V. Ferák

2.0k total citations
21 papers, 937 citations indexed

About

V. Ferák is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, V. Ferák has authored 21 papers receiving a total of 937 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Ophthalmology. Recurrent topics in V. Ferák's work include Metabolism and Genetic Disorders (4 papers), Forensic and Genetic Research (4 papers) and Glaucoma and retinal disorders (4 papers). V. Ferák is often cited by papers focused on Metabolism and Genetic Disorders (4 papers), Forensic and Genetic Research (4 papers) and Glaucoma and retinal disorders (4 papers). V. Ferák collaborates with scholars based in Slovakia, United States and Switzerland. V. Ferák's co-authors include Eva Feráková, L Kádasi, A Genĉík, Martina Plášilová, H Poláková, Mansoor Sarfarazi, Ivaylo Stoilov, Toomas Kivisild, Jüri Parik and Richard Villems and has published in prestigious journals such as Current Biology, The American Journal of Human Genetics and Journal of Medical Genetics.

In The Last Decade

V. Ferák

21 papers receiving 887 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
V. Ferák Slovakia 11 442 305 222 139 102 21 937
Missy Dixon United States 6 430 1.0× 361 1.2× 71 0.3× 12 0.1× 20 0.2× 8 839
P Aula Finland 11 292 0.7× 615 2.0× 40 0.2× 13 0.1× 219 2.1× 13 936
Olga Derbeneva United States 15 461 1.0× 1.0k 3.4× 35 0.2× 15 0.1× 412 4.0× 21 1.5k
Patcharee Lertrit Thailand 17 131 0.3× 625 2.0× 87 0.4× 28 0.2× 254 2.5× 41 770
A. Adam Israel 16 226 0.5× 277 0.9× 23 0.1× 37 0.3× 110 1.1× 41 966
Nance We United States 12 185 0.4× 205 0.7× 20 0.1× 6 0.0× 14 0.1× 38 498
Olga L. Posukh Russia 13 421 1.0× 303 1.0× 4 0.0× 12 0.1× 6 0.1× 58 846
J.-M. Lalouel United States 16 334 0.8× 377 1.2× 25 0.1× 12 0.1× 21 0.2× 54 859
Denis Pierron France 15 160 0.4× 268 0.9× 5 0.0× 5 0.0× 42 0.4× 28 533
Ellen E. Quillen United States 11 218 0.5× 177 0.6× 4 0.0× 14 0.1× 18 0.2× 29 577

Countries citing papers authored by V. Ferák

Since Specialization
Citations

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

Fields of papers citing papers by V. Ferák

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of V. Ferák

This figure shows the co-authorship network connecting the top 25 collaborators of V. Ferák. A scholar is included among the top collaborators of V. Ferák 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 V. Ferák. V. Ferák 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.
Ferák, V., et al.. (2018). Population genetic data for 16 STR loci in Slovakia. Legal Medicine. 34. 36–40. 1 indexed citations
2.
Rootsi, Siiri, Lev A. Zhivotovsky, Marián Baldovič, et al.. (2006). A counter-clockwise northern route of the Y-chromosome haplogroup N from Southeast Asia towards Europe. European Journal of Human Genetics. 15(2). 204–211. 120 indexed citations
3.
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
4.
Hollox, Edward J., Mark Poulter, V. Ferák, et al.. (2001). Lactase Haplotype Diversity in the Old World. The American Journal of Human Genetics. 68(1). 160–172. 125 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.
Kivisild, Toomas, Michael J. Bamshad, Katrin Kaldma, et al.. (1999). Deep common ancestry of Indian and western-Eurasian mitochondrial DNA lineages. Current Biology. 9(22). 1331–1334. 209 indexed citations
8.
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
9.
Varon, Raymonda, Manfred Stuhrmann, Milan Maçek, et al.. (1995). Pancreatic insufficiency and pulmonary disease in German and Slavic cystic fibrosis patients with the R347P mutation. Human Mutation. 6(3). 219–225. 9 indexed citations
10.
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
11.
Ferák, V., et al.. (1994). Population Genetic Study in Gypsies (Roms) from Slovakia: Distribution of Blood Group Genetie Markers.. Anthropological Science. 102(4). 409–419. 3 indexed citations
12.
Gécz, Jozef, et al.. (1993). TaqI Digestion of PCR Product Increases the Informativity of St14 Vntr for the Diagnosis of Hemophilia A. Disease Markers. 11(2-3). 139–141. 1 indexed citations
13.
Kádaši, Ľudevít, et al.. (1992). Deletion ΔF508 and haplotype analysis of CFTR gene region in Slovak CF patients. Human Genetics. 89(3). 305–306. 3 indexed citations
14.
Genĉík, A, et al.. (1982). Population genetical aspects of primary congenital glaucoma. I. Incidence, prevalence, gene frequency, and age of onset. Human Genetics. 61(3). 193–197. 81 indexed citations
15.
Ferák, V., et al.. (1982). Population genetic aspects of primary congenital glaucoma. II. Fitness, parental consanguinity, founder effect. Human Genetics. 61(3). 198–200. 11 indexed citations
16.
Ferák, V., et al.. (1981). Are population-genetic mechanisms responsible for clustering of cases of Creutzfeldt-Jakob disease?. BMJ. 282(6263). 521.2–522. 6 indexed citations
17.
Ferák, V., et al.. (1980). Genetic distances, geographic distances and migration between four villages of a single region in Slovakia. Journal of Human Evolution. 9(7). 573–581. 4 indexed citations
18.
Ferák, V., et al.. (1969). Haptoglobin Types in Gypsies from Slovakia (Czechoslovakia). Human Heredity. 19(5). 480–485. 11 indexed citations
19.
Ferák, V., et al.. (1968). Endogamy, exogamy, and stature. Eugenics Quarterly. 15(4). 273–276. 9 indexed citations
20.
Ferák, V., et al.. (1965). Genetik der Ataxie - Teleangiectasie. Acta geneticae medicae et gemellologiae. 14(1). 57–72. 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.

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