Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 32 Records) |
Query Trace: CHRNA2[original query] |
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A major role of the nicotinic acetylcholine receptor gene CHRNA2 in autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) is unlikely. Neuroscience letters 2007 Jul 422 (1): 74-6. Gu Wenli, Bertrand Daniel, Steinlein Ortrud |
Why do young women smoke? V. Role of direct and interactive effects of nicotinic cholinergic receptor gene variation on neurocognitive function. Genes, brain, and behavior 2008 Mar 7 (2): 164-72. Rigbi A, Kanyas K, Yakir A, Greenbaum L, Pollak Y, Ben-Asher E, Lancet D, Kertzman S, Lerer |
No evidence for association between 19 cholinergic genes and bipolar disorder. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2007 Sep 144B (6): 715-23. Shi Jiajun, Hattori Eiji, Zou Hongwei, Badner Judith A, Christian Susan L, Gershon Elliot S, Liu Chun |
Association of CHRNA2 polymorphisms with overweight/obesity and clinical characteristics in a Korean population. Clinical chemistry and laboratory medicine : CCLM / FESCC 2008 46 (8): 1085-9. Kim Jin |
Association of candidate genes with antisocial drug dependence in adolescents. Drug and alcohol dependence 2008 Jul 96 (1-2): 90-8. Corley Robin P, Zeiger Joanna S, Crowley Thomas, Ehringer Marissa A, Hewitt John K, Hopfer Christian J, Lessem Jeffrey, McQueen Matthew B, Rhee Soo Hyun, Smolen Andrew, Stallings Michael C, Young Susan E, Krauter Kenne |
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 |
CHRNA2 mutations are rare in the NFLE population: evaluation of a large cohort of Italian patients. Sleep medicine 2009 Jan 10 (1): 139-42. Combi Romina, Ferini-Strambi Luigi, Tenchini Maria Lui |
Identification of pharmacogenetic markers in smoking cessation therapy. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008 Sep 147B (6): 712-9. Heitjan Daniel F, Guo Mengye, Ray Riju, Wileyto E Paul, Epstein Leonard H, Lerman Car |
Examination of the nicotine dependence (NICSNP) consortium findings in the Iowa adoption studies population. Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco 2009 Mar . Philibert RA, Todorov A, Andersen A, Hollenbeck N, Gunter T, Heath A, Madden P |
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 |
Effect of neuronal nicotinic acetylcholine receptor genes (CHRN) on longitudinal cigarettes per day in adolescents and young adults. Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco 2014 Feb 16 (2): 137-44. Cannon Dale S, Mermelstein Robin J, Hedeker Donald, Coon Hilary, Cook Edwin H, McMahon William M, Hamil Cindy, Dunn Diane, Weiss Robert |
Significant associations of CHRNA2 and CHRNA6 with nicotine dependence in European American and African American populations. Human genetics 2013 Nov . Wang S, D van der Vaart A, Xu Q, Seneviratne C, Pomerleau OF, Pomerleau CS, Payne TJ, Ma JZ, Li MD |
The contribution of rare and common variants in 30 genes to risk nicotine dependence. Molecular psychiatry 2014 Dec . Yang J, Wang S, Yang Z, Hodgkinson C A, Iarikova P, Ma J Z, Payne T J, Goldman D, Li M |
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 |
Genome-wide association study identifies common genetic variants associated with salivary gland carcinoma and its subtypes.
Cancer 2015 Jul 121 (14): 2367-74. Xu Li, Tang Hongwei, Chen Diane W, El-Naggar Adel K, Wei Peng, Sturgis Erich |
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 |
Natural killer cells and single nucleotide polymorphisms of specific ion channels and receptor genes in myalgic encephalomyelitis/chronic fatigue syndrome. The application of clinical genetics 2016 9 39-47. Marshall-Gradisnik Sonya, Huth Teilah, Chacko Anu, Johnston Samantha, Smith Pete, Staines Dona |
Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes.
