Boyan Dimitrov

982 total citations
32 papers, 472 citations indexed

About

Boyan Dimitrov is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Boyan Dimitrov has authored 32 papers receiving a total of 472 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 17 papers in Genetics and 10 papers in Plant Science. Recurrent topics in Boyan Dimitrov's work include Genomic variations and chromosomal abnormalities (9 papers), Prenatal Screening and Diagnostics (6 papers) and Plant Genetic and Mutation Studies (6 papers). Boyan Dimitrov is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Prenatal Screening and Diagnostics (6 papers) and Plant Genetic and Mutation Studies (6 papers). Boyan Dimitrov collaborates with scholars based in Bulgaria, Belgium and Netherlands. Boyan Dimitrov's co-authors include Joris Vermeesch, J. P. Fryns, Koenraad Devriendt, Jean‐Pierre Fryns, Radka Stoeva, Thomy de Ravel, Иван Иванов, M Stefanova, Christina Fagerberg and Hanne Rose and has published in prestigious journals such as Human Molecular Genetics, Journal of Investigative Dermatology and Journal of Medical Genetics.

In The Last Decade

Boyan Dimitrov

30 papers receiving 414 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Boyan Dimitrov Bulgaria 11 257 232 97 80 52 32 472
M. Crippa Italy 12 145 0.6× 203 0.9× 40 0.4× 43 0.5× 23 0.4× 37 396
Isabelle Gicquel France 13 236 0.9× 312 1.3× 24 0.2× 93 1.2× 29 0.6× 21 453
Maxine J. Sutcliffe United States 13 375 1.5× 316 1.4× 129 1.3× 130 1.6× 8 0.2× 27 676
Anna Maria Nardone Italy 13 213 0.8× 380 1.6× 55 0.6× 35 0.4× 10 0.2× 38 552
Annelyse Mertz Germany 9 752 2.9× 663 2.9× 174 1.8× 53 0.7× 31 0.6× 9 947
Cornelia Daumer‐Haas Germany 8 264 1.0× 245 1.1× 62 0.6× 73 0.9× 6 0.1× 10 451
T. Lukusa Belgium 10 287 1.1× 214 0.9× 89 0.9× 70 0.9× 4 0.1× 32 397
N. Créau-Goldberg France 14 298 1.2× 323 1.4× 103 1.1× 80 1.0× 6 0.1× 29 581
Jacques Puechberty France 17 458 1.8× 355 1.5× 311 3.2× 221 2.8× 8 0.2× 43 729
Jean Pierre Siffroi France 16 483 1.9× 387 1.7× 93 1.0× 171 2.1× 7 0.1× 35 792

Countries citing papers authored by Boyan Dimitrov

Since Specialization
Citations

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

Fields of papers citing papers by Boyan Dimitrov

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Boyan Dimitrov. 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 Boyan Dimitrov. The network helps show where Boyan Dimitrov may publish in the future.

