Human Genome Epidemiology Literature Finder
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Records 1 - 9 (of 9 Records) |
| Query Trace: Disease and CACNB2[original query] |
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Genome-wide association study of blood pressure and hypertension.
Nature genetics 2009 Jun 41 (6): 677-87. Levy Daniel, Ehret Georg B, Rice Kenneth, Verwoert Germaine C, Launer Lenore J, Dehghan Abbas, Glazer Nicole L, Morrison Alanna C, Johnson Andrew D, Aspelund Thor, Aulchenko Yurii, Lumley Thomas, Köttgen Anna, Vasan Ramachandran S, Rivadeneira Fernando, Eiriksdottir Gudny, Guo Xiuqing, Arking Dan E, Mitchell Gary F, Mattace-Raso Francesco U S, Smith Albert V, Taylor Kent, Scharpf Robert B, Hwang Shih-Jen, Sijbrands Eric J G, Bis Joshua, Harris Tamara B, Ganesh Santhi K, O'Donnell Christopher J, Hofman Albert, Rotter Jerome I, Coresh Josef, Benjamin Emelia J, Uitterlinden André G, Heiss Gerardo, Fox Caroline S, Witteman Jacqueline C M, Boerwinkle Eric, Wang Thomas J, Gudnason Vilmundur, Larson Martin G, Chakravarti Aravinda, Psaty Bruce M, van Duijn Cornelia |
| Genetic variation in the beta2 subunit of the voltage-gated calcium channel and pharmacogenetic association with adverse cardiovascular outcomes in the INternational VErapamil SR-Trandolapril STudy GENEtic Substudy (INVEST-GENES). Circulation. Cardiovascular genetics 2010 Dec 3 (6): 548-55. Niu Yuxin, Gong Yan, Langaee Taimour Y, Davis Heather M, Elewa Hazem, Beitelshees Amber L, Moss James I, Cooper-Dehoff Rhonda M, Pepine Carl J, Johnson Julie |
| Genome-wide meta-analysis of systolic blood pressure in children with sickle cell disease.
PloS one 2013 8 (9): e74193. Bhatnagar Pallav, Barron-Casella Emily, Bean Christopher J, Milton Jacqueline N, Baldwin Clinton T, Steinberg Martin H, Debaun Michael, Casella James F, Arking Dan |
| Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.
Lancet (London, England) 2013 Apr 381 (9875): 1371-9. Authors are not available |
| Genetic variations in MOV10 and CACNB2 are associated with hypertension in a Chinese Han population. Genetics and molecular research : GMR 2013 12 (4): 6220-7. Hong G L, Chen X Z, Liu Y, Liu Y H, Fu X, Lin S B, Zhu |
| Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder. Translational psychiatry 2015 5 e678. Forstner A J, Hofmann A, Maaser A, Sumer S, Khudayberdiev S, Mühleisen T W, Leber M, Schulze T G, Strohmaier J, Degenhardt F, Treutlein J, Mattheisen M, Schumacher J, Breuer R, Meier S, Herms S, Hoffmann P, Lacour A, Witt S H, Reif A, Müller-Myhsok B, Lucae S, Maier W, Schwarz M, Vedder H, Kammerer-Ciernioch J, Pfennig A, Bauer M, Hautzinger M, Moebus S, Priebe L, Sivalingam S, Verhaert A, Schulz H, Czerski P M, Hauser J, Lissowska J, Szeszenia-Dabrowska N, Brennan P, McKay J D, Wright A, Mitchell P B, Fullerton J M, Schofield P R, Montgomery G W, Medland S E, Gordon S D, Martin N G, Krasnov V, Chuchalin A, Babadjanova G, Pantelejeva G, Abramova L I, Tiganov A S, Polonikov A, Khusnutdinova E, Alda M, Cruceanu C, Rouleau G A, Turecki G, Laprise C, Rivas F, Mayoral F, Kogevinas M, Grigoroiu-Serbanescu M, Propping P, Becker T, Rietschel M, Cichon S, Schratt G, Nöthen M |
| Does Sudden Unexplained Nocturnal Death Syndrome Remain the Autopsy-Negative Disorder: A Gross, Microscopic, and Molecular Autopsy Investigation in Southern China. Mayo Clinic proceedings 2016 Oct . Zhang Liyong, Tester David J, Lang Di, Chen Yili, Zheng Jinxiang, Gao Rui, Corliss Robert F, Tang Shuangbo, Kyle John W, Liu Chao, Ackerman Michael J, Makielski Jonathan C, Cheng Jiandi |
| The genetic overlap between mood disorders and cardiometabolic diseases: a systematic review of genome wide and candidate gene studies. Translational psychiatry 2017 Jan 7 (1): e1007. Amare A T, Schubert K O, Klingler-Hoffmann M, Cohen-Woods S, Baune B |
| Bifid T waves on the ECG and genetic variation in calcium channel voltage-dependent beta 2 subunit gene (CACNB2) in acute Kawasaki disease. Congenital heart disease 2019 Mar 14 (2): 213-220. Oyamada Jun, Shimizu Chisato, Kim Jihoon, Williams Matthew R, Png Eileen, Hibberd Martin L, Tremoulet Adriana H, Perry James C, Burns Jane |
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