Author: Francesco Cucca

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Preprints

Enhanced genetic analysis of type 1 diabetes by selecting variants on both effect size and significance, and by integration with autoimmune thyroid disease

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A reference panel of 64,976 haplotypes for genotype imputation

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Population history of the Sardinian people inferred from whole-genome sequencing

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Genetic analysis of over one million people identifies 535 novel loci for blood pressure.

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Population history from the Neolithic to present on the Mediterranean island of Sardinia: An ancient DNA perspective

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Genetic Associations with Subjective Well-Being Also Implicate Depression and Neuroticism

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Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility

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Narrow-sense heritability estimation of complex traits using identity-by-descent information.

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Sequencing and Imputation in GWAS: Cost-Effective Strategies to Increase Power and Genomic Coverage Across Diverse Populations

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Genetic dysregulation of gene expression and splicing during a ten-year period of human aging

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Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation

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Loss-of-function genomic variants with impact on liver-related blood traits highlight potential therapeutic targets for cardiovascular disease

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The Trans-Ancestral Genomic Architecture of Glycaemic Traits

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Multi-ancestry GWAS of the electrocardiographic PR interval identifies 210 loci underlying cardiac conduction

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Discovering patterns of pleiotropy in genome-wide association studies

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Exome chip meta-analysis elucidates the genetic architecture of rare coding variants in smoking and drinking behavior

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Genome-wide association meta-analysis of PR interval identifies 47 novel loci associated with atrial and atrioventricular electrical activity

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Evidence of polygenic adaptation at height-associated loci in mainland Europeans and Sardinians

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Genetic insights into the biological mechanisms governing human ovarian ageing

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Analysis of overlapping genetic association in type 1 and type 2 diabetes

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Meta-MultiSKAT: Multiple phenotype meta-analysis for region-based association test

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A Sardinian founder mutation in GP1BB that impacts thrombocytopenia.

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