Expanding the genetic basis of copy number variation in familial breast cancer

- Masson, Amy L., Talseth-Palmer, Bente A., Evans, Tiffany-Jane, Grice, Desma M., Hannan, Garry N., Scott, Rodney J.

Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients

- Talseth-Palmer, Bente A., Holliday, Elizabeth G., Evans, Tiffany-Jane, McEvoy, Mark, Attia, John, Grice, Desma M., Masson, Amy L., Meldrum, Cliff, Spigelman, Allan, Scott, Rodney J.

Copy number variation in hereditary non-polyposis colorectal cancer

- Masson, Amy L., Talseth-Palmer, Bente A., Evans, Tiffany-Jane, Grice, Desma M., Duesing, Konsta, Hannan, Garry N., Scott, Rodney J.

Genetic modifiers of cancer risk in Lynch syndrome: a review

- Talseth-Palmer, Bente A., Wijnen, Juul T., Grice, Desma M., Scott, Rodney J.

STaRRRT: a table of short tandem repeats in regulatory regions of the human genome

- Bolton, Katherine A., Ross, Jason P., Grice, Desma M., Bowden, Nikola A., Holliday, Elizabeth G., Avery-Kiejda, Kelly A., Scott, Rodney J.