selected publications academic article Correction: Uveitis and Multiple Sclerosis: Potential Common Causal Mutations (Molecular Neurobiology, (2019), 56, 12, (8008-8017), 10.1007/s12035-019-1630-2) 2023-5-1 Pharmacogenomic profile of actionable molecular variants related to drugs commonly used in anesthesia 2023-1-1 Frequency of actionable Exomic secondary findings in 160 Colombian patients Impact in the healthcare system 2022-9-5 Performance Comparison of a Duplex Implementation of the CDC EUA 2019-nCoV Assay with the Seegene Allplex-SARS-CoV-2 Assay for the Detection of SARS-CoV-2 in Nasopharyngeal Swab Samples 2022-9-21 Characterization of ADME Gene Variation in Colombian Population by Exome Sequencing 2022-6-30 Association Between the LZTFL1 rs11385942 Polymorphism and COVID-19 Severity in Colombian Population 2022-6-20 Ataxia with Ocular Apraxia Type 1 (AOA1) (APTX, W279* Mutation) 2022-6-1 Correction to 2022-6-1 Genetic and molecular aspects of drug-induced QT interval prolongation 2021-7-28 Genetic profile of the dystrophin gene reveals new mutations in colombian patients affected with muscular dystrophinopathy 2021-10-1 Noonan Syndrome with Multiple Lentigines and PTPN11 Mutation: A Case with Intracerebral Hemorrhage 2021-1-27 Possible Genetic Determinants of Response to Phenytoin in a Group of Colombian Patients With Epilepsy 2020-5-7 Síndrome Nefrótico: “De la teoría al manejo” 2020-2-27 A Novel Splice-Site Mutation in the ELN Gene Suggests an Alternative Mechanism for Vascular Elastinopathies 2020-12-17 Uveitis and multiple sclerosis: potential common causal mutations 2019-6-3 Congenital leptin deficiency and leptin gene missense mutation found in two colombian sisters with severe obesity 2019-5-1 Identification of a New Candidate Locus for Ebstein Anomaly in 1p36.2 2018-5-1 A combined linkage, microarray and exome analysis suggests MAP3K11 as a candidate gene for left ventricular hypertrophy 2018-3-5 Identification of clinically relevant phenotypes in patients with Ebstein anomaly 2018-3-1 A GHEP-ISFG collaborative study on the genetic variation of 38 autosomal indels for human identification in different continental populations 2018-1-1 Creating and validating a warfarin pharmacogenetic dosing algorithm for colombian patients 2018-1-1 Meningioma rabdoide Grado III, en paciente pediátrico: Reporte de caso 2017-5-28 Improving the evaluation of milestones for students completing a clinical genetics elective 2017-12-1 A novel TGM1 mutation, leading to multiple splicing rearrangements, is associated with autosomal recessive congenital ichthyosis 2015-10-1 Biallelic HERC1 mutations in a syndromic form of overgrowth and intellectual disability 2015-10-1 Frecuencia de mutación y de variantes de secuencia para los genes BRCA1 y BRCA2 en una muestra de mujeres colombianas con sospecha de síndrome de cáncer de mama hereditario: serie de casos 2015-1-1 Transcriptional regulator PRDM12 is essential for human pain perception 2015-1-1 BMP15 c.-9C>G promoter sequence variant may contribute to the cause of non-syndromic premature ovarian failure 2014-1-1 AFLP Polymorphisms Allow High Resolution Genetic Analysis of American Tegumentary Leishmaniasis Agents Circulating in Panama and Other Members of the Leishmania Genus 2013-9-9 Whole-Exome Sequencing Enables Rapid Determination of Xeroderma Pigmentosum Molecular Etiology 2013-6-3 A pseudopterane diterpene isolated from the octocoral Pseudopterogorgia acerosa inhibits the inflammatory response mediated by TLR-ligands and TNF-alpha in macrophages 2013-12-16 Sequence analysis of the ADRA2A coding region in children affected by attention deficit hyperactivity disorder 2013-12-1 A novel familial case of diffuse leukodystrophy related to NDUFV1 compound heterozygous mutations 2013-11-1 Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis 2012-8-1 A de novo 14q12q13.3 interstitial deletion in a patient affected by a severe neurodevelopmental disorder of unknown origin 2012-3-1 Screening for mutations of the FOXO4 gene in premature ovarian failure patients 2012-3-1 CITED2 mutations potentially cause idiopathic premature ovarian failure 2012-11-1 DNA repair mechanisms as drug targets in prokaryotes 2011-7-1 Sequence analysis of the CDKN1B gene in patients with premature ovarian failure reveals a novel mutation potentially related to the phenotype 2011-6-30 Amplified fragment length polymorphisms reveals high intraspecific variability in field isolates of Leishmania panamensis 2011-4-1 Analisis de marcadores STR sobre el cromosoma X en una poblacion de Bogota 2010-1-1 Population data on 15 autosomal STRs in a sample from Colombia 2009-6-1 Identificación de deleciones en portadoras de distrofia muscular de Duchenne 2008-1-1 Hemofilia: diagnostico molecular y alternativas de tratamiento 2007-9-1 Mutation study of spanish patients with hereditary hemorrhagic telangiectasia and expression analysis of endoglin and ALK1 2006-3-1 PCR-heterodúplex por agrupamiento: Implementación de un método de identificación de portadores de la mutación más común causal de fibrosis quística en Colombia 2006-1-1 Distrofia Muscular de Duchenne y Becker: Una visión molecular 2005-9-5 ADN fetal en sangre materna: Implicaciones para el diagnóstico prenatal 2005-1-1 Falla Ovarica Prematura y Síndrome X Fragil 2005-1-1 Aspectos clínico moleculares de la hiperplasia suprarrenal congénita 2004-1-1 Deleciones en el gen de la Distrofina en 62 familias colombianas correlación genotipo-fenotipo para la Distrofia Muscular de Duchenne y Becker. 