Karlijn Pellikaan
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- Genetic Syndromes and Imprinting 16
- Genetics and Neurodevelopmental Disorders 9
- Genomic variations and chromosomal abnormalities 2
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- Prenatal Screening and Diagnostics 5
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- Adolescent and Pediatric Healthcare 2
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- Epigenetics and DNA Methylation 4
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- Child and Adolescent Health 2
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- Pancreatic function and diabetes 2
- Co-authors
- Laura C. G. de GraaffAnna G. W. RosenbergA. J. van der LelySjoerd A.A. van den BergAart Jan van der LelyDaniël BosRogier KersseboomTania Markovic
- Journals
- The Journal of Clinical Endocrinology & Metabolism (5 papers)Stroke (1 paper)Physics in Medicine and Biology (1 paper)
- Partner nations
- NetherlandsItalySweden
In The Last Decade
Karlijn Pellikaan
20 papers receiving 235 citations
Peers
Comparison fields: 5 of 46
- Genetics 156
- Pediatrics, Perinatology and Child Health 65
- Endocrine and Autonomic Systems 10
- Speech and Hearing 9
- Pulmonary and Respiratory Medicine 35
Countries citing papers authored by Karlijn Pellikaan
This map shows the geographic impact of Karlijn Pellikaan'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 Karlijn Pellikaan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Karlijn Pellikaan more than expected).
Fields of papers citing papers by Karlijn Pellikaan
This network shows the impact of papers produced by Karlijn Pellikaan. 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 Karlijn Pellikaan. The network helps show where Karlijn Pellikaan may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Karlijn Pellikaan, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2023 | 1 | |
| 2 | 2023 | 2 | |
| 3 | 2023 | 4 | |
| 4 | 2022 | 9 | |
| 5 | 2022 | 13 | |
| 6 | 2021 | 2 | |
| 7 | 2021 | 12 | |
| 8 | 2021 | 11 | |
| 9 | 2021 | 19 | |
| 10 | 2021 | 8 | |
| 11 | Supplementary data for: Growth hormone treatment for adults with Prader-Willi syndrome - a meta-analysis | 2021 | 1 |
| 12 | 2021 | 3 | |
| 13 | 2021 | 3 | |
| 14 | 2021 | 2 | |
| 15 | 2021 | 15 | |
| 16 | 2020 | 39 | |
| 17 | 2020 | 0 | |
| 18 | 2020 | 27 | |
| 19 | 2017 | 24 | |
| 20 | 2016 | 25 |
About Karlijn Pellikaan
Karlijn Pellikaan is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Speech and Hearing, having authored 21 papers that have together received 235 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (16 papers), Genetics and Neurodevelopmental Disorders (9 papers), Prenatal Screening and Diagnostics (5 papers), Epigenetics and DNA Methylation (4 papers), Child and Adolescent Health (2 papers), Adolescent and Pediatric Healthcare (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Pancreatic function and diabetes (2 papers). The work is most often cited by research in Genetics (156 citations), Pediatrics, Perinatology and Child Health (65 citations) and Endocrine and Autonomic Systems (10 citations). Karlijn Pellikaan has collaborated with scholars based in Netherlands, Italy and Sweden. Frequent co-authors include Laura C. G. de Graaff, Anna G. W. Rosenberg, A. J. van der Lely, Sjoerd A.A. van den Berg, Aart Jan van der Lely, Daniël Bos, Rogier Kersseboom, Tania Markovic, Muriel Coupaye and Charlotte Höybye. Their work appears in journals such as The Journal of Clinical Endocrinology & Metabolism, Stroke and Physics in Medicine and Biology.
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.