Transducción de señales en bacterias
Hospital de la Santa Creu i Sant Pau
Barcelona, EspañaPublicaciones en colaboración con investigadores/as de Hospital de la Santa Creu i Sant Pau (11)
2024
-
Genetic and clinical characterization of a novel FH founder mutation in families with hereditary leiomyomatosis and renal cell cancer syndrome
Orphanet Journal of Rare Diseases, Vol. 19, Núm. 1
-
SpadaHC: a database to improve the classification of variants in hereditary cancer genes in the Spanish population
Database : the journal of biological databases and curation, Vol. 2024
2021
-
A multilayered post-GWAS assessment on genetic susceptibility to pancreatic cancer
Genome Medicine, Vol. 13, Núm. 1
-
Deciphering the complex interplay between pancreatic cancer, diabetes mellitus subtypes and obesity/BMI through causal inference and mediation analyses
Gut, Vol. 70, Núm. 2, pp. 319-329
2020
-
Comprehensive constitutional genetic and epigenetic characterization of lynch-like individuals
Cancers, Vol. 12, Núm. 7, pp. 1-32
-
Pancreatic Cancer Risk in Relation to Lifetime Smoking Patterns, Tobacco Type, and Dose-Response Relationships
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, Vol. 29, Núm. 5, pp. 1009-1018
2019
-
Pancreatic cancer and autoimmune diseases: An association sustained by computational and epidemiological case–control approaches
International Journal of Cancer, Vol. 144, Núm. 7, pp. 1540-1549
2018
-
Risk of pancreatic cancer associated with family history of cancer and other medical conditions by accounting for smoking among relatives
International Journal of Epidemiology, Vol. 47, Núm. 2, pp. 473-483
2017
-
Reduced risk of pancreatic cancer associated with asthma and nasal allergies
Gut, Vol. 66, Núm. 2, pp. 314-322
2014
-
Prevalence of germline MUTYH mutations among Lynch-like syndrome patients
European Journal of Cancer, Vol. 50, Núm. 13, pp. 2241-2250
2004
-
Germline mutational dynamics in myotonic dystrophy type 1 males: Allele length and age effects
Neurology, Vol. 62, Núm. 2, pp. 269-274