M Stefanova
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Chronic Lymphocytic Leukemia Research
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Reproductive Medicine top 10%
- Hypothalamic control of reproductive hormones
Papers in
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- Congenital heart defects research 5
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- Lymphoma Diagnosis and Treatment 6
- Co-authors
- Radka Stoeva (4 shared papers)Judith Dierlamm (10 shared papers)Lucienne Michaux (8 shared papers)Dieter K. Hossfeld (7 shared papers)Kristina Hinz (6 shared papers)Iwona Włodarska (6 shared papers)Herman Van den Berghe (4 shared papers)Jean‐Pierre Fryns (1 shared paper)
In The Last Decade
M Stefanova
28 papers receiving 442 citations
Peers
Comparison fields: 5 of 61
- Genetics 71
- Genetics 190
- Reproductive Medicine 48
- Pharmacy 24
- Pathology and Forensic Medicine 81
Countries citing papers authored by M Stefanova
This map shows the geographic impact of M Stefanova'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 M Stefanova with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M Stefanova more than expected).
Fields of papers citing papers by M Stefanova
This network shows the impact of papers produced by M Stefanova. 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 M Stefanova. The network helps show where M Stefanova may publish in the future.
Co-authors
The 25 scholars most cited alongside M Stefanova, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 29 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2009 | 92 | |
| 2 | Three cases of two unrelated families with a microduplication 22q11.2: developmental skull defects and phenotype variability | 2011 | 74 |
| 3 | 2000 | 65 | |
| 4 | 2014 | 38 | |
| 5 | 2003 | 23 | |
| 6 | 2014 | 18 | |
| 7 | 2010 | 18 | |
| 8 | 1990 | 17 | |
| 9 | 2001 | 13 | |
| 10 | 2000 | 13 | |
| 11 | 2005 | 13 | |
| 12 | 2008 | 13 | |
| 13 | 2019 | 11 | |
| 14 | 2018 | 11 | |
| 15 | 2007 | 9 | |
| 16 | 2019 | 7 | |
| 17 | 1993 | 7 | |
| 18 | 1999 | 6 | |
| 19 | 2013 | 6 | |
| 20 | A novel SOX9 nonsense mutation, q401x, in a case of campomelic dysplasia with XY sex reversal. | 2011 | 6 |
About M Stefanova
M Stefanova is a scholar working on Molecular Biology, Pathology and Forensic Medicine, Genetics, Genetics and Hematology, having authored 29 papers that have together received 474 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Lymphoma Diagnosis and Treatment (6 papers), Congenital heart defects research (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Chronic Lymphocytic Leukemia Research (4 papers), Viral-associated cancers and disorders (3 papers), Acute Myeloid Leukemia Research (3 papers) and Chronic Myeloid Leukemia Treatments (3 papers). The work is most often cited by research in Genetics (71 citations), Genetics (190 citations), Reproductive Medicine (48 citations), Pharmacy (24 citations) and Pathology and Forensic Medicine (81 citations). M Stefanova has collaborated with scholars based in Germany, Bulgaria and Belgium. Frequent co-authors include Radka Stoeva, Judith Dierlamm, Lucienne Michaux, Dieter K. Hossfeld, Kristina Hinz, Iwona Włodarska, Herman Van den Berghe, Jean‐Pierre Fryns, Anne Hagemeijer and Catarina Darnfors. Their work appears in journals such as Blood, Hematological Oncology, European Journal of Medical Genetics, Journal of Investigative Dermatology and Biochimie.
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.