Inge B. Mathijssen
Impact in
- Genetics top 10%
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 11
- Genomic variations and chromosomal abnormalities 5
- Genetic Syndromes and Imprinting 4
- Connective tissue disorders research 3
- Genomics and Rare Diseases 3
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- Prenatal Screening and Diagnostics 5
- Co-authors
- Eva Pajkrt (6 shared papers)Alex V. Postma (4 shared papers)Phil Barnett (3 shared papers)Aho Ilgun (3 shared papers)Jan Lam (2 shared papers)Lidewij Henneman (6 shared papers)Vincent M. Christoffels (1 shared paper)Arthur A.M. Wilde (1 shared paper)
- Journals
- European Journal of Human Genetics (7 papers)Prenatal Diagnosis (4 papers)Genetics in Medicine (4 papers)European Journal of Medical Genetics (3 papers)Human Mutation (2 papers)
- Partner nations
- NetherlandsGermanyUnited States
In The Last Decade
Inge B. Mathijssen
34 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 79
- Genetics 389
- Pediatrics, Perinatology and Child Health 179
- Molecular Biology 547
- Genetics 50
- Cardiology and Cardiovascular Medicine 94
Countries citing papers authored by Inge B. Mathijssen
This map shows the geographic impact of Inge B. Mathijssen'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 Inge B. Mathijssen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Inge B. Mathijssen more than expected).
Fields of papers citing papers by Inge B. Mathijssen
This network shows the impact of papers produced by Inge B. Mathijssen. 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 Inge B. Mathijssen. The network helps show where Inge B. Mathijssen may publish in the future.
Co-authors
The 25 scholars most cited alongside Inge B. Mathijssen, 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 37 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2008 | 149 | |
| 2 | 2013 | 107 | |
| 3 | 2016 | 96 | |
| 4 | 2015 | 81 | |
| 5 | 2018 | 51 | |
| 6 | 2008 | 46 | |
| 7 | 2004 | 45 | |
| 8 | 2011 | 42 | |
| 9 | 2018 | 42 | |
| 10 | 2010 | 39 | |
| 11 | 2016 | 39 | |
| 12 | 2014 | 39 | |
| 13 | 2014 | 37 | |
| 14 | 2021 | 37 | |
| 15 | 2011 | 36 | |
| 16 | 2016 | 29 | |
| 17 | 2015 | 27 | |
| 18 | 2011 | 26 | |
| 19 | 2021 | 24 | |
| 20 | 2018 | 23 |
About Inge B. Mathijssen
Inge B. Mathijssen is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Pulmonary and Respiratory Medicine, Molecular Biology and Rheumatology, having authored 37 papers that have together received 1.2k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (5 papers), RNA modifications and cancer (5 papers), Genetic Syndromes and Imprinting (4 papers), Cystic Fibrosis Research Advances (4 papers), Connective tissue disorders research (3 papers), Congenital Heart Disease Studies (3 papers) and Genomics and Rare Diseases (3 papers). The work is most often cited by research in Genetics (389 citations), Pediatrics, Perinatology and Child Health (179 citations), Molecular Biology (547 citations), Genetics (50 citations) and Cardiology and Cardiovascular Medicine (94 citations). Inge B. Mathijssen has collaborated with scholars based in Netherlands, Germany and United States. Frequent co-authors include Eva Pajkrt, Alex V. Postma, Phil Barnett, Aho Ilgun, Jan Lam, Lidewij Henneman, Vincent M. Christoffels, Arthur A.M. Wilde, Antoon F.M. Moorman and Phillis Lakeman. Their work appears in journals such as European Journal of Human Genetics, Prenatal Diagnosis, Genetics in Medicine, European Journal of Medical Genetics 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.