Nature genetics 2017 Jun . McKay James D, Hung Rayjean J, Han Younghun, Zong Xuchen, Carreras-Torres Robert, Christiani David C, Caporaso Neil E, Johansson Mattias, Xiao Xiangjun, Li Yafang, Byun Jinyoung, Dunning Alison, Pooley Karen A, Qian David C, Ji Xuemei, Liu Geoffrey, Timofeeva Maria N, Bojesen Stig E, Wu Xifeng, Le Marchand Loic, Albanes Demetrios, Bickeböller Heike, Aldrich Melinda C, Bush William S, Tardon Adonina, Rennert Gad, Teare M Dawn, Field John K, Kiemeney Lambertus A, Lazarus Philip, Haugen Aage, Lam Stephen, Schabath Matthew B, Andrew Angeline S, Shen Hongbing, Hong Yun-Chul, Yuan Jian-Min, Bertazzi Pier Alberto, Pesatori Angela C, Ye Yuanqing, Diao Nancy, Su Li, Zhang Ruyang, Brhane Yonathan, Leighl Natasha, Johansen Jakob S, Mellemgaard Anders, Saliba Walid, Haiman Christopher A, Wilkens Lynne R, Fernandez-Somoano Ana, Fernandez-Tardon Guillermo, van der Heijden Henricus F M, Kim Jin Hee, Dai Juncheng, Hu Zhibin, Davies Michael P A, Marcus Michael W, Brunnström Hans, Manjer Jonas, Melander Olle, Muller David C, Overvad Kim, Trichopoulou Antonia, Tumino Rosario, Doherty Jennifer A, Barnett Matt P, Chen Chu, Goodman Gary E, Cox Angela, Taylor Fiona, Woll Penella, Brüske Irene, Wichmann H-Erich, Manz Judith, Muley Thomas R, Risch Angela, Rosenberger Albert, Grankvist Kjell, Johansson Mikael, Shepherd Frances A, Tsao Ming-Sound, Arnold Susanne M, Haura Eric B, Bolca Ciprian, Holcatova Ivana, Janout Vladimir, Kontic Milica, Lissowska Jolanta, Mukeria Anush, Ognjanovic Simona, Orlowski Tadeusz M, Scelo Ghislaine, Swiatkowska Beata, Zaridze David, Bakke Per, Skaug Vidar, Zienolddiny Shanbeh, Duell Eric J, Butler Lesley M, Koh Woon-Puay, Gao Yu-Tang, Houlston Richard S, McLaughlin John, Stevens Victoria L, Joubert Philippe, Lamontagne Maxime, Nickle David C, Obeidat Ma'en, Timens Wim, Zhu Bin, Song Lei, Kachuri Linda, Artigas María Soler, Tobin Martin D, Wain Louise V, , Rafnar Thorunn, Thorgeirsson Thorgeir E, Reginsson Gunnar W, Stefansson Kari, Hancock Dana B, Bierut Laura J, Spitz Margaret R, Gaddis Nathan C, Lutz Sharon M, Gu Fangyi, Johnson Eric O, Kamal Ahsan, Pikielny Claudio, Zhu Dakai, Lindströem Sara, Jiang Xia, Tyndale Rachel F, Chenevix-Trench Georgia, Beesley Jonathan, Bossé Yohan, Chanock Stephen, Brennan Paul, Landi Maria Teresa, Amos Christopher |
Genome-wide association study of familial lung cancer.
Carcinogenesis 2018 Jun . Byun Jinyoung, Schwartz Ann G, Lusk Christine, Wenzlaff Angela S, de Andrade Mariza, Mandal Diptasri, Gaba Colette, Yang Ping, You Ming, Kupert Elena Y, Anderson Marshall W, Han Younghun, Li Yafang, Qian David, Stilp Adrienne, Laurie Cathy, Nelson Sarah, Zheng Wenying, Hung Rayjean J, Gaborieau Valerie, Mckay James, Brennan Paul, Caporaso Neil E, Landi Maria Teresa, Wu Xifeng, McLaughlin John R, Brhane Yonathan, Bossé Yohan, Pinney Susan M, Bailey-Wilson Joan E, Amos Christopher |
Cholinergic receptor nicotinic alpha 5 subunit polymorphisms are associated with smoking cessation success in women. BMC medical genetics 2018 Apr 19 (1): 55. Tomaz Paulo Roberto Xavier, Santos Juliana Rocha, Scholz Jaqueline, Abe Tânia Ogawa, Gaya Patrícia Viviane, Negrão André Brooking, Krieger José Eduardo, Pereira Alexandre Costa, Santos Paulo Caleb Júnior Li |
Genome-wide association study implicates CHRNA2 in cannabis use disorder.
Nature neuroscience 2019 Jun . Demontis Ditte, Rajagopal Veera Manikandan, Thorgeirsson Thorgeir E, Als Thomas D, Grove Jakob, Leppälä Kalle, Gudbjartsson Daniel F, Pallesen Jonatan, Hjorthøj Carsten, Reginsson Gunnar W, Tyrfingsson Thorarinn, Runarsdottir Valgerdur, Qvist Per, Christensen Jane Hvarregaard, Bybjerg-Grauholm Jonas, Bækvad-Hansen Marie, Huckins Laura M, Stahl Eli A, Timmermann Allan, Agerbo Esben, Hougaard David M, Werge Thomas, Mors Ole, Mortensen Preben Bo, Nordentoft Merete, Daly Mark J, Stefansson Hreinn, Stefansson Kari, Nyegaard Mette, Børglum Anders |
A large-scale genome-wide association study meta-analysis of cannabis use disorder.
