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Dr Bente Talseth-Palmer

Work Phone	(02) 4042 0328
Email	Bente.Talseth-palmer@newcastle.edu.au
Office	Level 3 West, HMRI, Hmri

Highlighted Publications

Year	Citation	Nova
2009	Talseth-Palmer Bente, Bowden Nikola Ann, Meldrum C, Nicholl J, Thompson E, Friend K, Liebelt J, Bratkovic D, Haan E, Yu S, Scott Rodney, 'A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technology', Cytogenetic and Genome Research, 124 94-101 (2009) [C1]
2008	Talseth-Palmer Bente, Ashton Katie Ann, Meldrum Cliff, Suchy Janina, Kurzawski Grzegorz, Lubinski Jan, Scott Rodney, 'Aurora-A and Cyclin D1 polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer', International Journal of Cancer, 122 1273-1277 (2008) [C1]
2008	Talseth-Palmer Bente, McPhillips M, Meldrum C, Groombridge C, Spigelman A, Scott Rodney, 'Hereditary nonpolyposis colorectal cancer in families: Mutations, age of diagnosis of cancer and cancer incidence', Conference on Translational Cancer Research: Abstracts, Newcastle, NSW (2008) [E3]
2007	Talseth-Palmer Bente, Meldrum C, Suchy J, Kurzawski G, Lubinski J, Scott Rodney, 'MDM2 SNP309 T > G alone or in combination with the TP53 R72P polymorphism does not appear to influence disease expression and age of diagnosis of colorectal cancer in HNPCC patients', International Journal of Cancer, 120 563-565 (2007) [C1]
2006	Talseth-Palmer Bente, Meldrum C, Suchy J, Kurzawski G, Lubinski J, Scott Rodney, 'Age of diagnosis of colorectal cancer in HNPCC patients is more complex than that predicted by R72P polymorphism in TP53', International Journal of Cancer, 118 2479-2484 (2006) [C1]
2003	LOUKA A S, LIE B A, TALSETH B, ASCHER H, EK J, GUDJONSDOTTIR A H, SOLLID L M, 'Coeliac disease patients carry conserved HLA-DR3-DQ2 haplotypes revealed by association of TNF alleles', Immunogenetics, 55 339-343 (2003) [C1]
2001	KRISTINSSON S, THOROLFSDOTTIR E, TALSETH B, STEINGRIMSSON E, THORSSON A, HELGASON T, HREIDARSSON A, ARNGRIMSSON R, 'MODY in Iceland is associated with mutations in HNF-1alpha and a novel mutation in NeuroD1. (2001) [C1]

Publications

For items published while at an institution other that the University of Newcastle, details are shown in italics.

Click on a category title below to expand the list of citations for that specific category.

Chapters In A Book (1 outputs)

Chapter in A1 Book (B1) (1 outputs)

Year	Citation	Nova
2012	Scott Rodney, Reeves Stuart Glen, Talseth-Palmer Bente, 'The role of modifier genes in Lynch Syndrome', Colorectal Cancer Biology From Genes To Tumor, InTech, Slovenia, 37-58 (2012) [B1]

Journal Articles (18 outputs)

Refereed Article in a Scholarly Journal (C1) (17 outputs)

