Erika Souche

2.6k total citations
31 papers, 765 citations indexed

About

Erika Souche is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Erika Souche has authored 31 papers receiving a total of 765 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 16 papers in Molecular Biology and 4 papers in Surgery. Recurrent topics in Erika Souche's work include Genomics and Rare Diseases (7 papers), Genomic variations and chromosomal abnormalities (5 papers) and Identification and Quantification in Food (4 papers). Erika Souche is often cited by papers focused on Genomics and Rare Diseases (7 papers), Genomic variations and chromosomal abnormalities (5 papers) and Identification and Quantification in Food (4 papers). Erika Souche collaborates with scholars based in Belgium, United States and France. Erika Souche's co-authors include Gert Matthijs, Anniek Corveleyn, Hans Scheffer, Marjan M. Weiss, Helger G. Yntema, Mariëlle Alders, Egbert Bakker, Sebastian Eck, Marc Sturm and Erik A. Sistermans and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Scientific Reports.

In The Last Decade

Erika Souche

28 papers receiving 754 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Erika Souche Belgium 13 349 299 109 79 68 31 765
James T. Lu United States 14 417 1.2× 407 1.4× 106 1.0× 40 0.5× 52 0.8× 26 843
Andrew Crenshaw United States 8 182 0.5× 236 0.8× 73 0.7× 43 0.5× 49 0.7× 12 664
Valerie C. L. Lin Singapore 21 431 1.2× 505 1.7× 135 1.2× 209 2.6× 46 0.7× 52 1.1k
Urko M. Marigorta Spain 16 506 1.4× 319 1.1× 61 0.6× 83 1.1× 43 0.6× 29 812
Yujuan Liu China 14 136 0.4× 421 1.4× 172 1.6× 91 1.2× 95 1.4× 43 819
Toshiro Mizuno Japan 20 192 0.6× 829 2.8× 80 0.7× 59 0.7× 46 0.7× 69 1.4k
Pedro Flores Mexico 9 122 0.3× 507 1.7× 114 1.0× 143 1.8× 50 0.7× 20 825
Ryszard Pawłowski Poland 20 416 1.2× 465 1.6× 165 1.5× 61 0.8× 37 0.5× 56 1.1k
John Ziniti United States 9 215 0.6× 347 1.2× 69 0.6× 106 1.3× 34 0.5× 15 721
Bruce Moran Ireland 16 138 0.4× 300 1.0× 137 1.3× 136 1.7× 29 0.4× 42 720

