Publicaciones en colaboración con investigadores/as de University College London (22)

2023

  1. A second update on mapping the human genetic architecture of COVID-19

    Nature

  2. Erratum to: Mapping the human genetic architecture of COVID-19 (Nature, (2021), 600, 7889, (472-477), 10.1038/s41586-021-03767-x)

    Nature

  3. Use of aequorin-based indicators for monitoring Ca2+ in acidic organelles

    Biochimica et Biophysica Acta - Molecular Cell Research, Vol. 1870, Núm. 6

2022

  1. Whole-genome sequencing reveals host factors underlying critical COVID-19

    Nature, Vol. 607, Núm. 7917, pp. 97-103

2021

  1. Guidelines for the use of flow cytometry and cell sorting in immunological studies (third edition)

    European Journal of Immunology, Vol. 51, Núm. 12, pp. 2708-3145

  2. Mapping the human genetic architecture of COVID-19

    Nature, Vol. 600, Núm. 7889, pp. 472-477

  3. Smart Nanoparticles as Advanced Anti-Akt Kinase Delivery Systems for Pancreatic Cancer Therapy

    ACS Applied Materials and Interfaces, Vol. 13, Núm. 47, pp. 55790-55805

2020

  1. Deletions of specific exons of FHOD3 detected by next-generation sequencing are associated with hypertrophic cardiomyopathy

    Clinical Genetics, Vol. 98, Núm. 1, pp. 86-90

2019

  1. Corrigendum to Supplemental Material: ‘D242N, a K V 7.1 LQTS mutation uncovers a key residue for I Ks voltage dependence’ [Journal of Molecular and Cellular Cardiology, Volume 110, September 2017, Pages 61–69](S0022282817301633)(10.1016/j.yjmcc.2017.07.009)

    Journal of Molecular and Cellular Cardiology

2018

  1. Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy

    Journal of the American College of Cardiology, Vol. 72, Núm. 20, pp. 2457-2467

2017

  1. D242N, a KV7.1 LQTS mutation uncovers a key residue for IKs voltage dependence

    Journal of Molecular and Cellular Cardiology, Vol. 110, pp. 61-69

  2. IKs computational modeling to enforce the investigation of D242N, a KV7.1 LQTS mutation

    Computing in Cardiology

  3. Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

    Nature Genetics, Vol. 49, Núm. 5, pp. 680-691

2014

  1. Consensus guidelines for the detection of immunogenic cell death

    OncoImmunology, Vol. 3, Núm. 9

2013

  1. Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk

    PLoS Genetics, Vol. 9, Núm. 3

2011

  1. Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers

    Journal of the National Cancer Institute, Vol. 103, Núm. 2, pp. 105-116

2010

  1. Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: Implications for risk prediction

    Cancer Research, Vol. 70, Núm. 23, pp. 9742-9754

  2. Common genetic variants and modification of penetrance of BRCA2-associated breast cancer

    PLoS Genetics, Vol. 6, Núm. 10, pp. 1-12

2009

  1. Notch controls embryonic Schwann cell differentiation, postnatal myelination and adult plasticity

    Nature Neuroscience, Vol. 12, Núm. 7, pp. 839-847

2007

  1. Regulation of the immature Schwann cell phenotype by Notch signalling

    NEURON GLIA BIOLOGY