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Talseth-Palmer, Bente A.

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Whole genome amplification and its impact on CGH array profiles 98 93 3
Haemochromatosis HFE gene polymorphisms as potential modifiers of hereditary nonpolyposis colorectal cancer risk and onset age 112 107 0
MSH6 and PMS2 mutation positive Australian Lynch syndrome families: novel mutations, cancer risk and age of diagnosis of colorectal cancer 140 135 2
Copy number variation in hereditary non-polyposis colorectal cancer 53 51 0
P53 in human melanoma fails to regulate target genes associated with apoptosis and the cell cycle and may contribute to proliferation 52 51 2
Genetic variation and its role in malignancy 31 25 3
Meta-analysis of mismatch repair polymorphisms within the cogent consortium for colorectal cancer susceptibility 74 71 0
Colorectal cancer susceptibility loci on chromosome 8q23.3 and 11q23.1 as modifiers for disease expression in lynch syndrome 22 21 0
The importance of a large sample cohort for studies on modifier genes influencing disease severity in FAP patients 40 37 0
Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients 29 26 0
Expanding the genetic basis of copy number variation in familial breast cancer 2 2 0
Confirmation of childhood acute lymphoblastic leukemia variants, ARID5B and IKZF1, and interaction with parental environmental exposures 4 3 0
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Talseth-Palmer, Bente A.

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Talseth-Palmer, Bente A.

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