Vili K. Stoyanova

Plovdiv, 4000, Bulgaria

Last Updated: 09/26/2026

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Found 11 publications

Neuronal Heterotopy in a Patient with Wiedemann-Steiner Syndrome Caused by a Truncating KMT2A Variant: Clinical and Genetic Correlations.

Neuronal Heterotopy in a Patient with Wiedemann-Steiner Syndrome Caused by a Truncating KMT2A Variant: Clinical and Genetic Correlations.

Journal: Reports (MDPI)

Published: January 06, 2026

Analysis and evaluation of correlation between DNA polymorphism in the genes MTHFR, PAI-1 and serum creatinine, creatinine clearance and albumin/creatinine ratio in morning urine of patients with type 2 diabetes mellitus and diabetic nephropathy.

Analysis and evaluation of correlation between DNA polymorphism in the genes MTHFR, PAI-1 and serum creatinine, creatinine clearance and albumin/creatinine ratio in morning urine of patients with type 2 diabetes mellitus and diabetic nephropathy.

Journal: Folia medica

Published: April 26, 2021

Application of pharmacogenetics in oncology.

Application of pharmacogenetics in oncology.

Journal: Biomarker research

Published: May 28, 2020

Mutations Associated with Imatinib Mesylate Resistance - Review.

Mutations Associated with Imatinib Mesylate Resistance - Review.

Journal: Folia medica

Published: October 11, 2017

Investigation of fasciculation and elongation protein ζ-1 (FEZ1) in peripheral blood reveals differences in gene expression in patients with schizophrenia.

Investigation of fasciculation and elongation protein ζ-1 (FEZ1) in peripheral blood reveals differences in gene expression in patients with schizophrenia.

Journal: Balkan journal of medical genetics : BJMG

Published: March 02, 2016

FREQUENCIES OF FETAL CHROMOSOMAL ABERRATIONS DETECTED BY AMNIOCENTESIS: OUR 15-YEARS EXPERIENCE

FREQUENCIES OF FETAL CHROMOSOMAL ABERRATIONS DETECTED BY AMNIOCENTESIS: OUR 15-YEARS EXPERIENCE

Journal: Akusherstvo i ginekologiia

Published: September 29, 2015

CYTOGENETIC ANALYSIS OF PATIENTS WITH PRIMARY AMENORRHEA

CYTOGENETIC ANALYSIS OF PATIENTS WITH PRIMARY AMENORRHEA

Journal: Akusherstvo i ginekologiia

Published: July 04, 2015

PRENATAL DIAGNOSIS OF FOETAL TRISOMY 3Q WITH PATERNAL ORIGIN

PRENATAL DIAGNOSIS OF FOETAL TRISOMY 3Q WITH PATERNAL ORIGIN

Journal: Akusherstvo i ginekologiia

Published: July 04, 2015

Autism Spectrum Disorder - A Complex Genetic Disorder.

Autism Spectrum Disorder - A Complex Genetic Disorder.

Journal: Folia medica

Published: December 01, 2014

Founder p.Arg 446* mutation in the PDHX gene explains over half of cases with congenital lactic acidosis in Roma children.

Founder p.Arg 446* mutation in the PDHX gene explains over half of cases with congenital lactic acidosis in Roma children.

Journal: Molecular genetics and metabolism

Published: May 30, 2014

Epigenetic aspects in schizophrenia etiology and pathogenesis.

Epigenetic aspects in schizophrenia etiology and pathogenesis.

Journal: Folia medica

Published: October 30, 2012

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Last Updated: 09/26/2026