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Review 1. 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

Review 2. Rett syndrome and MeCP2.

Authors: Vichithra R B Liyanage; Mojgan Rastegar
Journal: Neuromolecular Med Date: 2014-03-11 Impact factor: 3.843

3. Heterogeneity in residual function of MeCP2 carrying missense mutations in the methyl CpG binding domain.

Authors: S Kudo; Y Nomura; M Segawa; N Fujita; M Nakao; C Schanen; M Tamura
Journal: J Med Genet Date: 2003-07 Impact factor: 6.318

4. Abnormalities of cell packing density and dendritic complexity in the MeCP2 A140V mouse model of Rett syndrome/X-linked mental retardation.

Authors: Garilyn M Jentarra; Shannon L Olfers; Stephen G Rice; Nishit Srivastava; Gregg E Homanics; Mary Blue; Sakkubai Naidu; Vinodh Narayanan
Journal: BMC Neurosci Date: 2010-02-17 Impact factor: 3.288

Review 5. The role of MeCP2 in brain development and neurodevelopmental disorders.

Authors: Michael L Gonzales; Janine M LaSalle
Journal: Curr Psychiatry Rep Date: 2010-04 Impact factor: 5.285

6. Early life stress exacerbates behavioural and neuronal alterations in adolescent male mice lacking methyl-CpG binding protein 2 (Mecp2).

Authors: Jose Vicente Torres-Pérez; Elena Martínez-Rodríguez; Anabel Forte; Carlos Blanco-Gómez; Oliver Stork; Enrique Lanuza; Mónica Santos; Carmen Agustín-Pavón
Journal: Front Behav Neurosci Date: 2022-08-23 Impact factor: 3.617

6 in total