Libor Kozák

1.1k total citations
37 papers, 769 citations indexed

About

Libor Kozák is a scholar working on Molecular Biology, Clinical Biochemistry and Surgery. According to data from OpenAlex, Libor Kozák has authored 37 papers receiving a total of 769 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 11 papers in Clinical Biochemistry and 9 papers in Surgery. Recurrent topics in Libor Kozák's work include Metabolism and Genetic Disorders (11 papers), Amino Acid Enzymes and Metabolism (5 papers) and Cholesterol and Lipid Metabolism (5 papers). Libor Kozák is often cited by papers focused on Metabolism and Genetic Disorders (11 papers), Amino Acid Enzymes and Metabolism (5 papers) and Cholesterol and Lipid Metabolism (5 papers). Libor Kozák collaborates with scholars based in Czechia, Italy and United States. Libor Kozák's co-authors include Marek Borský, Giovanni Neri, Pietro Chiurazzi, Jin Ho Yoon, Anjan Thakurta, Ravi Dhar, Viera Kuhrová, František Foret, Maurizio Genuardi and David T. Croke and has published in prestigious journals such as Journal of Biological Chemistry, The EMBO Journal and Molecular Biology of the Cell.

In The Last Decade

Libor Kozák

34 papers receiving 752 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Libor Kozák Czechia	17	333	209	158	150	110	37	769
Ching‐Wan Lam Hong Kong	14	237 0.7×	77 0.4×	76 0.5×	95 0.6×	50 0.5×	32	593
Shanti Balasubramaniam Australia	17	487 1.5×	248 1.2×	80 0.5×	134 0.9×	40 0.4×	39	926
Ben Pode‐Shakked Israel	15	330 1.0×	85 0.4×	73 0.5×	172 1.1×	30 0.3×	54	620
Marianne Grüneberg Germany	14	335 1.0×	97 0.5×	66 0.4×	91 0.6×	21 0.2×	30	553
T. Ohura Japan	15	495 1.5×	543 2.6×	41 0.3×	93 0.6×	22 0.2×	33	959
Janine Reunert Germany	20	507 1.5×	90 0.4×	76 0.5×	115 0.8×	21 0.2×	45	880
Brian M. Clancy United States	13	537 1.6×	137 0.7×	33 0.2×	51 0.3×	26 0.2×	17	881
Jitka Sokolová Czechia	17	316 0.9×	232 1.1×	29 0.2×	45 0.3×	8 0.1×	33	900
Parvin Justice United States	14	219 0.7×	140 0.7×	39 0.2×	150 1.0×	6 0.1×	36	639
Annette L. Regec United States	13	328 1.0×	49 0.2×	36 0.2×	24 0.2×	34 0.3×	18	560

Countries citing papers authored by Libor Kozák

Since Specialization

Citations

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

Fields of papers citing papers by Libor Kozák

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Libor Kozák

This figure shows the co-authorship network connecting the top 25 collaborators of Libor Kozák. A scholar is included among the top collaborators of Libor Kozák 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 Libor Kozák. Libor Kozák 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

Kozák, Libor, et al.. (2017). Dynamics of physical development of young schoolchildren in Lviv.. Medicni perspektivi. 21(4). 116–122.

Kozák, Libor, et al.. (2017). Peculiarities of Physical Development of Primary School Age Children in Lviv. 2017(1). 44–49.

