Magdalena Danyel

562 total citations
12 papers, 87 citations indexed

About

Magdalena Danyel is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Magdalena Danyel has authored 12 papers receiving a total of 87 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 5 papers in Molecular Biology and 3 papers in Surgery. Recurrent topics in Magdalena Danyel's work include Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Magdalena Danyel is often cited by papers focused on Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Magdalena Danyel collaborates with scholars based in Germany, Austria and United States. Magdalena Danyel's co-authors include Denise Horn, Claus‐Eric Ott, Martin A. Mensah, Jean Tori Pantel, Kerstin Kutsche, Fanny Kortüm, Katarina Dathe, Ursula Kassner, Bastian Salewsky and Christian Fuchsberger and has published in prestigious journals such as Nucleic Acids Research, Scientific Reports and Journal of Medical Internet Research.

In The Last Decade

Magdalena Danyel

11 papers receiving 86 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Magdalena Danyel Germany 6 42 41 15 8 7 12 87
Burçak Otlu Türkiye 5 23 0.5× 59 1.4× 7 0.5× 26 3.3× 5 0.7× 11 110
Xiao Bao China 4 45 1.1× 57 1.4× 8 0.5× 7 0.9× 16 2.3× 10 103
Charlotte Pöe France 5 56 1.3× 41 1.0× 10 0.7× 10 1.3× 3 0.4× 6 86
Melissa M. Formosa Malta 7 36 0.9× 31 0.8× 12 0.8× 5 0.6× 15 2.1× 12 86
Ursula M. Schick United States 4 43 1.0× 36 0.9× 7 0.5× 19 2.4× 4 0.6× 6 102
Daniel Trejo Baños Austria 7 43 1.0× 57 1.4× 7 0.5× 15 1.9× 5 0.7× 7 118
Claire Searle United Kingdom 4 26 0.6× 28 0.7× 9 0.6× 4 0.5× 8 1.1× 8 66
Abdulrahman Swaid Saudi Arabia 5 66 1.6× 59 1.4× 8 0.5× 5 0.6× 4 0.6× 6 112
Fotios Karagiannis Germany 5 18 0.4× 53 1.3× 38 2.5× 11 1.4× 8 1.1× 6 174
Christina Loley Germany 5 89 2.1× 32 0.8× 12 0.8× 5 0.6× 5 0.7× 5 142

Countries citing papers authored by Magdalena Danyel

Since Specialization
Citations

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

Fields of papers citing papers by Magdalena Danyel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Magdalena Danyel

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

All Works

12 of 12 papers shown
1.
Pantel, Jean Tori, et al.. (2024). Validation of 3 Computer-Aided Facial Phenotyping Tools (DeepGestalt, GestaltMatcher, and D-Score): Comparative Diagnostic Accuracy Study. Journal of Medical Internet Research. 26. e42904–e42904. 6 indexed citations
2.
Nieminen, Mikko, R. Adam, Magdalena Danyel, et al.. (2024). REEV: review, evaluate and explain variants. Nucleic Acids Research. 52(W1). W148–W158. 1 indexed citations
3.
Funk, E. M., Christian Witzel, Nils Rouven Hansmeier, et al.. (2023). Three-Dimensional Histological Characterization of the Placental Vasculature Using Light Sheet Microscopy. Biomolecules. 13(6). 1009–1009. 4 indexed citations
4.
Danyel, Magdalena, Benno Kohlmaier, Christoph J. Mache, et al.. (2023). Biallelic known and novel DCDC2 variants in cholestatic liver disease: Phenotype–genotype observations in four children. Liver International. 43(5). 1089–1095. 3 indexed citations
5.
Danyel, Magdalena, Nina Erdmann, Felix Boschann, et al.. (2023). Case report: KPTN gene-related syndrome associated with a spectrum of neurodevelopmental anomalies including severe epilepsy. Frontiers in Neurology. 13. 1113811–1113811.
6.
Schmid, Alexander, Ashar Ahmad, Alexej Knaus, et al.. (2021). CADA: phenotype-driven gene prioritization based on a case-enriched knowledge graph. NAR Genomics and Bioinformatics. 3(3). lqab078–lqab078. 15 indexed citations
7.
Danyel, Magdalena, et al.. (2021). Genetik und Diagnostik des primären Lymphödems. Phlebologie. 50(2). 105–114. 1 indexed citations
8.
Pantel, Jean Tori, Magdalena Danyel, Stefan Mundlos, et al.. (2020). Efficiency of Computer-Aided Facial Phenotyping (DeepGestalt) in Individuals With and Without a Genetic Syndrome: Diagnostic Accuracy Study. Journal of Medical Internet Research. 22(10). e19263–e19263. 20 indexed citations
9.
Danyel, Magdalena, Zhuo Cheng, Christine Jung, et al.. (2019). Differentiation of MISSLA and Fanconi anaemia by computer-aided image analysis and presentation of two novel MISSLA siblings. European Journal of Human Genetics. 27(12). 1827–1835. 6 indexed citations
10.
11.
Danyel, Magdalena, Claus‐Eric Ott, Bastian Salewsky, et al.. (2019). Evaluation of the role of STAP1 in Familial Hypercholesterolemia. Scientific Reports. 9(1). 11995–11995. 15 indexed citations
12.
Danyel, Magdalena, Fanny Kortüm, Katarina Dathe, Kerstin Kutsche, & Denise Horn. (2018). Autosomal dominant Robinow syndrome associated with a novel DVL3 splice mutation. American Journal of Medical Genetics Part A. 176(4). 992–996. 13 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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