Gregory J. Pelka

Mutations of CDKL5 Cause a Severe Neurodevelopmental Disorder with Infantile Spasms and Mental Retardation

Linda S. Weaving, John Christodoulou, Sarah Williamson et al. · The American Journal of Human Genetics · 2004 · 498 citations · Full text

Neurodevelopmental Disorders, Developmental Biology, Genetic Disorder +12

Mecp2 deficiency is associated with learning and cognitive deficits and altered gene activity in the hippocampal region of mice

Gregory J. Pelka, Catherine M. Watson, Tania Radziewic et al. · Brain · 2006 · 206 citations · Full text

Brain Function, Developmental Cognitive Neuroscience, Rett Syndrome +23

Environmental enrichment ameliorates a motor coordination deficit in a mouse model of Rett syndrome –<i>Mecp2</i>gene dosage effects and BDNF expression

Mari Kondo, Laura Gray, Gregory J. Pelka et al. · European Journal of Neuroscience · 2008 · 185 citations

Mitochondrial dysfunction in the skeletal muscle of a mouse model of Rett syndrome (RTT): Implications for the disease phenotype

Wendy Gold, Sarah Williamson, Simranpreet Kaur et al. · Mitochondrion · 2014 · 75 citations

Mitochondrial Myopathy, Disease Mechanism, Mitochondrial Function +8

Chromatin context and ncRNA highlight targets of MeCP2 in brain

Scott Maxwell, Gregory J. Pelka, Patrick Tam et al. · RNA Biology · 2013 · 53 citations · Full text

Epigenetic Change, Genetics, Genomic Mechanism +20