The lancet. Psychiatry 2020 Oct . Johnson Emma C, Demontis Ditte, Thorgeirsson Thorgeir E, Walters Raymond K, Polimanti Renato, Hatoum Alexander S, Sanchez-Roige Sandra, Paul Sarah E, Wendt Frank R, Clarke Toni-Kim, Lai Dongbing, Reginsson Gunnar W, Zhou Hang, He June, Baranger David A A, Gudbjartsson Daniel F, Wedow Robbee, Adkins Daniel E, Adkins Amy E, Alexander Jeffry, Bacanu Silviu-Alin, Bigdeli Tim B, Boden Joseph, Brown Sandra A, Bucholz Kathleen K, Bybjerg-Grauholm Jonas, Corley Robin P, Degenhardt Louisa, Dick Danielle M, Domingue Benjamin W, Fox Louis, Goate Alison M, Gordon Scott D, Hack Laura M, Hancock Dana B, Hartz Sarah M, Hickie Ian B, Hougaard David M, Krauter Kenneth, Lind Penelope A, McClintick Jeanette N, McQueen Matthew B, Meyers Jacquelyn L, Montgomery Grant W, Mors Ole, Mortensen Preben B, Nordentoft Merete, Pearson John F, Peterson Roseann E, Reynolds Maureen D, Rice John P, Runarsdottir Valgerdur, Saccone Nancy L, Sherva Richard, Silberg Judy L, Tarter Ralph E, Tyrfingsson Thorarinn, Wall Tamara L, Webb Bradley T, Werge Thomas, Wetherill Leah, Wright Margaret J, Zellers Stephanie, Adams Mark J, Bierut Laura J, Boardman Jason D, Copeland William E, Farrer Lindsay A, Foroud Tatiana M, Gillespie Nathan A, Grucza Richard A, Harris Kathleen Mullan, Heath Andrew C, Hesselbrock Victor, Hewitt John K, Hopfer Christian J, Horwood John, Iacono William G, Johnson Eric O, Kendler Kenneth S, Kennedy Martin A, Kranzler Henry R, Madden Pamela A F, Maes Hermine H, Maher Brion S, Martin Nicholas G, McGue Matthew, McIntosh Andrew M, Medland Sarah E, Nelson Elliot C, Porjesz Bernice, Riley Brien P, Stallings Michael C, Vanyukov Michael M, Vrieze Scott, , Davis Lea K, Bogdan Ryan, Gelernter Joel, Edenberg Howard J, Stefansson Kari, Børglum Anders D, Agrawal Arpa |
Colocalization of association signals at nicotinic acetylcholine receptor genes between schizophrenia and smoking traits. Drug and alcohol dependence 2021 1 220 108517. Al-Soufi Laila, Costas Javi |
Several nAChRs gene variants are associated with phenotypes of heroin addiction in Chinese Han population. Neuroscience letters 2022 Feb 774 136532. Cai Xintong, Zhang Jianbo, Li Yunxiao, Deji Cuola, Zhou Jinting, Li Shengb |
Analysis of the Pathogenic Variants of Genes Using a Gene Panel in Turkish Epilepsy Patients. Clinical laboratory 2022 Jun 68 (6): . Gun-Bilgic Dilek, Polat Muzaff |
Whole-Genome Sequencing Among Kazakhstani Children with Early-Onset Epilepsy Revealed New Gene Variants and Phenotypic Variability. Molecular neurobiology 2023 4 . Mirgul Bayanova, Aidos K Bolatov, Assiya Bazenova, Lyazzat Nazarova, Alissa Nauryzbayeva, Naanlep Matthew Tanko, Saule Rakhimova, Nazerke Satvaldina, Diana Samakyzy, Ulan Kozhamkulov, Ulykbek Kairov, Ainur Akilzhanova, Dos Sarbass |
Relationship Between FERMT2, CELF1, COPI, CHRNA2, and ABCA7 Genetic Polymorphisms and Alzheimer's Disease Risk in the Southern Chinese Population. Journal of Alzheimer's disease reports 2023 11 7 (1): 1247-1257. Yanfei Ding, Haijuan Chen, Yi Yan, Yinghui Qiu, Aonan Zhao, Binyin Li, Wei Xu, Yulei De |
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