Kurinnaia Oxana
机构: Mental Health Research Center, Russian Academy of Medical Sciences, Moscow, Russia
每年引用次数
引用次数
引用: 742
H-指数: 15
I10-指数 : 20
出版物: 143
Diagnosis of Genome Pathology in Children with Mental Retardation and Autism by SNP-Oligonucleotide Molecular Karyotyping
IY Iourov , SG Vorsanova , SA Korostelev , MA Zelenova
YAKUT MEDICAL JOURNAL ( 2) 101 -105
2014
Molecular karyotyping by array CGH in a Russian cohort of children with intellectual disability, autism, epilepsy and congenital anomalies
Ivan Y Iourov , Svetlana G Vorsanova , Oxana S Kurinnaia , Maria A Zelenova
Molecular Cytogenetics 5 ( 1) 46 -46
45
2012
Xq28 (MECP2) microdeletions are common in mutation-negative females with Rett syndrome and cause mild subtypes of the disease.
Ivan Y Iourov , Svetlana G Vorsanova , Victoria Y Voinova , Oxana S Kurinnaia
Molecular Cytogenetics 6 ( 1) 53 -53
20
2013
FISH-Based Analysis of Mosaic Aneuploidy and Chromosome Instability for Investigating Molecular and Cellular Mechanisms of Disease
Svetlana G Vorsanova , Yuri B Yurov , Ilia V Soloviev , Alexei D Kolotii
OBM Genetics 3 ( 1)
3
2019
Somatic mosaicism in the diseased brain
Ivan Y Iourov , Svetlana G Vorsanova , Oxana S Kurinnaia , Sergei I Kutsev
Molecular Cytogenetics 15 ( 1) 1 -11
1
2022
An Interstitial Deletion at 10q26.2q26.3
Ivan Y Iourov , Svetlana G Vorsanova , Oxana S Kurinnaia , Yuri B Yurov
Case reports in genetics 2014 505832 -505832
6
2014
An Interstitial 20q11.21 Microdeletion Causing Mild Intellectual Disability and Facial Dysmorphisms
Ivan Y Iourov , Svetlana G Vorsanova , Oxana S Kurinnaia , Yuri B Yurov
Case reports in genetics 2013 353028 -353028
4
2013
Twenty-first century fish: focus on interphase chromosomes
Svetlana G Vorsanova , Yuri B Yurov , Oxana S Kurinnaia , Alexei D Kolotii
Human Interphase Chromosomes: Biomedical Aspects 131 -145
2
2020
Clinical characterization of 72 patients with del (22)(q11. 2q11. 2) from different ethnic backgrounds
Luis A Méndez-Rosado , Norma de León-Ojeda , Alina García , Frenny Sheth
Egyptian Journal of Medical Human Genetics 23 ( 1) 158 -158
1
2022
Algoritmo para la delineación clínica del Síndrome del22q11. 2.
Luis A Méndez Rosado , Yara Silva Gonzalez , Odalis Molina Gamboa , Oxana S Kurinnaia
Chromosomal mosaicism in spontaneous abortions: Analysis of 650 cases
S. G. Vorsanova , I. Yu. Iourov , A. D. Kolotii , A. K. Beresheva
Russian Journal of Genetics 46 ( 10) 1197 -1200
12
2010
Cytogenetic, molecular-cytogenetic, and clinical-genealogical studies of the mothers of children with autism: a search for familial genetic markers for autistic disorders.
SG Vorsanova , V Yu Voinova , I Yu Yurov , OS Kurinnaya
Neuroscience and Behavioral Physiology 40 ( 7) 745 -756
22
2010
BIOINFORMATIC ANALYSIS OF MICRODUPLICATIONS AT 5P15.33: IDENTIFICATION OF TPPP AS A CANDIDATE GENE FOR AUTISM AND INTELLECTUAL DISABILITY
Victoria Y. Voinova , Kirill S. Vasin , Svetlana G. Vorsanova , Oksana S. Kurinnaia
Научные результаты биомедицинских исследований 6 ( 4)
2020
Turner's syndrome mosaicism in girls with neurodevelopmental disorders: a cohort study and hypothesis.
Yuri B. Yurov , Svetlana G. Vorsanova , Oksana S. Kurinnaia , Victor S. Kravets
Molecular Cytogenetics 14 ( 1) 9 -9
15
2021
Epigenomic variations manifesting as a loss of heterozygosity affecting imprinted genes represent a molecular mechanism of autism spectrum disorders and intellectual disability in children
I. Y. Iourov , S. G. Vorsanova , M. A. Zelenova , K. S. Vasin
Zhurnal Nevrologii I Psikhiatrii Imeni S S Korsakova 119 ( 5) 91 -97
2
2019
Structural variations of the genome in autistic spectrum disorders with intellectual disability
I. Yu. Iourov , S. G. Vorsanova , S. A. Korostelev , K. S. Vasin
Zhurnal Nevrologii I Psikhiatrii Imeni S S Korsakova 116 ( 7) 50 -54
6
2016
Chromothripsis as a mechanism driving genomic instability mediating brain diseases
Ivan Iourov , Svetlana Vorsanova , Thomas Liehr , Maria Zelenova
MOLECULAR CYTOGENETICS 10
7
2017
Somatic chromosomal mosaicism and instability in neurodevelopmental diseases from brain to blood and back again
Ivan Iourov , Svetlana Vorsanova , Maria Zelenova , Oxana Kurinnaia
MOLECULAR CYTOGENETICS 12
2019
The Y chromosome disomy syndrome (47, XYY) in children with mental retardation, deviations of sex development and different genome anomalies: molecular cytogenetic studies
SG Vorsanova , IV Solovyev , OS Kurinnaya , VS Kravets
Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics) 65 ( 2) 40 -48
1
2020
High rate of chromosomal mosaicism in spontaneously aborted fetuses: Analysis of 715 consecutive cases with special emphasis to IVF.
SG Vorsanova , IY Iourov , OS Kurinnaya , AD Kolotii
Reproductive BioMedicine Online (Reproductive Healthcare Limited) 20
2010