Year	Citation	Nova
2012	Talseth-Palmer Bente, Wijnen Juul T, Brenne Ingvild S, Jagmohan-Changur Shantie, Barker Daniel Jacob, Ashton Katie Ann, Tops Carli M, Evans Tiffany-Jane, McPhillips Mary, Groombridge Claire, Suchy Janina, Kurzawski Grzegorz, The Dutch Cancer Genetics Group, Spigelman Allan, Moller Pal, Morreau Hans M, Van Wezel Tom, Lubinski Jan, Vasen Hans F A, Scott Rodney, '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, 132 1487-1729 (2012) [C1]
2011	Kiejda Kelly Anne, Bowden Nikola Ann, Croft Amanda J, Scurr Lyndee L, Kairupan Carla Felly, Ashton Katie Ann, Talseth-Palmer Bente, Rizos Helen, Zhang Xu Dong, Scott Rodney, Hersey Peter, 'P53 in human melanoma fails to regulate target genes associated with apoptosis and the cell cycle and may contribute to proliferation', BMC Cancer, 11 203-219 (2011) [C1]
2011	Talseth-Palmer Bente, Brenne Ingvild S, Ashton Katie Ann, Evans Tiffany-Jane, McPhillips Mary, Groombridge Claire, Suchy Janina, Kurzawski Grzegorz, Spigelman Allan, Lubinski Jan, Scott Rodney, 'Colorectal cancer susceptibility loci on chromosome 8q23.3 and 11q23.1 as modifiers for disease expression in lynch syndrome', Journal of Medical Genetics, 48 279-284 (2011) [C1]
2011	Talseth-Palmer Bente, Scott Rodney, 'Genetic variation and its role in malignancy', International Journal of Biomedical Science, 7 158-171 (2011) [C1]
2011	Wong-Brown Michelle, Nordfors Cecilia, Mossman David, Pecenpetelovska Gordana, Kiejda Kelly Anne, Talseth-Palmer Bente, Bowden Nikola Ann, Scott Rodney, 'BRIP1, PALB2, and RAD51C mutation analysis reveals their relative importance as genetic susceptibility factors for breast cancer', Breast Cancer Research and Treatment, 127 853-859 (2011) [C1]
2010	Talseth-Palmer Bente, McPhillips Mary, Groombridge Claire, Spigelman Allan, Scott Rodney, 'MSH6 and PMS2 mutation positive Australian Lynch syndrome families: Novel mutations, cancer risk and age of diagnosis of colorectal cancer', Hereditary Cancer in Clinical Practice, 8 1-10 (2010) [C1]
2009	Shi Zumin, Johnstone Daniel McKenzie, Talseth-Palmer Bente, Evans Tiffany-Jane, Spigelman Allan D, Groombridge Claire, Milward Adrienne Elizabeth, Olynyk John K, Suchy Janina, Kurzawski Grzegorz, Lubinski Jan, Scott Rodney, 'Haemochromatosis HFE gene polymorphisms as potential modifiers of hereditary nonpolyposis colorectal cancer risk and onset age', International Journal of Cancer, 125 78-83 (2009) [C1]
2009	Talseth-Palmer Bente, Bowden Nikola Ann, Meldrum C, Nicholl J, Thompson E, Friend K, Liebelt J, Bratkovic D, Haan E, Yu S, Scott Rodney, 'A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technology', Cytogenetic and Genome Research, 124 94-101 (2009) [C1]
2008	Talseth-Palmer Bente, Ashton Katie Ann, Meldrum Cliff, Suchy Janina, Kurzawski Grzegorz, Lubinski Jan, Scott Rodney, 'Aurora-A and Cyclin D1 polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer', International Journal of Cancer, 122 1273-1277 (2008) [C1]
2008	Talseth-Palmer Bente, Bowden Nikola Ann, Hill Alyssa, Meldrum Cliff, Scott Rodney, 'Whole genome amplification and its impact on CGH array profiles', BMC Research Notes, 1 108 (2008) [C1]
2007	Talseth-Palmer Bente, Meldrum C, Suchy J, Kurzawski G, Lubinski J, Scott Rodney, 'Lack of association between genetic polymorphisms in cytokine genes and disease expression in patients with hereditary non-polyposis colorectal cancer', Scandinavian Journal of Gastroenterology, 42 628-632 (2007) [C1]
2007	Talseth-Palmer Bente, Meldrum C, Suchy J, Kurzawski G, Lubinski J, Scott Rodney, 'MDM2 SNP309 T > G alone or in combination with the TP53 R72P polymorphism does not appear to influence disease expression and age of diagnosis of colorectal cancer in HNPCC patients', International Journal of Cancer, 120 563-565 (2007) [C1]
2006	Talseth-Palmer Bente, Meldrum C, Suchy J, Kurzawski G, Lubinski J, Scott Rodney, 'Age of diagnosis of colorectal cancer in HNPCC patients is more complex than that predicted by R72P polymorphism in TP53', International Journal of Cancer, 118 2479-2484 (2006) [C1]
2006	Talseth-Palmer Bente, Meldrum C, Suchy J, Kurzawski G, Lubinski J, Scott Rodney, 'Genetic polymorphisms in xenobiotic clearance genes and their influence on disease expression in hereditary nonpolyposis colorectal cancer patients', Cancer Epidemiology Biomarkers & Prevention, 15 2307-2310 (2006) [C1]
2003	LOUKA A S, LIE B A, TALSETH B, ASCHER H, EK J, GUDJONSDOTTIR A H, SOLLID L M, 'Coeliac disease patients carry conserved HLA-DR3-DQ2 haplotypes revealed by association of TNF alleles', Immunogenetics, 55 339-343 (2003) [C1]
2002	LOUKA A, NILSSON S, OLSSON M, TALSETH B, LIE B, EK J, GUDJONSDOTTIR A, ASCHER H, SOLLIED L, 'HLA in coeliac disease families: a novel test of risk modification by the 'other' haplotype when at least one DQA105-DQB102 haplotype is carried. (2002) [C1]
2001	KRISTINSSON S, THOROLFSDOTTIR E, TALSETH B, STEINGRIMSSON E, THORSSON A, HELGASON T, HREIDARSSON A, ARNGRIMSSON R, 'MODY in Iceland is associated with mutations in HNF-1alpha and a novel mutation in NeuroD1. (2001) [C1]

