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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 3, 2023. (Total: 221687Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Cognition and UFD1L[original query]
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
Polymorphisms in schizophrenia candidate gene UFD1L may contribute to cognitive deficits.
Psychiatry research 2013 Aug 209 (1): 110-3.
Ota Vanessa K, Berberian Arthur A, Gadelha Ary, Santoro Marcos L, Ottoni Gustavo L, Matsuzaka Camila T, Mari Jair J, Melaragno Maria I, Lara Diogo R, Smith Marília A C, Belangero Sintia I, Bressan Rodrigo
Association of genetic variants at 22q11.2 chromosomal region with cognitive performance in Japanese patients with schizophrenia.
Schizophrenia research. Cognition 2019 Sep 17 100134.
Akiyama Kazufumi, Saito Atsushi, Saito Satoshi, Ozeki Yuji, Watanabe Takashi, Fujii Kumiko, Shimoda Kazuta
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