Serena Lattante

Loss of function of C9orf72 causes motor deficits in a zebrafish model of amyotrophic lateral sclerosis

Sorana Ciura, Serena Lattante, Isabelle Le Ber et al. · Annals of Neurology · 2013 · 324 citations

Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype

Marcella Zollino, Daniela Orteschi, Marina Murdolo et al. · Nature Genetics · 2012 · 160 citations

Mendelian Disorder, Microdeletion Syndrome Phenotype, Genetic Disorder +4

P525L FUS mutation is consistently associated with a severe form of juvenile Amyotrophic Lateral Sclerosis

Amelia Conte, Serena Lattante, Marcella Zollino et al. · Neuromuscular Disorders · 2011 · 132 citations

Neurodegenerative Diseases, Amyotrophic Lateral Sclerosis, Neurological Disorder +10

Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease

Serena Lattante, Amelia Conte, Marcella Zollino et al. · Neurology · 2012 · 110 citations

Sporadic Als, Neurological Disorder, Genetics +17

Mutations in the 3′ untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis

Mario Sabatelli, Alice Moncada, Amelia Conte et al. · Human Molecular Genetics · 2013 · 107 citations · Full text

Neurodegenerative Diseases, Als Genes, Amyotrophic Lateral Sclerosis +15