Transcriptome and genome sequencing uncovers functional variation in humans

作者：Tuuli Lappalainen, Michael Sammeth, Marc R. Friedländer, Peter A.C. ’t Hoen, Jean Monlong, Manuel A. Rivas, Mar Gonzàlez-Porta, Natalja Kurbatova, Thasso Griebel, Pedro Gabriel Ferreira, Matthias Barann, Thomas Wieland, Liliana Greger, Maarten van Iterson, Jonas Carlsson Almlöf, Paolo Ribeca, Irina Pulyakhina, Daniela Esser, Thomas Giger, Andrew Tikhonov, Marc Sultan, Gabrielle Bertier, Daniel G. MacArthur, Monkol Lek, Esther Lizano, Henk P.J. Buermans, Ismaël Padioleau, Thomas Schwarzmayr, Olof Karlberg, Halit Ongen, Helena Kilpinen, Sergi Beltrán, Marta Gut, Katja Kahlem, Vyacheslav S. Amstislavskiy, Oliver Stegle, Matti Pirinen, Stephen B. Montgomery, Peter Donnelly, Mark I. McCarthy, Paul Flicek, Tim Matthias Strom, Hans R. Lehrach, Stefan Schreiber, Ralf Sudbrak, Ángel Carracedo, Stylianos E. Antonarakis, Robert Häsler, Ann‐Christine Syvänen, Gert‐Jan B. van Ommen, Alvis Brāzma, Thomas Meitinger, Philip C Rosenstiel, Roderic Guigó, Ivo Glynne Gut, Xavier Estivill, Emmanouil T. Dermitzakis · 发表于：Nature · 年份：2013 · DOI：10.1038/nature12531 · 被引用次数：2200 · 研究领域：RNA Research and Splicing、RNA modifications and cancer、Genetic Associations and Epidemiology