M Stefanova

883 total citations
29 papers, 474 citations indexed

About

M Stefanova is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, M Stefanova has authored 29 papers receiving a total of 474 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 9 papers in Genetics and 8 papers in Pathology and Forensic Medicine. Recurrent topics in M Stefanova's work include Genomic variations and chromosomal abnormalities (7 papers), Lymphoma Diagnosis and Treatment (6 papers) and Congenital heart defects research (5 papers). M Stefanova is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Lymphoma Diagnosis and Treatment (6 papers) and Congenital heart defects research (5 papers). M Stefanova collaborates with scholars based in Germany, Bulgaria and Sweden. M Stefanova's co-authors include Radka Stoeva, Judith Dierlamm, Lucienne Michaux, Dieter K. Hossfeld, Kristina Hinz, Iwona Włodarska, Herman Van den Berghe, Torbjörn Olausson, Jean‐Pierre Fryns and Catarina Darnfors and has published in prestigious journals such as Blood, Annals of Oncology and Journal of Investigative Dermatology.

In The Last Decade

M Stefanova

28 papers receiving 442 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
M Stefanova Germany 12 208 196 87 77 55 29 474
Shlomit Rienstein Israel 14 161 0.8× 277 1.4× 33 0.4× 69 0.9× 107 1.9× 28 559
Mamoru Ozaki Japan 12 142 0.7× 152 0.8× 56 0.6× 38 0.5× 63 1.1× 38 389
Susan Sheldon United States 13 149 0.7× 128 0.7× 95 1.1× 81 1.1× 20 0.4× 21 508
Ghislaine Plessis France 18 341 1.6× 431 2.2× 32 0.4× 129 1.7× 55 1.0× 31 810
Marie Trková Czechia 13 145 0.7× 272 1.4× 50 0.6× 110 1.4× 76 1.4× 33 589
Monica Hrynchak Canada 13 178 0.9× 124 0.6× 67 0.8× 58 0.8× 50 0.9× 25 368
A M van den Ouweland Netherlands 13 286 1.4× 312 1.6× 52 0.6× 32 0.4× 87 1.6× 19 737
Ruth A. Heim United States 13 117 0.6× 155 0.8× 36 0.4× 80 1.0× 46 0.8× 21 643
Nicole L. Hoppman United States 14 279 1.3× 279 1.4× 57 0.7× 78 1.0× 115 2.1× 62 704
Silvia Majore Italy 16 319 1.5× 427 2.2× 26 0.3× 133 1.7× 33 0.6× 48 808

