Lucas Fares-Taie

7PUBLICATIONS
110CO-AUTHORS
NeonatologyEpigenetics (incl. genome methylation and epigenomics)Vision scienceCellular nervous systemNeurology and neuromuscular diseases
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Publications (7)

|Mar 23, 2026
Novel PCDH12 pathogenic missense variants cause neurodevelopmental disorders with ocular malformation.

Jennifer Rakotomamonjy, Lucas Fares-Taie, Raman Kumar

|Nov 21, 2024
GPATCH11 variants cause mis-splicing and early-onset retinal dystrophy with neurological impairment.

Andrea Zanetti, Gwendal Dujardin, Lucas Fares-Taie

|Jun 19, 2024
Four Unique Genetic Variants in Three Genes Account for 62.7% of Early-Onset Severe Retinal Dystrophy in Chile: Diagnostic and Therapeutic Consequences.

Rene Moya, Clémentine Angée, Sylvain Hanein

|Apr 25, 2024
Ciliopathy patient variants reveal organelle-specific functions for TUBB4B in axonemal microtubules.

Daniel O Dodd, Sabrina Mechaussier, Patricia L Yeyati

|Mar 13, 2024
Structural Variant Disrupting the Expression of the Remote FOXC1 Gene in a Patient with Syndromic Complex Microphthalmia.

Julie Plaisancié, Bertrand Chesneau, Lucas Fares-Taie

|Aug 04, 2021
Expanding the KIF4A-associated phenotype.

Silvia Kalantari, Colleen Carlston, Norah Alsaleh

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