Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: MED15[original query] |
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Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data. Circulation research 2014 Oct 115 (10): 884-96. Glessner Joseph T, Bick Alexander G, Ito Kaoru, Homsy Jason G, Rodriguez-Murillo Laura, Fromer Menachem, Mazaika Erica, Vardarajan Badri, Italia Michael, Leipzig Jeremy, DePalma Steven R, Golhar Ryan, Sanders Stephan J, Yamrom Boris, Ronemus Michael, Iossifov Ivan, Willsey A Jeremy, State Matthew W, Kaltman Jonathan R, White Peter S, Shen Yufeng, Warburton Dorothy, Brueckner Martina, Seidman Christine, Goldmuntz Elizabeth, Gelb Bruce D, Lifton Richard, Seidman Jonathan, Hakonarson Hakon, Chung Wendy |
Somatic MED12 mutations in prostate cancer and uterine leiomyomas promote tumorigenesis through distinct mechanisms. The Prostate 2015 Sep . Kämpjärvi Kati, Kim Nam Hee, Keskitalo Salla, Clark Alison D, von Nandelstadh Pernilla, Turunen Mikko, Heikkinen Tuomas, Park Min Ju, Mäkinen Netta, Kivinummi Kati, Lintula Susanna, Hotakainen Kristina, Nevanlinna Heli, Hokland Peter, Böhling Tom, Bützow Ralf, Böhm Jan, Mecklin Jukka-Pekka, Järvinen Heikki, Kontro Mika, Visakorpi Tapio, Taipale Jussi, Varjosalo Markku, Boyer Thomas G, Vahteristo P |
A genome-wide association study identifies a new locus associated with the response to anti-TNF therapy in rheumatoid arthritis. The pharmacogenomics journal 2015 Apr . Julià A, Fernandez-Nebro A, Blanco F, Ortiz A, Cañete J D, Maymó J, Alperi-López M, Fernández-Gutierrez B, Olivè A, Corominas H, Erra A, Acosta-Colman I, Alonso A, López-Lasanta M, Tortosa R, Tornero J, Marsal |
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- Page last updated:Apr 29, 2024
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