Detalhe da pesquisa
1.
Deep Resequencing of the 1q22 Locus in Non-Lobar Intracerebral Hemorrhage.
Ann Neurol
; 95(2): 325-337, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37787451
2.
COVID-19 and systemic lupus erythematosus genetics: A balance between autoimmune disease risk and protection against infection.
PLoS Genet
; 18(11): e1010253, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36327221
3.
A Genomic Risk Score Identifies Individuals at High Risk for Intracerebral Hemorrhage.
Stroke
; 54(4): 973-982, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36799223
4.
Sex differences in human adipose tissue gene expression and genetic regulation involve adipogenesis.
Genome Res
; 30(10): 1379-1392, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32967914
5.
Transcriptome-wide analyses of adipose tissue in outbred rats reveal genetic regulatory mechanisms relevant for human obesity.
Physiol Genomics
; 54(6): 206-219, 2022 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35467982
6.
A plausibly causal functional lupus-associated risk variant in the STAT1-STAT4 locus.
Hum Mol Genet
; 27(13): 2392-2404, 2018 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29912393
7.
Genome-wide association studies suggest that APOL1-environment interactions more likely trigger kidney disease in African Americans with nondiabetic nephropathy than strong APOL1-second gene interactions.
Kidney Int
; 94(3): 599-607, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29885931
8.
Lupus Risk Variant Increases pSTAT1 Binding and Decreases ETS1 Expression.
Am J Hum Genet
; 96(5): 731-9, 2015 May 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-25865496
9.
Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND).
PLoS Genet
; 11(8): e1005352, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26305897
10.
Trans-Ethnic Mapping of BANK1 Identifies Two Independent SLE-Risk Linkage Groups Enriched for Co-Transcriptional Splicing Marks.
Int J Mol Sci
; 19(8)2018 Aug 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30096841
11.
Use of Statins and Outcomes in Intracerebral Hemorrhage Patients.
Stroke
; 48(8): 2098-2104, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28663510
12.
Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage.
Am J Hum Genet
; 94(4): 511-21, 2014 Apr 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-24656865
13.
Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes.
PLoS Genet
; 10(8): e1004517, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25102180
14.
Factors Considered by Clinicians when Prognosticating Intracerebral Hemorrhage Outcomes.
Neurocrit Care
; 27(3): 316-325, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-28744847
15.
APOL1 renal-risk genotypes associate with longer hemodialysis survival in prevalent nondiabetic African American patients with end-stage renal disease.
Kidney Int
; 90(2): 389-395, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27157696
16.
Mapping adipose and muscle tissue expression quantitative trait loci in African Americans to identify genes for type 2 diabetes and obesity.
Hum Genet
; 135(8): 869-80, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27193597
17.
Preferential association of a functional variant in complement receptor 2 with antibodies to double-stranded DNA.
Ann Rheum Dis
; 75(1): 242-52, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25180293
18.
Prophylactic Antiepileptic Drug Use and Outcome in the Ethnic/Racial Variations of Intracerebral Hemorrhage Study.
Stroke
; 46(12): 3532-5, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26470777
19.
Identification of IRF8, TMEM39A, and IKZF3-ZPBP2 as susceptibility loci for systemic lupus erythematosus in a large-scale multiracial replication study.
Am J Hum Genet
; 90(4): 648-60, 2012 Apr 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-22464253
20.
Differential effects of MYH9 and APOL1 risk variants on FRMD3 Association with Diabetic ESRD in African Americans.
PLoS Genet
; 7(6): e1002150, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21698141