Eric Smeets
Impact in
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Cognitive Neuroscience top 5%
- Autism Spectrum Disorder Research
Papers in
- Genetics 53
- Genetics and Neurodevelopmental Disorders 34
- Genomic variations and chromosomal abnormalities 17
- Connective tissue disorders research 4
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- Epigenetics and DNA Methylation 4
- Co-authors
- Leopold Curfs (20 shared papers)J. P. Fryns (8 shared papers)Herman Van den Berghe (8 shared papers)Karine Pelc (2 shared papers)Bernard Dan (2 shared papers)J. Herbergs (3 shared papers)Ute Moog (4 shared papers)Connie Schrander‐Stumpel (3 shared papers)
- Journals
- Journal of Developmental and Physical Disabilities (4 papers)Clinical Genetics (4 papers)Journal of Medical Genetics (3 papers)Brain and Development (3 papers)European Journal of Paediatric Neurology (2 papers)
- Partner nations
- NetherlandsBelgiumUnited States
In The Last Decade
Eric Smeets
62 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 80
- Genetics 923
- Cognitive Neuroscience 380
- Clinical Psychology 179
- Occupational Therapy 29
- Developmental Biology 16
Countries citing papers authored by Eric Smeets
This map shows the geographic impact of Eric Smeets'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 Eric Smeets with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eric Smeets more than expected).
Fields of papers citing papers by Eric Smeets
This network shows the impact of papers produced by Eric Smeets. 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 Eric Smeets. The network helps show where Eric Smeets may publish in the future.
Co-authors
The 25 scholars most cited alongside Eric Smeets, 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 62 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2003 | 84 | |
| 2 | 2011 | 75 | |
| 3 | 2009 | 67 | |
| 4 | 2018 | 62 | |
| 5 | 2016 | 57 | |
| 6 | 2009 | 56 | |
| 7 | 1994 | 54 | |
| 8 | 2008 | 51 | |
| 9 | 2009 | 49 | |
| 10 | 2011 | 49 | |
| 11 | 2006 | 47 | |
| 12 | 2015 | 47 | |
| 13 | 2003 | 46 | |
| 14 | 1998 | 41 | |
| 15 | 2008 | 39 | |
| 16 | Strong variable clinical presentation in 3 patients with 7q terminal deletion. | 1998 | 33 |
| 17 | 2011 | 32 | |
| 18 | 2009 | 31 | |
| 19 | 2006 | 29 | |
| 20 | 2011 | 27 |
About Eric Smeets
Eric Smeets is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Clinical Psychology and Pediatrics, Perinatology and Child Health, having authored 62 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (34 papers), Genomic variations and chromosomal abnormalities (17 papers), Autism Spectrum Disorder Research (16 papers), Family and Disability Support Research (10 papers), Prenatal Screening and Diagnostics (7 papers), Chromosomal and Genetic Variations (6 papers), Connective tissue disorders research (4 papers) and Epigenetics and DNA Methylation (4 papers). The work is most often cited by research in Genetics (923 citations), Cognitive Neuroscience (380 citations), Clinical Psychology (179 citations), Occupational Therapy (29 citations) and Developmental Biology (16 citations). Eric Smeets has collaborated with scholars based in Netherlands, Belgium and United States. Frequent co-authors include Leopold Curfs, J. P. Fryns, Herman Van den Berghe, Karine Pelc, Bernard Dan, J. Herbergs, Ute Moog, Connie Schrander‐Stumpel, Friederike Ehrhart and Elisa Cirillo. Their work appears in journals such as Journal of Developmental and Physical Disabilities, Clinical Genetics, Journal of Medical Genetics, Brain and Development and European Journal of Paediatric Neurology.
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.