Jasmin Beygo

2.8k total citations
32 papers, 690 citations indexed

About

Jasmin Beygo is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Jasmin Beygo has authored 32 papers receiving a total of 690 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 25 papers in Genetics and 16 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Jasmin Beygo's work include Genetic Syndromes and Imprinting (23 papers), Epigenetics and DNA Methylation (23 papers) and Prenatal Screening and Diagnostics (16 papers). Jasmin Beygo is often cited by papers focused on Genetic Syndromes and Imprinting (23 papers), Epigenetics and DNA Methylation (23 papers) and Prenatal Screening and Diagnostics (16 papers). Jasmin Beygo collaborates with scholars based in Germany, Netherlands and United Kingdom. Jasmin Beygo's co-authors include Karin Buiting, Bernhard Horsthemke, Thomas Eggermann, Deniz Kanber, Gabriele Gillessen‐Kaesbach, Reiner Siebert, Matthias Begemann, Sabine Hoffjan, Jörg T. Epplen and Dirk Prawitt and has published in prestigious journals such as PLoS ONE, Scientific Reports and Human Molecular Genetics.

In The Last Decade

Jasmin Beygo

31 papers receiving 685 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jasmin Beygo Germany 18 506 479 313 91 48 32 690
Derek Lim United Kingdom 13 546 1.1× 651 1.4× 293 0.9× 74 0.8× 63 1.3× 24 928
Deniz Kanber Germany 17 662 1.3× 712 1.5× 403 1.3× 51 0.6× 84 1.8× 33 999
Alina T. Midro Poland 16 575 1.1× 436 0.9× 244 0.8× 25 0.3× 77 1.6× 74 943
Jiangzhen Li United States 8 751 1.5× 418 0.9× 294 0.9× 40 0.4× 24 0.5× 8 946
Simona Cavani Italy 16 393 0.8× 313 0.7× 160 0.5× 21 0.2× 94 2.0× 31 692
Maxine J. Sutcliffe United States 13 375 0.7× 316 0.7× 130 0.4× 36 0.4× 136 2.8× 27 676
Cristina Molinatto Italy 10 296 0.6× 270 0.6× 196 0.6× 22 0.2× 28 0.6× 12 472
Samantha A. Schrier Vergano United States 18 331 0.7× 451 0.9× 85 0.3× 113 1.2× 40 0.8× 52 736
Carolina Sismani Cyprus 19 735 1.5× 515 1.1× 266 0.8× 14 0.2× 29 0.6× 75 984
Silvia Maitz Italy 17 319 0.6× 330 0.7× 123 0.4× 22 0.2× 32 0.7× 40 617

Countries citing papers authored by Jasmin Beygo

Since Specialization
Citations

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

Fields of papers citing papers by Jasmin Beygo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jasmin Beygo

