Florian Harmuth

698 total citations
11 papers, 235 citations indexed

About

Florian Harmuth is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Florian Harmuth has authored 11 papers receiving a total of 235 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Cellular and Molecular Neuroscience and 4 papers in Neurology. Recurrent topics in Florian Harmuth's work include Genetic Neurodegenerative Diseases (6 papers), Mitochondrial Function and Pathology (4 papers) and Neurological diseases and metabolism (2 papers). Florian Harmuth is often cited by papers focused on Genetic Neurodegenerative Diseases (6 papers), Mitochondrial Function and Pathology (4 papers) and Neurological diseases and metabolism (2 papers). Florian Harmuth collaborates with scholars based in Germany, United States and Spain. Florian Harmuth's co-authors include Matthis Synofzik, Peter Bauer, Lüdger Schöls, Dagmar Timmann, Martin A. Giese, Winfried Ilg, Rebecca Schüle, Holger Hengel, Christina Gerth‐Kahlert and Miriam Stampfer and has published in prestigious journals such as Movement Disorders, Breast Cancer Research and Treatment and Journal of Neurology.

In The Last Decade

Florian Harmuth

11 papers receiving 234 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Florian Harmuth Germany	8	120	117	58	52	49	11	235
Maartje Pennings Netherlands	10	134 1.1×	112 1.0×	48 0.8×	44 0.8×	76 1.6×	21	272
Claire Guissart France	12	174 1.4×	76 0.6×	65 1.1×	35 0.7×	73 1.5×	22	301
María Jesús Sobrido Spain	8	158 1.3×	100 0.9×	53 0.9×	29 0.6×	25 0.5×	20	224
Elly F. Ippel Netherlands	9	139 1.2×	96 0.8×	49 0.8×	26 0.5×	58 1.2×	10	254
Michiel R. Fokkens Netherlands	9	206 1.7×	176 1.5×	64 1.1×	47 0.9×	25 0.5×	11	312
Neven Maksemous Australia	12	121 1.0×	89 0.8×	81 1.4×	50 1.0×	134 2.7×	28	362
Gia Tuong Tran Norway	7	210 1.8×	104 0.9×	114 2.0×	60 1.2×	39 0.8×	8	328
Marie‐France Rioux Canada	6	140 1.2×	117 1.0×	22 0.4×	48 0.9×	38 0.8×	8	270
Marc Corral‐Juan Spain	11	260 2.2×	206 1.8×	74 1.3×	37 0.7×	60 1.2×	15	336

Countries citing papers authored by Florian Harmuth

Since Specialization

Citations

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

Fields of papers citing papers by Florian Harmuth

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Florian Harmuth

This figure shows the co-authorship network connecting the top 25 collaborators of Florian Harmuth. A scholar is included among the top collaborators of Florian Harmuth 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 Florian Harmuth. Florian Harmuth is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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11 of 11 papers shown

Harmuth, Florian, Martin A. Giese, Lüdger Schöls, et al.. (2025). Capture of Longitudinal Change in Real‐Life Walking in Cerebellar Ataxia Increases Patient Relevance and Effect Size. Movement Disorders. 40(7). 1343–1355. 1 indexed citations

Gutmann, Daniel A.P., Florian Harmuth, Tobias B. Haack, et al.. (2023). First case of adult onset neuronal intranuclear inclusion disease with both typical radiological signs and NOTCH2NLC repeat expansions in a Caucasian individual. European Journal of Neurology. 30(9). 2854–2858. 6 indexed citations

Harmuth, Florian, Martin A. Giese, Rebecca Schüle, et al.. (2022). Real‐Life Turning Movements Capture Subtle Longitudinal and Preataxic Changes in Cerebellar Ataxia. Movement Disorders. 37(5). 1047–1058. 24 indexed citations

Park, Joohyun, Jan Niklas Petry‐Schmelzer, Petra Stöbe, et al.. (2021). Transcript-Specific Loss-of-Function Variants in VPS16 Are Enriched in Patients With Dystonia. Neurology Genetics. 8(1). e644–e644. 7 indexed citations

Tüngler, Victoria, Peter Kaufmann, Christine Wolf, et al.. (2019). Aicardi-Goutières syndrome due to a paternal mosaic IFIH1 mutation. Neurology Genetics. 6(1). e384–e384. 6 indexed citations

Synofzik, Matthis, Katherine L. Helbig, Florian Harmuth, et al.. (2018). De novo ITPR1 variants are a recurrent cause of early-onset ataxia, acting via loss of channel function. European Journal of Human Genetics. 26(11). 1623–1634. 30 indexed citations

Schüle, Rebecca, Adriana Rebelo, María‐Jesús Sobrido, et al.. (2017). PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia. Clinical Genetics. 92(5). 534–539. 34 indexed citations

Ilg, Winfried, Cornelia Schatton, Holger Hengel, et al.. (2016). Individual changes in preclinical spinocerebellar ataxia identified via increased motor complexity. Movement Disorders. 31(12). 1891–1900. 42 indexed citations

Synofzik, Matthis, Florian Harmuth, Miriam Stampfer, et al.. (2015). NPC1 is enriched in unexplained early onset ataxia: a targeted high-throughput screening. Journal of Neurology. 262(11). 2557–2563. 22 indexed citations

10.

Faust, Ulrike, Marc Sturm, Karl Hackmann, et al.. (2015). HBOC multi-gene panel testing: comparison of two sequencing centers. Breast Cancer Research and Treatment. 152(1). 129–136. 35 indexed citations

11.

Tarnutzer, Alexander A., Christina Gerth‐Kahlert, Dagmar Timmann, et al.. (2014). Boucher–Neuhäuser syndrome: cerebellar degeneration, chorioretinal dystrophy and hypogonadotropic hypogonadism: two novel cases and a review of 40 cases from the literature. Journal of Neurology. 262(1). 194–202. 28 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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