Iourov IY - Search Results

1

Iourov IY, Gerasimov AP, Zelenova MA, Ivanova NE, Kurinnaia OS, Zabrodskaya YM, Demidova IA, Barantsevich ER, Vasin KS, Kolotii AD, Ushanov VV, Sitovskaya DA, Lobzhanidze TB, Iuditskaia ME, Iakushev NS, Zhumatov MM, Vorsanova SG, Samochernyh KA. Iourov IY, et al. Mol Cytogenet. 2023 Jan 5;16(1):1. doi: 10.1186/s13039-022-00634-w. Mol Cytogenet. 2023. PMID: 36600272 Free PMC article. Review.

2

Chromosomal mosaicism goes global.

Iourov IY, Vorsanova SG, Yurov YB. Iourov IY, et al. Mol Cytogenet. 2008 Nov 25;1:26. doi: 10.1186/1755-8166-1-26. Mol Cytogenet. 2008. PMID: 19032785 Free PMC article.

3

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

Iourov IY, Vorsanova SG, Kurinnaia OS, Zelenova MA, Silvanovich AP, Yurov YB. Iourov IY, et al. Mol Cytogenet. 2012 Dec 31;5(1):46. doi: 10.1186/1755-8166-5-46. Mol Cytogenet. 2012. PMID: 23272938 Free PMC article.

4

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

Iourov IY, Vorsanova SG, Voinova VY, Kurinnaia OS, Zelenova MA, Demidova IA, Yurov YB. Iourov IY, et al. Mol Cytogenet. 2013 Nov 27;6(1):53. doi: 10.1186/1755-8166-6-53. Mol Cytogenet. 2013. PMID: 24283533 Free PMC article.

5

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

Iourov IY, Vorsanova SG, Yurov YB. Iourov IY, et al. Mol Cytogenet. 2014 Dec 9;7(1):98. doi: 10.1186/s13039-014-0098-z. eCollection 2014. Mol Cytogenet. 2014. PMID: 25525469 Free PMC article.

6

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

Iourov IY, Vorsanova SG, Korostelev SA, Zelenova MA, Yurov YB. Iourov IY, et al. Mol Cytogenet. 2015 Oct 15;8:77. doi: 10.1186/s13039-015-0182-z. eCollection 2015. Mol Cytogenet. 2015. PMID: 26478745 Free PMC article.

7

Pathway-based classification of genetic diseases.

Iourov IY, Vorsanova SG, Yurov YB. Iourov IY, et al. Mol Cytogenet. 2019 Feb 4;12:4. doi: 10.1186/s13039-019-0418-4. eCollection 2019. Mol Cytogenet. 2019. PMID: 30766616 Free PMC article.

8

The variome concept: focus on CNVariome.

Iourov IY, Vorsanova SG, Yurov YB. Iourov IY, et al. Mol Cytogenet. 2019 Dec 19;12:52. doi: 10.1186/s13039-019-0467-8. eCollection 2019. Mol Cytogenet. 2019. PMID: 31890032 Free PMC article.

9

Laundering CNV data for candidate process prioritization in brain disorders.

Zelenova MA, Yurov YB, Vorsanova SG, Iourov IY. Zelenova MA, et al. Among authors: iourov iy. Mol Cytogenet. 2019 Dec 26;12:54. doi: 10.1186/s13039-019-0468-7. eCollection 2019. Mol Cytogenet. 2019. PMID: 31890034 Free PMC article.

10

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

Vorsanova SG, Yurov YB, Iourov IY. Vorsanova SG, et al. Among authors: iourov iy. Mol Cytogenet. 2020 May 7;13:16. doi: 10.1186/s13039-020-00488-0. eCollection 2020. Mol Cytogenet. 2020. PMID: 32411302 Free PMC article.

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