Koenraad Devriendt

30.9k total citations
444 papers, 12.6k citations indexed

About

Koenraad Devriendt is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Koenraad Devriendt has authored 444 papers receiving a total of 12.6k indexed citations (citations by other indexed papers that have themselves been cited), including 256 papers in Genetics, 222 papers in Molecular Biology and 87 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Koenraad Devriendt's work include Genomic variations and chromosomal abnormalities (123 papers), Congenital heart defects research (92 papers) and Prenatal Screening and Diagnostics (72 papers). Koenraad Devriendt is often cited by papers focused on Genomic variations and chromosomal abnormalities (123 papers), Congenital heart defects research (92 papers) and Prenatal Screening and Diagnostics (72 papers). Koenraad Devriendt collaborates with scholars based in Belgium, United States and Netherlands. Koenraad Devriendt's co-authors include Joris Vermeesch, Ann Swillen, Hilde Van Esch, Jean‐Pierre Fryns, Annick Vogels, Marc Gewillig, Gert Matthijs, Hilde Peeters, Eric Legius and J P Fryns and has published in prestigious journals such as Nature, Circulation and Journal of Clinical Investigation.

In The Last Decade

Koenraad Devriendt

433 papers receiving 12.2k citations

Peers

Koenraad Devriendt

GENET

PPCH

PRM

SURGE

John C. Carey United States

Joris A. Veltman Netherlands

Maximilian Muenke United States

Joris Vermeesch Belgium

Raoul C. M. Hennekam Netherlands

Valérie Cormier‐Daire France

Beverly S. Emanuel United States

Eric Legius Belgium

Stanislas Lyonnet France

Elaine Lyon United States

John C. Carey United States

Koenraad Devriendt

5.2k ×0.8

4.5k ×0.7

GENET

2.2k ×1.2

PPCH

1.2k ×0.8

PRM

2.0k ×1.4

SURGE

Citations per year, relative to Koenraad Devriendt Koenraad Devriendt (= 1×) peers John C. Carey

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-authorship network of co-authors of Koenraad Devriendt

This figure shows the co-authorship network connecting the top 25 collaborators of Koenraad Devriendt. A scholar is included among the top collaborators of Koenraad 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 Koenraad Devriendt. Koenraad Devriendt is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Matthews, Harold, Hanne Hoskens, Karlijne Indencleef, et al.. (2024). Toward 3D facial analysis for recognizing Mendelian causes of autism spectrum disorder. Clinical Genetics. 106(5). 603–613.

Hindryckx, An, et al.. (2024). Antenatal presentation and early postnatal treatment of infantile hypercalcemia type 2. Pediatric Nephrology. 39(10). 2911–2913. 1 indexed citations

Dierckxsens, Nicolas, Erika Souche, Tracy Heung, et al.. (2024). Multiple paralogs and recombination mechanisms contribute to the high incidence of 22q11.2 deletion syndrome. Genome Research. 35(4). 786–797. 1 indexed citations

Kayembe‐Kitenge, Tony, Aimé Lumaka, Oscar Numbi Luboya, et al.. (2023). Usefulness of automated image analysis for recognition of the fragile X syndrome gestalt in Congolese subjects. European Journal of Medical Genetics. 66(9). 104819–104819. 2 indexed citations

Lannoo, Lore, Nathalie Brison, Ilse Parijs, et al.. (2023). What helps define outcomes in persistent uninterpretable non‐invasive prenatal testing: Maternal factors, fetal fraction or quality scores?. Prenatal Diagnosis. 43(10). 1333–1343. 1 indexed citations

Che, Huiwen, Qian Yu, Lore Lannoo, et al.. (2023). Cell-free DNA methylome analysis for early preeclampsia prediction. Nature Medicine. 29(9). 2206–2215. 46 indexed citations

