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Author Details

Nicole Soranzo
Wellcome Sanger Institute
1998
237
104
Andrej Sali (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
36136759GWAS of genetic factors affecting white blood cell morphological parameters in Sardinians uncovers influence of chromosome 11 innate immunity gene cluster on eosinophil morphology.Hum Mol Genet2023
36136759GWAS of genetic factors affecting white blood cell morphological parameters in Sardinians uncovers influence of chromosome 11 innate immunity gene cluster on eosinophil morphology.Hum Mol Genet2023
37596262A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology.Nat Commun2023
37196361Methods and Insights from Single-Cell Expression Quantitative Trait Loci.Annu Rev Genomics Hum Genet2023
37066137Building pangenome graphs.bioRxiv2023
36991119An atlas of genetic scores to predict multi-omic traits.Nature2023
37596262A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology.Nat Commun2023
36991119An atlas of genetic scores to predict multi-omic traits.Nature2023
37196361Methods and Insights from Single-Cell Expression Quantitative Trait Loci.Annu Rev Genomics Hum Genet2023
37066137Building pangenome graphs.bioRxiv2023
34753797An Expanded Genome-Wide Association Study of Fructosamine Levels Identifies RCN3 as a Replicating Locus and Implicates FCGRT as the Effector Transcript.Diabetes2022
36357675Rare and common genetic determinants of metabolic individuality and their effects on human health.Nat Med2022
35568032Whole-exome sequencing identifies rare genetic variants associated with human plasma metabolites.Am J Hum Genet2022
36327219Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.PLoS Genet2022
35288711Genetic associations at regulatory phenotypes improve fine-mapping of causal variants for 12 immune-mediated diseases.Nat Genet2022
34753797An Expanded Genome-Wide Association Study of Fructosamine Levels Identifies RCN3 as a Replicating Locus and Implicates FCGRT as the Effector Transcript.Diabetes2022
35072137Machine learning optimized polygenic scores for blood cell traits identify sex-specific trajectories and genetic correlations with disease.Cell Genom2022
35331647Colocalization analysis of pancreas eQTLs with risk loci from alcoholic and novel non-alcoholic chronic pancreatitis GWAS suggests potential disease causing mechanisms.Pancreatology2022
35138379Transcriptome-wide association study in UK Biobank Europeans identifies associations with blood cell traits.Hum Mol Genet2022
35068290Higher body mass index raises immature platelet count: potential contribution to obesity-related thrombosis.Platelets2022
35568032Whole-exome sequencing identifies rare genetic variants associated with human plasma metabolites.Am J Hum Genet2022
36357675Rare and common genetic determinants of metabolic individuality and their effects on human health.Nat Med2022
36327219Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.PLoS Genet2022
35288711Genetic associations at regulatory phenotypes improve fine-mapping of causal variants for 12 immune-mediated diseases.Nat Genet2022
35072137Machine learning optimized polygenic scores for blood cell traits identify sex-specific trajectories and genetic correlations with disease.Cell Genom2022
35068290Higher body mass index raises immature platelet count: potential contribution to obesity-related thrombosis.Platelets2022
35331647Colocalization analysis of pancreas eQTLs with risk loci from alcoholic and novel non-alcoholic chronic pancreatitis GWAS suggests potential disease causing mechanisms.Pancreatology2022
35138379Transcriptome-wide association study in UK Biobank Europeans identifies associations with blood cell traits.Hum Mol Genet2022
32989287Genome-wide association study identifies 48 common genetic variants associated with handedness.Nat Hum Behav2021
34226637Effects of adiposity on the human plasma proteome: observational and Mendelian randomisation estimates.Int J Obes (Lond)2021
34215830FUT6 deficiency compromises basophil function by selectively abrogating their sialyl-Lewis x expression.Commun Biol2021
33558525Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.Nat Commun2021
34087167Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.Am J Hum Genet2021
34083789A map of transcriptional heterogeneity and regulatory variation in human microglia.Nat Genet2021
33863903Genetic perturbation of PU.1 binding and chromatin looping at neutrophil enhancers associates with autoimmune disease.Nat Commun2021
32989287Genome-wide association study identifies 48 common genetic variants associated with handedness.Nat Hum Behav2021
33402679Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.Nat Commun2021
34426706Mitochondrial DNA variants modulate N-formylmethionine, proteostasis and risk of late-onset human diseases.Nat Med2021
34750571Integrative analysis of the plasma proteome and polygenic risk of cardiometabolic diseases.Nat Metab2021
34582791Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program.Am J Hum Genet2021
33863903Genetic perturbation of PU.1 binding and chromatin looping at neutrophil enhancers associates with autoimmune disease.Nat Commun2021
33558525Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.Nat Commun2021
34582791Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program.Am J Hum Genet2021
34426706Mitochondrial DNA variants modulate N-formylmethionine, proteostasis and risk of late-onset human diseases.Nat Med2021
34750571Integrative analysis of the plasma proteome and polygenic risk of cardiometabolic diseases.Nat Metab2021
34215830FUT6 deficiency compromises basophil function by selectively abrogating their sialyl-Lewis x expression.Commun Biol2021
34087167Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.Am J Hum Genet2021
34083789A map of transcriptional heterogeneity and regulatory variation in human microglia.Nat Genet2021
34226637Effects of adiposity on the human plasma proteome: observational and Mendelian randomisation estimates.Int J Obes (Lond)2021
33402679Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.Nat Commun2021
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Collaborators

Tim D Spector
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Andr?? G Uitterlinden
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National Institute on Aging, National Institutes of Health
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Ozren Polasek
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Nilesh J Samani
Co-authored papers 36
Kari Stefansson
University of Iceland
Co-authored papers 36
Veikko Salomaa
Co-authored papers 35
Vilmundur Gudnason
Co-authored papers 35
Inês Barroso
Co-authored papers 35
Peter Vollenweider
Lausanne University Hospital and University of Lausanne
Co-authored papers 35
Release 1.2