Author: Penelope A. Lind

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

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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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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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Genome-wide association and functional studies identify 46 novel loci for alcohol consumption and suggest common genetic mechanisms with neuropsychiatric disorders

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

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Genetic variation in the Major Histocompatibility Complex and association with depression

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