Mari A. Hachmeriyan

1 Hristo Smirnenski Blvd
Varna, 9010, Bulgaria

Last Updated: 09/26/2026

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Found 20 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

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

Clinical Utility of Multiplex Ligation-Dependent Probe Amplification in the Genetic Assessment of Patients with Myelodysplastic Syndrome.

Clinical Utility of Multiplex Ligation-Dependent Probe Amplification in the Genetic Assessment of Patients with Myelodysplastic Syndrome.

Journal: Biomedicines

Published: October 30, 2025

Post-Transplant Double Malignancy: Multiple Myeloma and Papillary Renal Cell Carcinoma-A Case Report.

Post-Transplant Double Malignancy: Multiple Myeloma and Papillary Renal Cell Carcinoma-A Case Report.

Journal: Reports (MDPI)

Published: September 28, 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

Multifaceted Primary Ciliary Dyskinesia-A Case Report.

Multifaceted Primary Ciliary Dyskinesia-A Case Report.

Journal: Reports (MDPI)

Published: January 13, 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 20

Last Updated: 09/26/2026