Search
14/10/2025
Ending diagnostic odyssey by reanalysis of whole exome sequencing data: reclassification of suspected Fanconi anemia cases to dyskeratosis congenita and Diamond-Blackfan anemia
Tejero, E, de Haro, MJR, Pujol, R, Bogliolo, M, Rodríguez-Santiago, B, Surrallés, J. Ending diagnostic odyssey by reanalysis of whole exome sequencing data: reclassification of suspected Fanconi anemia cases to dyskeratosis congenita and Diamond-Blackfan anemia. Orphanet Journal of Rare Diseases. 2025; 20(1)DOI:10.1186/s13023-025-03928-5. PMID:41088272. IF:3.500(Q2/4D).
10/10/2025
VEGFA sex-specific signature is associated to long COVID symptom persistence
Farré, X, Blay, N, Iraola-Guzmán, S, Fernández-Jiménez, F, Alzate-Piñol, S, Llucià-Carol, L, Espinosa, A, Castaño-Vinyals, G, Dobaño, C, Moncunill, G, Karachaliou, M, Garcia-Aymerich, J, Kogevinas, M, Barceló, C, Cadenas, I, de Cid, R. VEGFA sex-specific signature is associated to long COVID symptom persistence. BMC Medicine. 2025; 23(1)DOI:10.1186/s12916-025-04402-6. PMID:41074076. IF:8.300(Q1/1D).
09/10/2025
Serum KL-6 as a biomarker to predict progression at one year in interstitial lung disease
Bonella, F, Sanchez, MCV, d'Alessandro, M, Millan-Billi, P, Santos, RF, Schroeder, N, Bastos, HN, Molina-Molina, M, Pernaute, OS, Villegas, DC, Bargagli, E. Serum KL-6 as a biomarker to predict progression at one year in interstitial lung disease. Scientific Reports. 2025; 15(1)DOI:10.1038/s41598-025-22483-4. PMID:41068354. IF:3.900(Q1/2D).
08/10/2025
Single-Nucleotide Polymorphisms, PITX2 and Abnormal Electrical Activity in Atrial Fibrillation
Jiménez-Sábado, V, Hove-Madsen, L. Single-Nucleotide Polymorphisms, PITX2 and Abnormal Electrical Activity in Atrial Fibrillation. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES. 2025; 26(19)DOI:10.3390/ijms26199780. PMID:41097045. IF:4.900(Q1/3D).