Liliana Fernández-Hernández

10PUBLICATIONS
19CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Genetic immunologyNutrigenomics and personalised nutritionMedical biochemistry - inorganic elements and compoundsNeonatology
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Publications (10)

|Feb 27, 2026
Reassessing Benign ASXL1 Variants in Bohring-Opitz Syndrome: The Role of Population Databases in Variant Reinterpretation.

Liliana Fernández-Hernández, Sergio Enríquez-Flores, Nancy L Hernández-Martínez

|Aug 28, 2025
Biparental and Androgenetic Somatic Mosaicism with Presentation of Non-Syndromic Severe Neonatal Hyperinsulinemia.

Miguel Angel Alcántara-Ortigoza, Marcela Vela-Amieva, Ariadna González-Del Angel

|Nov 09, 2024
Concordance Between Biochemical and Molecular Diagnosis Obtained by WES in Mexican Patients with Inborn Errors of Intermediary Metabolism: Utility for Therapeutic Management.

Marcela Vela-Amieva, Miguel Angel Alcántara-Ortigoza, Ariadna González-Del Angel

|Dec 23, 2023
In Silico Structural Protein Evaluation of the Phenylalanine Hydroxylase p.(Tyr77His) Variant Associated with Benign Hyperphenylalaninemia as Identified through Mexican Newborn Screening.

Marcela Vela-Amieva, Miguel Angel Alcántara-Ortigoza, Ariadna González-Del Angel

|Nov 11, 2022
The Enigmatic Etiology of Oculo-Auriculo-Vertebral Spectrum (OAVS): An Exploratory Gene Variant Interaction Approach in Candidate Genes.

Bernardette Estandia-Ortega, Miriam Erandi Reyna-Fabián, José Antonio Velázquez-Aragón

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