F. H. Menko

594 total citations
12 papers, 396 citations indexed

About

F. H. Menko is a scholar working on Pathology and Forensic Medicine, Genetics and Cancer Research. According to data from OpenAlex, F. H. Menko has authored 12 papers receiving a total of 396 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Pathology and Forensic Medicine, 6 papers in Genetics and 4 papers in Cancer Research. Recurrent topics in F. H. Menko's work include Genetic factors in colorectal cancer (6 papers), BRCA gene mutations in cancer (3 papers) and Cancer Genomics and Diagnostics (3 papers). F. H. Menko is often cited by papers focused on Genetic factors in colorectal cancer (6 papers), BRCA gene mutations in cancer (3 papers) and Cancer Genomics and Diagnostics (3 papers). F. H. Menko collaborates with scholars based in Netherlands, United Kingdom and Slovakia. F. H. Menko's co-authors include K. Madan, Hans F. A. Vasen, Katharina Wimmer, Noémie Lavoine, Yael Goldberg, Odile Cabaret, Jan Loeffen, Denisa Ilenčíková, Laurence Brugières and Chrystelle Colas and has published in prestigious journals such as Journal of Clinical Pathology, Journal of Medical Genetics and Gynecologic Oncology.

In The Last Decade

F. H. Menko

12 papers receiving 379 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
F. H. Menko Netherlands	8	250	137	135	131	116	12	396
Amelia Reichmann United States	11	206 0.8×	189 1.4×	139 1.0×	187 1.4×	147 1.3×	12	474
Gabriel M. Mulcahy United States	6	89 0.4×	135 1.0×	129 1.0×	95 0.7×	128 1.1×	11	328
Stefan Furgyik Sweden	9	73 0.3×	131 1.0×	68 0.5×	144 1.1×	114 1.0×	13	364
Agnès Chompret France	5	68 0.3×	171 1.2×	219 1.6×	120 0.9×	252 2.2×	5	441
Deborah Packham Australia	11	288 1.2×	89 0.6×	195 1.4×	202 1.5×	245 2.1×	14	490
Erika L.D. Mitchell United Kingdom	11	67 0.3×	139 1.0×	93 0.7×	107 0.8×	206 1.8×	15	352
Valeria Pensotti Italy	13	138 0.6×	200 1.5×	153 1.1×	111 0.8×	155 1.3×	30	451
Izabela Brożek Poland	15	95 0.4×	429 3.1×	97 0.7×	108 0.8×	353 3.0×	23	583
Elizabeth L. Schubert United States	8	85 0.3×	251 1.8×	125 0.9×	171 1.3×	241 2.1×	9	466
Anna Rohlin Sweden	10	285 1.1×	139 1.0×	170 1.3×	171 1.3×	176 1.5×	18	478

Countries citing papers authored by F. H. Menko

Since Specialization

Citations

This map shows the geographic impact of F. 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 F. 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 F. H. Menko more than expected).

Fields of papers citing papers by F. H. Menko

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by F. 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 F. H. Menko. The network helps show where F. H. Menko may publish in the future.

Co-authorship network of co-authors of F. H. Menko

This figure shows the co-authorship network connecting the top 25 collaborators of F. H. Menko. A scholar is included among the top collaborators of F. H. Menko based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with F. H. Menko. F. H. Menko is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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12 of 12 papers shown

Vasen, Hans F. A., Franck Bourdeaut, Odile Cabaret, et al.. (2014). Guidelines for surveillance of individuals with constitutional mismatch repair-deficiency proposed by the European Consortium “Care for CMMR-D” (C4CMMR-D). Journal of Medical Genetics. 51(5). 283–293. 142 indexed citations

Keller, Josbert J., Alex R. Musler, Marnix Jansen, et al.. (2005). STRAD in Peutz-Jeghers syndrome and sporadic cancers. Journal of Clinical Pathology. 58(10). 1091–1095. 19 indexed citations

Keller, Josbert J., G. J. A. Offerhaus, Francis M. Giardiello, & F. H. Menko. (2001). Jan Peutz, Harold Jeghers and a remarkable combination of polyposis and pigmentation of the skin and mucous membranes. Familial Cancer. 1(3-4). 181–185. 12 indexed citations

Hogervorst, Frans B.L., M J Ligtenberg, Gijs R. van den Brink, et al.. (1997). 0-8. Germ-line mutations in BRCA1 and BRCA2 are seldom found in `unilateral breast cancer only' families. The Breast. 6(4). 227–227. 1 indexed citations

Wijnen, Juul, P. Meera Khan, Hans F. A. Vasen, et al.. (1996). Majority of hMLH1 mutations responsible for hereditary nonpolyposis colorectal cancer cluster at the exonic region 15-16.. PubMed. 58(2). 300–7. 104 indexed citations

Wijker, Mario, F. Schoute, Gerard Pals, et al.. (1995). The gene for hereditary bullous dystrophy, X-linked macular type, maps to the Xq27.3-qter region.. PubMed. 56(5). 1096–100. 8 indexed citations

Vasen, Hans F. A., Hanne Meijers-Heijboer, M. van Vliet, et al.. (1995). Age at diagnosis as an indicator of eligibility for BRCA1 DNA testing in familial breast cancer. Human Genetics. 95(5). 539–544. 19 indexed citations

Menko, F. H., René H.M. Verheijen, Leoni A. Louwé, et al.. (1994). Endometrial Cancer in Four Sisters: Report of a Kindred with Presumed Cancer Family Syndrome. Gynecologic Oncology. 54(2). 171–174. 7 indexed citations

Zwaan, C. Michel, F. C. de Waal, F. H. Menko, et al.. (1994). A giant congenital orbital tumor: An unusual presentation of retinoblastoma. Medical and Pediatric Oncology. 23(6). 507–511. 1 indexed citations

10.

Madan, K. & F. H. Menko. (1992). Intrachromosomal insertions: a case report and a review. Human Genetics. 89(1). 1–9. 62 indexed citations

11.

Menko, F. H., et al.. (1992). Robin sequence and a deficiency of the left forearm in a girl with a deletion of chromosome 4q33‐qter. American Journal of Medical Genetics. 44(5). 696–698. 18 indexed citations

12.

Menko, F. H., et al.. (1988). Van der Woude syndrome--recognition of lesser expressions: case report.. PubMed. 25(3). 318–21. 3 indexed citations

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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