Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 46 Records) |
Query Trace: CHRNB2[original query] |
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A novel mutation of the nicotinic acetylcholine receptor gene CHRNA4 in sporadic nocturnal frontal lobe epilepsy. Epilepsy research 2009 Feb 83 (2-3): 152-6. Chen Yan, Wu Liwen, Fang Yue, He Zhiyi, Peng Bingwei, Shen Yan, Xu |
Alpha4 and beta2 subunits of neuronal nicotinic acetylcholine receptor genes are not associated with methamphetamine-use disorder in the Japanese population. Annals of the New York Academy of Sciences 2008 Oct 1139 70-82. Kishi Taro, Ikeda Masashi, Kitajima Tsuyoshi, Yamanouchi Yoshio, Kinoshita Yoko, Kawashima Kunihiro, Inada Toshiya, Harano Mutsuo, Komiyama Tokutaro, Hori Toru, Yamada Mitsuhiko, Iyo Masaomi, Sora Ichiro, Sekine Yoshimoto, Ozaki Norio, Ujike Hiroshi, Iwata Nak |
Association of nAChR gene haplotypes with heavy alcohol use and body mass. Brain research 2009 Dec 1305 Suppl S72-9. Landgren Sara, Engel Jörgen A, Andersson Malin E, Gonzalez-Quintela Arturo, Campos Joaquin, Nilsson Staffan, Zetterberg Henrik, Blennow Kaj, Jerlhag Elisab |
Association of genes coding for the alpha-4, alpha-5, beta-2 and beta-3 subunits of nicotinic receptors with cigarette smoking and nicotine dependence. Addictive behaviors 2009 Sep 34 (9): 772-5. Etter Jean-François, Hoda Jean-Charles, Perroud Nader, Munafò Marcus, Buresi Catherine, Duret Claudette, Neidhart Elisabeth, Malafosse Alain, Bertrand Dani |
CHRNB2 promoter region: association with subjective effects to nicotine and gene expression differences. Genes, brain, and behavior 2011 Mar 10 (2): 176-85. Hoft N R, Stitzel J A, Hutchison K E, Ehringer M |
Resequencing of nicotinic acetylcholine receptor genes and association of common and rare variants with the Fagerström test for nicotine dependence. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 2010 Nov 35 (12): 2392-402. Wessel Jennifer, McDonald Sarah M, Hinds David A, Stokowski Renee P, Javitz Harold S, Kennemer Michael, Krasnow Ruth, Dirks William, Hardin Jill, Pitts Steven J, Michel Martha, Jack Lisa, Ballinger Dennis G, McClure Jennifer B, Swan Gary E, Bergen Andrew |
Systematic analysis of candidate genes for Alzheimer's disease in a French, genome-wide association study. Journal of Alzheimer's disease : JAD 2010 20 (4): 1181-8. Laumet Geoffroy, Chouraki Vincent, Grenier-Boley Benjamin, Legry Vanessa, Heath Simon, Zelenika Diana, Fievet Nathalie, Hannequin Didier, Delepine Marc, Pasquier Florence, Hanon Olivier, Brice Alexis, Epelbaum Jacques, Berr Claudine, Dartigues Jean-Francois, Tzourio Christophe, Campion Dominique, Lathrop Mark, Bertram Lars, Amouyel Philippe, Lambert Jean-Charl |
Varenicline for smoking cessation: nausea severity and variation in nicotinic receptor genes. The pharmacogenomics journal 2012 Aug 12 (4): 349-58. Swan G E, Javitz H S, Jack L M, Wessel J, Michel M, Hinds D A, Stokowksi R P, McClure J B, Catz S L, Richards J, Zbikowski S M, Deprey M, McAfee T, Conti D V, Bergen A |
Associations of nicotine intake measures with CHRN genes in Finnish smokers. Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco 2011 Aug 13 (8): 686-90. Keskitalo-Vuokko Kaisu, Pitkäniemi Janne, Broms Ulla, Heliövaara Markku, Aromaa Arpo, Perola Markus, Ripatti Samuli, Salminen Outi, Salomaa Veikko, Loukola Anu, Kaprio Jaak |