Countries citing papers authored by Erika Souche

Since Specialization
Citations

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

Fields of papers citing papers by Erika Souche

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Erika Souche

This figure shows the co-authorship network connecting the top 25 collaborators of Erika Souche. A scholar is included among the top collaborators of Erika Souche 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 Erika Souche. Erika Souche 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.
Souche, Erika, Jeroen Breckpot, Koenraad Devriendt, et al.. (2025). Clinical evaluation of long-read sequencing-based episignature detection in developmental disorders. Genome Medicine. 17(1). 1–1. 10 indexed citations
2.
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
3.
Kentache, Takfarinas, Erika Souche, Céline Schulz, et al.. (2024). Absence of the dolichol synthesis gene DHRSX leads to N-glycosylation defects in Lec5 and Lec9 Chinese hamster ovary cells. Journal of Biological Chemistry. 300(12). 107875–107875. 2 indexed citations
4.
Tüysüz, Beyhan, Philippe Debeer, Erika Souche, et al.. (2024). Gollop–Wolfgang Complex Is Associated with a Monoallelic Variation in WNT11. Genes. 15(1). 129–129. 1 indexed citations
5.
Souche, Erika, Prosper Lukusa-Tshilobo, Chris Van Geet, et al.. (2024). Genetic modulators of diversity in biological expression of sickle cell anemia in patients from democratic republic of Congo. Mediterranean Journal of Hematology and Infectious Diseases. 17(1). e2025001–e2025001.
6.
Blommaert, Eline, Romain Péanne, Н. А. Черепанова, et al.. (2019). Mutations in MAGT1 lead to a glycosylation disorder with a variable phenotype. Proceedings of the National Academy of Sciences. 116(20). 9865–9870. 61 indexed citations
7.
Weehaeghe, Donatienne Van, Michel Koole, Mark E. Schmidt, et al.. (2019). [11C]JNJ54173717, a novel P2X7 receptor radioligand as marker for neuroinflammation: human biodistribution, dosimetry, brain kinetic modelling and quantification of brain P2X7 receptors in patients with Parkinson’s disease and healthy volunteers. European Journal of Nuclear Medicine and Molecular Imaging. 46(10). 2051–2064. 58 indexed citations
8.
Soto, José Luís, Ignacio Blanco, Orland Dı́ez, et al.. (2018). Documento de consenso sobre la implementación de la secuenciación masiva de nueva generación en el diagnóstico genético de la predisposición hereditaria al cáncer. Medicina Clínica. 151(2). 80.e1–80.e10. 8 indexed citations
9.
Soto, José Luís, Ignacio Blanco, Orland Dı́ez, et al.. (2018). Consensus document on the implementation of next generation sequencing in the genetic diagnosis of hereditary cancer. Medicina Clínica (English Edition). 151(2). 80.e1–80.e10. 7 indexed citations
10.
Roelens, Filip, et al.. (2017). SPG20 mutation in three siblings with familial hereditary spastic paraplegia. Molecular Case Studies. 3(4). a001537–a001537. 11 indexed citations
11.
Robyns, Tomas, Cuno Kuipéri, Jeroen Breckpot, et al.. (2017). Repeat genetic testing with targeted capture sequencing in primary arrhythmia syndrome and cardiomyopathy. European Journal of Human Genetics. 25(12). 1313–1323. 9 indexed citations
12.
Louw, Jacoba, Jeroen Breckpot, Bert Callewaert, et al.. (2015). The diagnostic value of next generation sequencing in familial nonsyndromic congenital heart defects. American Journal of Medical Genetics Part A. 167(8). 1822–1829. 36 indexed citations
13.
Matthijs, Gert, Erika Souche, Mariëlle Alders, et al.. (2015). Guidelines for diagnostic next-generation sequencing. European Journal of Human Genetics. 24(1). 2–5. 337 indexed citations
14.
Matthijs, Gert, Mariëlle Alders, Peter Bauer, et al.. (2014). EuroGentest guidelines for diagnostic next generation sequencing. European Journal of Human Genetics. 22. 566–566. 3 indexed citations
15.
Mensah, Martin A., Matthew S. Hestand, Maarten Larmuseau, et al.. (2014). Pseudoautosomal Region 1 Length Polymorphism in the Human Population. PLoS Genetics. 10(11). e1004578–e1004578. 21 indexed citations
16.
Ardeshirdavani, Amin, Erika Souche, Luc De Raedt, et al.. (2014). NGS-Logistics: federated analysis of NGS sequence variants across multiple locations. Genome Medicine. 6(9). 71–71. 15 indexed citations
17.
Houdt, Jeroen Van, et al.. (2013). High-throughput sample identification and tracking for exome and custom targeted sequencing projects. European Journal of Human Genetics. 21. 165–165. 2 indexed citations
18.
Lechat, P, Erika Souche, & Ivan Moszer. (2013). SynTView — an interactive multi-view genome browser for next-generation comparative microorganism genomics. BMC Bioinformatics. 14(1). 277–277. 21 indexed citations
19.
Orsini, Luisa, Mieke Jansen, Erika Souche, Sarah Geldof, & Luc De Meester. (2011). Single nucleotide polymorphism discovery from expressed sequence tags in the waterflea Daphnia magna. BMC Genomics. 12(1). 309–309. 18 indexed citations
20.
Louro, Bruno, Erika Souche, Costas S. Tsigenopoulos, et al.. (2010). Gilthead sea bream (Sparus auratus) and European sea bass (Dicentrarchus labrax) expressed sequence tags: Characterization, tissue-specific expression and gene markers. Marine Genomics. 3(3-4). 179–191. 22 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 James T. Lu Breakdown of academic impact, for papers by Andrew Crenshaw Breakdown of academic impact, for papers by Valerie C. L. Lin Breakdown of academic impact, for papers by Urko M. Marigorta Breakdown of academic impact, for papers by Yujuan Liu Breakdown of academic impact, for papers by Toshiro Mizuno Breakdown of academic impact, for papers by Pedro Flores Breakdown of academic impact, for papers by Ryszard Pawłowski Breakdown of academic impact, for papers by John Ziniti Breakdown of academic impact, for papers by Bruce Moran
Rankless by CCL
2026