Detalhe da pesquisa
1.
Limb development genes underlie variation in human fingerprint patterns.
Cell
; 185(1): 95-112.e18, 2022 01 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34995520
2.
Osteoclasts recycle via osteomorphs during RANKL-stimulated bone resorption.
Cell
; 184(5): 1330-1347.e13, 2021 03 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33636130
3.
Osteoclasts recycle via osteomorphs during RANKL-stimulated bone resorption.
Cell
; 184(7): 1940, 2021 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33798441
4.
Genome-wide association study of circulating interleukin 6 levels identifies novel loci.
Hum Mol Genet
; 30(5): 393-409, 2021 04 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-33517400
5.
Regenerating zebrafish scales express a subset of evolutionary conserved genes involved in human skeletal disease.
BMC Biol
; 20(1): 21, 2022 01 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-35057801
6.
Mendelian randomization analysis of factors related to ovulation and reproductive function and endometrial cancer risk.
BMC Med
; 20(1): 419, 2022 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36320039
7.
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders.
Am J Hum Genet
; 103(5): 691-706, 2018 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30388399
8.
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
9.
Development of a polygenic risk score to improve screening for fracture risk: A genetic risk prediction study.
PLoS Med
; 17(7): e1003152, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32614825
10.
Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero.
Hum Mol Genet
; 27(11): 2025-2038, 2018 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29659830
11.
Evaluation of shared genetic aetiology between osteoarthritis and bone mineral density identifies SMAD3 as a novel osteoarthritis risk locus.
Hum Mol Genet
; 26(19): 3850-3858, 2017 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28934396
12.
LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis.
Bioinformatics
; 33(2): 272-279, 2017 01 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27663502
13.
Genetic variants in adult bone mineral density and fracture risk genes are associated with the rate of bone mineral density acquisition in adolescence.
Hum Mol Genet
; 24(14): 4158-66, 2015 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25941325
14.
Genome-wide association study of blood lead shows multiple associations near ALAD.
Hum Mol Genet
; 24(13): 3871-9, 2015 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25820613
15.
A novel common variant in DCST2 is associated with length in early life and height in adulthood.
Hum Mol Genet
; 24(4): 1155-68, 2015 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25281659
16.
Cis and trans effects of human genomic variants on gene expression.
PLoS Genet
; 10(7): e1004461, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25010687
17.
Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment.
PLoS Genet
; 10(6): e1004423, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24945404
18.
Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index.
PLoS Genet
; 10(7): e1004508, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25078964
19.
Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error.
Am J Hum Genet
; 93(2): 264-77, 2013 Aug 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-24144296
20.
Common variants in left/right asymmetry genes and pathways are associated with relative hand skill.
PLoS Genet
; 9(9): e1003751, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24068947