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Milena Stoyanova

Observed names: Stoyanova M, Stoyanova, Milena, Стоянова, Милена
ORCID: 0000-0001-8604-2057
Observed ORCID: 0000-0001-8604-2057
OpenAlex ID: A5040110652
The clinical significance of A2ML1 variants in Noonan syndrome has to be reconsidered
2020 · Julia Brinkmann, Christina Lissewski, et al. · European Journal of Human Genetics · 14
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Diagnostic Yield of Next-Generation Sequencing for Rare Pediatric Genetic Disorders: A Single-Center Experience
2025 · Milena Stoyanova, Dinnar Yahya, et al. · Medical Sciences · 7
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Ethical and Psychosocial Issues Associated with Genetic Testing for Hereditary Tumor Predisposition Syndromes
2025 · Mari Hachmeriyan, Mariya Levkova, et al. · Healthcare · 7
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Variants of uncertain significance in the era of next-generation sequencing
2022 · Mariya Levkova, Milena Stoyanova, et al. · Journal of the American Association of Nurse Practitioners · 4
Comparison between thrombophilic gene polymorphisms among high risk patients
2019 · Mariya Levkova, Mari Hachmeriyan, et al. · Romanian Journal of Internal Medicine · 4
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Two Decades of Huntington’s Disease in Varna, Bulgaria: A Retrospective Single-Centre Study of Clinical Trends and Challenges
2025 · Mariya Levkova, Mihael Tsalta-Mladenov, et al. · Neurology International · 3
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16p11.2 Duplication Syndrome - a Case Report
2021 · Mariya Levkova, Milena Stoyanova, et al. · Folia Medica · 3
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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 Study
2026 · Andreya Yaneva, Mariya Levkova, et al. · Children · 2
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Genetic counseling for hereditary cancer syndromes: a 5-year experience from a single center in Bulgaria
2025 · Mari Hachmeriyan, Mariya Levkova, et al. · Oncology Reviews · 2
The application of the facial analysis program Face2Gene in a single genetic counseling center: a retrospective study
2025 · Dinnar Yahya, Milena Stoyanova, et al. · Egyptian Pediatric Association Gazette · 2
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Standard karyotyping - a look through the European guidelines
2019 · Mari Hachmeriyan, Maria Levkova, et al. · Varna Medical Forum · 2
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Genomic Evaluation of AML—Main Techniques and Novel Approaches
2025 · Dinnar Yahya, Milena Stoyanova, et al. · Journal of Clinical Medicine · 1
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NIPT Integration as a Patient-Paid Prenatal Screening Option—Observations and Challenges from a Bulgarian Genetic Counseling Center
2024 · Dinnar Yahya, Mari Hachmeriyan, et al. · Medical Sciences · 1
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Genetic Counseling for Childhood Cancer Predisposition Syndromes: A Six-Year Retrospective Study
2026 · Milena Stoyanova, Dinnar Yahya, et al. · Children
Case report: A detour in diagnosis—Waardenburg syndrome
2025 · Andreya Yaneva, Milena Stoyanova, et al. · Scripta Scientifica Medica
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Autosomal dominant macrocephaly, acquired with impaired intellectual development: a report of an ultra-rare disease
2025 · Dinnar Yahya, Milena Stoyanova, et al. · Egyptian Journal of Medical Human Genetics
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Genetic Tumor Risk Syndromes: Current Aspects of Diagnosis and Genetic Counseling
2025 · Mari Hachmeriyan, Mariya Levkova, et al. · Scripta Scientifica Medica
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A cost-efficient algorithm for diagnosing children with dysmorphic features
2024 · Mariya Levkova, Milena Stoyanova, et al. · Egyptian Journal of Medical Human Genetics
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The significance of follow-up in patients with dysmorphic features: a case from clinical practice
2024 · Mariya Levkova, Milena Stoyanova, et al. · Romanian Journal of Pediatrics
Genetic Diagnostic Study among Pediatric Patients with Hereditary Pathology Who Received Genetic Counselling
2022 · Стоянова, Милена, Stoyanova, Milena · Bulgarian Portal for Open Science
Molecular genetic markers in acute myelogenous leukemia—the good, the bad, and the intermediate
2022 · Dinnar Ali Yahya, Mari Hachmeriyan, et al. · Varna Medical Forum
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Noonan syndrome patients with short stature at a single paediatric endocrinology centre
2022 · Yana Deyanova, Violeta Iotova, et al. · Scripta Scientifica Medica
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Molecular screening for fragile X syndrome in children with unexplained intellectual disability and/or autistic behaviour
2022 · Milena Stoyanova, Mari Hachmeriyan, et al. · Folia Medica
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Genetic Diagnostic Study among Pediatric Patients with Hereditary Pathology Who Received Genetic Counselling // Генетико-диагностично проучване при лица в детска възраст с наследствена патология, преминали през кабинета за генетично консултиране
2022 · Стоянова, Милена, Stoyanova, Milena · Medical University of Varna Repository
Noonan syndrome patients with short stature at a single pediatric endocrinology centre
2021 · Y. Deyanova, Violeta Iotova, et al. · 59th ESPE Annual Meeting (ESPE 2021 Online)
Works count: 33
Citation count: 52
H-index: 4
I10-index: 1
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