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.
Published in Molecular genetics & genomic medicine (01.08.2019)
Published in Molecular genetics & genomic medicine (01.08.2019)
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Journal Article
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.
Published in Cancer medicine (Malden, MA) (01.05.2016)
Published in Cancer medicine (Malden, MA) (01.05.2016)
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Journal Article
TAPES: A tool for assessment and prioritisation in exome studies
Xavier, Alexandre, Scott, Rodney J, Talseth-Palmer, Bente A
Published in PLoS computational biology (01.10.2019)
Published in PLoS computational biology (01.10.2019)
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Journal Article
Use of multigene‐panel identifies pathogenic variants in several CRC‐predisposing genes in patients previously tested for Lynch Syndrome
Hansen, Maren F., Johansen, Jostein, Sylvander, Anna E., Bjørnevoll, Inga, Talseth‐Palmer, Bente A., Lavik, Liss A. S., Xavier, Alexandre, Engebretsen, Lars F., Scott, Rodney J., Drabløs, Finn, Sjursen, Wenche
Published in Clinical genetics (01.10.2017)
Published in Clinical genetics (01.10.2017)
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Journal Article
MTHFR C677T and A1298C polymorphism’s effect on risk of colorectal cancer in Lynch syndrome
Wiik, Mariann Unhjem, Negline, Mia, Beisvåg, Vidar, Clapham, Matthew, Holliday, Elizabeth, Dueñas, Nuria, Brunet, Joan, Pineda, Marta, Bonifaci, Nuria, Aretz, Stefan, Klinkhammer, Hannah, Spier, Isabel, Perne, Claudia, Mayr, Andreas, Valle, Laura, Lubinski, Jan, Sjursen, Wenche, Scott, Rodney J, Talseth-Palmer, Bente A
Published in Scientific reports (01.11.2023)
Published in Scientific reports (01.11.2023)
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Journal Article
A genetic variant in telomerase reverse transcriptase (TERT) modifies cancer risk in Lynch syndrome patients harbouring pathogenic MSH2 variants
Wiik, Mariann Unhjem, Evans, Tiffany-Jane, Belhadj, Sami, Bolton, Katherine A., Dymerska, Dagmara, Jagmohan-Changur, Shantie, Capellá, Gabriel, Kurzawski, Grzegorz, Wijnen, Juul T., Valle, Laura, Vasen, Hans F. A., Lubinski, Jan, Scott, Rodney J., Talseth-Palmer, Bente A.
Published in Scientific reports (31.05.2021)
Published in Scientific reports (31.05.2021)
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Journal Article
P53 in human melanoma fails to regulate target genes associated with apoptosis and the cell cycle and may contribute to proliferation
Avery-Kiejda, Kelly A, Bowden, Nikola A, Croft, Amanda J, Scurr, Lyndee L, Kairupan, Carla F, Ashton, Katie A, Talseth-Palmer, Bente A, Rizos, Helen, Zhang, Xu D, Scott, Rodney J, Hersey, Peter
Published in BMC cancer (27.05.2011)
Published in BMC cancer (27.05.2011)
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Journal Article
Confirmation of childhood acute lymphoblastic leukemia variants, ARID5B and IKZF1, and interaction with parental environmental exposures
Evans, Tiffany-Jane, Milne, Elizabeth, Anderson, Denise, de Klerk, Nicholas H, Jamieson, Sarra E, Talseth-Palmer, Bente A, Bowden, Nikola A, Holliday, Elizabeth G, Rudant, Jérémie, Orsi, Laurent, Richardson, Ebony, Lavis, Laura, Catchpoole, Daniel, Attia, John R, Armstrong, Bruce K, Clavel, Jacqueline, Scott, Rodney J
Published in PloS one (13.10.2014)
Published in PloS one (13.10.2014)
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Journal Article
Combined analysis of three lynch syndrome cohorts confirms the modifying effects of 8q23.3 and 11q23.1 in MLH1 mutation carriers
Talseth‐Palmer, Bente A., Wijnen, Juul T., Brenne, Ingvild S., Jagmohan‐Changur, Shantie, Barker, Daniel, Ashton, Katie A., Tops, Carli M., Evans, Tiffany‐Jane, McPhillips, Mary, Groombridge, Claire, Suchy, Janina, Kurzawski, Grzegorz, Spigelman, Allan, Møller, Pål, Morreau, Hans M., Van Wezel, Tom, Lubinski, Jan, Vasen, Hans F.A., Scott, Rodney J.
Published in International journal of cancer (01.04.2013)
Published in International journal of cancer (01.04.2013)
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Journal Article
Reply to Win and Jenkins
Talseth‐Palmer, Bente A., Wijnen, Juul T., Barker, Daniel, Vasen, Hans F. A., Scott, Rodney J.
Published in International journal of cancer (01.10.2013)
Published in International journal of cancer (01.10.2013)
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Journal Article
Haemochromatosis HFE gene polymorphisms as potential modifiers of hereditary nonpolyposis colorectal cancer risk and onset age
Shi, Zumin, Johnstone, Daniel, Talseth‐Palmer, Bente A., Evans, Tiffany‐Jane, Spigelman, Allan D., Groombridge, Claire, Milward, Elizabeth A., Olynyk, John K., Suchy, Janina, Kurzawski, Grzegorz, Lubinski, Jan, Scott, Rodney J.
Published in International journal of cancer (01.07.2009)
Published in International journal of cancer (01.07.2009)
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Journal Article
MSH6 and PMS2 mutation positive Australian Lynch syndrome families: novel mutations, cancer risk and age of diagnosis of colorectal cancer
Talseth-Palmer, Bente A, McPhillips, Mary, Groombridge, Claire, Spigelman, Allan, Scott, Rodney J
Published in Hereditary cancer in clinical practice (21.05.2010)
Published in Hereditary cancer in clinical practice (21.05.2010)
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Journal Article
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
Published in Genes (26.09.2013)
Published in Genes (26.09.2013)
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Journal Article
Whole genome amplification and its impact on CGH array profiles
Talseth-Palmer, Bente A, Bowden, Nikola A, Hill, Alyssa, Meldrum, Cliff, Scott, Rodney J
Published in BMC research notes (29.07.2008)
Published in BMC research notes (29.07.2008)
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Journal Article
Colorectal cancer susceptibility loci on chromosome 8q23.3 and 11q23.1 as modifiers for disease expression in lynch syndrome
Talseth-Palmer, Bente A, Brenne, Ingvild S, Ashton, Katie A, Evans, Tiffany-Jane, McPhillips, Mary, Groombridge, Claire, Suchy, Janina, Kurzawski, Grzegorz, Spigelman, Allan, Lubinski, Jan, Scott, Rodney J
Published in Journal of medical genetics (01.04.2011)
Published in Journal of medical genetics (01.04.2011)
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