Publicacións en colaboración con investigadores/as de Hospital General Universitario Gregorio Marañón (11)

2024

  1. Novel risk loci for COVID-19 hospitalization among admixed American populations

    eLife, Vol. 13

2023

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

    Nature

2022

  1. Corticospinal tract and motor cortex degeneration in pure hereditary spastic paraparesis type 4 (SPG4)

    Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, Vol. 23, Núm. 1-2, pp. 25-34

  2. Novel genes and sex differences in COVID-19 severity

    Human molecular genetics, Vol. 31, Núm. 22, pp. 3789-3806

  3. Tract-specific damage at spinal cord level in pure hereditary spastic paraplegia type 4: a diffusion tensor imaging study

    Journal of Neurology, Vol. 269, Núm. 6, pp. 3189-3203

2021

  1. Thalamic atrophy in patients with pure hereditary spastic paraplegia type 4

    Journal of Neurology, Vol. 268, Núm. 7, pp. 2429-2440

2018

  1. Role of copy number variants in sudden cardiac death and related diseases: Genetic analysis and translation into clinical practice

    European Journal of Human Genetics, Vol. 26, Núm. 7, pp. 1014-1025

2001

  1. Sau3A in situ digestion of human chromosome 3 pericentromeric heterochromatin. I. Differential digestion of α-satellite and satellite 1 DNA sequences

    Genome, Vol. 44, Núm. 1, pp. 120-127

2000

  1. A PCR product derived from female DNA with regional localization on the Y chromosome

    Genome, Vol. 43, Núm. 3, pp. 580-583

1999

  1. Chimerism quantification after sex-matched BMT: How probable is it to find donor/recipient pairs with distinguishable cells?

    Cancer Genetics and Cytogenetics, Vol. 113, Núm. 2, pp. 152-155

  2. Polymorphisms for the size of heterochromatic regions allow sex- independent quantification of post-BMT chimerism targeting metaphase and interphase cells

    Haematologica, Vol. 84, Núm. 2, pp. 138-141