Radim Mazanec

2.6k total citations
66 papers, 1.1k citations indexed

About

Radim Mazanec is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Radim Mazanec has authored 66 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Cellular and Molecular Neuroscience, 24 papers in Molecular Biology and 17 papers in Neurology. Recurrent topics in Radim Mazanec's work include Hereditary Neurological Disorders (33 papers), Genetic Neurodegenerative Diseases (24 papers) and Neurological diseases and metabolism (15 papers). Radim Mazanec is often cited by papers focused on Hereditary Neurological Disorders (33 papers), Genetic Neurodegenerative Diseases (24 papers) and Neurological diseases and metabolism (15 papers). Radim Mazanec collaborates with scholars based in Czechia, United States and Germany. Radim Mazanec's co-authors include Pavel Seeman, Martin Bojar, Radek Pádr, Aleš Homola, Petr Kobylka, J Neuwirth, V. Komrska, Jan Štulík, Eva Syková and T Maríková and has published in prestigious journals such as PLoS ONE, Neurology and Annals of Neurology.

In The Last Decade

Radim Mazanec

59 papers receiving 1.1k citations

Peers

Countries citing papers authored by Radim Mazanec

Since Specialization

Citations

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

Fields of papers citing papers by Radim Mazanec

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Radim Mazanec

This figure shows the co-authorship network connecting the top 25 collaborators of Radim Mazanec. A scholar is included among the top collaborators of Radim Mazanec 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 Radim Mazanec. Radim Mazanec 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	Genetic findings in Czech patients with limb girdle muscular dystrophy 2023 ·Clinical Genetics ·(unknown), (unknown), (unknown), Kamila Réblová, Jana Haberlová, Radim Mazanec, Stanislav Voháňka, (unknown), (unknown), Tomáš Honzík, (unknown), Hana Ošlejšková, (unknown), (unknown), Lenka Fajkusová	1
2	Diagnostic utility of neurofilament markers for MND is limited in restricted disease phenotype and for differentiation from compressive myeloradiculopathies 2022 ·Journal of Neurology ·(unknown), Radim Mazanec, (unknown)	1
3	Novel SBF2 mutations and clinical spectrum of Charcot‐Marie‐Tooth neuropathy type 4B2 2018 ·Clinical Genetics ·Petra Laššuthová, Katharina Vill, Sevim Erdem‐Özdamar, J. M. Schröder, Haluk Topaloğlu, Rita Horváth, Wolfgang Müller‐Felber, Boglárka Bánsági, Beate Schlotter‐Weigel, Dieter Gläser, Jana Neupauerová, Lucie Sedláčková, (unknown), Radim Mazanec, Joachim Weis, Pavel Seeman, Jan Senderek	7
4	Autosomal recessive hereditary spastic paraplegia type SPG35 due to a novel variant in the FA2H gene in a Czech patient 2018 ·Journal of Clinical Neuroscience ·(unknown), Dana Šafka Brožková, Martin Vyhnálek, Radim Mazanec, (unknown), Marie Trková, (unknown), (unknown), Pavel Seeman	3
5	Hereditary spastic paraplegias: clinical and genetic aspects 2016 ·Neurologie pro praxi ·(unknown), Radim Mazanec, Pavel Seeman	1
6	Evaluation of muscle strength and manual dexterity in patients with Charcot-Marie-Tooth disease 2015 ·Journal of Hand Therapy ·Alena Kobesová, (unknown), Josef Kraus, Pavel Kolář, (unknown), Radim Mazanec, Ross Andel	7
7	Autosomal recessive limb-girdle muscular dystrophies in theCzech Republic 2014 ·BMC Neurology ·(unknown), (unknown), (unknown), Lenka Mrázová, Petr Vondráček, Radim Mazanec, Stanislav Voháňka, Jana Haberlová, Markéta Hermanová, Josef Zámečnı́k, Ondřej Souček, Hana Ošlejšková, (unknown), (unknown), Lenka Fajkusová	1
