Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer

Whilst common genetic variation in many non-coding genomic regulatory regions are known to impart risk of colorectal cancer (CRC), much of the heritability of CRC remains unexplained. To examine the role of recurrent coding sequence variation in CRC aetiology, we genotyped 12,638 CRCs cases and 29,0...

Descripción completa

Detalles Bibliográficos
Autores principales: Timofeeva, Maria N., Kinnersley, Ben, Farrington, Susan M., Whiffin, Nicola, Palles, Claire, Svinti, Victoria, Lloyd, Amy, Gorman, Maggie, Ooi, Li-Yin, Hosking, Fay, Barclay, Ella, Zgaga, Lina, Dobbins, Sara, Martin, Lynn, Theodoratou, Evropi, Broderick, Peter, Tenesa, Albert, Smillie, Claire, Grimes, Graeme, Hayward, Caroline, Campbell, Archie, Porteous, David, Deary, Ian J., Harris, Sarah E., Northwood, Emma L., Barrett, Jennifer H., Smith, Gillian, Wolf, Roland, Forman, David, Morreau, Hans, Ruano, Dina, Tops, Carli, Wijnen, Juul, Schrumpf, Melanie, Boot, Arnoud, Vasen, Hans F A, Hes, Frederik J., van Wezel, Tom, Franke, Andre, Lieb, Wolgang, Schafmayer, Clemens, Hampe, Jochen, Buch, Stephan, Propping, Peter, Hemminki, Kari, Försti, Asta, Westers, Helga, Hofstra, Robert, Pinheiro, Manuela, Pinto, Carla, Teixeira, Manuel, Ruiz-Ponte, Clara, Fernández-Rozadilla, Ceres, Carracedo, Angel, Castells, Antoni, Castellví-Bel, Sergi, Campbell, Harry, Bishop, D. Timothy, Tomlinson, Ian P M, Dunlop, Malcolm G., Houlston, Richard S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4639776/
https://www.ncbi.nlm.nih.gov/pubmed/26553438
http://dx.doi.org/10.1038/srep16286

Ejemplares similares

Ejemplares similares