Francesca Lantieri

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

Josephine Elia, Xiaowu Gai, Hongbo Xie et al. · Molecular Psychiatry · 2009 · 526 citations · Full text

Genetics, Disease Gene Identification, Social Sciences +19

Differential Contributions of Rare and Common, Coding and Noncoding Ret Mutations to Multifactorial Hirschsprung Disease Liability

E Emison, Mercè Garcia-Barceló, Elizabeth A. Grice et al. · The American Journal of Human Genetics · 2010 · 241 citations · Full text

Somatic Variant, Noncoding Ret Mutations, Mendelian Disorder +10

TNF-α Gene Polymorphisms: Association with Disease Susceptibility and Response to Anti-TNF-α Treatment in Psoriatic Arthritis

Giuseppe Murdaca, Rossella Gulli, Francesca Spanò et al. · Journal of Investigative Dermatology · 2014 · 98 citations · Full text

Rheumatology, Disease Susceptibility, Autoimmune Disease +12

High prevalence of the G101W germline mutation in the <i>CDKN2A</i> (P16^ink4a) gene in 62 Italian malignant melanoma families

Michela Mantelli, Monica Barile, Paola Ciotti et al. · American Journal of Medical Genetics · 2002 · 73 citations

Genetic Testing, Cancer Pathology, Genetics +16

Parental origin and somatic mosaicism of PHOX2B mutations in Congenital Central Hypoventilation Syndrome

Sara Parodi, Tiziana Bachetti, Francesca Lantieri et al. · Human Mutation · 2007 · 59 citations · Full text