Literature DB >> 9792883

Rett syndrome: confirmation of X-linked dominant inheritance, and localization of the gene to Xq28.

N Sirianni, S Naidu, J Pereira, R F Pillotto, E P Hoffman.   

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Year:  1998        PMID： 9792883      PMCID： PMC1377565          DOI： 10.1086/302105

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  33 in total

Review 1.  Rett syndrome and the MECP2 gene.

Authors:  T Webb; F Latif
Journal:  J Med Genet       Date:  2001-04       Impact factor: 6.318

Review 2.  Sex Chromosome Genetics '99. The X chromosome and recurrent spontaneous abortion: the significance of transmanifesting carriers.

Authors:  M C Lanasa; W A Hogge; E P Hoffman
Journal:  Am J Hum Genet       Date:  1999-04       Impact factor: 11.025

Review 3.  MicroRNA dysregulation in neuropsychiatric disorders and cognitive dysfunction.

Authors:  Bin Xu; Pei-Ken Hsu; Maria Karayiorgou; Joseph A Gogos
Journal:  Neurobiol Dis       Date:  2012-03-03       Impact factor: 5.996

4.  Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome without MECP2 mutation: implications for the disease.

Authors:  L Villard; N Lévy; F Xiang; A Kpebe; V Labelle; C Chevillard; Z Zhang; C E Schwartz; M Tardieu; J Chelly; M Anvret; M Fontès
Journal:  J Med Genet       Date:  2001-07       Impact factor: 6.318

Review 5.  Rett syndrome and MeCP2: linking epigenetics and neuronal function.

Authors:  Mona D Shahbazian; Huda Y Zoghbi
Journal:  Am J Hum Genet       Date:  2002-11-19       Impact factor: 11.025

6.  Inhibitors of differentiation (ID1, ID2, ID3 and ID4) genes are neuronal targets of MeCP2 that are elevated in Rett syndrome.

Authors:  Sailaja Peddada; Dag H Yasui; Janine M LaSalle
Journal:  Hum Mol Genet       Date:  2006-05-08       Impact factor: 6.150

7.  A mutation hot spot for nonspecific X-linked mental retardation in the MECP2 gene causes the PPM-X syndrome.

Authors:  Sabine M Klauck; Susan Lindsay; Kim S Beyer; Miranda Splitt; John Burn; Annemarie Poustka
Journal:  Am J Hum Genet       Date:  2002-02-15       Impact factor: 11.025

Review 8.  MicroRNAs in psychiatric and neurodevelopmental disorders.

Authors:  Bin Xu; Maria Karayiorgou; Joseph A Gogos
Journal:  Brain Res       Date:  2010-04-10       Impact factor: 3.252

9.  White matter impairment in Rett syndrome: diffusion tensor imaging study with clinical correlations.

Authors:  A Mahmood; G Bibat; A-L Zhan; I Izbudak; L Farage; A Horska; S Mori; S Naidu
Journal:  AJNR Am J Neuroradiol       Date:  2009-10-15       Impact factor: 3.825

10.  X-chromosome inactivation patterns are unbalanced and affect the phenotypic outcome in a mouse model of rett syndrome.

Authors:  Juan I Young; Huda Y Zoghbi
Journal:  Am J Hum Genet       Date:  2004-02-17       Impact factor: 11.025
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