Т. Тодоров

404 total citations
26 papers, 258 citations indexed

About

Т. Тодоров is a scholar working on Molecular Biology, Health, Toxicology and Mutagenesis and Nutrition and Dietetics. According to data from OpenAlex, Т. Тодоров has authored 26 papers receiving a total of 258 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 5 papers in Health, Toxicology and Mutagenesis and 5 papers in Nutrition and Dietetics. Recurrent topics in Т. Тодоров's work include Trace Elements in Health (5 papers), Muscle Physiology and Disorders (5 papers) and Heavy Metal Exposure and Toxicity (5 papers). Т. Тодоров is often cited by papers focused on Trace Elements in Health (5 papers), Muscle Physiology and Disorders (5 papers) and Heavy Metal Exposure and Toxicity (5 papers). Т. Тодоров collaborates with scholars based in Bulgaria, Germany and Poland. Т. Тодоров's co-authors include Hartmut Schmidt, Andree Zibert, Vanio Mitev, Ivailo Tournev, Antonia Todorova, Veneta Bojinova, Velina Guergueltcheva, Margarita Raycheva, Teodora Chamova and Annu Aggarwal and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Biochemical and Biophysical Research Communications.

In The Last Decade

Т. Тодоров

24 papers receiving 255 citations

Peers

Countries citing papers authored by Т. Тодоров

Since Specialization

Citations

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

Fields of papers citing papers by Т. Тодоров

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Т. Тодоров

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Characterization of Streptococcus pyogenes Strains from Tonsillopharyngitis and Scarlet Fever Resurgence, 2023—FIRST Detection of M1UK in Bulgaria 2025 ·Microorganisms ·Emma Keuleyan, Т. Тодоров, (unknown), (unknown), Radoslava Vazharova, (unknown), (unknown), (unknown), Iskra Altankova, (unknown)	1
2	Molecular-genetic profile in patients with cardiomyopathy in Bulgaria 2024 ·SHILAP Revista de lepidopterología ·(unknown), (unknown), Vasil Velchev, (unknown), (unknown), Т. Тодоров, (unknown), Мариана Господинова, (unknown), (unknown), (unknown), (unknown), Ivailo Tournev, Vanio Mitev, (unknown)	0
3	Novel mutation in the COL11A1 gene causing Marshall-Stickler syndrome in three generations of a Bulgarian family 2021 ·SHILAP Revista de lepidopterología ·(unknown), Т. Тодоров, (unknown), Vanio Mitev, (unknown)	4
4	Molecular-Genetic Characteristics and Genotype-Phenotype Correlations in Bulgarian Patients with Tuberous Sclerosis Complex 2021 ·Acta Medica Bulgarica ·Bilyana Georgieva, (unknown), Т. Тодоров, Veneta Bojinova, (unknown), (unknown), (unknown), (unknown), (unknown), Vanio Mitev, (unknown)	1
5	Molecular-Genetic Diagnostics of Angelman Syndrome – The Bulgarian Experience 2020 ·SHILAP Revista de lepidopterología ·Bilyana Georgieva, (unknown), (unknown), Т. Тодоров, (unknown), (unknown), Vanio Mitev	1
6	Three Novel NF1 Gene Mutations in a Cohort of Bulgarian Neurofibromatoses Patients 2018 ·Russian Journal of Genetics ·(unknown), (unknown), Т. Тодоров, Veneta Bojinova, (unknown), Petia Dimova, Ivailo Tournev, (unknown), (unknown), Vanio Mitev	1
7	Limb girdle muscular dystrophy 2G in a religious minority of Bulgarian muslims homozygous for the c.75G>A, p.Trp25* TCAP mutation 2017 ·Neuromuscular Disorders ·Teodora Chamova, (unknown), Мариана Господинова, Dora Zlatareva, (unknown), (unknown), Т. Тодоров, (unknown), (unknown)	1
