Grace Vassallo
Manchester University NHS Foundation Trust(GB)Royal Manchester Children's Hospital(GB)Lombardia Informatica (Italy)(IT)
Publications by Year
Research Areas
Neurofibromatosis and Schwannoma Cases, Meningioma and schwannoma management, Epilepsy research and treatment, Metabolism and Genetic Disorders, Vascular Malformations Diagnosis and Treatment
Most-Cited Works
- → Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature(2012)928 cited
- → Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study(2013)433 cited
- → Use of Whole-Exome Sequencing to Determine the Genetic Basis of Multiple Mitochondrial Respiratory Chain Complex Deficiencies(2014)361 cited
- → Mutations in SLC12A5 in epilepsy of infancy with migrating focal seizures(2015)177 cited
- → Clinical features, course, and outcomes of a UK cohort of pediatric moyamoya(2018)116 cited
- → Phospholipase C beta 1 deficiency is associated with early-onset epileptic encephalopathy(2010)104 cited