Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Intellectual Disability and NRXN1[original query] |
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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 |
Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literature. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2013 Jun 162B (4): 388-403. Béna Frédérique, Bruno Damien L, Eriksson Mats, van Ravenswaaij-Arts Conny, Stark Zornitza, Dijkhuizen Trijnie, Gerkes Erica, Gimelli Stefania, Ganesamoorthy Devika, Thuresson Ann Charlotte, Labalme Audrey, Till Marianne, Bilan Frédéric, Pasquier Laurent, Kitzis Alain, Dubourgm Christele, Rossi Massimiliano, Bottani Armand, Gagnebin Maryline, Sanlaville Damien, Gilbert-Dussardier Brigitte, Guipponi Michel, van Haeringen Arie, Kriek Marjolein, Ruivenkamp Claudia, Antonarakis Stylianos E, Anderlid Britt Marie, Slater Howard R, Schoumans Jacqueli |
Mutation screening of the neurexin 1 gene in thai patients with intellectual disability and autism spectrum disorder. Genetic testing and molecular biomarkers 2014 Jul 18 (7): 510-5. Yangngam Supaporn, Plong-On Oradawan, Sripo Thanya, Roongpraiwan Rawiwan, Hansakunachai Tippawan, Wirojanan Juthamas, Sombuntham Tasnawat, Ruangdaraganon Nichara, Limprasert Pornpr |
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 |
Etiological yield of SNP microarrays in idiopathic intellectual disability. European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2014 May 18 (3): 327-37. Utine G Eda, Halilo?lu Göknur, Volkan-Salanc? Bilge, Çetinkaya Arda, Kiper Pelin Ö, Alanay Yasemin, Akta? Dilek, Anlar Banu, Topçu Meral, Boduro?lu Koray, Alika?ifo?lu Mehm |
Assessment of Potential Clinical Role for Exome Sequencing in Schizophrenia. Schizophrenia bulletin 2019 5 46 (2): 328-335. Balakrishna Thivia, Curtis Dav |
Both rare and common genetic variants contribute to autism in the Faroe Islands.
NPJ genomic medicine 2019 4 1. Leblond Claire S, Cliquet Freddy, Carton Coralie, Huguet Guillaume, Mathieu Alexandre, Kergrohen Thomas, Buratti Julien, Lemière Nathalie, Cuisset Laurence, Bienvenu Thierry, Boland Anne, Deleuze Jean-François, Stora Tormodur, Biskupstoe Rannva, Halling Jónrit, Andorsdóttir Guðrið, Billstedt Eva, Gillberg Christopher, Bourgeron Thom |
The clinical relevance of intragenic NRXN1 deletions. Journal of medical genetics 2020 1 57 (5): 347-355. Cosemans Nele, Vandenhove Laura, Vogels Annick, Devriendt Koenraad, Van Esch Hilde, Van Buggenhout Griet, Olivié Hilde, de Ravel Thomy, Ortibus Els, Legius Eric, Aerssens Peter, Breckpot Jeroen, R Vermeesch Joris, Shen Sanbing, Fitzgerald Jacqueline, Gallagher Louise, Peeters Hil |
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- Page last updated:Apr 29, 2024
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