List of works - Antonio Cao

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

scientific article

Newly identified loci that influence lipid concentrations and risk of coronary artery disease

scientific article

Variants in MTNR1B influence fasting glucose levels

scientific article

Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia

scientific article

Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals

scientific article

Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways

scientific article

Common variants in the GDF5-UQCC region are associated with variation in human height

scientific article

Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development

scientific journal article

The GLUT9 gene is associated with serum uric acid levels in Sardinia and Chianti cohorts

scientific article

A genome-wide association search for type 2 diabetes genes in African Americans

scientific article published on 4 January 2012

Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia

scientific article

IRAK-M is involved in the pathogenesis of early-onset persistent asthma

scientific article

Phosphodiesterase 8B gene variants are associated with serum TSH levels and thyroid function

scientific article published on June 2008

The central arterial burden of the metabolic syndrome is similar in men and women: the SardiNIA Study

scientific article

Alpha-thalassemia

scientific article (publication date: 5 January 2011)

COL4A1 is associated with arterial stiffness by genome-wide association scan

scientific article

Crisponi syndrome is caused by mutations in the CRLF1 gene and is allelic to cold-induced sweating syndrome type 1

scientific article

FOXL2 inactivation by a translocation 171 kb away: analysis of 500 kb of chromosome 3 for candidate long-range regulatory sequences

scientific article

The forkhead transcription factor Foxl2 is sumoylated in both human and mouse: sumoylation affects its stability, localization, and activity

scientific article

DAXX is a new AIRE-interacting protein

scientific article

Cloning MafF by recognition site screening with the NFE2 tandem repeat of HS2: analysis of its role in globin and GCSl genes regulation

scientific article

Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

scientific article published in May 2010

List of works by Antonio Cao

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

Newly identified loci that influence lipid concentrations and risk of coronary artery disease

Variants in MTNR1B influence fasting glucose levels

Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia

Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals

Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways

Common variants in the GDF5-UQCC region are associated with variation in human height

Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development

The GLUT9 gene is associated with serum uric acid levels in Sardinia and Chianti cohorts

A genome-wide association search for type 2 diabetes genes in African Americans

Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia

IRAK-M is involved in the pathogenesis of early-onset persistent asthma

Phosphodiesterase 8B gene variants are associated with serum TSH levels and thyroid function

The central arterial burden of the metabolic syndrome is similar in men and women: the SardiNIA Study

Alpha-thalassemia

COL4A1 is associated with arterial stiffness by genome-wide association scan

Crisponi syndrome is caused by mutations in the CRLF1 gene and is allelic to cold-induced sweating syndrome type 1

FOXL2 inactivation by a translocation 171 kb away: analysis of 500 kb of chromosome 3 for candidate long-range regulatory sequences

The forkhead transcription factor Foxl2 is sumoylated in both human and mouse: sumoylation affects its stability, localization, and activity

DAXX is a new AIRE-interacting protein

Cloning MafF by recognition site screening with the NFE2 tandem repeat of HS2: analysis of its role in globin and GCSl genes regulation

Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk