Aarno V Palotie


Ontology type: schema:Person     


Person Info

NAME

Aarno V

SURNAME

Palotie

Publications in SciGraph latest 50 shown

  • 2022-10-17 Genome-wide association study meta-analysis of suicide death and suicidal behavior in MOLECULAR PSYCHIATRY
  • 2022-09-16 Efficient and accurate frailty model approach for genome-wide survival association analysis in large-scale biobanks in NATURE COMMUNICATIONS
  • 2022-08-29 Large-scale sequencing identifies multiple genes and rare variants associated with Crohn’s disease susceptibility in NATURE GENETICS
  • 2022-08-17 Inframe insertion and splice site variants in MFGE8 associate with protection against coronary atherosclerosis in COMMUNICATIONS BIOLOGY
  • 2022-08-16 Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning in MOLECULAR PSYCHIATRY
  • 2022-08-03 A first update on mapping the human genetic architecture of COVID-19 in NATURE
  • 2022-06-27 The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia in NATURE COMMUNICATIONS
  • 2022-06-09 Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci in NATURE COMMUNICATIONS
  • 2022-04-08 Rare coding variants in ten genes confer substantial risk for schizophrenia in NATURE
  • 2022-04-08 Mapping genomic loci implicates genes and synaptic biology in schizophrenia in NATURE
  • 2022-03-28 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci in NATURE COMMUNICATIONS
  • 2022-02-23 Implementation of CYP2D6 copy-number imputation panel and frequency of key pharmacogenetic variants in Finnish individuals with a psychotic disorder in THE PHARMACOGENOMICS JOURNAL
  • 2022-02-23 Genetic associations of protein-coding variants in human disease in NATURE
  • 2022-02-23 Integration of questionnaire-based risk factors improves polygenic risk scores for human coronary heart disease and type 2 diabetes in COMMUNICATIONS BIOLOGY
  • 2022-02-03 Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles in NATURE GENETICS
  • 2022-01-28 A novel variant in SMG9 causes intellectual disability, confirming a role for nonsense-mediated decay components in neurocognitive development in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2021-09-30 A cross-population atlas of genetic associations for 220 human phenotypes in NATURE GENETICS
  • 2021-06-07 Mitochondrial genome copy number measured by DNA sequencing in human blood is strongly associated with metabolic traits via cell-type composition differences in HUMAN GENOMICS
  • 2021-05-25 Identifying nootropic drug targets via large-scale cognitive GWAS and transcriptomics in NEUROPSYCHOPHARMACOLOGY
  • 2021-04-12 Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices in NATURE COMMUNICATIONS
  • 2021-02-24 Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries in NATURE COMMUNICATIONS
  • 2021-02-01 Polygenic burden has broader impact on health, cognition, and socioeconomic outcomes than most rare and high-risk copy number variants in MOLECULAR PSYCHIATRY
  • 2021-02-01 Combined effects of genotype and childhood adversity shape variability of DNA methylation across age in TRANSLATIONAL PSYCHIATRY
  • 2021-01-22 Author Correction: The effect of LRRK2 loss-of-function variants in humans in NATURE MEDICINE
  • 2021-01-15 Independent and cumulative coeliac disease-susceptibility loci are associated with distinct disease phenotypes in JOURNAL OF HUMAN GENETICS
  • 2020-12-14 The role of polygenic risk and susceptibility genes in breast cancer over the course of life in NATURE COMMUNICATIONS
  • 2020-11-28 High-resolution population-specific recombination rates and their effect on phasing and genotype imputation in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2020-10-27 An expanded analysis framework for multivariate GWAS connects inflammatory biomarkers to functional variants and disease in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2020-10-14 Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells in NATURE
  • 2020-09-28 Genome-wide association study identifies 48 common genetic variants associated with handedness in NATURE HUMAN BEHAVIOUR
  • 2020-09-25 A data-driven medication score predicts 10-year mortality among aging adults in SCIENTIFIC REPORTS
  • 2020-08-07 GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer in NATURE COMMUNICATIONS
  • 2020-05-27 The effect of LRRK2 loss-of-function variants in humans in NATURE MEDICINE
  • 2020-04-07 Polygenic and clinical risk scores and their impact on age at onset and prediction of cardiometabolic diseases and common cancers in NATURE MEDICINE
  • 2020-03-17 Gene family information facilitates variant interpretation and identification of disease-associated genes in neurodevelopmental disorders in GENOME MEDICINE
  • 2020-01-21 Genomic prediction of alcohol-related morbidity and mortality in TRANSLATIONAL PSYCHIATRY
  • 2019-11-04 Author Correction: Exome sequencing of Finnish isolates enhances rare-variant association power in NATURE
  • 2019-10-21 Correction: Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation in MOLECULAR PSYCHIATRY
  • 2019-09-24 Genetic architecture of human plasma lipidome and its link to cardiovascular disease in NATURE COMMUNICATIONS
  • 2019-09-13 Author Correction: Leveraging European infrastructures to access 1 million human genomes by 2022 in NATURE REVIEWS GENETICS
  • 2019-09-10 Correction: Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2019-08-27 Leveraging European infrastructures to access 1 million human genomes by 2022 in NATURE REVIEWS GENETICS
  • 2019-07-31 Exome sequencing of Finnish isolates enhances rare-variant association power in NATURE
  • 2019-07-29 Assessment of genetic variant burden in epilepsy-associated brain lesions in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2019-07-15 Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa in NATURE GENETICS
  • 2019-05-14 Association analyses identify 31 new risk loci for colorectal cancer susceptibility in NATURE COMMUNICATIONS
  • 2019-05-01 Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function in NATURE COMMUNICATIONS
  • 2019-04-15 Roadmap for a precision-medicine initiative in the Nordic region in NATURE GENETICS
  • 2019-03-26 Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2019-03-19 Impact of constitutional TET2 haploinsufficiency on molecular and clinical phenotype in humans in NATURE COMMUNICATIONS
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