Aarno Palotie


Ontology type: schema:Person     


Person Info

NAME

Aarno

SURNAME

Palotie

Publications in SciGraph latest 50 shown

  • 2018-12 Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits in NATURE GENETICS
  • 2018-12 Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function in NATURE COMMUNICATIONS
  • 2018-10 Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits in NATURE GENETICS
  • 2018-08-14 Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation in MOLECULAR PSYCHIATRY
  • 2018-07 Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence in NATURE GENETICS
  • 2018-01 Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks in NATURE GENETICS
  • 2017-12 CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits in NATURE COMMUNICATIONS
  • 2017-12 Genome-wide association study of bronchopulmonary dysplasia: a potential role for variants near the CRP gene in SCIENTIFIC REPORTS
  • 2017-08 The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability in NATURE GENETICS
  • 2017-06 Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panel in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2017-04 Whole-genome view of the consequences of a population bottleneck using 2926 genome sequences from Finland and United Kingdom in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2017-03-21 Genetic correlation between amyotrophic lateral sclerosis and schizophrenia in NATURE COMMUNICATIONS
  • 2017-03 GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium in MOLECULAR PSYCHIATRY
  • 2017-01 Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects in NATURE GENETICS
  • 2016-12 New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk in NATURE COMMUNICATIONS
  • 2016-12 Migraine genetics: from genome-wide association studies to translational insights in GENOME MEDICINE
  • 2016-12 Ultra-rare disruptive and damaging mutations influence educational attainment in the general population in NATURE NEUROSCIENCE
  • 2016-11-23 A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape in NATURE COMMUNICATIONS
  • 2016-10 Enrichment of rare variants in population isolates: single AICDA mutation responsible for hyper-IgM syndrome type 2 in Finland in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2016-09 Genome-wide association study of antisocial personality disorder in TRANSLATIONAL PSYCHIATRY
  • 2016-04 Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders in NATURE NEUROSCIENCE
  • 2016-04 Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain Atlas in HUMAN GENETICS
  • 2016-03 Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium in BEHAVIOR GENETICS
  • 2016-02 GWAS for executive function and processing speed suggests involvement of the CADM2 gene in MOLECULAR PSYCHIATRY
  • 2016-02-01 Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels in NATURE COMMUNICATIONS
  • 2015-12 Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel in NATURE COMMUNICATIONS
  • 2015-12 TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport in NATURE COMMUNICATIONS
  • 2015-12 Whole-genome sequence-based analysis of thyroid function in NATURE COMMUNICATIONS
  • 2015-12 Towards a European consensus for reporting incidental findings during clinical NGS testing in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2015-10 Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study in MOLECULAR PSYCHIATRY
  • 2015-06 Genetic background of extreme violent behavior in MOLECULAR PSYCHIATRY
  • 2015-04 De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy in NATURE GENETICS
  • 2015-02 Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53 949) in MOLECULAR PSYCHIATRY
  • 2014-12 A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans in NATURE COMMUNICATIONS
  • 2014-10 A genome-wide association study of anorexia nervosa in MOLECULAR PSYCHIATRY
  • 2014-09 A framework for the interpretation of de novo mutation in human disease in NATURE GENETICS
  • 2014-07 Biological insights from 108 schizophrenia-associated genetic loci in NATURE
  • 2014-07 Harmonization of Neuroticism and Extraversion phenotypes across inventories and cohorts in the Genetics of Personality Consortium: an application of Item Response Theory in BEHAVIOR GENETICS
  • 2014-02 De novo mutations in schizophrenia implicate synaptic networks in NATURE
  • 2014-02 Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: a report from the Cognitive Genomics consorTium (COGENT) in MOLECULAR PSYCHIATRY
  • 2013-11 Common variants associated with plasma triglycerides and risk for coronary artery disease in NATURE GENETICS
  • 2013-11 Discovery and refinement of loci associated with lipid levels in NATURE GENETICS
  • 2013-09 Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders in NATURE NEUROSCIENCE
  • 2013-08 Genome-wide meta-analysis identifies new susceptibility loci for migraine in NATURE GENETICS
  • 2013-05 Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture in NATURE GENETICS
  • 2013-04 Identification of seven loci affecting mean telomere length and their association with disease in NATURE GENETICS
  • 2013-02 Migraine without aura: genome-wide association analysis identifies several novel susceptibility in THE JOURNAL OF HEADACHE AND PAIN
  • 2012-11 Toward a roadmap in global biobanking for health in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2012-08 A mutation in APP protects against Alzheimer’s disease and age-related cognitive decline in NATURE
  • 2012-05 A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales in TRANSLATIONAL PSYCHIATRY
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