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Maya Koleva
Observed names:
Koleva, Maya,
M. Koleva
Observed institutions:
Medical University of Sofia,
Multiprofile Hospital for Active Treatment in Neurology and Psychiatry St. Naum
ORCID:
0009-0004-8352-8739
Observed ORCID:
0009-0004-8352-8739
OpenAlex ID:
A5034887485
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
Involvement of mental health professionals in the treatment of tuberous sclerosis complex–associated neuropsychiatric disorders (TAND): results of a multinational European electronic survey
2021
·
Robert Waltereit
, Guillaume Beaure d’Augères
, et al.
·
Orphanet Journal of Rare Diseases
·
5
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
Epilepsy and Mental Retardation in Children with Cerebral Palsy – Bulgarian Study
2022
·
Elena Rodopska
, Nikolay Topalov
, et al.
·
Proceedings of the Bulgarian Academy of Sciences
·
1
PDF
Molecular-Genetic Characteristics and Genotype-Phenotype Correlations in Bulgarian Patients with Tuberous Sclerosis Complex
2021
·
B. Georgieva
, M. Koleva
, et al.
·
Acta Medica Bulgarica
·
1
PDF
From genome to chromatin: identification of a de novo SATB2 variant by trio whole-genome sequencing
2026
·
Maya Atanasoska
, Lubomir Balabanski
, et al.
The Clinical Spectrum of Malformations of Cortical Development in a Cohort of Bulgarian Patients
2025
·
Daniela Deneva-Todorova
, Veneta Bojinova
, et al.
·
Proceedings of the Bulgarian Academy of Sciences
Clinical and genetic variability among Bulgarian patients with autosomal recessive spastic ataxia of Charlevoix–Saguenay
2024
·
Teodora Chamova
, Neviana Ivanova
, et al.
·
Molecular Genetics & Genomic Medicine
PDF
Influence network analysis: the individuals in media coverage of global issues (2013 and 2017)
2019
·
Колева, Мая
, Koleva, Maya
·
Bulgarian Portal for Open Science
Hypomelanosis of Ito and De novo Interstitial 15q11.2q13.3 Triplication in Bulgarian Family
2019
·
M Mladenova
, Maya Koleva
, et al.
·
Journal of Clinical & Medical Genomics
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Works count:
36
Citation count:
15
H-index:
2
I10-index:
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