H Poláková

600 total citations
29 papers, 450 citations indexed

About

H Poláková is a scholar working on Molecular Biology, Clinical Biochemistry and Cancer Research. According to data from OpenAlex, H Poláková has authored 29 papers receiving a total of 450 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Clinical Biochemistry and 7 papers in Cancer Research. Recurrent topics in H Poláková's work include Metabolism and Genetic Disorders (7 papers), Carcinogens and Genotoxicity Assessment (6 papers) and Cystic Fibrosis Research Advances (4 papers). H Poláková is often cited by papers focused on Metabolism and Genetic Disorders (7 papers), Carcinogens and Genotoxicity Assessment (6 papers) and Cystic Fibrosis Research Advances (4 papers). H Poláková collaborates with scholars based in Slovakia, Russia and Spain. H Poláková's co-authors include Eva Feráková, V. Ferák, Ľudevít Kádaši, Mária Vargová, L Kádasi, Andrea Zaťková, Gabriel Minárik, Andrej Ficek, Santiago Rodrı́guez de Córdoba and Daniel Beltrán Valero de Bernabé and has published in prestigious journals such as Scientific Reports, The American Journal of Human Genetics and International Journal of Nanomedicine.

In The Last Decade

H Poláková

29 papers receiving 429 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
H Poláková Slovakia 11 221 153 60 57 54 29 450
D. T. Brown United Kingdom 9 677 3.1× 408 2.7× 55 0.9× 7 0.1× 5 0.1× 10 747
Helen Swalwell United Kingdom 11 407 1.8× 165 1.1× 18 0.3× 35 0.6× 9 0.2× 13 596
P.E. Peterson United States 13 297 1.3× 88 0.6× 27 0.5× 16 0.3× 2 0.0× 17 525
Ralf M. Zerbes Germany 12 819 3.7× 292 1.9× 14 0.2× 38 0.7× 7 0.1× 15 912
Juanjuan Zhang China 21 923 4.2× 312 2.0× 23 0.4× 42 0.7× 9 0.2× 60 1.0k
José L. Guevara United States 6 329 1.5× 19 0.1× 42 0.7× 22 0.4× 97 1.8× 7 571
Rajarshi Chakrabarti United States 12 504 2.3× 102 0.7× 27 0.5× 36 0.6× 7 0.1× 18 687
Elham Jaberi Iran 10 175 0.8× 34 0.2× 8 0.1× 29 0.5× 9 0.2× 16 347
Reetta Hinttala Finland 16 455 2.1× 219 1.4× 8 0.1× 37 0.6× 5 0.1× 49 653
Chen-Wei Tsai United States 11 516 2.3× 54 0.4× 25 0.4× 18 0.3× 11 0.2× 14 607

Countries citing papers authored by H Poláková

Since Specialization
Citations

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

Fields of papers citing papers by H Poláková

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of H Poláková

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

All Works

20 of 20 papers shown
1.
Samish, Ilan, et al.. (2017). A single residue controls electron transfer gating in photosynthetic reaction centers. Scientific Reports. 7(1). 44580–44580. 11 indexed citations
2.
Šoltýsová, Andrea, et al.. (2017). Comprehensive genetic study of cystic fibrosis in Slovak patients in 25 years of genetic diagnostics. The Clinical Respiratory Journal. 12(3). 1197–1206. 4 indexed citations
3.
Skopalík, Josef, Kateřina Poláková, Markéta Havrdová, et al.. (2014). Mesenchymal stromal cell labeling by new uncoated superparamagnetic maghemite nanoparticles in comparison with commercial Resovist – an initial in vitro study. International Journal of Nanomedicine. 9. 5355–5355. 35 indexed citations
4.
Baldovič, Marián, et al.. (2011). Mutation analysis of PMP22 in Slovak patients with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies. General Physiology and Biophysics. 30(4). 379–388. 2 indexed citations
5.
Poláková, H, et al.. (2011). Study of the effect of DNA polymorphisms in the mannose-binding lectin gene (MBL2) on disease severity in Slovak cystic fibrosis patients. General Physiology and Biophysics. 30(4). 373–378. 2 indexed citations
6.
Zaťková, Andrea, Tatiana Sedláčková, H Poláková, et al.. (2011). Identification of 11 Novel Homogentisate 1,2 Dioxygenase Variants in Alkaptonuria Patients and Establishment of a Novel LOVD-Based HGD Mutation Database. JIMD Reports. 4. 55–65. 43 indexed citations
7.
Zmetakova, Iveta, Gabriel Minárik, Andrej Ficek, et al.. (2007). Identification of the deletions in the UGT1A1 gene of the patients with Crigler-Najjar syndrome type I from Slovakia.. PubMed. 26(4). 306–10. 3 indexed citations
8.
Zaťková, Andrea, et al.. (2003). Rapid detection methods for five HGO gene mutations causing alkaptonuria. Clinical Genetics. 63(2). 145–149. 20 indexed citations
9.
Minárik, Gabriel, V. Ferák, Eva Feráková, et al.. (2003). High frequency of GJB2 mutation W24X among Slovak Romany (Gypsy) patients with non-syndromic hearing loss (NSHL).. PubMed. 22(4). 549–56. 59 indexed citations
10.
Poláková, H, Iveta Zmetakova, & Ľudevít Kádaši. (2003). Long distance PCR in detection of inversion mutations of F8C gene in hemophilia A patients.. PubMed. 22(2). 243–53. 12 indexed citations
11.
Zaťková, Andrea, Daniel Beltrán Valero de Bernabé, H Poláková, et al.. (2000). High Frequency of Alkaptonuria in Slovakia: Evidence for the Appearance of Multiple Mutations in HGO Involving Different Mutational Hot Spots. The American Journal of Human Genetics. 67(5). 1333–1339. 67 indexed citations
12.
Poláková, H, et al.. (1998). Factor VIII Gene Inversions in Haemophilia A Patients of Slovakia. Human Heredity. 48(1). 34–37. 5 indexed citations
13.
Plášilová, Martina, Eva Feráková, L Kádasi, et al.. (1998). Linkage of Autosomal Recessive Primary Congenital Glaucoma to the GLC3A Locus in Roms (Gypsies) from Slovakia. Human Heredity. 48(1). 30–33. 43 indexed citations
14.
Poláková, H, et al.. (1998). [Analysis of inversion in intron 22 of the factor F VIII:C gene in patients with hemophilia A in the Slovak population].. PubMed. 99(10). 538–42. 3 indexed citations
15.
Kádasi, L, H Poláková, Eva Feráková, et al.. (1995). PKU in Slovakia: mutation screening and haplotype analysis. Human Genetics. 95(1). 112–114. 4 indexed citations
16.
Feráková, Eva, et al.. (1992). A unique RFLP haplotype at the phenylalanine hydroxylase locus in Czechoslovak Gypsies with phenylketonuria.. PubMed. 2(2). 139–40. 3 indexed citations
17.
18.
Poláková, H, et al.. (1988). Analysis of chromosomes in peripheral blood lymphocytes of styrene-exposed workers. Mutation Research/Genetic Toxicology. 206(2). 167–169. 9 indexed citations
19.
Vargová, Mária, et al.. (1987). Monitoring of workers occupationally exposed to mankozeb. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 181(2). 318–318. 1 indexed citations
20.
Vargová, Mária, et al.. (1980). Evaluation of the mutagenic effect of the new fungicide trimorphamide. Mutation Research/Genetic Toxicology. 78(4). 361–367. 5 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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