Matias Wagner

4.6k total citations
83 papers, 792 citations indexed

About

Matias Wagner is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Matias Wagner has authored 83 papers receiving a total of 792 indexed citations (citations by other indexed papers that have themselves been cited), including 54 papers in Molecular Biology, 41 papers in Genetics and 13 papers in Clinical Biochemistry. Recurrent topics in Matias Wagner's work include Genomics and Rare Diseases (27 papers), Genetics and Neurodevelopmental Disorders (25 papers) and Metabolism and Genetic Disorders (13 papers). Matias Wagner is often cited by papers focused on Genomics and Rare Diseases (27 papers), Genetics and Neurodevelopmental Disorders (25 papers) and Metabolism and Genetic Disorders (13 papers). Matias Wagner collaborates with scholars based in Germany, Austria and United States. Matias Wagner's co-authors include Thomas Meitinger, Tim M. Strom, Saskia B. Wortmann, Holger Prokisch, Julia Hoefele, Martin Krenn, Thomas Klopstock, Elisabeth Graf, Fritz Zimprich and Korbinian M. Riedhammer and has published in prestigious journals such as Journal of Clinical Investigation, SHILAP Revista de lepidopterología and Scientific Reports.

In The Last Decade

Matias Wagner

74 papers receiving 780 citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Matias Wagner 447 225 133 96 73 83 792
Amal Alhashem 616 1.4× 447 2.0× 163 1.2× 90 0.9× 111 1.5× 76 1.1k
Almundher Al‐Maawali 312 0.7× 142 0.6× 57 0.4× 62 0.6× 60 0.8× 55 605
Caroline Sevin 551 1.2× 268 1.2× 121 0.9× 71 0.7× 180 2.5× 54 1.4k
Periyasamy Govindaraj 488 1.1× 206 0.9× 199 1.5× 41 0.4× 33 0.5× 59 831
Carolina Fischinger Moura de Souza 507 1.1× 183 0.8× 362 2.7× 70 0.7× 103 1.4× 110 1.2k
Gözde Yeşil 290 0.6× 205 0.9× 30 0.2× 30 0.3× 88 1.2× 78 679
Solaf M. Elsayed 548 1.2× 471 2.1× 44 0.3× 50 0.5× 109 1.5× 63 1.1k
Fuad Al Mutairi 342 0.8× 225 1.0× 195 1.5× 48 0.5× 70 1.0× 47 674
Tiina Tyni 796 1.8× 130 0.6× 645 4.8× 35 0.4× 158 2.2× 34 1.3k
Geetha Anand 303 0.7× 105 0.5× 77 0.6× 58 0.6× 36 0.5× 34 565

Countries citing papers authored by Matias Wagner

Since Specialization
Citations

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

Fields of papers citing papers by Matias Wagner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matias Wagner

