Konstantin Khrapko

6.7k total citations · 2 hit papers
74 papers, 4.8k citations indexed

About

Konstantin Khrapko is a scholar working on Molecular Biology, Clinical Biochemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, Konstantin Khrapko has authored 74 papers receiving a total of 4.8k indexed citations (citations by other indexed papers that have themselves been cited), including 67 papers in Molecular Biology, 19 papers in Clinical Biochemistry and 13 papers in Cellular and Molecular Neuroscience. Recurrent topics in Konstantin Khrapko's work include Mitochondrial Function and Pathology (45 papers), Metabolism and Genetic Disorders (19 papers) and Genetic Neurodegenerative Diseases (13 papers). Konstantin Khrapko is often cited by papers focused on Mitochondrial Function and Pathology (45 papers), Metabolism and Genetic Disorders (19 papers) and Genetic Neurodegenerative Diseases (13 papers). Konstantin Khrapko collaborates with scholars based in United States, Russia and United Kingdom. Konstantin Khrapko's co-authors include Yevgenya Kraytsberg, William G. Thilly, Kevin S. King, Christine P. Donahue, Anna M. Krichevsky, Kenneth S. Kosik, Hilary A. Coller, Elena Kudryavtseva, Neil W. Kowall and Ann C. McKee and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Konstantin Khrapko

71 papers receiving 4.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A microRNA array reveals extensive regulation of microRNAs during brain development

2003 844 citations Konstantin Khrapko et al. profile →
Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neurons

2006 712 citations Yevgenya Kraytsberg, Elena Kudryavtseva et al. Nature Genetics profile →

Peers

Konstantin Khrapko

CMN

GENET

Robert N. Lightowlers United Kingdom

Ian Holt United Kingdom

Peter J. McKinnon United States

Ming Guo United States

Marc Hild United States

Ody C.M. Sibon Netherlands

Sabine Dietmann United Kingdom

Lynne Chantranupong United States

Christian Grimm Switzerland

Robert N. Lightowlers United Kingdom

Konstantin Khrapko

7.0k ×1.8

392 ×0.4

2.4k ×2.7

585 ×1.1

CMN

463 ×1.1

GENET

Citations per year, relative to Konstantin Khrapko Konstantin Khrapko (= 1×) peers Robert N. Lightowlers

Countries citing papers authored by Konstantin Khrapko

Since Specialization

Citations

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

Fields of papers citing papers by Konstantin Khrapko

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Konstantin Khrapko

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

Saparbaev, Murat, Bakhyt Matkarimov, Ilya Mazunin, et al.. (2025). Deciphering the Foundations of Mitochondrial Mutational Spectra: Replication-Driven and Damage-Induced Signatures Across Chordate Classes. Molecular Biology and Evolution. 42(2). 2 indexed citations

Annis, Sofia, et al.. (2023). Reanalysis of mtDNA mutations of human primordial germ cells (PGCs) reveals NUMT contamination and suggests that selection in PGCs may be positive. Mitochondrion. 74. 101817–101817. 3 indexed citations

Popadin, Konstantin, Konstantin Gunbin, Leonid Peshkin, et al.. (2022). Mitochondrial Pseudogenes Suggest Repeated Inter-Species Hybridization among Direct Human Ancestors. Genes. 13(5). 810–810. 9 indexed citations

Macdonald, J., Sofia Annis, Somak Ray, et al.. (2019). A nanoscale, multi-parametric flow cytometry-based platform to study mitochondrial heterogeneity and mitochondrial DNA dynamics. Communications Biology. 2(1). 258–258. 30 indexed citations

Safdar, Adeel, Sofia Annis, Yevgenya Kraytsberg, et al.. (2016). Amelioration of premature aging in mtDNA mutator mouse by exercise: the interplay of oxidative stress, PGC-1α, p53, and DNA damage. A hypothesis. Current Opinion in Genetics & Development. 38. 127–132. 34 indexed citations

