Publications by authors named "Fred H Menko"

68Publications

Do Preferred Risk Formats Lead to Better Understanding? A Multicenter Controlled Trial on Communicating Familial Breast Cancer Risks Using Different Risk Formats.

Patient Prefer Adherence 2020 19;14:333-342. Epub 2020 Feb 19.

Department of Public and Occupational Health, Amsterdam UMC, Vrije Universiteit, Amsterdam, the Netherlands.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.2147/PPA.S232941DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7036980PMC
February 2020

[BRCAmutations more frequent in people of Jewish ancestry].

Ned Tijdschr Geneeskd 2019 03 1;163. Epub 2019 Mar 1.

Antoni van Leeuwenhoek, polikliniek Familiaire Tumoren en afd. Pathologie, Amsterdam.

View Article

Download full-text PDF

Source
March 2019

The uptake of presymptomatic genetic testing in hereditary breast-ovarian cancer and Lynch syndrome: a systematic review of the literature and implications for clinical practice.

Fam Cancer 2019 01;18(1):127-135

Department of Psychosocial Research and Epidemiology, Antoni van Leeuwenhoek Hospital and The Netherlands Cancer Institute, Amsterdam, The Netherlands.

View Article

Download full-text PDF

Source
http://link.springer.com/10.1007/s10689-018-0089-z
Publisher Site
http://dx.doi.org/10.1007/s10689-018-0089-zDOI Listing
January 2019

How to support cancer genetics counselees in informing at-risk relatives? Lessons from a randomized controlled trial.

Patient Educ Couns 2018 09 8;101(9):1611-1619. Epub 2018 May 8.

Department of Medical Psychology, Academic Medical Centre, University of Amsterdam, The Netherlands. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.pec.2018.05.009DOI Listing
September 2018

Design and Feasibility of an Intervention to Support Cancer Genetic Counselees in Informing their At-Risk Relatives.

J Genet Couns 2016 12 22;25(6):1179-1187. Epub 2016 Apr 22.

Department of Medical Psychology, Academic Medical Centre, University of Amsterdam, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s10897-016-9948-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5114329PMC
December 2016

Diagnosis and Management of Hereditary Renal Cell Cancer.

Recent Results Cancer Res 2016 ;205:85-104

Department of Medical Genetics, University of Cambridge, Cambridge, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/978-3-319-29998-3_6DOI Listing
July 2016

Fine mapping of the uterine leiomyoma locus on 1q43 close to a lncRNA in the RGS7-FH interval.

Endocr Relat Cancer 2015 Aug 25;22(4):633-43. Epub 2015 Jun 25.

Department of EpidemiologyR217JDepartment of BiostatisticsSchool of Public Health, University of Alabama at Birmingham, 1665 University Boulevard, Birmingham, Alabama 35294-0022, USADepartment of Human GeneticsRadboud University Medical Center Nijmegen, Nijmegen, The NetherlandsNetherlands Cancer InstituteAmsterdam, The Netherlands.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1530/ERC-15-0208DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4526794PMC
August 2015

Prevalence of Birt-Hogg-Dubé syndrome in patients with apparently primary spontaneous pneumothorax.

Eur Respir J 2015 Apr 23;45(4):1191-4. Epub 2014 Dec 23.

Dept of Pulmonary Diseases, VU University Medical Center, Amsterdam, The Netherlands

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1183/09031936.00196914DOI Listing
April 2015

Development of the Informing Relatives Inventory (IRI): Assessing Index Patients' Knowledge, Motivation and Self-Efficacy Regarding the Disclosure of Hereditary Cancer Risk Information to Relatives.

Int J Behav Med 2015 Aug;22(4):551-60

Department of Medical Psychology, Academic Medical Centre, University of Amsterdam, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands,

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s12529-014-9455-xDOI Listing
August 2015

Lynch syndrome caused by germline PMS2 mutations: delineating the cancer risk.

J Clin Oncol 2015 Feb 15;33(4):319-25. Epub 2014 Dec 15.

