about
Rare and low-frequency coding variants alter human adult heightGenetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.Salt-inducible kinase 3, SIK3, is a new gene associated with hearing.A reference panel of 64,976 haplotypes for genotype imputation.1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.Common variants in UMOD associate with urinary uromodulin levels: a meta-analysisA rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans.A general approach for haplotype phasing across the full spectrum of relatednessIdentification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease.Pharmacogenetics driving personalized medicine: analysis of genetic polymorphisms related to breast cancer medications in Italian isolated populations.Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney.Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.COL6A5 variants in familial neuropathic chronic itch.Erratum: A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans.Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure.MCM8 and MCM9 Nucleotide Variants in Women With Primary Ovarian Insufficiency.Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability.Association of HFE and TMPRSS6 genetic variants with iron and erythrocyte parameters is only in part dependent on serum hepcidin concentrations.Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traitsPublisher Correction: Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritabilityGenome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuriaGenome-wide association meta-analysis identifies five novel loci for age-related hearing impairmentAssociations of autozygosity with a broad range of human phenotypesA bird's-eye view of Italian genomic variation through whole-genome sequencingA catalog of genetic loci associated with kidney function from analyses of a million individuals
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description
hulumtues
@sq
researcher
@en
wetenschapper
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հետազոտող
@hy
name
Massimiliano Cocca
@ast
Massimiliano Cocca
@en
Massimiliano Cocca
@es
Massimiliano Cocca
@nl
Massimiliano Cocca
@sl
type
label
Massimiliano Cocca
@ast
Massimiliano Cocca
@en
Massimiliano Cocca
@es
Massimiliano Cocca
@nl
Massimiliano Cocca
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prefLabel
Massimiliano Cocca
@ast
Massimiliano Cocca
@en
Massimiliano Cocca
@es
Massimiliano Cocca
@nl
Massimiliano Cocca
@sl
P1053
J-2951-2018
P106
P1153
51763347100
P21
P31
P496
0000-0002-1127-7596