Jolanda Schieving
Impact in
- Genetics top 10%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Glioma Diagnosis and Treatment
- Genetics and Neurodevelopmental Disorders
- BRCA gene mutations in cancer
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- Genetic factors in colorectal cancer
Papers in
-
- PI3K/AKT/mTOR signaling in cancer 4
- Genetics 8
- Genomics and Rare Diseases 7
- Genetics and Neurodevelopmental Disorders 3
- Genomic variations and chromosomal abnormalities 3
- Co-authors
- Michèl A.A.P. Willemsen (8 shared papers)Simone van der Burg (4 shared papers)Joris A. Veltman (5 shared papers)Lisenka E.L.M. Vissers (5 shared papers)Tjitske Kleefstra (4 shared papers)Lotte Krabbenborg (3 shared papers)Erik-Jan Kamsteeg (2 shared papers)Gert Jan van der Wilt (4 shared papers)
- Journals
- European Journal of Paediatric Neurology (5 papers)European Journal of Medical Genetics (2 papers)Value in Health (1 paper)International Journal of Radiation Oncology*Biology*Physics (1 paper)Genome Medicine (1 paper)
- Partner nations
- NetherlandsUnited KingdomPoland
In The Last Decade
Jolanda Schieving
26 papers receiving 718 citations
Peers
Comparison fields: 5 of 84
- Genetics 117
- Genetics 298
- Pathology and Forensic Medicine 85
- Clinical Biochemistry 29
- Neurology 64
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 | 168 | |
| 2 | 2013 | 78 | |
| 3 | 2014 | 75 | |
| 4 | 2016 | 73 | |
| 5 | 2013 | 54 | |
| 6 | 2013 | 51 | |
| 7 | 2014 | 36 | |
| 8 | 2013 | 33 | |
| 9 | 2016 | 30 | |
| 10 | 2022 | 25 | |
| 11 | 2015 | 24 | |
| 12 | 2015 | 17 | |
| 13 | 2021 | 12 | |
| 14 | 2016 | 11 | |
| 15 | 1999 | 9 | |
| 16 | 2011 | 6 | |
| 17 | 2023 | 5 | |
| 18 | 2017 | 4 | |
| 19 | 2011 | 3 | |
| 20 | 2019 | 2 |
About Jolanda Schieving
Jolanda Schieving is a scholar working on Molecular Biology, Genetics, Genetics, Pediatrics, Perinatology and Child Health and Surgery, having authored 29 papers that have together received 726 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (7 papers), PI3K/AKT/mTOR signaling in cancer (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Metabolism and Genetic Disorders (2 papers), Genetic factors in colorectal cancer (2 papers), Family and Disability Support Research (2 papers) and Epilepsy research and treatment (2 papers). The work is most often cited by research in Genetics (117 citations), Genetics (298 citations), Pathology and Forensic Medicine (85 citations), Clinical Biochemistry (29 citations) and Neurology (64 citations). Jolanda Schieving has collaborated with scholars based in Netherlands, United Kingdom and Poland. Frequent co-authors include Michèl A.A.P. Willemsen, Simone van der Burg, Joris A. Veltman, Lisenka E.L.M. Vissers, Tjitske Kleefstra, Lotte Krabbenborg, Erik-Jan Kamsteeg, Gert Jan van der Wilt, Janneke P.C. Grutters and Han G. Brunner. Their work appears in journals such as European Journal of Paediatric Neurology, European Journal of Medical Genetics, Value in Health, International Journal of Radiation Oncology*Biology*Physics and Genome Medicine.
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.