Marián Baldovič

768 total citations
20 papers, 362 citations indexed

About

Marián Baldovič is a scholar working on Genetics, Archeology and Molecular Biology. According to data from OpenAlex, Marián Baldovič has authored 20 papers receiving a total of 362 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 8 papers in Archeology and 4 papers in Molecular Biology. Recurrent topics in Marián Baldovič's work include Forensic Anthropology and Bioarchaeology Studies (8 papers), Forensic and Genetic Research (6 papers) and Yersinia bacterium, plague, ectoparasites research (3 papers). Marián Baldovič is often cited by papers focused on Forensic Anthropology and Bioarchaeology Studies (8 papers), Forensic and Genetic Research (6 papers) and Yersinia bacterium, plague, ectoparasites research (3 papers). Marián Baldovič collaborates with scholars based in Slovakia, Czechia and Estonia. Marián Baldovič's co-authors include Э. К. Хуснутдинова, Toomas Kivisild, Peter A. Underhill, Siiri Rootsi, Ildus Kutuev, Alice Lin, Richard Villems, Jacques Chiaroni, Julie Di Cristofaro and Mari Järve and has published in prestigious journals such as American Journal of Physical Anthropology, European Journal of Human Genetics and Mitochondrion.

In The Last Decade

Marián Baldovič

17 papers receiving 337 citations

Peers

Marián Baldovič

GENET

ARCHE

PALEO

PRM

Avinash Arvind Rasalkar India

V. N. Kharkov Russia

Tanya M. Simms United States

Sheyla Mirabal United States

Ralph Garcia‐Bertrand United States

Rafael Bisso‐Machado Brazil

Óscar Acosta Peru

Ghania Hariti Algeria

Rifat Hadžiselimović Bosnia and Herzegovina

Marina Gubina Russia

Avinash Arvind Rasalkar India

Marián Baldovič

216 ×0.8

GENET

89 ×1.1

ARCHE

143 ×2.0

30 ×1.0

PALEO

10 ×0.8

PRM

Citations per year, relative to Marián Baldovič Marián Baldovič (= 1×) peers Avinash Arvind Rasalkar

Countries citing papers authored by Marián Baldovič

Since Specialization

Citations

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

Fields of papers citing papers by Marián Baldovič

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marián Baldovič

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

Baldovič, Marián, et al.. (2023). Population genetic analysis of 12 X-STR markers in Slovakia. Annals of Human Biology. 50(1). 431–435. 1 indexed citations

Pastorek, Michal, Július Hodosy, Katarı́na Šebeková, et al.. (2023). Mitochondrial DNA variability and Covid-19 in the Slovak population. Mitochondrion. 75. 101827–101827. 5 indexed citations

Beňuš, Radoslav, et al.. (2023). Pilot study of correlation of selected genetic factors with cribra orbitalia in individuals from a medieval population from Slovakia. International Journal of Paleopathology. 41. 1–7. 2 indexed citations

Baldovič, Marián, et al.. (2022). Unusual find of osteolytic lesion on skeleton from the Middle Bronze Age—Possible case of peritoneal abscess. International Journal of Osteoarchaeology. 32(4). 923–931.

Baldovič, Marián, et al.. (2022). A unique find of juvenile cleft lip and palate in the post-mediaeval impious burial of two males in Dunajská Streda, Slovakia. Archaeological and Anthropological Sciences. 14(4). 1 indexed citations

Baldovič, Marián, et al.. (2022). Mutational analysis of 16 STR markers in the Slovak population. Annals of Human Biology. 49(5-6). 248–253.

Konečný, M, et al.. (2021). The results of multigene panel sequencing in Slovak HBOC families. Neoplasma. 68(3). 652–664.

Zikmund, Tomáš, et al.. (2018). Serious chronic disease of the cervical spine and trauma in a young female from the middle ages (Czech Republic). International Journal of Paleopathology. 24. 185–196. 2 indexed citations

Baldovič, Marián, et al.. (2018). Detection of mitochondrial haplogroups in a small avar‐slavic population from the eigth–ninth century AD. American Journal of Physical Anthropology. 165(3). 536–553. 10 indexed citations

10.

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

11.

Daňková, Zuzana, et al.. (2016). Genetic and Environmental Biomarkers Associated with Triglyceride Levels in Two Groups of Slovak Women. Genetic Testing and Molecular Biomarkers. 21(1). 46–52. 3 indexed citations

12.

Baldovič, Marián, et al.. (2016). Molecular detection of Mycobacterium tuberculosis complex in the 8th century skeletal remains from the territory of Slovakia. Biologia. 71(6). 613–619. 1 indexed citations

13.

Baldovič, Marián, et al.. (2013). Analysis of Leucine-rich repeat kinase 2 (LRRK2) and Parkinson protein 2 (parkin, PARK2) genes mutations in Slovak Parkinson disease patients. General Physiology and Biophysics. 32(1). 55–66. 5 indexed citations

14.

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

15.

Myres, Natalie M., Siiri Rootsi, Alice Lin, et al.. (2010). A major Y-chromosome haplogroup R1b Holocene era founder effect in Central and Western Europe. European Journal of Human Genetics. 19(1). 95–101. 169 indexed citations

16.

Kovács, László, et al.. (2010). Elevated immunoglobulin D levels in children with PFAPA syndrome.. PubMed. 31(6). 743–6. 11 indexed citations

17.

Baldovič, Marián, et al.. (2008). A database of mitochondrial DNA hypervariable regions I and II sequences of individuals from Slovakia. Forensic Science International Genetics. 2(4). e53–e59. 11 indexed citations

18.

Kolesár, Peter, Gabriel Minárik, Marián Baldovič, et al.. (2008). Mutation analysis of the CFTR gene in Slovak cystic fibrosis patients by DHPLC and subsequent sequencing: identification of four novel mutations.. PubMed. 27(4). 299–305. 7 indexed citations

19.

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

20.

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

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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