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English
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For å registrere i Cristin må du være vitenskapelig eller administrativt ansatt.
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2023
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1. |
Singh, Ashish Kumar; Talseth-Palmer, Bente Anita; Xavier, Alexandre; Scott, Rodney J.; Drabløs, Finn Sverre; Sjursen, Wenche. Detection of germline variants with pathogenic potential in 48 patients with familial colorectal cancer by using whole exome sequencing. BMC Medical Genomics 2023 ;Volum 16. s. 1-13 STO NTNU HMR
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2. |
Wiik, Mariann Unhjem; Negline, Mia; Beisvag, 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 Anita. MTHFR C677T and A1298C polymorphism’s effect on risk of colorectal cancer in Lynch syndrome. Scientific Reports 2023 ;Volum 13. s. 1-10 NTNU HMR STO
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2022
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3. |
Driller, Bardo; Talseth-Palmer, Bente Anita; Hole, Torstein; Strømskag, Kjell Erik; Brenne, Anne-Tove. Cancer patients spend more time at home and more often die at home with advance care planning conversations in primary health care: a retrospective observational cohort study. BMC Palliative Care 2022 ;Volum 21.(1) s. 1-10 HMR NTNU STO
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2021
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4. |
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 Anita. A genetic variant in telomerase reverse transcriptase (TERT) modifies cancer risk in Lynch syndrome patients harbouring pathogenic MSH2 variants. Scientific Reports 2021 ;Volum 11:11401. s. 1-9 HMR
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2020
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5. |
Singh, Ashish Kumar; Talseth-Palmer, Bente Anita; McPhillips, Mary; Lavik, Liss Ane; Xavier, Alexandre; Drabløs, Finn; Sjursen, Wenche. Targeted sequencing of genes associated with the mismatch repair pathway in patients with endometrial cancer. PLOS ONE 2020 s. 1-19 STO NTNU HMR
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6. |
Wiik, Mariann Unhjem; Talseth-Palmer, Bente Anita. Familial Adenomatuos Polyposis. I: Handbook of Tumor Syndromes. CRC Press 2020 ISBN 978-0-8153-9380-1. s. 137-149 HMR
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2019
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7. |
Andersen-Hollekim, Tone Elisabeth; Kvangarsnes, Marit; Landstad, Bodil; Talseth-Palmer, Bente Anita; Hole, Torstein. Patient participation in the clinical pathway – nurses' perceptions of adults' involvement in haemodialysis. Nursing Open 2019 ;Volum 6.(2) s. 574-582 HMR HNT NTNU
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8. |
Røyset, Bodil; Talseth-Palmer, Bente Anita; Lydersen, Stian; Farup, Per Grønaas. Effects of a fall prevention program in elderly: A pragmatic observational study in two orthopedic departments. Clinical Interventions in Aging 2019 ;Volum 14. s. 145-154 HMR NTNU SI
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9. |
Xavier, Alexandre; Olsen, Maren Fridtjofsen; Lavik, Liss Ane; Johansen, Jostein; Singh, Ashish Kumar; Sjursen, Wenche; Scott, Rodney J.; Talseth-Palmer, Bente Anita. Comprehensive mismatch repair gene panel identifies variants in patients with Lynch-like syndrome. Molecular Genetics & Genomic Medicine 2019 ;Volum 7.(8) s. e850- STO NTNU HMR
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10. |
Xavier, Alexandre; Scott, Rodney J; Talseth-Palmer, Bente Anita. TAPES: A tool for assessment and prioritisation in exome studies. PLoS Computational Biology 2019 ;Volum 15:e1007453.(10) s. 1-9 HMR