The identification of a novel mutation of nicotinic acetylcholine receptor gene CHRNB2 in a Chinese patient: Its possible implication in non-familial nocturnal frontal lobe epilepsy. Epilepsy research 2011 Jun 95 (1-2): 94-9. Liu Hui, Lu Cailing, Li Zhenzhong, Zhou Shiyi, Li Xiaoqiao, Ji Liri, Lu Qiang, Lv Ruijuan, Wu Liwen, Ma |
[Mutational analysis of CHRNB2 and CHRNA2 genes in southern Chinese population with autosomal dominant nocturnal frontal lobe epilepsy]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2011 Feb 28 (1): 14-8. Chen Zhi-hong, Zhai Qiong-xiang, Gui Juan, Zhang Yu-xin, Guo Yu-xiong, Ding Jian, Hao Yi |
Genetics of late-onset Alzheimer's disease: update from the alzgene database and analysis of shared pathways. International journal of Alzheimer's disease 2011 2011 . Olgiati P, Politis AM, Papadimitriou GN, De Ronchi D, Serretti A |
Smoking cessation pharmacogenetics: analysis of varenicline and bupropion in placebo-controlled clinical trials. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 2012 Feb 37 (3): 641-50. King David P, Paciga Sara, Pickering Eve, Benowitz Neal L, Bierut Laura J, Conti David V, Kaprio Jaakko, Lerman Caryn, Park Peter |
Possible association of nicotinic acetylcholine receptor gene (CHRNA4 and CHRNB2) polymorphisms with nicotine dependence in Japanese males: an exploratory study. Pharmacopsychiatry 2012 Oct . Chen HI, Shinkai T, Utsunomiya K, Yamada K, Sakata S, Fukunaka Y, Hwang R, De Luca V, Ohmori O, Kennedy JL, Chuang HY, Nakamura J |
Relationship between nicotine dependence and the endophenotype-related trait of cognitive function but not acoustic startle reponses in Japanese patients with schizophrenia. Human psychopharmacology 2013 May 28 (3): 220-9. Kishi Taro, Fukuo Yasuhisa, Okochi Tomo, Kawashima Kunihiro, Moriwaki Masatsugu, Furukawa Osamu, Musso Giovanna M, Fujita Kiyoshi, Correll Christoph U, Iwata Nak |
The association between CHRN genetic variants and dizziness at first inhalation of cigarette smoke. Addictive behaviors 2014 Jan 39 (1): 316-20. Pedneault Maxime, Labbe Aurélie, Roy-Gagnon Marie-Hélène, Low Nancy C, Dugas Erika, Engert James C, O'Loughlin Jennif |
Nominal association with CHRNA4 variants and nicotine dependence. Genes, brain, and behavior 2013 Jan . Kamens HM, Corley RP, McQueen MB, Stallings M, Hopfer C, Crowley T, Brown SA, Hewitt J, Ehringer MA |
Mutational analysis of CHRNB2, CHRNA2 and CHRNA4 genes in Chinese population with autosomal dominant nocturnal frontal lobe epilepsy. International journal of clinical and experimental medicine 2015 8 (6): 9063-70. Chen Zhihong, Wang Lingan, Wang Chun, Chen Qian, Zhai Qiongxiang, Guo Yuxiong, Zhang Yux |
Effect of genetic variation in the nicotinic receptor genes on risk for posttraumatic stress disorder. Psychiatry research 2015 Sep 229 (1-2): 326-31. Kimbrel Nathan A, Garrett Melanie E, Dennis Michelle F, Liu Yutao, Patanam Ilyas, Workgroup Va Mid-Atlantic Mirecc, Ashley-Koch Allison E, Hauser Michael A, Beckham Jean |
CHRNA4 rs1044396 is associated with smoking cessation in varenicline therapy. Frontiers in genetics 2015 6 46. Rocha Santos Juliana, Tomaz Paulo R X, Issa Jaqueline S, Abe Tânia O, Krieger José E, Pereira Alexandre C, Santos Paulo C J |
The possible role of maternal bonding style and CHRNB2 gene polymorphisms in nicotine dependence and related depressive phenotype. Progress in neuro-psychopharmacology & biological psychiatry 2015 Jun 59 84-90. Csala Iren, Egervari Luca, Dome Peter, Faludi Gabor, Dome Balazs, Lazary Jud |