Co-authorship network of co-authors of Boyan Dimitrov

This figure shows the co-authorship network connecting the top 25 collaborators of Boyan Dimitrov. A scholar is included among the top collaborators of Boyan Dimitrov 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 Boyan Dimitrov. Boyan Dimitrov 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.
Keymolen, Kathelijn, et al.. (2024). Prenatal phenotype of a homozygous nonsense MPDZ variant in a fetus with severe congenital hydrocephalus. Prenatal Diagnosis. 44(5). 657–660.
2.
Tüysüz, Beyhan, Philippe Debeer, Erika Souche, et al.. (2024). Gollop–Wolfgang Complex Is Associated with a Monoallelic Variation in WNT11. Genes. 15(1). 129–129. 1 indexed citations
3.
Keymolen, Kathelijn, et al.. (2023). Searching for a sense of closure: parental experiences of recontacting after a terminated pregnancy for congenital malformations. European Journal of Human Genetics. 32(6). 673–680. 1 indexed citations
4.
Parijs, Ilse, Nathalie Brison, Leen Vancoillie, et al.. (2023). Population screening for 15q11-q13 duplications: corroboration of the difference in impact between maternally and paternally inherited alleles. European Journal of Human Genetics. 32(1). 31–36. 2 indexed citations
5.
Irving, Melita, Boyan Dimitrov, Marja W. Wessels, et al.. (2016). Rodriguez acrofacial dysostosis is caused by apparently de novo heterozygous mutations in the SF3B4 gene. American Journal of Medical Genetics Part A. 170(12). 3133–3137. 12 indexed citations
6.
Dimitrov, Boyan, Irina Balikova, Thomy de Ravel, et al.. (2010). 2q31.1 microdeletion syndrome: redefining the associated clinical phenotype. Journal of Medical Genetics. 48(2). 98–104. 38 indexed citations
7.
Dimitrov, Boyan, Thierry Voet, Luc De Smet, et al.. (2010). Genomic rearrangements of the GREM1-FMN1 locus cause oligosyndactyly, radio-ulnar synostosis, hearing loss, renal defects syndrome and Cenani–Lenz-like non-syndromic oligosyndactyly. Journal of Medical Genetics. 47(8). 569–574. 27 indexed citations
8.
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
9.
Maas, Nicole, Tom Van de Putte, Cindy Melotte, et al.. (2009). TheC20orf133gene is disrupted in a patient with Kabuki syndrome. BMJ Case Reports. 2009. bcr0620091994–bcr0620091994. 3 indexed citations
10.
Dimitrov, Boyan, et al.. (2008). Genotoxic effects of the pesticides Rubigan, Omite and Rovral in root-meristem cells of Crepis capillaris L.. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 652(2). 191–197. 25 indexed citations
11.
Zeevaert, Renate, François Foulquier, Boyan Dimitrov, et al.. (2008). Cerebrocostomandibular-like syndrome and a mutation in the conserved oligomeric Golgi complex, subunit 1. Human Molecular Genetics. 18(3). 517–524. 40 indexed citations
12.
Balikova, Irina, et al.. (2005). A boy with facial dysmorphism, macrocephaly, and Dandy-Walker malformation due to familial unbalanced translocation der(18)(t(11;18)(q23.3;p11.21)mat. European Journal of Human Genetics. 13. 112–112. 2 indexed citations
13.
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
14.
Dimitrov, Boyan, et al.. (2005). Acrofacial dysostosis type Rodríguez. American Journal of Medical Genetics Part A. 135A(1). 81–85. 12 indexed citations
15.
Dimitrov, Boyan, et al.. (2004). Mesomelic form of short stature, congenital cataract, patent ductus arteriosus and muscular hypotonia associated with de novo translocation (13;18)(q14;q23). 15(1). 130–130.
16.
Dimitrov, Boyan, et al.. (1999). RESISTANCE RESPONSES OF PLANTS REGENERATED FROM TOMATO ANTHER AND SOMATIC TISSUE CULTURES TO CLAVIBACTER MICHIGANENSE SUBSP. MICHIGANENSE. Israel Journal of Plant Sciences. 47(4). 237–243. 8 indexed citations
17.
Popov, Peter & Boyan Dimitrov. (1996). Comparative karyotype analysis of 24-chromosomeRanaspecies (R. chensinensisandR. arvalis, Amphibia, Anura). Caryologia. 49(2). 163–173. 1 indexed citations
18.
Dimitrov, Boyan, et al.. (1994). Comparative analysis of sister-chromatid exchanges in plant and human chromosomes. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 304(2). 187–192. 6 indexed citations
19.
Dimitrov, Boyan. (1985). Intrachromosomal distribution patterns of SCEs and structural chromosome aberrations in Crepis capillaris. Mutation Research/Environmental Mutagenesis and Related Subjects. 147(5). 291–291. 1 indexed citations
20.
Dimitrov, Boyan. (1979). Effect of caffeine on intrachromosomal distribution of chromatid aberrations induced by chemical mutagens in Crepis capillaris L. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 62(2). 267–277. 4 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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