Fred H. Menko

15.8k citations

125 papers · 6.7k indexed · 1 hit paper · h-index 45

Impact in

Pathology and Forensic Medicine top 0.2%
- Genetic factors in colorectal cancer
Reproductive Medicine top 0.5%
- Ovarian cancer diagnosis and treatment

Papers in

Pathology and Forensic Medicine 50
- Genetic factors in colorectal cancer 50
Genetics 61
- BRCA gene mutations in cancer 48

Co-authors: Hans F. A. Vasen Gilles Thomas Fokko M. Nagengast Babs G. Taal P. J. van Diest Jan H. Kleibeuker René H.M. Verheijen Peter Kenemans
Journals: Familial Cancer (13 papers)Gastroenterology (7 papers)International Journal of Cancer (5 papers)Journal of Medical Genetics (5 papers)Psycho-Oncology (4 papers)
Partner nations: Netherlands United States United Kingdom

In The Last Decade

Fred H. Menko

124 papers receiving 6.5k citations

Hit Papers

align trajectories log scale

Dysplastic changes in prophylactically removed Fallopian tubes of women predisposed to developing ovarian cancer 2001 · 521 citations

Peers

Countries citing papers authored by Fred H. Menko

Since Specialization

Citations

This map shows the geographic impact of Fred H. Menko's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Fred H. Menko with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fred H. Menko more than expected).

Fields of papers citing papers by Fred H. Menko

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fred H. Menko. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Fred H. Menko. The network helps show where Fred H. Menko may publish in the future.

