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Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications.
Gur RC, Bearden CE, Jacquemont S, Swillen A, van Amelsvoort T, van den Bree M, Vorstman J, Sebat J, Ruparel K, Gallagher RS, McClellan E, White L, Crowley TB, Giunta V, Kushan L, O'Hora K, Verbesselt J, Vandensande A, Vingerhoets C, van Haelst M, Hall J, Harwood J, Chawner SJRA, Patel N, Palad K, Hong O, Guevara J, Martin CO, Jizi K, Bélanger AM, Scherer SW, Bassett AS, McDonald-McGinn DM, Gur RE. Gur RC, et al. Among authors: vorstman j. Mol Psychiatry. 2024 Jul 24. doi: 10.1038/s41380-024-02661-y. Online ahead of print. Mol Psychiatry. 2024. PMID: 39048645
No evidence that common genetic risk variation is shared between schizophrenia and autism.
Vorstman JA, Anney RJ, Derks EM, Gallagher L, Gill M, de Jonge MV, van Engeland H, Kahn RS, Ophoff RA; Autism Genome Project, the International Schizophrenia Consortium. Vorstman JA, et al. Am J Med Genet B Neuropsychiatr Genet. 2013 Jan;162B(1):55-60. doi: 10.1002/ajmg.b.32121. Epub 2012 Nov 28. Am J Med Genet B Neuropsychiatr Genet. 2013. PMID: 23193033 Free article.
Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders.
Anney RJ, Kenny EM, O'Dushlaine C, Yaspan BL, Parkhomenka E, Buxbaum JD, Sutcliffe J, Gill M, Gallagher L; Autism Genome Project; Buxbaum JD, Sutcliffe J, Gill M, Gallagher L. Anney RJ, et al. Eur J Hum Genet. 2011 Oct;19(10):1082-9. doi: 10.1038/ejhg.2011.75. Epub 2011 Apr 27. Eur J Hum Genet. 2011. PMID: 21522181 Free PMC article.
168 results