Medicina Xenómica
GMX - USC
University Hospital of Lausanne
Lausana, SuizaPublicacións en colaboración con investigadores/as de University Hospital of Lausanne (13)
2023
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A second update on mapping the human genetic architecture of COVID-19
Nature
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Erratum: Author Correction: Common variants in Alzheimer's disease and risk stratification by polygenic risk scores (Nature communications (2021) 12 1 (3417))
Nature communications
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Genomic investigations of unexplained acute hepatitis in children
Nature, Vol. 617, Núm. 7961, pp. 564-573
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The relationship between genetic liability, childhood maltreatment, and IQ: findings from the EU-GEI multicentric case–control study
Social Psychiatry and Psychiatric Epidemiology, Vol. 58, Núm. 10, pp. 1573-1580
2022
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Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers
Acta Neuropathologica, Vol. 144, Núm. 5, pp. 821-842
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New insights into the genetic etiology of Alzheimer's disease and related dementias
Nature genetics, Vol. 54, Núm. 4, pp. 412-436
2021
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Common variants in Alzheimer's disease and risk stratification by polygenic risk scores
Nature communications, Vol. 12, Núm. 1, pp. 3417
2019
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Identification of regulatory variants associated with genetic susceptibility to meningococcal disease
Scientific Reports, Vol. 9, Núm. 1
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Plasma lipid profiles discriminate bacterial from viral infection in febrile children
Scientific Reports, Vol. 9, Núm. 1
2018
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Inferring biogeographic ancestry with compound markers of slow and fast evolving polymorphisms
European Journal of Human Genetics, Vol. 26, Núm. 11, pp. 1697-1707
2016
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A European spectrum of pharmacogenomic biomarkers: Implications for clinical pharmacogenomics
PLoS ONE, Vol. 11, Núm. 9
2015
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Completion of a worldwide reference panel of samples for an ancestry informative Indel assay
Forensic Science International: Genetics, Vol. 17, pp. 75-80