Marina Manvelyan
- Genetics top 10%
- Genomic variations and chromosomal abnormalities 11
- Mesenchymal stem cell research 4
- Genomics and Rare Diseases 2
- Genetic Syndromes and Imprinting 1
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- Prenatal Screening and Diagnostics 8
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- Chromosomal and Genetic Variations 8
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- Genomic variations and chromosomal abnormalities 11
- Mesenchymal stem cell research 4
- Genomics and Rare Diseases 2
- Genetic Syndromes and Imprinting 1
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- Genomics and Chromatin Dynamics 4
- Advanced biosensing and bioanalysis techniques 2
In The Last Decade
Marina Manvelyan
21 papers receiving 386 citations
Peers
Comparison fields: 5 of 52
- Genetics 228
- Pediatrics, Perinatology and Child Health 93
- Plant Science 131
- Genetics 36
- Reproductive Medicine 27
Countries citing papers authored by Marina Manvelyan
This map shows the geographic impact of Marina Manvelyan'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 Marina Manvelyan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marina Manvelyan more than expected).
Fields of papers citing papers by Marina Manvelyan
This network shows the impact of papers produced by Marina Manvelyan. 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 Marina Manvelyan. The network helps show where Marina Manvelyan may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Marina Manvelyan, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2025 | 0 | |
| 2 | 2020 | 15 | |
| 3 | 2020 | 1 | |
| 4 | 2016 | 2 | |
| 5 | 2015 | 1 | |
| 6 | 2015 | 13 | |
| 7 | 2014 | 68 | |
| 8 | 2013 | 6 | |
| 9 | 2012 | 14 | |
| 10 | 2011 | 6 | |
| 11 | 2011 | 15 | |
| 12 | 2011 | 47 | |
| 13 | 2010 | 30 | |
| 14 | 2010 | 20 | |
| 15 | 2010 | 15 | |
| 16 | 2010 | 41 | |
| 17 | 2008 | 20 | |
| 18 | 2008 | 14 | |
| 19 | 2008 | 62 | |
| 20 | 2007 | 2 |
About Marina Manvelyan
Marina Manvelyan is a scholar working on Genetics, Genetics and Pediatrics, Perinatology and Child Health, having authored 22 papers that have together received 402 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (8 papers), Chromosomal and Genetic Variations (8 papers), Mesenchymal stem cell research (4 papers), Genomics and Chromatin Dynamics (4 papers), Genomics and Rare Diseases (2 papers), Advanced biosensing and bioanalysis techniques (2 papers) and Genetic Syndromes and Imprinting (1 paper). The work is most often cited by research in Genetics (228 citations), Pediatrics, Perinatology and Child Health (93 citations) and Plant Science (131 citations). Marina Manvelyan has collaborated with scholars based in Germany, Armenia and France. Frequent co-authors include Thomas Liehr, Anja Weise, Kristin Mrasek, Elisabeth Ewers, Samarth Bhatt, Nadezda Kosyakova, Ahmed B. Hamid, Franck Pellestor, Rouben Aroutiounian and Aria Baniahmad. Their work appears in journals such as Journal of Clinical Oncology, PLoS ONE and Molecular Cancer.
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.