Publicacións en colaboración con investigadores/as de Newcastle University (17)

2024

  1. A genome-wide association meta-analysis of all-cause and vascular dementia

    Alzheimer's and Dementia, Vol. 20, Núm. 9, pp. 5973-5995

  2. Guidelines for minimal information on cellular senescence experimentation in vivo

    Cell, Vol. 187, Núm. 16, pp. 4150-4175

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

2021

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

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

  2. Markers of Right Ventricular Dysfunction Predict Maximal Exercise Capacity After Left Ventricular Assist Device Implantation

    ASAIO journal (American Society for Artificial Internal Organs : 1992), Vol. 67, Núm. 3, pp. 284-289

  3. Mitochondrial DNA variants modulate N-formylmethionine, proteostasis and risk of late-onset human diseases

    Nature Medicine, Vol. 27, Núm. 9, pp. 1564-1575

2020

  1. Metabolic shift underlies recovery in reversible infantile respiratory chain deficiency

    EMBO Journal, Vol. 39, Núm. 23

2019

  1. Author Correction: Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing (Nature Genetics, (2019), 51, 3, (414-430), 10.1038/s41588-019-0358-2)

    Nature Genetics

  2. Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

    Nature Genetics, Vol. 51, Núm. 3, pp. 414-430

2017

  1. Characterisation of the genomic landscape of CRLF2-rearranged acute lymphoblastic leukemia

    Genes Chromosomes and Cancer, Vol. 56, Núm. 5, pp. 363-372

  2. Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia

    Nature Communications, Vol. 8

  3. International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases

    American Journal of Human Genetics

2016

  1. The mitochondrial protein CHC HD2 primes the differentiation potential of human induced pluripotent stem cells to neuroectodermal lineages

    Journal of Cell Biology, Vol. 215, Núm. 2, pp. 187-202

2014

  1. Synaptic, transcriptional and chromatin genes disrupted in autism

    Nature, Vol. 515, Núm. 7526, pp. 209-215

2013

  1. Altered 2-thiouridylation impairs mitochondrial translation in reversible infantile respiratory chain deficiency

    Human Molecular Genetics, Vol. 22, Núm. 22, pp. 4602-4615

2010

  1. Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk

    Nature Genetics, Vol. 42, Núm. 2, pp. 132-136

2009

  1. Association of mitochondrial haplogroup J and mtDNA oxidative damage in two different North Spain elderly populations

    Biogerontology, Vol. 10, Núm. 4, pp. 435-442