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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 10, 2024. (Total: 234259Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Autistic Disorder and CNTNAP2[original query]
Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders.
European journal of human genetics : EJHG 2013 Mar 21 (3): 310-6.
Boccuto Luigi, Lauri Maria, Sarasua Sara M, Skinner Cindy D, Buccella Daniela, Dwivedi Alka, Orteschi Daniela, Collins Julianne S, Zollino Marcella, Visconti Paola, Dupont Barb, Tiziano Danilo, Schroer Richard J, Neri Giovanni, Stevenson Roger E, Gurrieri Fiorella, Schwartz Charles
Variants of the CNTNAP2 5' promoter as risk factors for autism spectrum disorders: a genetic and functional approach.
Molecular psychiatry 2015 Jul 20 (7): 839-49.
Chiocchetti A G, Kopp M, Waltes R, Haslinger D, Duketis E, Jarczok T A, Poustka F, Voran A, Graab U, Meyer J, Klauck S M, Fulda S, Freitag C
A common variant of CNTNAP2 is associated with sub-threshold autistic traits and intellectual disability.
PloS one 2021 12 16 (12): e0260548.
Shiota Yuka, Hirosawa Tetsu, Yoshimura Yuko, Tanaka Sanae, Hasegawa Chiaki, Iwasaki Sumie, An Kyung-Min, Soma Daiki, Sano Masuhiko, Yokoyama Shigeru, Kikuchi Mitsu
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