Publications by authors named "Paul Laissue"

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MIEN1 promoter deletion leads to impaired migration and invasion potential via actin cytoskeleton rearrangement in colorectal cancer.
Payal Ranade, Rucha Trivedi, Diana Carolina Sierra-Díaz, Paul Laissue, Jamboor K Vishwanatha

Sci Rep· September 2025

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Linking genotype to trophoblast phenotype in preeclampsia and HELLP syndrome associated with genetic variants.
Lorenzo Costa, Luis Bermudez-Guzman, Ikram Benouda, Paul Laissue, Adrien Morel

iScience· March 2024

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Structural Modelling of KCNQ1 and KCNH2 Double Mutant Proteins, Identified in Two Severe Long QT Syndrome Cases, Reveals New Insights into Cardiac Channelopathies.
William A Agudelo, Sebastian Ramiro Gil-Quiñones, Alejandra Fonseca, Alvaro Arenas, Laura Castro, Paul Laissue

Int J Mol Sci· November 2021

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A Pharmacogenetic Study of in Acute Coronary Syndrome Patients of Colombian Origin Reveals New Polymorphisms Potentially Related to Clopidogrel Therapy.
Mariana Angulo-Aguado, Karen Panche, Caroll Andrea Tamayo-Agudelo, Daniel-Armando Ruiz-Torres, Santiago Sambracos-Parrado, Paul Laissue

J Pers Med· May 2021

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Whole-Exome Sequencing in Patients Affected by Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Reveals New Variants Potentially Contributing to the Phenotype.
Dora Janeth Fonseca, Adrien Morel, Kevin Llinás-Caballero, David Bolívar-Salazar, Paul Laissue

Pharmgenomics Pers Med· March 2021

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DHH pathogenic variants involved in 46,XY disorders of sex development differentially impact protein self-cleavage and structural conformation.
Maëva Elzaiat, Delphine Flatters, Diana Carolina Sierra-Díaz, Berangère Legois, Paul Laissue

Hum Genet· November 2020

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Identifying new potential genetic biomarkers for HELLP syndrome using massive parallel sequencing.
Karen Marcela Jiménez, Adrien Morel, Laura Parada-Niño, María Alejandra González-Rodriguez, Stephanie Flórez, Paul Laissue

Pregnancy Hypertens· October 2020

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Genetic Variants Contributing to Early Recurrent Pregnancy Loss Etiology Identified by Sequencing Approaches.
Paula Quintero-Ronderos, Paul Laissue

Reprod Sci· August 2020

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Molecular Mechanisms of Trophoblast Dysfunction Mediated by Imbalance between STOX1 Isoforms.
Aurélien Ducat, Betty Couderc, Anthony Bouter, Louise Biquard, Rajaa Aouache, Paul Laissue

iScience· May 2020

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Possible Genetic Determinants of Response to Phenytoin in a Group of Colombian Patients With Epilepsy.
Carlos Alberto Calderon-Ospina, Jubby Marcela Galvez, Claudia López-Cabra, Natalia Morales, Carlos Martín Restrepo, Paul Laissue

Front Pharmacol· May 2020

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BMPR1A and BMPR1B Missense Mutations Cause Primary Ovarian Insufficiency.
Lucie Renault, Liliana C Patiño, Françoise Magnin, Brigitte Delemer, Jacques Young, Paul Laissue

J Clin Endocrinol Metab· April 2020

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Exploring the Molecular Aetiology of Preeclampsia by Massive Parallel Sequencing of DNA.
Paul Laissue, Daniel Vaiman

Curr Hypertens Rep· March 2020

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A Pharmacogenomic Dissection of a Rosuvastatin-Induced Rhabdomyolysis Case Evokes the Polygenic Nature of Adverse Drug Reactions.
Carlos Alberto Calderon-Ospina, Mario Hernández-Sómerson, Ana María García, Adriana Mejia, Caroll Tamayo-Agudelo, Paul Laissue

Pharmgenomics Pers Med· March 2020

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Mutant GNLY is linked to Stevens-Johnson syndrome and toxic epidermal necrolysis.
Dora Janeth Fonseca, Luz Adriana Caro, Diana Carolina Sierra-Díaz, Carlos Serrano-Reyes, Olga Londoño, Paul Laissue

Hum Genet· December 2019

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FOXD1 mutations are related to repeated implantation failure, intra-uterine growth restriction and preeclampsia.
Paula Quintero-Ronderos, Karen Marcela Jiménez, Clara Esteban-Pérez, Diego A Ojeda, Sandra Bello, Paul Laissue

Mol Med· August 2019

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Copy number variation profiling in pharmacogenetics CYP-450 and GST genes in Colombian population.
Brian Ramírez, María José Niño-Orrego, Daniel Cárdenas, Kevin Enrique Ariza, Karol Quintero, Paul Laissue

BMC Med Genomics· July 2019

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ATG7 and ATG9A loss-of-function variants trigger autophagy impairment and ovarian failure.
Clémence Delcour, Larbi Amazit, Liliana C Patino, Françoise Magnin, Jérôme Fagart, Paul Laissue

Genet Med· April 2019

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Genetic Variants Contributing to Early Recurrent Pregnancy Loss Etiology Identified by Sequencing Approaches.
Paula Quintero-Ronderos, Paul Laissue

Reprod Sci· March 2019

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Functional evidence implicating NOTCH2 missense mutations in primary ovarian insufficiency etiology.
Liliana C Patiño, Isabelle Beau, Adrien Morel, Brigitte Delemer, Jacques Young, Paul Laissue

Hum Mutat· January 2019

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The forkhead-box family of transcription factors: key molecular players in colorectal cancer pathogenesis.
Paul Laissue

Mol Cancer· January 2019

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Creating and validating a warfarin pharmacogenetic dosing algorithm for Colombian patients.
Jubby Marcela Galvez, Carlos Martin Restrepo, Nora Constanza Contreras, Clara Alvarado, Carlos-Alberto Calderón-Ospina, Paul Laissue

Pharmgenomics Pers Med· October 2018

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A novel mutation in KHDRBS1 in a patient affected by primary ovarian insufficiency.
Carolina Carlosama, Liliana Catherine Patiño, Isabelle Beau, Adrien Morel, Brigitte Delemer, Paul Laissue

Clin Endocrinol (Oxf)· August 2018

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The multisystemic functions of FOXD1 in development and disease.
Paula Quintero-Ronderos, Paul Laissue

J Mol Med (Berl)· August 2018

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Transcriptomic analysis of FUCA1 knock-down in keratinocytes reveals new insights into the pathogenesis of fucosidosis skin lesions.
Danyela Valero-Rubio, Karen Marcela Jiménez, Dora Janeth Fonseca, César Payán-Gómez, Paul Laissue

Exp Dermatol· June 2018

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Identification of a New Candidate Locus for Ebstein Anomaly in 1p36.2.
Marta-Catalina Miranda-Fernández, Silvia Ramírez-Oyaga, Carlos M Restrepo, Victor-Manuel Huertas-Quiñones, Magally Barrera-Castañeda, Paul Laissue

Mol Syndromol· May 2018

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