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Items: 1 to 20 of 133

1.

Pathway-based classification of genetic diseases.

Iourov IY, Vorsanova SG, Yurov YB.

Mol Cytogenet. 2019 Feb 4;12:4. doi: 10.1186/s13039-019-0418-4. eCollection 2019.

2.

Opening up new horizons for psychiatric genetics in the Russian Federation: moving toward a national consortium.

Fedorenko OY, Golimbet VE, Ivanova SА, Levchenko А, Gainetdinov RR, Semke AV, Simutkin GG, Gareeva АE, Glotov АS, Gryaznova A, Iourov IY, Krupitsky EM, Lebedev IN, Mazo GE, Kaleda VG, Abramova LI, Oleichik IV, Nasykhova YA, Nasyrova RF, Nikolishin AE, Kasyanov ED, Rukavishnikov GV, Timerbulatov IF, Brodyansky VM, Vorsanova SG, Yurov YB, Zhilyaeva TV, Sergeeva AV, Blokhina EA, Zvartau EE, Blagonravova AS, Aftanas LI, Bokhan NА, Kekelidze ZI, Klimenko TV, Anokhina IP, Khusnutdinova EK, Klyushnik TP, Neznanov NG, Stepanov VA, Schulze TG, Kibitov АО.

Mol Psychiatry. 2019 Jan 21. doi: 10.1038/s41380-019-0354-z. [Epub ahead of print] Review.

PMID:
30664668
3.

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

Iourov IY, Vorsanova SG, Yurov YB, Bertrand T.

Mol Cytogenet. 2018 Dec 24;11:61. doi: 10.1186/s13039-018-0412-2. eCollection 2018. Review.

4.

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

Iourov IY, Zelenova MA, Vorsanova SG, Voinova VV, Yurov YB.

Curr Genomics. 2018 Apr;19(3):173-178. doi: 10.2174/1389202918666170717161426. Review.

5.

Mosaic Brain Aneuploidy in Mental Illnesses: An Association of Low-level Post-zygotic Aneuploidy with Schizophrenia and Comorbid Psychiatric Disorders.

Yurov YB, Vorsanova SG, Demidova IA, Kolotii AD, Soloviev IV, Iourov IY.

Curr Genomics. 2018 Apr;19(3):163-172. doi: 10.2174/1389202918666170717154340. Review.

6.

Behavioral Variability and Somatic Mosaicism: A Cytogenomic Hypothesis.

Vorsanova SG, Zelenova MA, Yurov YB, Iourov IY.

Curr Genomics. 2018 Apr;19(3):158-162. doi: 10.2174/1389202918666170719165339. Review.

7.

Serologic Markers of Autism Spectrum Disorder.

Khramova TV, Kaysheva AL, Ivanov YD, Pleshakova TO, Iourov IY, Vorsanova SG, Yurov YB, Schetkin AA, Archakov AI.

J Mol Neurosci. 2017 Aug;62(3-4):420-429. doi: 10.1007/s12031-017-0950-9. Epub 2017 Jul 20. Review.

PMID:
28730336
8.

[Genomic instability in the brain: chromosomal mosaicism in schizophrenia].

Yurov YB, Vorsanova SG, Demidova IA, Kravets VS, Vostrikov VM, Soloviev IV, Uranova NA, Iourov IY.

Zh Nevrol Psikhiatr Im S S Korsakova. 2016;116(11):86-91. doi: 10.17116/jnevro201611611186-91. Russian.

PMID:
28091506
9.

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

Iourov IY, Vorsanova SG, Korostelev SA, Vasin KS, Zelenova MA, Kurinnaia OS, Yurov YB.

Zh Nevrol Psikhiatr Im S S Korsakova. 2016;116(7):50-54. doi: 10.17116/jnevro20161167150-54. Russian.

PMID:
27500877
10.

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

Iourov IY, Vorsanova SG, Demidova IA, Aliamovskaia GA, Keshishian ES, Yurov YB.

Springerplus. 2015 Oct 15;4:616. doi: 10.1186/s40064-015-1399-3. eCollection 2015.

11.

[Clinical and genetic characteristics of the X chromosome distal long arm microduplications encompassing the MECP2 gene].

Voinova VY, Vorsanova SG, Yurov YB, Kolotiy AD, Davidova YI, Demidova IA, Novikov PV, Iourov IY.

Zh Nevrol Psikhiatr Im S S Korsakova. 2015;115(10):10-16. doi: 10.17116/jnevro201511510110-16. Russian.

PMID:
26525614
12.

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

Iourov IY, Vorsanova SG, Voinova VY, Yurov YB.

Mol Cytogenet. 2015 Oct 31;8:82. doi: 10.1186/s13039-015-0185-9. eCollection 2015.

13.

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.

Mol Cytogenet. 2015 Oct 15;8:77. doi: 10.1186/s13039-015-0182-z. eCollection 2015.

14.

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

Iourov IY, Vorsanova SG, Zelenova MA, Korostelev SA, Yurov YB.

Int J Genomics. 2015;2015:757680. doi: 10.1155/2015/757680. Epub 2015 Sep 1.

15.

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.

Mol Cytogenet. 2014 Dec 9;7(1):98. doi: 10.1186/s13039-014-0098-z. eCollection 2014.

16.

An interstitial deletion at 10q26.2q26.3.

Iourov IY, Vorsanova SG, Kurinnaia OS, Yurov YB.

Case Rep Genet. 2014;2014:505832. doi: 10.1155/2014/505832. Epub 2014 Feb 6.

17.

[The use of molecular cytogenetic and cytogenetic techniques for the diagnosis of Prader-Willi and Angelman syndrome].

Iourov IY, Vorsanova SG, Kurinnaaya OS, Kolotii AD, Demidova IA, Kravets VS, Yurov YB.

Zh Nevrol Psikhiatr Im S S Korsakova. 2014;114(1):49-53. Russian.

PMID:
24637817
18.

X chromosome aneuploidy in the Alzheimer's disease brain.

Yurov YB, Vorsanova SG, Liehr T, Kolotii AD, Iourov IY.

Mol Cytogenet. 2014 Mar 6;7(1):20. doi: 10.1186/1755-8166-7-20.

19.

[Subchromosomal microdeletion identified by molecular karyotyping using DNA microarrays (array CGH) in Rett syndrome girls negative for MECP2 gene mutations].

Vorsanova SG, Iurov IIu, Voinova VIu, Kurinnaia OS, Zelenova MA, Demidova IA, Ulas EV, Iurov IuB.

Zh Nevrol Psikhiatr Im S S Korsakova. 2013;113(10):63-8. Russian.

PMID:
24300809
20.

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.

Mol Cytogenet. 2013 Nov 27;6(1):53. doi: 10.1186/1755-8166-6-53.

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