Sarah Vergult

2.5k total citations
28 papers, 541 citations indexed

About

Sarah Vergult is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Sarah Vergult has authored 28 papers receiving a total of 541 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 14 papers in Genetics and 3 papers in Genetics. Recurrent topics in Sarah Vergult's work include Genomic variations and chromosomal abnormalities (12 papers), RNA modifications and cancer (6 papers) and Genomics and Rare Diseases (4 papers). Sarah Vergult is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), RNA modifications and cancer (6 papers) and Genomics and Rare Diseases (4 papers). Sarah Vergult collaborates with scholars based in Belgium, Netherlands and United States. Sarah Vergult's co-authors include Björn Menten, Annelies Dheedene, Tim De Meyer, Tom Sante, Pieter‐Jan Volders, Rudy Van Coster, Sandra Janssens, Frank Speleman, Willy Lissens and Alfred Meurs and has published in prestigious journals such as Nature Communications, PLoS ONE and Scientific Reports.

In The Last Decade

Sarah Vergult

28 papers receiving 525 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sarah Vergult Belgium 14 334 218 91 63 53 28 541
Shehla Mohammed United Kingdom 12 497 1.5× 248 1.1× 92 1.0× 61 1.0× 54 1.0× 25 680
Julien Thévenon France 15 450 1.3× 474 2.2× 41 0.5× 30 0.5× 54 1.0× 51 798
Tracy Brandt United States 10 286 0.9× 399 1.8× 42 0.5× 27 0.4× 82 1.5× 14 581
Eva Rossier Germany 13 406 1.2× 392 1.8× 26 0.3× 39 0.6× 73 1.4× 21 644
Birgitte Bertelsen Denmark 13 244 0.7× 195 0.9× 73 0.8× 23 0.4× 29 0.5× 26 525
Antonio Vitobello France 13 446 1.3× 212 1.0× 71 0.8× 79 1.3× 22 0.4× 36 595
Karen M. Lower Australia 15 625 1.9× 400 1.8× 66 0.7× 91 1.4× 53 1.0× 34 927
Karin Writzl Slovenia 12 219 0.7× 238 1.1× 20 0.2× 24 0.4× 42 0.8× 33 466
Chantal Missirian France 16 404 1.2× 418 1.9× 24 0.3× 41 0.7× 100 1.9× 39 720

Countries citing papers authored by Sarah Vergult

Since Specialization
Citations

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

Fields of papers citing papers by Sarah Vergult

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sarah Vergult

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

All Works

20 of 20 papers shown
1.
2.
Martínez‐García, Pedro Manuel, Silvia Naranjo, Sarah Vergult, et al.. (2024). Comparative 3D genome analysis between neural retina and retinal pigment epithelium reveals differential cis-regulatory interactions at retinal disease loci. Genome biology. 25(1). 123–123. 1 indexed citations
3.
Wilderman, Andrea, Machteld Baetens, Ellen Roets, et al.. (2024). A distant global control region is essential for normal expression of anterior HOXA genes during mouse and human craniofacial development. Nature Communications. 15(1). 3 indexed citations
4.
Dahan, Idit, Sarah Vergult, Marta Vidal‐García, et al.. (2022). HDAC9structural variants disruptingTWIST1transcriptional regulation lead to craniofacial and limb malformations. Genome Research. 32(7). 1242–1253. 11 indexed citations
5.
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
6.
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
7.
Vergult, Sarah, et al.. (2020). Interpreting the impact of noncoding structural variation in neurodevelopmental disorders. Genetics in Medicine. 23(1). 34–46. 41 indexed citations
8.
Smet, Joél, Arnaud Vanlander, Sarah Vergult, et al.. (2018). Severe hepatopathy and neurological deterioration after start of valproate treatment in a 6-year-old child with mitochondrial tryptophanyl-tRNA synthetase deficiency. Orphanet Journal of Rare Diseases. 13(1). 80–80. 14 indexed citations
9.
Warrier, Sharat, Pieter‐Jan Volders, Margot Van der Jeught, et al.. (2017). CRISPR/Cas9-mediated genome editing in naïve human embryonic stem cells. Scientific Reports. 7(1). 16650–16650. 7 indexed citations
10.
Larson, Austin, Marisa W. Friederich, Michael A. Swanson, et al.. (2017). New insights into the phenotype of FARS2 deficiency. Molecular Genetics and Metabolism. 122(4). 172–181. 35 indexed citations
11.
Volders, Pieter‐Jan, et al.. (2016). Identification of long non-coding RNAs involved in neuronal development and intellectual disability. Scientific Reports. 6(1). 28396–28396. 42 indexed citations
12.
Vergult, Sarah, Annelies Dheedene, Alfred Meurs, et al.. (2014). Genomic aberrations of the CACNA2D1 gene in three patients with epilepsy and intellectual disability. European Journal of Human Genetics. 23(5). 628–632. 53 indexed citations
13.
Vanlander, Arnaud, Björn Menten, Joél Smet, et al.. (2014). Two Siblings with Homozygous Pathogenic Splice-Site Variant in Mitochondrial Asparaginyl-tRNA Synthetase (NARS2). Human Mutation. 36(2). 222–231. 43 indexed citations
14.
Vergult, Sarah, Ellen van Binsbergen, Tom Sante, et al.. (2013). Mate pair sequencing for the detection of chromosomal aberrations in patients with intellectual disability and congenital malformations. European Journal of Human Genetics. 22(5). 652–659. 25 indexed citations
15.
Stouffs, Katrien, et al.. (2012). Array comparative genomic hybridization in male infertility. Human Reproduction. 27(3). 921–929. 33 indexed citations
16.
Vergult, Sarah, A. Jeannette M. Hoogeboom, Emilia K. Bijlsma, et al.. (2012). Complex genetics of radial ray deficiencies: screening of a cohort of 54 patients. Genetics in Medicine. 15(3). 195–202. 22 indexed citations
17.
Vergult, Sarah, Andrew Dauber, Barbara Delle Chiaie, et al.. (2011). 17q24.2 microdeletions: a new syndromal entity with intellectual disability, truncal obesity, mood swings and hallucinations. European Journal of Human Genetics. 20(5). 534–539. 27 indexed citations
18.
Fieuw, Annelies, Candy Kumps, Alexander Schramm, et al.. (2011). Identification of a novel recurrent 1q42.2‐1qter deletion in high risk MYCN single copy 11q deleted neuroblastomas. International Journal of Cancer. 130(11). 2599–2606. 34 indexed citations
19.
Vergult, Sarah, Bart Loeys, Stanislas Lyonnet, et al.. (2011). Nasal speech and hypothyroidism are common hallmarks of 12q15 microdeletions. European Journal of Human Genetics. 19(10). 1032–1037. 8 indexed citations
20.
Buysse, Karen, Sarah Vergult, Chantal Ceuterick‐de Groote, et al.. (2010). Giant axonal neuropathy caused by compound heterozygosity for a maternally inherited microdeletion and a paternal mutation within the GAN gene. American Journal of Medical Genetics Part A. 152A(11). 2802–2804. 20 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Shehla Mohammed Breakdown of academic impact, for papers by Julien Thévenon Breakdown of academic impact, for papers by Tracy Brandt Breakdown of academic impact, for papers by Eva Rossier Breakdown of academic impact, for papers by Birgitte Bertelsen Breakdown of academic impact, for papers by Antonio Vitobello Breakdown of academic impact, for papers by Karen M. Lower Breakdown of academic impact, for papers by Karin Writzl Breakdown of academic impact, for papers by Chantal Missirian
Rankless by CCL
2026