karen marcela jimenez

Publicaciones

Linking genotype to trophoblast phenotype in preeclampsia and HELLP syndrome associated with STOX1 genetic variants
2024-3-15
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
Identifying new potential genetic biomarkers for HELLP syndrome using massive parallel sequencing
2020-10-1
FOXD1 mutations are related to repeated implantation failure, intra-uterine growth restriction and preeclampsia
2019-8-8
Transcriptomic analysis of FUCA1 knock-down in keratinocytes reveals new insights into the pathogenesis of fucosidosis skin lesions
2018-6-1
Next generation sequencing in women affected by nonsyndromic premature ovarian failure displays new potential causative genes and mutations
2015-7-1

Coinvestigador

Genómica funcional para la identificación de biomarcadores genéticos aplicables al diagnóstico temprano de la preeclampsia 2017-12-26 - 2019-12-26

Mejore su perfil