Non Refereed Article in a Professional Journal (C3) (1 outputs)

Year	Citation	Nova
2012	Talseth-Palmer Bente, Scott Rodney, 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, 20 487-488 (2012) [C3]

Conference Publication (16 outputs)

Extract of Paper (E3) (16 outputs)

Year	Citation	Nova
2012	Talseth-Palmer Bente, Holliday Elizabeth Gaye, Evans Tiffany-Jane, McEvoy Mark Anthony, Attia John Richard, Grice Desma M, Masson Amy L, Meldrum Cliff, Spigelman Allan David, Scott Rodney, 'A genome-wide CNV association study of Australian HNPCC/Lynch syndrome patients', Proceedings of the Australian Health & Medical Research Congress 2012, Adelaide, SA (2012) [E3]
2012	Talseth-Palmer Bente, Scott Rodney, 'A step closer to personalised medicine for Lynch Syndrome patients - Personalised screening can prevent cancer development in MLH1 mutation carriers', BDC 2012. 2nd Biomarker Discovery Conference, Shoal Bay, NSW (2012) [E3]
2012	Talseth-Palmer Bente, Wijen J, Brenne I, Jagomohan-Changur S, Baker D, Ashton Katie Ann, Tops C, Evans Tiffany-Jane, McPhillips M, Groombridge Claire, Suchy J, Kurzawski G, Group T, Spigelman A, Moller P, Morreau H, Van Wezel T, Lubinski J, Vasen H, Scott Rodney, 'Colorectal cancer risk modification in Lynch syndrome', Human Genome Meeting 2012: Genetics and Genomics in Personalised Medicine. Abstract Book, Sydney, NSW (2012) [E3]
2011	Martin Amy Louise, Talseth-Palmer Bente, Grice Desma Marie, Hannan Gary, Scott Rodney, 'Elucidating the genetic predisposition to colorectal cancer', XIX NSW Scientific Meeting. Programme, Sydney, NSW (2011) [E3]
2011	Talseth-Palmer Bente, Wijnen Juul T, Brenne Ingvild S, Jagmohan-Changur Shantie, Ashton Katie Ann, Tops Carli M, Evans Tiffany-Jane, McPhillips Mary, Groombridge Claire, Suchy Janina, Kurzawski Grzegorz, The Dutch Cancer Genetics Group, Spigelman Allan, Moller Pal, Morreau Hans M, Van Wezel Tom, Lubinski Jan, Vasen Hans F A, Scott Rodney, 'Chromosome 8q23.3, 10p14 and 11q23.1 variants modify colorectal cancer risk in Lynch syndrome - a combined analysis of the Australian, Dutch and Polish Lynch syndrome cohorts', Familial Aspects of Cancer: Research and Practice 2011, Kingscliff, NSW (2011) [E3]
2011	Talseth-Palmer Bente, Wijnen Juul T, Brenne Ingvild S, Jagmohan-Changur Shanty, Ashton Katie Ann, Tops Carli M, Evans Tiffany-Jane, McPhillips Mary, Groombridge Claire, Suchy Janina, Kurzawski Grzegorz, Spigelman Allan, Moller Pal, Van Wezel Tom, Lubinski Jan, Vasen Hans F A, Scott Rodney, 'Chromosome 8q23.3 AND 11q23.1 variants modify colorectal cancer risk in Lynch syndrome: A meta-analysis of the Dutch and Australian Lynch syndrome cohorts', Abstracts: 4th Biennial Meeting: International Society for Gastrointestinal Hereditary Tumours, San Antonio, TX (2011) [E3]
