Common genetic variants on 5p14.1 associate with autism spectrum disorders.

Wang K, Zhang H, Ma D, Bucan M, Glessner JT, Abrahams BS, Salyakina D, Imielinski M, Bradfield JP, Sleiman PM, Kim CE, Hou C, Frackelton E, Chiavacci R, Takahashi N, Sakurai T, Rappaport E, Lajonchere CM, Munson J, Estes A, Korvatska O, Piven J, Sonnenblick LI, Alvarez Retuerto AI, Herman EI, Dong H, Hutman T, Sigman M, Ozonoff S, Klin A, Owley T, Sweeney JA, Brune CW, Cantor RM, Bernier R, Gilbert JR, Cuccaro ML, McMahon WM, Miller J, State MW, Wassink TH, Coon H, Levy SE, Schultz RT, Nurnberger JI, Haines JL, Sutcliffe JS, Cook EH, Minshew NJ, Buxbaum JD, Dawson G, Grant SF, Geschwind DH, Pericak-Vance MA, Schellenberg GD, Hakonarson H
Nature. 2009 459 (7246): 528-33

PMID: 19404256 · PMCID: PMC2943511 · DOI:10.1038/nature07999

MeSH Terms (16)

Autistic Disorder Brain Cadherins Case-Control Studies Cell Adhesion Cell Adhesion Molecules, Neuronal Chromosomes, Human, Pair 5 Cohort Studies Genetic Markers Genetic Predisposition to Disease Genetic Variation Genome-Wide Association Study Genotype Humans Polymorphism, Single Nucleotide Reproducibility of Results

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