A.K. Beresheva
- Co-authors
- Svetlana G. VorsanovaYuri B. YurovIvan Y. IourovDemidova IaIlia V. SolovievAlexei D. KolotiiFranck PellestorThomas Liehr
- Topics
- Genomic variations and chromosomal abnormalities (3 papers)Prenatal Screening and Diagnostics (3 papers)Congenital Anomalies and Fetal Surgery (1 paper)
- Cited by
- GeneticsCell BiologyCancer Research
- Journals
- PLoS ONERussian Journal of GeneticsPubMed
In The Last Decade
A.K. Beresheva
5 papers receiving 189 citations
Peers
Comparison fields: 5 of 27
- Genetics 136
- Molecular Biology 96
- Cell Biology 44
- Pediatrics, Perinatology and Child Health 36
- Plant Science 33
Countries citing papers authored by A.K. Beresheva
This map shows the geographic impact of A.K. Beresheva'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 A.K. Beresheva with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A.K. Beresheva more than expected).
Fields of papers citing papers by A.K. Beresheva
This network shows the impact of papers produced by A.K. Beresheva. 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 A.K. Beresheva. The network helps show where A.K. Beresheva may publish in the future.
Co-authorship network of co-authors of A.K. Beresheva
This figure shows the co-authorship network connecting the top 25 collaborators of A.K. Beresheva. A scholar is included among the top collaborators of A.K. Beresheva 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 A.K. Beresheva. A.K. Beresheva is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 9 | |
| 2 | 160 | |
| 3 | Non-disjunction of chromosome 21, alphoid DNA variation, and sociogenetic features of Down syndrome. | 20 |
| 4 | [Diagnosis of numerical chromosomal aberrations in the cells of spontaneous abortions by multicolor fluorescence in situ hybridization (MFISH)]. | 2 |
| 5 | [Current methods of molecular cytogenetics in pre- and postnatal diagnosis of chromosome aberrations]. | 2 |
About A.K. Beresheva
A.K. Beresheva is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Surgery, having authored 5 papers that have together received 193 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Prenatal Screening and Diagnostics (3 papers) and Congenital Anomalies and Fetal Surgery (1 paper). The work is most often cited by research in Genetics (136 citations), Cell Biology (44 citations) and Cancer Research (32 citations). A.K. Beresheva has collaborated with scholars based in Russia, France and Germany. Frequent co-authors include Svetlana G. Vorsanova, Yuri B. Yurov, Ivan Y. Iourov, Demidova Ia, Ilia V. Soloviev, Alexei D. Kolotii, Franck Pellestor, Thomas Liehr, Sergey I. Kutsev and Rune Male. Their work appears in journals such as PLoS ONE, Russian Journal of Genetics and PubMed.
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.