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

por Laissue, Paul
Publicado 2019

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

por Fonseca, Dora Janeth, Morel, Adrien, Llinás-Caballero, Kevin, Bolívar-Salazar, David, Laissue, Paul
Publicado 2021

MON-235 Bone Morphogenic Protein Receptor Variants: A New Cause of Primary Ovarian Insufficiency

por Beau, Isabelle, Renault, Lucie, Clémence, Delcour, Patino, Liliana, Delemer, Brigitte, Laissue, Paul, Young, Jacques, Binart, Nadine
Publicado 2019

Exome Sequencing Is an Efficient Tool for Variant Late-Infantile Neuronal Ceroid Lipofuscinosis Molecular Diagnosis

por Patiño, Liliana Catherine, Battu, Rajani, Ortega-Recalde, Oscar, Nallathambi, Jeyabalan, Anandula, Venkata Ramana, Renukaradhya, Umashankar, Laissue, Paul
Publicado 2014

Refined Mapping of a Quantitative Trait Locus on Chromosome 1 Responsible for Mouse Embryonic Death

por Vatin, Magalie, Burgio, Gaetan, Renault, Gilles, Laissue, Paul, Firlej, Virginie, Mondon, Françoise, Montagutelli, Xavier, Vaiman, Daniel, Serres, Catherine, Ziyyat, Ahmed
Publicado 2012

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

por Calderon-Ospina, Carlos Alberto, Hernández-Sómerson, Mario, García, Ana María, Mejia, Adriana, Tamayo-Agudelo, Caroll, Laissue, Paul, Fonseca Mendoza, Dora Janeth
Publicado 2020

Novel genes and mutations in patients affected by recurrent pregnancy loss

por Quintero-Ronderos, Paula, Mercier, Eric, Fukuda, Michiko, González, Ronald, Suárez, Carlos Fernando, Patarroyo, Manuel Alfonso, Vaiman, Daniel, Gris, Jean-Christophe, Laissue, Paul
Publicado 2017

A first description of the Colombian national registry for rare diseases

por Mateus, Heidi Eliana, Pérez, Ana María, Mesa, Martha Lucía, Escobar, Germán, Gálvez, Jubby Marcela, Montaño, José Ivo, Ospina, Martha Lucía, Laissue, Paul
Publicado 2017

THBD sequence variants potentially related to recurrent pregnancy loss

por Quintero-Ronderos, Paula, Mercier, Eric, Gris, Jean-Christophe, Esteban-Perez, Clara, Moreno-Ortiz, Harold, Fonseca, Dora Janeth, Lucena, Elkin, Vaiman, Daniel, Laissue, Paul
Publicado 2017

Creating and validating a warfarin pharmacogenetic dosing algorithm for Colombian patients

por Galvez, Jubby Marcela, Restrepo, Carlos Martin, Contreras, Nora Constanza, Alvarado, Clara, Calderón-Ospina, Carlos-Alberto, Peña, Nidia, Cifuentes, Ricardo A, Duarte, Daniela, Laissue, Paul, Fonseca, Dora Janeth
Publicado 2018

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

por Agudelo, William A., Gil-Quiñones, Sebastian Ramiro, Fonseca, Alejandra, Arenas, Alvaro, Castro, Laura, Sierra-Díaz, Diana Carolina, Patarroyo, Manuel A., Laissue, Paul, Suárez, Carlos F., Cabrera, Rodrigo
Publicado 2021

Copy number variation profiling in pharmacogenetics CYP-450 and GST genes in Colombian population

por Ramírez, Brian, Niño-Orrego, María José, Cárdenas, Daniel, Ariza, Kevin Enrique, Quintero, Karol, Contreras Bravo, Nora Constanza, Tamayo-Agudelo, Caroll, González, María Alejandra, Laissue, Paul, Fonseca Mendoza, Dora Janeth
Publicado 2019

