Human Genome Epidemiology Literature Finder
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Records 1 - 8 (of 8 Records) |
| Query Trace: Disease and CHRNA2[original query] |
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| 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 |
| 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 |
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 |
| 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 |
| Clinical application of sparse canonical correlation analysis to detect genetic associations with cortical thickness in Alzheimer's disease. Frontiers in neuroscience 2024 10 18 1428900. Bo-Hyun Kim, Sang Won Seo, Yu Hyun Park, JiHyun Kim, Hee Jin Kim, Hyemin Jang, Jihwan Yun, Mansu Kim, Jun Pyo K |
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