Koen Devriendt

595 total citations
13 papers, 290 citations indexed

About

Koen Devriendt is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Koen Devriendt has authored 13 papers receiving a total of 290 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Molecular Biology and 2 papers in Surgery. Recurrent topics in Koen Devriendt's work include Genomic variations and chromosomal abnormalities (4 papers), Genomics and Rare Diseases (3 papers) and Genetic Syndromes and Imprinting (2 papers). Koen Devriendt is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Genomics and Rare Diseases (3 papers) and Genetic Syndromes and Imprinting (2 papers). Koen Devriendt collaborates with scholars based in Belgium, United States and Austria. Koen Devriendt's co-authors include J. P. Fryns, Philippe Debeer, Joris Vermeesch, Heather E. Cunliffe, Kiyoshi Imaizumi, Lisa A. Schimmenti, Leslie A. McNoe, Boyan Dimitrov, Teresa Ward and Stephen R. Braddock and has published in prestigious journals such as PLoS ONE, Scientific Reports and Gene.

In The Last Decade

Koen Devriendt

13 papers receiving 275 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Koen Devriendt Belgium 9 205 137 61 31 24 13 290
Herbert Reichenbach Germany 6 308 1.5× 145 1.1× 72 1.2× 38 1.2× 26 1.1× 9 411
Kiyoshi Kikkawa Japan 12 182 0.9× 211 1.5× 103 1.7× 32 1.0× 14 0.6× 27 378
Daniele De Brasi Italy 14 224 1.1× 256 1.9× 86 1.4× 38 1.2× 6 0.3× 44 478
Susan J. Kirkpatrick United States 10 154 0.8× 211 1.5× 120 2.0× 31 1.0× 7 0.3× 13 430
Lailá Bastaki Kuwait 11 142 0.7× 104 0.8× 83 1.4× 16 0.5× 15 0.6× 35 308
Mahmoud Taleb Al‐Ali United Arab Emirates 10 174 0.8× 150 1.1× 44 0.7× 15 0.5× 28 1.2× 34 312
Barbara Delle Chiaie Belgium 7 195 1.0× 251 1.8× 136 2.2× 14 0.5× 5 0.2× 10 423
Birsen Karaman Türkiye 12 180 0.9× 157 1.1× 57 0.9× 33 1.1× 6 0.3× 58 345
Margo Whiteford United Kingdom 11 194 0.9× 193 1.4× 43 0.7× 43 1.4× 4 0.2× 15 398
Winnie Courtens Belgium 16 256 1.2× 431 3.1× 158 2.6× 22 0.7× 39 1.6× 29 587

Countries citing papers authored by Koen Devriendt

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Koen Devriendt

This figure shows the co-authorship network connecting the top 25 collaborators of Koen Devriendt. A scholar is included among the top collaborators of Koen Devriendt based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Koen Devriendt. Koen Devriendt is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

13 of 13 papers shown
1.
Devriendt, Koen, Kris Van Den Bogaert, Björn Cools, et al.. (2025). Chromosomal analysis and short-term outcome of prenatally diagnosed congenital heart disease. Scientific Reports. 15(1). 3923–3923. 1 indexed citations
2.
D’Alessandro, Lisa C.A., Saeed Al Turki, Ashok Kumar Manickaraj, et al.. (2015). Exome sequencing identifies rare variants in multiple genes in atrioventricular septal defect. Genetics in Medicine. 18(2). 189–198. 29 indexed citations
3.
Vandewalle, Joke, Marijke Bauters, Hilde Van Esch, et al.. (2013). The mitochondrial solute carrier SLC25A5 at Xq24 is a novel candidate gene for non-syndromic intellectual disability. Human Genetics. 132(10). 1177–1185. 22 indexed citations
4.
Izzi, Benedetta, Inge François, Veerle Labarque, et al.. (2012). Methylation Defect in Imprinted Genes Detected in Patients with an Albright's Hereditary Osteodystrophy Like Phenotype and Platelet Gs Hypofunction. PLoS ONE. 7(6). e38579–e38579. 19 indexed citations
5.
Dimitrov, Boyan, Irina Balikova, Thomy de Ravel, et al.. (2010). 2q31.1 microdeletion syndrome: redefining the associated clinical phenotype. Journal of Medical Genetics. 48(2). 98–104. 38 indexed citations
6.
Dimitrov, Boyan, Thierry Voet, Luc De Smet, et al.. (2010). Genomic rearrangements of the GREM1-FMN1 locus cause oligosyndactyly, radio-ulnar synostosis, hearing loss, renal defects syndrome and Cenani–Lenz-like non-syndromic oligosyndactyly. Journal of Medical Genetics. 47(8). 569–574. 27 indexed citations
7.
Thienpont, Bernard, Marc Gewillig, J. P. Fryns, Koen Devriendt, & Joris Vermeesch. (2006). Molecular cytogenetic characterization of a constitutional complex intrachromosomal 4q rearrangement in a patient with multiple congenital anomalies. Cytogenetic and Genome Research. 114(3-4). 338–341. 8 indexed citations
8.
Debeer, Anne, et al.. (2005). Scalp skin lesion in Turner syndrome: more than lymphoedema?. Clinical Dysmorphology. 14(3). 149–150. 4 indexed citations
9.
Debeer, Philippe, et al.. (2003). Melorheostosis in a family with autosomal dominant osteopoikilosis: Report of a third family. American Journal of Medical Genetics Part A. 119A(2). 188–193. 26 indexed citations
10.
Devriendt, Koen, et al.. (1997). Regional localization of two genes for nonspecific X‐linked mental retardation to Xp22.3–p22.2 (MRX49) and Xp11.3–p11.21 (MRX50). American Journal of Medical Genetics. 73(4). 474–479. 1 indexed citations
11.
Schimmenti, Lisa A., Heather E. Cunliffe, Leslie A. McNoe, et al.. (1997). Further delineation of renal-coloboma syndrome in patients with extreme variability of phenotype and identical PAX2 mutations.. PubMed. 60(4). 869–78. 98 indexed citations
12.
Zhang, Ji, et al.. (1990). Chromosome mapping using polymerase chain reaction on somatic cell hybrids. Cancer Genetics and Cytogenetics. 45(2). 217–221. 1 indexed citations
13.

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.

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