Sanne W. ten Broeke, Carli M. Tops, Heleen M. van der Klift, Manon Suerink, Frederik J. Hes, Hans F. Vasen, Maartje Nielsen, and Juul T. Wijnen, Leiden University Medical Center; Hans F. Vasen, The Netherlands Foundation for the Detection of Hereditary Tumors, Leiden; Richard M. Brohet, Research Center Linnaeus Institute, Spaarne Hospital, Hoofddorp; Mary E. Velthuizen and Tom G.W. Letteboer, University Medical Center Utrecht, Utrecht; Encarna Gomez Garcia, Maastricht University Medical Center, Maastricht; Nicoline Hoogerbrugge, Arjen R. Mensenkamp, and Liesbeth Spruijt, Radboud University Medical Center, Nijmegen; Fred H. Menko, Vrije Universiteit, University Medical Center; Theo A. van Os and Bert J.W. Redeker, Academic Medical Center, Amsterdam; Rolf H. Sijmons and Yvonne J. Vos, University of Groningen, University Medical Center Groningen, Groningen; Anja Wagner, Erasmus University Medical Center, Rotterdam, the Netherlands; Inge Bernstein, Aalborg University Hospital, Aalborg; Inge Bernstein, Danish Hereditary Nonpolyposis Colorectal Cancer Registry, Hvidovre University Hospital Copenhagen, Denmark; Gabriel Capellá Munar, Hereditary Cancer Program, Catalan Institute of Oncology-Institut D'Investigació Biomèdica de Bellvitge, l'Hospitalet de Llobregat, Spain; Annika Lindblom, Karolinska Institutet, Karolinska University Hospital, Solna; Pal Moller, Research Group Inherited Cancer, Oslo University Hospital, Oslo, Norway; and Nils Rahner, Institute of Human Genetics, University of Dusseldorf, Dusseldorf, Germany.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1200/JCO.2014.57.8088DOI Listing
February 2015

Establishing a clinical and molecular diagnosis for hereditary colorectal cancer syndromes: Present tense, future perfect?

Gastrointest Endosc 2014 Dec;80(6):1145-55

Department of Pathology, University Medical Centre Utrecht, Utrecht, the Netherlands.

View Article

Download full-text PDF

Source
https://linkinghub.elsevier.com/retrieve/pii/S00165107140204
Publisher Site
http://dx.doi.org/10.1016/j.gie.2014.07.049DOI Listing
December 2014

The pathogenesis of pneumothorax in Birt-Hogg-Dubé syndrome: a hypothesis.

Respirology 2014 Nov;19(8):1248-50

Department of Pulmonary Diseases, VU University Medical Center, Amsterdam, The Netherlands.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/resp.12405DOI Listing
November 2014

[A young man with intestinal polyposis and epistaxis].

Ned Tijdschr Geneeskd 2014 ;158:A7398

VU medisch centrum, afd. Klinische genetica, Amsterdam.

View Article

Download full-text PDF

Source
April 2015

In-flight pneumothorax: diagnosis may be missed because of symptom delay.

Am J Respir Crit Care Med 2014 Sep;190(6):704-5

1 Vrije Universiteit (VU) University Medical Center Amsterdam, The Netherlands.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1164/rccm.201404-0698LEDOI Listing
September 2014

Topical rapamycin as a treatment for fibrofolliculomas in Birt-Hogg-Dubé syndrome: a double-blind placebo-controlled randomized split-face trial.

PLoS One 2014 9;9(6):e99071. Epub 2014 Jun 9.

Department of Dermatology, GROW School for Oncology and Developmental Biology, Maastricht University Medical Centre+, Maastricht, The Netherlands; Department of Clinical Genetics, GROW School for Oncology and Developmental Biology, Maastricht University Medical Centre+, Maastricht, The Netherlands; Institute of Medical Biology, Singapore, Singapore.

View Article

Download full-text PDF

Source
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0099071PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4049818PMC
October 2015

The effectiveness of a graphical presentation in addition to a frequency format in the context of familial breast cancer risk communication: a multicenter controlled trial.

BMC Med Inform Decis Mak 2013 Apr 29;13:55. Epub 2013 Apr 29.

Department of Public and Occupational Health, EMGO Institute for Health and Care Research, VU University Medical Center, Amsterdam, The Netherlands.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1186/1472-6947-13-55DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3644257PMC
April 2013

Genetic counseling does not fulfill the counselees' need for certainty in hereditary breast/ovarian cancer families: an explorative assessment.

Psychooncology 2013 May 9;22(5):1167-76. Epub 2012 Jul 9.

Department of Clinical Genetics, Center for Human and Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/pon.3125DOI Listing
May 2013

The counselees' self-reported request for psychological help in genetic counseling for hereditary breast/ovarian cancer: not only psychopathology matters.

Psychooncology 2013 Apr 27;22(4):902-10. Epub 2012 Jun 27.

Department of Clinical Genetics, Center for Human and Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/pon.3081DOI Listing
April 2013

Exploring the short-term impact of DNA-testing in breast cancer patients: the counselees' perception matters, but the actual BRCA1/2 result does not.

Patient Educ Couns 2012 Feb 27;86(2):239-51. Epub 2011 Dec 27.

Department of Clinical Genetics, Center for Human and Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.pec.2011.04.017DOI Listing
February 2012

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-result.

Psychooncology 2012 Jan 11;21(1):29-42. Epub 2010 Nov 11.

Department of Clinical Genetics, Center for Human and Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/pon.1864DOI Listing
January 2012

Informing family members about a hereditary predisposition to cancer: attitudes and practices among clinical geneticists.

