Lindor, Noralane M.

Association of Type and Location of BRCA1 and BRCA2 Mutations With Risk of Breast and Ovarian Cancer

Rebbeck, T. R., Mitra, N., Wan, F., Sinilnikova, O. M., Healey, S., McGuffog, L., Mazoyer, S., Chenevix-Trench, G., Easton, D. F., Antoniou, A. C., et al. (2015) · JAMA

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Identification of six new susceptibility loci for invasive epithelial ovarian cancer

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KRAS-mutation status in relation to colorectal cancer survival: The joint impact of correlated tumour markers

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Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170

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RECQL4 is essential for the transport of p53 to mitochondria in normal human cells in the absence of exogenous stress

De, S., Kumari, J., Mudgal, R., Modi, P., Gupta, S., Futami, K., Goto, H., Lindor, N. M., Furuichi, Y., Mohanty, D., et al. (2012) · Journal of Cell Science

Cancer-related Molecular PathwaysDNA Repair Mechanisms

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Tenascin‐X deficiency in autosomal recessive Ehlers–Danlos syndrome

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