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2018
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11. |
Holmes, Merran; Connor, Toni; Oldmeadow, Christopher; Pockney, Peter; Scott, Rodney J.; Talseth-Palmer, Bente Anita. CD36 - a plausible modifier of disease phenotype in familial adenomatous polyposis. Hereditary Cancer in Clinical Practice 2018 ;Volum 16:14. s. 1-7 HMR NTNU
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2017
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12. |
Hansen, Maren; Johansen, Jostein; Sylvander, Anna Elisabeth; Bjørnevoll, Inga; Talseth-Palmer, Bente Anita; Lavik, Liss Ane; Xavier, Alexandre; Engebretsen, Lars Fredri; Scott, Rodney; Drabløs, Finn Sverre; Sjursen, Wenche. Use of multigene-panel identifies pathogenic variants in several CRC-predisposing genes in patients previously tested for Lynch Syndrome. Clinical Genetics 2017 ;Volum 92.(4) s. 405-414 HMR NTNU STO
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13. |
Talseth-Palmer, Bente. The genetic basis of colonic adenomatous polyposis syndromes. Hereditary Cancer in Clinical Practice 2017 ;Volum 15:5. s. 1-7 NTNU HMR
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2016
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14. |
Hansen, Grete; Talseth-Palmer, Bente. Norsk bioingeniør ble kreftforsker i Australia. Bioingeniøren 2016 ;Volum 51.(3) s. 28-29 NTNU HMR
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15. |
Sjursen, Wenche; McPhillips, Mary; Scott, Rodney J.; Talseth-Palmer, Bente. Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations. Molecular Genetics & Genomic Medicine 2016 ;Volum 4.(2) s. 223-231 STO HMR NTNU
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16. |
Talseth-Palmer, Bente; Bauer, Denis; Sjursen, Wenche; Evans, Tiffany-Jane; McPhillips, Mary; Proietto, Anthony; Otten, Geoffrey; Spigelman, Allan D.; Scott, Rodney J.. Targeted next-generation sequencing of 22 mismatch repair genes identifies Lynch syndrome families. Cancer Medicine 2016 ;Volum 5.(5) s. 929-941 STO NTNU
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2015
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17. |
Masson, Amy; Talseth-Palmer, Bente; Evans, Tiffany-Jane; McElduff, Patrick; Spigelman, Allan D.; Hannan, Garry N.; Scott, Rodney J.. Copy number variants associated with 18p11.32, DCC and the promoter 1B region of APC in colorectal polyposis patients. Meta Gene 2015
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2014
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18. |
Evans, Tiffany-Jane; Milne, Elizabeth; Anderson, Denise; de Klerk, Nicolas; Jamieson, Sarra; Talseth-Palmer, Bente; Bowden, Nikola; Holliday, Elizabeth G.; Rudant, Jeremie; Orsi, Laurent; Richardson, Ebony; Lavis, Laura; Catchpoole, Daniel; Attia, John; Clavel, Jacqueline; Armstrong, Bruce; Scott, Rodney J.. Confirmation of Childhood Acute Lymphoblastic Leukemia Variants, ARID5B and IKZF1, and Interaction with Parental Environmental Exposures. PLOS ONE 2014 ;Volum 9.(10) NTNU
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19. |
Masson, Amy; Talseth-Palmer, Bente; Evans, Tiffany-Jane; Grice, Desma M.; Hannan, Garry N.; Scott, Rodney J.. Expanding the genetic basis of copy number variation in familial breast cancer. Hereditary Cancer in Clinical Practice 2014 ;Volum 12.(1) s. 15- NTNU
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2013
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20. |
Chen, Jinyun; Pande, Mala; Huang, Yu-Jing; Wei, Chongjuan; Amos, Christopher I.; Talseth-Palmer, Bente; Meldrum, Cliff; Chen, Wei V.; Gorlov, Ivan P.; Lynch, Patrick M.; Scott, Rodney J.; Frazier, Marsha L.. Cell cycle–related genes as modifiers of age of onset of colorectal cancer in Lynch syndrome: a large-scale study in non-Hispanic white patients.. Carcinogenesis 2013 ;Volum 34.(2) s. 299-306 NTNU
