Human Genome Epidemiology Literature Finder
Records 1 - 22 (of 22 Records) |
Query Trace: STX1A[original query] |
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Search for genetic variants of the SYNTAXIN 1A (STX1A) gene: the -352 A>T variant in the STX1A promoter associates with impaired glucose metabolism in an Italian obese population. International journal of obesity (2005) 2008 Mar 32 (3): 413-20. Romeo S, Sentinelli F, Cavallo M G, Leonetti F, Fallarino M, Mariotti S, Baroni M |
Genetic and expression analyses reveal elevated expression of syntaxin 1A ( STX1A) in high functioning autism. The international journal of neuropsychopharmacology / official scientific journal of the Collegium Internationale Neuropsychopharmacologicum (CINP) 2008 Dec 11 (8): 1073-84. Nakamura Kazuhiko, Anitha Ayyappan, Yamada Kazuo, Tsujii Masatsugu, Iwayama Yoshimi, Hattori Eiji, Toyota Tomoko, Suda Shiro, Takei Noriyoshi, Iwata Yasuhide, Suzuki Katsuaki, Matsuzaki Hideo, Kawai Masayoshi, Sekine Yoshimoto, Tsuchiya Kenji J, Sugihara Gen-Ichi, Ouchi Yasuomi, Sugiyama Toshiro, Yoshikawa Takeo, Mori Nor |
No association between tagging SNPs of SNARE complex genes (STX1A, VAMP2 and SNAP25) and schizophrenia in a Japanese population. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008 Oct 147B (7): 1327-31. Kawashima Kunihiro, Kishi Taro, Ikeda Masashi, Kitajima Tsuyoshi, Yamanouchi Yoshio, Kinoshita Yoko, Takahashi Nagahide, Saito Shinichi, Ohi Kazutaka, Yasuda Yuka, Hashimoto Ryota, Takeda Masatoshi, Inada Toshiya, Ozaki Norio, Iwata Nak |
De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy. Annals of neurology 2009 Jun 65 (6): 748-53. Hamdan Fadi F, Piton Amélie, Gauthier Julie, Lortie Anne, Dubeau François, Dobrzeniecka Sylvia, Spiegelman Dan, Noreau Anne, Pellerin Stéphanie, Côté Mélanie, Henrion Edouard, Fombonne Eric, Mottron Laurent, Marineau Claude, Drapeau Pierre, Lafrenière Ronald G, Lacaille Jean Claude, Rouleau Guy A, Michaud Jacques |
Contribution of syntaxin 1A to the genetic susceptibility to migraine: a case-control association study in the Spanish population. Neuroscience letters 2009 May 455 (2): 105-9. Corominas Roser, Ribasés Marta, Cuenca-León Ester, Narberhaus Bernat, Serra Selma A, del Toro Mireia, Roig Manuel, Fernández-Fernández José M, Macaya Alfons, Cormand B |
Evidence of syntaxin 1A involvement in migraine susceptibility: a Portuguese study. Archives of neurology 2010 Apr 67 (4): 422-7. Lemos Carolina, Pereira-Monteiro José, Mendonça Denisa, Ramos Eliana Marisa, Barros José, Sequeiros Jorge, Alonso Isabel, Sousa Al |
Replication study of Japanese cohorts supports the role of STX1A in autism susceptibility. Progress in neuro-psychopharmacology & biological psychiatry 2011 Mar 35 (2): 454-8. Nakamura Kazuhiko, Iwata Yasuhide, Anitha Ayyappan, Miyachi Taishi, Toyota Tomoko, Yamada Satoru, Tsujii Masatsugu, Tsuchiya Kenji J, Iwayama Yoshimi, Yamada Kazuo, Hattori Eiji, Matsuzaki Hideo, Matsumoto Kaori, Suzuki Katsuaki, Suda Shiro, Takebayashi Kiyokazu, Takei Nori, Ichikawa Hironobu, Sugiyama Toshiro, Yoshikawa Takeo, Mori Nor |
Candidate pathway association study in cocaine dependence: the control of neurotransmitter release. The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry 2012 Feb 13 (2): 126-34. Fernàndez-Castillo Noèlia, Cormand Bru, Roncero Carlos, Sánchez-Mora Cristina, Grau-Lopez Lara, Gonzalvo Begoña, Miquel Laia, Corominas Roser, Ramos-Quiroga Josep Antoni, Casas Miquel, Ribasés Mar |
Association of GTF2i in the Williams-Beuren syndrome critical region with autism spectrum disorders. Journal of autism and developmental disorders 2012 Jul 42 (7): 1459-69. Malenfant Patrick, Liu Xudong, Hudson Melissa L, Qiao Ying, Hrynchak Monica, Riendeau Noémie, Hildebrand M Jeannette, Cohen Ira L, Chudley Albert E, Forster-Gibson Cynthia, Mickelson Elizabeth C R, Rajcan-Separovic Evica, Lewis M E Suzanne, Holden Jeanette J |
