Federico Ferraro

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 7

Top Topics

Pluripotent Stem Cells

Intellectual Disability

Top Venues

Clinical genetics

Brain : a journal of neurology

Disease models & mechanisms

Movement disorders : official journal of the Movement Disorder Society

This page only lists publications with an associated author ORCID identifier.

Publications

Rachel Schot, Federico Ferraro, Geert Geeven, Karin E M Diderich, Tahsin Stefan Barakat
Re-analysis of whole genome sequencing ends a diagnostic odyssey: Case report of an RNU4-2 related neurodevelopmental disorder. Clinical genetics 106 (4) (2024)
Rachel Schot, Federico Ferraro, Geert Geeven, Karin E M Diderich, Tahsin Stefan Barakat
Re-analysis of whole genome sequencing ends a diagnostic odyssey: Case report of an RNU4-2 related neurodevelopmental disorder. Clinical genetics (2024)
Martyna M Grochowska, Federico Ferraro, Ana Carreras Mascaro, Domenico Natale, Amber Winkelaar, Valerie Boumeester, Guido J Breedveld, Vincenzo Bonifati, Wim Mandemakers
deCLUTTER2+ pipeline to analyze calcium traces in a novel stem cell model for ventral midbrain patterned astrocytes. Disease models & mechanisms (2023)
Alessandra Fanciulli, Fabian Leys, Fabienne Lehner, Victoria Sidoroff, Viktoria C Ruf, Cecilia Raccagni, Philipp Mahlknecht, Demy J S Kuipers, Wilfred F J Van IJcken, Heike Stockner, Thomas Musacchio, Jens Volkmann, Camelia Maria Monoranu, Iva Stankovic, Guido Breedveld, Federico Ferraro, Christina Fevga, Otto Windl, Jochen Herms, Stefan Kiechl, Werner Poewe, Klaus Seppi, Nadia Stefanova, Sonja W Scholz, Vincenzo Bonifati, Gregor K Wenning
A multiplex pedigree with pathologically confirmed multiple system atrophy and Parkinson's disease with dementia. Brain communications 4 (4) (2022)
Federico Ferraro, Christina Fevga, Vincenzo Bonifati, Wim Mandemakers, Ahmed Mahfouz, Marcel J T Reinders
Correcting Differential Gene Expression Analysis for Cyto-Architectural Alterations in Substantia Nigra of Parkinson's Disease Patients Reveals Known and Potential Novel Disease-Associated Genes and Pathways. Cells 11 (2) (2022)
Christina Fevga, Christelle Tesson, Ana Carreras Mascaro, Thomas Courtin, Riaan van Coller, Salma Sakka, Federico Ferraro, Nouha Farhat, Soraya Bardien, Mariem Damak, Jonathan Carr, Mélanie Ferrien, Valerie Boumeester, Jasmijn Hundscheid, Nicola Grillenzoni, Irini A Kessissoglou, Demy J S Kuipers, Marialuisa Quadri, null null, null null, Jean Christophe Corvol, Chokri Mhiri, Bassem A Hassan, Guido J Breedveld, Suzanne Lesage, Wim Mandemakers, Alexis Brice, Vincenzo Bonifati
PTPA variants and impaired PP2A activity in early-onset parkinsonism with intellectual disability. Brain : a journal of neurology (2022)
Christina Fevga, Federico Ferraro, Guido J Breedveld, Charulata S Sankhla, Vincenzo Bonifati
AOPEP Homozygous Loss-of-Function Variant in an Indian Patient with Early-Onset Generalized Dystonia. Movement disorders : official journal of the Movement Disorder Society 37 (4) (2022)