M. Mannens
Impact in
- Genetics top 10%
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
-
- Prenatal Screening and Diagnostics
Papers in
-
- Epigenetics and DNA Methylation 12
- Renal and related cancers 8
- Cancer-related gene regulation 4
- RNA modifications and cancer 3
- Genetics 19
- Genetic Syndromes and Imprinting 13
- Genomic variations and chromosomal abnormalities 4
- Co-authors
- A. Westerveld (11 shared papers)Marja Steenman (3 shared papers)Jet Bliek (8 shared papers)Mariëlle Alders (8 shared papers)J.M.N. Hoovers (9 shared papers)Peter Little (5 shared papers)N. J. Leschot (3 shared papers)Veronica van Heyningen (3 shared papers)
- Journals
- Genomics (6 papers)Human Molecular Genetics (2 papers)European Journal of Human Genetics (2 papers)Genes Chromosomes and Cancer (2 papers)Cytogenetic and Genome Research (1 paper)
- Partner nations
- NetherlandsUnited KingdomUnited States
In The Last Decade
M. Mannens
32 papers receiving 818 citations
Peers
Comparison fields: 5 of 64
- Genetics 294
- Pediatrics, Perinatology and Child Health 173
- Molecular Biology 543
- Cardiology and Cardiovascular Medicine 112
- Immunology 85
Countries citing papers authored by M. Mannens
This map shows the geographic impact of M. Mannens'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 M. Mannens with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. Mannens more than expected).
Fields of papers citing papers by M. Mannens
This network shows the impact of papers produced by M. Mannens. 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 M. Mannens. The network helps show where M. Mannens may publish in the future.
Co-authors
The 25 scholars most cited alongside M. Mannens, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 32 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1992 | 115 | |
| 2 | 1993 | 115 | |
| 3 | 2000 | 81 | |
| 4 | 1998 | 73 | |
| 5 | 1997 | 73 | |
| 6 | 1999 | 70 | |
| 7 | 1999 | 54 | |
| 8 | 1993 | 31 | |
| 9 | 1991 | 26 | |
| 10 | 1994 | 23 | |
| 11 | 1999 | 22 | |
| 12 | 1991 | 20 | |
| 13 | 2004 | 19 | |
| 14 | 1998 | 15 | |
| 15 | 1999 | 14 | |
| 16 | 1997 | 14 | |
| 17 | 1996 | 12 | |
| 18 | 1995 | 12 | |
| 19 | 1993 | 12 | |
| 20 | 2008 | 11 |
About M. Mannens
M. Mannens is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Immunology and Pathology and Forensic Medicine, having authored 32 papers that have together received 849 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (13 papers), Epigenetics and DNA Methylation (12 papers), Renal and related cancers (8 papers), Prenatal Screening and Diagnostics (7 papers), Cancer-related gene regulation (4 papers), Genomic variations and chromosomal abnormalities (4 papers), RNA modifications and cancer (3 papers) and Cardiac electrophysiology and arrhythmias (2 papers). The work is most often cited by research in Genetics (294 citations), Pediatrics, Perinatology and Child Health (173 citations), Molecular Biology (543 citations), Cardiology and Cardiovascular Medicine (112 citations) and Immunology (85 citations). M. Mannens has collaborated with scholars based in Netherlands, United Kingdom and United States. Frequent co-authors include A. Westerveld, Marja Steenman, Jet Bliek, Mariëlle Alders, J.M.N. Hoovers, Peter Little, N. J. Leschot, Veronica van Heyningen, David J. Porteous and Rosalind M. John. Their work appears in journals such as Genomics, Human Molecular Genetics, European Journal of Human Genetics, Genes Chromosomes and Cancer and Cytogenetic and Genome Research.
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.