J Med Ethics 2010 Jul;36(7):391-5

University of Amsterdam/Centre for Society and Genomics, Nijmegen, Amsterdam, The Netherlands.

View Article

Download full-text PDF

Source
http://jme.bmj.com/cgi/doi/10.1136/jme.2009.033324
Publisher Site
http://dx.doi.org/10.1136/jme.2009.033324DOI Listing
July 2010

Investigation of the Birt-Hogg-Dube tumour suppressor gene (FLCN) in familial and sporadic colorectal cancer.

J Med Genet 2010 Jun;47(6):385-90

Department of Medical & Molecular Genetics, School of Clinical and Experimental Medicine, University of Birmingham College of Medical and Dental Sciences, Edgbaston, Birmingham B15 2TT, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1136/jmg.2009.073304DOI Listing
June 2010

[Spontaneous pneumothorax as the first manifestation of a hereditary condition with an increased renal cancer risk].

Ned Tijdschr Geneeskd 2009 ;153:A581

VU Medisch Centrum, Afd. Longziekten, Amsterdam, The Netherlands.

View Article

Download full-text PDF

Source
February 2010

A new locus-specific database (LSDB) for mutations in the folliculin (FLCN) gene.

Hum Mutat 2010 Jan;31(1):E1043-51

Department of Medical & Molecular Genetics, School of Clinical and Experimental Medicine, University of Birmingham College of Medical and Dental Sciences, Edgbaston, Birmingham B15 2TT, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/humu.21130DOI Listing
January 2010

The contribution of CHEK2 to the TP53-negative Li-Fraumeni phenotype.

Hered Cancer Clin Pract 2009 Feb 17;7(1). Epub 2009 Feb 17.

Family Cancer Clinic, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1186/1897-4287-7-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2664322PMC
February 2009

[Desmoid tumour as indication of familial adenomatous polyposis].

Ned Tijdschr Geneeskd 2010 ;154:A2235

Stichting Opsporing Erfelijke Tumoren, Leids Universitair Medisch Centrum, Afd. Heelkunde, Leiden, the Netherlands.

View Article

Download full-text PDF

Source
November 2010

High frequency of HIF-1alpha overexpression in BRCA1 related breast cancer.

Breast Cancer Res Treat 2008 Oct 21;111(3):475-80. Epub 2007 Nov 21.

Department of Pathology, University Medical Center, 3508 GA, Utrecht, The Netherlands.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s10549-007-9817-zDOI Listing
October 2008

Biallelic germline mutations of mismatch-repair genes: a possible cause for multiple pediatric malignancies.

Cancer 2007 Jun;109(11):2349-56

Department of Gastroenterology and Hepatology, Erasmus MC University Medical Center, Rotterdam, the Netherlands.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/cncr.22697DOI Listing
June 2007

Colorectal cancer in the family: psychosocial distress and social issues in the years following genetic counselling.

Hered Cancer Clin Pract 2007 Jun 15;5(2):59-66. Epub 2007 Jun 15.

Division of Psychosocial Research and Epidemiology, The Netherlands Cancer Institute, Amsterdam.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1186/1897-4287-5-2-59DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2736993PMC
June 2007

Late-onset common cancers in a kindred with an Arg213Gln TP53 germline mutation.

Fam Cancer 2006 ;5(2):169-74

Family Cancer Clinic, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s10689-005-4789-9DOI Listing
August 2006

Screening behavior of individuals at high risk for colorectal cancer.

Gastroenterology 2005 Feb;128(2):280-7

Division of Psychosocial Research and Epidemiology, The Netherlands Cancer Institute - Antoni van Leewenhoek Hospital, Amsterdam, The Netherlands.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1053/j.gastro.2004.11.002DOI Listing
February 2005

A homozygous MSH6 mutation in a child with café-au-lait spots, oligodendroglioma and rectal cancer.

Fam Cancer 2004 ;3(2):123-7

Department of Clinical Genetics and Human Genetics, VU University Medical Center, Amsterdam, The Netherlands.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1023/B:FAME.0000039893.19289.18DOI Listing
November 2004

Surveillance for hereditary nonpolyposis colorectal cancer: a long-term study on 114 families.

Dis Colon Rectum 2002 Dec;45(12):1588-94

Department of Gastroenterology, Leiden University Medical Center Leiden, The Netherlands,

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s10350-004-7244-3DOI Listing
December 2002

Atypical MEN type 2B associated with two germline RET mutations on the same allele not involving codon 918.

J Clin Endocrinol Metab 2002 Jan;87(1):393-7

Department of Clinical Genetics and Human Genetics, Vrije Universiteit Medical Center, 1007 MB Amsterdam, The Netherlands.

View Article

Download full-text PDF

Source
https://academic.oup.com/jcem/article-lookup/doi/10.1210/jce
Publisher Site
http://dx.doi.org/10.1210/jcem.87.1.8136DOI Listing
January 2002