Che, Huiwen, Tatjana Jatsenko, Lore Lannoo, et al.. (2022). Machine learning-based detection of immune-mediated diseases from genome-wide cell-free DNA sequencing datasets. npj Genomic Medicine. 7(1). 55–55. 9 indexed citations

Kempers, Marlies, Koenraad Devriendt, Luc De Catte, et al.. (2021). Two novel presentations of KCNMA1‐related pathology––Expanding the clinical phenotype of a rare channelopathy. Molecular Genetics & Genomic Medicine. 9(10). 5 indexed citations

Kumps, Candy, Sarah Vergult, Rudy Van Coster, et al.. (2020). Phenotypic spectrum of the RBM10 ‐mediated intellectual disability and congenital malformation syndrome beyond classic TARP syndrome features. Clinical Genetics. 99(3). 449–456. 10 indexed citations

10.

Lévy, Jonathan, Yline Capri, Céline Dupont, et al.. (2020). LEF1 haploinsufficiency causes ectodermal dysplasia. Clinical Genetics. 97(4). 595–600. 12 indexed citations

11.

Louw, Jacoba, Ricardo Bastos, Anniek Corveleyn, et al.. (2018). Compound heterozygous loss-of-function mutations in KIF20A are associated with a novel lethal congenital cardiomyopathy in two siblings. PLoS Genetics. 14(1). e1007138–e1007138. 16 indexed citations

12.

Hens, Greet, et al.. (2015). Congenital sternoclavicular dermoid sinus. International Journal of Pediatric Otorhinolaryngology. 81. 65–67. 10 indexed citations

13.

Louw, Jacoba, et al.. (2015). MEIS2 involvement in cardiac development, cleft palate, and intellectual disability. American Journal of Medical Genetics Part A. 167(5). 1142–1146. 40 indexed citations

14.

Ghassibe‐Sabbagh, Michella, Nicole Revençu, Odile Boute, et al.. (2012). IRF6 Screening of Syndromic and a priori Non-Syndromic Cleft Lip and Palate Patients: Identification of a New Type of Minor VWS Sign. Data Archiving and Networked Services (DANS). 59. 1 indexed citations

15.

Claes, Erna, Lieve Denayer, Gerry Evers‐Kiebooms, et al.. (2005). Predictive Testing for Hereditary Nonpolyposis Colorectal Cancer: Subjective Perception Regarding Colorectal and Endometrial Cancer, Distress, and Health-related Behavior at One Year Post-Test. Genetic Testing. 9(1). 54–65. 52 indexed citations

16.

Devriendt, Koenraad, Eric Legius, Yves Sznajer, et al.. (2005). Syndromic clefting : broadening the clinical spectrum of an “old” syndrome, confirmation of a rare syndrome and description of a novel entity. 16(1). 211–212. 2 indexed citations

17.

Menten, Björn, Cindy Melotte, Bernard Thienpont, et al.. (2005). Molecular karkyotyping detecs structural low grade mosaics in 4 % of patietns with idiopathic mental retardation and multiple congenital aberrations. European Journal of Human Genetics. 13. 63. 2 indexed citations

18.

Lévy, Nicolas, Claire Navarro, Irène Boccaccio, et al.. (2003). Functional exploration of A type lamins and associated proteins in patients affected with Hutchinson-Gilford progeria syndrome caused by G608G mutation in LMNA. The American Journal of Human Genetics. 73(5). 554. 1 indexed citations

19.

Vogels, Annick, Gert Matthijs, Koenraad Devriendt, et al.. (2002). Psychosis in Prader Willi syndrome and chromosomal 15 maternal uniparental disomy. American Journal of Medical Genetics Part A. 114(7). 824–824. 1 indexed citations

20.

Lukusa, T., Koenraad Devriendt, & J. P. Fryns. (1999). A 3p deletion syndrome in a child with both del(3)(p25-->pter) and dup(17)(q23-->qter).. PubMed. 42(2). 91–4. 4 indexed citations

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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