Yulia V. Fomicheva

2, Akkuratova Street, 197341
Saint Petersburg, SPE, Russian Federation

Last Updated: 09/26/2026

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Found 11 publications

The clinical and genetic spectrum of pediatric hypertrophic cardiomyopathy manifesting before one year of age.

The clinical and genetic spectrum of pediatric hypertrophic cardiomyopathy manifesting before one year of age.

Journal: Pediatric research

Published: January 12, 2025

A Comprehensive Target Panel Allows to Extend the Genetic Spectrum of Neuroendocrine Tumors.

A Comprehensive Target Panel Allows to Extend the Genetic Spectrum of Neuroendocrine Tumors.

Journal: Neuroendocrinology

Published: April 09, 2024

Shift of N-MYC Oncogene Expression in AML Patients Carrying the FLT3-ITD Mutation.

Shift of N-MYC Oncogene Expression in AML Patients Carrying the FLT3-ITD Mutation.

Journal: Pathophysiology : the official journal of the International Society for Pathophysiology

Published: May 05, 2023

Characterization of the novel heterozygous SCN5A genetic variant Y739D associated with Brugada syndrome.

Characterization of the novel heterozygous SCN5A genetic variant Y739D associated with Brugada syndrome.

Journal: Biochemistry and biophysics reports

Published: December 01, 2021

Different Expressions of Pericardial Fluid MicroRNAs in Patients With Arrhythmogenic Right Ventricular Cardiomyopathy and Ischemic Heart Disease Undergoing Ventricular Tachycardia Ablation.

Different Expressions of Pericardial Fluid MicroRNAs in Patients With Arrhythmogenic Right Ventricular Cardiomyopathy and Ischemic Heart Disease Undergoing Ventricular Tachycardia Ablation.

Journal: Frontiers in cardiovascular medicine

Published: December 30, 2020

Generation of two iPSC lines (FAMRCi007-A and FAMRCi007-B) from patient with Emery-Dreifuss muscular dystrophy and heart rhythm abnormalities carrying genetic variant LMNA p.Arg249Gln.

Generation of two iPSC lines (FAMRCi007-A and FAMRCi007-B) from patient with Emery-Dreifuss muscular dystrophy and heart rhythm abnormalities carrying genetic variant LMNA p.Arg249Gln.

Journal: Stem cell research

Published: June 04, 2020

A 300-kb microduplication of 7q36.3 in a patient with triphalangeal thumb-polysyndactyly syndrome combined with congenital heart disease and optic disc coloboma: a case report.

A 300-kb microduplication of 7q36.3 in a patient with triphalangeal thumb-polysyndactyly syndrome combined with congenital heart disease and optic disc coloboma: a case report.

Journal: BMC medical genomics

Published: June 01, 2020

Genetic Spectrum of Left Ventricular Non-Compaction in Paediatric Patients.

Genetic Spectrum of Left Ventricular Non-Compaction in Paediatric Patients.

Journal: Cardiology

Published: May 20, 2020

Generation of two induced pluripotent stem cell lines (FAMRCi005-A and FAMRCi005-B) from patient carrying genetic variant LMNA p.Asp357Val.

Generation of two induced pluripotent stem cell lines (FAMRCi005-A and FAMRCi005-B) from patient carrying genetic variant LMNA p.Asp357Val.

Journal: Stem cell research

Published: November 30, 2019

Generation of two iPSC lines (FAMRCi006-A and FAMRCi006-B) from patient with dilated cardiomyopathy and Emery-Dreifuss muscular dystrophy associated with genetic variant LMNAp.Arg527Pro.

Generation of two iPSC lines (FAMRCi006-A and FAMRCi006-B) from patient with dilated cardiomyopathy and Emery-Dreifuss muscular dystrophy associated with genetic variant LMNAp.Arg527Pro.

Journal: Stem cell research

Published: November 30, 2019

Truncating Variant in Myof Gene Is Associated With Limb-Girdle Type Muscular Dystrophy and Cardiomyopathy.

Truncating Variant in Myof Gene Is Associated With Limb-Girdle Type Muscular Dystrophy and Cardiomyopathy.

Journal: Frontiers in genetics

Published: November 26, 2018

Showing 1-11 of 11

Last Updated: 09/26/2026