Rare germline copy number deletions of likely functional importance are implicated in endometrial cancer predisposition

- Moir-Meyer, Gemma L., Pearson, John F., Pharoah, Paul D., Dunning, Alison M., Thompson, Deborah J., Easton, Douglas F., Spurdle, Amanda B., Walker, Logan C., Lose, Felicity, The Australian National Endometrial Cancer Study Group,, Scott, Rodney J., McEvoy, Mark, Attia, John, Holliday, Elizabeth G., The Hunter Community Study,, Studies of Epidemiology and Risk Factors in Cancer Heredity,

Genome-wide association study identifies a common variant associated with risk of endometrial cancer

- Spurdle, Amanda B., Thompson, Deborah J., Fahey, Paul, Montgomery, Grant W., Webb, Penelope M., Fasching, Peter A., Beckmann, Matthias W., Ekici, Arif B., Hein, Alexander, Lambrechts, Diether, Coenegrachts, Lieve, Vergote, Ignace, Ahmed, Shahana, Amant, Frederic, Salvesen, Helga B., Trovik, Jone, Njolstad, Tormund S., Helland, Harald, Scott, Rodney J., Ashton, Katie, Proietto, Tony, Otton, Geoffrey, National Study of Endometrial Cancer Genetics Group,, Ferguson, Kaltin, Tomlinson, Ian, Gorman, Maggie, Howarth, Kimberley, Hodgson, Shirley, Garcia-Closas, Montserrat, Wentzensen, Nicolas, Yang, Hannah, Chanock, Stephen, Hall, Per, Czene, Kamila, Healey, Catherine S., Liu, Jianjun, Li, Jingmei, Shu, Xiao-Ou, Zheng, Wei, Long, Jirong, Xiang, Yong-Bing, Shah, Mitul, Morrison, Jonathan, Michailidou, Kyriaki, Pharoah, Paul D., O'Mara, Tracy, Dunning, Alison M., Easton, Douglas F., Walker, Logan C,, Montgomery, Stephen B., Dermitzakis, Emmanouil T., Australian National Endometrial Cancer Study Group,