Holger Prokisch

48.9k total citations
221 papers, 8.6k citations indexed

About

Holger Prokisch is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Holger Prokisch has authored 221 papers receiving a total of 8.6k indexed citations (citations by other indexed papers that have themselves been cited), including 179 papers in Molecular Biology, 75 papers in Clinical Biochemistry and 39 papers in Genetics. Recurrent topics in Holger Prokisch's work include Mitochondrial Function and Pathology (107 papers), Metabolism and Genetic Disorders (75 papers) and RNA modifications and cancer (42 papers). Holger Prokisch is often cited by papers focused on Mitochondrial Function and Pathology (107 papers), Metabolism and Genetic Disorders (75 papers) and RNA modifications and cancer (42 papers). Holger Prokisch collaborates with scholars based in Germany, Austria and United States. Holger Prokisch's co-authors include Thomas Meitinger, Tobias B. Haack, Sarah L. Stenton, Thomas Klopstock, Johannes A. Mayr, Tim M. Strom, Mirjana Gušić, Walter Neupert, Uwe Ahting and Laura S. Kremer and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Holger Prokisch

212 papers receiving 8.5k citations

Author Peers

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

Author Last Decade Papers Cites
Holger Prokisch 6.6k 2.2k 923 842 793 221 8.6k
Rita Horváth 7.1k 1.1× 3.2k 1.5× 823 0.9× 695 0.8× 454 0.6× 280 9.4k
Anne Lombès 7.1k 1.1× 3.5k 1.6× 431 0.5× 814 1.0× 337 0.4× 145 9.5k
Stephan Kemp 6.3k 1.0× 1.6k 0.7× 573 0.6× 259 0.3× 332 0.4× 110 7.5k
Gino Cortopassi 4.8k 0.7× 1.3k 0.6× 434 0.5× 242 0.3× 414 0.5× 64 6.5k
Mariusz Karbowski 7.9k 1.2× 1.6k 0.7× 221 0.2× 741 0.9× 305 0.4× 62 9.5k
Katsuyoshi Mihara 10.7k 1.6× 2.4k 1.1× 415 0.4× 555 0.7× 230 0.3× 107 12.8k
Niels Gregersen 5.4k 0.8× 3.1k 1.4× 762 0.8× 245 0.3× 190 0.2× 200 7.9k
David A. Antonetti 5.6k 0.9× 1.4k 0.6× 260 0.3× 407 0.5× 2.9k 3.7× 124 12.7k
Brett H. Graham 3.3k 0.5× 1.0k 0.5× 574 0.6× 210 0.2× 253 0.3× 91 4.6k
Ann B. Moser 10.2k 1.5× 3.8k 1.8× 741 0.8× 325 0.4× 495 0.6× 215 12.3k

Countries citing papers authored by Holger Prokisch

Since Specialization
Citations

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

Fields of papers citing papers by Holger Prokisch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Holger Prokisch

This figure shows the co-authorship network connecting the top 25 collaborators of Holger Prokisch. A scholar is included among the top collaborators of Holger Prokisch 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 Holger Prokisch. Holger Prokisch 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.
Andreasi, Nico Golfrè, Sara Rinaldo, Zvi Israel, et al.. (2025). Spiking Patterns in the Globus Pallidus Highlight Convergent Neural Dynamics across Diverse Genetic Dystonia Syndromes. Annals of Neurology. 97(5). 826–844. 3 indexed citations
2.
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.
3.
Pauli, Jessica, Nadja Sachs, Katja Steiger, et al.. (2025). Single cell spatial transcriptomics integration deciphers the morphological heterogeneity of atherosclerotic carotid arteries. Nature Communications. 16(1). 11282–11282. 1 indexed citations
4.
Maalmi, Haïfa, Holger Prokisch, Barbara Thorand, et al.. (2024). Interpretable multimodal machine learning (IMML) framework reveals pathological signatures of distal sensorimotor polyneuropathy. SHILAP Revista de lepidopterología. 4(1). 265–265.
5.
Gramer, Gwendolyn, Saskia B. Wortmann, Junmin Fang‐Hoffmann, et al.. (2024). New Cases of Maleylacetoacetate Isomerase Deficiency with Detection by Newborn Screening and Natural History over 32 Years: Experience from a German Newborn Screening Center. International Journal of Neonatal Screening. 10(1). 17–17. 2 indexed citations
6.
Mayr, Johannes A., Nadja Fratzl‐Zelman, Stéphane Blouin, et al.. (2023). Investigating the role of ASCC1 in the causation of bone fragility. Frontiers in Endocrinology. 14. 1137573–1137573. 4 indexed citations
7.
Indelicato, Elisabetta, Sylvia Boesch, Niccolò E. Mencacci, et al.. (2023). Dystonia in ATP Synthase Defects: Reconnecting Mitochondria and Dopamine. Movement Disorders. 39(1). 29–35. 3 indexed citations
8.
Prokisch, Holger, et al.. (2023). Integrative omics approaches to advance rare disease diagnostics. Journal of Inherited Metabolic Disease. 46(5). 824–838. 13 indexed citations
9.
Wagner, Nils, Muhammed Hasan Çelik, Christian Mertes, et al.. (2023). Aberrant splicing prediction across human tissues. Nature Genetics. 55(5). 861–870. 34 indexed citations
10.
Frenzel, Stefan, Alexander Teumer, Katharina Wittfeld, et al.. (2022). TREML2 Gene Expression and Its Missense Variant rs3747742 Associate with White Matter Hyperintensity Volume and Alzheimer’s Disease-Related Brain Atrophy in the General Population. International Journal of Molecular Sciences. 23(22). 13764–13764. 4 indexed citations
11.
Berutti, Riccardo, et al.. (2022). Guidelines for clinical interpretation of variant pathogenicity using RNA phenotypes. Human Mutation. 43(8). 1056–1070. 14 indexed citations
12.
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
13.
Casaroli‐Marano, Ricardo P., Judit García‐Villoria, Vicente A. Yépez, et al.. (2022). Diagnostic Odyssey in an Adult Patient with Ophthalmologic Abnormalities and Hearing Loss: Contribution of RNA-Seq to the Diagnosis of a PEX1 Deficiency. International Journal of Molecular Sciences. 23(20). 12367–12367. 3 indexed citations
14.
Yépez, Vicente A., Christian Mertes, Michaela Müller, et al.. (2021). Detection of aberrant gene expression events in RNA sequencing data. Nature Protocols. 16(2). 1276–1296. 65 indexed citations
15.
Kostić, Marko, Essam A. Assali, Yael Amitai, et al.. (2021). Author Correction: Aberrant activity of mitochondrial NCLX is linked to impaired synaptic transmission and is associated with mental retardation. Communications Biology. 4(1). 755–755. 2 indexed citations
16.
Kopajtich, Robert, et al.. (2021). RNA-seq count and proteomics intensity data used in the Kopajtich, Smirnov, Stenton et al study. Zenodo (CERN European Organization for Nuclear Research).
17.
Mertes, Christian, Ines F. Scheller, Vicente A. Yépez, et al.. (2021). Detection of aberrant splicing events in RNA-seq data using FRASER. Nature Communications. 12(1). 529–529. 84 indexed citations
18.
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
19.
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
20.
Prokisch, Holger, Christophe Andréoli, Curt Scharfe, Lars M. Steinmetz, & Thomas Meitinger. (2004). Integrative analysis of the mitochondrial proteome. mediaTUM (Technical University of Munich). 2 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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