Fred H. Menko

Overview

Best Publications

• Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13

  Richard Wooster;Susan L. Neuhausen;Jonathan Mangion;Yvette Quirk

  2719
  Citations

• Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis.

  HF Vasen;JT Wijnen;FH Menko;JH Kleibeuker

  1045
  Citations

• Frequency and Spectrum of Cancers in the Peutz-Jeghers Syndrome

  Nicholas Hearle;Valérie Schumacher;Fred H. Menko;Sylviane Olschwang

  1020
  Citations

• Dysplastic changes in prophylactically removed Fallopian tubes of women predisposed to developing ovarian cancer

  J M Piek;P J van Diest;R P Zweemer;J W Jansen

  940
  Citations

• Birt-Hogg-Dubé syndrome: diagnosis and management

  Fred H Menko;Maurice Am van Steensel;Sophie Giraud;Lennart Friis-Hansen

  645
  Citations

• Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance.

  Yvonne M C Hendriks;Anja Wagner;Hans Morreau;Fred Menko

  514
  Citations

• Familial endometrial cancer in female carriers of MSH6 germline mutations

  J Wijnen;W de Leeuw;H Vasen;H van der Klift

  499
  Citations

• Clinical findings with implications for genetic testing in families with clustering of colorectal cancer.

  JT Wijnen;Hfa Vasen;PM Khan;AH Zwinderman

  498
  Citations

• Cancer risks in BRCA2 families: estimates for sites other than breast and ovary

  C J van Asperen;R M Brohet;E J Meijers-Heijboer;N Hoogerbrugge

  497
  Citations

• MSH2 mutation carriers are at higher risk of cancer than MLH1 mutation carriers : A study of hereditary nonpolyposis colorectal cancer families

  H. F.A. Vasen;A. Stormorken;F. H. Menko;F. M. Nagengast

  492
  Citations

• Rapid detection of BRCA1 mutations by the protein truncation test

  Fbl Hogervorst;RS Cornelis;M Bout;M van Vliet

  414
  Citations

• Large genomic deletions and duplications in the BRCA1 gene identified by a novel quantitative method

  Frans B. L. Hogervorst;Petra M. Nederlof;Johan J. P. Gille;Cathal J. McElgunn

  404
  Citations

• TP53 germline mutation testing in 180 families suspected of Li–Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes

  Marielle W. G. Ruijs;Senno Verhoef;Matti A. Rookus;Roelof Pruntel

  362
  Citations

• Risks of Less Common Cancers in Proven Mutation Carriers With Lynch Syndrome

  Christoph Engel;Markus Loeffler;Verena Steinke;Nils Rahner

  338
  Citations

• Hereditary leiomyomatosis and renal cell cancer (HLRCC): renal cancer risk, surveillance and treatment

  Fred H. Menko;Eamonn R. Maher;Laura S. Schmidt;Lindsay A. Middelton

  321
  Citations

• Relative frequency and morphology of cancers in STK11 mutation carriers.

  Wendy Lim;Sylviane Olschwang;Josbert J. Keller;Anne Marie Westerman

  320
  Citations

• Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. Effects of mutant gene dosage on phenotype.

  M R Pollak;Y H Chou;S J Marx;B Steinmann

  282
  Citations

• MSH2 genomic deletions are a frequent cause of HNPCC.

  Wijnen J;van der Klift H;Vasen H;Khan Pm

  281
  Citations

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

  Wouter H de Vos tot Nederveen Cappel;Fokko M Nagengast;Gerrit Griffioen;Fred H Menko

  273
  Citations

• Prediction of a mismatch repair gene defect by microsatellite instability and immunohistochemical analysis in endometrial tumours from HNPCC patients

  Wiljo J. F. de Leeuw;Wiljo J. F. de Leeuw;JanWillem Dierssen;Hans F. A. Vasen;Juul Th. Wijnen

  263
  Citations