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Erika Tenderini
Observed names:
E Tenderini,
Tenderini, E.
Institution:
Telethon Institute Of Genetics And Medicine
Observed institutions:
University of Milan,
Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico,
The San Raffaele Telethon Institute for Gene Therapy,
IRCCS Eugenio Medea,
Telethon Institute Of Genetics And Medicine,
European Institute of Oncology
show all 6
ORCID:
0000-0002-4073-8259
Observed ORCID:
0000-0002-4073-8259
OpenAlex ID:
A5009057517
From cohorts to molecules: Adverse impacts of endocrine disrupting mixtures
2022
·
Nicolò Caporale
, Michelle Leemans
, et al.
·
Science
·
385
PDF
Mutations in the motor and stalk domains of KIF5A in spastic paraplegia type 10 and in axonal Charcot–Marie–Tooth type 2
2011
·
C Crimella
, C Baschirotto
, et al.
·
Clinical Genetics
·
165
Human Cortical Organoids Expose a Differential Function of GSK3 on Cortical Neurogenesis
2019
·
Alejandro López-Tobón
, Carlo Emanuele Villa
, et al.
·
Stem Cell Reports
·
62
PDF
Immunotherapy of acute leukemia by chimeric antigen receptor-modified lymphocytes using an improved Sleeping Beauty transposon platform
2016
·
Chiara F. Magnani
, Nice Turazzi
, et al.
·
Oncotarget
·
50
Brain malformations and mutations in α ‐ and β ‐tubulin genes: a review of the literature and description of two new cases
2014
·
Romina Romaniello
, Filippo Arrigoni
, et al.
·
Developmental Medicine & Child Neurology
·
48
PDF
KMT2B Is Selectively Required for Direct Neuronal Reprogramming and Its Loss Exposes Dystonia-Relevant Targets
2018
·
Giulia Barbagiovanni
, Pierre-Luc Germain
, et al.
·
Cell Reports
·
47
PDF
Clinical phenotype variability in patients with hereditary spastic paraplegia type 5 associated with CYP7B1 mutations
2011
·
A Arnoldi
, C Crimella
, et al.
·
Clinical Genetics
·
47
Benchmarking brain organoid recapitulation of fetal corticogenesis
2022
·
Cristina Cheroni
, Sebastiano Trattaro
, et al.
·
Translational Psychiatry
·
45
PDF
GTF2I dosage regulates neuronal differentiation and social behavior in 7q11.23 neurodevelopmental disorders
2023
·
Alejandro Lopez-Tobon
, Reinald Shyti
, et al.
·
Science Advances
·
40
PDF
A Novel Mutation in STXBP1 Gene in a Child With Epileptic Encephalopathy and an Atypical Electroclinical Pattern
2013
·
Romina Romaniello
, Claudio Zucca
, et al.
·
Journal of Child Neurology
·
20
A 66-year-old patient with vanishing white matter disease due to the p.Ala87Val EIF2B3 mutation
2012
·
Laura Ghezzi
, Elio Scarpini
, et al.
·
Neurology
·
19
adLIMS: a customized open source software that allows bridging clinical and basic molecular research studies
2015
·
Andrea Calabria
, Giulio Spinozzi
, et al.
·
BMC Bioinformatics
·
15
PDF
Multiscale modeling uncovers 7q11.23 copy number variation–dependent changes in ribosomal biogenesis and neuronal maturation and excitability
2024
·
Marija Mihailovich
, Pierre-Luc Germain
, et al.
·
Journal of Clinical Investigation
·
13
PDF
YY1 mutations disrupt corticogenesis through a cell type specific rewiring of cell-autonomous and non-cell-autonomous transcriptional programs
2025
·
Marlene F. Pereira
, Veronica Finazzi
, et al.
·
Molecular Psychiatry
·
10
KMT2D haploinsufficiency in Kabuki syndrome disrupts neuronal function through transcriptional and chromatin rewiring independent of H3K4-monomethylation
2021
·
Michele Gabriele
, Alessandro Vitriolo
, et al.
·
bioRxiv (Cold Spring Harbor Laboratory)
·
10
PDF
γ-TRIS: a graph-algorithm for comprehensive identification of vector genomic insertion sites
2019
·
Andrea Calabria
, Stefano Beretta
, et al.
·
Bioinformatics
·
10
PDF
Uncovering mitochondrial defects in photoreceptors opens therapeutic opportunities for Stargardt disease
2026
·
Simona Brillante
, Mariagrazia Volpe
, et al.
·
Proceedings of the National Academy of Sciences
·
2
Human cortical organoids expose a differential function of GSK3 on direct and indirect neurogenesis
2018
·
Alejandro López-Tobón
, Carlo Emanuele Villa
, et al.
·
bioRxiv (Cold Spring Harbor Laboratory)
·
2
PDF
Disruption of ADNP-KDM1A-GTF2I complex drives neural differentiation imbalance in Helsmoortel-Van der Aa syndrome
2025
·
Ludovico Rizzuti
, Alessandro Vitriolo
, et al.
·
bioRxiv (Cold Spring Harbor Laboratory)
·
1
Targeting cryptic splicing variants in SDCCAG8, CEP290, and ABCA4: A translational workflow from diagnosis to ASO-based therapy
2026
·
Mariia Zadorozhna
, Simona Rossi
, et al.
·
Molecular Therapy — Nucleic Acids
AB012. Transcriptional and chromatin profiling reveals the molecular architecture and druggable vulnerabilities of thymic epithelial tumors (TETs)
2021
·
Pierluigi Giuseppe Manti
, Sebastiano Trattaro
, et al.
·
Mediastinum
PDF
2. Identification and Ranking of Different Chromatin Insulators to Block Vector-Driven Enhancer-Mediated Insertional Mutagenesis In Vivo
2016
·
Monica Volpin
, Andrea Calabria
, et al.
·
Molecular Therapy
PDF
537. New Graph-Based Algorithm for Comprehensive Identification and Tracking Retroviral Integration Sites
2016
·
Andrea Calabria
, Stefano Beretta
, et al.
·
Molecular Therapy
PDF
212. Lentiviral Insertional Mutagenesis Helps to Uncover the Mechanisms of Resistance to AZD9291 and CO-1686 in EGFR-Mutant Lung Adenocarcinoma
2016
·
Valentina Pirazzoli
, Giulio Spinozzi
, et al.
·
Molecular Therapy
PDF
674. Insertional Mutagenesis to Identify Mechanisms of Cetuximab Resistance in Colorectal Cancer
2016
·
Riccardo Biavasco
, Valentina Pirazzoli
, et al.
·
Molecular Therapy
PDF
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Works count:
30
Citation count:
991
H-index:
13
I10-index:
16
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