Publicaciones en colaboración con investigadores/as de French Institute of Health and Medical Research (25)

2022

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

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

2021

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

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

  2. Iron status influences non-alcoholic fatty liver disease in obesity through the gut microbiome

    Microbiome, Vol. 9, Núm. 1

2020

  1. Budding yeast complete DNA synthesis after chromosome segregation begins

    Nature Communications, Vol. 11, Núm. 1

  2. Congenital anomalies from a physics perspective. The key role of “manufacturing” volatility

    Physica A: Statistical Mechanics and its Applications, Vol. 537

  3. Impact of chromosome fusions on 3D genome organization and gene expression in budding yeast

    Genetics, Vol. 214, Núm. 3, pp. 651-667

  4. Modulation of Cell Identity by Modification of Nuclear Pore Complexes

    Frontiers in Genetics, Vol. 10

  5. Physical models of infant mortality: implications for defects in biological systems

    Journal of Biological Physics, Vol. 46, Núm. 4, pp. 371-394

  6. The budding yeast Start repressor Whi7 differs in regulation from Whi5, emerging as a major cell cycle brake in response to stress

    Journal of Cell Science, Vol. 133, Núm. 24

2019

  1. Infant mortality across species. A global probe of congenital abnormalities

    Physica A: Statistical Mechanics and its Applications, Vol. 535

2018

  1. Daughter-cell-specific modulation of nuclear pore complexes controls cell cycle entry during asymmetric division

    Nature Cell Biology, Vol. 20, Núm. 4, pp. 432-442

  2. RbFOX1/MBNL1 competition for CCUG RNA repeats binding contributes to myotonic dystrophy type 1/type 2 differences

    Nature Communications, Vol. 9, Núm. 1

2017

  1. Inflammatory demyelination induces ependymal modifications concomitant to activation of adult (SVZ) stem cell proliferation

    GLIA, Vol. 65, Núm. 5, pp. 756-772

2014

  1. The oral-facial-digital syndrome gene C2CD3 encodes a positive regulator of centriole elongation

    Nature Genetics, Vol. 46, Núm. 8, pp. 905-911

2011

  1. Disruption of a ciliary B9 protein complex causes meckel syndrome

    American Journal of Human Genetics, Vol. 89, Núm. 1, pp. 94-110

  2. Inflammation-induced subventricular zone dysfunction leads to olfactory deficits in a targeted mouse model of multiple sclerosis

    Journal of Clinical Investigation, Vol. 121, Núm. 12, pp. 4722-4734

  3. Maternal germline-specific effect of DNA ligase I on CTG/CAG instability

    Human Molecular Genetics, Vol. 20, Núm. 11, pp. 2131-2143

  4. Vascular endothelial growth factor receptor 3 directly regulates murine neurogenesis

    Genes and Development, Vol. 25, Núm. 8, pp. 831-844

2010

  1. Ikaros-1 couples cell cycle arrest of late striatal precursors with neurogenesis of enkephalinergic neurons

    Journal of Comparative Neurology, Vol. 518, Núm. 3, pp. 329-351

  2. The USH2A c.2299delG mutation: Dating its common origin in a Southern European population

    European Journal of Human Genetics, Vol. 18, Núm. 7, pp. 788-793