T Maríková

401 total citations
16 papers, 294 citations indexed

About

T Maríková is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, T Maríková has authored 16 papers receiving a total of 294 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Cellular and Molecular Neuroscience and 5 papers in Genetics. Recurrent topics in T Maríková's work include Muscle Physiology and Disorders (5 papers), Hereditary Neurological Disorders (4 papers) and Genetic Neurodegenerative Diseases (4 papers). T Maríková is often cited by papers focused on Muscle Physiology and Disorders (5 papers), Hereditary Neurological Disorders (4 papers) and Genetic Neurodegenerative Diseases (4 papers). T Maríková collaborates with scholars based in Czechia, Denmark and Germany. T Maríková's co-authors include Radim Mazanec, Josef Zámečnı́k, Josef Kraus, Zdeněk Sedláček, Petr Vondráček, Lenka Fajkusová, Markéta Hermanová, Anna Křepelová, Zuzana Mušová and Tomáš Procházka and has published in prestigious journals such as Annals of the New York Academy of Sciences, Muscle & Nerve and Human Mutation.

In The Last Decade

T Maríková

15 papers receiving 290 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
T Maríková Czechia	8	252	173	60	49	34	16	294
Zuzana Mušová Czechia	8	221 0.9×	166 1.0×	15 0.3×	61 1.2×	35 1.0×	21	261
D.E. Wilcox United Kingdom	8	250 1.0×	165 1.0×	14 0.2×	60 1.2×	30 0.9×	10	286
Emilia K. Bijlsma Netherlands	10	273 1.1×	295 1.7×	30 0.5×	141 2.9×	47 1.4×	15	395
Eduardo Calpena Spain	11	153 0.6×	114 0.7×	39 0.7×	25 0.5×	42 1.2×	21	272
Tatsushi Toda Japan	10	268 1.1×	115 0.7×	47 0.8×	39 0.8×	100 2.9×	29	382
Maartje Pennings Netherlands	10	134 0.5×	112 0.6×	33 0.6×	48 1.0×	76 2.2×	21	272
Isabel Banchs Spain	11	229 0.9×	309 1.8×	18 0.3×	117 2.4×	51 1.5×	19	424
Aline Huguet France	8	324 1.3×	302 1.7×	14 0.2×	66 1.3×	23 0.7×	11	362
Mei‐Ling Qi Japan	10	239 0.9×	150 0.9×	29 0.5×	24 0.5×	44 1.3×	13	336
M. Chaouch France	6	244 1.0×	128 0.7×	68 1.1×	20 0.4×	28 0.8×	8	295

Countries citing papers authored by T Maríková

Since Specialization

Citations

This map shows the geographic impact of T Maríková'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 T Maríková with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T Maríková more than expected).

Fields of papers citing papers by T Maríková

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of T Maríková

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

All Works

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16 of 16 papers shown

Nazaryan‐Petersen, Lusine, Mana M. Mehrjouy, Miroslava Hančárová, et al.. (2018). Very short DNA segments can be detected and handled by the repair machinery during germline chromothriptic chromosome reassembly. Human Mutation. 39(5). 709–716. 16 indexed citations

Neupauerová, Jana, Katalin Štěrbová, Markéta Vlčková, et al.. (2017). Two Novel Variants Affecting CDKL5 Transcript Associated with Epileptic Encephalopathy. Genetic Testing and Molecular Biomarkers. 21(10). 613–618. 10 indexed citations

Laššuthová, Petra, et al.. (2009). Emery-Dreifuss Muscular Dystrophy: A Novel Mutation in the LMNA Gene. Pediatric Neurology. 41(2). 127–130. 3 indexed citations

Sedláčková, Jana, Petr Vondráček, Markéta Hermanová, et al.. (2009). Point mutations in Czech DMD/BMD patients and their phenotypic outcome. Neuromuscular Disorders. 19(11). 749–753. 16 indexed citations

Mušová, Zuzana, Radim Mazanec, Anna Křepelová, et al.. (2009). Highly unstable sequence interruptions of the CTG repeat in the myotonic dystrophy gene. American Journal of Medical Genetics Part A. 149A(7). 1365–1374. 110 indexed citations

Bendová, Šárka, et al.. (2007). Novel mutations in the NF1 gene in Czech patients with neurofibromatosis type 1. Journal of Molecular Neuroscience. 31(3). 273–279. 3 indexed citations

Sedláčková, Jana, Markéta Hermanová, Petr Vondráček, et al.. (2006). Quantitative analysis of CAPN3 transcripts in LGMD2A patients: Involvement of nonsense-mediated mRNA decay. Neuromuscular Disorders. 17(2). 143–147. 18 indexed citations

Hermanová, Markéta, Jana Sedláčková, Josef Zámečnı́k, et al.. (2005). Analysis of histopathologic and molecular pathologic findings in Czech LGMD2A patients. Muscle & Nerve. 33(3). 424–432. 35 indexed citations

Bauer, Peter, Alena Zumrová, Václav Maťoška, et al.. (2005). Absence of spinocerebellar ataxia type 3/Machado–Joseph disease within ataxic patients in the Czech population. European Journal of Neurology. 12(11). 851–857. 16 indexed citations

10.

Bauer, Peter, Václav Maťoška, Alena Zumrová, et al.. (2005). Genotype/phenotype correlation in a SCA1 family: anticipation without CAG expansion.. PubMed. 46(3). 325–8. 7 indexed citations

11.

Hermanová, Markéta, Petr Vondráček, T Maríková, et al.. (2004). Mutations in Czech LGMD2A patients revealed by analysis of calpain3 mRNA and their phenotypic outcome. Neuromuscular Disorders. 14(10). 659–665. 45 indexed citations

12.

Seeman, Pavel, Radim Mazanec, T Maríková, & Bernd Rautenstrauß. (1999). Charcot‐Marie‐Tooth 1A: Heterozygous T118M Mutation over a CMT1A Duplication Has No Influence on the Phenotype. Annals of the New York Academy of Sciences. 883(1). 485–489. 7 indexed citations

13.

Mareš, J., Heike Görgens, Zdeněk Sedláček, et al.. (1998). Oncogene amplification and expression in pediatric solid tumors.. PubMed. 45(3). 123–7. 5 indexed citations

14.

Mareš, J., Zdeněk Sedláček, T Maríková, et al.. (1996). [Amplification of oncogenes in solid tumors in children].. PubMed. 135(15). 493–6. 1 indexed citations

15.

Seemanová, E, A. Schmidt, Ivan Šubrt, et al.. (1987). [The fragile X chromosome syndrome].. PubMed. 42(11). 650–4. 1 indexed citations

16.

Seemanová, E, et al.. (1983). [Macro-orchism. A significant symptom in the detection of the fragile X chromosome syndrome].. PubMed. 122(7). 215–7. 1 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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