Larysa Sivitskaya

Work

Genomed (Poland)

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clinical variant analyst

Poland

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National Academy of Sciences of Belarus

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PhD, senior researcher

Belarus

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Education

Institute of Genetics and Cytology

Belarus
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PhD

Belarussian State University

Belarus
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Publications

Optimised, Broad NGS Panel for Inherited Eye Diseases to Diagnose 1000 Patients in Poland

Biomedicines

journal-article

Optimised, Broad NGS Panel for Inherited Eye Diseases to Diagnose 1000 Patients in Poland

Biomedicines

journal-article

Genetic spectrum of familial and sporadic dilated cardiomyopathy: arrhythmic phenotypes associated with mutations in the lamin A/C (LMNA) gene

Eurasian heart journal

journal-article

Sporadic Dilated Cardiomyopathy: Real Prevalence of the Familial Disease as a Result of Cascade Screening of the “Idiopathic” Dilated Cardiomyopathy

Kardiologija v Belarusi

journal-article

New deletion in LAMP2 causing familial Danon disease. Effect of the X-chromosome inactivation

Folia Medica

journal-article

Non-compaction and dilated cardiomyopathy: genotypic, phenotypic and prognostic differences

Russian Journal of Cardiology

journal-article

Non-compaction and dilated cardiomyopathy: genotypic, phenotypic and prognostic differences

Russian Journal of Cardiology

journal-article

New Deletion in LAMP2 Causing Familial Danon Disease. Effect of X-Chromosome Inactivation,Новая делеция в LAMP2, связанная с семейным случаем болезни Данона. Эффект инактивации Х-хромосомы

Folia Medica

journal-article

AHR-dependent genes and response to MTX therapy in rheumatoid arthritis patients

Pharmacogenomics Journal

journal-article

Genetic risk factors for dilated cardiomyopathy

Russian Journal of Cardiology

journal-article

Genetic risk factors for dilated cardiomyopathy

Russian Journal of Cardiology

journal-article

AHR-dependent genes and response to MTX therapy in rheumatoid arthritis patients

The Pharmacogenomics Journal

journal-article

Application of NGS Technology in Understanding the Pathology of Autoimmune Diseases

Journal of Clinical Medicine

journal-article

Application of NGS Technology in Understanding the Pathology of Autoimmune Diseases

Journal of Clinical Medicine

journal-article

Application of ngs technology in understanding the pathology of autoimmune diseases

Journal of Clinical Medicine

journal-article

Application of Massive Parallel DNA Sequencing to Diagnose Drug-Resistant Epilepsy in Children

Molecular Genetics, Microbiology and Virology

journal-article

Arrhythmogenic cardiomyopathy. Part ii: Clinical and genetic assessment of the new phenotypes

Kardiologija v Belarusi

journal-article

New opportunities of electrocardiography for diagnostics and prediction of dilated cardiomyopathy

Kardiologija v Belarusi

journal-article

Splicing mutation in TAZ gene leading to exon skipping and Barth syndrome

Acta Myologica

journal-article

Arrhythmogenic cardiomyopathy. Part i: Change of the concept, new phenotypes and diagnostic criteria

Kardiologija v Belarusi

journal-article

Long QT syndrome: Clinical and genetic diagnostic complications

Kardiologija v Belarusi

journal-article

Atrial cardiomyopathy — a new concept with a long history

Russian Journal of Cardiology

journal-article

Atrial cardiomyopathy — a new concept with a long history

Russian Journal of Cardiology

journal-article

Non-compaction cardiomyopathy. Part II: limitations of imaging techniques and genetic screening, clinical observations

Russian Journal of Cardiology

journal-article

Non-compaction cardiomyopathy. Part ii: Limitations of imaging techniques and genetic screening, clinical observations

Russian Journal of Cardiology

journal-article

Non-compaction cardiomyopathy. Part I: clinical and genetic heterogeneity and predictors of unfavorable prognosis

Russian Journal of Cardiology

journal-article

Non-compaction cardiomyopathy. Part i: Clinical and genetic heterogeneity and predictors of unfavorable prognosis

Russian Journal of Cardiology

journal-article

A paradigm shift in the concept of arrhythmogenic cardiomyopathy: expanding the clinical and genetic spectrum, new diagnostic criteria for left ventricular phenotypes

Russian Journal of Cardiology

journal-article

A paradigm shift in the concept of arrhythmogenic cardiomyopathy: Expanding the clinical and genetic spectrum, new diagnostic criteria for left ventricular phenotypes

Russian Journal of Cardiology

journal-article

Splicing mutation in LAMP2 gene leading to exon skipping and cardiomyopathy development

Gene Reports

journal-article

Splicing mutation in LAMP2 gene leading to exon skipping and cardiomyopathy development

Gene Reports

journal-article

Non-compact cardiomyopathy: Clinical-genetic analysis (the first experience in Belarus)

