K Devriendt
Impact in
- Genetics top 10%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
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- Congenital heart defects research
Papers in
- Genetics 4
- Genomic variations and chromosomal abnormalities 3
- Genetics and Neurodevelopmental Disorders 2
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- Congenital heart defects research 1
- Co-authors
- Marc Gewillig (2 shared papers)Eric Legius (1 shared paper)J P Fryns (1 shared paper)Bénédicte Eyskens (1 shared paper)M Dumoulin (1 shared paper)Ann Swillen (1 shared paper)Teruhisa Miike (1 shared paper)Hiroyo Mabe (1 shared paper)
- Journals
- Clinical Genetics (1 paper)The Journal of Pediatrics (1 paper)Journal of Medical Genetics (1 paper)Genomics (1 paper)PubMed (2 papers)
- Partner nations
- BelgiumUnited StatesJapan
In The Last Decade
K Devriendt
6 papers receiving 460 citations
Peers
Comparison fields: 5 of 47
- Genetics 185
- Molecular Biology 384
- Pulmonary and Respiratory Medicine 181
- Epidemiology 151
- Developmental Neuroscience 17
Countries citing papers authored by K Devriendt
This map shows the geographic impact of K 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 K Devriendt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites K Devriendt more than expected).
Fields of papers citing papers by K Devriendt
This network shows the impact of papers produced by K 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 K Devriendt. The network helps show where K Devriendt may publish in the future.
Co-authors
The 20 scholars most cited alongside K 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 | 1997 | 283 | |
| 2 | 2000 | 122 | |
| 3 | 1998 | 31 | |
| 4 | 2002 | 16 | |
| 5 | Terminal deletion of chromosome 10q26: delineation of two clinical phenotypes. | 1998 | 13 |
| 6 | Unusual de novo t(13;15)(q12.1;p13) translocation leading to complex mosaicism including jumping translocation. | 1998 | 10 |
About K Devriendt
K Devriendt is a scholar working on Genetics, Molecular Biology, Pulmonary and Respiratory Medicine, Surgery and Pediatrics, Perinatology and Child Health, having authored 6 papers that have together received 475 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Congenital heart defects research (1 paper), Thyroid Disorders and Treatments (1 paper), Congenital Heart Disease Studies (1 paper), Neonatal Respiratory Health Research (1 paper), Chromosomal and Genetic Variations (1 paper) and Coronary Artery Anomalies (1 paper). The work is most often cited by research in Genetics (185 citations), Molecular Biology (384 citations), Pulmonary and Respiratory Medicine (181 citations), Epidemiology (151 citations) and Developmental Neuroscience (17 citations). K Devriendt has collaborated with scholars based in Belgium, United States and Japan. Frequent co-authors include Marc Gewillig, Eric Legius, J P Fryns, Bénédicte Eyskens, M Dumoulin, Ann Swillen, Teruhisa Miike, Hiroyo Mabe, Noritaka Iwatani and Wim J.M. Van de Ven. Their work appears in journals such as Clinical Genetics, The Journal of Pediatrics, Journal of Medical Genetics, Genomics and PubMed.
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.