Marjan Boter
Impact in
- Virology top 5%
- Poxvirus research and outbreaks
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- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
Papers in
- Genetics 15
- Genomic variations and chromosomal abnormalities 12
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
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- Prenatal Screening and Diagnostics 13
- Fetal and Pediatric Neurological Disorders 6
- Co-authors
- Diane Van Opstal (13 shared papers)Robert‐Jan H. Galjaard (10 shared papers)Malgorzata I. Srebniak (12 shared papers)Leendert H. J. Looijenga (3 shared papers)Marieke Joosten (9 shared papers)Lutgarde Govaerts (8 shared papers)J. Wolter Oosterhuis (2 shared papers)Katja P. Wolffenbuttel (2 shared papers)
- Journals
- European Journal of Human Genetics (4 papers)Molecular Cytogenetics (3 papers)Eurosurveillance (3 papers)Prenatal Diagnosis (2 papers)Human Mutation (2 papers)
- Partner nations
- NetherlandsRwandaSpain
In The Last Decade
Marjan Boter
27 papers receiving 898 citations
Marjan Boter's Hit Papers
Peers
Comparison fields: 5 of 88
- Virology 83
- Pediatrics, Perinatology and Child Health 316
- Genetics 416
- Modeling and Simulation 49
- Infectious Diseases 179
Countries citing papers authored by Marjan Boter
This map shows the geographic impact of Marjan Boter'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 Marjan Boter with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marjan Boter more than expected).
Fields of papers citing papers by Marjan Boter
This network shows the impact of papers produced by Marjan Boter. 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 Marjan Boter. The network helps show where Marjan Boter may publish in the future.
Co-authors
The 25 scholars most cited alongside Marjan Boter, 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 28 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2020 | 175 | |
| 2 | 2005 | 140 | |
| 3 | 2011 | 81 | |
| 4 | 2002 | 59 | |
| 5 | Ongoing mpox outbreak in Kamituga, South Kivu province, associated with monkeypox virus of a novel Clade I sub-lineage, Democratic Republic of the Congo, 2024 Hit paper breakdown → | 2024 | 56 |
| 6 | 2012 | 55 | |
| 7 | 2015 | 55 | |
| 8 | 2008 | 51 | |
| 9 | 2014 | 37 | |
| 10 | 2015 | 35 | |
| 11 | 2007 | 25 | |
| 12 | 2011 | 22 | |
| 13 | 2013 | 20 | |
| 14 | 2017 | 18 | |
| 15 | 2011 | 14 | |
| 16 | 2025 | 11 | |
| 17 | 2023 | 11 | |
| 18 | 2018 | 11 | |
| 19 | 2024 | 10 | |
| 20 | 2019 | 10 |
About Marjan Boter
Marjan Boter is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Infectious Diseases and Virology, having authored 28 papers that have together received 932 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (13 papers), Genomic variations and chromosomal abnormalities (12 papers), Fetal and Pediatric Neurological Disorders (6 papers), Poxvirus research and outbreaks (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), COVID-19 Clinical Research Studies (3 papers), SARS-CoV-2 and COVID-19 Research (3 papers) and Testicular diseases and treatments (3 papers). The work is most often cited by research in Virology (83 citations), Pediatrics, Perinatology and Child Health (316 citations), Genetics (416 citations), Modeling and Simulation (49 citations) and Infectious Diseases (179 citations). Marjan Boter has collaborated with scholars based in Netherlands, Rwanda and Spain. Frequent co-authors include Diane Van Opstal, Robert‐Jan H. Galjaard, Malgorzata I. Srebniak, Leendert H. J. Looijenga, Marieke Joosten, Lutgarde Govaerts, J. Wolter Oosterhuis, Katja P. Wolffenbuttel, Martine Cools and Stenvert L. S. Drop. Their work appears in journals such as European Journal of Human Genetics, Molecular Cytogenetics, Eurosurveillance, Prenatal Diagnosis and Human Mutation.
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.