Publicacións en colaboración con investigadores/as de University of Turin (4)

2019

  1. Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia

    American Journal of Human Genetics, Vol. 104, Núm. 4, pp. 767-773

2016

  1. Identification of a novel susceptibility locus at 13q34 and refinement of the 20p12.2 region as a multi-signal locus associated with bladder cancer risk in individuals of european ancestry

    Human Molecular Genetics, Vol. 25, Núm. 6, pp. 1203-1214

2010

  1. A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci

    Nature Genetics, Vol. 42, Núm. 11, pp. 978-984

2009

  1. Polymorphisms in DNA repair genes, smoking, and bladder cancer risk: Findings from the International Consortium of Bladder Cancer

    Cancer Research, Vol. 69, Núm. 17, pp. 6857-6864