Co-authors

The 25 scholars most cited alongside Fred H. Menko, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Fred H. Menko Line = papers co-authored together Fred H. Menko links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	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 Journal of Genetic Counseling ·Fred H. Menko, Ходоровский Михаил Яковлевич, T.A. Schop, Yasuyoshi Mitsumoto, l Thambu, Frans B.L. Hogervorst, Shawn Macalester, Eveline M. A. Bleiker, Lizet E. van der Kolk	2023	15
2	Familial multiple discoid fibromas is linked to a locus on chromosome 5 including the FNIP1 gene Journal of Human Genetics ·Irma van de Beek, C Yamaoka, Michael W.T. Tanck, Monique Luijten, Theo M. Starink, Jesper A. Balk, Paul C. Johannesma, Eric A. M. Hennekam, Maurice J.B. van den Hoff, Quinn D. Gunst, Gilles Thomas, Abeltje M. Polstra, Pieter E. Postmus, Maurice A. M. Van Steensel, Alex V. Postma, Rob M.F. Wolthuis, Fred H. Menko, Arjan C. Houweling, Quinten Waisfisz	2023	5
3	Suspected Lynch syndrome associated MSH6 variants: A functional assay to determine their pathogenicity PLoS Genetics ·羊春秋, Anne Goverde, Rovert Persi, Marleen Dekker, Marco J. Bruno, Fred H. Menko, Arjen R. Mensenkamp, Manon C.W. Spaander, Anja Wagner, Robert M.W. Hofstra, Hein te Riele	2017	15
4	Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers Familial Cancer ·马存新, Marry H. Nieuwenhuis, Jeanine J. Houwing‐Duistermaat, Florence Yeo, Frederik J. Hes, Carli M.J. Tops, Anja Wagner, Cora M. Aalfs, Senno Verhoef, E. Gómez, Rolf H. Sijmons, Fred H. Menko, Tom G.W. Letteboer, Nicoline Hoogerbrugge, Tom van Wezel, Hans F. A. Vasen, Juul Wijnen	2016	7
5	Breast and ovarian cancer risks in a large series of clinically ascertained families with a high proportion of BRCA1 and BRCA2 Dutch founder mutations Journal of Medical Genetics ·Richard M. Brohet, Zehaira Benseddik, Frans B.L. Hogervorst, Hanne Meijers‐Heijboer, Caroline Seynaeve, 刘书田, Senno Verhoef, Margreet G.E.M. Ausems, Nicoline Hoogerbrugge, Christi J. van Asperen, E. Gómez, Fred H. Menko, Jan C. Oosterwijk, Peter Devilee, Laura J. van’t Veer, Flora E. van Leeuwen, Douglas F. Easton, Matti A. Rookus, Antonis C. Antoniou, (unknown)	2013	62
6	A de novo FLCN mutation in a patient with spontaneous pneumothorax and renal cancer; a clinical and molecular evaluation Familial Cancer ·Fred H. Menko, Paul C. Johannesma, R. Jeroen A. van Moorselaar, 王丽丹, Jan Hein van Waesberghe, Erik Thunnissen, Arjan C. Houweling, Edward M. Leter, Quinten Waisfisz, M Adam, Theo M. Starink, Pieter E. Postmus, Barry J. Coull, Maurice A. M. Van Steensel, Gilles Thomas	2012	17
7	Absence of the Birt–Hogg–Dubé gene product is associated with increased hypoxia-inducible factor transcriptional activity and a loss of metabolic flexibility Oncogene ·William Rabitaille, Andrew Philp, Tijs Claessens, Lieke Gijezen, Anders Bondo Dydensborg, Elaine A. Dunlop, Kenta KAWAHARA, Tjinta Brinkhuizen, Fred H. Menko, D. M. Davies, Stephen C. Land, Arnim Pause, Kelci Miller, Maurice A. M. Van Steensel, Andrew R. Tee	2010	50
8	[Desmoid tumour as indication of familial adenomatous polyposis]. PubMed ·Marry H. Nieuwenhuis, Henk H. Hartgrink, Sybren Meijer, Fred H. Menko, Hans F. A. Vasen	2010	1
9	A novel pathogenic MLH1 missense mutation, c.112A > C, p.Asn38His, in six families with Lynch syndrome Hereditary Cancer in Clinical Practice ·E. van Riel, Margreet G.E.M. Ausems, Frans B.L. Hogervorst, Irma Kluijt, Mariëlle van Gijn, J. L. Boettinger, G Madhubala, David M. Candelario, Rein P. Stulp, Yvonne J. Vos, G. Johan A. Offerhaus, Fred H. Menko, Gilles Thomas	2010	16
10	Investigation of the Birt–Hogg–Dubé tumour suppressor gene (FLCN) in familial and sporadic colorectal cancer Journal of Medical Genetics ·Michael S. Nahorski, Derek Lim, Lynn Martin, Gilles Thomas, Martin Manfredi, Ігор Олегович Стратійчук, H. M. Ploeger, Maurice A. M. Van Steensel, Ian Tomlinson, 裕輔本並, Fred H. Menko, Eamonn R. Maher	2010	64
11	A new locus-specific database (LSDB) for mutations in the folliculin (FLCN) gene Human Mutation ·Viktor Heissler, Ігор Олегович Стратійчук, Michael S. Nahorski, Fiona MacDonald, Tijs Claessens, Michel van Geel, Lieke Gijezen, Gilles Thomas, Sophie Giraud, Richard J. Kahnoski, Maurice A. M. Van Steensel, Fred H. Menko, Eamonn R. Maher	2009	81