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21. |
Masson, Amy; Talseth-Palmer, Bente; Evans, Tiffany-Jane; Grice, Desma M.; Duesing, Konsta; Hannan, Garry N.; Scott, Rodney J.. Copy number variation in hereditary non-polypsis colorectal cancer. Genes 2013 ;Volum 4.(4) s. 536-555 NTNU
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22. |
Picelli, S; Lorenzo Bermejo, J; Chang-Claude, J; Hoffmeister, M; Fernandez-Rozadilla, C; Carracedo, A; Castells, A; Castellvi-Bel, Sergi; the EPICOLON Consortium, Members of; Naccarati, A; Pardini, Barbara; Vodickova, Ludmila; Muller, H.; Talseth-Palmer, Bente; Stibbard, G.; Peterlongo, P; Nici, C.; Veneroni, S.; Li, L.; Casey, G.; Tenesa, A.; Farrington, SM; Tomlinson, I.; Moreno, V.; Van Wezel, Tom; Wijnen, Juul; Dunlop, M.; Radice, P; Scott, Rodney J.; Vodicka, Pavel; Ruiz-Ponte, C.; Brenner, H.; Buch, S; Volzke, H; Hampe, J.; Schafmayer, Clemens; Lindblom, Annika. Meta-analysis of mismatch repair polymorphisms within the cogent consortium for colorectal cancer susceptibility. PLOS ONE 2013 ;Volum 8.(9) s. e72091- NTNU
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23. |
Talseth-Palmer, Bente; Holliday, Elizabeth G.; Evans, Tiffany-Jane; McEvoy, Mark; Attia, John; Grice, Desma M.; Masson, Amy; Meldrum, Cliff; Spigelman, Allan D.; Scott, Rodney J.. Continuing difficulties in interpreting CNV data: Lessons from a genome-wide CNV association study of Australian HNPCC/Lynch syndrome patients.. BMC Medical Genomics 2013 ;Volum 26. s. 6-10 NTNU
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24. |
Talseth-Palmer, Bente; Wijnen, Juul T.; Andreassen, Eva K.; Barker, Daniel; Jagmohan-Changur, Shanti; Tops, Carli M.J.; Meldrum, Cliff; The Dutch Cancer Genetics Grou, .; Spigelman, Allan D.; Hes, Fredrik J.; Van Wezel, Tom; Vasen, Hans F.A.; Scott, Rodney J.. The importance of a large sample cohort for studies on modifier genes influencing disease severity in FAP patients.. Hereditary Cancer in Clinical Practice 2013 ;Volum 11.(1) s. 20- NTNU
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25. |
Talseth-Palmer, Bente; Wijnen, Juul T.; Brenne, Ingvild S.; Jagmohan-Changur, S; Barker, Daniel; Ashton, Katie A.; Tops, Carli M.J.; Evans, Tiffany-Jane; McPhillips, Mary; Groombridge, Claire; Suchy, Janina; Kurzawski, Grzegorz; Dutch Cancer Genetics Group, The; Spigelman, Allan D.; Møller, Pål; Morreau, HM; Van Wezel, Tom; Vasen, Hans F.A.; Scott, Rodney J.. Combined analysis of three Lynch syndrome cohorts confirms the modifying effects of 8q23.3 and 11q23.1 in MLH1 mutation carriers.. International Journal of Cancer 2013 ;Volum 132.(7) s. 1556-1564 NTNU
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26. |
Talseth-Palmer, Bente; Wijnen, Juul T.; Grice, Desma M.; Scott, Rodney J.. Genetic Modifiers of Cancer risk in Lynch syndrome: A Review.. Familial Cancer 2013 ;Volum 12.(2) s. 207-216 NTNU
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27. |
Talseth-Palmer, Bente; Wijnen, Juul T.; Vasen, Hans F.A.; Scott, Rodney J.. Letter to the Editor: Reply to Win and Jenkins.. International Journal of Cancer 2013 ;Volum 133.(7) s. 1764- NTNU
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2012
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28. |
Scott, Rodney J.; Reeves, Stuart; Talseth-Palmer, Bente. The role of modifier genes in Lynch syndrome. : INTECH 2012 (ISBN 978-953-51-0062-1) ;Volum 2012.21 s. Colorectal Cancer Biology - From Genes to Tumor(1) NTNU
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29. |
Talseth-Palmer, Bente; Scott, Rodney J.; Vasen, Hans F.A.; Wijnen, Juul T.. 8q23.3 and 11q23.1 as modifying loci influencing the risk for CRC in Lynch syndrome. European Journal of Human Genetics 2012 ;Volum 20.(5) s. 487-488 NTNU
