Variants in the 1q21 risk region are associated with a visual endophenotype of autism and schizophrenia

Genome-Wide Linkage Analyses of 12 Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia

(2013) Tiffany A. Greenwood et al.   AMERICAN JOURNAL OF PSYCHIATRY

Marked selective impairment in autism on an index of magnocellular function

(2013) R. Greenaway et al.   NEUROPSYCHOLOGIA

Genome-Wide Association Study of Multiplex Schizophrenia Pedigrees

(2012) Douglas F. Levinson et al.   AMERICAN JOURNAL OF PSYCHIATRY

Genetic association suggests that SMOC1 mediates between prenatal sex hormones and digit ratio

(2012) Adam J. Lawrance-Owen et al.   HUMAN GENETICS

ENCODE Data in the UCSC Genome Browser: year 5 update

(2012) Kate R. Rosenbloom et al.   NUCLEIC ACIDS RESEARCH

Association Analysis of 94 Candidate Genes and Schizophrenia-Related Endophenotypes

(2012) Tiffany A. Greenwood et al.   PLoS One

Do different 'magnocellular tasks' probe the same neural substrate?

(2012) P. T. Goodbourn et al.   PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES

Analysis of 94 Candidate Genes and 12 Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia

(2011) Tiffany A. Greenwood et al.   AMERICAN JOURNAL OF PSYCHIATRY

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

(2011) Douglas F. Levinson et al.   AMERICAN JOURNAL OF PSYCHIATRY

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

(2011) Jillian P. Casey et al.   HUMAN GENETICS

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

Genotype Imputation with Thousands of Genomes

(2011) Bryan Howie et al.   G3-Genes Genomes Genetics

Inference of Unexpected Genetic Relatedness among Individuals in HapMap Phase III

(2010) Trevor J. Pemberton et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Association of MouseDlg4(PSD-95) Gene Deletion and HumanDLG4Gene Variation With Phenotypes Relevant to Autism Spectrum Disorders and Williams' Syndrome

(2010) Michael Feyder et al.   AMERICAN JOURNAL OF PSYCHIATRY

Vision in developmental disorders: Is there a dorsal stream deficit?

(2010) Emma J. Grinter et al.   BRAIN RESEARCH BULLETIN

Integrating common and rare genetic variation in diverse human populations

(2010)   NATURE

Functional impact of global rare copy number variation in autism spectrum disorders

(2010) Dalila Pinto et al.   NATURE

A map of human genome variation from population-scale sequencing

(2010) Richard M. Durbin et al.   NATURE

A synaptic trek to autism

(2009) Thomas Bourgeron   CURRENT OPINION IN NEUROBIOLOGY

Vision in autism spectrum disorders

(2009) David R. Simmons et al.   VISION RESEARCH

A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies

(2009) Bryan N. Howie et al.   PLoS Genetics

Visual Perception and Its Impairment in Schizophrenia

(2008) Pamela D. Butler et al.   BIOLOGICAL PSYCHIATRY

Neuroligins and neurexins link synaptic function to cognitive disease

(2008) Thomas C. Südhof   NATURE

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

Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes

(2008) Heather C. Mefford et al.   NEW ENGLAND JOURNAL OF MEDICINE

Gene–Environment Interactions and Aging Visual Function

(2008) Ruth E. Hogg et al.   OPHTHALMOLOGY