Ariele Spanhol-Rosseto

FOXG1 Is Responsible for the Congenital Variant of Rett Syndrome

Francesca Ariani, Dalila Rondinella, Rosangela Artuso et al. · The American Journal of Human Genetics · 2008 · 434 citations · Full text

Life Sciences, Genetics, Molecular Genetics +7

Whole-exome sequencing identifies somatic mutations of BCOR in acute myeloid leukemia with normal karyotype

Enrico Tiacci, Antony B. Holmes, Alexander Kohlmann et al. · Blood · 2011 · 268 citations · Full text

Life Sciences, Genetics, Oncology +14

Novel <i>FOXG1</i> mutations associated with the congenital variant of Rett syndrome

Maria Antonietta Mencarelli, Ariele Spanhol-Rosseto, Rosangela Artuso et al. · Journal of Medical Genetics · 2009 · 109 citations

Life Sciences, Genetics, Molecular Genetics +14

BRAF inhibitors reverse the unique molecular signature and phenotype of hairy cell leukemia and exert potent antileukemic activity

Valentina Pettirossi, Alessia Santi, Elisa Imperi et al. · Blood · 2014 · 96 citations · Full text

Medicine, Oncology, Pharmacology +5

New Recurrently Mutated Genes in Classical Hodgkin Lymphoma Revealed By Whole-Exome Sequencing of Microdissected Tumor Cells

Enrico Tiacci, Alexander Penson, Gianluca Schiavoni et al. · Blood · 2016 · 11 citations

Medicine, Molecular Genetics, Oncology +16