Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: Epilepsy and NRXN1[original query] |
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Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications. The American journal of psychiatry 2011 Mar 168 (3): 302-16. Levinson Douglas F, Duan Jubao, Oh Sang, Wang Kai, Sanders Alan R, Shi Jianxin, Zhang Nancy, Mowry Bryan J, Olincy Ann, Amin Farooq, Cloninger C Robert, Silverman Jeremy M, Buccola Nancy G, Byerley William F, Black Donald W, Kendler Kenneth S, Freedman Robert, Dudbridge Frank, Pe'er Itsik, Hakonarson Hakon, Bergen Sarah E, Fanous Ayman H, Holmans Peter A, Gejman Pablo |
High frequency of known copy number abnormalities and maternal duplication 15q11-q13 in patients with combined schizophrenia and epilepsy. BMC medical genetics 2011 Nov 12 (1): 1. Stewart LR, Hall AL, Kang SH, Shaw CA, Beaudet AL |
Investigation of NRXN1 deletions: clinical and molecular characterization. American journal of medical genetics. Part A 2013 Apr 161 (4): 4. Dabell MP, Rosenfeld JA, Bader P, Escobar LF, El-Khechen D, Vallee SE, Dinulos MB, Curry C, Fisher J, Tervo R, Hannibal MC, Siefkas K, Wyatt PR, Hughes L, Smith R, Ellingwood S, Lacassie Y, Stroud T, Farrell SA, Sanchez-Lara PA, Randolph LM, Niyazov D, Stevens CA, Schoonveld C, Skidmore D, Mackay S, Miles JH, Moodley M, Huillet A, Neill NJ, Ellison JW, Ballif BC, Shaffer LG |
Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy. Epilepsia 2013 Jan . Møller RS, Weber YG, Klitten LL, Trucks H, Muhle H, Kunz WS, Mefford HC, Franke A, Kautza M, Wolf P, Dennig D, Schreiber S, Rückert IM, Wichmann HE, Ernst JP, Schurmann C, Grabe HJ, Tommerup N, Stephani U, Lerche H, Hjalgrim H, Helbig I, Sander T |
Identification of candidate single-nucleotide polymorphisms in NRXN1 related to antipsychotic treatment response in patients with schizophrenia. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 2014 Aug 39 (9): 2170-8. Jenkins Aaron, Apud José A, Zhang Fengyu, Decot Heather, Weinberger Daniel R, Law Amanda |
Burden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsies. PLoS genetics 2015 May 11 (5): e1005226. Lal Dennis, Ruppert Ann-Kathrin, Trucks Holger, Schulz Herbert, de Kovel Carolien G, Kasteleijn-Nolst Trenité Dorothée, Sonsma Anja C M, Koeleman Bobby P, Lindhout Dick, Weber Yvonne G, Lerche Holger, Kapser Claudia, Schankin Christoph J, Kunz Wolfram S, Surges Rainer, Elger Christian E, Gaus Verena, Schmitz Bettina, Helbig Ingo, Muhle Hiltrud, Stephani Ulrich, Klein Karl M, Rosenow Felix, Neubauer Bernd A, Reinthaler Eva M, Zimprich Fritz, Feucht Martha, Møller Rikke S, Hjalgrim Helle, De Jonghe Peter, Suls Arvid, Lieb Wolfgang, Franke Andre, Strauch Konstantin, Gieger Christian, Schurmann Claudia, Schminke Ulf, Nürnberg Peter, , Sander Thom |
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- Page last updated:Apr 16, 2024
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