Edwin Reyniers
Impact in
- Genetics top 0.5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Cognitive Neuroscience top 2%
- Autism Spectrum Disorder Research
Papers in
- Genetics 48
- Genetics and Neurodevelopmental Disorders 41
- Genomic variations and chromosomal abnormalities 22
- Genomics and Rare Diseases 7
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- Congenital heart defects research 11
- Epigenetics and DNA Methylation 5
- RNA modifications and cancer 5
- Ubiquitin and proteasome pathways 4
- Co-authors
- R. Frank Kooy (42 shared papers)Ben A. Oostra (13 shared papers)Kristel De Boulle (15 shared papers)Patrick J. Willems (20 shared papers)Lieve Vits (9 shared papers)Annemieke J.M.H. Verkerk (5 shared papers)Esther de Graaff (4 shared papers)Bernadette Van Roy (3 shared papers)
- Journals
- European Journal of Medical Genetics (4 papers)Human Genetics (4 papers)Human Molecular Genetics (4 papers)Human Mutation (4 papers)Nature Genetics (4 papers)
- Partner nations
- BelgiumNetherlandsUnited States
In The Last Decade
Edwin Reyniers
67 papers receiving 3.5k citations
Peers
Comparison fields: 5 of 101
- Genetics 2.6k
- Cognitive Neuroscience 1.1k
- Developmental Neuroscience 144
- Molecular Biology 2.1k
- Cellular and Molecular Neuroscience 412
Countries citing papers authored by Edwin Reyniers
This map shows the geographic impact of Edwin Reyniers'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 Edwin Reyniers with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Edwin Reyniers more than expected).
Fields of papers citing papers by Edwin Reyniers
This network shows the impact of papers produced by Edwin Reyniers. 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 Edwin Reyniers. The network helps show where Edwin Reyniers may publish in the future.
Co-authors
The 25 scholars most cited alongside Edwin Reyniers, 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 67 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1993 | 484 | |
| 2 | 2006 | 307 | |
| 3 | 1993 | 222 | |
| 4 | 1997 | 163 | |
| 5 | FMR1 Knockout mice: A model to study fragile X mental retardation | 1994 | 156 |
| 6 | 1996 | 141 | |
| 7 | 1996 | 139 | |
| 8 | 1994 | 135 | |
| 9 | 2005 | 131 | |
| 10 | 2000 | 116 | |
| 11 | 1993 | 114 | |
| 12 | 1994 | 110 | |
| 13 | Fmrl Knockout Mice: A Model to Study Fragile X Mental Retardation The Dutch-Belgian Fragile X Consortium* | 1994 | 96 |
| 14 | 1993 | 87 | |
| 15 | 2003 | 79 | |
| 16 | 2011 | 55 | |
| 17 | 1999 | 54 | |
| 18 | Refinement of the multiple exostoses locus (EXT2) to a 3-cM interval on chromosome 11. | 1995 | 54 |
| 19 | 1999 | 52 | |
| 20 | 2005 | 51 |
About Edwin Reyniers
Edwin Reyniers is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Cellular and Molecular Neuroscience and Rheumatology, having authored 67 papers that have together received 3.6k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (41 papers), Genomic variations and chromosomal abnormalities (22 papers), Autism Spectrum Disorder Research (18 papers), Congenital heart defects research (11 papers), Genomics and Rare Diseases (7 papers), Epigenetics and DNA Methylation (5 papers), RNA modifications and cancer (5 papers) and Ubiquitin and proteasome pathways (4 papers). The work is most often cited by research in Genetics (2.6k citations), Cognitive Neuroscience (1.1k citations), Developmental Neuroscience (144 citations), Molecular Biology (2.1k citations) and Cellular and Molecular Neuroscience (412 citations). Edwin Reyniers has collaborated with scholars based in Belgium, Netherlands and United States. Frequent co-authors include R. Frank Kooy, Ben A. Oostra, Kristel De Boulle, Patrick J. Willems, Lieve Vits, Annemieke J.M.H. Verkerk, Esther de Graaff, Bernadette Van Roy, C.E. Bakker and Liesbeth Rooms. Their work appears in journals such as European Journal of Medical Genetics, Human Genetics, Human Molecular Genetics, Human Mutation and Nature 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.