Identification of molecular signatures and pathways involved in Rett syndrome using a multi-omics approach

被引:0
作者
Ainhoa Pascual-Alonso
Clara Xiol
Dmitrii Smirnov
Robert Kopajtich
Holger Prokisch
Judith Armstrong
机构
[1] Fundació Per La Recerca Sant Joan de Déu,Institute of Human Genetics
[2] Institut de Recerca Sant Joan de Déu,Institute of Neurogenomics
[3] Technical University of Munich,CIBER
[4] Helmholtz Zentrum München,ER (Biomedical Network Research Center for Rare Diseases)
[5] Instituto de Salud Carlos III (ISCIII),Genomic Unit, Molecular and Genetic Medicine Section
[6] Hospital Sant Joan de Déu,undefined
来源
Human Genomics | / 17卷
关键词
Rett syndrome; MECP2 duplication syndrome; Rett-like phenotypes; Multi-omics; Transcriptomics; Proteomics; Differential expression;
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[1]  
Ehrhart F(2016)Rett syndrome - Biological pathways leading from MECP2 to disorder phenotypes Orphanet J Rare Dis 11 158-950
[2]  
Coort SLM(2010)Rett syndrome: revised diagnostic criteria and nomenclature Ann Neurol 68 944-1321
[3]  
Cirillo E(2008)Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome Neurology 70 1313-2661
[4]  
Smeets E(2008)Key clinical features to identify girls with CDKL5 mutations Brain 131 2647-93
[5]  
Evelo CT(2008)FOXG1 is responsible for the congenital variant of Rett syndrome Am J Hum Genet 83 89-230
[6]  
Curfs LMG(2019)Genetic landscape of Rett syndrome spectrum: improvements and challenges Int J Mol Sci 20 3925-108
[7]  
Neul JL(2019)Clinician’s guide to genes associated with Rett-like phenotypes—Investigation of a Danish cohort and review of the literature Clin Genet 1 221-136
[8]  
Kaufmann WE(2018)Current developments in the genetics of Rett and Rett-like syndrome Curr Opin Psychiatry 31 103-581
[9]  
Glaze DG(2011)MECP2 duplication syndrome Mol Syndromol 2 128-2764
[10]  
Christodoulou J(2019)Characterizing the phenotypic effect of Xq28 duplication size in MECP2 duplication syndrome Clin Genet 95 575-24