Eva Feráková

518 total citations
13 papers, 395 citations indexed

About

Eva Feráková is a scholar working on Clinical Biochemistry, Molecular Biology and Genetics. According to data from OpenAlex, Eva Feráková has authored 13 papers receiving a total of 395 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Clinical Biochemistry, 5 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in Eva Feráková's work include Metabolism and Genetic Disorders (6 papers), Glaucoma and retinal disorders (2 papers) and Amino Acid Enzymes and Metabolism (1 paper). Eva Feráková is often cited by papers focused on Metabolism and Genetic Disorders (6 papers), Glaucoma and retinal disorders (2 papers) and Amino Acid Enzymes and Metabolism (1 paper). Eva Feráková collaborates with scholars based in Slovakia, United States and Spain. Eva Feráková's co-authors include V. Ferák, L Kádasi, H Poláková, Martina Plášilová, Ivaylo Stoilov, Mansoor Sarfarazi, Andrea Zaťková, Ľudevít Kádaši, Gabriel Minárik and Andrej Ficek and has published in prestigious journals such as The American Journal of Human Genetics, Journal of Medical Genetics and Human Genetics.

In The Last Decade

Eva Feráková

12 papers receiving 378 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eva Feráková Slovakia 8 210 139 116 79 58 13 395
John M. Strother United States 4 247 1.2× 239 1.7× 55 0.5× 92 1.2× 3 0.1× 6 420
K.–G. Schmidt Germany 13 185 0.9× 364 2.6× 14 0.1× 172 2.2× 6 0.1× 28 540
Clive N. Graymore Mexico 13 330 1.6× 169 1.2× 28 0.2× 91 1.2× 3 0.1× 33 517
T.K. Van Ells United States 3 188 0.9× 268 1.9× 54 0.5× 124 1.6× 2 0.0× 4 397
Darya V. Telegina Russia 12 248 1.2× 182 1.3× 22 0.2× 51 0.6× 2 0.0× 33 431
Yanling Su China 8 252 1.2× 232 1.7× 11 0.1× 61 0.8× 2 0.0× 14 390
Cynthia A. Koutz United States 14 261 1.2× 93 0.7× 7 0.1× 42 0.5× 4 0.1× 17 409
J. Harned United States 11 205 1.0× 63 0.5× 16 0.1× 32 0.4× 16 366
Hyang-Sook Kim South Korea 11 222 1.1× 13 0.1× 9 0.1× 7 0.1× 24 0.4× 26 366
Xiaoxia Zeng China 5 185 0.9× 234 1.7× 44 0.4× 79 1.0× 11 379

Countries citing papers authored by Eva Feráková

Since Specialization
Citations

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

Fields of papers citing papers by Eva Feráková

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eva Feráková

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

All Works

13 of 13 papers shown
1.
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
2.
Poláková, H, Gabriel Minárik, Eva Feráková, et al.. (2007). Detection of His1069Gln mutation in Wilson disease by bidirectional PCR amplification of specific alleles (BI-PASA) test.. PubMed. 26(2). 91–6. 8 indexed citations
3.
Zaťková, Andrea, et al.. (2003). Rapid detection methods for five HGO gene mutations causing alkaptonuria. Clinical Genetics. 63(2). 145–149. 20 indexed citations
4.
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
5.
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
6.
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 inHGOInvolving Different Mutational Hot Spots. The American Journal of Human Genetics. 67(5). 1333–1339. 25 indexed citations
7.
Bernasovská, Jarmila, et al.. (1999). Romany Population Data on Two Loci (D1S80, Apo BII) from East Slovakia. Journal of Human Ecology. 10(5-6). 341–347.
8.
Plášilová, Martina, Ivaylo Stoilov, Mansoor Sarfarazi, et al.. (1999). Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucoma. Journal of Medical Genetics. 36(4). 290–294. 143 indexed citations
9.
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
10.
Richards, Robert I., Joanna Crawford, Kouji Narahara, et al.. (1996). Dynamic mutation loci: allele distributions in different populations. Annals of Human Genetics. 60(5). 391–400. 17 indexed citations
11.
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
12.
Kádasi, L, et al.. (1994). Distribution of ApoBII, MCT118 (D1S80), YNZ22 (D17S30), and COL2A1 Amp-FLPs (amplified fragment length polymorphisms) in Caucasoid population of Slovakia.. PubMed. 8(2). 121–7. 3 indexed citations
13.
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

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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by John M. Strother Breakdown of academic impact, for papers by K.–G. Schmidt Breakdown of academic impact, for papers by Clive N. Graymore Breakdown of academic impact, for papers by T.K. Van Ells Breakdown of academic impact, for papers by Darya V. Telegina Breakdown of academic impact, for papers by Yanling Su Breakdown of academic impact, for papers by Cynthia A. Koutz Breakdown of academic impact, for papers by J. Harned Breakdown of academic impact, for papers by Hyang-Sook Kim Breakdown of academic impact, for papers by Xiaoxia Zeng
Rankless by CCL
2026