Gregory J. Pelka
Children's Medical Research Institute(AU)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, RNA modifications and cancer, Chromatin Remodeling and Cancer, Autism Spectrum Disorder Research, Genomic variations and chromosomal abnormalities
Most-Cited Works
- → Mutations of CDKL5 Cause a Severe Neurodevelopmental Disorder with Infantile Spasms and Mental Retardation(2004)498 cited
- → Mecp2 deficiency is associated with learning and cognitive deficits and altered gene activity in the hippocampal region of mice(2006)207 cited
- → Environmental enrichment ameliorates a motor coordination deficit in a mouse model of Rett syndrome –Mecp2gene dosage effects and BDNF expression(2008)190 cited
- → Mitochondrial dysfunction in the skeletal muscle of a mouse model of Rett syndrome (RTT): Implications for the disease phenotype(2014)76 cited
- → Chromatin context and ncRNA highlight targets of MeCP2 in brain(2013)53 cited
- → Distinct expression profiles of Mecp2 transcripts with different lengths of 3′UTR in the brain and visceral organs during mouse development(2005)52 cited
- → A novel transcript of cyclin-dependent kinase-like 5 (CDKL5) has an alternative C-terminus and is the predominant transcript in brain(2011)50 cited
- → Generation of Mice Deficient in both KLF3/BKLF and KLF8 Reveals a Genetic Interaction and a Role for These Factors in Embryonic Globin Gene Silencing(2013)47 cited
- → Alleviating Transcriptional Inhibition of the NorepinephrineSlc6a2Transporter Gene in Depolarized Neurons(2010)31 cited
- → Application of lacZ Transgenic Mice to Cell Lineage Studies(2008)31 cited