Publications by authors named "Fred Menko"

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ERN GENTURIS clinical practice guidelines for the diagnosis, surveillance and management of people with Birt-Hogg-Dubé syndrome.
Marianne Geilswijk, Maurizio Genuardi, Emma R Woodward, Katie Nightingale, Jazzmin Huber, Fred H Menko

Eur J Hum Genet· December 2024

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Does a proactive procedure lead to a higher uptake of predictive testing in families with a pathogenic BRCA1/BRCA2 variant? A family cancer clinic evaluation.
Fred H Menko, Sophie L van der Velden, Diana N Griffioen, Daoud Ait Moha, Kiki N Jeanson

J Genet Couns· June 2024

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Familial multiple discoid fibromas is linked to a locus on chromosome 5 including the FNIP1 gene.
Irma van de Beek, Iris E Glykofridis, Michael W T Tanck, Monique N H Luijten, Theo M Starink, Fred H Menko

J Hum Genet· April 2023

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Update of penetrance estimates in Birt-Hogg-Dubé syndrome.
Fiona Jane Bruinsma, James G Dowty, Aung Ko Win, Laura C Goddard, Prachi Agrawal, Fred H Menko

J Med Genet· April 2023

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European collaboration on genetic tumour risk syndromes.
Hildegunn H Vetti, Ignacio Blanco, Fred H Menko

Eur J Med Genet· February 2023

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Challenges in breast cancer genetic testing. A call for novel forms of multidisciplinary care and long-term evaluation.
Fred H Menko, Kim Monkhorst, Frans B L Hogervorst, Efraim H Rosenberg, Muriel A Adank

Crit Rev Oncol Hematol· August 2022

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Oral contraceptive use and ovarian cancer risk for BRCA1/2 mutation carriers: an international cohort study.
Lieske H Schrijver, Antonis C Antoniou, Håkan Olsson, Thea M Mooij, Marie-José Roos-Blom, Fred H Menko

Am J Obstet Gynecol· July 2021

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The uptake of predictive DNA testing in 40 families with a pathogenic BRCA1/BRCA2 variant. An evaluation of the proband-mediated procedure.
Fred H Menko, Kiki N Jeanson, Eveline M A Bleiker, Carla W M van Tiggelen, Frans B L Hogervorst

Eur J Hum Genet· August 2020

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Do Preferred Risk Formats Lead to Better Understanding? A Multicenter Controlled Trial on Communicating Familial Breast Cancer Risks Using Different Risk Formats.
Lidewij Henneman, Christi J van Asperen, Jan C Oosterwijk, Fred H Menko, Liesbeth Claassen

Patient Prefer Adherence· February 2020

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[BRCAmutations more frequent in people of Jewish ancestry].
Fred H Menko, Efraim H Rosenberg, Lizet E van der Kolk

Ned Tijdschr Geneeskd· March 2019

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Constitutional mismatch repair deficiency as a differential diagnosis of neurofibromatosis type 1: consensus guidelines for testing a child without malignancy.
Manon Suerink, Tim Ripperger, Ludwine Messiaen, Fred H Menko, Franck Bourdeaut

J Med Genet· February 2019

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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.
Fred H Menko, Jacqueline A Ter Stege, Lizet E van der Kolk, Kiki N Jeanson, Winnie Schats

Fam Cancer· January 2019

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How to support cancer genetics counselees in informing at-risk relatives? Lessons from a randomized controlled trial.
Willem Eijzenga, Eveline de Geus, Cora M Aalfs, Fred H Menko, Rolf H Sijmons

Patient Educ Couns· September 2018

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CDC73-Related Disorders: Clinical Manifestations and Case Detection in Primary Hyperparathyroidism.
Karin van der Tuin, Carli M J Tops, Muriel A Adank, Jan-Maarten Cobben, Neveen A T Hamdy, Fred H Menko

J Clin Endocrinol Metab· December 2017

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Suspected Lynch syndrome associated MSH6 variants: A functional assay to determine their pathogenicity.
Hellen Houlleberghs, Anne Goverde, Jarnick Lusseveld, Marleen Dekker, Marco J Bruno, Fred H Menko

PLoS Genet· May 2017

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Design and Feasibility of an Intervention to Support Cancer Genetic Counselees in Informing their At-Risk Relatives.
Eveline de Geus, Willem Eijzenga, Fred H Menko, Rolf H Sijmons, Hanneke C J M de Haes

J Genet Couns· December 2016

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Hereditary cancer registries improve the care of patients with a genetic predisposition to cancer: contributions from the Dutch Lynch syndrome registry.
Hans F A Vasen, Mary E Velthuizen, Jan H Kleibeuker, Fred H Menko, Fokke M Nagengast

Fam Cancer· July 2016

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Diagnosis and Management of Hereditary Renal Cell Cancer.
Fred H Menko, Eamonn R Maher

Recent Results Cancer Res· July 2016

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The effect of genotypes and parent of origin on cancer risk and age of cancer development in PMS2 mutation carriers.
Manon Suerink, Heleen M van der Klift, Sanne W Ten Broeke, Olaf M Dekkers, Inge Bernstein, Fred H Menko

Genet Med· April 2016

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Are lung cysts in renal cell cancer (RCC) patients an indication for FLCN mutation analysis?
Paul C Johannesma, Arjan C Houweling, Fred H Menko, I van de Beek, Rinze Reinhard

Fam Cancer· April 2016

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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.
Eveline de Geus, Cora M Aalfs, Fred H Menko, Rolf H Sijmons, Mathilde G E Verdam

Int J Behav Med· August 2015

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Fine mapping of the uterine leiomyoma locus on 1q43 close to a lncRNA in the RGS7-FH interval.
Brahim Aissani, Kui Zhang, Arjen R Mensenkamp, Fred H Menko, Howard W Wiener

Endocr Relat Cancer· August 2015

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Prevalence of Birt-Hogg-Dubé syndrome in patients with apparently primary spontaneous pneumothorax.
Paul C Johannesma, Rinze Reinhard, Yael Kon, Jincey D Sriram, Hans J Smit, Fred H Menko

Eur Respir J· April 2015

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Lynch syndrome caused by germline PMS2 mutations: delineating the cancer risk.
Sanne W ten Broeke, Richard M Brohet, Carli M Tops, Heleen M van der Klift, Mary E Velthuizen, Fred H Menko

J Clin Oncol· February 2015

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Establishing a clinical and molecular diagnosis for hereditary colorectal cancer syndromes: Present tense, future perfect?
Marnix Jansen, Fred H Menko, Lodewijk A A Brosens, Francis M Giardiello, G Johan Offerhaus

Gastrointest Endosc· December 2014

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