Detalhe da pesquisa
1.
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations.
Cell;
184(18): 4784-4818.e17, 2021 09 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34450027
2.
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations.
Cell;
184(24): 6003-6005, 2021 11 24.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34822786
3.
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology.
Nature;
627(8003): 347-357, 2024 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38374256
4.
An epigenome-wide view of osteoarthritis in primary tissues.
Am J Hum Genet;
109(7): 1255-1271, 2022 07 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35679866
5.
A molecular map of long non-coding RNA expression, isoform switching and alternative splicing in osteoarthritis.
Hum Mol Genet;
31(12): 2090-2105, 2022 06 22.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35088088
6.
Primary osteoarthritis chondrocyte map of chromatin conformation reveals novel candidate effector genes.
Ann Rheum Dis;
2024 Mar 13.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38479789
7.
Causal relationships between anthropometric traits, bone mineral density, osteoarthritis and spinal stenosis: A Mendelian randomisation investigation.
Osteoarthritis Cartilage;
32(6): 719-729, 2024 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38160745
8.
Linking chondrocyte and synovial transcriptional profile to clinical phenotype in osteoarthritis.
Ann Rheum Dis;
80(8): 1070-1074, 2021 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33903094
9.
Genome-wide association of phenotypes based on clustering patterns of hand osteoarthritis identify WNT9A as novel osteoarthritis gene.
Ann Rheum Dis;
80(3): 367-375, 2021 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33055079
10.
A Genome-wide Association Study of Dupuytren Disease Reveals 17 Additional Variants Implicated in Fibrosis.
Am J Hum Genet;
101(3): 417-427, 2017 Sep 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28886342
11.
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.
Am J Hum Genet;
100(6): 865-884, 2017 Jun 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28552196
12.
Very low-depth whole-genome sequencing in complex trait association studies.
Bioinformatics;
35(15): 2555-2561, 2019 08 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30576415
13.
Pathways to understanding the genomic aetiology of osteoarthritis.
Hum Mol Genet;
26(R2): R193-R201, 2017 10 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28977450
14.
The 2018 Otto Aufranc Award: How Does Genome-wide Variation Affect Osteolysis Risk After THA?
Clin Orthop Relat Res;
477(2): 297-309, 2019 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30794219
15.
Very low-depth sequencing in a founder population identifies a cardioprotective APOC3 signal missed by genome-wide imputation.
Hum Mol Genet;
25(11): 2360-2365, 2016 06 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27146844
16.
Analysis with the exome array identifies multiple new independent variants in lipid loci.
Hum Mol Genet;
25(18): 4094-4106, 2016 09 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27466198
17.
Widespread epigenomic, transcriptomic and proteomic differences between hip osteophytic and articular chondrocytes in osteoarthritis.
Rheumatology (Oxford);
57(8): 1481-1489, 2018 08 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29741735
18.
Combination therapy as a potential risk factor for the development of type 2 diabetes in patients with schizophrenia: the GOMAP study.
BMC Psychiatry;
18(1): 249, 2018 08 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30071838
19.
Radiographic endophenotyping in hip osteoarthritis improves the precision of genetic association analysis.
Ann Rheum Dis;
76(7): 1199-1206, 2017 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27974301
20.
Genome-wide meta-analysis of common variant differences between men and women.
Hum Mol Genet;
21(21): 4805-15, 2012 Nov 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22843499