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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 190 164 3
Confirmation of childhood acute lymphoblastic leukemia variants, ARID5B and IKZF1, and interaction with parental environmental exposures 125 100 0
Whole genome amplification and its impact on CGH array profiles 139 124 4
Genetic modifiers of cancer risk in Lynch syndrome: a review 23 16 0
Genetic variation and its role in malignancy 50 38 4
Meta-analysis of mismatch repair polymorphisms within the cogent consortium for colorectal cancer susceptibility 225 196 0
P53 in human melanoma fails to regulate target genes associated with apoptosis and the cell cycle and may contribute to proliferation 121 102 3
Colorectal cancer susceptibility loci on chromosome 8q23.3 and 11q23.1 as modifiers for disease expression in lynch syndrome 54 49 0
The importance of a large sample cohort for studies on modifier genes influencing disease severity in FAP patients 100 85 0
Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients 90 77 2
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 33 25 0
Expanding the genetic basis of copy number variation in familial breast cancer 40 32 0
8q23.3 and 11q23.1 as modifying loci influencing the risk for CRC in Lynch syndrome 21 14 0
Combined analysis of three lynch syndrome cohorts confirms the modifying effects of 8q23.3 and 11q23.1 in MLH1 mutation carriers 47 32 0
Haemochromatosis HFE gene polymorphisms as potential modifiers of hereditary nonpolyposis colorectal cancer risk and onset age 183 160 0
Copy number variation in hereditary non-polyposis colorectal cancer 123 99 1
Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations 11 9 0
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