Publicaciones en colaboración con investigadores/as de University of Helsinki (15)

2023

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

    Nature

  2. Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations

    Nature genetics, Vol. 55, Núm. 3, pp. 369-376

2022

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

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

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

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

  3. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

    Nature Genetics, Vol. 54, Núm. 9, pp. 1320-1331

2021

  1. Arcuate fasciculus architecture is associated with individual differences in pre-attentive detection of unpredicted music changes

    NeuroImage, Vol. 229

2020

  1. Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

    Cell, Vol. 180, Núm. 3, pp. 568-584.e23

2017

  1. Cognitive impairments in patients with first episode psychosis: The relationship between neurophysiological and neuropsychological assessments

    Journal of Clinical Neuroscience, Vol. 36, pp. 80-87

2016

  1. Sensory gating deficits in first-episode psychosis

    Journal of Nervous and Mental Disease, Vol. 204, Núm. 12, pp. 877-884

2015

  1. Large-scale recent expansion of European patrilineages shown by population resequencing

    Nature Communications, Vol. 6

  2. The Y-chromosome tree bursts into leaf: 13,000 high-confidence SNPs covering the majority of known clades

    Molecular Biology and Evolution, Vol. 32, Núm. 3, pp. 661-673

2014

  1. Common variant at 16p11.2 conferring risk of psychosis

    Molecular Psychiatry, Vol. 19, Núm. 1, pp. 108-114

  2. Synaptic, transcriptional and chromatin genes disrupted in autism

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

2011

  1. Common variants at VRK2 and TCF4 conferring risk of schizophrenia

    Human Molecular Genetics, Vol. 20, Núm. 20, pp. 4076-4081

  2. Magnetoencephalography as a putative biomarker for Alzheimer's disease

    International Journal of Alzheimer's Disease