Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Intellectual Disability and CHRNA7[original query] |
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| 15q13.3 microdeletions increase risk of idiopathic generalized epilepsy. Nature genetics 2009 Feb 41 (2): 160-2. Helbig Ingo, Mefford Heather C, Sharp Andrew J, Guipponi Michel, Fichera Marco, Franke Andre, Muhle Hiltrud, de Kovel Carolien, Baker Carl, von Spiczak Sarah, Kron Katherine L, Steinich Ines, Kleefuss-Lie Ailing A, Leu Costin, Gaus Verena, Schmitz Bettina, Klein Karl M, Reif Philipp S, Rosenow Felix, Weber Yvonne, Lerche Holger, Zimprich Fritz, Urak Lydia, Fuchs Karoline, Feucht Martha, Genton Pierre, Thomas Pierre, Visscher Frank, de Haan Gerrit-Jan, Møller Rikke S, Hjalgrim Helle, Luciano Daniela, Wittig Michael, Nothnagel Michael, Elger Christian E, Nürnberg Peter, Romano Corrado, Malafosse Alain, Koeleman Bobby P C, Lindhout Dick, Stephani Ulrich, Schreiber Stefan, Eichler Evan E, Sander Thom |
| Analysis of CHRNA7 rare variants in autism spectrum disorder susceptibility. American journal of medical genetics. Part A 2015 Apr 167A (4): 715-23. Bacchelli Elena, Battaglia Agatino, Cameli Cinzia, Lomartire Silvia, Tancredi Raffaella, Thomson Susanne, Sutcliffe James S, Maestrini Ele |
| Evaluation of multiple putative risk alleles within the 15q13.3 region for genetic generalized epilepsy. Epilepsy research 2015 Sep 117 70-73. Damiano John A, Mullen Saul A, Hildebrand Michael S, Bellows Susannah T, Lawrence Kate M, Arsov Todor, Dibbens Leanne, Major Heather, Dahl Hans-Henrik M, Mefford Heather C, Darbro Benjamin W, Scheffer Ingrid E, Berkovic Samuel |
| Chrna7 deficient mice manifest no consistent neuropsychiatric and behavioral phenotypes. Scientific reports 2017 1 7 39941. Yin Jiani, Chen Wu, Yang Hongxing, Xue Mingshan, Schaaf Christian |
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- Page last updated:Jun 02, 2023
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