Katja Aktan-Collan

Katja Aktan-Collan

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Katja Aktan-Collan

Katja Aktan-Collan

Publications by authors named "Katja Aktan-Collan"

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7Publications

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Psychosocial consequences of predictive genetic testing for Lynch syndrome and associations to surveillance behaviour in a 7-year follow-up study.

Fam Cancer 2013 Dec;12(4):639-46

Department of Medical Genetics, Haartman Institute Biomedicum, University of Helsinki, PO Box 63, FIN-00014, Helsinki, Finland,

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http://link.springer.com/10.1007/s10689-013-9628-9
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http://dx.doi.org/10.1007/s10689-013-9628-9DOI Listing
December 2013

A microduplication on chromosome 17p13.1p13.3 including the PAFAH1B1 (LIS1) gene.

Am J Med Genet A 2011 Apr 15;155A(4):875-9. Epub 2011 Mar 15.

Vaestoliitto, The Family Federation of Finland, Department of Medical Genetics, Helsinki, Finland.

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http://dx.doi.org/10.1002/ajmg.a.33944DOI Listing
April 2011

Sharing genetic risk with next generation: mutation-positive parents' communication with their offspring in Lynch Syndrome.

Fam Cancer 2011 Mar;10(1):43-50

Department of Medical Genetics, Haartman Institute Biomedicum, University of Helsinki, Helsinki, Finland.

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http://dx.doi.org/10.1007/s10689-010-9386-xDOI Listing
March 2011

Ten years after mutation testing for Lynch syndrome: cancer incidence and outcome in mutation-positive and mutation-negative family members.

J Clin Oncol 2009 Oct 31;27(28):4793-7. Epub 2009 Aug 31.

Department of Surgery, University of Helsinki, FI-00029 HUS, Helsinki, Finland.

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http://dx.doi.org/10.1200/JCO.2009.23.7784DOI Listing
October 2009

Adolescents at risk for MODY3 diabetes prefer genetic testing before adulthood.

Diabetes Care 2007 Jun 10;30(6):1571-3. Epub 2007 Mar 10.

Research Program for Molecular Medicine, Folkhälsan Research Center, Helsinki University and Genetic Institute, Helsinki, Finland.

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http://dx.doi.org/10.2337/dc06-1744DOI Listing
June 2007

Life and health insurance behaviour of individuals having undergone a predictive genetic testing programme for hereditary non-polyposis colorectal cancer.

Community Genet 2001 ;4(4):219-24

Department of Medical Genetics, Family Federation of Finland, PO Box 849, FIN-00101 Helsinki (Finland).

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http://dx.doi.org/10.1159/000064196DOI Listing
June 2003