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  1. Pubblicazioni

NATURE GENETICS

Rivista
Codice:
E116310
ISSN:
1061-4036
  • Dati Generali

Dati Generali

Pubblicazioni (42)

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A functional variant of lymphoid tyrosine phosphatase is associated with type 1 diabetes
Articolo
A male-female bias in type 1 diabetes and linkage to chromosome Xp in MHC HLA-DR3-positive patients
Articolo
A reference panel of 64,976 haplotypes for genotype imputation
Articolo
A search for type 1 diabetes susceptibility genes in families from the United Kingdom
Articolo
Application of comparative functional genomics to identify best-fit mouse models to study human cancer
Articolo
Autoimmune-associated lymphoid tyrosine phosphatase is a gain-of-function variant
Articolo
Common variants at 30 loci contribute to polygenic dyslipidemia.
Articolo
Common variants at ten loci modulate the QT interval duration in the QTSCD Study.
Articolo
Complex genetic signatures in immune cells underlie autoimmunity and inform therapy
Articolo
Genetic Investigation of ANthropometric Traits Consortium. Six new loci associated with body mass index highlight a neuronal influence on body weight regulation.
Articolo
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses
Articolo
Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers
Articolo
Genome-wide analysis identifies 12 loci influencing human reproductive behavior
Articolo
Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels
Articolo
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations
Articolo
Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes
Articolo
Genome-wide association study identifies eight loci associated with blood pressure.
Articolo
Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma
Articolo
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
Articolo
Genomic history of the Sardinian population
Articolo
Height-reducing variants and selection for short stature in Sardinia
Articolo
Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.
Articolo
Insulin VNTR allele-specific effect in type 1 diabetes depends on identity of untransmitted paternal allele
Articolo
Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways
Articolo
Linkage disequilibrium mapping of a type 1 diabetes susceptibility gene (IDDM7) to chromosome 2q31-q33
Articolo
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways
Articolo
Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations
Articolo
Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque.
Articolo
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
Articolo
Newly identified loci that influence lipid concentrations and risk of coronary artery disease
Articolo
Next-generation genotype imputation service and methods
Articolo
Parameters for reliable results in genetic association studies in common disease
Articolo
Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals
Articolo
Population- and individual-specific regulatory variation in Sardinia
Articolo
Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry
Articolo
The genetically isolated populations of Finland and Sardinia may not be a panacea for linkage disequilibrium mapping of common disease genes
Articolo
The trans-ancestral genomic architecture of glycemic traits
Articolo
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies
Articolo
Understanding the genetic complexity of puberty timing across the allele frequency spectrum
Articolo
Variants in MTNR1B influence fasting glucose levels
Articolo
Variants within the immunoregulatory CBLB gene are associated with multiple sclerosis
Articolo
Y chromosome sequence variation and the history of human populations
Articolo
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