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NPJ Precision Oncology|October 28, 2021
GD2 CAR T cells against human glioblastomaMalvina Prapa, Chiara Chiavelli, Giulia Golinelli, et al.European Journal of Human Genetics : EJHG|August 16, 2012
Prevalence of SHANK3 variants in patients with different subtypes of autism spectrum disordersLuigi Boccuto, Maria Lauri, Sara M Sarasua, et al.Human Genetics|January 11, 2020
Altered mitochondrial function in cells carrying a premutation or unmethylated full mutation of the FMR1 geneVeronica Nobile, Federica Palumbo, Stella Lanni, et al.Cell|May 12, 2015
Disruptions of topological chromatin domains cause pathogenic rewiring of gene-enhancer interactionsDarío G Lupiáñez, Katerina Kraft, Verena Heinrich, et al.American Journal of Medical Genetics. Part A|February 21, 2008
A double-blind, parallel, multicenter comparison of L-acetylcarnitine with placebo on the attention deficit hyperactivity disorder in fragile X syndrome boysM Giulia Torrioli, Silvia Vernacotola, Laura Peruzzi, et al.Human Mutation|October 21, 2006
Diversity, parental germline origin, and phenotypic spectrum of de novo HRAS missense changes in Costello syndromeGiuseppe Zampino, Francesca Pantaleoni, Claudio Carta, et al.Psychiatry Research. Neuroimaging|August 29, 2022
Incidental findings on brain MRI in patients with first-episode and chronic psychosisMarcella Bellani, Cinzia Perlini, Niccolò Zovetti, et al.Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|August 10, 2012
Replication of association of CHRNA4 rare variants with sporadic amyotrophic lateral sclerosis: the Italian multicentre studyMario Sabatelli, Serena Lattante, Amelia Conte, et al.Human Genetics|August 7, 2007
Wolf-Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene clusters nor by inversion polymorphism on 4p16Marcella Zollino, Rosetta Lecce, Marina Murdolo, et al.European Journal of Human Genetics : EJHG|October 16, 2008
Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndromeThomas E Neumann, Judith Allanson, Ines Kavamura, et al.Pageof 33