Mariya Levkova

Varna, 9000, Bulgaria

Last Updated: 09/26/2026

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Found 28 publications

Genetic Counseling for Childhood Cancer Predisposition Syndromes: A Six-Year Retrospective Study.

Genetic Counseling for Childhood Cancer Predisposition Syndromes: A Six-Year Retrospective Study.

Journal: Children (Basel, Switzerland)
Published: April 18, 2026

A Lightweight Workflow for Targeted Long-Read Transcriptomic Profiling Using Oxford Nanopore Sequencing.

A Lightweight Workflow for Targeted Long-Read Transcriptomic Profiling Using Oxford Nanopore Sequencing.

Journal: Methods and protocols
Published: March 14, 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 Study.

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.

Journal: Children (Basel, Switzerland)
Published: February 23, 2026

A Novel Frameshift Variant in the SPAST Gene Causing Hereditary Spastic Paraplegia in a Bulgarian-Turkish Family.

A Novel Frameshift Variant in the SPAST Gene Causing Hereditary Spastic Paraplegia in a Bulgarian-Turkish Family.

Journal: Neurology international
Published: August 24, 2025

Genetic counselors' perspectives on the expanded use of non-invasive prenatal testing.

Genetic counselors' perspectives on the expanded use of non-invasive prenatal testing.

Journal: Journal of community genetics
Published: July 30, 2025

Genomic Evaluation of AML-Main Techniques and Novel Approaches.

Genomic Evaluation of AML-Main Techniques and Novel Approaches.

Journal: Journal of clinical medicine
Published: July 08, 2025

Two Decades of Huntington's Disease in Varna, Bulgaria: A Retrospective Single-Centre Study of Clinical Trends and Challenges.

Two Decades of Huntington's Disease in Varna, Bulgaria: A Retrospective Single-Centre Study of Clinical Trends and Challenges.

Journal: Neurology international
Published: May 03, 2025

Diagnostic Yield of Next-Generation Sequencing for Rare Pediatric Genetic Disorders: A Single-Center Experience.

Diagnostic Yield of Next-Generation Sequencing for Rare Pediatric Genetic Disorders: A Single-Center Experience.

Journal: Medical sciences (Basel, Switzerland)
Published: April 25, 2025

Genetic counseling for hereditary cancer syndromes: a 5-year experience from a single center in Bulgaria.

Genetic counseling for hereditary cancer syndromes: a 5-year experience from a single center in Bulgaria.

Journal: Oncology reviews
Published: April 03, 2025

An Ultra-Rare Disorder: Case Report on Cerebrotendinous Xanthomatosis.

An Ultra-Rare Disorder: Case Report on Cerebrotendinous Xanthomatosis.

Journal: Reports (MDPI)
Published: March 20, 2025

Ethical and Psychosocial Issues Associated with Genetic Testing for Hereditary Tumor Predisposition Syndromes.

Ethical and Psychosocial Issues Associated with Genetic Testing for Hereditary Tumor Predisposition Syndromes.

Journal: Healthcare (Basel, Switzerland)
Published: March 11, 2025

NIPT Integration as a Patient-Paid Prenatal Screening Option-Observations and Challenges from a Bulgarian Genetic Counseling Center.

NIPT Integration as a Patient-Paid Prenatal Screening Option-Observations and Challenges from a Bulgarian Genetic Counseling Center.

Journal: Medical sciences (Basel, Switzerland)
Published: December 02, 2024
Showing 1-12 of 28

Last Updated: 09/26/2026