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BMC Medical Informatics and Decision Making|May 1, 2013
The effectiveness of a graphical presentation in addition to a frequency format in the context of familial breast cancer risk communication: a multicenter controlled trialLidewij Henneman, Jan C Oosterwijk, Christi J van Asperen, et al.
Gastroenterology|February 3, 2005
Screening behavior of individuals at high risk for colorectal cancerEveline M A Bleiker, Fred H Menko, Babs G Taal, et al.
Patient Education and Counseling|June 21, 2011
Exploring the short-term impact of DNA-testing in breast cancer patients: the counselees' perception matters, but the actual BRCA1/2 result does notJoël Vos, Jan C Oosterwijk, Encarna Gomez-Garcia, et al.
International Journal of Behavioral Medicine|December 18, 2014
Development of the Informing Relatives Inventory (IRI): Assessing Index Patients' Knowledge, Motivation and Self-Efficacy Regarding the Disclosure of Hereditary Cancer Risk Information to RelativesEveline de Geus, Cora M Aalfs, Fred H Menko, et al.
Psycho-Oncology|November 13, 2010
Opening the psychological black box in genetic counseling. The psychological impact of DNA testing is predicted by the counselees' perception, the medical impact by the pathogenic or uninformative BRCA1/2-resultJoël Vos, Encarna Gómez-García, Jan C Oosterwijk, et al.
The Lancet. Oncology|December 5, 2009
Birt-Hogg-Dubé syndrome: diagnosis and managementFred H Menko, Maurice A M van Steensel, Sophie Giraud, et al.
Hereditary Cancer in Clinical Practice|April 3, 2009
The contribution of CHEK2 to the TP53-negative Li-Fraumeni phenotypeMarielle W G Ruijs, Annegien Broeks, Fred H Menko, et al.
Respirology (Carlton, Vic.)|October 11, 2014
The pathogenesis of pneumothorax in Birt-Hogg-Dubé syndrome: a hypothesisPaul Christiaan Johannesma, Arjan C Houweling, Jan-Hein T M van Waesberghe, et al.
Familial Cancer|October 24, 2003
Histopathological characteristics of BRCA1- and BRCA2-associated intraperitoneal cancer: a clinic-based studyJurgen M J Piek, Bas Torrenga, Brenda Hermsen, et al.
The Journal of Clinical Endocrinology and Metabolism|January 15, 2002
Atypical MEN type 2B associated with two germline RET mutations on the same allele not involving codon 918Fred H Menko, Rob B van der Luijt, Irene A J de Valk, et al.
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