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

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

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

Confirmation of childhood acute lymphoblastic leukemia variants, ARID5B and IKZF1, and interaction with parental environmental exposures

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

CD36-a plausible modifier of disease phenotype in familial adenomatous polyposis

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

Copy number variation in hereditary non-polyposis colorectal cancer

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

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

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

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

Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations

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

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

Genetic variation and its role in malignancy

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

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

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

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

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