Martin Krenn

2.1k total citations
36 papers, 394 citations indexed

About

Martin Krenn is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Martin Krenn has authored 36 papers receiving a total of 394 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 13 papers in Genetics and 11 papers in Neurology. Recurrent topics in Martin Krenn's work include Genomics and Rare Diseases (9 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Peripheral Neuropathies and Disorders (5 papers). Martin Krenn is often cited by papers focused on Genomics and Rare Diseases (9 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Peripheral Neuropathies and Disorders (5 papers). Martin Krenn collaborates with scholars based in Austria, Germany and United States. Martin Krenn's co-authors include Fritz Zimprich, Jakob Rath, Hakan Çetin, Anna Grisold, Gudrun Zulehner, Matias Wagner, Klaus Groschner, Christoph Romanin, Tim M. Strom and Alexander Zimprich and has published in prestigious journals such as Journal of Biological Chemistry, Scientific Reports and The FASEB Journal.

In The Last Decade

Martin Krenn

32 papers receiving 392 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Martin Krenn Austria 13 135 103 86 60 54 36 394
Michela Ripolone Italy 13 349 2.6× 72 0.7× 121 1.4× 63 1.1× 27 0.5× 40 526
Dustin Shilling United States 11 177 1.3× 33 0.3× 89 1.0× 28 0.5× 30 0.6× 15 501
Katie Mayne United Kingdom 8 164 1.2× 56 0.5× 91 1.1× 42 0.7× 6 0.1× 10 397
Asma I. Tahir Saudi Arabia 11 129 1.0× 34 0.3× 21 0.2× 90 1.5× 16 0.3× 19 294
Esther Nibbeling Netherlands 10 191 1.4× 73 0.7× 116 1.3× 107 1.8× 5 0.1× 15 408
Emily Bonkowski United States 4 118 0.9× 37 0.4× 37 0.4× 72 1.2× 5 0.1× 11 277
Bird Td United States 6 162 1.2× 25 0.2× 35 0.4× 90 1.5× 7 0.1× 244 342
Mefford Hc 6 163 1.2× 24 0.2× 35 0.4× 90 1.5× 7 0.1× 239 337
Eleonora Di Zanni Italy 14 312 2.3× 47 0.5× 34 0.4× 24 0.4× 10 0.2× 23 471
Vijay K. Ulaganathan Germany 7 145 1.1× 25 0.2× 28 0.3× 22 0.4× 22 0.4× 11 483

Countries citing papers authored by Martin Krenn

Since Specialization
Citations

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

Fields of papers citing papers by Martin Krenn

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martin Krenn

This figure shows the co-authorship network connecting the top 25 collaborators of Martin Krenn. A scholar is included among the top collaborators of Martin Krenn 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 Martin Krenn. Martin Krenn 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.
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
2.
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.
3.
Krenn, Martin, Karl‐Heinz Nenning, Susanne Aull‐Watschinger, et al.. (2025). ADAM23 haploinsufficiency as a putative oligogenic contributor in an individual with focal epilepsy. Seizure. 131. 454–457.
4.
Siegert, Sandy, Anna Grisold, Franco Laccone, et al.. (2024). Developmental, Cognitive, Ocular Motor, and Neuroimaging Findings Related to SUFU Haploinsufficiency: Unraveling Subtle and Highly Variable Phenotypes. Pediatric Neurology. 160. 38–44. 3 indexed citations
5.
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
6.
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
7.
Krenn, Martin, et al.. (2022). A de novo truncating variant in CSDE1 in an adult-onset neuropsychiatric phenotype without intellectual disability. European Journal of Medical Genetics. 65(3). 104423–104423. 3 indexed citations
8.
Krenn, Martin, Gudrun Zulehner, Jakob Rath, et al.. (2021). Incidence and clinical spectrum of rhabdomyolysis in general neurology: a retrospective cohort study. Neuromuscular Disorders. 31(12). 1227–1234. 2 indexed citations
9.
Rath, Jakob, Gudrun Zulehner, Anna Grisold, et al.. (2021). Cerebrospinal fluid analysis in Guillain–Barré syndrome: value of albumin quotients. Journal of Neurology. 268(9). 3294–3300. 16 indexed citations
10.
Krenn, Martin, Ekaterina Pataraia, Ellen Gelpí, et al.. (2021). Delineation of epileptic and neurodevelopmental phenotypes associated with variants in STX1B. Seizure. 87. 25–29. 4 indexed citations
11.
Rath, Jakob, Gudrun Zulehner, Anna Grisold, et al.. (2020). Nerve conduction studies in Guillain-Barré syndrome: Influence of timing and value of repeated measurements. Journal of the Neurological Sciences. 420. 117267–117267. 13 indexed citations
12.
Krenn, Martin, Matias Wagner, Christoph Hotzy, et al.. (2020). Diagnostic exome sequencing in non-acquired focal epilepsies highlights a major role of GATOR1 complex genes. Journal of Medical Genetics. 57(9). 624–633. 18 indexed citations
13.
Ittiwut, Chupong, Martin Krenn, Fritz Zimprich, et al.. (2020). ATP1A3-related epilepsy: Report of seven cases and literature-based analysis of treatment response. Journal of Clinical Neuroscience. 72. 31–38. 12 indexed citations
14.
Grisold, Anna, Gerda Ricken, Martin Krenn, et al.. (2019). Retinal and Corneal Neurodegeneration and Their Association with Systemic Signs of Peripheral Neuropathy in Type 2 Diabetes. American Journal of Ophthalmology. 209. 197–205. 24 indexed citations
15.
Rath, Jakob, Gudrun Zulehner, Eva Hilger, et al.. (2019). Frequency and clinical features of treatment-refractory myasthenia gravis. Journal of Neurology. 267(4). 1004–1011. 23 indexed citations
16.
Krenn, Martin, Gudrun Zulehner, Christoph Hotzy, et al.. (2017). Hereditary spastic paraplegia caused by compound heterozygous mutations outside the motor domain of the KIF1A gene. European Journal of Neurology. 24(5). 741–747. 17 indexed citations
17.
Krenn, Martin, Geoff Keir, & Udo Wieshmann. (2014). CANOMAD responding to weekly treatment with intravenous immunoglobulin (IVIg). BMJ Case Reports. 2014. bcr2013202545–bcr2013202545. 7 indexed citations
18.
Graziani, Annarita, Michael Poteser, Wolfgang-Moritz Heupel, et al.. (2009). Cell-Cell Contact Formation Governs Ca2+ Signaling by TRPC4 in the Vascular Endothelium. Journal of Biological Chemistry. 285(6). 4213–4223. 44 indexed citations
19.
Schindl, Rainer, Irene Frischauf, Heike Kahr, et al.. (2007). The first ankyrin-like repeat is the minimum indispensable key structure for functional assembly of homo- and heteromeric TRPC4/TRPC5 channels. Cell Calcium. 43(3). 260–269. 30 indexed citations
20.
Kaiser, Hans, Martin Krenn, B Bödey, & B Bödey. (2000). Involution and neoplasms of the thymus.. PubMed. 14(1). 189–98.

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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