2004-1-1 Bases Genéticas de la Preclampsia 2003-1-1 Estudio Citogenético en líquido Amniótico para la detección de Anomalías Cromosómicas del Feto 2003-1-1 Identificación de portadoras de hemofilia A para asesoramiento genético mediante análisis en el ADN de polimorfismos intragénicos del gen del factor VIII de la coagulación 2003-1-1 CFTR mutations in three Latin American countries 2000-4-24 FALLA OVARICA PREMATURA 1995-1-1 Tandem duplication of proximal 5q 1990-1-1 Síndrome de Meckel en dos hermanos. Aspectos clínicos, anatomopatológicos y genéticos. 1988-9-1 Incidencia familiar de la glomerulonefritis postestrepotocócica. 1981-1-1 Performance verification (secondary validation) of the real-time molecular PCR (RT-qPCR) test on the Vivalytic One * (Vivalytic SARS-CoV-2) platform for point-of-care (POC) detection of SARS-CoV-2. chapter Genética del retraso mental. 301-310. 2017-5-31 editorial article Is genetic counseling a practice that stimulates eugenics? 2018-1-1 comment Erratum. 962. 2015-8-30 Genetics and genomic medicine in colombia. 84-91. 2015-1-1 letter A severe familial phenotype of Ichthyosis Curth-Macklin caused by a novel mutation in the KRT1 gene. 456-458. 2013-2-1 review Hemophilia: Molecular diagnosis and alternatives of treatment. 308-315. 2007-7-1
principal investigator on Genómica funcional para la descripción de mutaciones en el diagnóstico molecular del cáncer de seno esporádico en población colombiana 2022-02-01 - 2023-08-31 Genetic mapping of cardiac conduction disorders - Genetic architecture of ECG 2011-07-01 - 2017-12-01 Creation of a DNA bank referring to pathologies associated with human reproduction and frequent neurological dysfunctions. 2011-01-01 - 2012-01-01 Analysis of haplotypes constructed with microsatellites linked to the FMR-1 gene in families with Fragile X Syndrome in Cundinamarca, Eje Cafetero and Valle del Cauca. 2006-01-01 - 2012-01-01 New algorithm for warfarin dosage. Genetic and non-genetic factors. 2010-08-01 - 2011-04-15 Clinical cases with relevance in medical genetics 2006-01-01 - 2009-12-31 Development of a new simple and inexpensive diagnostic method for Fragil X syndrome -Evaluation of a diagnostic concept 2004-01-01 - 2006-06-01 Analysis of genetic ligation in a Colombian family with diagnosis of DYGGVE-MELCHIOR-CLAUSEN and/or late spondyloepiphyseal dysplasia. 2005-02-01 - 2006-04-01
co-principal investigator on A method to identify rare diseases with translational research in biogeographic isolates from the Boyacá department exploring ancestry. 2021-12-23 - 2024-11-26 Factores genéticos asociados a la severidad clínica en población colombiana afectada por SARS-CoV-2 2022-02-01 - 2023-08-31 Functional genomics for the description of mutations in the molecular diagnosis of sporadic colon and rectal cancer in a Colombian population. 2021-01-01 - 2022-12-31 Implication of 3'UTR sequence variation in breast cancer. 2021-11-23 - 2022-11-23 Impact of genetic and non-genetic factors on the severity of SARS-CoV-2 infection: towards the generation of a risk prediction model in a Colombian population. 2021-03-01 - 2022-03-31 missing activity
Tutor of Análisis genómico en pacientes con anomalía de Ebstein Thesis Desarrollo de una aplicación de computador para analizar parámetros estadísticos genético-poblacionales de microsatélites en poblaciones humanas Thesis El papel de polimorfismos del gen COMT en la susceptibilidad a la Depresión Mayor Thesis Genotipificación de HLA-B en pacientes colombianos afectados por el síndrome Stevens-Johnson y la Necrólisis Epidérmica Tóxica Thesis Hallazgos secundarios en la secuenciación del exoma según las recomendaciones del Colegio Americano de Genética Médica y Genómica (ACMG) en una muestra de la población colombiana Thesis Impacto de la tecnología de secuencia de nueva generación (NGS) sobre el análisis genético de casos complejos en identificación de personas desaparecidas en el conflicto armado colombiano Thesis Medicina genómica en el diagnóstico de enfermedades raras Thesis Mutaciones bialélicas en HERC1 en una forma sindrómica de sobrecrecimiento y retraso mental Thesis Nuevos datos estadísticos genético-poblacionales para microsatélites en Colombia Thesis Polimorfismos del gen Butirilcolinesterasa responsables de reacciones adversas en pacientes consumidores de “cocaína” Thesis Pruebas de diagnóstico y cribado genético Thesis Tamizaje combinado de aneuploidía durante el primer trimestre del embarazo en Colombia Thesis Understanding the heritability of heart rhythm and conduction disorders Thesis
mailing address Universidad del Rosario. Sede Quinta de Mutis. Carrera 24 # 63C-69. Bogotá, Colombia.
CVLAC http://scienti.colciencias.gov.co:8081/cvlac/visualizador/generarCurriculoCv.do?cod_rh=0000173100