Works by Yurov, Yuri B.

Results: 27

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

Published in:

International Journal of Genomics, 2015, v. 2015, p. 1, doi. 10.1155/2015/757680

By:

Iourov, Ivan Y.;
Vorsanova, Svetlana G.;
Zelenova, Maria A.;
Korostelev, Sergei A.;
Yurov, Yuri B.

Publication type:

Article

Ontogenetic and Pathogenetic Views on Somatic Chromosomal Mosaicism.

Published in:

Genes, 2019, v. 10, n. 5, p. 379, doi. 10.3390/genes10050379

By:

Iourov, Ivan Y.;
Vorsanova, Svetlana G.;
Yurov, Yuri B.;
Kutsev, Sergei I.

Publication type:

Article

Turner's syndrome mosaicism in girls with neurodevelopmental disorders: a cohort study and hypothesis.

Published in:

Molecular Cytogenetics (17558166), 2021, v. 14, n. 1, p. 1, doi. 10.1186/s13039-021-00529-2

By:

Vorsanova, Svetlana G.;
Kolotii, Alexey D.;
Kurinnaia, Oksana S.;
Kravets, Victor S.;
Demidova, Irina A.;
Soloviev, Ilya V.;
Yurov, Yuri B.;
Iourov, Ivan Y.

Publication type:

Article

Dynamic nature of somatic chromosomal mosaicism, genetic-environmental interactions and therapeutic opportunities in disease and aging.

Published in:

Molecular Cytogenetics (17558166), 2020, v. 13, n. 1, p. 1, doi. 10.1186/s13039-020-00488-0

By:

Vorsanova, Svetlana G.;
Yurov, Yuri B.;
Iourov, Ivan Y.

Publication type:

Article

Laundering CNV data for candidate process prioritization in brain disorders.

Published in:

Molecular Cytogenetics (17558166), 2019, v. 12, n. 1, p. 1, doi. 10.1186/s13039-019-0468-7

By:

Zelenova, Maria A.;
Yurov, Yuri B.;
Vorsanova, Svetlana G.;
Iourov, Ivan Y.

Publication type:

Article

The variome concept: focus on CNVariome.

Published in:

Molecular Cytogenetics (17558166), 2019, v. 12, n. 1, p. 1, doi. 10.1186/s13039-019-0467-8

By:

Iourov, Ivan Y.;
Vorsanova, Svetlana G.;
Yurov, Yuri B.

Publication type:

Article

VIII World Rett Syndrome Congress & Symposium of rare diseases, Kazan, Russia.

Published in:

Molecular Cytogenetics (17558166), 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13039-018-0412-2

By:

Vorsanova, Svetlana G.;
Yurov, Yuri B.;
Iourov, Ivan Y.;
Bertrand, Thomas

Publication type:

Article

Pathway-based classification of genetic diseases.

Published in:

Molecular Cytogenetics (17558166), 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s13039-019-0418-4

By:

Iourov, Ivan Y.;
Vorsanova, Svetlana G.;
Yurov, Yuri B.

Publication type:

Article

3p22.1p21.31 microdeletion identifies CCK as Asperger syndrome candidate gene and shows the way for therapeutic strategies in chromosome imbalances.

Published in:

Molecular Cytogenetics (17558166), 2015, v. 8, p. 1, doi. 10.1186/s13039-015-0185-9

By:

Iourov, Ivan Y.;
Vorsanova, Svetlana G.;
Voinova, Victoria Y.;
Yurov, Yuri B.

Publication type:

Article

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

Published in:

Molecular Cytogenetics (17558166), 2015, v. 8, p. 2, doi. 10.1186/s13039-015-0182-z

By:

Iourov, Ivan Y.;
Vorsanova, Svetlana G.;
Korostelev, Sergei A.;
Zelenova, Maria A.;
Yurov, Yuri B.

Publication type:

Article

Mosaike im Gehirn des Menschen.

Published in:

Medizinische Genetik, 2014, v. 26, n. 3, p. 342, doi. 10.1007/s11825-014-0010-6

By:

Iourov, Ivan Y.;
Vorsanova, Svetlana G.;
Liehr, Thomas;
Yurov, Yuri B.

Publication type:

Article

Prenatal diagnosis of trisomy 21 using interphase fluorescence in situ hybridization of post-replicated cells with site-specific cosmid and cosmid contig probes.

Published in:

1995

By:

Soloviev, Ilia V.;
Yurov, Yuri B.;
Vorsanova, Svetlana G.;
Fayet, Florance;
Roizes, Gerard;
Malet, Paul;
Soloviev, I V;
Yurov, Y B;
Vorsanova, S G;
Fayet, F;
Roizes, G;
Malet, P

Publication type:

journal article

Increased chromosome instability dramatically disrupts neural genome integrity and mediates cerebellar degeneration in the ataxia-telangiectasia brain.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 14, p. 2656, doi. 10.1093/hmg/ddp207

By:

Iourov, Ivan Y.;
Vorsanova, Svetlana G.;
Liehr, Thomas;
Kolotii, Alexei D.;
Yurov, Yuri B.

Publication type:

Article

In silico molecular cytogenetics: a bioinformatic approach to prioritization of candidate genes and copy number variations for basic and clinical genome research.

Published in:

Molecular Cytogenetics (17558166), 2014, v. 7, n. 1, p. 143, doi. 10.1186/s13039-014-0098-z

By:

Iourov, Ivan Y.;
Vorsanova, Svetlana G.;
Yurov, Yuri B.

