Francesca Lantieri
University of Genoa(IT)
Publications by Year
Research Areas
Congenital gastrointestinal and neural anomalies, Digestive system and related health, Intestinal Malrotation and Obstruction Disorders, RNA regulation and disease, Attention Deficit Hyperactivity Disorder
Most-Cited Works
- → Hirschsprung disease, associated syndromes and genetics: a review(2007)1,197 cited
- → Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes(2009)530 cited
- → Differential Contributions of Rare and Common, Coding and Noncoding Ret Mutations to Multifactorial Hirschsprung Disease Liability(2010)243 cited
- → TNF-α Gene Polymorphisms: Association with Disease Susceptibility and Response to Anti-TNF-α Treatment in Psoriatic Arthritis(2014)99 cited
- → High prevalence of the G101W germline mutation in the CDKN2A (P16ink4a) gene in 62 Italian malignant melanoma families(2002)73 cited
- → Parental origin and somatic mosaicism of PHOX2B mutations in Congenital Central Hypoventilation Syndrome(2007)60 cited
- → CDKN2A and CDK4 mutation analysis in Italian melanoma-prone families: functional characterization of a novel CDKN2A germ line mutation(2001)56 cited
- → Induction of RET Dependent and Independent Pro-Inflammatory Programs in Human Peripheral Blood Mononuclear Cells from Hirschsprung Patients(2013)55 cited
- → Novel MC1R variants in Ligurian melanoma patients and controls(2004)49 cited
- → A prospective observational study of associated anomalies in Hirschsprung’s disease(2013)48 cited