Human Genome Epidemiology Literature Finder
Records 1 - 20 (of 20 Records) |
Query Trace: VAMP2[original query] |
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Association study between vesicle-associated membrane protein 2 gene polymorphisms and fluvoxamine response in Japanese major depressive patients. Neuropsychobiology 2006 54 (4): 226-30. Saito Shinichi, Takahashi Nagahide, Ishihara Ryoko, Ikeda Masashi, Suzuki Tatsuyo, Kitajima Tsuyoshi, Yamanouchi Yoshio, Iwata Nakao, Yamada Mitsuhiko, Yoshida Keizo, Inada Toshiya, Ozaki Nor |
Association study between genetic variants at the VAMP2 and VAMP3 loci and bipolar affective disorder. Psychiatric genetics 2008 Aug 18 (4): 199-203. Abou Jamra Rami, Gobina Carl Motinda, Becker Tim, Georgi Alexander, Schulze Thomas G, Schmael Christine, Cichon Sven, Propping Peter, Rietschel Marcella, Nöthen Markus M, Schumacher Johann |
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 |
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 |
Genetic variants of synaptic vesicle and presynaptic plasma membrane proteins in idiopathic generalized epilepsy. Journal of receptor and signal transduction research 2014 Feb 34 (1): 38-43. Yilmaz Mustafa, Edgunlu Tuba Gokdogan, Yilmaz Nigar, Cetin Esin Sakalli, Celik Sevim Karakas, Emir Gülser Karadaban, Sözen Ay |
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 |
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 |
Novel SNARE Complex Polymorphisms Associated with Multiple Sclerosis: Signs of Synaptopathy in Multiple Sclerosis. Balkan medical journal 2019 05 36 (3): 174-178. Yal?n Osman Özgür, Gökdo?an Edgünlü Tuba, Karaka? Çelik Sevim, Emre Ufuk, Güne? Ta?k?n, Erdal Yüksel, Ero?lu Ünal Ays |
The Syntaxin-1A gene single nucleotide polymorphism rs4717806 associates with the risk of ischemic heart disease. Medicine 2019 Jun 98 (24): e15846. Guerini Franca R, Ripamonti Enrico, Costa Andrea S, Zanzottera Milena, Agliardi Cristina, Bolognesi Elisabetta, Clerici Mario, Racca Vittor |
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 |
Going Deep into Synaptic Vesicle Machinery Genes and Migraine Susceptibility - A Case-Control Association Study. Headache 2020 9 60 (10): 2152-2165. Quintas Marlene, Neto João Luís, Sequeiros Jorge, Sousa Alda, Pereira-Monteiro José, Lemos Carolina, Alonso Isab |
New genes involved in Angelman syndrome-like: Expanding the genetic spectrum. PloS one 2021 16 (10): e0258766. Aguilera Cinthia, Gabau Elisabeth, Ramirez-Mallafré Ariadna, Brun-Gasca Carme, Dominguez-Carral Jana, Delgadillo Veronica, Laurie Steve, Derdak Sophia, Padilla Natàlia, de la Cruz Xavier, Capdevila Núria, Spataro Nino, Baena Neus, Guitart Miriam, Ruiz An |
Variants in clock genes could be associated with lower risk of type 2 diabetes in an elderly Greek population. Maturitas 2021 Oct 152 20-25. Tsekmekidou Xanthippi, Tsetsos Fotis, Koufakis Theocharis, Georgitsi Marianthi, Papanas Nikolaos, Papazoglou Dimitrios, Roumeliotis Athanasios, Panagoutsos Stylianos, Thodis Elias, Theodoridis Marios, Passadakis Ploumis, Maltezos Efstratios, Paschou Peristera, Kotsa Kallio |
VAMP2 Expression and Genotype Are Possible Discriminators in Different Forms of Dementia. Frontiers in aging neuroscience 2022 4 14 858162. Costa Andrea Saul, Ferri Evelyn, Guerini Franca Rosa, Rossi Paolo Dionigi, Arosio Beatrice, Clerici Mar |
EXOC6 (Exocyst Complex Component 6) Is Associated with the Risk of Type 2 Diabetes and Pancreatic ?-Cell Dysfunction. Biology 2022 3 11 (3): . Sulaiman Nabil, Yaseen Hachim Mahmood, Khalique Anila, Mohammed Abdul Khader, Al Heialy Saba, Taneera Jal |
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 |
VAMP2 Gene-Related Neurodevelopmental Disorder: A Differential Diagnosis for Rett/Angelman-Type Spectrum of Disorders. Molecular syndromology 2023 10 14 (5): 449-456. Danielle Bogue, Gavin Ryan, Evangeline Wassmer, Genomics England Research Consortium, Swati Na |
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- Page last updated:Mar 25, 2024
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