Skip to Main Content

Author Details

Lynne J Hocking
2000
91
51
PMIDPaper TitleJournal TitlePublished Year
30700811Genome-wide association study of antidepressant treatment resistance in a population-based cohort using health service prescription data and meta-analysis with GENDEP.Pharmacogenomics J2020
29892015Multi-ethnic genome-wide association study for atrial fibrillation.Nat Genet2018
28146470Rare and low-frequency coding variants alter human adult height.Nature2017
28809859Do regional brain volumes and major depressive disorder share genetic architecture? A study of Generation Scotland (n=19â¿¿762), UK Biobank (n=24â¿¿048) and the English Longitudinal Study of Ageing (n=5766).Transl Psychiatry2017
28416818Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.Nat Genet2017
28448500Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.PLoS Genet2017
28747752Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.Nat Genet2017
28443625Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.Nat Commun2017
28832619Correction: Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.PLoS Genet2017
27422368A Combined Pathway and Regional Heritability Analysis Indicates NETRIN1 Pathway Is Associated With Major Depressive Disorder.Biol Psychiatry2017
27480393Investigating shared aetiology between type 2 diabetes and major depressive disorder in a population based cohort.Am J Med Genet B Neuropsychiatr Genet2017
28270201Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.Genome Med2017
27519822Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium.Biol Psychiatry2017
27920155<i>SOS2</i> and <i>ACP1</i> Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function.J Am Soc Nephrol2017
28040731Quantifying the extent to which index event biases influence large genetic association studies.Hum Mol Genet2017
28225781Chronic pain, depression and cardiovascular disease linked through a shared genetic predisposition: Analysis of a family-based cohort and twin study.PLoS ONE2017
27911795KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference.Proc Natl Acad Sci U S A2016
25754080Common polygenic risk for autism spectrum disorder (ASD) is associated with cognitive ability in the general population.Mol Psychiatry2016
25869804GWAS for executive function and processing speed suggests involvement of the CADM2 gene.Mol Psychiatry2016
25865819Polygenic risk for alcohol dependence associates with alcohol consumption, cognitive function and social deprivation in a population-based cohort.Addict Biol2016
26917578Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12.Thorax2016
27225129Genome-wide association study identifies 74 loci associated with educational attainment.Nature2016
27036123Meta-analysis of 49â¿¿549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels.J Med Genet2016
26275430MICL controls inflammation in rheumatoid arthritis.Annals of the Rheumatic Diseases2016
26691832Systems genetics identifies a convergent gene network for cognition and neurodevelopmental disease.Nat Neurosci2016
27529168Genetic and Environmental Risk for Chronic Pain and the Contribution of Risk Variants for Major Depressive Disorder: A Family-Based Mixed-Model Analysis.PLoS Med2016
27838479Shared Genetics and Couple-Associated Environment Are Major Contributors to the Risk of Both Clinical and Self-Declared Depression.eBioMedicine2016
26674845Corrigendum: Rare coding variants and X-linked loci associated with age at menarche.Nat Commun2015
25751400Genome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels.Nat Commun2015
26228839Association between cognition and gene polymorphisms involved in thrombosis and haemostasis.2015
26131930Directional dominance on stature and cognition in diverse human populations.Nature2015
26125155Major depressive disorder and current psychological distress moderate the effect of polygenic risk for obesity on body mass index.Transl Psychiatry2015
26635082Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation.Nat Commun2015
26414677Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair.Nat Genet2015
26239645Rare coding variants and X-linked loci associated with age at menarche.Nat Commun2015
24554214Common genetic variants explain the majority of the correlation between height and intelligence: the generation Scotland study.Behav Genet2014
24449572Novel rheumatoid arthritis susceptibility locus at 22q12 identified in an extended UK genome-wide association study.Arthritis and Rheumatology2014
24343915A genome-wide copy number association study of osteoporotic fractures points to the 6p25.1 locus.J Med Genet2014
24909125Editorial overview: Musculoskeletal: Are we on the road to personalised medicine in musculoskeletal diseases?Current Opinion in Pharmacology2014
24944428Molecular genetic contributions to socioeconomic status and intelligence.Intelligence2014
24577799Does a history of depression actually mediate smoking-related pain? Findings from a cross-sectional general population-based study.European Journal of Pain2014
24880767Stratified medicine approaches for the treatment of musculoskeletal disorders.Curr Opin Pharmacol2014
23707277Cardiovascular risk factors associated with the metabolic syndrome are more prevalent in people reporting chronic pain: results from a cross-sectional general population study.Pain2013
22786799Cohort Profile: Generation Scotland: Scottish Family Health Study (GS:SFHS). The study, its participants and their potential for genetic research on health and illness.Int J Epidemiol2013
22956598Genome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 region.Ann Rheum Dis2013
24068971Predicting the risk of rheumatoid arthritis and its age of onset through modelling genetic risk variants with smoking.PLoS Genetics2013
24022229Identification of BACH2 and RAD51B as rheumatoid arthritis susceptibility loci in a meta-analysis of genome-wide data.2013
22234152Polymorphisms in the P2X7 receptor gene are associated with low lumbar spine bone mineral density and accelerated bone loss in post-menopausal women.European Journal of Human Genetics2012
22706899Autophagy: a new player in skeletal maintenance?Journal of Bone and Mineral Research2012
22440825Relationship between area-level socio-economic deprivation and autoantibody status in patients with rheumatoid arthritis: multicentre cross-sectional study.Annals of the Rheumatic Diseases2012
  • 1 - 50 of 91

Recommended Authors

Collaborators

Co-authored papers 32
Co-authored papers 31
Co-authored papers 22
Co-authored papers 22
Co-authored papers 22
Co-authored papers 22
Co-authored papers 22
Co-authored papers 22
Co-authored papers 21
Erasmus University Medical Center
Co-authored papers 21
Co-authored papers 20
Co-authored papers 18
University Medicine Greifswald
Co-authored papers 18
Harvard T.H. Chan School of Public Health
Co-authored papers 18
Co-authored papers 17
National Institute on Aging
Co-authored papers 17
University of Michigan School of Public Health ann arbor
Co-authored papers 16
Co-authored papers 16
Co-authored papers 16
Co-authored papers 16
Co-authored papers 16
Co-authored papers 15
Harvard Medical School, Harvard University
Co-authored papers 15
Co-authored papers 15
Co-authored papers 14
Finnish Cardiovascular Research Center-Tampere - FCRCT, Tampere University
Co-authored papers 14
University Medical Center Rotterdam
Co-authored papers 14
Co-authored papers 13
University of Oxford
Co-authored papers 13
Co-authored papers 13