Publication type:

Article

X chromosome aneuploidy in the Alzheimer's disease brain.

Published in:

Molecular Cytogenetics (17558166), 2014, v. 7, n. 1, p. 1, doi. 10.1186/1755-8166-7-20

By:

Yurov, Yuri B.;
Vorsanova, Svetlana G.;
Liehr, Thomas;
Kolotii, Alexei D.;
Iourov, Ivan Y.

Publication type:

Article

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

Published in:

Molecular Cytogenetics (17558166), 2013, v. 6, n. 1, p. 1, doi. 10.1186/1755-8166-6-53

By:

Iourov, Ivan Y.;
Vorsanova, Svetlana G.;
Voinova, Victoria Y.;
Kurinnaia, Oxana S.;
Zelenova, Maria A.;
Demidova, Irina A.;
Yurov, Yuri B.

Publication type:

Article

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

Published in:

Molecular Cytogenetics (17558166), 2012, v. 5, n. 1, p. 46, doi. 10.1186/1755-8166-5-46

By:

Iourov, Ivan Y.;
Vorsanova, Svetlana G.;
Kurinnaia, Oxana S.;
Zelenova, Maria A.;
Silvanovich, Alexandra P.;
Yurov, Yuri B.

Publication type:

Article

Human interphase chromosomes: a review of available molecular cytogenetic technologies.

Published in:

Molecular Cytogenetics (17558166), 2010, v. 3, p. 1, doi. 10.1186/1755-8166-3-1

By:

Vorsanova, Svetlana G.;
Yurov, Yuri B.;
Iourov, Ivan Y.

Publication type:

Article

First case of del(1)(p36.2p33) in a fetus delivered stillborn.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 11, p. 1092, doi. 10.1002/pd.1571

By:

Iourov, Ivan Y.;
Vorsanova, Svetlana G.;
Kirillova, Elena A.;
Yurov, Yuri B.

Publication type:

Article

Somatic mosaicism in the diseased brain.

Published in:

Molecular Cytogenetics (17558166), 2022, v. 15, n. 1, p. 1, doi. 10.1186/s13039-022-00624-y

By:

Iourov, Ivan Y.;
Vorsanova, Svetlana G.;
Kurinnaia, Oxana S.;
Kutsev, Sergei I.;
Yurov, Yuri B.

Publication type:

Article

Klinefelter syndrome mosaicism in boys with neurodevelopmental disorders: a cohort study and an extension of the hypothesis.

Published in:

Molecular Cytogenetics (17558166), 2022, v. 15, n. 1, p. 1, doi. 10.1186/s13039-022-00588-z

By:

Vorsanova, Svetlana G.;
Demidova, Irina A.;
Kolotii, Alexey D.;
Kurinnaia, Oksana S.;
Kravets, Victor S.;
Soloviev, Ilya V.;
Yurov, Yuri B.;
Iourov, Ivan Y.

Publication type:

Article

Chromosome Instability, Aging and Brain Diseases.

Published in:

Cells (2073-4409), 2021, v. 10, n. 5, p. 1256, doi. 10.3390/cells10051256

By:

Iourov, Ivan Y.;
Yurov, Yuri B.;
Vorsanova, Svetlana G.;
Kutsev, Sergei I.;
Jin, Kunlin;
Su, Huanxing;
Yang, Guo-Yuan

Publication type:

Article

An Interstitial Deletion at 10q26.2q26.3.

Published in:

2014

By:

Iourov, Ivan Y.;
Vorsanova, Svetlana G.;
Kurinnaia, Oxana S.;
Yurov, Yuri B.

Publication type:

Case Study

An Interstitial 20q11.21 Microdeletion Causing Mild Intellectual Disability and Facial Dysmorphisms.

Published in:

Case Reports in Genetics, 2013, p. 1, doi. 10.1155/2013/353028

By:

Iourov, Ivan Y.;
Vorsanova, Svetlana G.;
Kurinnaia, Oxana S.;
Yurov, Yuri B.

Publication type:

Article

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

Published in:

International Journal of Molecular Sciences, 2020, v. 21, n. 21, p. 8328, doi. 10.3390/ijms21218328

By:

Iourov, Ivan Y.;
Vorsanova, Svetlana G.;
Yurov, Yuri B.;
Zelenova, Maria A.;
Kurinnaia, Oxana S.;
Vasin, Kirill S.;
Kutsev, Sergei I.

Publication type:

Article

Genomic Landscape of the Alzheimer's Disease Brain: Chromosome Instability - Aneuploidy, but Not Tetraploidy - Mediates Neurodegeneration.

Published in:

Neurodegenerative Diseases, 2010, v. 8, n. 1/2, p. 35, doi. 10.1159/000315398

By:

Iourov, Ivan Y.;
Vorsanova, Svetlana G.;
Yurov, Yuri B.

Publication type:

Article

The Evolutionary Origin of Man Can Be Traced in the Layers of Defunct Ancestral Alpha Satellites Flanking the Active Centromeres of Human Chromosomes.

Published in:

PLoS Genetics, 2009, v. 5, n. 9, p. 1, doi. 10.1371/journal.pgen.1000641

By:

Shepelev, Valery A.;
Alexandrov, Alexander A.;
Yurov, Yuri B.;
Alexandrov, Ivan A.

Publication type:

Article