Detalhe da pesquisa
1.
Genome-wide association study of antidepressant treatment resistance in a population-based cohort using health service prescription data and meta-analysis with GENDEP.
Pharmacogenomics J
; 20(2): 329-341, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30700811
2.
Quantifying the extent to which index event biases influence large genetic association studies.
Hum Mol Genet
; 26(5): 1018-1030, 2017 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28040731
3.
Meta-analysis of 49â 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels.
J Med Genet
; 53(7): 441-9, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27036123
4.
Investigating shared aetiology between type 2 diabetes and major depressive disorder in a population based cohort.
Am J Med Genet B Neuropsychiatr Genet
; 174(3): 227-234, 2017 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-27480393
5.
Genetic and Environmental Risk for Chronic Pain and the Contribution of Risk Variants for Major Depressive Disorder: A Family-Based Mixed-Model Analysis.
PLoS Med
; 13(8): e1002090, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27529168
6.
Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12.
Thorax
; 71(6): 501-9, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-26917578
7.
MICL controls inflammation in rheumatoid arthritis.
Ann Rheum Dis
; 75(7): 1386-91, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-26275430
8.
Polygenic risk for alcohol dependence associates with alcohol consumption, cognitive function and social deprivation in a population-based cohort.
Addict Biol
; 21(2): 469-80, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25865819
9.
Predicting the risk of rheumatoid arthritis and its age of onset through modelling genetic risk variants with smoking.
PLoS Genet
; 9(9): e1003808, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24068971
10.
A genome-wide copy number association study of osteoporotic fractures points to the 6p25.1 locus.
J Med Genet
; 51(2): 122-31, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24343915
11.
Informed conditioning on clinical covariates increases power in case-control association studies.
PLoS Genet
; 8(11): e1003032, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23144628
12.
Common genetic variants explain the majority of the correlation between height and intelligence: the generation Scotland study.
Behav Genet
; 44(2): 91-6, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24554214
13.
Identification of BACH2 and RAD51B as rheumatoid arthritis susceptibility loci in a meta-analysis of genome-wide data.
Arthritis Rheum
; 65(12): 3058-62, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24022229
14.
Molecular genetic contributions to socioeconomic status and intelligence.
Intelligence
; 44(100): 26-32, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24944428
15.
Genome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 region.
Ann Rheum Dis
; 72(3): 427-36, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22956598
16.
Genome sequencing with gene panel-based analysis for rare inherited conditions in a publicly funded healthcare system: implications for future testing.
Eur J Hum Genet
; 31(2): 231-238, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36474026
17.
Relationship between area-level socio-economic deprivation and autoantibody status in patients with rheumatoid arthritis: multicentre cross-sectional study.
Ann Rheum Dis
; 71(10): 1640-5, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22440825
18.
Identification of AF4/FMR2 family, member 3 (AFF3) as a novel rheumatoid arthritis susceptibility locus and confirmation of two further pan-autoimmune susceptibility genes.
Hum Mol Genet
; 18(13): 2518-22, 2009 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-19359276
19.
Combined effects of three independent SNPs greatly increase the risk estimate for RA at 6q23.
Hum Mol Genet
; 18(14): 2693-9, 2009 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19417005
20.
Common genetic determinants of vitamin D insufficiency: a genome-wide association study.
Lancet
; 376(9736): 180-8, 2010 Jul 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-20541252