A quantitative association study of SLC25A12 and restricted repetitive behavior traits in autism spectrum disorders

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

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

The Simons Simplex Collection: A Resource for Identification of Autism Genetic Risk Factors

(2010) Gerald D. Fischbach et al.   NEURON

Genetics in psychiatry: common variant association studies

(2010) Joseph D Buxbaum et al.   Molecular Autism

Slc25a12 Disruption Alters Myelination and Neurofilaments: A Model for a Hypomyelination Syndrome and Childhood Neurodevelopmental Disorders

(2009) Takeshi Sakurai et al.   BIOLOGICAL PSYCHIATRY

AGC1 Deficiency Associated with Global Cerebral Hypomyelination

(2009) Rolf Wibom et al.   NEW ENGLAND JOURNAL OF MEDICINE

Failure to Replicate a Genetic Association May Provide Important Clues About Genetic Architecture

(2009) Casey S. Greene et al.   PLoS One

Association study of the SLC25A12 gene and autism in Han Chinese in Taiwan

(2009) Wei-Hsien Chien et al.   PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY

Mitochondrial aspartate/glutamate carrier SLC25A12 gene is associated with autism

(2008) Joni A. Turunen et al.   Autism Research

SLC25A12 expression is associated with neurite outgrowth and is upregulated in the prefrontal cortex of autistic subjects

(2008) A-M Lepagnol-Bestel et al.   MOLECULAR PSYCHIATRY