M. Zelenova

发表

The Cytogenomic “Theory of Everything”: Chromohelkosis May Underlie Chromosomal Instability and Mosaicism in Disease and Aging

Y. Yurov, S. Vorsanova, I. Iourov, 2020, International journal of molecular sciences.

Black Carbon Emissions from the Siberian Fires 2019: Modelling of the Atmospheric Transport and Possible Impact on the Radiation Balance in the Arctic Region

A. Revokatova, S. Kostrykin, A. Chernenkov, 2021, Atmosphere.

Analysis of 329,942 SARS-CoV-2 records retrieved from GISAID database

M. Zelenova, S. Semyonov, Y. Gankin, 2021, bioRxiv.

Long contiguous stretches of homozygosity spanning shortly the imprinted loci are associated with intellectual disability, autism and/or epilepsy

Y. Yurov, S. Vorsanova, I. Iourov, 2015, Molecular Cytogenetics.

[Epigenomic variations manifesting as a loss of heterozygosity affecting imprinted genes represent a molecular mechanism of autism spectrum disorders and intellectual disability in children].

Y. Yurov, I. Iourov, M. Zelenova, 2019, Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova.

The Cytogenomic “Theory of Everything”: Chromohelkosis May Underlie Chromosomal Instability and Mosaicism in Disease and Aging

Y. Yurov, S. Vorsanova, I. Iourov, 2020, International journal of molecular sciences.

Algorithm of diagnostics of cognitive functions development violation in children born extremally premature

I. Iourov, I. Demidova, E. Keshishyan, 2020, Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics).

COVID-19: a crash test for biomedical publishing?

I. Iourov, M. Zelenova, S. Vorsanova, 2020, medRxiv.

CHROMOHELKOSIS — A UNUSUAL FORM OF CHROMOSOME INSTABILITY AND SOMATIC MOSAICISM ASSOCIATED WITH CENTRAL NERVOUS SYSTEM DISEASES IN CHILDREN

Y. Yurov, S. Vorsanova, I. Iourov, 2021, Современные проблемы науки и образования (Modern Problems of Science and Education).

4q21.2q21.3 Duplication: Molecular and Neuropsychological Aspects

Y. Yurov, S. Vorsanova, I. Iourov, 2017, Current genomics.

Molecular karyotyping by array CGH in a Russian cohort of children with intellectual disability, autism, epilepsy and congenital anomalies

Y. Yurov, S. Vorsanova, I. Iourov, 2012, Molecular Cytogenetics.

Cytogenomic epileptology

S. Vorsanova, I. Iourov, I. Demidova, 2023, Molecular Cytogenetics.

Long contiguous stretches of homozygosity spanning shortly the imprinted loci are associated with intellectual disability, autism and/or epilepsy

Y. Yurov, S. Vorsanova, I. Iourov, 2015, Molecular Cytogenetics.

DEVELOPMENTAL SPEECH DELAY AND AUTISM IN AN INFANT WITH CHROMOSOME 18P DELETION: PRIORITIZING CANDIDATE PROCESSES

M. Zelenova, K. S. Vasin, R. G. Kuramagomedova, 2022, Современные проблемы науки и образования (Modern Problems of Science and Education).

[Structural variations of the genome in autistic spectrum disorders with intellectual disability].

Y. Yurov, S. Vorsanova, I. Iourov, 2016, Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova.

Genomic Copy Number Variation Affecting Genes Involved in the Cell Cycle Pathway: Implications for Somatic Mosaicism

Y. Yurov, S. Vorsanova, I. Iourov, 2015, International journal of genomics.

Cytogenetic analysis in the era of highresolution molecular-cytogenetic methods: the potential of «reverse» karyotyping

Y. Yurov, S. Vorsanova, I. Iourov, 2019, Research Results in Biomedicine.

Xq28 (MECP2) microdeletions are common in mutation-negative females with Rett syndrome and cause mild subtypes of the disease

Y. Yurov, S. Vorsanova, I. Iourov, 2013, Molecular Cytogenetics.

Xq28 (MECP2) microdeletions are common in mutation-negative females with Rett syndrome and cause mild subtypes of the disease

Y. Yurov, S. Vorsanova, I. Iourov, 2013, Molecular Cytogenetics.

Laundering CNV data for candidate process prioritization in brain disorders

Y. Yurov, S. Vorsanova, I. Iourov, 2019, Molecular Cytogenetics.

Causes and Consequences of Genome Instability in Psychiatric and Neurodegenerative Diseases

Y. Yurov, I. Iourov, M. Zelenova, 2021 .

Causes and Consequences of Genome Instability in Psychiatric and Neurodegenerative Diseases

Y. Yurov, I. Iourov, M. Zelenova, 2021, Molecular Biology.

Behavioral Phenotypes in Genetic Syndromes Associated with Intellectual Disability and Autism. Clin Neuro Neurological Res Int J 2018, 1(1): 180001

M. Zelenova, S. Vorsanova, I. Iourov, 2018 .

Candidate processes for autism spectrum disorders revealed by copy number variation analysis

I. Iourov, M. Zelenova, S. Vorsanova, 2019 .

Laundering CNV data for candidate process prioritization in brain disorders

Y. Yurov, S. Vorsanova, I. Iourov, 2019, Molecular Cytogenetics.

Behavioral Variability and Somatic Mosaicism: A Cytogenomic Hypothesis

Y. Yurov, S. Vorsanova, I. Iourov, 2017, Current genomics.