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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 7, 2024. (Total: 232297Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Efficiency and CNTNAP2[original query]
Genome-wide association study with DNA pooling identifies variants at CNTNAP2 associated with pseudoexfoliation syndrome.
European journal of human genetics : EJHG 2011 Feb 19 (2): 186-93.
Krumbiegel Mandy, Pasutto Francesca, Schlötzer-Schrehardt Ursula, Uebe Steffen, Zenkel Matthias, Mardin Christian Y, Weisschuh Nicole, Paoli Daniela, Gramer Eugen, Becker Christian, Ekici Arif B, Weber Bernhard H F, Nürnberg Peter, Kruse Friedrich E, Reis And
Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample.
Journal of neurodevelopmental disorders 2011 Mar 3 (1): 39-49.
Peter Beate, Raskind Wendy H, Matsushita Mark, Lisowski Mark, Vu Tiffany, Berninger Virginia W, Wijsman Ellen M, Brkanac Zor
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
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