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Author: Sarah E Medland

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    • genomics: 5,198 (rank: 3,448 (tie) out of 41,981)
    • neuroscience: 3,918 (rank: 3,487 (tie) out of 65,936)

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Preprints

Understanding science communication in human genetics using text mining

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

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

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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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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

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

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Dynamics of Brain Structure and its Genetic Architecture over the Lifespan

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

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Genome-wide meta-analysis of cognitive empathy: heritability, and correlates with sex, neuropsychiatric conditions and brain anatomy

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

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

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

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The genetic architecture of sporadic and recurrent miscarriage

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Genetic markers of ADHD-related variations in intracranial volume

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

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Planar cell polarity pathway and development of the human visual cortex

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Novel genetic loci affecting facial shape variation in humans

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Genetic Association Study of Childhood Aggression across raters, instruments and age

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Higher genetic risk for schizophrenia is associated with living in urban and populated areas

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

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Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity

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

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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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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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Genetic variants for head size share genes and pathways with cancer

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

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