Amabile, Giovanni, Robert S. Welner, César Nombela‐Arrieta, et al.. (2012). In vivo generation of transplantable human hematopoietic cells from induced pluripotent stem cells. Blood. 121(8). 1255–1264. 160 indexed citations

Guo, Xinhong, Elena Kudryavtseva, Natalya D. Bodyak, et al.. (2010). Mitochondrial DNA deletions in mice in men: Substantia nigra is much less affected in the mouse. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1797(6-7). 1159–1162. 18 indexed citations

Nicholas, Adeline K., João Pedro de Magalhães, Yevgenya Kraytsberg, et al.. (2010). Age-related gene-specific changes of A-to-I mRNA editing in the human brain. Mechanisms of Ageing and Development. 131(6). 445–447. 41 indexed citations

Zsurka, Gábor, Tatiana A. Kudina, Viktoriya Peeva, et al.. (2010). Distinct patterns of mitochondrial genome diversity in bonobos (Pan paniscus) and humans. BMC Evolutionary Biology. 10(1). 270–270. 22 indexed citations

10.

Kraytsberg, Yevgenya, et al.. (2009). Collection of Isolated Cells for Studying Mitochondrial DNA Mutations Within Individual Cells. Methods in molecular biology. 554. 315–327. 3 indexed citations

11.

Ekstrøm, Per Olaf, Konstantin Khrapko, Xiaocheng Li-Sucholeiki, Ian W. Hunter, & William G. Thilly. (2008). Analysis of mutational spectra by denaturing capillary electrophoresis. Nature Protocols. 3(7). 1153–1166. 27 indexed citations

12.

Khrapko, Konstantin & Jan Vijg. (2008). Mitochondrial DNA mutations and aging: devils in the details?. Trends in Genetics. 25(2). 91–98. 87 indexed citations

13.

Zsurka, Gábor, Kevin G. Hampel, Tatiana A. Kudina, et al.. (2007). Inheritance of Mitochondrial DNA Recombinants in Double-Heteroplasmic Families: Potential Implications for Phylogenetic Analysis. The American Journal of Human Genetics. 80(2). 298–305. 19 indexed citations

14.

Morozova, Nadya, Konstantin Khrapko, Jun Panee, et al.. (2007). Glutathione depletion in hippocampal cells increases levels of H and L ferritin and glutathione S‐transferase mRNAs. Genes to Cells. 12(5). 561–567. 15 indexed citations

15.

Zheng, Weiming, Konstantin Khrapko, Hilary A. Coller, William G. Thilly, & William C. Copeland. (2006). Origins of human mitochondrial point mutations as DNA polymerase γ-mediated errors. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 599(1-2). 11–20. 101 indexed citations

16.

Khrapko, Konstantin, et al.. (2006). Does premature aging of the mtDNA mutator mouse prove that mtDNA mutations are involved in natural aging?. Aging Cell. 5(3). 279–282. 65 indexed citations

17.

Kraytsberg, Yevgenya, Elena Kudryavtseva, Ann C. McKee, et al.. (2006). Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neurons. Nature Genetics. 38(5). 518–520. 712 indexed citations breakdown →

18.

Khrapko, Konstantin, Konstantin K. Ebralidse, & Yevgenya Kraytsberg. (2004). Where and When Do Somatic mtDNA Mutations Occur?. Annals of the New York Academy of Sciences. 1019(1). 240–244. 10 indexed citations

19.

Khrapko, Konstantin, et al.. (2003). Clonal expansions of mitochondrial genomes: implications for in vivo mutational spectra. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 522(1-2). 13–19. 27 indexed citations

20.

Kraytsberg, Yevgenya, et al.. (2002). mtLOH (mitochondrial loss of heteroplasmy), aging, and ‘surrogate self’. Mechanisms of Ageing and Development. 123(8). 891–898. 7 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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