Human Genome Epidemiology Literature Finder
|
Records 1 - 7 (of 7 Records) |
| Query Trace: Disease and CHRM2[original query] |
|---|
| A missense mutation in the CHRM2 gene is associated with familial dilated cardiomyopathy. Circulation research 2008 Jun 102 (11): 1426-32. Zhang Lin, Hu Aihua, Yuan Haixin, Cui Liang, Miao Guobin, Yang Xinchun, Wang Lefeng, Liu Jinchun, Liu Xiulan, Wang Shuyan, Zhang Zhiyong, Liu Lisheng, Zhao Rongrui, Shen Y |
| Most reported genetic associations with general intelligence are probably false positives. Psychological science 2012 23 (11): 1314-23. Chabris Christopher F, Hebert Benjamin M, Benjamin Daniel J, Beauchamp Jonathan, Cesarini David, van der Loos Matthijs, Johannesson Magnus, Magnusson Patrik K E, Lichtenstein Paul, Atwood Craig S, Freese Jeremy, Hauser Taissa S, Hauser Robert M, Christakis Nicholas, Laibson Dav |
| Identifying genetic variants for heart rate variability in the acetylcholine pathway. PloS one 2014 9 (11): e112476. Riese Harriëtte, Muñoz Loretto M, Hartman Catharina A, Ding Xiuhua, Su Shaoyong, Oldehinkel Albertine J, van Roon Arie M, van der Most Peter J, Lefrandt Joop, Gansevoort Ron T, van der Harst Pim, Verweij Niek, Licht Carmilla M M, Boomsma Dorret I, Hottenga Jouke-Jan, Willemsen Gonneke, Penninx Brenda W J H, Nolte Ilja M, de Geus Eco J C, Wang Xiaoling, Snieder Haro |
| Genome-wide association study of metabolic syndrome in koreans. Genomics & informatics 2014 Dec 12 (4): 187-94. Jeong Seok Won, Chung Myungguen, Park Soo-Jung, Cho Seong Beom, Hong Kyung-W |
| Genetic Polymorphism of CHRM2 in COPD: Clinical Significance and Therapeutic Implications. Journal of cellular physiology 2015 Dec . Cherubini Emanuela, Esposito Maria Cristina, Scozzi Davide, Terzo Fabrizio, Osman Giorgia Amira, Mariotta Salvatore, Mancini Rita, Bruno Pierdonato, Ricci Alber |
| Polymorphisms in the Cholinergic Receptors Muscarinic (CHRM2 and CHRM3) Genes and Alzheimer's Disease. Avicenna journal of medical biotechnology 0 10 (3): 196-199. Chee Lim Ya, Cumming Alaista |
| Genetic polymorphisms of CYP3A5, CHRM2, and ZNF498 and their association with epilepsy susceptibility: a pharmacogenetic and case-control study. Pharmacogenomics and personalized medicine 2019 12 225-233. Al-Eitan Laith N, Al-Dalalah Islam M, Mustafa Mohamed M, Alghamdi Mansour A, Elshammari Afrah K, Khreisat Wael H, Al-Quasmi Mohammed N, Aljamal Hanan |
- Page last reviewed:Feb 1, 2024
- Content source: