Rob van Luijk
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
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- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
Papers in
- Genetics 9
- Genomic variations and chromosomal abnormalities 8
- Genetics and Neurodevelopmental Disorders 6
- Genomics and Rare Diseases 3
- Blood disorders and treatments 1
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- Phosphodiesterase function and regulation 1
- Co-authors
- J. Wauters (8 shared papers)Stefaan Scheers (7 shared papers)R. Frank Kooy (8 shared papers)Edwin Reyniers (7 shared papers)Liesbeth Rooms (7 shared papers)Berten Ceulemans (4 shared papers)Yolande van Bever (2 shared papers)Jenneke van den Ende (2 shared papers)
In The Last Decade
Rob van Luijk
9 papers receiving 346 citations
Peers
Comparison fields: 5 of 37
- Genetics 247
- Pediatrics, Perinatology and Child Health 81
- Psychiatry and Mental health 59
- Molecular Biology 124
- Cellular and Molecular Neuroscience 30
Countries citing papers authored by Rob van Luijk
This map shows the geographic impact of Rob van Luijk'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 Rob van Luijk with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rob van Luijk more than expected).
Fields of papers citing papers by Rob van Luijk
This network shows the impact of papers produced by Rob van Luijk. 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 Rob van Luijk. The network helps show where Rob van Luijk may publish in the future.
Co-authors
The 25 scholars most cited alongside Rob van Luijk, 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 | 2006 | 95 | |
| 2 | 2003 | 82 | |
| 3 | 2005 | 52 | |
| 4 | 2005 | 49 | |
| 5 | 2006 | 34 | |
| 6 | 2007 | 20 | |
| 7 | 2003 | 9 | |
| 8 | 2006 | 8 | |
| 9 | 2007 | 5 |
About Rob van Luijk
Rob van Luijk is a scholar working on Genetics, Molecular Biology, Plant Science, Pediatrics, Perinatology and Child Health and Psychiatry and Mental health, having authored 9 papers that have together received 354 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (6 papers), Genomics and Rare Diseases (3 papers), Chromosomal and Genetic Variations (3 papers), Epilepsy research and treatment (1 paper), Prenatal Screening and Diagnostics (1 paper), Phosphodiesterase function and regulation (1 paper) and Blood disorders and treatments (1 paper). The work is most often cited by research in Genetics (247 citations), Pediatrics, Perinatology and Child Health (81 citations), Psychiatry and Mental health (59 citations), Molecular Biology (124 citations) and Cellular and Molecular Neuroscience (30 citations). Rob van Luijk has collaborated with scholars based in Belgium, Croatia and India. Frequent co-authors include J. Wauters, Stefaan Scheers, R. Frank Kooy, Edwin Reyniers, Liesbeth Rooms, Berten Ceulemans, Yolande van Bever, Jenneke van den Ende, Annick Laridon and Winnie Courtens. Their work appears in journals such as Human Mutation, Cytogenetic and Genome Research, European Journal of Human Genetics, European Journal of Medical Genetics and Clinical Genetics.
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.