Simona Mellone

A novel peripherin gene (PRPH) mutation identified in one sporadic amyotrophic lateral sclerosis patient

Lucia Corrado, Yari Carlomagno, Luca Falasco et al. · Neurobiology of Aging · 2010 · 68 citations

Life Sciences, Neurology, Neuroscience +12

Association of osteopontin regulatory polymorphisms with systemic sclerosis

Nadia Barizzone, Maurizio Marchini, Francesca Cappiello et al. · Human Immunology · 2011 · 35 citations

Medicine, Molecular Genetics, Bone Metabolism +10

Rare Variants in the<i>TREX1</i>Gene and Susceptibility to Autoimmune Diseases

Nadia Barizzone, Sara Monti, Simona Mellone et al. · BioMed Research International · 2013 · 32 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

A Recurrent Signal Peptide Mutation in the Growth Hormone Releasing Hormone Receptor with Defective Translocation to the Cell Surface and Isolated Growth Hormone Deficiency

Michela Godi, Simona Mellone, Antonella Petri et al. · The Journal of Clinical Endocrinology & Metabolism · 2009 · 26 citations

Medicine, Endocrinology, Genetics +15

Two new PROP1 gene mutations responsible for compound pituitary hormone deficiency

R. Paracchini, Mara Giordano, Andrea Corrias et al. · Clinical Genetics · 2003 · 25 citations

Medicine, Genetics, Molecular Genetics +17