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Bente A. Talseth‐Palmer

Observed names: B. Talseth, B.A. Talseth-Palmer, Bente A Talseth-Palmer, Bente A. Talseth, Bente A. Talseth-Palmer, Bente Talseth, Bente Talseth-Palmer, Bente Talseth‐Palmer, Talseth-Palmer, Bente
Observed institutions: Universidad Complutense de Madrid, Oslo University Hospital, University of Oslo, Norwegian University of Science and Technology, Innlandet Hospital Trust, Leiden University Medical Center, John Hunter Hospital, Hunter Medical Research Institute, Molde Hospital, Ålesund Hospital, St Olav's University Hospital, Helse Møre og Romsdal HF, NSW Health Pathology, University of Newcastle Australia, Newcastle University
ORCID: 0000-0003-0286-7161
Observed ORCID: 0000-0003-0286-7161
OpenAlex ID: A5056125067
P53 in human melanoma fails to regulate target genes associated with apoptosis and the cell cycle and may contribute to proliferation
2011 · Kelly A Avery-Kiejda, Nikola A Bowden, et al. · BMC Cancer · 119
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MODY in Iceland is associated with mutations in HNF -1? and a novel mutation in NeuroD1
2001 · S. Y. Kristinsson, B. Talseth, et al. · Diabetologia · 113
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The genetic basis of colonic adenomatous polyposis syndromes
2017 · Bente A. Talseth-Palmer · Hereditary Cancer in Clinical Practice · 105
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BRIP1, PALB2, and RAD51C mutation analysis reveals their relative importance as genetic susceptibility factors for breast cancer
2011 · Michelle W. Wong, Cecilia Nordfors, et al. · Breast Cancer Research and Treatment · 105
Genetic Variation and its Role in Malignancy
2011 · Bente A. Talseth-Palmer, Rodney J. Scott, et al. · International Journal of Biomedical Science · 69
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HLA in coeliac disease families: A novel test of risk modification by the ‘other’ haplotype when at least one DQA1*05‐DQB1*02 haplotype is carried
2002 · A.S. Louka, S. Nilsson, et al. · Tissue Antigens · 53
Comprehensive mismatch repair gene panel identifies variants in patients with Lynch‐like syndrome
2019 · Alexandre Xavier, Maren Fridtjofsen Olsen, et al. · Molecular Genetics & Genomic Medicine · 48
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MSH6 and PMS2 mutation positive Australian Lynch syndrome families: novel mutations, cancer risk and age of diagnosis of colorectal cancer
2010 · Bente A Talseth-Palmer, Mary McPhillips, et al. · Hereditary Cancer in Clinical Practice · 48
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TAPES: A tool for assessment and prioritisation in exome studies
2019 · Alexandre Xavier, Rodney J. Scott, et al. · PLoS Computational Biology · 46
Use of multigene‐panel identifies pathogenic variants in several CRC ‐predisposing genes in patients previously tested for Lynch Syndrome
2017 · Maren F. Hansen, Jostein Johansen, et al. · Clinical Genetics · 46
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Colorectal cancer susceptibility loci on chromosome 8q23.3 and 11q23.1 as modifiers for disease expression in lynch syndrome
2010 · Bente A Talseth-Palmer, Ingvild S Brenne, et al. · Journal of Medical Genetics · 44
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
2006 · Bente A. Talseth, Cliff Meldrum, et al. · International Journal of Cancer · 44
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Haemochromatosis HFE gene polymorphisms as potential modifiers of hereditary nonpolyposis colorectal cancer risk and onset age
2009 · Zumin Shi, Daniel Johnstone, et al. · International Journal of Cancer · 43
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Confirmation of Childhood Acute Lymphoblastic Leukemia Variants, ARID5B and IKZF1, and Interaction with Parental Environmental Exposures
2014 · Tiffany-Jane Evans, Elizabeth Milne, et al. · PLoS ONE · 36
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Combined analysis of three lynch syndrome cohorts confirms the modifying effects of 8q23.3 and 11q23.1 in MLH1 mutation carriers
2012 · Bente A. Talseth‐Palmer, Juul T. Wijnen, et al. · International Journal of Cancer · 35
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Age of diagnosis of colorectal cancer in HNPCC patients is more complex than that predicted by R72P polymorphism in TP53
2005 · Bente A. Talseth, Cliff Meldrum, et al. · International Journal of Cancer · 34
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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
2022 · Bardo Driller, Bente Talseth-Palmer, et al. · BMC Palliative Care · 33
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Targeted next‐generation sequencing of 22 mismatch repair genes identifies Lynch syndrome families
2016 · Bente A. Talseth‐Palmer, Denis C. Bauer, et al. · Cancer Medicine · 31
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Coeliac disease patients carry conserved HLA-DR3-DQ2 haplotypes revealed by association of TNF alleles
2003 · Andrew S. Louka, Benedicte A. Lie, et al. · Immunogenetics · 31
Aurora‐A and Cyclin D1 polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer
2007 · Bente A. Talseth, Katie A. Ashton, et al. · International Journal of Cancer · 28
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Genetic modifiers of cancer risk in Lynch syndrome: a review
2013 · Bente A. Talseth-Palmer, Juul T. Wijnen, et al. · Familial Cancer · 27
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Whole genome amplification and its impact on CGH array profiles
2008 · Bente A Talseth-Palmer, Nikola A Bowden, et al. · BMC Research Notes · 24
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Effects of a fall prevention program in elderly: a pragmatic observational study in two orthopedic departments
2019 · Bodil Røyset, Bente A. Talseth-Palmer, et al. · Clinical Interventions in Aging · 23
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Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients
2013 · Bente A Talseth-Palmer, Elizabeth G Holliday, et al. · BMC Medical Genomics · 23
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Genetic Polymorphisms in Xenobiotic Clearance Genes and Their Influence on Disease Expression in Hereditary Nonpolyposis Colorectal Cancer Patients
2006 · Bente A. Talseth, Cliff Meldrum, et al. · Cancer Epidemiology Biomarkers & Prevention · 23
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Works count: 64
Citation count: 1,460
H-index: 23
I10-index: 37
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