Author: Sarah E. Medland

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Preprints

Cohort profile: The Australian Parkinson's Genetics Study (APGS)

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Shared genetic etiology between cortical brain morphology and tobacco, alcohol, and cannabis use

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Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

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The genetic architecture of the human cerebral cortex

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Genomewide association study identifies 30 loci associated with bipolar disorder

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GWAS meta-analysis (N=279,930) identifies new genes and functional links to intelligence

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Detection and interpretation of shared genetic influences on 40 human traits

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Case-control association mapping without cases

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

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Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology

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Trans-ancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

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Dynamics of Brain Structure and its Genetic Architecture over the Lifespan

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Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide

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

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Brain Aging in Major Depressive Disorder: Results from the ENIGMA Major Depressive Disorder working group

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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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Genetic Determinants of Cortical Structure (Thickness, Surface Area and Volumes) among Disease Free Adults in the CHARGE Consortium

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

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Cell-type specific open chromatin profiling in human postmortem brain infers functional roles for non-coding schizophrenia loci

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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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Genome-wide association study of offspring birth weight in 86,577 women highlights maternal genetic effects that are independent of fetal genetics

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The genetic architecture of sporadic and recurrent miscarriage

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The Evolutionary History of Common Genetic Variants Influencing Human Cortical Surface Area

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Genetic regulatory effects modified by immune activation contribute to autoimmune disease associations

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Mega-analysis of 31,396 individuals from 6 countries uncovers strong gene-environment interaction for human fertility

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An epigenome-wide association study of educational attainment (n = 10,767)

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Do Candidate Genes Affect the Brain's White Matter Microstructure? Large-Scale Evaluation of 6,165 Diffusion MRI Scans

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Genetic markers of ADHD-related variations in intracranial volume

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Planar cell polarity pathway and development of the human visual cortex

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Subcortical Volume Trajectories across the Lifespan: Data from 18,605 healthy individuals aged 3-90 years

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Shared Genetic Risk between Eating Disorder- and Substance-Use-Related Phenotypes: Evidence from Genome-Wide Association Studies

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Evidence of causal effect of major depression on alcohol dependence: Findings from the Psychiatric Genomics Consortium

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Symptom-level genetic modelling identifies novel risk loci and unravels the shared genetic architecture of anxiety and depression

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  • In genetic and genomic medicine: 112
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Novel genetic loci affecting facial shape variation in humans

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The Australian Genetics of Depression Study: Study Description and Sample Characteristics

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Within-sibship GWAS improve estimates of direct genetic effects

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Altered structural brain asymmetry in autism spectrum disorder: large-scale analysis via the ENIGMA Consortium

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  • In neuroscience: 6,029
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Genetic insights into the biological mechanisms governing human ovarian ageing

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Dissecting the shared genetic architecture of suicide attempt, psychiatric disorders and known risk factors

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Investigating the causal nature of the relationship of subcortical brain volume with smoking and alcohol use

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Genetic variants for head size share genes and pathways with cancer

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Altered cortical brain structure and increased risk for disease seen decades after perinatal exposure to maternal smoking: A study of 9,000 adults in the UK Biobank

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Concordance Of Genetic Variation That Increases Risk For Tourette Syndrome And That Influences Its Underlying Neurocircuitry

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Understanding science communication in human genetics using text mining

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Analysis of structural brain asymmetries in Attention-Deficit/Hyperactivity Disorder in 39 datasets

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Brain correlates of suicide attempt in 18,925 participants across 18 international cohorts

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Comorbid chronic pain and depression: Shared risk factors and differential antidepressant effectiveness

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