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Víctor Faundes

8PUBLICATIONS

103CO-AUTHORS

Counselling, wellbeing and community servicesGene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Regenerative medicine (incl. stem cells)Microelectromechanical systems (MEMS)

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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

|Jan 13, 2023

<i>Letter to the Editor:</i> How Spermidine and Targeting Eukaryotic Initiator Factor 5A Might Help to Both a Novel Congenital Disorder and Brain Aging.

Víctor Faundes

|Nov 09, 2022

Tissue mosaicism, FMR1 expression and intellectual functioning in males with fragile X syndrome.

Emma K Baker, Marta Arpone, Minh Bui

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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

Lorenza Mistura

Frequent Collaborators

2 joint publications

Siddharth Banka

1 joint publications

Lluis Serra-Majem

1 joint publications

António Raposo

1 joint publications

Carmen Pérez-Rodrigo

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