Whole-Exome Sequencing Enables Rapid Determination of Xeroderma Pigmentosum Molecular Etiology

por Ortega-Recalde, Oscar, Vergara, Jéssica Inés, Fonseca, Dora Janeth, Ríos, Xiomara, Mosquera, Hernando, Bermúdez, Olga María, Medina, Claudia Liliana, Vargas, Clara Inés, Pallares, Argemiro Enrique, Restrepo, Carlos Martín, Laissue, Paul
Publicado 2013

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

por Calderon-Ospina, Carlos Alberto, Galvez, Jubby Marcela, López-Cabra, Claudia, Morales, Natalia, Restrepo, Carlos Martín, Rodríguez, Jesús, Aristizábal-Gutiérrez, Fabio Ancízar, Velez-van-Meerbeke, Alberto, Laissue, Paul, Fonseca-Mendoza, Dora Janeth
Publicado 2020

Genome-Wide Linkage in a Highly Consanguineous Pedigree Reveals Two Novel Loci on Chromosome 7 for Non-Syndromic Familial Premature Ovarian Failure

por Caburet, Sandrine, Zavadakova, Petra, Ben-Neriah, Ziva, Bouhali, Kamal, Dipietromaria, Aurélie, Charon, Céline, Besse, Céline, Laissue, Paul, Chalifa-Caspi, Vered, Christin-Maitre, Sophie, Vaiman, Daniel, Levi, Giovanni, Veitia, Reiner A., Fellous, Marc
Publicado 2012

Endothelial cell dysfunction and cardiac hypertrophy in the STOX1 model of preeclampsia

por Ducat, Aurélien, Doridot, Ludivine, Calicchio, Rosamaria, Méhats, Celine, Vilotte, Jean-Luc, Castille, Johann, Barbaux, Sandrine, Couderc, Betty, Jacques, Sébastien, Letourneur, Franck, Buffat, Christophe, Le Grand, Fabien, Laissue, Paul, Miralles, Francisco, Vaiman, Daniel
Publicado 2016

Success stories in genomic medicine from resource-limited countries

por Mitropoulos, Konstantinos, Al Jaibeji, Hayat, Forero, Diego A., Laissue, Paul, Wonkam, Ambroise, Lopez-Correa, Catalina, Mohamed, Zahurin, Chantratita, Wasun, Lee, Ming Ta Michael, Llerena, Adrian, Brand, Angela, Ali, Bassam R., Patrinos, George P.
Publicado 2015

FOXD1 mutations are related to repeated implantation failure, intra-uterine growth restriction and preeclampsia

por Quintero-Ronderos, Paula, Jiménez, Karen Marcela, Esteban-Pérez, Clara, Ojeda, Diego A., Bello, Sandra, Fonseca, Dora Janeth, Coronel, María Alejandra, Moreno-Ortiz, Harold, Sierra-Díaz, Diana Carolina, Lucena, Elkin, Barbaux, Sandrine, Vaiman, Daniel, Laissue, Paul
Publicado 2019

Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans

por Laissue, Paul, Lakhal, Besma, Vatin, Magalie, Batista, Frank, Burgio, Gaëtan, Mercier, Eric, Santos, Esther Dos, Buffat, Christophe, Sierra-Diaz, Diana Carolina, Renault, Gilles, Montagutelli, Xavier, Salmon, Jane, Monget, Philippe, Veitia, Reiner A., Méhats, Céline, Fellous, Marc, Gris, Jean-Christophe, Cocquet, Julie, Vaiman, Daniel
Publicado 2016

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

por Angulo-Aguado, Mariana, Panche, Karen, Tamayo-Agudelo, Caroll Andrea, Ruiz-Torres, Daniel-Armando, Sambracos-Parrado, Santiago, Niño-Orrego, Maria Jose, Páez, Nathaly, Piñeros-Hernandez, Laura B, Castillo-León, Luisa-Fernanda, Pardo-Oviedo, Juan Mauricio, Abaunza, Katherine Parra, Laissue, Paul, Contreras, Nora, Calderón-Ospina, Carlos Alberto, Fonseca-Mendoza, Dora Janeth
Publicado 2021