F. H. Menko
Impact in
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- Genetic factors in colorectal cancer
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- Cancer Genomics and Diagnostics
Papers in
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- Genetic factors in colorectal cancer 6
- Genetics 6
- BRCA gene mutations in cancer 3
- Genomic variations and chromosomal abnormalities 3
- Craniofacial Disorders and Treatments 2
- Co-authors
- K. Madan (2 shared papers)Hans F. A. Vasen (4 shared papers)Franck Bourdeaut (1 shared paper)Laurence Brugières (1 shared paper)P. Meera Khan (2 shared papers)Natacha Entz‐Werlé (1 shared paper)Jan Loeffen (1 shared paper)Martine Muleris (1 shared paper)
- Journals
- Human Genetics (2 papers)Journal of Clinical Pathology (1 paper)Familial Cancer (1 paper)Gynecologic Oncology (1 paper)Journal of Medical Genetics (1 paper)
- Partner nations
- NetherlandsUnited KingdomSlovakia
In The Last Decade
F. H. Menko
12 papers receiving 379 citations
Peers
Comparison fields: 5 of 40
- Pathology and Forensic Medicine 250
- Cancer Research 131
- Oncology 135
- Genetics 137
- Pediatrics, Perinatology and Child Health 46
Countries citing papers authored by F. H. Menko
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
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-authors
The 25 scholars most cited alongside F. H. Menko, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2014 | 142 | |
| 2 | Majority of hMLH1 mutations responsible for hereditary nonpolyposis colorectal cancer cluster at the exonic region 15-16. | 1996 | 104 |
| 3 | 1992 | 62 | |
| 4 | 2005 | 19 | |
| 5 | 1995 | 19 | |
| 6 | 1992 | 18 | |
| 7 | 2001 | 12 | |
| 8 | The gene for hereditary bullous dystrophy, X-linked macular type, maps to the Xq27.3-qter region. | 1995 | 8 |
| 9 | 1994 | 7 | |
| 10 | Van der Woude syndrome--recognition of lesser expressions: case report. | 1988 | 3 |
| 11 | 1994 | 1 | |
| 12 | 1997 | 1 |
About F. H. Menko
F. H. Menko is a scholar working on Pathology and Forensic Medicine, Genetics, Cancer Research, Surgery and Oncology, having authored 12 papers that have together received 396 indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (6 papers), Cancer Genomics and Diagnostics (3 papers), BRCA gene mutations in cancer (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Craniofacial Disorders and Treatments (2 papers), Colorectal Cancer Screening and Detection (2 papers), Neuroblastoma Research and Treatments (1 paper) and Colorectal Cancer Treatments and Studies (1 paper). The work is most often cited by research in Pathology and Forensic Medicine (250 citations), Cancer Research (131 citations), Oncology (135 citations), Genetics (137 citations) and Pediatrics, Perinatology and Child Health (46 citations). F. H. Menko has collaborated with scholars based in Netherlands, United Kingdom and Slovakia. Frequent co-authors include K. Madan, Hans F. A. Vasen, Franck Bourdeaut, Laurence Brugières, P. Meera Khan, Natacha Entz‐Werlé, Jan Loeffen, Martine Muleris, Christian P. Kratz and Noémie Lavoine. Their work appears in journals such as Human Genetics, Journal of Clinical Pathology, Familial Cancer, Gynecologic Oncology and Journal of Medical Genetics.
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.