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, Holger Prokisch, Saskia B. Wortmann, 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

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Estimating Lifetime Risk of Autosomal Recessive Kidney Diseases Using Population-Based Genotypic Data 2025 ·Kidney International Reports ·Matthias C. Braunisch, (unknown), (unknown), (unknown), Riccardo Berutti, (unknown), Roman Günthner, Lutz Renders, Christoph Schmaderer, Uwe Heemann, Korbinian M. Riedhammer, Matias Wagner, Julia Hoefele	0
2	Antisense oligonucleotide therapies for monogenic disorders 2025 ·Medizinische Genetik ·Ilona Krey, Irene Zarra‐Ferro, Matias Wagner	1
3	AlphaMissense prediction for the evaluation of missense variants in the diagnostic setting of neuromuscular disorders 2025 ·Journal of Neuromuscular Diseases ·Martin Krenn, Axel Schmidt, Matias Wagner, Margot Ernst, Elisabeth Graf, Gudrun Zulehner, Hakan Çetin, Fritz Zimprich, Jakob Rath	0
4	Holistic Exome-Based Genetic Testing in Adults With Epilepsy 2025 ·Neurology Genetics ·Martin Krenn, Matias Wagner, Karin Trimmel, Silvia Bonelli, Jakob Rath, (unknown), (unknown), Ivan Milenković, (unknown), Johannes Koren, Christoph Baumgartner, Melanie Brügger, Theresa Brunet, Elisabeth Graf, Juliane Winkelmann, Susanne Aull‐Watschinger, Fritz Zimprich, Ekaterina Pataraia	1
5	Hepatic Form of Dihydrolipoamide Dehydrogenase Deficiency ( DLDD ): Phenotypic Spectrum, Laboratory Findings, and Therapeutic Approaches in 52 Patients 2025 ·Journal of Inherited Metabolic Disease ·(unknown), Christian Staufner, (unknown), (unknown), René G. Feichtinger, Johannes Häberle, Norman Junge, Vassiliki Konstantopoulou, Robert Kopajtich, Valérie A. McLin, Daisy Rymen, Christoph Slavetinsky, Ekkehard Sturm, Johannes A. Mayr, Matias Wagner, (unknown), Holger Prokisch, Georg F. Hoffmann, Dominic Lenz	0
6	Clinical heterogeneity within the ALS‐FTD spectrum in a family with a homozygous optineurin mutation 2024 ·Annals of Clinical and Translational Neurology ·(unknown), Sigrid Klotz, (unknown), (unknown), (unknown), Theresa König, Lukas Haider, Tatjana Traub‐Weidinger, Matias Wagner, Theresa Brunet, Melanie Brügger, Alexander Zimprich, Jakob Rath, Elisabeth Stögmann, Ellen Gelpí, Hakan Çetin	1
7	Exome sequencing (ES) of a pediatric cohort with chronic endocrine diseases: a single-center study (within the framework of the TRANSLATE-NAMSE project) 2023 ·Endocrine ·(unknown), Matias Wagner, Theresa Brunet, (unknown), Melanie Brügger, Eva Maria Christina Schwaibold, Tobias B. Haack, Georg F. Hoffmann, Markus Bettendorf, Daniela Choukair	1
8	Fast versus slow disease progression in amyotrophic lateral sclerosis–clinical and genetic factors at the edges of the survival spectrum 2022 ·Neurobiology of Aging ·Simon Witzel, Matias Wagner, Chen Zhao, (unknown), Elisabeth Graf, Riccardo Berutti, Konrad Oexle, Dávid Brenner, Juliane Winkelmann, Albert C. Ludolph	6
9	The constitutional gain‐of‐function variant p. Glu1099Lys in NSD2 is associated with a novel syndrome 2022 ·Clinical Genetics ·Bernt Popp, Melanie Brügger, (unknown), Tobias Bartolomaeus, (unknown), Julia Hentschel, Nataliya Di Donato, Andreas Rump, Janina Gburek‐Augustat, Elisabeth Graf, Matias Wagner, Ina Sorge, Johannes R. Lemke, Thomas Meitinger, Rami Abou Jamra, Vincent Strehlow, Theresa Brunet	2
10	Clonal hematopoiesis as a pitfall in germline variant interpretation in the context of Mendelian disorders 2022 ·Human Molecular Genetics ·Theresa Brunet, Riccardo Berutti, Veronika Dill, Judith S. Hecker, Daniela Choukair, (unknown), Marcus Deschauer, Janine Diehl‐Schmid, Martin Krenn, Gertrud Eckstein, Elisabeth Graf, Thomas Gasser, Tim M. Strom, Julia Hoefele, Katharina S. Götze, Thomas Meitinger, Matias Wagner	4
