Publicaciones en colaboración con investigadores/as de King's College London (9)

2024

  1. MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study

    The Lancet Neurology, Vol. 23, Núm. 5, pp. 487-499

2023

  1. Erratum: Author Correction: Common variants in Alzheimer's disease and risk stratification by polygenic risk scores (Nature communications (2021) 12 1 (3417))

    Nature communications

2022

  1. New insights into the genetic etiology of Alzheimer's disease and related dementias

    Nature genetics, Vol. 54, Núm. 4, pp. 412-436

2021

  1. Common variants in Alzheimer's disease and risk stratification by polygenic risk scores

    Nature communications, Vol. 12, Núm. 1, pp. 3417

  2. Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1

    Autophagy, Vol. 17, Núm. 1, pp. 1-382

  3. Lipidomic traits of plasma and cerebrospinal fluid in amyotrophic lateral sclerosis correlate with disease progression

    Brain Communications, Vol. 3, Núm. 3

2018

  1. T-type calcium channels drive migration/invasion in BRAFV600E melanoma cells through Snail1

    Pigment Cell and Melanoma Research, Vol. 31, Núm. 4, pp. 484-495

2012

  1. Sprouty1 is a candidate tumor-suppressor gene in medullary thyroid carcinoma

    Oncogene, Vol. 31, Núm. 35, pp. 3961-3972

2009

  1. Loss of Sprouty1 rescues renal agenesis caused by ret mutation

    Journal of the American Society of Nephrology, Vol. 20, Núm. 2, pp. 255-259