Koen Devriendt

595 citations

13 papers · 290 indexed · h-index 9

Impact in

Developmental Biology top 10%
- Congenital limb and hand anomalies
Genetics
- Genomic variations and chromosomal abnormalities
- Dermatological and Skeletal Disorders

Papers in ⓘ

Developmental Biology 2
- Congenital limb and hand anomalies 2
Genetics 8
- Genomic variations and chromosomal abnormalities 4
- Genomics and Rare Diseases 3
- Genetics and Neurodevelopmental Disorders 2
- Genetic Syndromes and Imprinting 2

Co-authors: J. P. Fryns (4 shared papers)Joris Vermeesch (3 shared papers)Philippe Debeer (2 shared papers)Stephen R. Braddock (1 shared paper)Kiyoshi Imaizumi (1 shared paper)Leslie A. McNoe (1 shared paper)Michael R. Eccles (1 shared paper)Heather E. Cunliffe (1 shared paper)
Journals: Journal of Medical Genetics (2 papers)Gene (1 paper)Scientific Reports (1 paper)Genetics in Medicine (1 paper)Human Genetics (1 paper)
Partner nations: Belgium United States United Kingdom

In The Last Decade

Koen Devriendt

13 papers receiving 275 citations

Peers

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-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.

Border = papers with Koen Devriendt Line = papers co-authored together Koen Devriendt links everyone, so they are left out of the graph.

All Works

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13 of 13 papers shown

#	Work
1	Further delineation of renal-coloboma syndrome in patients with extreme variability of phenotype and identical PAX2 mutations. PubMed ·Lisa A. Schimmenti, Heather E. Cunliffe, Leslie A. McNoe, Teresa Ward, Michelle C. French, Heather H. Shim, Yao Hua Zhang, Willem Proesmans, Anita Leys, Kyna A. Byerly, Stephen R. Braddock, Mitsuno Masuno, Kiyoshi Imaizumi, Koen Devriendt, Michael R. Eccles	1997	98
2	2q31.1 microdeletion syndrome: redefining the associated clinical phenotype Journal of Medical Genetics ·Boyan Dimitrov, Irina Balikova, Thomy de Ravel, Hilde Van Esch, Maryse De Smedt, Emiel Baten, Joris Vermeesch, Irena Bradinova, E Simeonov, Koen Devriendt, J. P. Fryns, Philippe Debeer	2010	38
3	Exome sequencing identifies rare variants in multiple genes in atrioventricular septal defect Genetics in Medicine ·Lisa C.A. D’Alessandro, Saeed Al Turki, Ashok Kumar Manickaraj, Dorin Manase, Barbara J.M. Mulder, Lynn Bergin, Herschel Rosenberg, Tapas Mondal, Elaine Gordon, Jane Lougheed, John Smythe, Koen Devriendt, Shoumo Bhattacharya, Hugh Watkins, Jamie Bentham, Sarah Bowdin, Matthew E. Hurles, Seema Mital	2015	29
4	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 ·Boyan Dimitrov, Thierry Voet, Luc De Smet, Joris Vermeesch, Koen Devriendt, J. P. Fryns, Philippe Debeer	2010	27
5	Melorheostosis in a family with autosomal dominant osteopoikilosis: Report of a third family American Journal of Medical Genetics Part A ·Philippe Debeer, E. Pykels, Johan Lammens, Koen Devriendt, J. P. Fryns	2003	26
6	The mitochondrial solute carrier SLC25A5 at Xq24 is a novel candidate gene for non-syndromic intellectual disability Human Genetics ·Joke Vandewalle, Marijke Bauters, Hilde Van Esch, Stefanie Belet, Jelle Verbeeck, Nathalie Fieremans, Maureen Holvoet, Jodie M. Vento, Ana Spreiz, Dieter Kotzot, Edda Haberlandt, Jill A. Rosenfeld, Joris Andrieux, Bruno Delobel, Marie-Bertille Dehouck, Koen Devriendt, Jean‐Pierre Fryns, Peter Marynen, Amy Goldstein, Guy Froyen	2013	22
7	Methylation Defect in Imprinted Genes Detected in Patients with an Albright's Hereditary Osteodystrophy Like Phenotype and Platelet Gs Hypofunction PLoS ONE ·Benedetta Izzi, Inge François, Veerle Labarque, Chantal Thys, Christine Wittevrongel, Koen Devriendt, Eric Legius, Annick Van den Bruel, Marc D’Hooghe, Diether Lambrechts, Francis de Zegher, Chris Van Geet, Kathleen Freson	2012	19
8	A cluster of α2-macroglobulin-related genes (α2M) on human chromosome 12p: cloning of the pregnancy-zone protein gene and an α2M pseudogene Gene ·Koen Devriendt, Ji Zhang, F. Van Leuven, Herman Van den Berghe, J.J. Cassiman, Peter Marynen	1989	16
9	Molecular cytogenetic characterization of a constitutional complex intrachromosomal 4q rearrangement in a patient with multiple congenital anomalies Cytogenetic and Genome Research ·Bernard Thienpont, Marc Gewillig, J. P. Fryns, Koen Devriendt, Joris Vermeesch	2006	8
10	Scalp skin lesion in Turner syndrome: more than lymphoedema? Clinical Dysmorphology ·Anne Debeer, E. Steenkiste, Koen Devriendt, Marie‐Anne Morren	2005	4
11	Chromosomal analysis and short-term outcome of prenatally diagnosed congenital heart disease Scientific Reports ·Marcellino Verbeke, Laurens Hannes, Koen Devriendt, Kris Van Den Bogaert, Björn Cools, Luc De Catte, Marc Gewillig, Jeroen Breckpot	2025	1
12	Chromosome mapping using polymerase chain reaction on somatic cell hybrids Cancer Genetics and Cytogenetics ·Ji Zhang, Koen Devriendt, Peter Marynen, Herman Van Den Berghe, Jean‐Jacques Cassiman	1990	1
13	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 ·S. Claes, A. Vogels, M. Holvoet, Koen Devriendt, P. Raeymaekers, J.J. Cassiman, J.P. Fryns	1997	1

About Koen Devriendt

Koen Devriendt is a scholar working on Developmental Biology, Genetics, Molecular Biology, Cardiology and Cardiovascular Medicine and Rheumatology, having authored 13 papers that have together received 290 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Genomics and Rare Diseases (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Congenital limb and hand anomalies (2 papers), Congenital Heart Disease Studies (2 papers), Congenital heart defects research (2 papers), Genetic Syndromes and Imprinting (2 papers) and Pancreatic function and diabetes (1 paper). The work is most often cited by research in Developmental Biology (24 citations), Genetics (137 citations), Urology (22 citations), Pediatrics, Perinatology and Child Health (61 citations) and Molecular Biology (205 citations). Koen Devriendt has collaborated with scholars based in Belgium, United States and United Kingdom. Frequent co-authors include J. P. Fryns, Joris Vermeesch, Philippe Debeer, Stephen R. Braddock, Kiyoshi Imaizumi, Leslie A. McNoe, Michael R. Eccles, Heather E. Cunliffe, Michelle C. French and Anita Leys. Their work appears in journals such as Journal of Medical Genetics, Gene, Scientific Reports, Genetics in Medicine and Human 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.

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