The hunt for gene effects pertinent to behavioral traits and psychiatric disorders: From mouse to human

Behavior genetics and postgenomics

(2012) Evan Charney   BEHAVIORAL AND BRAIN SCIENCES

The mystery of missing heritability: Genetic interactions create phantom heritability

(2012) O. Zuk et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Behavioral profiles of mouse models for autism spectrum disorders

(2011) Elodie Ey et al.   Autism Research

Genetic analysis of complex traits in the emerging Collaborative Cross

(2011) David L. Aylor et al.   GENOME RESEARCH

Autism candidate genes via mouse phenomics

(2011) Terrence F. Meehan et al.   JOURNAL OF BIOMEDICAL INFORMATICS

Soluble tau Species, Not Neurofibrillary Aggregates, Disrupt Neural System Integration in a tau Transgenic Model

(2011) Leora M. Fox et al.   JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY

Genome-wide association studies establish that human intelligence is highly heritable and polygenic

(2011) G Davies et al.   MOLECULAR PSYCHIATRY

Evidence-based psychiatric genetics, AKA the false dichotomy between common and rare variant hypotheses

(2011) P M Visscher et al.   MOLECULAR PSYCHIATRY

Initial impact of the sequencing of the human genome

(2011) Eric S. Lander   NATURE

New mouse models of autism highlight need for standardized tests

(2011) Sarah C P Williams   NATURE MEDICINE

Mice line up for success

(2011) Mary Muers   NATURE REVIEWS GENETICS

High Frequencies of De Novo CNVs in Bipolar Disorder and Schizophrenia

(2011) Dheeraj Malhotra et al.   NEURON

Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders

(2011) Dan Levy et al.   NEURON

Rare De Novo Variants Associated with Autism Implicate a Large Functional Network of Genes Involved in Formation and Function of Synapses

(2011) Sarah R. Gilman et al.   NEURON

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

(2011) Stephan J. Sanders et al.   NEURON

The Meaning of the Human Genome Project for Neuropsychiatric Disorders

(2011) S. E. Hyman   SCIENCE

Genetics of autism spectrum disorders

(2011) Daniel H. Geschwind   TRENDS IN COGNITIVE SCIENCES

A comparison of selected quantitative trait loci associated with alcohol use phenotypes in humans and mouse models

(2010) Cindy L. Ehlers et al.   ADDICTION BIOLOGY

The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: Evidence from a large collaborative study totaling 4,963 Subjects

(2010) Thais S. Rizzi et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Genetic Heterogeneity in Human Disease

(2010) Jon McClellan et al.   CELL

A genome-wide scan for common alleles affecting risk for autism

(2010) R. Anney et al.   HUMAN MOLECULAR GENETICS

Phenothiazine-mediated rescue of cognition in tau transgenic mice requires neuroprotection and reduced soluble tau burden

(2010) John C O'Leary et al.   Molecular Neurodegeneration

Meta-analysis of genome-wide association studies for personality

(2010) M H M de Moor et al.   MOLECULAR PSYCHIATRY

The NIH Roadmap Epigenomics Mapping Consortium

(2010) Bradley E Bernstein et al.   NATURE BIOTECHNOLOGY

Behavioural phenotyping assays for mouse models of autism

(2010) Jill L. Silverman et al.   NATURE REVIEWS NEUROSCIENCE

A systems genetic analysis of alcohol drinking by mice, rats and men: Influence of brain GABAergic transmission

(2010) Laura M. Saba et al.   NEUROPHARMACOLOGY

Is Pharma Running Out of Brainy Ideas?

(2010) G. Miller   SCIENCE

Beyond genome-wide association studies: genetic heterogeneity and individual predisposition to cancer

(2010) Antonella Galvan et al.   TRENDS IN GENETICS

A method for mapping intralocus interactions influencing excessive alcohol drinking

(2009) Tamara J. Phillips et al.   MAMMALIAN GENOME

Systematic behavioral evaluation of Huntington's disease transgenic and knock-in mouse models

(2009) Liliana Menalled et al.   NEUROBIOLOGY OF DISEASE

The Impact of Genetic Research on our Understanding of Normal Cognitive Ageing: 1995 to 2009

(2009) Antony Payton   NEUROPSYCHOLOGY REVIEW

Genomewide Association Studies and Human Disease

(2009) John Hardy et al.   NEW ENGLAND JOURNAL OF MEDICINE

Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders

(2009) Jonathan Sebat et al.   TRENDS IN GENETICS

Rare chromosomal deletions and duplications increase risk of schizophrenia

(2008) Jennifer L. Stone et al.   NATURE

Large recurrent microdeletions associated with schizophrenia

(2008) Hreinn Stefansson et al.   NATURE

Copy Number Variation and Schizophrenia

(2008) D. St Clair   SCHIZOPHRENIA BULLETIN

Dissection of a QTL Hotspot on Mouse Distal Chromosome 1 that Modulates Neurobehavioral Phenotypes and Gene Expression

(2008) Khyobeni Mozhui et al.   PLoS Genetics