Andrej Ficek

917 total citations
31 papers, 616 citations indexed

About

Andrej Ficek is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Andrej Ficek has authored 31 papers receiving a total of 616 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 7 papers in Genetics and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in Andrej Ficek's work include Genetic Neurodegenerative Diseases (5 papers), Genomics and Rare Diseases (4 papers) and Sexual Differentiation and Disorders (4 papers). Andrej Ficek is often cited by papers focused on Genetic Neurodegenerative Diseases (5 papers), Genomics and Rare Diseases (4 papers) and Sexual Differentiation and Disorders (4 papers). Andrej Ficek collaborates with scholars based in Slovakia, Czechia and Austria. Andrej Ficek's co-authors include Ľudevít Kádaši, Gabriel Minárik, Daniela Ostatníková, Peter Celec, H Poláková, Andrea Šoltýsová, Eva Feráková, V. Ferák, Martina Drličková and P Bobek and has published in prestigious journals such as SHILAP Revista de lepidopterología, Bioinformatics and PLoS ONE.

In The Last Decade

Andrej Ficek

30 papers receiving 602 citations

Peers

Countries citing papers authored by Andrej Ficek

Since Specialization

Citations

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

Fields of papers citing papers by Andrej Ficek

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrej Ficek

This figure shows the co-authorship network connecting the top 25 collaborators of Andrej Ficek. A scholar is included among the top collaborators of Andrej Ficek 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 Andrej Ficek. Andrej Ficek 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	Prognostic Value of Genotype–Phenotype Correlations in X-Linked Myotubular Myopathy and the Use of the Face2Gene Application as an Effective Non-Invasive Diagnostic Tool 2023 ·Genes ·(unknown), Andrea Šoltýsová, Andrej Ficek, René G. Feichtinger, Johannes A. Mayr, Martina Škopková, Daniela Gašperíková, Miriam Kolníková, (unknown), Ognian Kalev, Serge Weis, (unknown)	0
2	The importance of defining the age-specific TREC/KREC levels for detection of various inborn errors of immunity in pediatric and adult patients 2022 ·Clinical Immunology ·(unknown), (unknown), (unknown), (unknown), Peter Čižnár, (unknown), (unknown), (unknown), Andrej Ficek, Andrea Šoltýsová	2
3	Clinical manifestation of CDKL5 deficiency disorder and identified mutations in a cohort of Slovak patients 2021 ·Epilepsy Research ·(unknown), Miriam Kolníková, (unknown), (unknown), (unknown), (unknown), (unknown), Ľudevít Kádaši, Andrea Šoltýsová, Andrej Ficek	1
4	Mathematical modeling based on RT-qPCR analysis of SARS-CoV-2 in wastewater as a tool for epidemiology 2021 ·Scientific Reports ·(unknown), Andrea Šoltýsová, (unknown), Zdenko Takáč, (unknown), Andrej Ficek, Miroslav Gál, Marián Gall, (unknown), (unknown), (unknown), (unknown), (unknown), Andrea Škulcová, Tomáš Mackuľak	28
5	A Study among the Genotype, Functional Alternations, and Phenotype of 9 SCN1A Mutations in Epilepsy Patients 2020 ·Scientific Reports ·(unknown), Miriam Kolníková, Ľubica Lacinová, (unknown), (unknown), Viktor Demko, Ľudevít Kádaši, Andrej Ficek, Andrea Šoltýsová	25
6	Variant c.2158-2A>G in MANBA is an important and frequent cause of hereditary hearing loss and beta-mannosidosis among the Czech and Slovak Roma population- evidence for a new ethnic-specific variant 2020 ·Orphanet Journal of Rare Diseases ·Dana Šafka Brožková, Lukáš Varga, (unknown), (unknown), Martina Škopková, Andrea Šoltýsová, Andrej Ficek, (unknown), (unknown), Daniela Gašperíková, Pavel Seeman	4
