Detection of germline variants with pathogenic potential in 48 patients with familial colorectal cancer by using whole exome sequencing

- Singh, Ashish Kumar, Talseth-Palmer, Bente, Xavier, Alexandre, Scott, Rodney J., Drabløs, Finn, Sjursen, Wenche

MTHFR C677T and A1298C polymorphism’s effect on risk of colorectal cancer in Lynch syndrome

- Wiik, Mariann Unhjem, Negline, Mia, Klinkhammer, Hannah, Spier, Isabel, Perne, Claudia, Mayr, Andreas, Valle, Laura, Lubinski, Jan, Sjursen, Wenche, Scott, Rodney J., Talseth-Palmer, Bente A., Beisvåg, Vidar, Clapham, Matthew, Holliday, Elizabeth, Dueñas, Nuria, Brunet, Joan, Pineda, Marta, Bonifaci, Nuria, Aretz, Stefan

Targeted sequencing of genes associated with the mismatch repair pathway in patients with endometrial cancer

- Singh, Ashish Kimar, Talseth-Palmer, Bente, McPhillips, Mary, Lavik, Liss Anne Solberg, Xavier, Alexandre, Drablos, Finn, Sjursen, Wenche

Comprehensive mismatch repair gene panel identifies variants in patients with Lynch-like syndrome

- Xavier, Alexandre, Olsen, Maren Fridtjofsen, Lavik, Liss A., Johansen, Jostein, Singh, Ashish Kumar, Sjursen, Wenche, Scott, Rodney J., Talseth-Palmer, Bente A.

Use of multigene-panel identifies pathogenic variants in several CRC-predisposing genes in patients previously tested for Lynch Syndrome

- Hansen, Maren F., Johansen, Jostein, Sjursen, Wenche, Sylvander, Anna E., Bjørnevoll, Inga, Talseth-Palmer, Bente A., Lavik, Liss A. S., Xavier, Alexandre, Engebretsen, Lars F., Scott, Rodney J., Drabløs, Finn

Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations

- Sjursen, Wenche, McPhillips, Mary, Scott, Rodney J., Talseth-Palmer, Bente A.

Targeted next-generation sequencing of 22 mismatch repair genes identifies Lynch syndrome families

- Talseth-Palmer, Bente A., Bauer, Denis C., Sjursen, Wenche, Evans, Tiffany J., McPhillips, Mary, Proietto, Anthony, Otton, Geoffrey, Spigelman, Allan D., Scott, Rodney J.