Koen Devriendt
Impact in
- Developmental Biology top 10%
- Congenital limb and hand anomalies
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- Genomic variations and chromosomal abnormalities
- Dermatological and Skeletal Disorders
Papers in
- Genetics 6
- Genomics and Rare Diseases 2
- Genetics and Neurodevelopmental Disorders 2
- Genetic Syndromes and Imprinting 2
- Genomic variations and chromosomal abnormalities 2
- Dermatological and Skeletal Disorders 1
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- RNA modifications and cancer 1
- Co-authors
- J. P. Fryns (4 shared papers)Philippe Debeer (2 shared papers)Joris Vermeesch (3 shared papers)Anita Leys (1 shared paper)Michelle C. French (1 shared paper)Leslie A. McNoe (1 shared paper)Lisa A. Schimmenti (1 shared paper)Heather E. Cunliffe (1 shared paper)
- Journals
- Journal of Medical Genetics (2 papers)PLoS ONE (1 paper)Cytogenetic and Genome Research (1 paper)Gene (1 paper)Scientific Reports (1 paper)
- Partner nations
- BelgiumUnited StatesIndia
In The Last Decade
Koen Devriendt
13 papers receiving 297 citations
Peers
Comparison fields: 5 of 48
- Developmental Biology 24
- Genetics 137
- Urology 24
- Pediatrics, Perinatology and Child Health 59
- Molecular Biology 203
Countries citing papers authored by Koen Devriendt
This map shows the geographic impact of Koen Devriendt'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 Koen Devriendt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Koen Devriendt more than expected).
Fields of papers citing papers by Koen Devriendt
This network shows the impact of papers produced by Koen Devriendt. 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 Koen Devriendt. The network helps show where Koen Devriendt may publish in the future.
Co-authors
The 25 scholars most cited alongside Koen Devriendt, 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 | Further delineation of renal-coloboma syndrome in patients with extreme variability of phenotype and identical PAX2 mutations. | 1997 | 115 |
| 2 | 2010 | 42 | |
| 3 | 2015 | 32 | |
| 4 | 2003 | 30 | |
| 5 | 2010 | 27 | |
| 6 | 2013 | 23 | |
| 7 | 2012 | 19 | |
| 8 | 1989 | 16 | |
| 9 | 2006 | 8 | |
| 10 | 2005 | 5 | |
| 11 | 1990 | 2 | |
| 12 | 2025 | 1 | |
| 13 | 1997 | 1 |
About Koen Devriendt
Koen Devriendt is a scholar working on Genetics, Molecular Biology, Surgery, Pathology and Forensic Medicine and Cardiology and Cardiovascular Medicine, having authored 13 papers that have together received 321 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Genetic Syndromes and Imprinting (2 papers), Genomic variations and chromosomal abnormalities (2 papers), RNA modifications and cancer (1 paper), Pancreatic function and diabetes (1 paper), Dermatological and Skeletal Disorders (1 paper) and Chromosomal and Genetic Variations (1 paper). The work is most often cited by research in Developmental Biology (24 citations), Genetics (137 citations), Urology (24 citations), Pediatrics, Perinatology and Child Health (59 citations) and Molecular Biology (203 citations). Koen Devriendt has collaborated with scholars based in Belgium, United States and India. Frequent co-authors include J. P. Fryns, Philippe Debeer, Joris Vermeesch, Anita Leys, Michelle C. French, Leslie A. McNoe, Lisa A. Schimmenti, Heather E. Cunliffe, Stephen R. Braddock and Teresa Ward. Their work appears in journals such as Journal of Medical Genetics, PLoS ONE, Cytogenetic and Genome Research, Gene and Scientific Reports.
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.