Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Attention and CNTN5[original query] |
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Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD. Science translational medicine 2011 Aug 3 (95): 95ra75. Lionel Anath C, Crosbie Jennifer, Barbosa Nicole, Goodale Tara, Thiruvahindrapuram Bhooma, Rickaby Jessica, Gazzellone Matthew, Carson Andrew R, Howe Jennifer L, Wang Zhuozhi, Wei John, Stewart Alexandre F R, Roberts Robert, McPherson Ruth, Fiebig Andreas, Franke Andre, Schreiber Stefan, Zwaigenbaum Lonnie, Fernandez Bridget A, Roberts Wendy, Arnold Paul D, Szatmari Peter, Marshall Christian R, Schachar Russell, Scherer Stephen |
CNTN6 copy number variations in 14 patients: a possible candidate gene for neurodevelopmental and neuropsychiatric disorders. Journal of neurodevelopmental disorders 2015 7 (1): 26. Hu Jie, Liao Jun, Sathanoori Malini, Kochmar Sally, Sebastian Jessica, Yatsenko Svetlana A, Surti Urvas |
CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders. Molecular psychiatry 2016 May . Mercati O, Huguet G, Danckaert A, André-Leroux G, Maruani A, Bellinzoni M, Rolland T, Gouder L, Mathieu A, Buratti J, Amsellem F, Benabou M, Van-Gils J, Beggiato A, Konyukh M, Bourgeois J-P, Gazzellone M J, Yuen R K C, Walker S, Delépine M, Boland A, Régnault B, Francois M, Van Den Abbeele T, Mosca-Boidron A L, Faivre L, Shimoda Y, Watanabe K, Bonneau D, Rastam M, Leboyer M, Scherer S W, Gillberg C, Delorme R, Cloëz-Tayarani I, Bourgeron |
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