Somatic Genome Variations: First Steps Towards a Deeper Understanding of an Underappreciated Source of Biodiversity and Disease

Por Yurov, Yuri B., Iourov, Ivan Y.
Publicado em 2010

Thoughts about SLC16A2, TSIX and XIST gene like sites in the human genome and a potential role in cellular chromosome counting

Por Rinčić, Martina, Iourov, Ivan Y., Liehr, Thomas
Publicado no Mol Cytogenet (2016)

Chromosomal mosaicism goes global

Por Iourov, Ivan Y, Vorsanova, Svetlana G, Yurov, Yuri B
Publicado em 2008

GIN'n'CIN hypothesis of brain aging: deciphering the role of somatic genetic instabilities and neural aneuploidy during ontogeny

Por Yurov, Yuri B, Vorsanova, Svetlana G, Iourov, Ivan Y
Publicado em 2009

Human interphase chromosomes: a review of available molecular cytogenetic technologies

Por Vorsanova, Svetlana G, Yurov, Yuri B, Iourov, Ivan Y
Publicado em 2010

The DNA Replication Stress Hypothesis of Alzheimer's Disease

Por Yurov, Yuri B., Vorsanova, Svetlana G., Iourov, Ivan Y.
Publicado em 2012

Single Cell Genomics of the Brain: Focus on Neuronal Diversity and Neuropsychiatric Diseases

Por Iourov, Ivan Y, Vorsanova, Svetlana G, Yurov, Yuri B
Publicado em 2012

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

Por Iourov, Ivan Y, Vorsanova, Svetlana G, Yurov, Yuri B
Publicado no Mol Cytogenet (2014)

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

Por Iourov, Ivan Y., Vorsanova, Svetlana G., Kurinnaia, Oxana S., Yurov, Yuri B.
Publicado em 2013

An Interstitial Deletion at 10q26.2q26.3

Por Iourov, Ivan Y., Vorsanova, Svetlana G., Kurinnaia, Oxana S., Yurov, Yuri B.
Publicado em 2014

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

Por Iourov, Ivan Y., Vorsanova, Svetlana G., Voinova, Victoria Y., Yurov, Yuri B.
Publicado no Mol Cytogenet (2015)

A new open access journal for a rapidly evolving biomedical field: introducing Molecular Cytogenetics

Por Yurov, Yuri B, Liehr, Thomas, Shaffer, Lisa G, Iourov, Ivan Y, Vorsanova, Svetlana G
Publicado em 2008

X chromosome aneuploidy in the Alzheimer’s disease brain

Por Yurov, Yuri B, Vorsanova, Svetlana G, Liehr, Thomas, Kolotii, Alexei D, Iourov, Ivan Y
Publicado em 2014

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

Por Iourov, Ivan Y., Vorsanova, Svetlana G., Zelenova, Maria A., Korostelev, Sergei A., Yurov, Yuri B.
Publicado no Int J Genomics (2015)

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

Por Iourov, Ivan Y., Vorsanova, Svetlana G., Korostelev, Sergei A., Zelenova, Maria A., Yurov, Yuri B.
Publicado no Mol Cytogenet (2015)

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

Por Iourov, Ivan Y, Vorsanova, Svetlana G, Kurinnaia, Oxana S, Zelenova, Maria A, Silvanovich, Alexandra P, Yurov, Yuri B
Publicado em 2012

5p13.3p13.2 duplication associated with developmental delay, congenital malformations and chromosome instability manifested as low-level aneuploidy

Por Iourov, Ivan Y., Vorsanova, Svetlana G., Demidova, Irina A., Aliamovskaia, Galina A., Keshishian, Elena S., Yurov, Yuri B.
Publicado no Springerplus (2015)

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

Por Iourov, Ivan Y, Vorsanova, Svetlana G, Voinova, Victoria Y, Kurinnaia, Oxana S, Zelenova, Maria A, Demidova, Irina A, Yurov, Yuri B
Publicado em 2013

Partial monosomy 7q34-qter and 21pter-q22.13 due to cryptic unbalanced translocation t(7;21) but not monosomy of the whole chromosome 21: a case report plus review of the literatur...

Por Vorsanova, Svetlana G, Iourov, Ivan Y, Voinova-Ulas, Victoria Y, Weise, Anja, Monakhov, Victor V, Kolotii, Alexei D, Soloviev, Ilia V, Novikov, Petr V, Yurov, Yuri B, Liehr, Thomas
Publicado em 2008

Aneuploidy and Confined Chromosomal Mosaicism in the Developing Human Brain

Por Yurov, Yuri B., Iourov, Ivan Y., Vorsanova, Svetlana G., Liehr, Thomas, Kolotii, Alexei D., Kutsev, Sergei I., Pellestor, Franck, Beresheva, Alfia K., Demidova, Irina A., Kravets, Viktor S., Monakhov, Viktor V., Soloviev, Ilia V.
Publicado em 2007