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Talseth-Palmer, Bente A.

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MSH6 and PMS2 mutation positive Australian Lynch syndrome families: novel mutations, cancer risk and age of diagnosis of colorectal cancer 174 158 3
Genetic variation and its role in malignancy 40 33 4
Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients 69 61 2
The importance of a large sample cohort for studies on modifier genes influencing disease severity in FAP patients 75 64 0
8q23.3 and 11q23.1 as modifying loci influencing the risk for CRC in Lynch syndrome 3 3 0
Haemochromatosis HFE gene polymorphisms as potential modifiers of hereditary nonpolyposis colorectal cancer risk and onset age 160 145 0
Genetic modifiers of cancer risk in Lynch syndrome: a review 12 9 0
Confirmation of childhood acute lymphoblastic leukemia variants, ARID5B and IKZF1, and interaction with parental environmental exposures 88 76 0
Expanding the genetic basis of copy number variation in familial breast cancer 29 24 0
Copy number variation in hereditary non-polyposis colorectal cancer 99 86 1
Whole genome amplification and its impact on CGH array profiles 131 120 4
Meta-analysis of mismatch repair polymorphisms within the cogent consortium for colorectal cancer susceptibility 160 149 0
Colorectal cancer susceptibility loci on chromosome 8q23.3 and 11q23.1 as modifiers for disease expression in lynch syndrome 44 40 0
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 11 11 0
P53 in human melanoma fails to regulate target genes associated with apoptosis and the cell cycle and may contribute to proliferation 90 85 3
Combined analysis of three lynch syndrome cohorts confirms the modifying effects of 8q23.3 and 11q23.1 in MLH1 mutation carriers 8 5 0
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Talseth-Palmer, Bente A.

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