Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: NLGN3[original query] |
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NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2005 Jan 132B (1): 74-5. Gauthier Julie, Bonnel Anna, St-Onge Judith, Karemera Liliane, Laurent Sandra, Mottron Laurent, Fombonne Eric, Joober Ridha, Rouleau Guy |
Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probands. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2004 Aug 129B (1): 82-4. Vincent John B, Kolozsvari Debbie, Roberts Wendy S, Bolton Patrick F, Gurling Hugh M D, Scherer Stephen |
Analysis of the neuroligin 4Y gene in patients with autism. Psychiatric genetics 2008 Aug 18 (4): 204-7. Yan Jin, Feng Jinong, Schroer Richard, Li Wenyan, Skinner Cindy, Schwartz Charles E, Cook Edwin H, Sommer Steve |
No evidence for involvement of genetic variants in the X-linked neuroligin genes NLGN3 and NLGN4X in probands with autism spectrum disorder on high functioning level. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008 Jun 147B (4): 535-7. Wermter Anne-Kathrin, Kamp-Becker Inge, Strauch Konstantin, Schulte-Körne Gerd, Remschmidt Helm |
A substitution involving the NLGN4 gene associated with autistic behavior in the Greek population. Genetic testing and molecular biomarkers 2009 Oct 13 (5): 611-5. Pampanos Andreas, Volaki Konstantina, Kanavakis Emmanuel, Papandreou Ourania, Youroukos Sotiris, Thomaidis Loretta, Karkelis Savvas, Tzetis Maria, Kitsiou-Tzeli Soph |
A sex-specific association of common variants of neuroligin genes (NLGN3 and NLGN4X) with autism spectrum disorders in a Chinese Han cohort. Behavioral and brain functions : BBF 2011 7 (1): 13. Yu Jindan, He Xue, Yao Dan, Li Zhongyue, Li Hui, Zhao Zhengy |
Identification of Four Novel Synonymous Substitutions in the X-Linked Genes Neuroligin 3 and Neuroligin 4X in Japanese Patients with Autistic Spectrum Disorder. Autism research and treatment 2012 2012 . Yanagi K, Kaname T, Wakui K, Hashimoto O, Fukushima Y, Naritomi K |
Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disorders. European journal of human genetics : EJHG 2013 Mar 21 (3): 310-6. Boccuto Luigi, Lauri Maria, Sarasua Sara M, Skinner Cindy D, Buccella Daniela, Dwivedi Alka, Orteschi Daniela, Collins Julianne S, Zollino Marcella, Visconti Paola, Dupont Barb, Tiziano Danilo, Schroer Richard J, Neri Giovanni, Stevenson Roger E, Gurrieri Fiorella, Schwartz Charles |
Mutation screening in the Greek population and evaluation of NLGN3 and NLGN4X genes causal factors for autism. Psychiatric genetics 2013 Oct 23 (5): 198-203. Volaki Konstantina, Pampanos Andreas, Kitsiou-Tzeli Sophia, Vrettou Christina, Oikonomakis Vasilis, Sofocleous Christalena, Kanavakis Emmanu |
Lack of association between NLGN3, NLGN4, SHANK2 and SHANK3 gene variants and autism spectrum disorder in a Chinese population. PloS one 2013 8 (2): e56639. Liu Yanyan, Du Yasong, Liu Wenwen, Yang Caohua, Liu Yan, Wang Hongyan, Gong Xiaoho |
Analysis of the genes encoding neuroligins NLGN3 and NLGN4 in Bulgarian patients with autism. Genetic counseling (Geneva, Switzerland) 2012 23 (4): 505-11. Avdjieva-Tzavella D M, Todorov T P, Todorova A P, Kirov A V, Hadjidekova S P, Rukova B B, Litvinenko I O, Hristova-Naydenova D N, Tincheva R S, Toncheva D |
Association Analysis of Noncoding Variants in Neuroligins 3 and 4X Genes with Autism Spectrum Disorder in an Italian Cohort. International journal of molecular sciences 2016 Oct 17 (10): . Landini Martina, Merelli Ivan, Raggi M Elisabetta, Galluccio Nadia, Ciceri Francesca, Bonfanti Arianna, Camposeo Serena, Massagli Angelo, Villa Laura, Salvi Erika, Cusi Daniele, Molteni Massimo, Milanesi Luciano, Marabotti Anna, Mezzelani Alessand |
Significance of neurexin and neuroligin polymorphisms in regulating risk of Hirschsprung's disease. Journal of investigative medicine : the official publication of the American Federation for Clinical Research 2018 Apr . Li Yanhong, Liu Hui, Dong Yub |
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- Page last updated:Apr 22, 2024
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