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Romanian Journal of Internal Medicine = Revue Roumaine De Medecine Interne|August 31, 2019
Comparison between thrombophilic gene polymorphisms among high risk patientsMariya Levkova, Mari Hachmeriyan, Milena Stoyanova, et al.
Biomedicines|December 30, 2025
Clinical Utility of Multiplex Ligation-Dependent Probe Amplification in the Genetic Assessment of Patients with Myelodysplastic SyndromeRadostina Valeva, Maria Levkova, Dinnar Yahya, et al.
Oncology Reviews|August 11, 2025
Genetic counseling for hereditary cancer syndromes: a 5-year experience from a single center in BulgariaMari Hachmeriyan, Mariya Levkova, Dinnar Yahya, et al.
Healthcare (Basel, Switzerland)|April 26, 2025
Ethical and Psychosocial Issues Associated with Genetic Testing for Hereditary Tumor Predisposition SyndromesMari Hachmeriyan, Mariya Levkova, Dinnar Yahya, et al.
Reports (MDPI)|July 25, 2025
An Ultra-Rare Disorder: Case Report on Cerebrotendinous XanthomatosisMariya Levkova, Mari Hachmeriyan, Margarita Grudkova, et al.
Children (Basel, Switzerland)|May 4, 2026
Diagnostic Yield and Genotype-Phenotype Overlap in Pediatric Autism Spectrum Disorder Patients Using Whole-Exome Sequencing and Phenotype-Driven Variant Interpretation: A Single-Center Cohort StudyAndreya Yaneva, Mariya Levkova, Milena Stoyanova, et al.
Neurology International|June 25, 2025
Two Decades of Huntington's Disease in Varna, Bulgaria: A Retrospective Single-Centre Study of Clinical Trends and ChallengesMariya Levkova, Mihael Tsalta-Mladenov, Milena Stoyanova, et al.
Journal of Clinical Research in Pediatric Endocrinology|February 2, 2023
Long-term Follow-up of a Late Diagnosed Patient with Temple SyndromeNikolinka Yordanova, Violeta Iotova, Deborah J G Mackay, et al.
Folia Medica|July 19, 2022
Molecular screening for fragile X syndrome in children with unexplained intellectual disability and/or autistic behaviourMilena Stoyanova, Mari Hachmeriyan, Mariya Levkova, et al.
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