8	Mutations in HINT1 are one of the most frequent causes of hereditary neuropathy among Czech patients and neuromyotonia is rather an underdiagnosed symptom 2014 ·Neurogenetics ·Petra Laššuthová, Dana Šafka Brožková, Marcela Krůtová, Jana Neupauerová, Jana Haberlová, Radim Mazanec, (unknown), (unknown), Pavel Seeman	31
9	Ulnar nerve at the elbow – normative nerve conduction study 2013 ·PubMed ·Edvard Ehler, Petr Ridzoň, Pavel Urban, Radim Mazanec, Marie Nakládalová, Bohumír Procházka, (unknown), (unknown), Pavel Otruba	6
10	Spectrum and frequencies of mutations in the MFN2 gene and its phenotypical expression in Czech hereditary motor and sensory neuropathy type II patients 2013 ·Molecular Medicine Reports ·Dana Šafka Brožková, (unknown), Petra Laššuthová, Radim Mazanec, Jana Haberlová, (unknown), (unknown), Jana Neupauerová, Pavel Seeman	10
11	Pulmonary function in patients with hereditary motor and sensory neuropathy: A comparison of patients with and without spinal deformity 2012 ·Neuromuscular Disorders ·(unknown), J Chlumský, Radim Mazanec, Pavel Kolář, Ross Andel, Alena Kobesová	4
12	Klinický standard pro farmakoterapii neuropatické bolesti 2011 ·Česká a slovenská neurologie a neurochirurgie ·Josef Bednařík, Zdeněk Ambler, J Opavský, O. Keller, Richard Rokyta, Radim Mazanec, Jan Lejčko, (unknown), (unknown), (unknown), (unknown)	9
13	Clinical and in silico evidence for and against pathogenicity of 11 new mutations in the MPZ gene 2010 ·Clinical Genetics ·Dana Šafka Brožková, Radim Mazanec, Jana Haberlová, (unknown), Pavel Seeman	6
14	Six New Gap Junction Beta 1 Gene Mutations and Their Phenotypic Expression in Czech Patients with Charcot-Marie-Tooth Disease 2009 ·Genetic Testing and Molecular Biomarkers ·Dana Šafka Brožková, Radim Mazanec, Jana Haberlová, (unknown), Ivan Šubrt, Pavel Seeman	11
15	Atrophy of type II fibres in myasthenia gravis muscle in thymectomized patients: steroid‐induced change with prognostic impact 2008 ·Journal of Cellular and Molecular Medicine ·Josef Zámečnı́k, (unknown), (unknown), (unknown), Jiří Piťha, J Schützner, Radim Mazanec	7
16	Muscle lymphocytic infiltrates in thymoma-associated myasthenia gravis are phenotypically different from those in polymyositis 2007 ·Neuromuscular Disorders ·Josef Zámečnı́k, (unknown), (unknown), (unknown), Jiří Piťha, J Schützner, Radim Mazanec, Hannes Vogel	17
17	Charcot‐Marie‐Tooth neuropathy type 1A combined with Duchenne muscular dystrophy 2007 ·European Journal of Neurology ·Petr Vondráček, Markéta Hermanová, Jana Sedláčková, Lenka Fajkusová, (unknown), (unknown), Renata Gaillyová, Pavel Seeman, Radim Mazanec	6
18	Concomitancy of mutation in FRDA gene and FMR1 premutation in 58 year-old woman. 2005 ·PubMed ·Alena Zumrová, Radim Mazanec, Martin Vyhnálek, Anna Křepelová, Zuzana Mušová, (unknown), (unknown), Markéta Havlovičová	3
19	Analysis of histopathologic and molecular pathologic findings in Czech LGMD2A patients 2005 ·Muscle & Nerve ·Markéta Hermanová, (unknown), Jana Sedláčková, (unknown), (unknown), (unknown), Josef Zámečnı́k, Petr Vondráček, Radim Mazanec, T Maríková, Stanislav Voháňka, Lenka Fajkusová	35
20	Charcot‐Marie‐Tooth 1A: Heterozygous T118M Mutation over a CMT1A Duplication Has No Influence on the Phenotype 1999 ·Annals of the New York Academy of Sciences ·Pavel Seeman, Radim Mazanec, T Maríková, Bernd Rautenstrauß	7

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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