Countries citing papers authored by M Stefanova

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of M Stefanova

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

All Works

20 of 20 papers shown
1.
2.
Danielsson, Ingela, et al.. (2019). NUP188 Biallelic Loss of Function May Underlie a New Syndrome: Nucleoporin 188 Insufficiency Syndrome?. Molecular Syndromology. 10(6). 313–319. 10 indexed citations
3.
Gréen, Anna, Jon Jonasson, Hartmut Vogt, et al.. (2018). Could Dissimilar Phenotypic Effects of ACTB Missense Mutations Reflect the Actin Conformational Change Two Novel Mutations and Literature Review. Molecular Syndromology. 9(5). 259–265. 11 indexed citations
4.
Samuelsson, Lena, et al.. (2014). UBE2A deficiency syndrome: A report of two unrelated cases with large Xq24 deletions encompassing UBE2A gene. American Journal of Medical Genetics Part A. 167(1). 204–210. 18 indexed citations
5.
Yamamoto, Toshiyuki, Anna Wilsdon, Shelagh Joss, et al.. (2014). An emerging phenotype of Xq22 microdeletions in females with severe intellectual disability, hypotonia and behavioral abnormalities. Journal of Human Genetics. 59(6). 300–306. 38 indexed citations
6.
Stoeva, Radka, et al.. (2011). Three cases of two unrelated families with a microduplication 22q11.2: developmental skull defects and phenotype variability. European Journal of Human Genetics. 17. 139–140. 74 indexed citations
7.
Kirchhoff, Maria, Anne‐Marie Bisgaard, Radka Stoeva, et al.. (2009). Phenotype and 244k array‐CGH characterization of chromosome 13q deletions: An update of the phenotypic map of 13q21.1‐qter. American Journal of Medical Genetics Part A. 149A(5). 894–905. 92 indexed citations
8.
Stefanova, M, Peter Meinecke, Andreas Gal, & Hanno J. Bolz. (2005). A novel 9 bp deletion in the filamin a gene causes an otopalatodigital-spectrum disorder with a variable, intermediate phenotype. American Journal of Medical Genetics Part A. 132A(4). 386–390. 13 indexed citations
9.
Stefanova, M, Boyan Dimitrov, Cristina Has, et al.. (2005). Disruption of ERBB2IP Is not Associated with Dystrophic Epidermolysis Bullosa in Both Father and Son Carrying a Balanced 5;13 Translocation. Journal of Investigative Dermatology. 125(4). 700–704. 2 indexed citations
10.
11.
Dierlamm, Judith, M Stefanova, Iwona Włodarska, et al.. (2001). Chromosomal gains and losses are uncommon in hairy cell leukemia. Cancer Genetics and Cytogenetics. 128(2). 164–167. 13 indexed citations
12.
Stefanova, M, et al.. (2000). Polysomy 13 with Concomitant Deletion of 13q13–14 Involving the Retinoblastoma Gene and the D13S25 Locus in a Case of Acute Myeloid Leukemia. Cancer Genetics and Cytogenetics. 119(2). 158–161. 2 indexed citations
13.
Dierlamm, Judith, M Stefanova, Iwona Włodarska, et al.. (2000). Analysis of the P53, RB/D13S25, and P16 Tumor Suppressor Genes in Marginal Zone B-cell Lymphoma. Cancer Genetics and Cytogenetics. 120(1). 1–5. 13 indexed citations
14.
Dierlamm, Judith, M Stefanova, Kristina Hinz, et al.. (1999). The t(11;18)(q21;q21) characterizes a subgroup of extranodal MALT lymphomas: a two-color fluor-escence in situ hybridization study using AP12 and MLT specific probes. Blood. 1 indexed citations
15.
Dierlamm, Judith, et al.. (1999). Unusual Clinical Course and Acquisition of del(11)(q23) in Second Lymphatic Blastic Phase of a Ph-Positive Chronic Myeloid Leukemia. Cancer Genetics and Cytogenetics. 113(1). 85–89. 3 indexed citations
16.
Dierlamm, Judith, Lucienne Michaux, M Stefanova, et al.. (1999). Novel Philadelphia Variant t(Y;9;22)(q12;q34;q11) in a Case of Chronic Myeloid Leukemia. Cancer Genetics and Cytogenetics. 114(2). 150–153. 6 indexed citations
17.
Stefanova, M, et al.. (1998). Polysomy 13 with deletion of the retinoblastoma gene and the D13S25 locus in a case of acute myeloid leukemia. Annals of Oncology. 9. 82–82. 1 indexed citations
18.
Dierlamm, Judith, Iwona Włodarska, M Stefanova, et al.. (1998). Molecular cytogenetic characterization of the chromosome 11 and 18 breakpoints in the t(11;18)(q21;q21) associated with malt lymphomas. Blood. 92(10). 1 indexed citations
19.
Galland, Franck, M Stefanova, Marina Lafage, & Daniel Birnbaum. (1992). Localization of the 5’ end of the MCF2 oncogene to human chromosome 15q15→q23. Cytogenetic and Genome Research. 60(2). 114–116. 15 indexed citations
20.
Galland, Franck, et al.. (1990). Characterization of a murine glyceraldehyde-3-phosphate dehydrogenase pseudogene. Biochimie. 72(10). 759–762. 17 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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