Roberta Oneda

A UV-sensitive syndrome patient with a specific <i>CSA</i> mutation reveals separable roles for CSA in response to UV and oxidative DNA damage

Tiziana Nardò, Roberta Oneda, Graciela Spivak et al. · Proceedings of the National Academy of Sciences · 2009 · 136 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Developmental alterations of the respiratory human retrotrapezoid nucleus in sudden unexplained fetal and infant death

Anna Maria Lavezzi, Debra E. Weese‐Mayer, Margaret Y. Yu et al. · Autonomic Neuroscience · 2012 · 56 citations

Medicine, Neurobiology, Neuroscience +16

Sudden Infant Death Syndrome and Sudden Intrauterine Unexplained Death: Correlation Between Hypoplasia of Raphé Nuclei and Serotonin Transporter Gene Promoter Polymorphism

Anna Maria Lavezzi, Valentina Casale, Roberta Oneda et al. · Pediatric Research · 2009 · 42 citations

Life Sciences, Genetics, Neuroscience +15

Obstructive sleep apnea syndrome (OSAS) in children with Class III malocclusion: involvement of the PHOX2B gene

Anna Maria Lavezzi, Valentina Casale, Roberta Oneda et al. · Sleep And Breathing · 2013 · 16 citations

Medicine, Orthodontics, Pediatrics +14

Optimisation of postmortem tissue preservation and alternative protocol for serotonin transporter gene polymorphisms amplification in SIDS and SIUD cases

Valentina Casale, Roberta Oneda, Anna Maria Lavezzi et al. · Experimental and Molecular Pathology · 2009 · 16 citations

Life Sciences, Molecular Medicine, Psychiatry +16