Diane Beysen

2.0k total citations
20 papers, 951 citations indexed

About

Diane Beysen is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Diane Beysen has authored 20 papers receiving a total of 951 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 6 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in Diane Beysen's work include Genomic variations and chromosomal abnormalities (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers) and Neurogenetic and Muscular Disorders Research (3 papers). Diane Beysen is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers) and Neurogenetic and Muscular Disorders Research (3 papers). Diane Beysen collaborates with scholars based in Belgium, United States and Netherlands. Diane Beysen's co-authors include Elfride De Baere, Ludwine Messiaen, Anne De Paepe, Ina Vandenbroucke, Geert Mortier, Nadine Van Roy, Tom Callens, Frank Speleman, Anne De Paepe and Reiner A. Veitia and has published in prestigious journals such as The American Journal of Human Genetics, Human Molecular Genetics and PLoS Genetics.

In The Last Decade

Diane Beysen

20 papers receiving 936 citations

Peers

Diane Beysen

GENET

NEURO

PRM

RHEUM

Paolo Simi Italy

Federica Natacci Italy

Boris G. Kousseff United States

Fady M. Mikhail United States

Constance K. Stein United States

Chin‐To Fong United States

Duane Superneau United States

James V. Higgins United States

H. Kruyer Spain

Anna Latos‐Bieleńska Poland

Paolo Simi Italy

Diane Beysen

633 ×1.6

571 ×1.6

GENET

79 ×0.2

NEURO

201 ×1.6

PRM

64 ×0.5

RHEUM

Citations per year, relative to Diane Beysen Diane Beysen (= 1×) peers Paolo Simi

Countries citing papers authored by Diane Beysen

Since Specialization

Citations

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

Fields of papers citing papers by Diane Beysen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Diane Beysen

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Rosenblum, Jessica, Diane Beysen, Anna Jansen, et al.. (2024). RNU4‐2 ‐Related Neurodevelopmental Disorder Is Associated With a Recognisable Facial Gestalt. Clinical Genetics. 107(1). 104–112. 3 indexed citations

Beysen, Diane, Berten Ceulemans, Filip Roelens, et al.. (2024). The Genetic Puzzle of Cerebral Palsy: Results of a Monocentric Study. Pediatric Neurology. 161. 1–8. 1 indexed citations

Meuwissen, Marije, et al.. (2023). Novel presentation of AADC deficiency as a mild phenotype with exercise-induced dystonic crises: A case report. Heliyon. 10(1). e23746–e23746. 2 indexed citations

Verlaet, Annelies, Annelies Breynaert, Tania Naessens, et al.. (2022). Clinical Investigation of French Maritime Pine Bark Extract on Attention-Deficit Hyperactivity Disorder as compared to Methylphenidate and Placebo: Part 1: Efficacy in a Randomised Trial. Journal of Functional Foods. 97. 105246–105246. 4 indexed citations

Schil, Kristof Van, et al.. (2022). A Severe Form of Familial Desminopathy Due to a Homozygous Nonsense DES Variant in Two Siblings. Neuropediatrics. 54(4). 279–286. 4 indexed citations

Beysen, Diane, et al.. (2021). Genetic Testing Contributes to Diagnosis in Cerebral Palsy: Aicardi-Goutières Syndrome as an Example. Frontiers in Neurology. 12. 617813–617813. 5 indexed citations

Stouffs, Katrien, Patrick Verloo, Luc Régal, et al.. (2020). Recurrent NEDD4L Variant in Periventricular Nodular Heterotopia, Polymicrogyria and Syndactyly. Frontiers in Genetics. 11. 26–26. 11 indexed citations

Beysen, Diane, et al.. (2019). Novel BRPF1 mutation in a boy with intellectual disability, coloboma, facial nerve palsy and hypoplasia of the corpus callosum. European Journal of Medical Genetics. 62(8). 103691–103691. 17 indexed citations

Bleyenheuft, Corinne, Philip Van Damme, Nathalie Goemans, et al.. (2018). Quantifying the changes in activity level of neuromuscular patients using the ACTIVLIM questionnaire: A 5-years study. Annals of Physical and Rehabilitation Medicine. 61. e541–e541. 1 indexed citations

10.

Banka, Siddharth, Damien Lederer, Valérie Benoît, et al.. (2014). Novel KDM6A (UTX) mutations and a clinical and molecular review of the X‐linked Kabuki syndrome (KS2). Clinical Genetics. 87(3). 252–258. 91 indexed citations

11.

Verdin, Hannah, Barbara D′haene, Diane Beysen, et al.. (2013). Microhomology-Mediated Mechanisms Underlie Non-Recurrent Disease-Causing Microdeletions of the FOXL2 Gene or Its Regulatory Domain. PLoS Genetics. 9(3). e1003358–e1003358. 56 indexed citations

12.

Beysen, Diane, Lara Moumné, Reiner A. Veitia, et al.. (2008). Missense mutations in the forkhead domain of FOXL2 lead to subcellular mislocalization, protein aggregation and impaired transactivation. Human Molecular Genetics. 17(13). 2030–2038. 66 indexed citations

13.

Beysen, Diane, Anne De Paepe, & Elfride De Baere. (2008). FOXL2mutations and genomic rearrangements in BPES. Human Mutation. 30(2). 158–169. 89 indexed citations

14.

Coppieters, Frauke, Bart P. Leroy, Diane Beysen, et al.. (2007). Recurrent Mutation in the First Zinc Finger of the Orphan Nuclear Receptor NR2E3 Causes Autosomal Dominant Retinitis Pigmentosa. The American Journal of Human Genetics. 81(1). 147–157. 96 indexed citations

15.

Jeyabalan, Nallathambi, Lara Moumné, Elfride De Baere, et al.. (2006). A novel polyalanine expansion in FOXL2: the first evidence for a recessive form of the blepharophimosis syndrome (BPES) associated with ovarian dysfunction. Human Genetics. 121(1). 107–112. 59 indexed citations

16.

Baere, Elfride De, Sandrine Caburet, Paul Laissue, et al.. (2005). Premature ovarian failure and forkhead transcription factor FOXL2: blepharophimosis-ptosis-epicanthus inversus syndrome and ovarian dysfunction.. PubMed. 2(4). 653–60. 21 indexed citations

17.

Beysen, Diane, Jean‐Pierre Fryns, Miranda Splitt, et al.. (2004). Genomic deletions account for more than 10% of the FOXL2 mutations in BPES families and can be revealed by MLPA analysis. European Journal of Human Genetics. 12. 248–248. 2 indexed citations

18.

Beysen, Diane, Jo Vandesompele, Ludwine Messiaen, Anne De Paepe, & Elfride De Baere. (2004). The humanFOXL2 mutation database. Human Mutation. 24(3). 189–193. 42 indexed citations

19.

Messiaen, Ludwine, Tom Callens, Geert Mortier, et al.. (2000). Exhaustive mutation analysis of theNF1 gene allows identification of 95% of mutations and reveals a high frequency of unusual splicing defects. Human Mutation. 15(6). 541–555. 350 indexed citations

20.

Messiaen, Ludwine, Tom Callens, Geert Mortier, et al.. (2000). Exhaustive mutation analysis of the NF1 gene allows identification of 95% of mutations and reveals a high frequency of unusual splicing defects. Human Mutation. 15(6). 541–541. 31 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