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Lista de obras de Bente A Talseth-Palmer

8q23.3 and 11q23.1 as modifying loci influencing the risk for CRC in Lynch syndrome.

artículo científico publicado en 2011

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.

artículo científico publicado en 2009

BRIP1, PALB2, and RAD51C mutation analysis reveals their relative importance as genetic susceptibility factors for breast cancer ⬇️

artículo científico publicado el 16 de marzo de 2011

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.

artículo científico publicado en 2012

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

article

Colorectal cancer susceptibility loci on chromosome 8q23.3 and 11q23.1 as modifiers for disease expression in Lynch syndrome

artículo científico publicado en 2010

Combined analysis of three lynch syndrome cohorts confirms the modifying effects of 8q23.3 and 11q23.1 in MLH1 mutation carriers

artículo científico publicado en 2012

Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients

artículo científico publicado en 2013

Copy number variants associated with 18p11.32, DCC and the promoter 1B region of APC in colorectal polyposis patients

artículo científico publicado en 2015

Copy number variation in hereditary non-polyposis colorectal cancer

artículo científico publicado en 2013

Effects of a fall prevention program in elderly: a pragmatic observational study in two orthopedic departments

artículo científico publicado en 2019

Expanding the genetic basis of copy number variation in familial breast cancer.

artículo científico publicado en 2014

Haemochromatosis HFE gene polymorphisms as potential modifiers of hereditary nonpolyposis colorectal cancer risk and onset age.

artículo científico publicado en 2009

MSH6 and PMS2 mutation positive Australian Lynch syndrome families: novel mutations, cancer risk and age of diagnosis of colorectal cancer.

artículo científico publicado en 2010

Meta-analysis of mismatch repair polymorphisms within the cogent consortium for colorectal cancer susceptibility

artículo científico publicado en 2013

P53 in human melanoma fails to regulate target genes associated with apoptosis and the cell cycle and may contribute to proliferation

artículo científico publicado en 2011

Patient participation in the clinical pathway-Nurses' perceptions of adults' involvement in haemodialysis

scientific article published on 14 February 2019

Reply to Win and Jenkins

artículo científico publicado en 2013

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

artículo científico publicado en 2016

The genetic basis of colonic adenomatous polyposis syndromes

artículo científico publicado en 2017

The importance of a large sample cohort for studies on modifier genes influencing disease severity in FAP patients

artículo científico publicado en 2013

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

artículo científico publicado en 2017

Whole genome amplification and its impact on CGH array profiles.

artículo científico publicado en 2008

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