8	Intragenic Deletions in ATP7B as an Unusual Molecular Genetics Mechanism of Wilson’s Disease Pathogenesis 2016 ·PLoS ONE ·Т. Тодоров, (unknown), Alexey Savov, Piotr Socha, Hartmut Schmidt	19
9	Non-deletion mutations in Egyptian patients with Duchenne muscular dystrophy 2014 ·Egyptian Journal of Medical Human Genetics ·Rabah M. Shawky, Solaf M. Elsayed, Т. Тодоров, Andree Zibert, (unknown), Hartmut Schmidt	7
10	A family with fragile X syndrome, Duchenne muscular dystrophy and ichthyosis transmitted by an asymptomatic carrier 2013 ·Clinical Genetics ·(unknown), Ivan Litvinenko, Т. Тодоров, Radka Tincheva, Daniela Avdjieva, (unknown), Vanio Mitev	5
11	Association Between Loss of Dp140 and Cognitive Impairment in Duchenne and Becker Dystrophies 2013 ·SHILAP Revista de lepidopterología ·Teodora Chamova, Velina Guergueltcheva, Margarita Raycheva, Т. Тодоров, (unknown), (unknown), Veneta Bojinova, Vanio Mitev, Ivailo Tournev, Antonia Todorova	57
12	Wilson Disease Mutation Pattern with Genotype‐Phenotype Correlations from Western India: Confirmation of p.C271* as a Common Indian Mutation and Identification of 14 Novel Mutations 2013 ·Annals of Human Genetics ·Annu Aggarwal, Gursimran Chandhok, Т. Тодоров, (unknown), (unknown), Andree Zibert, Mohit Bhatt, Hartmut Schmidt	38
13	Neurological Symptoms, Genotype-Phenotype Correlations and Ethnic-specific Differences in Bulgarian Patients With Wilson Disease 2012 ·The Neurologist ·Violeta Mihaylova, Т. Тодоров, (unknown), (unknown), (unknown), (unknown), G. Georgiev, (unknown), (unknown), (unknown), (unknown), Ivailo Tournev	20
14	Overexpressed ATP7B protects mesenchymal stem cells from toxic copper 2010 ·Biochemical and Biophysical Research Communications ·Vanessa Sauer, (unknown), Т. Тодоров, Andree Zibert, Hartmut Schmidt	17
15	Fragile X mosaic male full mutation/normal allele detected by PCR/MS-MLPA 2009 ·BMJ Case Reports ·Т. Тодоров, (unknown), Andrey Kirov, (unknown), R. Carvalho, Anders O.H. Nygren, (unknown), Vanio Mitev	12
16	Molecular Diagnostics of Duchenne/Becker Muscular Dystrophy Patients by Multiplex Ligation-Dependent Probe Amplification Analysis and Direct Sequencing 2009 ·Balkan Journal of Medical Genetics ·(unknown), Velina Guergueltcheva, (unknown), Violeta Mihaylova, Т. Тодоров, (unknown), Bilyana Georgieva, Ivo Kremensky, Ivailo Tournev, Vanio Mitev	1
17	Prevalence of Germline Mutations in the TTR Gene in a Consecutive Series of Surgical Pathology Specimens With ATTR Amyloid 2008 ·The American Journal of Surgical Pathology ·Magdalena Eriksson, Janine Büttner, Т. Тодоров, (unknown), Stefan Schönland, Ute Hegenbart, Arnt V. Kristen, Thomas J. Dengler, Peter Lohse, Burkhard Helmke, Hartmut Schmidt, Christoph Röcken	36
18	No association of the CARD8 (TUCAN) c.30T>A (p.C10X) variant with Crohnʼs disease: A study in 3 independent European cohorts 2007 ·Inflammatory Bowel Diseases ·Carsten Büning, Hartmut Schmidt, (unknown), Joost P.H. Drenth, Thomas Fiedler, Enno Gentz, Т. Тодоров, Daniel C. Baumgart, Andreas Sturm, Ferenc Nagy, János Lonovics, Dirk J. de Jong, Olfert Landt, Andreas Kage, Renate Nickel, Janine Büttner, Herbert Lochs, Heiko Witt	20
19	[Amyloidosis of the urinary tract--case report and review of the literature]. 2006 ·PubMed ·(unknown), (unknown), (unknown), Elenko Popov, (unknown), Т. Тодоров	1
20	[Primary hyperparathyroidism in childhood and adolescence]. 1982 ·PubMed ·(unknown), Т. Тодоров	0

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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