Glendon, Gord
University of Toronto · Lunenfeld-Tanenbaum Research Institute · Sinai Health System
4 papers on CoChatORCID 0000-0001-8630-6673
Most cited papers
- Verified
Identification of six new susceptibility loci for invasive epithelial ovarian cancer
EMBRACE, Kuchenbaecker, K. B., Collaborators, G. S., Breast Cancer Family Registry, HEBON, KConFab Investigators, Australian Cancer Study (Ovarian Cancer Investigators), Australian Ovarian Cancer Study Group, the Consortium of Investigators of Modifiers of BRCA1 and BRCA2, Ramus, S. J., et al. (2015) · Nature Genetics
BRCA gene mutations in cancerOvarian cancer diagnosis and treatment
Cited by 250
- Verified
Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170
EMBRACE, Dunning, A. M., Collaborators, G. S., HEBON, kConFab Investigators, Michailidou, K., Kuchenbaecker, K. B., Thompson, D., French, J. D., Beesley, J., et al. (2016) · Nature Genetics
Genetic Associations and EpidemiologyEstrogen and related hormone effects
Cited by 161
- Verified
Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32, 295 women
EMBRACE, Rebbeck, T. R., HEBON, Friebel, T. M., Mitra, N., Wan, F., Chen, S., Andrulis, I. L., Apostolou, P., Arnold, N., et al. (2016) · Breast Cancer Research
BRCA gene mutations in cancerMultiple and Secondary Primary Cancers
Cited by 71
- Verified
Assessing patient readiness for personalized genomic medicine
Frost, C. J., Andrulis, I. L., Buys, S. S., Hopper, J. L., John, E. M., Terry, M. B., Bradbury, A., Chung, W. K., Colbath, K., Quintana, N., et al. (2019) · Journal of Community Genetics
BRCA gene mutations in cancerPatient-Provider Communication in Healthcare
Cited by 14
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