Koenraad Devriendt

31.2k citations
456 papers · 14.0k · h-index 59

Impact in

  • Genetics top 0.1%
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Genomics and Rare Diseases
    • Genetic Syndromes and Imprinting
  • Pediatrics, Perinatology and Child Health top 0.2%
    • Prenatal Screening and Diagnostics

Papers in

  • Genetics 242
    • Genomic variations and chromosomal abnormalities 111
    • Genetics and Neurodevelopmental Disorders 52
    • Genomics and Rare Diseases 35
    • Cleft Lip and Palate Research 26
  • Molecular Biology 206
    • Congenital heart defects research 89
Co-authors
Joris Vermeesch (106 shared papers)Hilde Van Esch (51 shared papers)Ann Swillen (43 shared papers)Jean‐Pierre Fryns (55 shared papers)Annick Vogels (21 shared papers)Marc Gewillig (45 shared papers)Gert Matthijs (34 shared papers)Eric Legius (35 shared papers)
Journals
European Journal of Medical Genetics (31 papers)European Journal of Human Genetics (29 papers)Prenatal Diagnosis (21 papers)Journal of Medical Genetics (18 papers)Clinical Genetics (16 papers)
Partner nations
BelgiumUnited StatesNetherlands

In The Last Decade

Koenraad Devriendt

439 papers receiving 13.2k citations

Peers

Koenraad Devriendt
Comparison fields: 5 of 173
  • Genetics 5.8k
  • Pediatrics, Perinatology and Child Health 1.8k
  • Molecular Biology 6.6k
  • Genetics 763
  • Developmental Biology 140
Replace John C. Carey with:
John C. Carey United States
David Chitayat Canada
Stanislas Lyonnet France
Joris A. Veltman Netherlands
Ben C.J. Hamel Netherlands
David Bick United States
Jeanne Amiel France
Alain Verloès France
Valérie Cormier‐Daire France
Leslie G. Biesecker United States
Koenraad Devriendt relative to John C. Carey United States John C. Carey's profile →
Citations per field
00.5×1.5×
John C. Carey · 1×
Citations per year

Countries citing papers authored by Koenraad Devriendt

Since Specialization
Citations

This map shows the geographic impact of Koenraad 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 Koenraad Devriendt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Koenraad Devriendt more than expected).

Fields of papers citing papers by Koenraad Devriendt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Koenraad 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 Koenraad Devriendt. The network helps show where Koenraad Devriendt may publish in the future.

Co-authors

The 25 scholars most cited alongside Koenraad 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 Koenraad Devriendt Line = papers co-authored together Koenraad Devriendt links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 456 papers — load more, or switch the sort, to bring in the rest.