Oláh, Anna V., et al.. (2009). A patient with Smith–Lemli–Opitz syndrome: novel mutation of the DHCR7 gene and effects of therapy with simvastatin and cholesterol supplement. European Journal of Pediatrics. 169(1). 121–123. 22 indexed citations

Fajkusová, Lenka, et al.. (2008). MLPA in differential diagnostics of congenital adrenalhyperplasia. 1 indexed citations

Kozák, Libor, et al.. (2007). Analysis of point mutations in the SMN1 gene in SMA patients bearing a single SMN1 copy. Neuromuscular Disorders. 17(6). 476–481. 30 indexed citations

Petrášek, Jan, M Jirsa, Jan Šperl, et al.. (2006). Revised King's College score for liver transplantation in adult patients with Wilson's disease. Liver Transplantation. 13(1). 55–61. 40 indexed citations

Thakurta, Anjan, et al.. (2005). Homolog of BRCA2‐interacting Dss1p and Uap56p link Mlo3p and Rae1p for mRNA export in fission yeast. The EMBO Journal. 24(14). 2512–2523. 40 indexed citations

Kozák, Libor, et al.. (2005). Molecular Genetic Analysis of SLC3A1 and SLC7A9 Genes in Czech and Slovak Cystinuric Patients. Annals of Human Genetics. 69(5). 501–507. 23 indexed citations

Borský, Marek, et al.. (2005). Mutation analysis of the ATP7B gene and genotype/phenotype correlation in 227 patients with Wilson disease. Molecular Genetics and Metabolism. 86(1-2). 277–285. 107 indexed citations

10.

Kozák, Libor, et al.. (2004). Capillary electrophoresis and mass spectrometry for screening of metabolic disorders in newborns. Electrophoresis. 25(10-11). 1447–1456. 26 indexed citations

11.

Thakurta, Anjan, William Whalen, Jin Ho Yoon, et al.. (2002). Crp79p, Like Mex67p, Is an Auxiliary mRNA Export Factor in Schizosaccharomyces pombe. Molecular Biology of the Cell. 13(8). 2571–2584. 8 indexed citations

12.

Kozák, Libor, Jin Ho Yoon, Zuben E. Sauna, et al.. (2002). Elf1p, a Member of the ABC Class of ATPases, Functions as a mRNA Export Factor in Schizosacchromyces pombe. Journal of Biological Chemistry. 277(37). 33580–33589. 22 indexed citations

13.

Kuhrová, Viera, et al.. (2001). Spectrum of low density lipoprotein receptor mutations in Czech hypercholesterolemic patients. Human Mutation. 18(3). 253–253. 24 indexed citations

14.

Kuhrová, Viera, et al.. (2001). Spectrum of low density lipoprotein receptor mutations in Czech hypercholesterolemic patients. Human Mutation. 19(1). 80–80. 14 indexed citations

15.

Trbušek, Martin, et al.. (2001). Identification of three novel mutations in the PHKA2 gene in Czech patients with X‐linked liver glycogenosis. Journal of Inherited Metabolic Disease. 24(1). 85–87. 12 indexed citations

16.

Tyfield, Linda, Juergen Reichardt, David T. Croke, et al.. (1999). Classical galactosemia and mutations at the galactose-1-phosphate uridyl transferase (GALT) gene. Human Mutation. 13(6). 417–430. 104 indexed citations

17.

Chiurazzi, Pietro, Maurizio Genuardi, Libor Kozák, et al.. (1996). Fragile X founder chromosomes in Italy: A few initial events and possible explanation for their heterogeneity. American Journal of Medical Genetics. 64(1). 209–215. 36 indexed citations

18.

Chiurazzi, Pietro, Libor Kozák, & Giovanni Neri. (1994). Unstable triplets and their mutational mechanism: Size reduction of the CGG repeat vs. germline mosaicism in the fragile X syndrome. American Journal of Medical Genetics. 51(4). 517–521. 26 indexed citations

19.

Chiurazzi, Pietro, Esther de Graaff, Jessica M.Y. Ng, et al.. (1994). No apparent involvement of the FMR1 gene in five patients with phenotypic manifestations of the fragile X syndrome. American Journal of Medical Genetics. 51(4). 309–314. 14 indexed citations

20.

Apold, Jaran, Hans Geir Eiken, Elisabeth Svensson, et al.. (1993). The phenylketonuria G272X haplotype 7 mutation in European populations. Human Genetics. 92(2). 107–9. 7 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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