Hoai V. Tran

Lausanne, VD 1004, Switzerland

Last Updated: 09/26/2026

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Found 23 publications

Missense variants in KATNA1 alter microtubule dynamics and underlie dominant macular dystrophy.

Missense variants in KATNA1 alter microtubule dynamics and underlie dominant macular dystrophy.

Journal: Research square
Published: July 17, 2026

Resting-state electroretinography reveals pathological retinal oscillations in retinitis pigmentosa mice and patients.

Resting-state electroretinography reveals pathological retinal oscillations in retinitis pigmentosa mice and patients.

Journal: Nature communications
Published: November 04, 2025

Bi-allelic variants in three genes encoding distinct subunits of the vesicular AP-5 complex cause hereditary macular dystrophy.

Bi-allelic variants in three genes encoding distinct subunits of the vesicular AP-5 complex cause hereditary macular dystrophy.

Journal: American journal of human genetics
Published: September 12, 2024

GNB1-Related Rod-Cone Dystrophy: A Case Report.

GNB1-Related Rod-Cone Dystrophy: A Case Report.

Journal: Case reports in ophthalmology
Published: September 26, 2023

Mutations in SAMD7 cause autosomal-recessive macular dystrophy with or without cone dysfunction.

Mutations in SAMD7 cause autosomal-recessive macular dystrophy with or without cone dysfunction.

Journal: American journal of human genetics
Published: September 11, 2023

Genetics of Retinitis Pigmentosa and Other Hereditary Retinal Disorders in Western Switzerland.

Genetics of Retinitis Pigmentosa and Other Hereditary Retinal Disorders in Western Switzerland.

Journal: Ophthalmic research
Published: June 07, 2023

Cost-effective sequence analysis of 113 genes in 1,192 probands with retinitis pigmentosa and Leber congenital amaurosis.

Cost-effective sequence analysis of 113 genes in 1,192 probands with retinitis pigmentosa and Leber congenital amaurosis.

Journal: Frontiers in cell and developmental biology
Published: November 30, 2022

Enhancer of Zeste Homolog 2 (EZH2) Contributes to Rod Photoreceptor Death Process in Several Forms of Retinal Degeneration and Its Activity Can Serve as a Biomarker for Therapy Efficacy.

Enhancer of Zeste Homolog 2 (EZH2) Contributes to Rod Photoreceptor Death Process in Several Forms of Retinal Degeneration and Its Activity Can Serve as a Biomarker for Therapy Efficacy.

Journal: International journal of molecular sciences
Published: July 26, 2021

Different Phenotypes in Pseudodominant Inherited Retinal Dystrophies.

Different Phenotypes in Pseudodominant Inherited Retinal Dystrophies.

Journal: Frontiers in cell and developmental biology
Published: November 03, 2020

Retinal Structure in RPE65-Associated Retinal Dystrophy.

Retinal Structure in RPE65-Associated Retinal Dystrophy.

Journal: Investigative ophthalmology & visual science
Published: April 30, 2020

Malattia Leventinese: EFEMP1 R345W Variant Is a Hot Spot Mutation, Not a Founder Mutation.

Malattia Leventinese: EFEMP1 R345W Variant Is a Hot Spot Mutation, Not a Founder Mutation.

Journal: Ophthalmology. Retina
Published: April 13, 2020

Correction: Novel PDE6B Mutation Presenting with Retinitis Pigmentosa - A Case Series of Three Patients.

Correction: Novel PDE6B Mutation Presenting with Retinitis Pigmentosa - A Case Series of Three Patients.

Journal: Klinische Monatsblatter fur Augenheilkunde
Published: February 16, 2019
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Last Updated: 09/26/2026