New common variants affecting susceptibility to basal cell carcinoma

Simon N Stacey,Patrick Sulem,Gisli Masson,Sigurjon A Gudjonsson,Gudmar Thorleifsson,Margret Jakobsdottir,Asgeir Sigurdsson,Daniel F Gudbjartsson,Bardur Sigurgeirsson,Kristrun R Benediktsdottir,Kristin Thorisdottir,Rafn Ragnarsson,Dominique Scherer,Kari Hemminki,Peter Rudnai,Eugene Gurzau,Kvetoslava Koppova,Rafael Botella-Estrada,Virtudes Soriano,Pablo Juberias,Berta Saez,Yolanda Gilaberte,Victoria Fuentelsaz,Cristina Corredera,Matilde Grasa,Veronica Höiom,Annika Lindblom,Johannes J Bonenkamp,Michelle M van Rossum,Katja K H Aben,Esther de Vries,Mario Santinami,Maria G Di Mauro,Andrea Maurichi,Judith Wendt, Pia Hochleitner,Hubert Pehamberger,Julius Gudmundsson,Droplaug N Magnusdottir,Solveig Gretarsdottir,Hilma Holm,Valgerdur Steinthorsdottir,Michael L Frigge,Thorarinn Blondal,Jona Saemundsdottir,Hjördis Bjarnason,Kristleifur Kristjansson,Gyda Bjornsdottir,Ichiro Okamoto,Licia Rivoltini,Monica Rodolfo,Lambertus A Kiemeney,Johan Hansson,Eduardo Nagore,José I Mayordomo,Rajiv Kumar,Margaret R Karagas,Heather H Nelson,Jeffrey R Gulcher,Thorunn Rafnar,Unnur Thorsteinsdottir,Jon H Olafsson,Augustine Kong,Kari Stefansson

Nature Genetics（2009）

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摘要

Simon Stacey and colleagues report several new susceptibility variants for basal cell carcinoma, including coding variants in KRT5 , a variant at 9p21 near CDKN2A and CDKN2B and a variant at 7q32 near KLF14 . The latter is an imprinted gene, and the effect at this locus is dependent on the parental origin of the risk allele.

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