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Author Details

Andrea Ganna
Institute for Molecular Medicine Finland (FIMM), University of Helsinki
2008
94
41
PMIDPaper TitleJournal TitlePublished Year
36939312The lingering effects of Neanderthal introgression on human complex traits.Elife2023
37890904Risk factors for severe respiratory syncytial virus infection during the first year of life: development and validation of a clinical prediction model.Lancet Digit Health2023
37704630Quantifying the causal impact of biological risk factors on healthcare costs.Nat Commun2023
37689771ADuLT: An efficient and robust time-to-event GWAS.Nat Commun2023
36653562FinnGen provides genetic insights from a well-phenotyped isolated population.Nature2023
36829046Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population.Nature2023
36653479Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases.Nat Med2023
37386106Patterns of item nonresponse behaviour to survey questionnaires are systematic and associated with genetic loci.Nat Hum Behav2023
36939312The lingering effects of Neanderthal introgression on human complex traits.Elife2023
37117793Development and validation of DNA methylation scores in two European cohorts augment 10-year risk prediction of type 2 diabetes.Nat Aging2023
37365732Data Resource Profile: Nationwide registry data for high-throughput epidemiology and machine learning (FinRegistry).Int J Epidemiol2023
36670106Deep phenotyping and genomic data from a nationally representative study on dementia in India.Sci Data2023
36782352Polygenic Risk Scores for Alzheimer's Disease and General Cognitive Function Are Associated With Measures of Cognition in Older South Asians.J Gerontol A Biol Sci Med Sci2023
37704630Quantifying the causal impact of biological risk factors on healthcare costs.Nat Commun2023
37890904Risk factors for severe respiratory syncytial virus infection during the first year of life: development and validation of a clinical prediction model.Lancet Digit Health2023
37689771ADuLT: An efficient and robust time-to-event GWAS.Nat Commun2023
37386106Patterns of item nonresponse behaviour to survey questionnaires are systematic and associated with genetic loci.Nat Hum Behav2023
37117793Development and validation of DNA methylation scores in two European cohorts augment 10-year risk prediction of type 2 diabetes.Nat Aging2023
37365732Data Resource Profile: Nationwide registry data for high-throughput epidemiology and machine learning (FinRegistry).Int J Epidemiol2023
36653562FinnGen provides genetic insights from a well-phenotyped isolated population.Nature2023
36653479Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases.Nat Med2023
36782352Polygenic Risk Scores for Alzheimer's Disease and General Cognitive Function Are Associated With Measures of Cognition in Older South Asians.J Gerontol A Biol Sci Med Sci2023
36829046Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population.Nature2023
36670106Deep phenotyping and genomic data from a nationally representative study on dementia in India.Sci Data2023
34785567Effect of General Adiposity and Central Body Fat Distribution on the Circulating Metabolome: A Multicohort Nontargeted Metabolomics Observational and Mendelian Randomization Study.Diabetes2022
35591975Genome-wide risk prediction of common diseases across ancestries in one million people.Cell Genom2022
35396579Rare coding variants in ten genes confer substantial risk for schizophrenia.Nature2022
35708486Novel genes and sex differences in COVID-19 severity.Hum Mol Genet2022
36097220Genetic risk factors have a substantial impact on healthy life years.Nat Med2022
35760976The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia.Nat Commun2022
35501396The human genetic epidemiology of COVID-19.Nat Rev Genet2022
36327219Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.PLoS Genet2022
36198465Recontacting biobank participants to collect lifestyle, behavioural and cognitive information via online questionnaires: lessons from a pilot study within FinnGen.BMJ Open2022
36062073Cystatin C is associated with adverse COVID-19 outcomes in diverse populations.iScience2022
37118362Mendelian randomization of genetically independent aging phenotypes identifies LPA and VCAM1 as biological targets for human aging.Nat Aging2022
34861179Fast estimation of genetic correlation for biobank-scale data.Am J Hum Genet2022
34785567Effect of General Adiposity and Central Body Fat Distribution on the Circulating Metabolome: A Multicohort Nontargeted Metabolomics Observational and Mendelian Randomization Study.Diabetes2022
35027740Multi-ancestry fine mapping implicates OAS1 splicing in risk of severe COVID-19.Nat Genet2022
35708486Novel genes and sex differences in COVID-19 severity.Hum Mol Genet2022
35501396The human genetic epidemiology of COVID-19.Nat Rev Genet2022
35760976The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia.Nat Commun2022
35396579Rare coding variants in ten genes confer substantial risk for schizophrenia.Nature2022
35591975Genome-wide risk prediction of common diseases across ancestries in one million people.Cell Genom2022
37118362Mendelian randomization of genetically independent aging phenotypes identifies LPA and VCAM1 as biological targets for human aging.Nat Aging2022
36097220Genetic risk factors have a substantial impact on healthy life years.Nat Med2022
36062073Cystatin C is associated with adverse COVID-19 outcomes in diverse populations.iScience2022
36198465Recontacting biobank participants to collect lifestyle, behavioural and cognitive information via online questionnaires: lessons from a pilot study within FinnGen.BMJ Open2022
36327219Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.PLoS Genet2022
34861179Fast estimation of genetic correlation for biobank-scale data.Am J Hum Genet2022
35027740Multi-ancestry fine mapping implicates OAS1 splicing in risk of severe COVID-19.Nat Genet2022
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Collaborators

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William Harvey Research Institute, Queen Mary University of London
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Ulf de Faire
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Tamara B Harris
National Institute on Aging
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Kari E North
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Markku Laakso
Co-authored papers 9
Luigi Ferrucci
National Institute on Aging, National Institutes of Health
Co-authored papers 9
Stefania Bandinelli
Laboratory of Clinical Epidemiology
Co-authored papers 9
Release 1.2