Jolanda Schieving
Impact in
- Genetics top 10%
- Genomics and Rare Diseases
- Glioma Diagnosis and Treatment
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- BRCA gene mutations in cancer
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- RNA modifications and cancer
- RNA regulation and disease
- RNA Research and Splicing
Papers in
- Genetics 8
- Genomics and Rare Diseases 6
- Genetics and Neurodevelopmental Disorders 3
- Glioma Diagnosis and Treatment 2
- Co-authors
- MAAP Willemsen (9 shared papers)Joris A. Veltman (5 shared papers)Simone van der Burg (4 shared papers)Tjitske Kleefstra (4 shared papers)Lisenka E.L.M. Vissers (5 shared papers)Lotte Krabbenborg (3 shared papers)Erik-Jan Kamsteeg (2 shared papers)Janneke P.C. Grutters (4 shared papers)
- Journals
- European Journal of Paediatric Neurology (4 papers)European Journal of Medical Genetics (2 papers)Pediatric Neurology (1 paper)Familial Cancer (1 paper)International Journal of Cancer (1 paper)
- Partner nations
- NetherlandsUnited KingdomBelgium
In The Last Decade
Jolanda Schieving
26 papers receiving 805 citations
Peers
Comparison fields: 5 of 80
- Genetics 126
- Genetics 291
- Molecular Biology 247
- Neurology 50
- Cellular and Molecular Neuroscience 62
Countries citing papers authored by Jolanda Schieving
This map shows the geographic impact of Jolanda Schieving'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 Jolanda Schieving with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jolanda Schieving more than expected).
Fields of papers citing papers by Jolanda Schieving
This network shows the impact of papers produced by Jolanda Schieving. 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 Jolanda Schieving. The network helps show where Jolanda Schieving may publish in the future.
Co-authors
The 25 scholars most cited alongside Jolanda Schieving, 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 29 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2017 | 176 | |
| 2 | 2013 | 91 | |
| 3 | 2016 | 78 | |
| 4 | 2014 | 75 | |
| 5 | 2013 | 63 | |
| 6 | 2013 | 61 | |
| 7 | 2014 | 39 | |
| 8 | 2022 | 35 | |
| 9 | 2013 | 34 | |
| 10 | 2016 | 30 | |
| 11 | 2015 | 25 | |
| 12 | 2019 | 21 | |
| 13 | 2015 | 18 | |
| 14 | 2021 | 15 | |
| 15 | 2016 | 11 | |
| 16 | 1999 | 10 | |
| 17 | 2023 | 7 | |
| 18 | 2011 | 6 | |
| 19 | 2017 | 5 | |
| 20 | 2011 | 3 |
About Jolanda Schieving
Jolanda Schieving is a scholar working on Genetics, Genetics, Pediatrics, Perinatology and Child Health, Rheumatology and Psychiatry and Mental health, having authored 29 papers that have together received 813 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (6 papers), PI3K/AKT/mTOR signaling in cancer (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Glioma Diagnosis and Treatment (2 papers), Family and Disability Support Research (2 papers), Mast cells and histamine (1 paper), Cutaneous Melanoma Detection and Management (1 paper) and Cancer Genomics and Diagnostics (1 paper). The work is most often cited by research in Genetics (126 citations), Genetics (291 citations), Molecular Biology (247 citations), Neurology (50 citations) and Cellular and Molecular Neuroscience (62 citations). Jolanda Schieving has collaborated with scholars based in Netherlands, United Kingdom and Belgium. Frequent co-authors include MAAP Willemsen, Joris A. Veltman, Simone van der Burg, Tjitske Kleefstra, Lisenka E.L.M. Vissers, Lotte Krabbenborg, Erik-Jan Kamsteeg, Janneke P.C. Grutters, Gert Jan van der Wilt and Helger G. Yntema. Their work appears in journals such as European Journal of Paediatric Neurology, European Journal of Medical Genetics, Pediatric Neurology, Familial Cancer and International Journal of Cancer.
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.