HRS4R
Vull donar

ALEXANDRA PÉREZ SERRA

Firma
ALEXANDRA PÉREZ-SERRA
Posició
Tècnic/a Investigador/a
Tècnics/ques investigadors/es

Projectes

Codi oficial: 101095436 Data inici: 01/12/2022 Data fi: 31/05/2027 Investigador/a principal: EVA FRIGOLA CAPELL Organisme finançador: EUROPEAN HEALTH AND DIGITAL EXECUTIVE AGENCY (HADEA)

Publicacions

Polo-Alonso S, Hernáez Á, Dégano IR, Martí-Lluch R, Pinsach-Abuin ML, Elosua R, Subirana I, Puigmulé M, Pérez A, Cruz R, Diz-de Almeida S, Puigdecant E, Selga E, Nogues X, Masclans JR, Güerri-Fernández R, Cubero-Gallego H, Tizon-Marcos H, Vaquerizo B, Brugada R, Ramos R, Camps-Vilaró A, Marrugat J

Global and Sex-Stratified Genome-Wide Association Study of Long COVID Based on Patient-Driven Symptom Recall.

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2025, 26 dx.doi.org/10.3390/ijms26189252
Camps-Vilaró A, Pinsach-Abuin ML, Degano IR, Ramos R, Martí-Lluch R, Elosua R, Subirana I, Solà-Richarte C, Puigmulé M, Pérez A, Vilaró I, Cruz R, Diz-de Almeida S, Nogues X, Masclans JR, Güerri-Fernández R, Marin J, Tizon-Marcos H, Vaquerizo B, Brugada R, Marrugat J

Genetic characteristics involved in COVID-19 severity. The CARGENCORS case-control study and meta-analysis

JOURNAL OF MEDICAL VIROLOGY, 2024, 96 dx.doi.org/10.1002/jmv.29404
Perez-Serra, A, Toro, R, Martinez-Barrios, E, Iglesias, A, Fernandez-Falgueras, A, Alcalde, M, Coll, M, Puigmule, M, del Olmo, B, Pico, F, Lopez, L, Arbelo, E, Cesar, S, Llano, CTD, Mangas, A, Brugada, J, Sarquella-Brugada, G, Brugada, R, Campuzano, O

Implementing a New Algorithm for Reinterpretation of Ambiguous Variants in Genetic Dilated Cardiomyopathy

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2024, 25 dx.doi.org/10.3390/ijms25073807
Pérez-Jurado LA, Cáceres A, Balagué-Dobón L, Esko T, López de Heredia M, Quintela I, Cruz R, Lapunzina P, Carracedo Á, González JR

Clonal chromosomal mosaicism and loss of chromosome Y in elderly men increase vulnerability for SARS-CoV-2.

Communications Biology, 2024, 7, 202-202 dx.doi.org/10.1038/s42003-024-05805-6
Martinez-Barrios E, Sarquella-Brugada G, Perez-Serra A, Fernandez-Falgueras A, Cesar S, Alcalde M, Coll M, Puigmulé M, Iglesias A, Ferrer-Costa C, Del Olmo B, Picó F, Lopez L, Fiol V, Cruzalegui J, Hernandez C, Arbelo E, Díez-Escuté N, Cerralbo P, Grassi S, Oliva A, Toro R, Brugada J, Brugada R, Campuzano O

Reevaluation of ambiguous genetic variants in sudden unexplained deaths of a young cohort

INTERNATIONAL JOURNAL OF LEGAL MEDICINE, 2023, 137, 345-351 dx.doi.org/10.1007/s00414-023-02951-0
Cesar S, Coll M, Fiol V, Fernandez-Falgueras A, Cruzalegui J, Iglesias A, Moll I, Perez-Serra A, Martínez-Barrios E, Ferrer-Costa C, Del Olmo B, Puigmulè M, Alcalde M, Lopez L, Pico F, Berrueco R, Brugada J, Zschaeck I, Natera-de Benito D, Carrera-García L, Exposito-Escudero J, Ortez C, Nascimento A, Brugada R, Sarquella-Brugada G, Campuzano O

LMNA-related muscular dystrophy: Identification of variants in alternative genes and personalized clinical translation

Frontiers in Genetics, 2023, 14, 1135438-1135438 dx.doi.org/10.3389/fgene.2023.1135438
Martínez-Moreno R, Pérez-Serra A, Selga E, Carreras D, Aran B, Kuebler B, Scornik FS, Pérez GJ, Brugada R

Generation of the induced pluripotent stem cell line ESi108-A from a familial atrial fibrillation patient.

STEM CELL RESEARCH, 2023, 73, 103239-103239 dx.doi.org/10.1016/j.scr.2023.103239
Sarquella-Brugada G, Fernandez-Falgueras A, Cesar S, Arbelo E, Coll M, Perez-Serra A, Puigmulé M, Iglesias A, Alcalde M, Vallverdú-Prats M, Fiol V, Ferrer-Costa C, Del Olmo B, Picó F, Lopez L, García-Alvarez A, Jordà P, Tiron de Llano C, Toro R, Grassi S, Oliva A, Brugada J, Brugada R, Campuzano O

Clinical impact of rare variants associated with inherited channelopathies: a 5-year update

HUMAN GENETICS, 2022, 141, 1579-1589 dx.doi.org/10.1007/s00439-021-02370-4
Puigmulé M, Coll M, Pérez-Serra A, López L, Picó F, Neto N, Corona M, Pinsach-Abuin ML, Ferrer-Costa C, Buxó M, Queralt FX, Brugada R

High-quality RNA improves sensitivity of SARS-CoV-2 detection by colorimetric RT-LAMP

EXPERIMENTAL BIOLOGY AND MEDICINE, 2022, 247, 276-281 dx.doi.org/10.1177/15353702211054768
Martínez-Barrios E, Sarquella-Brugada G, Pérez-Serra A, Fernández-Falgueras A, Cesar S, Coll M, Puigmulé M, Iglesias A, Alcalde M, Vallverdú-Prats M, Ferrer-Costa C, Del Olmo B, Picó F, López L, Fiol V, Cruzalegui J, Hernández C, Arbelo E, Grassi S, Oliva A, Toro R, Brugada J, Brugada R, Campuzano O

Discerning the Ambiguous Role of Missense TTN Variants in Inherited Arrhythmogenic Syndromes

Journal of Personalized Medicine, 2022, 12 dx.doi.org/10.3390/jpm12020241

Formulari de contacte

Coneix l’IDIBGI!

menu