This figure shows the co-authorship network connecting the top 25 collaborators of Matias Wagner. A scholar is included among the top collaborators of Matias Wagner 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 Matias Wagner. Matias Wagner 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.
Braunisch, Matthias C., Riccardo Berutti, Roman Günthner, et al.. (2025). Estimating Lifetime Risk of Autosomal Recessive Kidney Diseases Using Population-Based Genotypic Data. Kidney International Reports. 10(7). 2384–2393.
2.
Krey, Ilona, Irene Zarra‐Ferro, & Matias Wagner. (2025). Antisense oligonucleotide therapies for monogenic disorders. Medizinische Genetik. 37(3). 179–187. 1 indexed citations
3.
Krenn, Martin, Matias Wagner, Karin Trimmel, et al.. (2025). Holistic Exome-Based Genetic Testing in Adults With Epilepsy. Neurology Genetics. 11(3). e200260–e200260. 1 indexed citations
4.
Staufner, Christian, René G. Feichtinger, Johannes Häberle, et al.. (2025). Hepatic Form of Dihydrolipoamide Dehydrogenase Deficiency ( DLDD ): Phenotypic Spectrum, Laboratory Findings, and Therapeutic Approaches in 52 Patients. Journal of Inherited Metabolic Disease. 48(3). e70035–e70035.
5.
Krenn, Martin, Axel Schmidt, Matias Wagner, et al.. (2025). AlphaMissense prediction for the evaluation of missense variants in the diagnostic setting of neuromuscular disorders. Journal of Neuromuscular Diseases. 708678093–708678093.
6.
Klotz, Sigrid, Theresa König, Lukas Haider, et al.. (2024). Clinical heterogeneity within the ALS‐FTD spectrum in a family with a homozygous optineurin mutation. Annals of Clinical and Translational Neurology. 11(6). 1579–1589. 1 indexed citations
7.
Wagner, Matias, Theresa Brunet, Melanie Brügger, et al.. (2023). Exome sequencing (ES) of a pediatric cohort with chronic endocrine diseases: a single-center study (within the framework of the TRANSLATE-NAMSE project). Endocrine. 85(1). 444–453. 1 indexed citations
8.
Vogel, Florian, Martin Krenn, Dominik S. Westphal, et al.. (2022). A de novo missense variant in GABRA4 alters receptor function in an epileptic and neurodevelopmental phenotype. Epilepsia. 63(4). e35–e41. 8 indexed citations
9.
Popp, Bernt, Melanie Brügger, Tobias Bartolomaeus, et al.. (2022). The constitutional gain‐of‐function variant p. Glu1099Lys in NSD2 is associated with a novel syndrome. Clinical Genetics. 103(2). 226–230. 2 indexed citations
10.
Witzel, Simon, Matias Wagner, Chen Zhao, et al.. (2022). Fast versus slow disease progression in amyotrophic lateral sclerosis–clinical and genetic factors at the edges of the survival spectrum. Neurobiology of Aging. 119. 117–126. 6 indexed citations
11.
Marina, Adela Della, Marina Flotats‐Bastardas, Felix Distelmaier, et al.. (2022). Mitochondrial diseases mimicking autoimmune diseases of the CNS and good response to steroids initially. European Journal of Paediatric Neurology. 41. 27–35. 6 indexed citations
12.
Brunet, Theresa, Riccardo Berutti, Veronika Dill, et al.. (2022). Clonal hematopoiesis as a pitfall in germline variant interpretation in the context of Mendelian disorders. Human Molecular Genetics. 31(14). 2386–2395. 4 indexed citations
13.
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
14.
Kreienkamp, Hans‐Jürgen, Matias Wagner, Heike Weigand, et al.. (2021). Variant-specific effects define the phenotypic spectrum of HNRNPH2-associated neurodevelopmental disorders in males. Human Genetics. 141(2). 257–272. 13 indexed citations
15.
Kotzaeridou, Urania, Sara K. Young, Vanessa Suckow, et al.. (2020). Novel pathogenic EIF2S3 missense variants causing clinically variable MEHMO syndrome with impaired eIF2γ translational function, and literature review. Clinical Genetics. 98(5). 507–514. 10 indexed citations
16.
Lenz, Dominic, Mirjam Stahl, Elias Seidl, et al.. (2020). Rescue of respiratory failure in pulmonary alveolar proteinosis due to pathogenic MARS1 variants. Pediatric Pulmonology. 55(11). 3057–3066. 19 indexed citations
17.
Brügger, Melanie, Theresa Brunet, Tim M. Strom, et al.. (2020). A homozygous truncating variant in CCDC186 in an individual with epileptic encephalopathy. Annals of Clinical and Translational Neurology. 8(1). 278–283. 4 indexed citations
18.
Wagner, Matias, Sarah L. Stenton, Tim M. Strom, et al.. (2020). Lifetime risk of autosomal recessive mitochondrial disorders calculated from genetic databases. EBioMedicine. 54. 102730–102730. 39 indexed citations
19.
Brunet, Theresa, Milena Radivojkov‐Blagojevic, Peter Lichtner, et al.. (2020). Biallelic loss‐of‐function variants in RBL2 in siblings with a neurodevelopmental disorder. Annals of Clinical and Translational Neurology. 7(3). 390–396. 8 indexed citations
20.
Westphal, Dominik S., Gloria Leszinski, Esther Rieger‐Fackeldey, et al.. (2019). Lessons from exome sequencing in prenatally diagnosed heart defects: A basis for prenatal testing. Clinical Genetics. 95(5). 582–589. 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.

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