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Author Details

Johanna Kuusisto
1991
312
95
PMIDPaper TitleJournal TitlePublished Year
37039676SARS-CoV-2 Infection of Human Neurons Is TMPRSS2 Independent, Requires Endosomal Cell Entry, and Can Be Blocked by Inhibitors of Host Phosphoinositol-5 Kinase.2023
37647564Cell-Type Composition Affects Adipose Gene Expression Associations With Cardiometabolic Traits.Diabetes2023
37961277Adipose tissue eQTL meta-analysis reveals the contribution of allelic heterogeneity to gene expression regulation and cardiometabolic traits.bioRxiv2023
37034649Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.medRxiv2023
36927868Late-onset and classic phenotypes of Fabry disease in males with the -Thr410Ala mutation.2023
34995504Subcutaneous adipose tissue splice quantitative trait loci reveal differences in isoform usage associated with cardiometabolic traits.Am J Hum Genet2022
35697829Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.Commun Biol2022
35571963Effects of age, amyloid, sex, and <i>APOE</i> ε4 on the CSF proteome in normal cognition.Alzheimers Dement (Amst)2022
35560802Prevalence, characteristics, and mortality of patients with transthyretin amyloid cardiomyopathy in the Nordic countries.ESC heart failure2022
35551307Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.Nat Genet2022
35365974Healthcare resource use of patients with transthyretin amyloid cardiomyopathy.ESC heart failure2022
35474963Multiparametric platform for profiling lipid trafficking in human leukocytes.Cell Rep Methods2022
36055244Integrating transcriptomics, metabolomics, and GWAS helps reveal molecular mechanisms for metabolite levels and disease risk.Am J Hum Genet2022
36477530Genetic diversity fuels gene discovery for tobacco and alcohol use.Nature2022
34645699Nationwide prevalence and characteristics of transthyretin amyloid cardiomyopathy in Sweden.Open Heart2021
33594006Machine Learning Reveals Time-Varying Microbial Predictors with Complex Effects on Glucose Regulation.mSystems2021
33798444Association of structural variation with cardiometabolic traits in Finns.Am J Hum Genet2021
34108472Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes.Nat Commun2021
34099068Mitochondrial genome copy number measured by DNA sequencing in human blood is strongly associated with metabolic traits via cell-type composition differences.Hum Genomics2021
33660951Novel biomarkers associated with incident heart failure in 10 106 Finnish men.ESC heart failure2021
33558525Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.Nat Commun2021
33602475Cardiac Involvement in Fabry Disease: JACC Review Topic of the Week.Journal of the American College of Cardiology2021
34346487The Association of 9 Amino Acids With Cardiovascular Events in Finnish Men in a 12-Year Follow-up Study.Journal of Clinical Endocrinology and Metabolism2021
33402679Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.Nat Commun2021
35011686Microglia-like Cells Promote Neuronal Functions in Cerebral Organoids.Cells2021
32611329Rotation and torsion of the left ventricle with cardiovascular magnetic resonance tagging: comparison of two analysis methods.BMC Medical Imaging2020
31949022Cardiomyopathy associated with the Ala143Thr variant of the gene.Heart2020
32546508Genetics of hypertrophic cardiomyopathy: what is the next step?Heart2020
32915782Adiponectin GWAS loci harboring extensive allelic heterogeneity exhibit distinct molecular consequences.PLoS Genet2020
32911327Generation of a human induced pluripotent stem cell line (UEFi003-A) carrying heterozygous A673T variant in amyloid precursor protein associated with a reduced risk of Alzheimer's disease.Stem Cell Research2020
31358974New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders.Nat Hum Behav2019
31564431Adipose Tissue Gene Expression Associations Reveal Hundreds of Candidate Genes for Cardiometabolic Traits.Am J Hum Genet2019
30976029CMR derived left ventricular septal convexity in carriers of the hypertrophic cardiomyopathy-causing MYBPC3-Q1061X mutation.Scientific Reports2019
31127295A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure.Hum Mol Genet2019
30734465Circulating RNAs as predictive markers for the progression of type 2 diabetes.Journal of Cellular and Molecular Medicine2019
31160809Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.Nat Genet2019
31118516Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls.Nature2019
31152163A catalog of genetic loci associated with kidney function from analyses of a million individuals.Nat Genet2019
30885989Nine Amino Acids Are Associated With Decreased Insulin Secretion and Elevated Glucose Levels in a 7.4-Year Follow-up Study of 5,181 Finnish Men.2019
30775854Genetic basis and outcome in a nationwide study of Finnish patients with hypertrophic cardiomyopathy.ESC heart failure2019
29807259Generation of a human induced pluripotent stem cell line from a patient with a rare A673T variant in amyloid precursor protein gene that reduces the risk for Alzheimer's disease.Stem Cell Research2018
28941595Lipidome as a predictive tool in progression to type 2 diabetes in Finnish men.Metabolism2018
29974557Fibrosis and wall thickness affect ventricular repolarization dynamics in hypertrophic cardiomyopathy.Annals of Noninvasive Electrocardiology2018
30497761Novel electrocardiographic features in carriers of hypertrophic cardiomyopathy causing sarcomeric mutations.Journal of Electrocardiology2018
30349858Decreased plasma C-reactive protein levels in 4 allele carriers.Annals of Clinical and Translational Neurology2018
30297969Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps.Nat Genet2018
30201759Systems Genetics Approach to Biomarker Discovery: GPNMB and Heart Failure in Mice and Humans.G3 (Bethesda)2018
29912962Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries.PLoS One2018
30375486Functional Variant in the GCKR Gene Affects Lactate Levels Differentially in the Fasting State and During Hyperglycemia.Scientific Reports2018
29893869Epigenome-wide association in adipose tissue from the METSIM cohort.Hum Mol Genet2018
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Stanford University School of Medicine
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The University of Manchester
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German Research Center for Cardiovascular Disease (DZHK)
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University of Oxford
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London NorthWest Healthcare NHS Trust
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Lee Kong Chian School of Medicine, Nanyang Technological University
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Regeneron Pharmaceuticals Inc.
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King's College London
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Pat Macpherson Centre for Pharmacogenomics and Pharmacogenetics, University of Dundee
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