Detalhe da pesquisa
1.
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids.
Am J Hum Genet
; 109(8): 1366-1387, 2022 08 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35931049
2.
A UVB-responsive common variant at chromosome band 7p21.1 confers tanning response and melanoma risk via regulation of the aryl hydrocarbon receptor, AHR.
Am J Hum Genet
; 108(9): 1611-1630, 2021 09 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34343493
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.
Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits.
PLoS Genet
; 16(10): e1008718, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33045005
5.
Genetic and Epigenetic Fine Mapping of Complex Trait Associated Loci in the Human Liver.
Am J Hum Genet
; 105(1): 89-107, 2019 07 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31204013
6.
IL-1 Transcriptional Responses to Lipopolysaccharides Are Regulated by a Complex of RNA Binding Proteins.
J Immunol
; 204(5): 1334-1344, 2020 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31953354
7.
Identifying differential regulatory control of APOE É4 on African versus European haplotypes as potential therapeutic targets.
Alzheimers Dement
; 18(10): 1930-1942, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34978147
8.
A trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesity.
Hum Mol Genet
; 28(19): 3327-3338, 2019 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31504550
9.
Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects.
Am J Hum Genet
; 102(1): 88-102, 2018 01 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29304378
10.
Canonical Notch signaling is required for bone morphogenetic protein-mediated human osteoblast differentiation.
Stem Cells
; 38(10): 1332-1347, 2020 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32535942
11.
Genetic potential and height velocity during childhood and adolescence do not fully account for shorter stature in cystic fibrosis.
Pediatr Res
; 89(3): 653-659, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32386398
12.
A Dementia-Associated Risk Variant near TMEM106B Alters Chromatin Architecture and Gene Expression.
Am J Hum Genet
; 101(5): 643-663, 2017 Nov 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29056226
13.
Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium.
PLoS Genet
; 13(4): e1006719, 2017 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-28430825
14.
Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index.
Hum Mol Genet
; 25(2): 389-403, 2016 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26604143
15.
Leveraging epigenomics and contactomics data to investigate SNP pairs in GWAS.
Hum Genet
; 137(5): 413-425, 2018 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-29797095
16.
A trans-ethnic genome-wide association study identifies gender-specific loci influencing pediatric aBMD and BMC at the distal radius.
Hum Mol Genet
; 24(17): 5053-9, 2015 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26041818
17.
Relative contribution of type 1 and type 2 diabetes loci to the genetic etiology of adult-onset, non-insulin-requiring autoimmune diabetes.
BMC Med
; 15(1): 88, 2017 04 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-28438156
18.
The type 2 diabetes presumed causal variant within TCF7L2 resides in an element that controls the expression of ACSL5.
Diabetologia
; 59(11): 2360-2368, 2016 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-27539148
19.
BMD Loci Contribute to Ethnic and Developmental Differences in Skeletal Fragility across Populations: Assessment of Evolutionary Selection Pressures.
Mol Biol Evol
; 32(11): 2961-72, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26226985
20.
A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories.
J Med Genet
; 51(6): 419-24, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24706941