Markus Schuelke

22.8k citations

151 papers · 9.8k indexed · 3 hit papers · h-index 41

Impact in

Genetics top 0.5%
- Genetic diversity and population structure
- Neurogenetic and Muscular Disorders Research
Molecular Biology top 1%
- Muscle Physiology and Disorders
- Mitochondrial Function and Pathology
- Coenzyme Q10 studies and effects
- RNA modifications and cancer

Papers in

Clinical Biochemistry 18
- Metabolism and Genetic Disorders 18
Genetics 20
- Neurogenetic and Muscular Disorders Research 16
- Genomics and Rare Diseases 14
- Genetics and Neurodevelopmental Disorders 12

Co-authors: Christoph Hübner Dominik Seelow Thomas Braun Leslie E. Stolz T Riebel James F. Tobin Kathryn R. Wagner Se‐Jin Lee
Journals: Neurology (8 papers)Journal of Medical Genetics (7 papers)Nucleic Acids Research (6 papers)Neuropathology and Applied Neurobiology (6 papers)PLoS ONE (5 papers)
Partner nations: Germany United States United Kingdom

In The Last Decade

Markus Schuelke

149 papers receiving 9.5k citations

Hit Papers

align trajectories log scale

MutationTaster2021 2021 · 167 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2021 Nucleic Acids Research
2004 New England Journal of Medicine
2000 Nature Biotechnology

