Author details

Full Name

Carlo Sidore

Affiliation

ORCID

Career Start Year

2010

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36739617	A fast linkage method for population GWAS cohorts with related individuals.	Genet Epidemiol	2023
36136759	GWAS 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 Genet	2023
35484151	Childhood body size directly increases type 1 diabetes risk based on a lifecourse Mendelian randomization approach.	Nat Commun	2022
34718232	Predicting physiological aging rates from a range of quantitative traits using machine learning.	Aging (Albany NY)	2021
33566725	<i>PRF1</i> mutation alters immune system activation, inflammation, and risk of autoimmunity.	Mult Scler	2021
33830302	Analysis of overlapping genetic association in type 1 and type 2 diabetes.	Diabetologia	2021
33216977	A Sardinian founder mutation in glycoprotein Ib platelet subunit beta (GP1BB) that impacts thrombocytopenia.	Br J Haematol	2020
32231244	The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis.	Nat Commun	2020
32094358	Genetic history from the Middle Neolithic to present on the Mediterranean island of Sardinia.	Nat Commun	2020
32929287	Complex genetic signatures in immune cells underlie autoimmunity and inform therapy.	Nat Genet	2020
32533944	Evidence of Polygenic Adaptation in Sardinia at Height-Associated Loci Ascertained from the Biobank Japan.	Am J Hum Genet	2020
32519380	Sequencing and imputation in GWAS: Cost-effective strategies to increase power and genomic coverage across diverse populations.	Genet Epidemiol	2020
33339817	Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease.	Nat Commun	2020
32948852	Author Correction: Complex genetic signatures in immune cells underlie autoimmunity and inform therapy.	Nat Genet	2020
30675526	Parent-of-origin effects on quantitative phenotypes in a large Hutterite pedigree.	Commun Biol	2019
30565766	Relative impact of indels versus SNPs on complex disease.	Genet Epidemiol	2019
31433078	Meta-MultiSKAT: Multiple phenotype meta-analysis for region-based association test.	Genet Epidemiol	2019
30388399	Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders.	Am J Hum Genet	2018
30224645	Genomic history of the Sardinian population.	Nat Genet	2018
28177087	Mitogenome Diversity in Sardinians: A Genetic Window onto an Island's Past.	Mol Biol Evol	2017
28552196	Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.	Am J Hum Genet	2017
28453676	fastMitoCalc: an ultra-fast program to estimate mitochondrial DNA copy number from whole-genome sequences.	Bioinformatics	2017
28934930	XCAVATOR: accurate detection and genotyping of copy number variants from second and third generation whole-genome sequencing experiments.	BMC Genomics	2017
28445677	Overexpression of the Cytokine BAFF and Autoimmunity Risk.	N Engl J Med	2017
28394350	Population- and individual-specific regulatory variation in Sardinia.	Nat Genet	2017
27548312	A reference panel of 64,976 haplotypes for genotype imputation.	Nat Genet	2016
27386562	Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation.	Sci Adv	2016
27571263	Next-generation genotype imputation service and methods.	Nat Genet	2016
26366551	Height-reducing variants and selection for short stature in Sardinia.	Nat Genet	2015
25926048	Detection of phylogenetically informative polymorphisms in the entire euchromatic portion of human Y chromosome from a Sardinian sample.	BMC Res Notes	2015
25293720	Rare variant genotype imputation with thousands of study-specific whole-genome sequences: implications for cost-effective study designs.	Eur J Hum Genet	2015
26172475	Assessing Mitochondrial DNA Variation and Copy Number in Lymphocytes of ~2,000 Sardinians Using Tailored Sequencing Analysis Tools.	PLoS Genet	2015
26418551	Correction: Assessing Mitochondrial DNA Variation and Copy Number in Lymphocytes of ~2,000 Sardinians Using Tailored Sequencing Analysis Tools.	PLoS Genet	2015
26366553	Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels.	Nat Genet	2015
26366554	Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers.	Nat Genet	2015
24809476	Population genomic analysis of ancient and modern genomes yields new insights into the genetic ancestry of the Tyrolean Iceman and the genetic structure of Europe.	PLoS Genet	2014
23669352	Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course.	Hum Mol Genet	2013
23908240	Low-pass DNA sequencing of 1200 Sardinians reconstructs European Y-chromosome phylogeny.	Science	2013
24074872	Genetic variants regulating immune cell levels in health and disease.	Cell	2013
24097068	Discovery and refinement of loci associated with lipid levels.	Nat Genet	2013
24097064	Common variants associated with plasma triglycerides and risk for coronary artery disease.	Nat Genet	2013
23064751	Genotype calling and haplotyping in parent-offspring trios.	Genome Res	2013
23055937	A likelihood-based framework for variant calling and de novo mutation detection in families.	PLoS Genet	2012
22885924	Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways.	Nat Genet	2012
22291609	A genome-wide association scan on the levels of markers of inflammation in Sardinians reveals associations that underpin its complex regulation.	PLoS Genet	2012
22876189	The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits.	PLoS Genet	2012
22982992	FTO genotype is associated with phenotypic variability of body mass index.	Nature	2012
21829380	Fine mapping of five loci associated with low-density lipoprotein cholesterol detects variants that double the explained heritability.	PLoS Genet	2011
21460063	Low-coverage sequencing: implications for design of complex trait association studies.	Genome Res	2011
20453840	Variants within the immunoregulatory CBLB gene are associated with multiple sclerosis.	Nat Genet	2010