11	A de novo missense variant in GABRA4 alters receptor function in an epileptic and neurodevelopmental phenotype 2022 ·Epilepsia ·Florian Vogel, Martin Krenn, Dominik S. Westphal, Elisabeth Graf, Matias Wagner, Steffen Leiz, (unknown), (unknown), (unknown), Petra Scholze, Margot Ernst	8
12	CADA: phenotype-driven gene prioritization based on a case-enriched knowledge graph 2021 ·NAR Genomics and Bioinformatics ·(unknown), (unknown), Alexander Schmid, Ashar Ahmad, Alexej Knaus, (unknown), (unknown), Birgit Zirn, Tobias B. Haack, Stephan Ossowski, Matias Wagner, Theresa Brunet, Nadja Ehmke, Magdalena Danyel, (unknown), Tom Kamphans, Guy Nadav, Nicole Fleischer, Holger Fröhlich, Peter Krawitz	15
13	Variant-specific effects define the phenotypic spectrum of HNRNPH2-associated neurodevelopmental disorders in males 2021 ·Human Genetics ·Hans‐Jürgen Kreienkamp, Matias Wagner, Heike Weigand, (unknown), Marie McDonald, Boris Keren, Cyril Mignot, Julie Gauthier, (unknown), Jacques L. Michaud, (unknown), Rosemarie Smith, Ulrike Löbel, Maja Hempel, Christian Kubisch, Jonas Denecke, Philippe M. Campeau, Jennifer Bain, Davor Lessel	13
14	Investigation of gamma secretase gene complex mutations in German population with Hidradenitis suppurativa designate a complex polygenic heritage 2021 ·Journal of the European Academy of Dermatology and Venereology ·Seçil Vural, Martina Baumgartner, Peter Lichtner, Gertrud Eckstein, (unknown), W. Chen, Thomas Ruzicka, Bodo C. Melnik, Gerd Plewig, Matias Wagner, Kathrin Giehl	12
15	Novel pathogenic EIF2S3 missense variants causing clinically variable MEHMO syndrome with impaired eIF2γ translational function, and literature review 2020 ·Clinical Genetics ·Urania Kotzaeridou, Sara K. Young, Vanessa Suckow, (unknown), Matias Wagner, Inga Harting, (unknown), Tim M. Strom, Thomas Dever, Vera M. Kalscheuer	10
16	A homozygous truncating variant in CCDC186 in an individual with epileptic encephalopathy 2020 ·Annals of Clinical and Translational Neurology ·Melanie Brügger, (unknown), Theresa Brunet, Tim M. Strom, Thomas Meitinger, Eberhard Lurz, Ingo Borggraefe, Matias Wagner	4
17	Lifetime risk of autosomal recessive mitochondrial disorders calculated from genetic databases 2020 ·EBioMedicine ·(unknown), Matias Wagner, Sarah L. Stenton, Tim M. Strom, Saskia B. Wortmann, Holger Prokisch, Thomas Meitinger, Konrad Oexle, Thomas Klopstock	39
18	Rescue of respiratory failure in pulmonary alveolar proteinosis due to pathogenic MARS1 variants 2020 ·Pediatric Pulmonology ·Dominic Lenz, Mirjam Stahl, Elias Seidl, (unknown), Heiko Brennenstuhl, (unknown), (unknown), Thomas Longerich, Marisa I. Mendes, Holger Prokisch, Gajja S. Salomons, (unknown), Desirée E.C. Smith, Olaf Sommerburg, Matias Wagner, Jens H. Westhoff, Karl Reiter, Christian Staufner, Matthias Griese	19
19	Biallelic loss‐of‐function variants in RBL2 in siblings with a neurodevelopmental disorder 2020 ·Annals of Clinical and Translational Neurology ·Theresa Brunet, Milena Radivojkov‐Blagojevic, Peter Lichtner, Verena Kraus, Thomas Meitinger, Matias Wagner	8
20	Lessons from exome sequencing in prenatally diagnosed heart defects: A basis for prenatal testing 2019 ·Clinical Genetics ·Dominik S. Westphal, Gloria Leszinski, Esther Rieger‐Fackeldey, Elisabeth Graf, Gregor Weirich, Thomas Meitinger, Eva Ostermayer, Renate Oberhoffer, Matias Wagner	22

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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