Associated Papers
Utilizing Genomically Targeted Molecular Data to Improve Patient-Specific Outcomes in Autism Spectrum Disorder.
Hausman-Cohen S et al.
International Journal of Molecular Sciences, 2022
Novel rare variations of the oxytocin receptor (OXTR) gene in autism spectrum disorder individuals.
Liu X et al.
Human Genome Variation, 2015
27081536 (PubMed )
Supplement: hgv201524-s2.xls › Supplenmentary_Table_2
TBX1 mutation identified by exome sequencing in a Japanese family with 22q11.2 deletion syndrome-like craniofacial features and hypocalcemia.
Ogata T et al.
Plos One, 2014
24637876 (PubMed )
Supplement: pone.0091598.s004.pdf
Evidence for the involvement of genetic variation in the oxytocin receptor gene (OXTR) in the etiology of autistic disorders on high-functioning level.
Wermter AK et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2010
Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families.
Ylisaukko-oja T et al.
Annals of Neurology, 2006
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