Get started
Author

Т. Тодоров

Observed names: T Todorov, T. Todorov, Teodor N. Todorov, Teodor Todorov, Theodor Todorov, Tihomir Todorov
Observed institutions: New Bulgarian University, University of Münster, Alexandrovska Hospital, Lozenetz Hospital, Medical University of Sofia, University Hospital Münster, Stiftung Charité, Sofia University "St. Kliment Ohridski", Technische Universität Dresden, Charité – Universitätsmedizin Berlin
ORCID: 0000-0002-0548-5487
Observed ORCIDs: 0000-0002-0548-5487, 0000-0001-9903-5251
OpenAlex ID: A5010037203
Association Between Loss of Dp140 and Cognitive Impairment in Duchenne and Becker Dystrophies
2013 · T Chamova, V Guergueltcheva, et al. · Balkan Journal of Medical Genetics · 86
PDF
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 · Annu Aggarwal, Gursimran Chandhok, et al. · Annals of Human Genetics · 59
Prevalence of Germline Mutations in the TTR Gene in a Consecutive Series of Surgical Pathology Specimens With ATTR Amyloid
2008 · Magdalena Eriksson, Janine Büttner, et al. · The American Journal of Surgical Pathology · 43
Neurological Symptoms, Genotype-Phenotype Correlations and Ethnic-specific Differences in Bulgarian Patients With Wilson Disease
2012 · Violeta Mihaylova, Teodor Todorov, et al. · The Neurologist · 31
Spectrum of mutations in the Wilson disease gene (ATP7B) in the Bulgarian population
2005 · T Todorov, A Savov, et al. · Clinical Genetics · 27
Intragenic Deletions in ATP7B as an Unusual Molecular Genetics Mechanism of Wilson’s Disease Pathogenesis
2016 · Theodor Todorov, Prahlad Balakrishnan, et al. · PLoS ONE · 25
PDF
No association of the CARD8 (TUCAN) c.30T>A (p.C10X) variant with Crohnʼs disease: A study in 3 independent European cohorts
2007 · Carsten Büning, Hartmut H.-J. Schmidt, et al. · Inflammatory Bowel Diseases · 22
A study in three European IBD cohorts confirms that the ATG16L1 c.898A>G (p.Thr300Ala) variant is a susceptibility factor for Crohn’s disease
2007 · Carsten Büning, Tahir Durmus, et al. · Journal of Crohn s and Colitis · 22
Overexpressed ATP7B protects mesenchymal stem cells from toxic copper
2010 · Vanessa Sauer, Ramsi Siaj, et al. · Biochemical and Biophysical Research Communications · 21
Synonymous mutation in adenosine triphosphatase copper‐transporting beta causes enhanced exon skipping in Wilson disease
2022 · Marlene Panzer, André Viveiros, et al. · Hepatology Communications · 17
PDF
Fragile X mosaic male full mutation/normal allele detected by PCR/MS-MLPA
2009 · Tihomir Todorov, Albena Todorova, et al. · BMJ Case Reports · 14
Influence of Botulinumtoxin A on the Expression of Adult MyHC Isoforms in the Masticatory Muscles in Dystrophin-Deficient Mice (Mdx-Mice)
2016 · Ute Ulrike Botzenhart, Constantin Wegenstein, et al. · BioMed Research International · 7
PDF
Non-deletion mutations in Egyptian patients with Duchenne muscular dystrophy
2014 · Rabah M. Shawky, Solaf M. Elsayed, et al. · Egyptian Journal of Medical Human Genetics · 7
PDF
A family with fragile X syndrome, Duchenne muscular dystrophy and ichthyosis transmitted by an asymptomatic carrier
2013 · A. Todorova, I. Litvinenko, et al. · Clinical Genetics · 7
Molecular genetic diagnostics of tuberous sclerosis complex in Bulgaria: six novel mutations in the TSC1 and TSC2 genes
2018 · M. Glushkova, V. Bojinova, et al. · Journal of Genetics · 6
Novel mutation in the COL11A1 gene causing Marshall-Stickler syndrome in three generations of a Bulgarian family
2021 · M Mladenova, T Todorov, et al. · Balkan Journal of Medical Genetics · 5
PDF
Wilson’s disease in two consecutive generations in a Bulgarian Roma family
2007 · V. Mihaylova, T. Todorov, et al. · Journal of Neurology · 5
Characterization of Streptococcus pyogenes Strains from Tonsillopharyngitis and Scarlet Fever Resurgence, 2023—FIRST Detection of M1UK in Bulgaria
2025 · Emma Keuleyan, Theodor Todorov, et al. · Microorganisms · 4
PDF
Evoked Potentials in Patients With Wilson Disease
2020 · Violeta M. Mihaylova, Olga R. Kosseva, et al. · Journal of Clinical Neurophysiology · 4
[Pregnancy outcome in women over the age of 35].
2014 · T Dakov, V Dimitrova, et al. · PubMed · 3
Ethnic specific background of mutations in Bulgarian patients with Wilson disease.
2007 · T Todorov, A Savov, et al. · PubMed · 3
Molecular-Genetic Diagnostics of Angelman Syndrome – The Bulgarian Experience
2020 · B. Georgieva, S. Atemin, et al. · Acta Medica Bulgarica · 2
PDF
Three Novel NF1 Gene Mutations in a Cohort of Bulgarian Neurofibromatoses Patients
2018 · M. Glushkova, I. Yordanova, et al. · Russian Journal of Genetics · 2
[Mode of conception, acompanying medical disorders and complications in the second half of pregnancy in women over the age of 35].
2014 · T Dakov, V Dimitrova, et al. · PubMed · 2
Molecular Diagnostics of Duchenne/Becker Muscular Dystrophy Patients by Multiplex Ligation-Dependent Probe Amplification Analysis and Direct Sequencing
2009 · A Todorova, V Guergueltcheva, et al. · Balkan Journal of Medical Genetics · 2
PDF
Works count: 49
Citation count: 432
H-index: 11
I10-index: 11
Year
Topic
Type