Vianey Labastida-Ordonez

Cuernavaca, MOR, Mexico

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 12 publications

The landscape of 605 genetically confirmed distinct rare diseases in a single center in Mexico (2005-2025).

The landscape of 605 genetically confirmed distinct rare diseases in a single center in Mexico (2005-2025).

Journal: Orphanet journal of rare diseases

Published: August 18, 2025

Diagnosis of inborn errors of metabolism through massive DNA sequencing: benefits and limitations.

Diagnosis of inborn errors of metabolism through massive DNA sequencing: benefits and limitations.

Journal: Gaceta medica de Mexico

Published: June 18, 2025

Resolving the Diagnostic Odyssey in Inherited Retinal Dystrophies Through Long-Read Genome Sequencing.

Resolving the Diagnostic Odyssey in Inherited Retinal Dystrophies Through Long-Read Genome Sequencing.

Journal: American journal of medical genetics. Part A

Published: April 07, 2025

ABCC6 gene mutational spectrum and ocular features in Mexican patients with pseudoxanthoma elasticum-related angioid streaks.

ABCC6 gene mutational spectrum and ocular features in Mexican patients with pseudoxanthoma elasticum-related angioid streaks.

Journal: Ophthalmic genetics

Published: March 05, 2025

Identification of Pathogenic Copy Number Variants in Mexican Patients With Inherited Retinal Dystrophies Applying an Exome Sequencing Data-Based Read-Depth Approach.

Identification of Pathogenic Copy Number Variants in Mexican Patients With Inherited Retinal Dystrophies Applying an Exome Sequencing Data-Based Read-Depth Approach.

Journal: Molecular genetics & genomic medicine

Published: May 21, 2024

Identification of Genetic Variants for Diabetic Retinopathy Risk Applying Exome Sequencing in Extreme Phenotypes.

Identification of Genetic Variants for Diabetic Retinopathy Risk Applying Exome Sequencing in Extreme Phenotypes.

Journal: BioMed research international

Published: November 08, 2023

Genotypic spectrum of ABCA4-associated retinal degenerations in 211 unrelated Mexican patients: identification of 22 novel disease-causing variants.

Genotypic spectrum of ABCA4-associated retinal degenerations in 211 unrelated Mexican patients: identification of 22 novel disease-causing variants.

Journal: Molecular genetics and genomics : MGG

Published: July 19, 2023

MTSS2-related neurodevelopmental disorder: Further delineation of the phenotype.

MTSS2-related neurodevelopmental disorder: Further delineation of the phenotype.

Journal: European journal of medical genetics

Published: June 12, 2023

USH2A mutational spectrum causing syndromic and non-syndromic retinal dystrophies in a large cohort of Mexican patients.

USH2A mutational spectrum causing syndromic and non-syndromic retinal dystrophies in a large cohort of Mexican patients.

Journal: Molecular vision

Published: November 04, 2022

Effectiveness of Whole-Exome Sequencing for the Identification of Causal Mutations in Patients with Suspected Inherited Ocular Diseases.

Effectiveness of Whole-Exome Sequencing for the Identification of Causal Mutations in Patients with Suspected Inherited Ocular Diseases.

Journal: Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion

Published: September 10, 2022

A novel homozygous ZNF469 variant causing brittle cornea syndrome is associated with corneal ectasias in heterozygous carriers.

A novel homozygous ZNF469 variant causing brittle cornea syndrome is associated with corneal ectasias in heterozygous carriers.

Journal: International ophthalmology

Published: January 12, 2022

Clinical, radiological, and molecular diagnosis of progressive fibrodysplasia ossificans.

Clinical, radiological, and molecular diagnosis of progressive fibrodysplasia ossificans.

Journal: Boletin medico del Hospital Infantil de Mexico

Published: May 03, 2021

Showing 1-12 of 12

Last Updated: 09/26/2026