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Healey, Catherine S., Ahmed, Shahana, O'Mara, Tracy A., Ferguson, Kaltin, Lambrechts, Diether, Garcia-Dios, Diego A., Vergote, Ignace, Amant, Frederic, Howarth, Kimberley, Gorman, Maggie, Hodgson, Shirley, Tomlinson, Ian, Yang, Hannah P., Lissowska, Jolanta, Brinton, Louise A., Chanock, Stephen, Garcia-Closas, Montserrat, Hall, Per, Liu, Jianjun, Shah, Mitul, Pharoah, Paul D. P., Thompson, Deborah J., Rebbeck, Timothy R., Strom, Brian L., Dunning, Alison M., Easton, Douglas F., Spurdle, Amanda B., ANECS Group and Obermair, Andreas (2011) Breast cancer susceptibility polymorphisms and endometrial cancer risk: A collaborative endometrial cancer study. Carcinogenesis, 32 12: 1862-1866. doi:10.1093/carcin/bgr214 58   2 Cited 3 times in Scopus3 0
O'Mara, Tracy A., Ferguson, Kaltin, Fahey, Paul, Marquart, Louise, Yang, Hannah P., Lissowska, Jolanta, Chanock, Stephen, Garcia-Closas, Montserrat, Thompson, Deborah J., Healey, Catherine S., Dunning, Alison M., Easton, Douglas F., ANECS, Webb, Penelope M., Spurdle, Amanda B. and Obermair, Andreas (2011) CHEK2,MGMT,SULT1E1 and SULT1A1 polymorphisms and endometrial cancer risk. Twin Research and Human Genetics, 14 4: 328-332. doi:10.1375/twin.14.4.328 95 1 5 Cited 5 times in Scopus5 1
Spurdle, Amanda B., Thompson, Deborah J., Ahmed, Shahana, Ferguson, Kaltin, Healey, Catherine S., O'Mara, Tracy, Walker, Logan C., Montgomery, Stephen B., Dermitzakis, Emmanouil T., The Australian National Endometrial Cancer Study Group, 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, 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, Tomlinson, Ian, Gorman, Maggie, Howarth, Kimberley, Hodgson, Shirley, Garcia-Closas, Montserrat, Wentzensen, Nicolas, Yang, Hannah, Chanock, Stephen, Hall, Per, Czene, Kamila, Liu, Jianjun, Li, Jingmei, Shu, Xiao-Ou, Zheng, Wei, Long, Jirong, Xiang, Yong-Bing, Shah, Mitul, Morrison, Jonathan, Michailidou, Kyriaki, Pharoah, Paul D., Dunning, Alison M. and Easton, Douglas F. (2011) Genome-wide association study identifies a common variant associated with risk of endometrial cancer. Nature Genetics, 43 5: 451-454. doi:10.1038/ng.812 177   36 Cited 37 times in Scopus37 6
Garcia-Dios, Diego A., Lambrechts, Diether, Coenegrachts, Lieve, Vandenput, Ingrid, Capoen, An, Webb, Penelope M., Ferguson, Kaltin, Akslen, Lars A., Claes, Bart, Vergote, Ignace, Moerman, Philippe, Van Robays, Johan, Marcickiewicz, Janusz, Salvesen, Helga B., Spurdle, Amanda B. and Amant, Frederic (2013) High-throughput interrogation of PIK3CA, PTEN, KRAS, FBXW7 and TP53 mutations in primary endometrial carcinoma. Gynecologic Oncology, 128 2: 327-334. doi:10.1016/j.ygyno.2012.11.037 34   9 Cited 11 times in Scopus11 0
Tan, Yen Y., McGaughran, Julie, Ferguson, Kaltin, Walsh, Michael D., Buchanan, Daniel D., Young, Joanne P., Webb, Penelope M., Obermair, Andreas and Spurdle, Amanda B. (2013) Improving identification of lynch syndrome patients: A comparison of research data with clinical records. International Journal of Cancer, 132 12: 2876-2883. doi:10.1002/ijc.27978 36   4 Cited 4 times in Scopus4 5
Newman, Beth, Lose, Felicity, Kedda, Mary-Anne, Francois, Mathias, Ferguson, Kaltin, Janda, Monika, Yates, Patsy, Spurdle, Amanda B. and Hayes, Sandra C. (2012) Possible genetic predisposition to lymphedema after breast cancer. Lymphatic Research and Biology, 10 1: 2-13. doi:10.1089/lrb.2011.0024 22   11 Cited 13 times in Scopus13 2
O'Mara, Tracy A., Fahey, Paul, Ferguson, Kaltin, Marquart, Louise, Lambrechts, Diether, Despierre, Evelyn, Vergote, Ignace, Amant, Frederic, Hall, Per, Liu, Jianjun, Czene, Kamila, SASBAC, Rebbeck, Timothy R., WISE Study Group, AOCS Management Group, SEARCH, Ahmed, Shahana, Dunning, Alison M., Gregory, Catherine S., Shah, Mitul, ANECS, Webb, Penelope M. and Spurdle, Amanda B. (2011) Progesterone receptor gene variants and risk of endometrial cancer. Carcinogenesis, 32 3: 331-335. doi:10.1093/carcin/bgq263 66   11 Cited 12 times in Scopus12 0
Brennan, Donal J., Hackethal, Andreas, Metcalf, Alex M., Coward, Jermaine, Ferguson, Kaltin, Oehler, Martin K., Quinn, Michael A., Janda, Monika, Leung, Yee, Freemantle, Michael, Webb, Penelope M., Spurdle, Amanda B., Obermair, Andreas, ANECS Group, Spurdle, A. B., Webb, P. M. and Young, J. (2014) Serum HE4 as a prognostic marker in endometrial cancer: a population based study. Gynecologic Oncology, 132 1: 159-165. doi:10.1016/j.ygyno.2013.10.036 39   1 Cited 1 times in Scopus1 1
Buchanan, Daniel D., Tan, Yen Y., Walsh, Michael D., Clendenning, Mark, Metcalf, Alexander M., Ferguson, Kaltin, Arnold, Sven T., Thompson, Bryony A., Lose, Felicity A., Parsons, Michael T., Walters, Rhiannon J., Pearson, Sally-Ann, Cummings, Margaret, Oehler, Martin K., Blomfield, Penelope B., Quinn, Michael A., Kirk, Judy A., Stewart, Colin J., Obermair, Andreas, Young, Joanne P., Webb, Penelope M. and Spurdle, Amanda B. (2014) Tumor mismatch repair immunohistochemistry and DNA MLH1 methylation testing of patients with endometrial cancer diagnosed at age younger than 60 years optimizes triage for population-level germline mismatch repair gene mutation testing. Journal of Clinical Oncology, 32 2: 90-100. doi:10.1200/JCO.2013.51.2129 20   7 Cited 9 times in Scopus9 8