Wilmar Saldarriaga-Gil

11PUBLICATIONS
24CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Pacific Peoples and disabilityAutoimmunityNeonatologyElectronic and magnetic properties of condensed matter; superconductivity
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Publications (11)

|Aug 27, 2026
Exploratory Analysis of Glaucoma-Associated SNPs in a Colombian Cohort Highlights Potential Involvement of Oxidative, Vascular, and Neurodegenerative Pathways.

|Jun 30, 2026
New variant in PLP1 gene associated with X-linked spastic paraplegia type 2: First report of a family in Colombia

|Nov 14, 2024
Phenotype-Genotype Correlation in Morquio A Syndrome: Protocol for a Meta-Analysis.

Lorena Diaz-Ordoñez, Paola Andrea Duque-Cordoba, Daniel Andrés Nieva-Posso

|Nov 08, 2023
Thoracic kidney and diaphragmatic hernia: prenatal diagnosis and successful management. Case report and review of the literature

Mario Fernando Ortega-Mafla, Valerye Viveros-Gonzalez, Wilmar Saldarriaga-Gil

|Sep 04, 2023
Fragile X Syndrome in children.

David O Acero-Garcés, Wilmar Saldarriaga, Ana M Cabal-Herrera

|Nov 23, 2022
Preliminary identification of pathogenic variants in an Afro-Colombian Raizal family with risk factors for glaucoma.

Harry Castillo-Plata, Nelson Rivera-Franco, Claudia Valencia-Peña

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Frequent Collaborators

2 joint publications

Lorena Diaz-Ordoñez

2 joint publications

Harry Pachajoa

2 joint publications

Ana Maria Cabal-Herrera

2 joint publications

Andres Castillo