperal cerebral venous thrombosis.
Clin Appl Thromb Hemost
; 21(8): 768-71, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24907135
16.
Influence of CYP2C9 polymorphism and phenytoin co-administration on acenocoumarol dose in patients with cerebral venous thrombosis.
Thromb Res
; 133(5): 729-35, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24530212
17.
Angiotensin-converting enzyme gene insertion/deletion polymorphism and small vessel cerebral stroke in Indian population.
Int J Vasc Med
; 2014: 305309, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24523965
18.
Janus kinase (JAK) 2 V617F mutation in Asian Indians with cerebral venous thrombosis and without overt myeloproliferative disorders.
J Neurol Sci
; 323(1-2): 178-82, 2012 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23031663
19.
Screening for inborn errors of metabolism using automated electrospray tandem mass spectrometry: study in high-risk Indian population.
Clin Biochem
; 43(6): 581-8, 2010 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-20026021
20.
The intron 7 -33T>C polymorphism in TFPI gene and cerebral venous thrombosis: evidence for a protective role.
Thromb Res
; 130(4): 687-9, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22836130