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Talseth-Palmer, Bente A.

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Whole genome amplification and its impact on CGH array profiles 100 95 3
MSH6 and PMS2 mutation positive Australian Lynch syndrome families: novel mutations, cancer risk and age of diagnosis of colorectal cancer 147 141 2
Genetic variation and its role in malignancy 32 26 3
Expanding the genetic basis of copy number variation in familial breast cancer 4 4 0
Haemochromatosis HFE gene polymorphisms as potential modifiers of hereditary nonpolyposis colorectal cancer risk and onset age 113 108 0
P53 in human melanoma fails to regulate target genes associated with apoptosis and the cell cycle and may contribute to proliferation 56 55 2
Meta-analysis of mismatch repair polymorphisms within the cogent consortium for colorectal cancer susceptibility 81 78 0
Copy number variation in hereditary non-polyposis colorectal cancer 54 52 0
The importance of a large sample cohort for studies on modifier genes influencing disease severity in FAP patients 44 41 0
Confirmation of childhood acute lymphoblastic leukemia variants, ARID5B and IKZF1, and interaction with parental environmental exposures 7 6 0
Colorectal cancer susceptibility loci on chromosome 8q23.3 and 11q23.1 as modifiers for disease expression in lynch syndrome 24 23 0
Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients 35 30 1
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Talseth-Palmer, Bente A.

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