Kardiologija v Belarusi

journal-article

Restrictive cardiomyopathy: difficulties desminopathy diagnostics

Russian Journal of Cardiology

journal-article

Dilated cardiomyopathy: reconceptualization of the problem

Russian Journal of Cardiology

journal-article

Dilated cardiomyopathy: Reconceptualization of the problem

Russian Journal of Cardiology

journal-article

Dilated cardiomyopathy: Genetic predictors in assessment of the risk of sudden death

Kardiologija v Belarusi

journal-article

Restrictive cardiomyopathy: Difficulties desminopathy diagnostics

Russian Journal of Cardiology

journal-article

Carvajal syndrome: a brief overview and clinical case of cardiomyopathy, associated with compound heterozygous mutations of the desmoplakin gene

Russian Journal of Cardiology

journal-article

Carvajal syndrome: a brief overview and clinical case of cardiomyopathy, associated with compound heterozygous mutations of the desmoplakin gene

Russian Journal of Cardiology

journal-article

Carvajal syndrome: A brief overview and clinical case of cardiomyopathy, associated with compound heterozygous mutations of the desmoplakin gene

Russian Journal of Cardiology

journal-article

LMNA-associated dilated cardiomyopathy: Variability of clinical manifestations

Kardiologija v Belarusi

journal-article

Left ventricular noncompaction: A distinct cardiomyopathy or a composite anatomical syndrome?

Kardiologiya

journal-article

Molecular-genetic diagnostics of sudden cardiac death: The first experience in Belarus

Kardiologija v Belarusi

journal-article

Novel desmoplakin mutations in familial Carvajal syndrome

Acta Myologica

journal-article

DANON DISEASE: A RARE SYSTEMIC DISORDER WITH THE LAMP2-CARDIOMYOPATHY

Russian Journal of Cardiology

journal-article

Danon disease: A rare systemic disorder with the LAMP2-cardiomyopathy

Russian Journal of Cardiology

journal-article

Three new cases of dilated cardiomyopathy caused by mutations in LMNA gene

Acta Myologica

journal-article

Case Report of Malouf Syndrome not Associated with LMNA Gene Mutation

MOJ Clinical & Medical Case Reports

journal-article

Lamin A/C hot spot codon 190: form various amino acid substitutions to clinical effects

Cardiovascular Research

conference-abstract

Dilatation of the Chambers of the Heart Caused by a Mutation of Lamin Gene (LMNA)

Kardiologiia

journal-article

Dilatation of the chambers of the heart caused by mutation in lamin gene (LMNA)

Kardiologiya

journal-article

[Dilatation of the Chambers of the Heart Caused by a Mutation of Lamin Gene (LMNA)].

Kardiologiia

journal-article

AN INDIVIDUALIZED RISK ASSESSMENT OF SUDDEN CARDIAC DEATH IN DILATION CARDIOMYOPATHY PATIENTS

Russian Journal of Cardiology

journal-article

An individualized risk assessment of sudden cardiac death in dilation cardiomyopathy patients

Russian Journal of Cardiology

journal-article

AN ORPHAN PHENOTYPE OF CARDIOGENITAL LAMINOPATHY — MALOUF SYNDROME

Russian Journal of Cardiology

journal-article

An orphan phenotype of cardiogenital laminopathy — Malouf syndrome

Russian Journal of Cardiology

journal-article

Dilated cardiomyopathy: clinical signs of the lamin-related phenotype and predictors of life-threatening tachyarrhythmia

Russian Heart Failure Journal

journal-article

Genotype-phenotype clinical cases of laminopathies by MOGE (S) classifying

Unpublished

other

Genotype-phenotype of laminopathies by MOGE (S) classifying

Unpublished

other

The multidisciplinary and multisystemic issue of laminopathies: many diseases, one gene

Russian Heart Failure Journal

journal-article

The algorithm of diagnosis and treatment for patients with dilated cardiomyopathy

Russian Heart Failure Journal

journal-article

LMNA-related dilated cardiomyopathy.

journal-article

LMNA-related dilated cardiomyopathy

Oxford Medical Case Reports

journal-article

AB0026 Genetic markers of secondary amyloidosis in belarusian patiens with rheumatoid arthitis

Annals of the Rheumatic Diseases

journal-article

HFE Gene Mutation Associated with the Severity of Gestational Diabetes Mellitus in Belarusian Women

Open Journal of Endocrine and Metabolic Diseases

journal-article

Uniparental genetic heritage of belarusians: encounter of rare middle eastern matrilineages with a central European mitochondrial DNA pool.

journal-article

Uniparental Genetic Heritage of Belarusians: Encounter of Rare Middle Eastern Matrilineages with a Central European Mitochondrial DNA Pool

PLoS ONE

journal-article

The Y chromosome R1A1A7 (M458) haplogroup of modern Belarusians and migrations of ancestors of Slavs on Belarus' territory

Russian Journal of Genetics: Applied Research

journal-article

[Gene polymorphism of the renin-angiotensin system in six ethnic/geographic regions of Belarus].

Genetika

journal-article

Gene polymorphism of the renin-angiotensin system in six ethnogeographic regions of Belarus

Russian Journal of Genetics

journal-article