Petr Pecina

3.2k total citations
49 papers, 2.3k citations indexed

About

Petr Pecina is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, Petr Pecina has authored 49 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Molecular Biology, 16 papers in Clinical Biochemistry and 6 papers in Physiology. Recurrent topics in Petr Pecina's work include Mitochondrial Function and Pathology (41 papers), ATP Synthase and ATPases Research (32 papers) and Metabolism and Genetic Disorders (16 papers). Petr Pecina is often cited by papers focused on Mitochondrial Function and Pathology (41 papers), ATP Synthase and ATPases Research (32 papers) and Metabolism and Genetic Disorders (16 papers). Petr Pecina collaborates with scholars based in Czechia, United States and United Kingdom. Petr Pecina's co-authors include J Houštěk, Maik Hüttemann, Icksoo Lee, Jeffrey W. Doan, Alena Pecinová, Tomáš Mráček, Valerian E. Kagan, Lobelia Samavati, Thomas H. Sanderson and J Zeman and has published in prestigious journals such as Blood, PLoS ONE and Biochemistry.

In The Last Decade

Petr Pecina

47 papers receiving 2.3k citations

Peers

Petr Pecina

PHYSI

Johan Palmfeldt Denmark

Edwin J. Vazquez United States

Irina V. Perevoshchikova United States

Lydie Plecitá‐Hlavatá Czechia

Gillian Hughes New Zealand

Casey L. Quinlan United States

Małgorzata Tokarska-Schlattner France

Gaetano Villani Italy

Marcella Canton Italy

Roberta Menabò Italy

Johan Palmfeldt Denmark

Petr Pecina

1.5k ×0.9

267 ×0.6

PHYSI

304 ×0.9

212 ×0.9

126 ×0.6

Citations per year, relative to Petr Pecina Petr Pecina (= 1×) peers Johan Palmfeldt

Countries citing papers authored by Petr Pecina

Since Specialization

Citations

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

Fields of papers citing papers by Petr Pecina

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Petr Pecina

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

Pecina, Petr, Vilma Kaplanová, Jan Šilhavý, et al.. (2024). Haplotype variability in mitochondrial rRNA predisposes to metabolic syndrome. Communications Biology. 7(1). 1116–1116. 2 indexed citations

Marković, Aleksandra Pavlović, Miroslava Šimáková, Petr Mlejnek, et al.. (2022). Genetic Complementation of ATP Synthase Deficiency Due to Dysfunction of TMEM70 Assembly Factor in Rat. Biomedicines. 10(2). 276–276. 4 indexed citations

Pak, Oleg, Fenja Knoepp, Luca Giordano, et al.. (2022). Mitochondrial oxygen sensing of acute hypoxia in specialized cells - Is there a unifying mechanism?. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1863(8). 148911–148911. 14 indexed citations

Reguera, David Pajuelo, Marek Vrbacký, Erika Fernández‐Vizarra, et al.. (2021). Loss of COX4I1 Leads to Combined Respiratory Chain Deficiency and Impaired Mitochondrial Protein Synthesis. Cells. 10(2). 369–369. 31 indexed citations

Reguera, David Pajuelo, et al.. (2020). Role of cytochrome c oxidase nuclear-encoded subunits in health and disease. Physiological Research. 69(6). 947–965. 33 indexed citations

Pecina, Petr, et al.. (2018). Role of the mitochondrial ATP synthase central stalk subunits γ and δ in the activity and assembly of the mammalian enzyme. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1859(5). 374–381. 17 indexed citations

Pecina, Petr, et al.. (2018). Cytochrome c oxidase subunit 4 isoform switch results in modulation of oxygen affinity. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1859. e21–e21. 1 indexed citations

Pecinová, Alena, Z Drahota, Petr Pecina, et al.. (2017). Pleiotropic Effects of Biguanides on Mitochondrial Reactive Oxygen Species Production. Oxidative Medicine and Cellular Longevity. 2017(1). 7038603–7038603. 21 indexed citations

Pecina, Petr, Hana Nůsková, Marek Vrbacký, et al.. (2016). Tissue- and species-specific differences in cytochrome c oxidase assembly induced by SURF1 defects. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1862(4). 705–715. 22 indexed citations

10.

Zhang, Kezhong, Guohui Wang, Xuebao Zhang, et al.. (2016). COX7AR is a Stress-inducible Mitochondrial COX Subunit that Promotes Breast Cancer Malignancy. Scientific Reports. 6(1). 31742–31742. 33 indexed citations

11.

Hejzlarová, Kateřina, Tomáš Mráček, Marek Vrbacký, et al.. (2014). Nuclear Genetic Defects of Mitochondrial ATP Synthase. Physiological Research. 63(Suppl 1). S57–S71. 36 indexed citations

12.

Mráček, Tomáš, Hana Nůsková, Marek Vrbacký, et al.. (2013). High Molecular Weight Forms of Mammalian Respiratory Chain Complex II. PLoS ONE. 8(8). e71869–e71869. 7 indexed citations

13.

Sanderson, Thomas H., Gargi Mahapatra, Petr Pecina, et al.. (2013). Cytochrome c Is Tyrosine 97 Phosphorylated by Neuroprotective Insulin Treatment. PLoS ONE. 8(11). e78627–e78627. 50 indexed citations

14.

Pecina, Petr, et al.. (2012). Adaptation of respiratory chain biogenesis to cytochrome c oxidase deficiency caused by SURF1 gene mutations. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1822(7). 1114–1124. 26 indexed citations

15.

Pecina, Petr, Hana Nůsková, Vendula Havlíčková, & J Houštěk. (2012). Role of the mitochondrial ATP synthase central stalk subunits γ and δ in the activity and assembly of the mammalian enzyme. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1817. S20–S21. 3 indexed citations

16.

Hüttemann, Maik, Petr Pecina, Thomas H. Sanderson, et al.. (2011). The multiple functions of cytochrome c and their regulation in life and death decisions of the mammalian cell: From respiration to apoptosis. Mitochondrion. 11(3). 369–381. 428 indexed citations

17.

Hüttemann, Maik, Scott E. Klewer, Icksoo Lee, et al.. (2011). Mice deleted for heart-type cytochrome c oxidase subunit 7a1 develop dilated cardiomyopathy. Mitochondrion. 12(2). 294–304. 38 indexed citations

18.

Lee, Icksoo, Arthur R. Salomon, Kebing Yu, et al.. (2009). Chapter 11 Isolation of Regulatory‐Competent, Phosphorylated Cytochrome c Oxidase. Methods in enzymology on CD-ROM/Methods in enzymology. 457. 193–210. 38 indexed citations

19.

Houštěk, J, et al.. (2006). Mitochondrial diseases and genetic defects of ATP synthase. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1757(9-10). 1400–1405. 101 indexed citations

20.

Pecina, Petr, Subir Roy Chowdhury, Z Drahota, et al.. (2003). Functional alteration of cytochrome c oxidase by SURF1 mutations in Leigh syndrome. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1639(1). 53–63. 46 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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