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2011
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30. |
Avery-Kiejda, Kelly A.; Bowden, Nikola A.; Kairupan, Carla; Croft, Amanda J.; Scurr, LL; Ashton, Katie A.; Talseth-Palmer, Bente; Rizos, H.; Zhang, XD; Scott, Rodney J.; Hersey, Peter. p53 in human melanoma fails to regulate target genes associated with apoptosis and the cell cycle and may contribute to cell proliferation.. BMC Cancer 2011 ;Volum 11.(1) s. 203- NTNU
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31. |
Talseth-Palmer, Bente; Brenne, Ingvild S.; Ashton, Katie A.; Evans, Tiffany-Jane; McPhillips, Mary; Groombridge, Claire; Suchy, Janina; Kurzawski, Grzegorz; Spigelman, Allan D.; Lubinski, Jan; Scott, Rodney J.. Colorectal cancer susceptibility loci on chromosome 8q23.3 and 11q23.1 as modifiers for disease expression in Lynch syndromes.. Journal of Medical Genetics 2011 ;Volum 48.(4) s. 279-284 NTNU
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32. |
Talseth-Palmer, Bente; Scott, Rodney J.. Genetic variation and its role in malignancy. International Journal of Biomedical Science 2011 ;Volum 7.(3) s. 158-171 NTNU
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33. |
Wong, Michelle W.; Norfors, Cecilie; Mossman, David; Pecenpetelovska, Gordana; Avery-Kiejda, Kelly A.; Talseth-Palmer, Bente; Bowden, Nikola A.; Scott, Rodney J.. BRIP1, PALB2 and RAD51C mutation analysis reveals their relative importance as genetic susceptibility factors for breast cancer.. Breast Cancer Research 2011 ;Volum 127.(3) s. 853-859 NTNU
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2010
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34. |
Talseth-Palmer, Bente; McPhillips, Mary; Meldrum, Cliff; Groombridge, Claire; Spigelman, Allan D.; Scott, Rodney J.. MSH6 and PMS2 Mutation Positive Australian Lynch Syndrome Families: Novel Mutations, Cancer Incidence and Age of Diagnosis of Colorectal Cancer.. Hereditary Cancer in Clinical Practice 2010 ;Volum 8. s. 5- NTNU
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2009
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35. |
Shi, Z.; Johnstone, Daniel; Talseth-Palmer, Bente; Evans, Tiffany-Jane; Spigelman, Allan D.; Groombridge, Claire; Milward, E.A.; Olynyk, J.K.; Suchy, Janina; Kurzawski, Grzegorz; Lubinski, Jan; Scott, Rodney J.. Haemochromatosis HFE gene polymorphism as potential modifiers of hereditary nonpolyposis colorectal cancer risk and onset age. International Journal of Cancer 2009 ;Volum 125.(1) s. 78-83 NTNU
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36. |
Talseth-Palmer, Bente; Bowden, Nikola A.; Meldrum, Cliff; Nicholl, J.; Thompson, E.; Friend, K.; Yu, S.; Scott, Rodney J.. A 1q44 deletion, paternal UPD of choromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technology. Cytogenetic and Genome Research 2009 ;Volum 124.(1) s. 94-101 NTNU
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2008
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37. |
Talseth-Palmer, Bente; Bowden, Nikola A.; Hill, Alyssa; Meldrum, Cliff; Scott, Rodney J.. Whole genome amplification and its impact on CGH array profiles.. BMC Research Notes 2008 ;Volum 1. s. 56- NTNU
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38. |
Talseth-Palmer, Bente; Talseth, Bente A.; Ashton, Katie A.; Meldrum, Cliff; Suchy, Janina; Kurzawski, Grzegorz; Lubinski, Jan; Scott, Rodney J.. Aurora-A and Cyclin D1 polymorphisms and age of onset of colorectal cancer in Hereditary Nonpolyposis Colorectal Cancer. International Journal of Cancer 2008 ;Volum 122.(6) s. 1273-1277 NTNU
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