Marcel Nelen
Impact in
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
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- Neurotransmitter Receptor Influence on Behavior
Papers in
-
- PI3K/AKT/mTOR signaling in cancer 5
- RNA modifications and cancer 5
- Mitochondrial Function and Pathology 4
- Genetics 21
- Genomic variations and chromosomal abnormalities 9
- Genomics and Rare Diseases 8
- Co-authors
- Bernard A. van Oost (8 shared papers)Hans‐Hilger Ropers (5 shared papers)Han G. Brunner (8 shared papers)Xandra O. Breakefield (1 shared paper)Ben C.J. Hamel (3 shared papers)Han G. Brunner (2 shared papers)A. H. van Gennip (1 shared paper)Erik Ch. Wolters (1 shared paper)
- Journals
- Human Mutation (4 papers)International Journal of Neonatal Screening (3 papers)Genomics (3 papers)European Journal of Human Genetics (3 papers)Molecular and Cellular Biology (2 papers)
- Partner nations
- NetherlandsUnited StatesGermany
In The Last Decade
Marcel Nelen
57 papers receiving 3.4k citations
Marcel Nelen's Hit Papers
Peers
Comparison fields: 5 of 135
- Genetics 992
- Cellular and Molecular Neuroscience 613
- Biological Psychiatry 66
- Molecular Biology 1.5k
- Behavioral Neuroscience 70
Countries citing papers authored by Marcel Nelen
This map shows the geographic impact of Marcel Nelen'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 Marcel Nelen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marcel Nelen more than expected).
Fields of papers citing papers by Marcel Nelen
This network shows the impact of papers produced by Marcel Nelen. 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 Marcel Nelen. The network helps show where Marcel Nelen may publish in the future.
Co-authors
The 25 scholars most cited alongside Marcel Nelen, 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 57 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Abnormal Behavior Associated with a Point Mutation in the Structural Gene for Monoamine Oxidase A Hit paper breakdown → | 1993 | 1091 |
| 2 | 1997 | 334 | |
| 3 | X-linked borderline mental retardation with prominent behavioral disturbance: phenotype, genetic localization, and evidence for disturbed monoamine metabolism. | 1993 | 254 |
| 4 | 1999 | 236 | |
| 5 | 2016 | 108 | |
| 6 | 1992 | 105 | |
| 7 | 1994 | 88 | |
| 8 | 2016 | 83 | |
| 9 | 2009 | 81 | |
| 10 | 2008 | 76 | |
| 11 | 2013 | 75 | |
| 12 | 2009 | 73 | |
| 13 | 1993 | 64 | |
| 14 | 1989 | 60 | |
| 15 | 2016 | 47 | |
| 16 | 1992 | 45 | |
| 17 | 1992 | 43 | |
| 18 | 1989 | 34 | |
| 19 | 1999 | 33 | |
| 20 | 2022 | 33 |
About Marcel Nelen
Marcel Nelen is a scholar working on Molecular Biology, Genetics, Surgery, Genetics and Pathology and Forensic Medicine, having authored 57 papers that have together received 3.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Genomics and Rare Diseases (8 papers), PI3K/AKT/mTOR signaling in cancer (5 papers), RNA modifications and cancer (5 papers), Cardiovascular Effects of Exercise (4 papers), Cancer Genomics and Diagnostics (4 papers), Metabolism and Genetic Disorders (4 papers) and Mitochondrial Function and Pathology (4 papers). The work is most often cited by research in Genetics (992 citations), Cellular and Molecular Neuroscience (613 citations), Biological Psychiatry (66 citations), Molecular Biology (1.5k citations) and Behavioral Neuroscience (70 citations). Marcel Nelen has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include Bernard A. van Oost, Hans‐Hilger Ropers, Han G. Brunner, Xandra O. Breakefield, Ben C.J. Hamel, Han G. Brunner, A. H. van Gennip, Erik Ch. Wolters, N.G.G.M. Abeling and Michaël Kuiper. Their work appears in journals such as Human Mutation, International Journal of Neonatal Screening, Genomics, European Journal of Human Genetics and Molecular and Cellular Biology.
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.