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Frederic H Menko
Frederic H Menko
Consultant Clinical Geneticist, Antoni van Leeuwenhoek Hospital/ Netherlands Cancer Institute
Verified email at nki.nl
Title
Cited by
Cited by
Year
Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis
HF Vasen, JT Wijnen, FH Menko, JH Kleibeuker, BG Taal, G Griffioen, ...
Gastroenterology 110 (4), 1020-1027, 1996
10651996
Frequency and spectrum of cancers in the Peutz-Jeghers syndrome
N Hearle, V Schumacher, FH Menko, S Olschwang, LA Boardman, ...
Clinical Cancer Research 12 (10), 3209-3215, 2006
10482006
Dysplastic changes in prophylactically removed Fallopian tubes of women predisposed to developing ovarian cancer
JMJ Piek, PJ Van Diest, RP Zweemer, JW Jansen, RJJ Poort‐Keesom, ...
The Journal of Pathology: A Journal of the Pathological Society of Great …, 2001
9912001
Birt-Hogg-Dubé syndrome: diagnosis and management
FH Menko, MAM Van Steensel, S Giraud, L Friis-Hansen, S Richard, ...
The lancet oncology 10 (12), 1199-1206, 2009
6352009
Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance
YMC Hendriks, A Wagner, H Morreau, F Menko, A Stormorken, ...
Gastroenterology 127 (1), 17-25, 2004
5132004
Cancer risks in BRCA2 families: estimates for sites other than breast and ovary
CJ Van Asperen, RM Brohet, EJ Meijers-Heijboer, N Hoogerbrugge, ...
Journal of medical genetics 42 (9), 711-719, 2005
5082005
Familial endometrial cancer in female carriers of MSH6 germline mutations
J Wijnen, W Leeuw, H Vasen, H Klift, P Møller, A Stormorken, ...
Nature genetics 23 (2), 142-144, 1999
4931999
MSH2 mutation carriers are at higher risk of cancer than MLH1 mutation carriers: a study of hereditary nonpolyposis colorectal cancer families.
HF Vasen, A Stormorken, FH Menko, FM Nagengast, JH Kleibeuker, ...
4912001
Clinical findings with implications for genetic testing in families with clustering of colorectal cancer
JT Wijnen, HFA Vasen, PM Khan, AH Zwinderman, H van der Klift, ...
New England Journal of Medicine 339 (8), 511-518, 1998
4911998
Large genomic deletions and duplications in the BRCA1 gene identified by a novel quantitative method
FBL Hogervorst, PM Nederlof, JJP Gille, CJ McElgunn, M Grippeling, ...
Cancer research 63 (7), 1449-1453, 2003
4112003
Rapid detection of BRCA1 mutations by the protein truncation test
FBL Hogervorst, RS Cornelis, M Bout, M Vliet, JC Oosterwijk, R Olmer, ...
Nature genetics 10 (2), 208-212, 1995
4091995
TP53 germline mutation testing in 180 families suspected of Li–Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes
MWG Ruijs, S Verhoef, MA Rookus, R Pruntel, AH van der Hout, ...
Journal of medical genetics 47 (6), 421-428, 2010
3602010
Risks of less common cancers in proven mutation carriers with lynch syndrome
C Engel, M Loeffler, V Steinke, N Rahner, E Holinski-Feder, W Dietmaier, ...
Journal of Clinical Oncology 30 (35), 4409-4415, 2012
3432012
Hereditary leiomyomatosis and renal cell cancer (HLRCC): renal cancer risk, surveillance and treatment
FH Menko, ER Maher, LS Schmidt, LA Middelton, K Aittomäki, I Tomlinson, ...
Familial cancer 13, 637-644, 2014
3272014
Relative frequency and morphology of cancers in STK11 mutation carriers
W Lim, S Olschwang, JJ Keller, AM Westerman, FH Menko, LA Boardman, ...
Gastroenterology 126 (7), 1788-1794, 2004
3232004
Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. Effects of mutant gene dosage on phenotype.
MR Pollak, YH Chou, SJ Marx, B Steinmann, DE Cole, ML Brandi, ...
The Journal of clinical investigation 93 (3), 1108-1112, 1994
2991994
MSH2 genomic deletions are a frequent cause of HNPCC
J Wijnen, H van der Klift, H Vasen, PM Khan, F Menko, C Tops, ...
Nature genetics 20 (4), 326-328, 1998
2671998
The role of mismatch repair gene defects in the development of adenomas in patients with HNPCC
AE De Jong, H Morreau, M Van Puijenbroek, PHC Eilers, J Wijnen, ...
Gastroenterology 126 (1), 42-48, 2004
2402004
Molecular evidence linking primary cancer of the fallopian tube to BRCA1 germline mutations
RP Zweemer, PJ Van Diest, RHM Verheijen, A Ryan, JJP Gille, ...
Gynecologic oncology 76 (1), 45-50, 2000
2282000
Lynch Syndrome Caused by Germline PMS2 Mutations: Delineating the Cancer Risk
SW Ten Broeke, RM Brohet, CM Tops, HM van der Klift, ME Velthuizen, ...
Journal of Clinical Oncology 33 (4), 319-325, 2015
2232015
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