Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia

A Genome-wide Association Study of Autism Reveals a Common Novel Risk Locus at 5p14.1

(2009) Deqiong Ma et al.   ANNALS OF HUMAN GENETICS

Recurrent Rearrangements in Synaptic and Neurodevelopmental Genes and Shared Biologic Pathways in Schizophrenia, Autism, and Mental Retardation

(2009) Audrey Guilmatre et al.   ARCHIVES OF GENERAL PSYCHIATRY

A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation

(2009) Patrick S Tarpey et al.   NATURE GENETICS

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

(2009) Jonathan Sebat et al.   TRENDS IN GENETICS

Contact in the genetics of autism and schizophrenia

(2009) J. Peter H. Burbach et al.   TRENDS IN NEUROSCIENCES

Novel de novo SHANK3 mutation in autistic patients

(2008) Julie Gauthier et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

A Model Incorporating Potential Skewed X-Inactivation in MZ Girls Suggests that X-Linked QTLs Exist for Several Social Behaviours Including Autism Spectrum Disorder

(2008) C. S. Loat et al.   ANNALS OF HUMAN GENETICS

Mid-frequency DFNA8/12 hearing loss caused by a synonymous TECTA mutation that affects an exonic splice enhancer

(2008) Rob W J Collin et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Mutations in the calcium-related gene IL1RAPL1 are associated with autism

(2008) A. Piton et al.   HUMAN MOLECULAR GENETICS

Association of A/G Polymorphism in Intron 13 of the Monoamine Oxidase B Gene with Schizophrenia in a Spanish Population

(2008) Patricia Gassó et al.   NEUROPSYCHOBIOLOGY

Cerebellar modulation of frontal cortex dopamine efflux in mice: Relevance to autism and schizophrenia

(2008) Guy Mittleman et al.   SYNAPSE

Genetic Variation in an Individual Human Exome

(2008) Pauline C. Ng et al.   PLoS Genetics