Stefanie Belet

785 total citations
10 papers, 252 citations indexed

About

Stefanie Belet is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Stefanie Belet has authored 10 papers receiving a total of 252 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Genetics and 2 papers in Cell Biology. Recurrent topics in Stefanie Belet's work include Genetics and Neurodevelopmental Disorders (8 papers), Genomic variations and chromosomal abnormalities (4 papers) and RNA modifications and cancer (2 papers). Stefanie Belet is often cited by papers focused on Genetics and Neurodevelopmental Disorders (8 papers), Genomic variations and chromosomal abnormalities (4 papers) and RNA modifications and cancer (2 papers). Stefanie Belet collaborates with scholars based in Belgium, United States and Brazil. Stefanie Belet's co-authors include Guy Froyen, Nathalie Fieremans, Jelle Verbeeck, Hilde Van Esch, Marijke Bauters, Jorge Duitama, Rita Gemayel, Kevin J. Verstrepen, An Jansen and Joris Vermeesch and has published in prestigious journals such as Nucleic Acids Research, PLoS ONE and PEDIATRICS.

In The Last Decade

Stefanie Belet

10 papers receiving 240 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stefanie Belet Belgium 9 153 148 31 24 22 10 252
Nathalie Fieremans Belgium 9 162 1.1× 154 1.0× 35 1.1× 10 0.4× 11 0.5× 10 264
Geena Skariah United States 10 107 0.7× 268 1.8× 22 0.7× 19 0.8× 29 1.3× 11 316
Shashidhar Pai United States 8 237 1.5× 278 1.9× 25 0.8× 35 1.5× 10 0.5× 13 391
Laurens Wiel Netherlands 5 134 0.9× 154 1.0× 20 0.6× 16 0.7× 21 1.0× 6 234
Salvatore Fioriniello Italy 8 107 0.7× 204 1.4× 22 0.7× 15 0.6× 10 0.5× 14 258
Seth M. Kelly United States 11 92 0.6× 425 2.9× 19 0.6× 18 0.8× 34 1.5× 14 475
Kiara N. Berríos United States 9 107 0.7× 252 1.7× 11 0.4× 15 0.6× 57 2.6× 11 337
Colin P. Florian United States 4 59 0.4× 249 1.7× 11 0.4× 18 0.8× 32 1.5× 6 298
Erick Loomis United States 7 191 1.2× 314 2.1× 16 0.5× 27 1.1× 72 3.3× 8 407
Л. П. Назаренко Russia 10 155 1.0× 141 1.0× 18 0.6× 55 2.3× 11 0.5× 45 244

Countries citing papers authored by Stefanie Belet

Since Specialization
Citations

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

Fields of papers citing papers by Stefanie Belet

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stefanie Belet

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

All Works

10 of 10 papers shown
1.
Santos-Rebouças, Cíntia Barros, Stefanie Belet, Márcia Gonçalves Ribeiro, et al.. (2015). Novel microduplications at Xp11.22 including HUWE1: clinical and molecular insights into these genomic rearrangements associated with intellectual disability. Journal of Human Genetics. 60(4). 207–211. 16 indexed citations
2.
Fieremans, Nathalie, Hilde Van Esch, Thomy de Ravel, et al.. (2015). Microdeletion of the escape genes KDM5C and IQSEC2 in a girl with severe intellectual disability and autistic features. European Journal of Medical Genetics. 58(5). 324–327. 25 indexed citations
3.
Fieremans, Nathalie, Marijke Bauters, Stefanie Belet, et al.. (2014). De novo MECP2 duplications in two females with intellectual disability and unfavorable complete skewed X-inactivation. Human Genetics. 133(11). 1359–1367. 33 indexed citations
4.
Duitama, Jorge, Rita Gemayel, An Jansen, et al.. (2014). Large-scale analysis of tandem repeat variability in the human genome. Nucleic Acids Research. 42(9). 5728–5741. 40 indexed citations
5.
Santos-Rebouças, Cíntia Barros, Stefanie Belet, Márcia Gonçalves Ribeiro, et al.. (2013). A novel in-frame deletion affecting the BAR domain of OPHN1 in a family with intellectual disability and hippocampal alterations. European Journal of Human Genetics. 22(5). 644–651. 22 indexed citations
6.
Vandewalle, Joke, Marijke Bauters, Hilde Van Esch, et al.. (2013). The mitochondrial solute carrier SLC25A5 at Xq24 is a novel candidate gene for non-syndromic intellectual disability. Human Genetics. 132(10). 1177–1185. 22 indexed citations
7.
Belet, Stefanie, Nathalie Fieremans, Xuan Yuan, et al.. (2013). Early Frameshift Mutation inPIGAIdentified in a Large XLID Family Without Neonatal Lethality. Human Mutation. 35(3). 350–355. 27 indexed citations
8.
Verbeeck, Jelle, Stefanie Belet, Anton Roebroek, et al.. (2013). Generation and Characterization of an Nxf7 Knockout Mouse to Study NXF5 Deficiency in a Patient with Intellectual Disability. PLoS ONE. 8(5). e64144–e64144. 6 indexed citations
9.
Giannandrea, Maila, Nathalie Fieremans, Jelle Verbeeck, et al.. (2013). Increased Dosage of RAB39B Affects Neuronal Development and Could Explain the Cognitive Impairment in Male Patients with Distal Xq28 Copy Number Gains. Human Mutation. 35(3). 377–383. 47 indexed citations
10.
Tejada, María‐Isabel, Cristina Martínez-Bouzas, Ainhoa García-Ribes, et al.. (2011). A Child With Mild X-Linked Intellectual Disability and a Microduplication at Xp22.12 Including RPS6KA3. PEDIATRICS. 128(4). e1029–e1033. 14 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 Nathalie Fieremans Breakdown of academic impact, for papers by Geena Skariah Breakdown of academic impact, for papers by Shashidhar Pai Breakdown of academic impact, for papers by Laurens Wiel Breakdown of academic impact, for papers by Salvatore Fioriniello Breakdown of academic impact, for papers by Seth M. Kelly Breakdown of academic impact, for papers by Kiara N. Berríos Breakdown of academic impact, for papers by Colin P. Florian Breakdown of academic impact, for papers by Erick Loomis Breakdown of academic impact, for papers by Л. П. Назаренко
Rankless by CCL
2026