SNPs in NRXN1 and CHRNA5 are associated to smoking and regulation of GABAergic and glutamatergic pathways. Pharmacogenomics 2016 Jun . Pérez-Rubio Gloria, Pérez-Rodríguez Martha E, Fernández-López Juan Carlos, Ramírez-Venegas Alejandra, García-Colunga Jesús, Ávila-Moreno Federico, Camarena Angel, Sansores Raúl H, Falfán-Valencia Ramc |
Genome-wide meta-analysis identifies a novel susceptibility signal at CACNA2D3 for nicotine dependence.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2017 Apr . Yin Xianyong, Bizon Chris, Tilson Jeffrey, Lin Yuan, Gizer Ian R, Ehlers Cindy L, Wilhelmsen Kirk |
Pharmacogenetic study of seven polymorphisms in three nicotinic acetylcholine receptor subunits in smoking-cessation therapies. Scientific reports 2017 Dec 7 (1): 16730. Pintarelli Giulia, Galvan Antonella, Pozzi Paolo, Noci Sara, Pasetti Giovanna, Sala Francesca, Pastorino Ugo, Boffi Roberto, Colombo Frances |
Association and cis-mQTL analysis of variants in CHRNA3-A5, CHRNA7, CHRNB2, and CHRNB4 in relation to nicotine dependence in a Chinese Han population. Translational psychiatry 2018 Apr 8 (1): 83. Liu Qiang, Han Haijun, Wang Maiqiu, Yao Yinghao, Wen Li, Jiang Keran, Ma Yunlong, Fan Rongli, Chen Jiali, Su Kunkai, Yang Zhongli, Cui Wenyan, Yuan Wenji, Jiang Xianzhong, Li Jingjing, Payne Thomas J, Wang Jundong, Li Ming |
[Maternal bonding style, cholinergic receptor gene polymorphisms in association with smoking-related depressive symptoms]. Neuropsychopharmacologia Hungarica : a Magyar Pszichofarmakologiai Egyesulet lapja = official journal of the Hungarian Association of Psychopharmacology 2017 Dec 19 (4): 189-196. Csala Iren, Dome Peter, Lazary Jud |
Genetic Analysis of Lung Cancer and the Germline Impact on Somatic Mutation Burden. Journal of the National Cancer Institute 2022 May . Gabriel Aurélie A G, Atkins Joshua R, Penha Ricardo C C, Smith-Byrne Karl, Gaborieau Valerie, Voegele Catherine, Abedi-Ardekani Behnoush, Milojevic Maja, Olaso Robert, Meyer Vincent, Boland Anne, Deleuze Jean François, Zaridze David, Mukeriya Anush, Swiatkowska Beata, Janout Vladimir, Schejbalová Miriam, Mates Dana, Stojši? Jelena, Ognjanovic Miodrag, , Witte John S, Rashkin Sara R, Kachuri Linda, Hung Rayjean J, Kar Siddhartha, Brennan Paul, Sertier Anne-Sophie, Ferrari Anthony, Viari Alain, Johansson Mattias, Amos Christopher I, Foll Matthieu, McKay James |
Cholinergic Synapse Pathway Gene Polymorphisms Associated With Late-Phase Responses in Allergic Rhinitis. Frontiers in allergy 2022 4 2 724328. Samra Simranjit K, Rajasekaran Ashwini, Sandford Andrew J, Ellis Anne K, Tebbutt Scott |
Rare coding variants in CHRNB2 reduce the likelihood of smoking. Nature genetics 2023 6 . Veera M Rajagopal, Kyoko Watanabe, Joelle Mbatchou, Ariane Ayer, Peter Quon, Deepika Sharma, Michael D Kessler, Kavita Praveen, Sahar Gelfman, Neelroop Parikshak, Jacqueline M Otto, Suying Bao, Shek Man Chim, Elias Pavlopoulos, Andreja Avbersek, Manav Kapoor, Esteban Chen, Marcus B Jones, Michelle Leblanc, Jonathan Emberson, Rory Collins, Jason Torres, Pablo Kuri Morales, Roberto Tapia-Conyer, Jesus Alegre, Jaime Berumen, , , Alan R Shuldiner, Suganthi Balasubramanian, Gonçalo R Abecasis, Hyun M Kang, Jonathan Marchini, Eli A Stahl, Eric Jorgenson, Robert Sanchez, Wolfgang Liedtke, Matthew Anderson, Michael Cantor, David Lederer, Aris Baras, Giovanni Coppo |
Familial Epilepsy Associated With Concurrent CHRNB2 Mutation and RBFOX1 Exon Deletion: A Case Report. Cureus 2023 4 15 (3): e35845. Xu Tony, Luong Dorris, Zhong Ni |
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- Page last updated:Apr 22, 2024
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