Associations between neurodevelopmental genes, neuroanatomy, and ultra high risk symptoms of psychosis in 22q11.2 deletion syndrome.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2017 Jan .
Thompson Carlie A, Karelis Jason, Middleton Frank A, Gentile Karen, Coman Ioana L, Radoeva Petya D, Mehta Rashi, Fremont Wanda P, Antshel Kevin M, Faraone Stephen V, Kates Wendy
Increased corpus callosum volume in children with chromosome 22q11.2 deletion syndrome is associated with neurocognitive deficits and genetic polymorphisms.
European journal of human genetics : EJHG 2012 Oct 20 (10): 1051-7.
Shashi Vandana, Francis Alan, Hooper Stephen R, Kranz Peter G, Zapadka Michael, Schoch Kelly, Ip Edward, Tandon Neeraj, Howard Timothy D, Keshavan Matcheri