#Work
1
GATA3 haplo-insufficiency causes human HDR syndrome
Nature ·Hilde Van Esch, Peter Groenen, M. Andrew Nesbit, Simone Schuffenhauer, Peter Lichtner, Gert Vanderlinden, Brian Harding, Rolf Beetz, Rudolf W. Bilous, I. M. Holdaway, Nicholas J Shaw, J P Fryns, Wim Van de Ven, Rajesh V. Thakker, Koenraad Devriendt
2000486
2
Practical Guidelines for Managing Patients with 22q11.2 Deletion Syndrome
The Journal of Pediatrics ·Anne S. Bassett, Donna M. McDonald‐McGinn, Koenraad Devriendt, Maria Cristina Digilio, Paula Goldenberg, Alex Habel, Bruno Marino, Sólveig Óskarsdóttir, Nicole Philip, Kathleen E. Sullivan, Ann Swillen, Jacob Vorstman
2011411
3
Constitutively activating mutation in WASP causes X-linked severe congenital neutropenia
Nature Genetics ·Koenraad Devriendt, Annette S. Kim, Gert Mathijs, Suzanna G.M. Frints, Marianne Schwartz, Joost J. van den Oord, Gregor Verhoef, Marc Boogaerts, J. P. Fryns, Daoqi You, Michael K. Rosen, Peter Vandenberghe
2001331
4
Congenital Hereditary Lymphedema Caused by a Mutation That Inactivates VEGFR3 Tyrosine Kinase
The American Journal of Human Genetics ·Alexandre Irrthum, Marika J. Karkkainen, Koenraad Devriendt, Kari Alitalo, Miikka Vikkula
2000325
5
Mutations in the Transcription Factor Gene SOX18 Underlie Recessive and Dominant Forms of Hypotrichosis-Lymphedema-Telangiectasia
The American Journal of Human Genetics ·Alexandre Irrthum, Koenraad Devriendt, David Chitayat, Gert Matthijs, Conrad P. Glade, Peter M. Steijlen, Jean‐Pierre Fryns, Maurice A. M. Van Steensel, Miikka Vikkula
2003324
6
Mutations in LRP2, which encodes the multiligand receptor megalin, cause Donnai-Barrow and facio-oculo-acoustico-renal syndromes
Nature Genetics ·Sibel Kantarci, Lihadh Al‐Gazali, R. Sean Hill, Dian Donnai, Graeme C. Black, Éric Bieth, Nicolas Chassaing, Didier Lacombe, Koenraad Devriendt, Ahmad S. Teebi, Marı́a Loscertales, Caroline D. Robson, Tianming Liu, David T. MacLaughlin, Kristin Noonan, Meaghan Russell, Christopher A. Walsh, Patricia K. Donahoe, Barbara R. Pober
2007249
7
Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant
Journal of Medical Genetics ·Femke Hannes, Andrew J. Sharp, Heather C. Mefford, Thomy de Ravel, Claudia Ruivenkamp, M.H. Breuning, JP Fryns, Koenraad Devriendt, Griet Van Buggenhout, Annick Vogels, Helen Stewart, Raoul C. M. Hennekam, Gregory M. Cooper, Regina Regan, Samantha J.L. Knight, Evan E. Eichler, Joris Vermeesch
2008230
8
Haploinsufficiency of TCF4 Causes Syndromal Mental Retardation with Intermittent Hyperventilation (Pitt-Hopkins Syndrome)
The American Journal of Human Genetics ·Christiane Zweier, Maarit Peippo, Juliane Hoyer, Sérgio B. Sousa, Armand Bottani, Jill Clayton‐Smith, William Reardon, Jorge Saraiva, Alexandra Cabral, Ina Göhring, Koenraad Devriendt, Thomy de Ravel, Emilia K. Bijlsma, Raoul C. M. Hennekam, Alfredo Orrico, Monika Cohen, Alexander Dreweke, André Reis, Peter Nürnberg, Anita Rauch
2007222
9
FOXL2 and BPES: Mutational Hotspots, Phenotypic Variability, and Revision of the Genotype-Phenotype Correlation
The American Journal of Human Genetics ·(unknown), Diane Beysen, Christine Oley, Birgit Lorenz, Julie Cocquet, Paul De Sutter, Koenraad Devriendt, Michael J. Dixon, Marc Fellous, Jean‐Pierre Fryns, Arturo Garza, Christoffer Jonsrud, Pasi A. Koivisto, Amanda Krause, Bart P. Leroy, Françoise Meire, Astrid S. Plomp, Lionel Van Maldergem, Anne De Paepe, Reiner A. Veitia, Ludwine Messiaen
2003199
10
Platelet characteristics in patients with X-linked macrothrombocytopenia because of a novel GATA1mutation
Blood ·Kathleen Freson, Koenraad Devriendt, Gert Matthijs, Achiel Van Hoof, Rita De Vos, Chantal Thys, Kristien Minner, Marc Hoylaerts, Jos Vermylen, Chris Van Geet
2001183
11
