Víctor Faundes
8PUBLICATIONS
103CO-AUTHORS
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Publications (8)
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|Sep 24, 2025
Impact of brief telehealth interventions on parental stress and challenging behaviors of children with fragile X syndrome.María Francisca Miranda, Víctor Faundes, María Angélica Alliende
|Mar 11, 2024
Discovery of novel genetic syndromes in Latin America: Opportunities and challenges.Víctor Faundes, Gabriela M Repetto, Leonardo E Valdivia
|Jan 04, 2024
Decoding complex inherited phenotypes in rare disorders: the DECIPHERD initiative for rare undiagnosed diseases in Chile.M Cecilia Poli, Boris Rebolledo-Jaramillo, Catalina Lagos
|Mar 10, 2023
Mechanism of KMT5B haploinsufficiency in neurodevelopment in humans and mice.Sarah E Sheppard, Laura Bryant, Rochelle N Wickramasekara
|Nov 09, 2022
Tissue mosaicism, FMR1 expression and intellectual functioning in males with fragile X syndrome.Emma K Baker, Marta Arpone, Minh Bui
|Feb 06, 2021
Impaired eIF5A function causes a Mendelian disorder that is partially rescued in model systems by spermidine.Víctor Faundes, Martin D Jennings, Siobhan Crilly
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Frequent Collaborators
2 joint publications
Siddharth Banka
1 joint publications
Lluis Serra-Majem
1 joint publications
António Raposo
1 joint publications
Carmen Pérez-Rodrigo
1 joint publications
Márcio Carocho
1 joint publications
Maria do Céu Costa
1 joint publications
Samuel Durán
1 joint publications
Carlo La Vecchia
1 joint publications
Ana María López-Sobaler
1 joint publications
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