7	Novel SCN1A variants in Dravet syndrome and evaluating a wide approach of patient selection 2016 ·General Physiology and Biophysics ·(unknown), Andrea Šoltýsová, Miriam Kolníková, (unknown), Denisa Ilenčíková, Andrej Ficek, Ján Radvánszky, Ľudevít Kádaši	4
8	MARVELD2 (DFNB49) Mutations in the Hearing Impaired Central European Roma Population - Prevalence, Clinical Impact and the Common Origin 2015 ·PLoS ONE ·(unknown), Andrea Šoltýsová, Lukáš Varga, (unknown), Andrej Ficek, Miloslava Hučková, (unknown), Dana Šafka Brožková, Saima Anwar, Judit Bene, (unknown), (unknown), Zubair M. Ahmed, Pavel Seeman, Béla Melegh, Milan Profant, I Klimeś, Saima Riazuddin, Ľudevít Kádaši, Daniela Gašperíková	16
9	Bacterial Communities in Rhizosphere of Maize Studied by T-RFLP 2014 ·SHILAP Revista de lepidopterología ·(unknown), Andrej Ficek, Daniel Mihálik, (unknown), (unknown), Hana Drahovská, Ján Kraic	1
10	Phenylalanine hydroxylase deficiency in the Slovak population: Genotype–phenotype correlations and genotype-based predictions of BH4-responsiveness 2013 ·Gene ·(unknown), Andrej Ficek, Ján Radvánszky, Andrea Šoltýsová, (unknown), (unknown), (unknown), Ľudevít Kádaši	33
11	Mental rotation in intellectually gifted boys is affected by the androgen receptor CAG repeat polymorphism 2013 ·Neuropsychologia ·Jaroslava Durdiaková, Silvia Lakatošová, (unknown), (unknown), Andrej Ficek, Daniela Ostatníková, Peter Celec	22
12	Repeat-Primed Polymerase Chain Reaction in Myotonic Dystrophy Type 2 Testing 2011 ·Genetic Testing and Molecular Biomarkers ·(unknown), Andrej Ficek, Ľudevít Kádaši	10
13	Effect of Unexpected Sequence Interruptions to Conventional PCR and Repeat Primed PCR in Myotonic Dystrophy Type 1 Testing 2011 ·Diagnostic Molecular Pathology ·(unknown), Andrej Ficek, Gabriel Minárik, Roland Pálffy, Ľudevít Kádaši	33
14	Upgrading molecular diagnostics of myotonic dystrophies: Multiplexing for simultaneous characterization of the DMPK and ZNF9 repeat motifs 2011 ·Molecular and Cellular Probes ·(unknown), Andrej Ficek, Ľudevít Kádaši	20
15	Polymorphisms of candidate genes in Slovak autistic patients 2010 ·Psychiatric Genetics ·(unknown), (unknown), Andrej Ficek, Peter Celec, (unknown), Daniela Ostatníková	40
16	High-resolution melting analysis for genotyping of the myotonic dystrophy type 1 associated Alu insertion/deletion polymorphism 2009 ·Analytical Biochemistry ·(unknown), (unknown), (unknown), Gabriel Minárik, Andrej Ficek, Ľudevít Kádaši	16
17	Identification of the deletions in the UGT1A1 gene of the patients with Crigler-Najjar syndrome type I from Slovakia. 2007 ·PubMed ·Iveta Zmetakova, (unknown), Gabriel Minárik, Andrej Ficek, H Poláková, Eva Feráková, Ľudevít Kádaši	3
18	Variability in occurrence of multiple prophage genes inSalmonellaTyphimurium strains isolated in Slovak Republic 2007 ·FEMS Microbiology Letters ·Hana Drahovská, (unknown), Tomáš Szemes, Andrej Ficek, (unknown), (unknown), (unknown)	15
19	RNA-based mutation analysis identifies an unusual MSH6 splicing defect and circumvents PMS2 pseudogene interference 2007 ·Human Mutation ·Julia Etzler, Andreas Peyrl, Andrea Zaťková, Hans‐Ulrich Schildhaus, Andrej Ficek, Sabine Merkelbach‐Bruse, (unknown), Andishe Attarbaschi, Johannes A. Hainfellner, (unknown), Ludwine Messiaen, Irene Slavc, Katharina Wimmer	54
20	High frequency of GJB2 mutation W24X among Slovak Romany (Gypsy) patients with non-syndromic hearing loss (NSHL). 2003 ·PubMed ·Gabriel Minárik, V. Ferák, Eva Feráková, Andrej Ficek, H Poláková, Ľudevít Kádaši	59

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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