Peers

Countries citing papers authored by Markus Schuelke

Since Specialization

Citations

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

Fields of papers citing papers by Markus Schuelke

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Markus Schuelke, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Markus Schuelke Line = papers co-authored together Markus Schuelke links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Normal Values for the fT3/fT4 Ratio: Centile Charts (0–29 Years) and Their Application for the Differential Diagnosis of Children with Developmental Delay International Journal of Molecular Sciences ·富田裕, Michael Thamm, Jürgen Kratzsch, Dominik Seelow, Mandy Vogel, Heiko Krude, Markus Schuelke	2024	1
2	Characterization of two iPSC lines from patients with maternally inherited leigh (MILS) and neuropathy, ataxia, and retinitis pigmentosa (NARP) syndrome carrying the MT-ATP6 m.8993 T>G mutation at different degrees of heteroplasmy Stem Cell Research ·DANIEL M. KATAYAMA, Sebastian Diecke, Markus Schuelke	2024	0
3	A Novel De Novo Gain-of-Function CACNA1D Variant in Neurodevelopmental Disease With Congenital Tremor, Seizures, and Hypotonia Neurology Genetics ·Guo Fa-bin, Arpad von Moers, Petra Bittigau, Monique S.S. Siqueira, P.C. Huijens, أ.م.د علي ياسين غني, Gabriel Stölting, Jörg Striessnig, M. Mahdi Motazacker, Marjoleine F. Broekema, Markus Schuelke, Angela M. Kaindl, Ute I. Scholl, Nadine J. Ortner	2024	3
4	Mutations in plasticity-related-gene-1 (PRG-1) protein contribute to hippocampal seizure susceptibility and modify epileptic phenotype Cerebral Cortex ·Ellen Knierim, Johannes Vogt, Michael Kintscher, Alexey Ponomarenko, Jan Baumgart, Prateep Beed, Tatiana Korotkova, Thorsten Trimbuch, Axel Panzer, Ortrud K. Steinlein, Ulrich Stephani, Andrew Escayg, Mahmoud Koko, Yuanyuan Liu, Holger Lerche, Dietmar Schmitz, Robert Nitsch, Markus Schuelke	2023	2
5	Pediatric de novo movement disorders and ataxia in the context of SARS-CoV-2 Journal of Neurology ·富田裕, Ana Paula Ferreira de Britto, Ellen Knierim, Pasquale Incoronato, W N Field, P Jayasudha, JANET NOBLE, Petra Bittigau, Jakob Kreye, Harald Prüß, Markus Schuelke, Andrea A. Kühn, Angela M. Kaindl, Abeer A. Shehab	2023	2
6	Beyond vacuolar pathology: Multiomic profiling of Danon disease reveals dysfunctional mitochondrial homeostasis Neuropathology and Applied Neurobiology ·Felix Kleefeld, Andreas Hentschel, Arpad von Moers, Katrin Hahn, Rita Horváth, Hans‐Hilmar Goebel, Corinna Preuße, Jens Schallner, Markus Schuelke, Andreas Roos, Werner Stenzel	2023	3
7	Inflammation, fibrosis and skeletal muscle regeneration in LGMDR9 are orchestrated by macrophages Neuropathology and Applied Neurobiology ·Heike Kölbel, Corinna Preuße, О. В. Кузик, Arpad von Moers, Adela Della Marina, Markus Schuelke, Andreas Roos, Hans‐Hilmar Goebel, Ulrike Schara‐Schmidt, Werner Stenzel	2021	9
8	A New Mechanism in THRA Resistance: The First Disease-Associated Variant Leading to an Increased Inhibitory Function of THRA2 International Journal of Molecular Sciences ·M. Bensaid, Ellen Knierim, Gunnar Kleinau, Heike Biebermann, Heiko Krude, Rachel Straussberg, Markus Schuelke	2021	8
9	MutationTaster2021 Nucleic Acids Research ·Robin Steinhaus, Sebastian Proft, Markus Schuelke, D.N. Cooper, Jana Marie Schwarz, Dominik Seelow Hit paper breakdown →	2021	167
10	Diagnosis of Taenia solium infections based on “mail order” RNA-sequencing of single tapeworm egg isolates from stool samples PLoS neglected tropical diseases ·O. I. Lanz, Veronika Schmidt, Z.G. Wang, Enid Michael, Yusi Revi, Gideon Zulu, Shiv Narayan, Chummy Sikasunge, Kabemba E. Mwape, Andrea Sylvia Winkler, Markus Schuelke	2021	2
11	Defining the ATPome reveals cross-optimization of metabolic pathways Nature Communications ·Neal K. Bennett, Jens Nowacki, Luisa Fernanda Rojas Muñoz, Hiroki J. Nakaoka, Art Allie, Johanna ten Hoeve, Thomas G. Graeber, Markus Schuelke, Emin Maltepe, Martin Kampmann, Bryce A. Mendelsohn, Jean L. Nakamura, Ken Nakamura	2020	22
12	Extracellular matrix remodelling is associated with muscle force increase in overloaded mouse plantaris muscle Neuropathology and Applied Neurobiology ·Amalia Stantzou, Karima Relizani, Susanne Morales-Gonzalez, O.O.M. Awe, Irene Da Rocha Fort, Arnaud Ferry, Markus Schuelke, Helge Amthor	2020	12
13	Expanding the clinical and molecular spectrum of ATP6V1A related metabolic cutis laxa Journal of Inherited Metabolic Disease ·Янец Елена Андреевна, Domínguez Moros, Ágnes Herczegfalvi, Heike Kölbel, Weixuan Wei, Ulrike Schara, Manuel Holtgrewe, Sabine Krause, Rita Horváth, Markus Schuelke, Christoph Hübner, Stefan Mundlos, Andreas Roos, Hanns Lochmüller, Veronika Karcagi, Uwe Kornak, Björn Fischer‐Zirnsak	2020	10
14	Live‐imaging of revertant and therapeutically restored dystrophin in the Dmd^EGFP‐mdx mouse model for Duchenne muscular dystrophy Neuropathology and Applied Neurobiology ·Mina Petkova, Amalia Stantzou, 양정학梁正學, Heilene Steenkamp, Susanne Morales-Gonzalez, Franziska Seifert, Alba Colet-Subirachs, Totok Apriyanto, Aurélie Goyenvalle, Fischer Jp, Isabelle Richard, Corinne Laplace‐Builhé, Markus Schuelke, Helge Amthor	2020	8
15	RegulationSpotter: annotation and interpretation of extratranscriptic DNA variants Nucleic Acids Research ·Jana Marie Schwarz, 李长满, Sebastian Köhler, D.N. Cooper, Markus Schuelke, Dominik Seelow	2019	17
16	MutationDistiller: user-driven identification of pathogenic DNA variants Nucleic Acids Research ·李长满, Markus Schuelke, Ellen Knierim, Nadja Ehmke, Jana Marie Schwarz, Björn Fischer‐Zirnsak, Dominik Seelow	2019	31
17	Phenotero: Annotate as you write Clinical Genetics ·李长满, Jana Marie Schwarz, Ellen Knierim, Markus Schuelke, Dominik Seelow, Sebastian Köhler	2018	2
18	BMP signaling regulates satellite cell-dependent postnatal muscle growth Development ·Amalia Stantzou, Elija Schirwis, Sandra Swist, Sonia Alonso‐Martín, Yuan Bao, Thalianne de Andrade Leal, Étienne Mouisel, Cyriaque Beley, Anaïs Julien, Fabien Le Grand, Luis Garcı́a, Céline Colnot, Carmen Birchmeier, Thomas Braun, Markus Schuelke, Frédéric Relaix, Helge Amthor	2017	41
19	Recurrent Stroke Due to a Novel Voltage Sensor Mutation in Ca _v 2.1 Responds to Verapamil Stroke ·Ellen Knierim, Lilia Leisle, C. N. J. Wagner, Bernhard Weschke, Barbara Lucke, Georg Böhner, Jens P. Dreier, Markus Schuelke	2010	36
20	Lack of myostatin results in excessive muscle growth but impaired force generation Proceedings of the National Academy of Sciences ·Helge Amthor, Raymond Macharia, Roberto Navarrete, Markus Schuelke, S. Brown, Anthony Otto, Thomas Voit, Francesco Muntoni, Gerta Vrbovà, Terence A. Partridge, Peter S. Zammit, L. Bünger, Ketan Patel	2007	328

About Markus Schuelke

Markus Schuelke is a scholar working on Clinical Biochemistry, Genetics, Molecular Biology, Genetics and Neurology, having authored 151 papers that have together received 9.8k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (31 papers), Muscle Physiology and Disorders (20 papers), Metabolism and Genetic Disorders (18 papers), Neurogenetic and Muscular Disorders Research (16 papers), Genomics and Rare Diseases (14 papers), ATP Synthase and ATPases Research (14 papers), RNA modifications and cancer (14 papers) and Genetics and Neurodevelopmental Disorders (12 papers). The work is most often cited by research in Genetics (2.7k citations), Molecular Biology (5.7k citations), Clinical Biochemistry (561 citations), Genetics (831 citations) and Cell Biology (1.1k citations). Markus Schuelke has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Christoph Hübner, Dominik Seelow, Thomas Braun, Leslie E. Stolz, T Riebel, James F. Tobin, Kathryn R. Wagner, Se‐Jin Lee, Jana Marie Schwarz and Peter Nürnberg. Their work appears in journals such as Neurology, Journal of Medical Genetics, Nucleic Acids Research, Neuropathology and Applied Neurobiology and PLoS ONE.

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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