Víctor Faundes

9PUBLICATIONS
116CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Counselling, wellbeing and community servicesGene expression (incl. microarray and other genome-wide approaches)Microelectromechanical systems (MEMS)Epidemiological modelling
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Publications (9)

|Oct 01, 2026
Computer-Aided Facial Analysis and Non-Coding Variants Detectable by Exome Sequencing Increase Its Diagnostic Yield: Results From the DECIPHERD Study.

|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

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Frequent Collaborators

2 joint publications

María Jesús Zavala

2 joint publications

Trinidad Hasbún

2 joint publications

Gonzalo Encina

2 joint publications

Gabriela M Repetto