Publicaciones en colaboración con investigadores/as de Johns Hopkins University (22)

2023

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

    Nature

  2. Genome-wide Association Study of Bladder Cancer Reveals New Biological and Translational Insights

    European Urology, Vol. 84, Núm. 1, pp. 127-137

  3. Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population

    Nature Communications, Vol. 14, Núm. 1

2022

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

    Nature

  2. Mapping genomic loci implicates genes and synaptic biology in schizophrenia

    Nature, Vol. 604, Núm. 7906, pp. 502-508

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

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

2021

  1. Assessing lung cancer absolute risk trajectory based on a polygenic risk model

    Cancer Research, Vol. 81, Núm. 6, pp. 1607-1615

2020

  1. Body mass index and weight change are associated with adult lung function trajectories: The prospective ECRHS study

    Thorax, Vol. 75, Núm. 4, pp. 313-320

  2. Diesel exhaust and bladder cancer risk by pathologic stage and grade subtypes

    Environment International, Vol. 135

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

  3. Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies

    The Lancet Neurology, Vol. 18, Núm. 12, pp. 1091-1102

  4. The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight

    Movement Disorders, Vol. 34, Núm. 12, pp. 1851-1863

2018

  1. Regional variation of Guillain-Barré syndrome

    Brain, Vol. 141, Núm. 10, pp. 2866-2877

2017

  1. International Guillain-Barré Syndrome Outcome Study: protocol of a prospective observational cohort study on clinical and biological predictors of disease course and outcome in Guillain-Barré syndrome

    Journal of the Peripheral Nervous System, Vol. 22, Núm. 2, pp. 68-76

2015

  1. Analysis of heritability and shared heritability based on genome-wide association studies for thirteen cancer types

    Journal of the National Cancer Institute, Vol. 107, Núm. 12

2014

  1. Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33

    Human Molecular Genetics, Vol. 23, Núm. 24, pp. 6616-6633

2012

  1. CT angiography helps to differentiate acute from chronic carotid occlusion: The "carotid ring sign"

    Neuroradiology, Vol. 54, Núm. 2, pp. 139-146

2011

  1. Response to letter regarding article, "primary results from the smartdelay determined AV optimization: A comparison to other AV delay methods used in cardiac resynchronization therapy (SMART-AV) trial: A randomized trial comparing empirical, echocardiography-guided and algorithmic atrioventricular delay programming in cardiac resynchronization therapy"

    Circulation

2010

  1. SmartDelay determined AV optimization: A comparison of AV delay methods used in cardiac resynchronization therapy (SMART-AV): Rationale and design

    PACE - Pacing and Clinical Electrophysiology, Vol. 33, Núm. 1, pp. 54-63