J.A.S. Vorstman
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic Associations and Epidemiology
- Cognitive Neuroscience top 10%
- Autism Spectrum Disorder Research
Papers in
- Genetics 4
- Genomic variations and chromosomal abnormalities 4
- Genetics and Neurodevelopmental Disorders 1
- Genomics and Rare Diseases 1
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- Congenital heart defects research 3
- Co-authors
- Wouter Staal (2 shared papers)Emma van Daalen (2 shared papers)Hermán van Engeland (2 shared papers)Ron Hochstenbach (1 shared paper)Jacobine E. Buizer‐Voskamp (1 shared paper)Roel A. Ophoff (1 shared paper)Lude Franke (1 shared paper)Carrie E. Bearden (1 shared paper)
- Partner nations
- NetherlandsUnited StatesGermany
In The Last Decade
J.A.S. Vorstman
4 papers receiving 292 citations
Peers
Comparison fields: 5 of 45
- Genetics 187
- Cognitive Neuroscience 113
- Developmental Neuroscience 7
- Molecular Biology 116
- Psychiatry and Mental health 14
Countries citing papers authored by J.A.S. Vorstman
This map shows the geographic impact of J.A.S. Vorstman'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 J.A.S. Vorstman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites J.A.S. Vorstman more than expected).
Fields of papers citing papers by J.A.S. Vorstman
This network shows the impact of papers produced by J.A.S. Vorstman. 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 J.A.S. Vorstman. The network helps show where J.A.S. Vorstman may publish in the future.
Co-authors
The 25 scholars most cited alongside J.A.S. Vorstman, 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 | 2005 | 112 | |
| 2 | 2011 | 80 | |
| 3 | 2017 | 57 | |
| 4 | 2010 | 51 |
About J.A.S. Vorstman
J.A.S. Vorstman is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Plant Science and Infectious Diseases, having authored 4 papers that have together received 300 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Congenital heart defects research (3 papers), Autism Spectrum Disorder Research (2 papers), Genetics and Neurodevelopmental Disorders (1 paper), Genomics and Rare Diseases (1 paper) and Chromosomal and Genetic Variations (1 paper). The work is most often cited by research in Genetics (187 citations), Cognitive Neuroscience (113 citations), Developmental Neuroscience (7 citations), Molecular Biology (116 citations) and Psychiatry and Mental health (14 citations). J.A.S. Vorstman has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include Wouter Staal, Emma van Daalen, Hermán van Engeland, Ron Hochstenbach, Jacobine E. Buizer‐Voskamp, Roel A. Ophoff, Lude Franke, Carrie E. Bearden, Thomas Lehner and Bernice E. Morrow. Their work appears in journals such as Molecular Psychiatry and Cytogenetic and Genome Research.
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.