Evaluation of common variants in 16 genes involved in the regulation of neurotransmitter release in ADHD. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 2013 Jun 23 (6): 426-35. Sánchez-Mora Cristina, Cormand Bru, Ramos-Quiroga Josep Antoni, Hervás Amaia, Bosch Rosa, Palomar Glòria, Nogueira Mariana, Gómez-Barros Núria, Richarte Vanesa, Corrales Montse, Garcia-Martinez Iris, Corominas Roser, Guijarro Silvina, Bigorra Aitana, Bayés Mònica, Casas Miguel, Ribasés Mar |
Association analysis of STX1A gene variants in common forms of migraine. Cephalalgia : an international journal of headache 2012 Feb 32 (3): 203-12. Tropeano Maria, Wöber-Bingöl Ciçek, Karwautz Andreas, Wagner Gudrun, Vassos Evangelos, Campos-de-Sousa Sara, Graggaber Andrea, Zesch Heidi E, Kienbacher Christian, Natriashvili Sofia, Kanbur Incifer, Wöber Christian, Collier David |
Clinical and molecular characterization of the potential CF disease modifier syntaxin 1A. European journal of human genetics : EJHG 2013 Dec 21 (12): 1462-6. von Kanel Thomas, Stanke Frauke, Weber Melanie, Schaller Andre, Racine Julien, Kraemer Richard, Chanson Marc, Tümmler Burkhard, Gallati Sabi |
Synaptosome-related (SNARE) genes and their interactions contribute to the susceptibility and working memory of attention-deficit/hyperactivity disorder in males. Progress in neuro-psychopharmacology & biological psychiatry 2015 Mar 57 132-9. Gao Qian, Liu Lu, Chen Yun, Li Haimei, Yang Li, Wang Yufeng, Qian Qiuj |
Synergistic association of STX1A and VAMP2 with cryptogenic epilepsy in North Indian population. Brain and behavior 2016 Jul 6 (7): e00490. Baghel Ruchi, Grover Sandeep, Kaur Harpreet, Jajodia Ajay, Parween Shama, Sinha Juhi, Srivastava Ankit, Srivastava Achal Kumar, Bala Kiran, Chandna Puneet, Kushwaha Suman, Agarwal Rachna, Kukreti Ritushr |
Molecular factors in migraine. Oncotarget 2016 May . Kowalska Marta, Prendecki MichaÅ, Kozubski Wojciech, Lianeri Margarita, Dorszewska Jolan |
Exocytosis-related genes and response to methylphenidate treatment in adults with ADHD. Molecular psychiatry 2018 06 23 (6): 1446-1452. da Silva B S, Cupertino R B, Rovaris D L, Schuch J B, Kappel D B, Müller D, Bandeira C E, Victor M M, Karam R G, Mota N R, Rohde L A, Contini V, Grevet E H, Bau C H |
Replicated association of Synaptotagmin (SYT1) with ADHD and its broader influence in externalizing behaviors. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 2017 Jan . Cupertino Renata Basso, Schuch Jaqueline Bohrer, Bandeira Cibele Edom, da Silva Bruna Santos, Rovaris Diego Luiz, Kappel Djenifer B, Contini Verônica, Salatino-Oliveira Angélica, Vitola Eduardo Schneider, Karam Rafael Gomes, Hutz Mara Helena, Rohde Luis Augusto, Grevet Eugenio Horacio, Bau Claiton Henrique Dotto, Mota Nina Ro |
The Molecular and Neuropathological Consequences of Genetic Risk for Alzheimer's Dementia. Frontiers in neuroscience 2018 12 699. Tasaki Shinya, Gaiteri Chris, Mostafavi Sara, De Jager Philip L, Bennett David |
SNARE Complex Polymorphisms Associate with Alterations of Visual Selective Attention in Alzheimer's Disease. Journal of Alzheimer's disease : JAD 2019 Apr . Costa Andrea Saul, Guerini Franca Rosa, Arosio Beatrice, Galimberti Daniela, Zanzottera Milena, Bianchi Anna, Nemni Raffaello, Clerici Mar |
STX1A gene variations contribute to the susceptibility of children attention-deficit/hyperactivity disorder: a case-control association study. European archives of psychiatry and clinical neuroscience 2019 Apr . Wang Min, Gu Xue, Huang Xin, Zhang Qi, Chen Xinzhen, Wu Ji |
Analysis of Genetic Variants in SCN1A, SCN2A, KCNK18, TRPA1 and STX1A as a Possible Marker of Migraine. Current genomics 2020 Apr 21 (3): 224-236. Kowalska Marta, Prendecki Micha?, Kapelusiak-Pielok Magdalena, Grzelak Teresa, ?agan-J?drzejczyk Urszula, Wiszniewska Ma?gorzata, Kozubski Wojciech, Dorszewska Jolan |
Non-coding variants in VAMP2 and SNAP25 affect gene expression: potential implications in migraine susceptibility. The journal of headache and pain 2023 6 24 (1): 78. Daniela Felício, Andreia Dias, Sandra Martins, Estefânia Carvalho, Alexandra M Lopes, Nádia Pinto, Carolina Lemos, Mariana Santos, Miguel Alves-Ferrei |
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- Page last updated:Apr 22, 2024
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