Paul Laissue

Carrera 24 N° 63C-69, CP 112111
Bogota, DC, Colombia

Last Updated: 09/26/2026

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Found 56 publications

MIEN1 promoter deletion leads to impaired migration and invasion potential via actin cytoskeleton rearrangement in colorectal cancer.

MIEN1 promoter deletion leads to impaired migration and invasion potential via actin cytoskeleton rearrangement in colorectal cancer.

Journal: Scientific reports
Published: April 04, 2025

Linking genotype to trophoblast phenotype in preeclampsia and HELLP syndrome associated with STOX1 genetic variants.

Linking genotype to trophoblast phenotype in preeclampsia and HELLP syndrome associated with STOX1 genetic variants.

Journal: iScience
Published: November 15, 2023

Structural Modelling of KCNQ1 and KCNH2 Double Mutant Proteins, Identified in Two Severe Long QT Syndrome Cases, Reveals New Insights into Cardiac Channelopathies.

Structural Modelling of KCNQ1 and KCNH2 Double Mutant Proteins, Identified in Two Severe Long QT Syndrome Cases, Reveals New Insights into Cardiac Channelopathies.

Journal: International journal of molecular sciences
Published: September 24, 2021

A Pharmacogenetic Study of CYP2C19 in Acute Coronary Syndrome Patients of Colombian Origin Reveals New Polymorphisms Potentially Related to Clopidogrel Therapy.

A Pharmacogenetic Study of CYP2C19 in Acute Coronary Syndrome Patients of Colombian Origin Reveals New Polymorphisms Potentially Related to Clopidogrel Therapy.

Journal: Journal of personalized medicine
Published: March 14, 2021

Whole-Exome Sequencing in Patients Affected by Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Reveals New Variants Potentially Contributing to the Phenotype.

Whole-Exome Sequencing in Patients Affected by Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Reveals New Variants Potentially Contributing to the Phenotype.

Journal: Pharmacogenomics and personalized medicine
Published: November 01, 2020

Genetic Variants Contributing to Early Recurrent Pregnancy Loss Etiology Identified by Sequencing Approaches.

Genetic Variants Contributing to Early Recurrent Pregnancy Loss Etiology Identified by Sequencing Approaches.

Journal: Reproductive sciences (Thousand Oaks, Calif.)
Published: May 21, 2020

DHH pathogenic variants involved in 46,XY disorders of sex development differentially impact protein self-cleavage and structural conformation.

DHH pathogenic variants involved in 46,XY disorders of sex development differentially impact protein self-cleavage and structural conformation.

Journal: Human genetics
Published: April 21, 2020

Exploring the Molecular Aetiology of Preeclampsia by Massive Parallel Sequencing of DNA.

Exploring the Molecular Aetiology of Preeclampsia by Massive Parallel Sequencing of DNA.

Journal: Current hypertension reports
Published: March 16, 2020

Identifying new potential genetic biomarkers for HELLP syndrome using massive parallel sequencing.

Identifying new potential genetic biomarkers for HELLP syndrome using massive parallel sequencing.

Journal: Pregnancy hypertension
Published: February 08, 2020

Possible Genetic Determinants of Response to Phenytoin in a Group of Colombian Patients With Epilepsy.

Possible Genetic Determinants of Response to Phenytoin in a Group of Colombian Patients With Epilepsy.

Journal: Frontiers in pharmacology
Published: January 15, 2020

Molecular Mechanisms of Trophoblast Dysfunction Mediated by Imbalance between STOX1 Isoforms.

Molecular Mechanisms of Trophoblast Dysfunction Mediated by Imbalance between STOX1 Isoforms.

Journal: iScience
Published: November 05, 2019

A Pharmacogenomic Dissection of a Rosuvastatin-Induced Rhabdomyolysis Case Evokes the Polygenic Nature of Adverse Drug Reactions.

A Pharmacogenomic Dissection of a Rosuvastatin-Induced Rhabdomyolysis Case Evokes the Polygenic Nature of Adverse Drug Reactions.

Journal: Pharmacogenomics and personalized medicine
Published: August 26, 2019
Showing 1-12 of 56

Last Updated: 09/26/2026