Edwin Mientjes
Impact in
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
- Developmental Neuroscience top 5%
Papers in
- Genetics 27
- Genetics and Neurodevelopmental Disorders 15
- Genetic Syndromes and Imprinting 10
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- Epigenetics and DNA Methylation 6
- DNA Repair Mechanisms 6
- Congenital heart defects research 4
- Glycosylation and Glycoproteins Research 3
- Cancer-related gene regulation 3
- Co-authors
- Ype Elgersma (14 shared papers)Gerard C. Grosveld (4 shared papers)Rob Willemsen (7 shared papers)Ben A. Oostra (5 shared papers)Geeske M. van Woerden (6 shared papers)Andrew D. Hollenbach (1 shared paper)Rekha V. Iyengar (1 shared paper)Craig J. McPherson (1 shared paper)
- Journals
- Molecular Psychiatry (3 papers)Molecular Autism (3 papers)Environmental and Molecular Mutagenesis (3 papers)Scientific Reports (2 papers)Neuron (1 paper)
- Partner nations
- NetherlandsUnited StatesSwitzerland
In The Last Decade
Edwin Mientjes
41 papers receiving 2.5k citations
Peers
Comparison fields: 5 of 104
- Genetics 1.5k
- Developmental Neuroscience 123
- Cognitive Neuroscience 596
- Molecular Biology 1.8k
- Cellular and Molecular Neuroscience 284
Countries citing papers authored by Edwin Mientjes
This map shows the geographic impact of Edwin Mientjes'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 Edwin Mientjes with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Edwin Mientjes more than expected).
Fields of papers citing papers by Edwin Mientjes
This network shows the impact of papers produced by Edwin Mientjes. 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 Edwin Mientjes. The network helps show where Edwin Mientjes may publish in the future.
Co-authors
The 25 scholars most cited alongside Edwin Mientjes, 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 44 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2005 | 338 | |
| 2 | 2002 | 219 | |
| 3 | 2015 | 195 | |
| 4 | 2005 | 192 | |
| 5 | 2004 | 118 | |
| 6 | 2006 | 113 | |
| 7 | 2000 | 111 | |
| 8 | 2005 | 104 | |
| 9 | 2008 | 88 | |
| 10 | 2015 | 78 | |
| 11 | 2019 | 77 | |
| 12 | 2014 | 76 | |
| 13 | 2015 | 72 | |
| 14 | 2018 | 61 | |
| 15 | 2021 | 61 | |
| 16 | Fragile X syndrome | 2005 | 58 |
| 17 | 2020 | 56 | |
| 18 | 2006 | 49 | |
| 19 | 1994 | 44 | |
| 20 | 2021 | 41 |
About Edwin Mientjes
Edwin Mientjes is a scholar working on Genetics, Molecular Biology, Cancer Research, Cellular and Molecular Neuroscience and Cell Biology, having authored 44 papers that have together received 2.6k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (15 papers), Genetic Syndromes and Imprinting (10 papers), Epigenetics and DNA Methylation (6 papers), DNA Repair Mechanisms (6 papers), Carcinogens and Genotoxicity Assessment (4 papers), Congenital heart defects research (4 papers), Glycosylation and Glycoproteins Research (3 papers) and Cancer-related gene regulation (3 papers). The work is most often cited by research in Genetics (1.5k citations), Developmental Neuroscience (123 citations), Cognitive Neuroscience (596 citations), Molecular Biology (1.8k citations) and Cellular and Molecular Neuroscience (284 citations). Edwin Mientjes has collaborated with scholars based in Netherlands, United States and Switzerland. Frequent co-authors include Ype Elgersma, Gerard C. Grosveld, Rob Willemsen, Ben A. Oostra, Geeske M. van Woerden, Andrew D. Hollenbach, Rekha V. Iyengar, Craig J. McPherson, David L. Nelson and Steven A. Kushner. Their work appears in journals such as Molecular Psychiatry, Molecular Autism, Environmental and Molecular Mutagenesis, Scientific Reports and Neuron.
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.