Giovanni Neri
Università Cattolica del Sacro Cuore(IT)University of Pisa(IT)Istituto Nazionale Tumori IRCCS "Fondazione G. Pascale"(IT)University of Naples Federico II(IT)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Genomic variations and chromosomal abnormalities, RNA modifications and cancer, Autism Spectrum Disorder Research, Epigenetics and DNA Methylation
Most-Cited Works
- → Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome(1996)763 cited
- → Epigenetic Modification of the FMR1 Gene in Fragile X Syndrome Is Associated with Differential Response to the mGluR5 Antagonist AFQ056(2011)611 cited
- → Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome(2006)598 cited
- → A new function for the fragile X mental retardation protein in regulation of PSD-95 mRNA stability(2007)356 cited
- → Fragile X syndrome: causes, diagnosis, mechanisms, and therapeutics(2012)322 cited
- → Molecular and Clinical Analyses of Greig Cephalopolysyndactyly and Pallister-Hall Syndromes: Robust Phenotype Prediction from the Type and Position of GLI3 Mutations(2005)276 cited