Hereditary Cancer in Clinical Practice


Open Access Research

Penetrance of HNPCC-related cancers in a retrolective cohort of 12 large Newfoundland families carrying a MSH2 founder mutation: an evaluation using modified segregation models

Karen A Kopciuk1*, Yun-Hee Choi2, Elena Parkhomenko3, Patrick Parfrey4, John McLaughlin5,6, Jane Green7 and Laurent Briollais6

Author Affiliations

1 Division of Population Health Research, Alberta Health Services Board, Calgary, Alberta, Canada

2 Department of Epidemiology and Biostatistics, The University of Western Ontario, London, Ontario, Canada

3 Research Institute, Hospital for Sick Children, Toronto, Ontario, Canada

4 Clinical Epidemiology Unit, Memorial University, St John's, Newfoundland, Canada

5 Population Studies and Surveillance, Cancer Care Ontario, Toronto, Ontario, Canada

6 Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Toronto, Ontario, Canada

7 Discipline of Genetics, Memorial University, St John's, Newfoundland, Canada

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Hereditary Cancer in Clinical Practice 2009, 7:16 doi:10.1186/1897-4287-7-16

Published: 28 October 2009

Additional files

Additional file 1:

General hazard specification for parametric regression model. The formulation of the hazard function based on a generalized log-Burr specification of the survival function.

Format: TEX Size: 7KB Download file

Open Data

Additional file 2:

Retrospective Ascertainment-Corrected Likelihood. Details on the derivation of the correction for ascertainment of high risk families.

Format: TEX Size: 8KB Download file

Open Data