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Papers published by Dr Adrien Morel:
Detection of a Novel Homozygous PEX5 Stop-Loss Variant Associated with Zellweger Syndrome in a Highly Endogamic Family
Bernal-Bonilla IT, Arias-Florez JS, Ramirez SX, Bayona-Gomez BA, Castro-Castillo L, Correa-Martinez V, Sanchez-Gomez Y, Santiago-Tovar N, Gaviria-Sabogal CC, Contreras Bravo NC, Cabrera R, Morel A, Fonseca-Mendoza DJ, Restrepo CM
The Application of Clinical Genetics 2025, 18:165-173
Published Date: 4 September 2025
Functional Analysis of BRCA1 3’UTR Variants Predisposing to Breast Cancer
Sierra-Díaz DC, Cabrera R, Gonzalez-Vasquez LA, Angulo-Aguado M, Llinás-Caballero K, Fonseca-Mendoza DJ, Contreras-Bravo NC, Restrepo CM, Ortega-Recalde O, Morel A
The Application of Clinical Genetics 2024, 17:57-62
Published Date: 23 May 2024
Whole-Exome Sequencing in Patients Affected by Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Reveals New Variants Potentially Contributing to the Phenotype
Fonseca DJ, Morel A, Llinás-Caballero K, Bolívar-Salazar D, Laissue P
Pharmacogenomics and Personalized Medicine 2021, 14:287-299
Published Date: 1 March 2021
A Novel Splice-Site Mutation in the ELN Gene Suggests an Alternative Mechanism for Vascular Elastinopathies
Velandia-Piedrahita CA, Morel A, Fonseca-Mendoza DJ, Huertas-Quiñones VM, Castillo D, Bonilla JD, Hernandez-Toro CJ, Miranda-Fernández MC, Restrepo CM, Cabrera R
The Application of Clinical Genetics 2020, 13:233-240
Published Date: 17 December 2020