Bert Callewaert

11.4k total citations · 1 hit paper
89 papers, 3.3k citations indexed

About

Bert Callewaert is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Bert Callewaert has authored 89 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Genetics, 34 papers in Molecular Biology and 17 papers in Surgery. Recurrent topics in Bert Callewaert's work include Connective tissue disorders research (49 papers), Dermatological and Skeletal Disorders (14 papers) and Congenital heart defects research (12 papers). Bert Callewaert is often cited by papers focused on Connective tissue disorders research (49 papers), Dermatological and Skeletal Disorders (14 papers) and Congenital heart defects research (12 papers). Bert Callewaert collaborates with scholars based in Belgium, United States and Netherlands. Bert Callewaert's co-authors include Bart Loeys, Julie De Backer, Anne De Paepe, Harry C. Dietz, Paul Coucke, Anne M. De Paepe, Dianna M. Milewicz, Guillaume Jondeau, Laurence Faivre and Alan C. Braverman and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and PLoS ONE.

In The Last Decade

Bert Callewaert

84 papers receiving 3.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

The revised Ghent nosology for the Marfan syndrome: Table 1

2010 1.4k citations Bart Loeys, Harry C. Dietz et al. Journal of Medical Genetics profile →

Peers

Bert Callewaert

GENET

PRM

CCM

SURGE

Melanie Pepin United States

Lesley C. Adès Australia

Philippe Duquesnoy France

Alessandro Pecci Italy

Paul Grossfeld United States

Mohamad Azhar United States

Russell A. Norris United States

Sharon A. Pawlowski United States

Marja W. Wessels Netherlands

David W. Hollister United States

Melanie Pepin United States

Bert Callewaert

2.2k ×1.0

GENET

667 ×0.5

PRM

366 ×0.5

CCM

567 ×0.7

482 ×0.9

SURGE

Citations per year, relative to Bert Callewaert Bert Callewaert (= 1×) peers Melanie Pepin

Countries citing papers authored by Bert Callewaert

Since Specialization

Citations

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

Fields of papers citing papers by Bert Callewaert

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bert Callewaert

This figure shows the co-authorship network connecting the top 25 collaborators of Bert Callewaert. A scholar is included among the top collaborators of Bert Callewaert 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 Bert Callewaert. Bert Callewaert 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

Beyens, Aude, et al.. (2025). Ocular Manifestations in Congenital Cutis Laxa: A Case Series. Cornea. 44(9). 1107–1112. 1 indexed citations

Schiavinato, Alvise, Alexandra V. Zuk, Sara F. Tufa, et al.. (2024). New insights into the structural role of EMILINs within the human skin microenvironment. Scientific Reports. 14(1). 30345–30345.

He, Yukun, et al.. (2024). A systematic review and cross-database analysis of single nucleotide polymorphisms underlying hip morphology and osteoarthritis reveals shared mechanisms. Osteoarthritis and Cartilage. 32(8). 872–885. 1 indexed citations

Beyens, Aude, Kathleen Claes, Elfride De Baere, et al.. (2023). HRAS ‐related epidermal nevus syndromes: Expansion of the spectrum with first branchial arch defects. Clinical Genetics. 103(6). 709–713. 1 indexed citations

Beyens, Aude, et al.. (2023). ATP7A‐related copper transport disorders: A systematic review and definition of the clinical subtypes. Journal of Inherited Metabolic Disease. 46(2). 163–173. 12 indexed citations

Kobbe, Birgit, Bert Callewaert, Gerhard Sengle, et al.. (2022). LTBP1 promotes fibrillin incorporation into the extracellular matrix. Matrix Biology. 110. 60–75. 15 indexed citations

Hoorens, Anne, Tassos Grammatikopoulos, Maesha Deheragoda, et al.. (2021). Two cases of DCDC2 ‐related neonatal sclerosing cholangitis with developmental delay and literature review. Clinical Genetics. 100(4). 447–452. 4 indexed citations

McKenzie, F. Ellis, Kym Mina, Bert Callewaert, et al.. (2021). Severe congenital cutis laxa: Identification of novel homozygous LOX gene variants in two families. Clinical Genetics. 100(2). 168–175. 1 indexed citations

Vergult, Sarah, Annelies Dheedene, Björn Menten, et al.. (2021). A Reassessment of Copy Number Variations in Congenital Heart Defects: Picturing the Whole Genome. Genes. 12(7). 1048–1048. 7 indexed citations

10.

Hanisch, Franz‐Georg, Geert Goeminne, Andreja Rajković, et al.. (2021). Loss of zebrafish atp6v1e1b, encoding a subunit of vacuolar ATPase, recapitulates human ARCL type 2C syndrome and identifies multiple pathobiological signatures. PLoS Genetics. 17(6). e1009603–e1009603. 6 indexed citations

11.

Boel, Annekatrien, Aude Beyens, Marjolijn Renard, et al.. (2020). Slc2a10 knock-out mice deficient in ascorbic acid synthesis recapitulate aspects of arterial tortuosity syndrome and display mitochondrial respiration defects. Human Molecular Genetics. 29(9). 1476–1488. 4 indexed citations

12.

Boel, Annekatrien, Wouter Steyaert, Bert Callewaert, et al.. (2018). CRISPR/Cas9-mediated homology-directed repair by ssODNs in zebrafish induces complex mutational patterns resulting from genomic integration of repair-template fragments. Disease Models & Mechanisms. 11(10). 68 indexed citations

13.

Symoens, Sofie, Andy Willaert, Tamer Essawi, et al.. (2017). Genetic analysis of osteogenesis imperfecta in the Palestinian population: molecular screening of 49 affected families. Molecular Genetics & Genomic Medicine. 6(1). 15–26. 25 indexed citations

14.

Hardin, Joshua S., Yuri A. Zárate, Bert Callewaert, & David Warner. (2017). Corneal Findings in Arterial Tortuosity Syndrome. Investigative Ophthalmology & Visual Science. 58(8). 5661–5661. 1 indexed citations

15.

Legendre, Marie, Florence Dastot, Nathalie Collot, et al.. (2016). Contribution of GHR and IGFALS Mutations to Growth Hormone Resistance - Identification of New Variants and Impact on the Inheritance Pattern. 86. 1 indexed citations

16.

Campens, Laurence, Marjolijn Renard, Bert Callewaert, et al.. (2013). New insights into the molecular diagnosis and management of heritable thoracic aortic aneurysms and dissections. Polskie Archiwum Medycyny Wewnętrznej. 123(12). 693–700. 4 indexed citations

17.

Chiaie, Barbara Delle, Roos Leroy, Bert Callewaert, et al.. (2012). Adults with Down syndrome: health/care considerations for health professionals. Ghent University Academic Bibliography (Ghent University).

18.

Wojciechowski, Marek, Tine Boiy, Bert Callewaert, et al.. (2012). Health problems in children with Down syndrome. Ghent University Academic Bibliography (Ghent University).

19.

Willaert, Andy, Bert Callewaert, Paul Coucke, et al.. (2011). GLUT10 is required for the development of the cardiovascular system and the notochord and connects mitochondrial function to TGFβ signaling. Human Molecular Genetics. 21(6). 1248–1259. 45 indexed citations

20.

Loeys, Bart, Harry C. Dietz, Alan C. Braverman, et al.. (2010). The revised Ghent nosology for the Marfan syndrome: Table 1. Journal of Medical Genetics. 47(7). 476–485. 1350 indexed citations breakdown →

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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