Author: Nicholas J. Timpson

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Preprints

Genome-wide association study identifies 48 common genetic variants associated with handedness

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Genetic Associations with Subjective Well-Being Also Implicate Depression and Neuroticism

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Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

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Systematic Mendelian randomization framework elucidates hundreds of genetic loci which may influence disease through changes in DNA methylation levels

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Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility

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Causal epigenome-wide association study identifies CpG sites that influence cardiovascular disease risk

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Body mass index and mortality in UK Biobank: revised estimates using Mendelian randomization

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Causal Analyses, Statistical Efficiency And Phenotypic Precision Through Recall-By-Genotype Study Design

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Using Y chromosomal haplogroups in genetic association studies and suggested implications

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Assessing the causal role of body mass index on cardiovascular health in young adults: Mendelian randomization and recall-by-genotype analyses

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Genetic architecture of early childhood growth phenotypes gives insights into their link with later obesity

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Early metabolic features of genetic liability to type 2 diabetes: cohort study with repeated metabolomics across early life

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Expanded genomic analyses for male voice-breaking highlights a shared phenotypic and genetic basis between puberty timing and hair colour

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Epigenetic regulation of PAR4-related platelet activation: mechanistic links between environmental exposure and cardiovascular disease

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Consortium genome-wide meta-analysis for childhood dental caries traits

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Testing the causal effects between subjective wellbeing and physical health using Mendelian randomisation

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Identifying Critical Points of Trajectories of Depressive Symptoms From Childhood to Young Adulthood: Evidence of Sex Differences from the Avon Longitudinal Study of Parents and Children (ALSPAC)

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Inference and visualization of phenome-wide causal relationships using genetic data: an application to dental caries and periodontitis

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Hypothesis-free analysis of deep vein thrombosis aetiology: a Mendelian randomization study

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Association of intrauterine alcohol exposure and offspring depression: A negative control analysis of maternal and partner consumption.

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Schizophrenia-associated variation at ZNF804A correlates with altered experience-dependent dynamics of sleep slow-waves and spindles in healthy young adults

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Exploration of the role of CHRNA5-A3-B4 genotype in smoking behaviours

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Common maternal and fetal genetic variants show expected polygenic effects on the probability of being born small- or large-for-gestational-age (SGA or LGA), except in the smallest 3% of babies

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