Analysis of meiotic recombination in 22q11.2, a region that frequently undergoes deletions and duplications

por Torres-Juan, Laura, Rosell, Jordi, Sánchez-de-la-Torre, Manuel, Fibla, Joan, Heine-Suñer, Damià
Publicado 2007

Identification of Driver Epistatic Gene Pairs Combining Germline and Somatic Mutations in Cancer

por Rocha, Jairo, Sastre, Jaume, Amengual-Cladera, Emilia, Hernandez-Rodriguez, Jessica, Asensio-Landa, Victor, Heine-Suñer, Damià, Capriotti, Emidio
Publicado 2023

Geographical genetic variability: a factor to consider when assessing clinical implications of PRDM9

por Alemany-Schmidt, Alexandra, Navarro-Palou, Maria, Voltes-Cobo, Adrià, Rosell, Jordi, Heine-Suñer, Damià, Picornell, Antònia, Oliver-Bonet, Maria
Publicado 2014

Angiotensin-converting-enzyme gene polymorphisms, smoking and chronic obstructive pulmonary disease

por Busquets, Xavier, MacFarlane, Niall G, Heine-Suñer, Damià, Morlá, Montse, Torres-Juan, Laura, Iglesias, Amanda, Lladó, Jeronia, Sauleda, Jaume, Agustí, Alvar GN
Publicado 2007

Familial Dilated Cardiomyopathy and Sudden Cardiac Arrest: New Association with a SCN5A Mutation

por Rico, Yolanda, Ramis, Maria Francisca, Massot, Montse, Torres-Juan, Laura, Pons, Jaume, Fortuny, Elena, Ripoll-Vera, Tomas, González, Rosa, Peral, Vicente, Rossello, Xavier, Heine Suñer, Damià
Publicado 2021

A deletion and a duplication in distal 22q11.2 deletion syndrome region. Clinical implications and review

por Fernández, Luis, Nevado, Julián, Santos, Fernando, Heine-Suñer, Damià, Martinez-Glez, Victor, García-Miñaur, Sixto, Palomo, Rebeca, Delicado, Alicia, Pajares, Isidora López, Palomares, María, García-Guereta, Luis, Valverde, Eva, Hawkins, Federico, Lapunzina, Pablo
Publicado 2009

The conserved ASTN2/BRINP1 locus at 9q33.1–33.2 is associated with major psychiatric disorders in a large pedigree from Southern Spain

por Pol-Fuster, Josep, Cañellas, Francesca, Ruiz-Guerra, Laura, Medina-Dols, Aina, Bisbal-Carrió, Bàrbara, Ortega-Vila, Bernat, Llinàs, Jaume, Hernandez-Rodriguez, Jessica, Lladó, Jerònia, Olmos, Gabriel, Strauch, Konstantin, Heine-Suñer, Damià, Vives-Bauzà, Cristòfol, Flaquer, Antònia
Publicado 2021

Familial Psychosis Associated With a Missense Mutation at MACF1 Gene Combined With the Rare Duplications DUP3p26.3 and DUP16q23.3, Affecting the CNTN6 and CDH13 Genes

por Pol-Fuster, Josep, Cañellas, Francesca, Ruiz-Guerra, Laura, Medina-Dols, Aina, Bisbal-Carrió, Bàrbara, Asensio, Víctor, Ortega-Vila, Bernat, Marzese, Diego, Vidal, Carme, Santos, Carmen, Lladó, Jerònia, Olmos, Gabriel, Heine-Suñer, Damià, Strauch, Konstantin, Flaquer, Antònia, Vives-Bauzà, Cristòfol
Publicado 2021