Jubby M. Galvez
Bogota, DC, Colombia
Last Updated: 09/26/2026
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Found 14 publications
Genetic Ancestry and Carrier Variant Frequency Enrichment in a Colombian Andean Population: Insights From the Eje Cafetero.
Journal: American journal of medical genetics. Part A
Published: January 28, 2026
Familial chylomicronemia syndrome caused by 2 genetic variants in the APOA5 gene: Severe hypertriglyceridemia that complicates pregnancy.
Journal: Journal of clinical lipidology
Published: August 24, 2024
Effectiveness of the Booster Dose in Protecting against COVID-19, Colombia 2022.
Journal: Vaccines
Published: July 01, 2023
Genomic characterization of SARS-CoV-2 and its association with clinical outcomes: a 1-year longitudinal study of the pandemic in Colombia.
Journal: International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases
Published: August 23, 2021
Machine Learning for Prediction of Stable Warfarin Dose in US Latinos and Latin Americans.
Journal: Frontiers in pharmacology
Published: July 29, 2021
Mutation profile of SARS-CoV-2 genome in a sample from the first year of the pandemic in Colombia.
Journal: Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases
Published: June 15, 2021
Possible Genetic Determinants of Response to Phenytoin in a Group of Colombian Patients With Epilepsy.
Journal: Frontiers in pharmacology
Published: January 15, 2020
Creating and validating a warfarin pharmacogenetic dosing algorithm for Colombian patients.
Journal: Pharmacogenomics and personalized medicine
Published: November 10, 2018
A first description of the Colombian national registry for rare diseases.
Journal: BMC research notes
Published: June 23, 2017
Ocular findings in Fabry disease in Colombian patients
Journal: Biomedica : revista del Instituto Nacional de Salud
Published: March 13, 2017
Lack of association of polymorphisms in six candidate genes in colombian adhd patients.
Journal: Annals of neurosciences
Published: November 04, 2015
Biallelic HERC1 mutations in a syndromic form of overgrowth and intellectual disability.
Journal: Clinical genetics
Published: April 29, 2015
Last Updated: 09/26/2026