This figure shows the co-authorship network connecting the top 25 collaborators of Jasmin Beygo. A scholar is included among the top collaborators of Jasmin Beygo 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 Jasmin Beygo. Jasmin Beygo 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.
Schaper, Jörg, Simon Thelen, Thomas Klenzner, et al.. (2023). FGF9-Associated Multiple Synostoses Syndrome Type 3 in a Multigenerational Family. Genes. 14(3). 724–724. 2 indexed citations
2.
Beygo, Jasmin, Silvia Russo, Pierpaola Tannorella, et al.. (2023). Prenatal testing for imprinting disorders: A laboratory perspective. Prenatal Diagnosis. 43(8). 973–982. 2 indexed citations
3.
Hummel, Elisabeth, Magdeldin Elgizouli, Maurizio Sicorello, et al.. (2022). No evidence for intervention-associated DNA methylation changes in monocytes of patients with posttraumatic stress disorder. Scientific Reports. 12(1). 17347–17347. 7 indexed citations
4.
Beygo, Jasmin, et al.. (2021). Beckwith–Wiedemann syndrome: Clinical, histopathological and molecular study of two Tunisian patients and review of literature. Molecular Genetics & Genomic Medicine. 9(10). e1796–e1796. 3 indexed citations
5.
Elgizouli, Magdeldin, Jasmin Beygo, Florian Erger, et al.. (2020). The adult phenotype of Schaaf-Yang syndrome. Orphanet Journal of Rare Diseases. 15(1). 294–294. 19 indexed citations
6.
Beygo, Jasmin, et al.. (2020). Common genetic variation in the Angelman syndrome imprinting centre affects the imprinting of chromosome 15. European Journal of Human Genetics. 28(6). 835–839. 10 indexed citations
7.
Beygo, Jasmin, Karin Buiting, Simon Ramsden, et al.. (2019). Update of the EMQN/ACGS best practice guidelines for molecular analysis of Prader-Willi and Angelman syndromes. European Journal of Human Genetics. 27(9). 1326–1340. 38 indexed citations
8.
Beygo, Jasmin, Joachim Bürger, Tim M. Strom, Sabine Kaya, & Karin Buiting. (2019). Disruption of KCNQ1 prevents methylation of the ICR2 and supports the hypothesis that its transcription is necessary for imprint establishment. European Journal of Human Genetics. 27(6). 903–908. 11 indexed citations
9.
Leitão, Elsa, Jasmin Beygo, Michael Zeschnigk, et al.. (2018). Locus-Specific DNA Methylation Analysis by Targeted Deep Bisulfite Sequencing. Methods in molecular biology. 1767. 351–366. 32 indexed citations
10.
Beygo, Jasmin, Benjamin Kamien, Jill Clayton‐Smith, et al.. (2017). Atypical Angelman syndrome due to a mosaic imprinting defect: Case reports and review of the literature. American Journal of Medical Genetics Part A. 173(3). 753–757. 18 indexed citations
11.
Beygo, Jasmin, Gabriele Gillessen‐Kaesbach, Beate Albrecht, et al.. (2017). New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome. European Journal of Human Genetics. 25(8). 935–945. 31 indexed citations
12.
Beygo, Jasmin, Ivana Joksić, Tim M. Strom, et al.. (2016). A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith–Wiedemann syndrome. European Journal of Human Genetics. 24(9). 1280–1286. 18 indexed citations
13.
Laurentino, Sandra, Jasmin Beygo, Verena Nordhoff, et al.. (2014). Epigenetic germline mosaicism in infertile men. Human Molecular Genetics. 24(5). 1295–1304. 49 indexed citations
14.
Beygo, Jasmin, Miriam Elbracht, Matthias Begemann, et al.. (2014). Novel deletions affecting the MEG3-DMR provide further evidence for a hierarchical regulation of imprinting in 14q32. European Journal of Human Genetics. 23(2). 180–188. 48 indexed citations
15.
Beygo, Jasmin, Ole Ammerpohl, Julia Richter, et al.. (2013). Deep Bisulfite Sequencing of Aberrantly Methylated Loci in a Patient with Multiple Methylation Defects. PLoS ONE. 8(10). e76953–e76953. 25 indexed citations
16.
Berland, Siren, Ove Bruland, Jasmin Beygo, et al.. (2013). Evidence for anticipation in Beckwith–Wiedemann syndrome. European Journal of Human Genetics. 21(12). 1344–1348. 22 indexed citations
17.
Beygo, Jasmin, Valentina Citro, Angela Sparago, et al.. (2012). The molecular function and clinical phenotype of partial deletions of the IGF2/H19 imprinting control region depends on the spatial arrangement of the remaining CTCF-binding sites. Human Molecular Genetics. 22(3). 544–557. 64 indexed citations
18.
Beygo, Jasmin, Karin Buiting, Saskia Seland, et al.. (2011). First Report of a Single Exon Deletion in TCOF1 Causing Treacher Collins Syndrome. Molecular Syndromology. 2(2). 53–59. 16 indexed citations
19.
Akkad, Denis A., Sabine Hoffjan, Elisabeth Petrasch‐Parwez, et al.. (2009). Variation in the IL7RA and IL2RA genes in German multiple sclerosis patients. Journal of Autoimmunity. 32(2). 110–115. 50 indexed citations
20.
Beygo, Jasmin, Qumar Parwez, Elisabeth Petrasch‐Parwez, Jörg T. Epplen, & Sabine Hoffjan. (2008). No evidence of an association between polymorphisms in the IRAK-M gene and atopic dermatitis in a German cohort. Molecular and Cellular Probes. 23(1). 16–19. 8 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.

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