2010	Evans Tiffany-Jane, Talseth-Palmer Bente, Brenne Ingvild S, Ashton Katie Ann, McPhillips Mary, Groombridge Claire, Kurzawski Grzegorz, Spigelman Alan, Lubinski Jan, Scott Rodney, 'Colorectal cancer suspectibility loci on chr 8q23.3 and 11q23.1 as modifiers for disease expression in Lynch syndrome', Sydney Cancer Conference 2010. Profiling Risk, Personalising Treatment and Predicting Outcomes. Conference Program and Abstract Book, Sydney, NSW (2010) [E3]
2010	Scott Rodney, Talseth-Palmer Bente, Reeves Stuart Glen, Meldrum, Groombridge Claire, Spigelman Allan David, Suchy Janina, Kurzawski Grezegroz, Lubiniski Jan, McElduff Patrick, 'MTHFR 677 C>T and 1298 A>C polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer', Familial Cancer, Dusseldorf, Germany (2010) [E3]
2010	Talseth-Palmer Bente, Holliday Elizabeth Gaye, Evans Tiffany-Jane, McPhillips M, McEvoy Mark Anthony, Attia John Richard, Scott Rodney, 'A modern approach to the search for modifying genetic loci infleuncing the high breast cancer incidence seen in an Australian HNPCC/Lynch Syndrome cohort', Proceedings of the Australian Health and Medical Research Congress 2010, Melbourne, Vic (2010) [E3]
2010	Talseth-Palmer Bente, Holliday Elizabeth Gaye, Evans Tiffany-Jane, McPhillips Mary, Groombridge Claire, Spigelman Allan David, Scott Rodney, 'Modifier genes influencing breast cancer incidence in HNPCC/Lynch syndrome', AMATA 2010 Conference: Conference Handbook, Hobart, Tasmania (2010) [E3]
2010	Talseth-Palmer Bente, McPhillips Mary, Meldrum Cliff, Groombridge Claire, Spigelman Allan David, Scott Rodney, 'Haemochromatosis HFE gene polymorphisms as ptential modifiers of hereditary nonpolyposis colorectal cancer risk and onset age', Familial Cancer, Dusseldorf, Germany (2010) [E3]
2010	Talseth-Palmer Bente, McPhillips Mary, Meldrum Cliff, Groombridge Claire, Spigelman Allan David, Scott Rodney, 'Hereditary nonpolyposis colorectal cancer in 688 families: Mutations, age of diagnosis and cancer incidence', Familial Cancer, Dusseldorf, Germany (2010) [E3]
2009	Evans Tiffany-Jane, Bowden Nikola Ann, Talseth-Palmer Bente, Catchpoole Daniel, Scott Rodney, 'Copy number variation in childhood acute lmphoblastic leukaemia', AMATA 2009, Katoomba, NSW (2009) [E3]
2008	Talseth-Palmer Bente, McPhillips M, Meldrum C, Groombridge C, Spigelman A, Scott Rodney, 'Hereditary nonpolyposis colorectal cancer in families: Mutations, age of diagnosis of cancer and cancer incidence', Conference on Translational Cancer Research: Abstracts, Newcastle, NSW (2008) [E3]
2005	Ashton Katie Ann, Talseth-Palmer Bente, Meldrum Cliff J, McPhillips Mary L, Scott Rodney, 'COMT polymorphism (V158M) and its association with endometrial cancer in HNPCC families that adhere to the Amsterdam or Bethesda criteria', Human Genetics Society of Australasia 29th Annual Conference, Newcastle, NSW (2005) [E3]
2005	Talseth-Palmer Bente, Meldrum Cliff, Ashton Katie Ann, Scott Rodney, 'Age of disease onset in HNPCC patients is more complex than that predicted by R72P polymorphism in TP53', Human Genetics Society of Australasia 29th Annual Conference, Newcastle, NSW (2005) [E3]