Medicina Legal, Psiquiatría y Patología
Département
University of Helsinki
Helsinki, FinlandiaPublications en collaboration avec des chercheurs de University of Helsinki (15)
2023
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A second update on mapping the human genetic architecture of COVID-19
Nature
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Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations
Nature genetics, Vol. 55, Núm. 3, pp. 369-376
2022
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Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Nature, Vol. 604, Núm. 7906, pp. 502-508
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Novel genes and sex differences in COVID-19 severity
Human molecular genetics, Vol. 31, Núm. 22, pp. 3789-3806
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Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
Nature Genetics, Vol. 54, Núm. 9, pp. 1320-1331
2021
2020
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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
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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
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Sensory gating deficits in first-episode psychosis
Journal of Nervous and Mental Disease, Vol. 204, Núm. 12, pp. 877-884
2015
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Large-scale recent expansion of European patrilineages shown by population resequencing
Nature Communications, Vol. 6
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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
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Common variant at 16p11.2 conferring risk of psychosis
Molecular Psychiatry, Vol. 19, Núm. 1, pp. 108-114
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Synaptic, transcriptional and chromatin genes disrupted in autism
Nature, Vol. 515, Núm. 7526, pp. 209-215
2011
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Common variants at VRK2 and TCF4 conferring risk of schizophrenia
Human Molecular Genetics, Vol. 20, Núm. 20, pp. 4076-4081
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Magnetoencephalography as a putative biomarker for Alzheimer's disease
International Journal of Alzheimer's Disease