Elena D. Markova

748 total citations
28 papers, 560 citations indexed

About

Elena D. Markova is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Elena D. Markova has authored 28 papers receiving a total of 560 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Cellular and Molecular Neuroscience, 13 papers in Neurology and 12 papers in Molecular Biology. Recurrent topics in Elena D. Markova's work include Genetic Neurodegenerative Diseases (14 papers), Neurological disorders and treatments (8 papers) and Mitochondrial Function and Pathology (6 papers). Elena D. Markova is often cited by papers focused on Genetic Neurodegenerative Diseases (14 papers), Neurological disorders and treatments (8 papers) and Mitochondrial Function and Pathology (6 papers). Elena D. Markova collaborates with scholars based in Russia, Japan and United Kingdom. Elena D. Markova's co-authors include I. A. Ivanova‐Smolenskaya, С. Н. Иллариошкин, Limborskaia Sa, Hajime Tanaka, P. A. Slominsky, В. С. Сухоруков, Shoji Tsuji, Cheryl R. Greenberg, Edward Nylen and Klaus Wrogemann and has published in prestigious journals such as SHILAP Revista de lepidopterología, Brain and Neurology.

In The Last Decade

Elena D. Markova

28 papers receiving 548 citations

Peers

Elena D. Markova

CMN

NEURO

PHYSI

CCM

Claude Mignard France

Angela Marsili Italy

Davina J. Hensman Moss United Kingdom

P. Thomas United States

Vitalie D. Lupu United States

Naonobu Futamura Japan

Daita Kaneda Japan

Andreas Dalski Germany

Cinzia Bertolin Italy

R. Liane Ramirez United States

Claude Mignard France

Elena D. Markova

690 ×2.2

688 ×2.2

CMN

238 ×0.9

NEURO

33 ×0.5

PHYSI

43 ×0.8

CCM

Citations per year, relative to Elena D. Markova Elena D. Markova (= 1×) peers Claude Mignard

Countries citing papers authored by Elena D. Markova

Since Specialization

Citations

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

Fields of papers citing papers by Elena D. Markova

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Elena D. Markova. 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 Elena D. Markova. The network helps show where Elena D. Markova may publish in the future.

Co-authorship network of co-authors of Elena D. Markova

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Иллариошкин, С. Н., et al.. (2007). Heterogeneity of sporadic Parkinson’s disease: molecular approach to solving the problem. SHILAP Revista de lepidopterología. 1 indexed citations

Иллариошкин, С. Н., М. И. Шадрина, P. A. Slominsky, et al.. (2007). A common leucine‐rich repeat kinase 2 gene mutation in familial and sporadic Parkinson's disease in Russia. European Journal of Neurology. 14(4). 413–417. 26 indexed citations

Иллариошкин, С. Н., I. A. Ivanova‐Smolenskaya, Elena D. Markova, et al.. (2004). Molecular Genetic Analysis of Hereditary Neurodegenerative Diseases. Russian Journal of Genetics. 40(6). 663–671. 9 indexed citations

Иллариошкин, С. Н., Magali Periquet, Nina Rawal, et al.. (2003). Mutation analysis of the parkin gene in Russian families with autosomal recessive juvenile parkinsonism. Movement Disorders. 18(8). 914–919. 24 indexed citations

Kramarenko, G. G., Elena D. Markova, I. A. Ivanova‐Smolenskaya, & А. А. Болдырев. (2001). Peculiarities of Carnosine Metabolism in a Patient with Pronounced Homocarnosinemia. Bulletin of Experimental Biology and Medicine. 132(4). 996–999. 6 indexed citations

Иллариошкин, С. Н., I. A. Ivanova‐Smolenskaya, Cheryl R. Greenberg, et al.. (2000). Identical dysferlin mutation in limb-girdle muscular dystrophy type 2B and distal myopathy. Neurology. 55(12). 1931–1933. 102 indexed citations

Иллариошкин, С. Н., et al.. (2000). Different phenotypes of Friedreich's ataxia within one ‘pseudo‐dominant’ genealogy: relationships between trinucleotide (GAA) repeat lengths and clinical features. European Journal of Neurology. 7(5). 535–540. 10 indexed citations

Иллариошкин, С. Н., et al.. (2000). Clinical and genetic study of familial essential tremor in an isolate of Northern Tajikistan. Movement Disorders. 15(5). 1020–1023. 14 indexed citations

Markova, Elena D., P. A. Slominsky, С. Н. Иллариошкин, et al.. (1999). A novel mutation in the GTP cyclohydrolase I gene associated with a broad range of clinical presentations in a family with autosomal dominant dopa‐responsive dystonia. European Journal of Neurology. 6(5). 605–608. 1 indexed citations

10.

Slominsky, P. A., Elena D. Markova, М. И. Шадрина, et al.. (1999). A common 3-bp deletion in theDYT1 gene in Russian families with early-onset torsion dystonia. Human Mutation. 14(3). 269–269. 22 indexed citations

11.

Brin, Mitchell F., D. de Leon, Limborskaia Sa, et al.. (1998). De Novo Mutations (GAG Deletion) in the DYT1 Gene in Two Non-Jewish Patients with Early-onset Dystonia. Human Molecular Genetics. 7(7). 1133–1136. 47 indexed citations

12.

Иллариошкин, С. Н., Elena D. Markova, P. A. Slominsky, et al.. (1998). The GTP Cyclohydrolase I Gene in Russian Families With Dopa-Responsive Dystonia. Archives of Neurology. 55(6). 789–789. 15 indexed citations

13.

Ozelius, Laurie J., Jeffrey Hewett, Patricia Kramer, et al.. (1997). Fine Localization of the Torsion Dystonia Gene (DYT1) on Human Chromosome 9q34: YAC Map and Linkage Disequilibrium. Genome Research. 7(5). 483–494. 50 indexed citations

14.

Ivanova‐Smolenskaya, I. A., et al.. (1997). 5-29-06 Molecular analysis in Russian families with Wilson's disease. Journal of the Neurological Sciences. 150. S314–S314. 1 indexed citations

15.

Иллариошкин, С. Н., et al.. (1997). Refined Genetic Location of the Chromosome 2p-Linked Progressive Muscular Dystrophy Gene. Genomics. 42(2). 345–348. 15 indexed citations

16.

Иллариошкин, С. Н., P. A. Slominsky, Igor V. Ovchinnikov, et al.. (1996). Spinocerebellar ataxia type 1 in Russia. Journal of Neurology. 243(7). 506–510. 25 indexed citations

17.

Иллариошкин, С. Н., I. A. Ivanova‐Smolenskaya, Hajime Tanaka, et al.. (1996). Clinical and molecular analysis of a large family with three distinct phenotypes of progressive muscular dystrophy. Brain. 119(6). 1895–1909. 58 indexed citations

18.

Иллариошкин, С. Н., et al.. (1996). X‐linked nonprogressive congenital cerebellar hypoplasia: Clinical description and mapping to chromosome Xq. Annals of Neurology. 40(1). 75–83. 27 indexed citations

19.

Ivanova‐Smolenskaya, I. A., et al.. (1995). Novel mutational mechanism in man: Expansion of trinucleotide repeats. Russian Journal of Genetics. 31(11). 194–203. 2 indexed citations

20.

Markova, Elena D., et al.. (1989). [Analysis of trace elements of the brain and liver tissues in Wilson's disease].. PubMed. 89(7). 69–73. 2 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