Maria Cristina Digilio - Genetic Mutations

Author Information

Maria Cristina Digilio is an esteemed researcher currently affiliated with the Genetics and Rare Diseases Research Division at Ospedale Pediatrico Bambino Gesù, IRCCS, located in Rome, Italy. Her work focuses on the field of genetics and rare diseases, where she has made significant contributions through her extensive research and numerous publications.

Research Contributions

Maria Cristina Digilio's research encompasses various aspects of genetics and rare diseases. In 2022, she published several noteworthy papers, including studies on Osteopathia striata with cranial sclerosis, the long-term outcomes in patients with repaired Tetralogy of Fallot, and the clinical characteristics and management of hypertrophic cardiomyopathy in RASopathies. Her work also extends to understanding the systemic disorders associated with cardiomyopathies in children, the molecular causes of neurodevelopmental disorders, and the cognitive and adaptive characteristics of children with KBG Syndrome. Additionally, she has explored the dual biocontrol potential of Beauveria bassiana in tomatoes and studied severe herpes virus 6 interstitial pneumonia in infants with genetic predispositions to lung disease.

Aliases

Maria Cristina Digilio has published under various aliases, including Maria Cristina Digilio, Mariacristina Digilio, M. Cristina Digilio, Maria C. Digilio, M C Digilio, M. C. Digilio, M Cristina Digilio, Maria Digilio, M Digilio, Maria C Digilio, and M C. Digilio.

Publication and Citation Metrics

Citation Count 15958
H-index 66
Paper Count 453

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