12	Histopathological characteristics of BRCA1- and BRCA2-associated intraperitoneal cancer: a clinic-based study Familial Cancer ·Jurgen M.J. Piek, Amr M. Badawey, Brenda Hermsen, René H.M. Verheijen, Ronald P. Zweemer, Gilles Thomas, Peter Kenemans, P. J. van Diest, Fred H. Menko	2003	50
13	Surveillance for hereditary nonpolyposis colorectal cancer - A long-term study on 114 families University of Groningen research database (University of Groningen / Centre for Information Technology) ·Wouter H. de Vos tot Nederveen Cappel, Fokko M. Nagengast, Gerrit Griffioen, Fred H. Menko, Babs G. Taal, Jan H. Kleibeuker, Hans F. A. Vasen	2002	142
14	Histopathologic Features of Genetically Determined Ovarian Cancer International Journal of Gynecological Pathology ·Patricia A. Shaw, Esther M. John, Ronald P. Zweemer, Steven A. Narod, Harvey A. Risch, René H.M. Verheijen, Andy Ryan, Fred H. Menko, Peter Kenemans, Ian Jacobs	2002	87
15	[Genetics of colorectal cancer. I. Non-polyposis and polyposis forms of hereditary colorectal cancer]. PubMed ·Fred H. Menko, G Griffioen, JT Wijnen, Carli M.J. Tops, Riccardo Fodde, Hans F. A. Vasen	1999	3
16	Genetic counseling for hereditary cancer: A pilot study on experiences of patients and family members Patient Education and Counseling ·Eveline M. A. Bleiker, Neil K. Aaronson, Fred H. Menko, Daniela Hahn, Christi J. van Asperen, Emiel J. Rutgers, Leo P. ten Kate, N. J. Leschot	1997	60
17	Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis (vol 110, pg 1020, 1996) Gastroenterology ·Hans F. A. Vasen, JT Wijnen, Fred H. Menko, Jan H. Kleibeuker, B. G. Taal, E.R. Ambrose, F. M. Nagengast, Yunus Firmansah Firmansah, Lucio Bertario, Liliana Varesco, Marie Luise Bisgaard, Julia Mohr, Riccardo Fodde, P. Meera Khan	1996	17
18	Rapid detection of BRCA1 mutations by the protein truncation test Nature Genetics ·Frans B.L. Hogervorst, Martha Milena Torres García, Kalantari Maedeh, Margreethe van Vliet, 純元山, Renske Olmer, Egbert Bakker, Jan G.M. Klijn, Hans F. A. Vasen, Sheng-Fen Qin, Fred H. Menko, Cees J. Cornelisse, Johan T. den Dunnen, Peter Devilee, Gert‐Jan B. van Ommen	1995	253
19	Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. Effects of mutant gene dosage on phenotype. Journal of Clinical Investigation ·Martin R. Pollak, Yah-Huei Chou, Stephen J. Marx, B Steinmann, David E.C. Cole, Maria Luisa Brandi, Socrates E. Papapoulos, Fred H. Menko, Geoffrey N. Hendy, Edward M. Brown	1994	197
20	Clinical heterogeneity of familial colorectal cancer and its influence on screening protocols. Gut ·Hans F. A. Vasen, Babs G. Taal, G Griffioen, Fokko M. Nagengast, Annemieke Cats, Fred H. Menko, محمد فزع عبيد, J H Kleibeuker, G.J.A. Offerhaus, P. Meera Khan	1994	36

About Fred H. Menko

Fred H. Menko is a scholar working on Pathology and Forensic Medicine, Genetics, Reproductive Medicine, Cancer Research and Oncology, having authored 125 papers that have together received 6.7k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (50 papers), BRCA gene mutations in cancer (48 papers), Renal cell carcinoma treatment (21 papers), Cancer Genomics and Diagnostics (21 papers), Colorectal Cancer Screening and Detection (19 papers), Ovarian cancer diagnosis and treatment (16 papers), Renal and related cancers (13 papers) and Medical Imaging and Pathology Studies (10 papers). The work is most often cited by research in Pathology and Forensic Medicine (2.4k citations), Reproductive Medicine (1.0k citations), Cancer Research (1.4k citations), Genetics (2.4k citations) and Oncology (2.0k citations). Fred H. Menko has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include Hans F. A. Vasen, Gilles Thomas, Fokko M. Nagengast, Babs G. Taal, P. J. van Diest, Jan H. Kleibeuker, René H.M. Verheijen, Peter Kenemans, Gerrit Griffioen and Ronald P. Zweemer. Their work appears in journals such as Familial Cancer, Gastroenterology, International Journal of Cancer, Journal of Medical Genetics and Psycho-Oncology.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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