Risk of psychiatric illness from advanced paternal age is not predominantly from de novo mutations

Evidence for Genetic Overlap Between Schizophrenia and Age at First Birth in Women

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Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

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A New Initiative on Precision Medicine

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Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu

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Most genetic risk for autism resides with common variation

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Defining the role of common variation in the genomic and biological architecture of adult human height

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The Rate of Nonallelic Homologous Recombination in Males Is Highly Variable, Correlated between Monozygotic Twins and Independent of Age

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A Comprehensive Assessment of Parental Age and Psychiatric Disorders

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“Selfish Spermatogonial Selection”: A Novel Mechanism for the Association Between Advanced Paternal Age and Neurodevelopmental Disorders

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Interpreting the role of de novo protein-coding mutations in neuropsychiatric disease

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Whole-Genome Sequencing in Autism Identifies Hot Spots for De Novo Germline Mutation

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(2012) Peter D. Keightley   GENETICS

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De novo mutations revealed by whole-exome sequencing are strongly associated with autism

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Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

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Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs

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Fecundity of Patients With Schizophrenia, Autism, Bipolar Disorder, Depression, Anorexia Nervosa, or Substance Abuse vs Their Unaffected Siblings

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Common genetic variants, acting additively, are a major source of risk for autism

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Autism spectrum disorders and autistic traits: A decade of new twin studies

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Copy Number Variants in Schizophrenia: Confirmation of Five Previous Findings and New Evidence for 3q29 Microdeletions and VIPR2 Duplications

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The Genetics of Autism Spectrum Disorders and Related Neuropsychiatric Disorders in Childhood

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Advancing paternal age and risk of autism: new evidence from a population-based study and a meta-analysis of epidemiological studies

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A map of human genome variation from population-scale sequencing

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Meta-analysis of Paternal Age and Schizophrenia Risk in Male Versus Female Offspring

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Risk of Autism and Increasing Maternal and Paternal Age in a Large North American Population

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Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study

(2009) Paul Lichtenstein et al.   LANCET

The role of genetic variation in the causation of mental illness: an evolution-informed framework

(2009) R Uher   MOLECULAR PSYCHIATRY

Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors

(2009) Anne Goriely et al.   NATURE GENETICS

Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia

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