Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
   dataset        GWAS Only
Filtered By:

Previous    

Records 1 - 3 (of 3 Records)

Query Trace: Disease and MYH7B[original query]
A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20. GWAS Catalog
Human molecular genetics 2016 Mar .
Hanchard Neil A, Swaminathan Shanker, Bucasas Kristine, Furthner Dieter, Fernbach Susan, Azamian Mahshid S, Wang Xueqing, Lewin Mark, Towbin Jeffrey A, D'Alessandro Lisa C A, Morris Shaine A, Dreyer William, Denfield Susan, Ayres Nancy A, Franklin Wayne J, Justino Henri, Lantin-Hermoso M Regina, Ocampo Elena C, Santos Alexia B, Parekh Dhaval, Moodie Douglas, Jeewa Aamir, Lawrence Emily, Allen Hugh D, Penny Daniel J, Fraser Charles D, Lupski James R, Popoola Mojisola, Wadhwa Lalita, Brook J David, Bu'Lock Frances A, Bhattacharya Shoumo, Lalani Seema R, Zender Gloria A, Fitzgerald-Butt Sara, Bowman Jessica, Corsmeier Don, White Peter, Lecerf Kelsey, Zapata Gladys, Hernandez Patricia, Goodship Judith A, Garg Vidu, Keavney Bernard D, Leal Suzanne M, Cordell Heather J, Belmont John W, McBride Kim
MYH7B variants cause hypertrophic cardiomyopathy by activating the CaMK-signaling pathway.
Science China. Life sciences 2020 3 63 (9): 1347-1362.
Chen Peng, Li Zongzhe, Nie Jiali, Wang Hong, Yu Bo, Wen Zheng, Sun Yang, Shi Xiaolu, Jin Li, Wang Dao-W
The Link between Type 2 Diabetes Mellitus and the Polymorphisms of Glutathione-Metabolizing Genes Suggests a New Hypothesis Explaining Disease Initiation and Progression.
Life (Basel, Switzerland) 2021 Aug 11 (9): .
Azarova Iuliia, Klyosova Elena, Polonikov Alex
TOP