The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence.
PubMed ·Ann Swillen, Koenraad Devriendt, Eric Legius, Peter Prinzie, Annick Vogels, Pol Ghesquière, Jean‐Pierre Fryns
1999159
12
Chromosome 22q11 deletion syndrome: Update and review of the clinical features, cognitive-behavioral spectrum, and psychiatric complications
American Journal of Medical Genetics ·Ann Swillen, Annick Vogels, Koenraad Devriendt, J P Fryns
2000151
13
Minimum prevalence, birth incidence and cause of death for Prader–Willi syndrome in Flanders
European Journal of Human Genetics ·Annick Vogels, Jenneke van den Ende, Kathelijn Keymolen, Geert Mortier, Koenraad Devriendt, Eric Legius, J P Fryns
2003146
14
Neuropsychological, Learning and Psychosocial Profile of Primary School Aged Children with the Velo-Cardio-Facial Syndrome (22q11 Deletion): Evidence for a Nonverbal Learning Disability?
Child Neuropsychology ·Ann Swillen, Leen Vandeputte, Joris Cracco, Bea Maes, Pol Ghesquière, Koenraad Devriendt, Jean‐Pierre Fryns
1999144
15
Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage ofXLMRgenes
Human Mutation ·Guy Froyen, Hilde Van Esch, Marijke Bauters, Karen Hollanders, Suzanna G.M. Frints, Joris Vermeesch, Koenraad Devriendt, Jean‐Pierre Fryns, Peter Marynen
2007143
16
To tell or not to tell? A systematic review of ethical reflections on incidental findings arising in genetics contexts
European Journal of Human Genetics ·Gabrielle Christenhusz, Koenraad Devriendt, Kris Dierickx
2012139
17
Intellectual abilities in a large sample of children with Velo–Cardio–Facial Syndrome: an update
Journal of Intellectual Disability Research ·Bert De Smedt, Koenraad Devriendt, J. P. Fryns, Annick Vogels, Marc Gewillig, Ann Swillen
2007137
18
Prenatal and pre-implantation genetic diagnosis
Nature Reviews Genetics ·Joris Vermeesch, Thierry Voet, Koenraad Devriendt
2016132
19
Human laterality disorders
European Journal of Medical Genetics ·Hilde Peeters, Koenraad Devriendt
2006131
20
Guidelines for molecular karyotyping in constitutional genetic diagnosis
European Journal of Human Genetics ·Joris Vermeesch, Heike Fiegler, Nicole de Leeuw, Károly Szuhai, Jacqueline Schoumans, Roberto Ciccone, Frank Speleman, Anita Rauch, Jill Clayton‐Smith, Conny van Ravenswaaij, Damien Sanlaville, Philippos C. Patsalis, Helen V. Firth, Koenraad Devriendt, Orsetta Zuffardi
2007123

About Koenraad Devriendt

Koenraad Devriendt is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Pulmonary and Respiratory Medicine, having authored 456 papers that have together received 14.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (111 papers), Congenital heart defects research (89 papers), Prenatal Screening and Diagnostics (64 papers), Genetics and Neurodevelopmental Disorders (52 papers), Genomics and Rare Diseases (35 papers), Congenital Heart Disease Studies (34 papers), Chromosomal and Genetic Variations (29 papers) and Cleft Lip and Palate Research (26 papers). The work is most often cited by research in Genetics (5.8k citations), Pediatrics, Perinatology and Child Health (1.8k citations), Molecular Biology (6.6k citations), Genetics (763 citations) and Developmental Biology (140 citations). Koenraad Devriendt has collaborated with scholars based in Belgium, United States and Netherlands. Frequent co-authors include Joris Vermeesch, Hilde Van Esch, Ann Swillen, Jean‐Pierre Fryns, Annick Vogels, Marc Gewillig, Gert Matthijs, Eric Legius, Hilde Peeters and J P Fryns. Their work appears in journals such as European Journal of Medical Genetics, European Journal of Human Genetics, Prenatal Diagnosis, Journal of Medical Genetics and Clinical 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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