CNR Institutional Research Information System

ANGIUS, ANDREA
 Distribuzione geografica
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Continente #
AS - Asia 289
EU - Europa 215
NA - Nord America 83
Totale 587
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Nazione #
SG - Singapore 248
IT - Italia 204
US - Stati Uniti d'America 83
KR - Corea 26
CN - Cina 15
ES - Italia 7
NL - Olanda 2
IE - Irlanda 1
SE - Svezia 1
Totale 587
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Città #
Singapore 169
Assemini 160
Santa Clara 29
Seoul 26
Cagliari 21
Guangzhou 14
Catania 3
Oristano 3
Amsterdam 2
Forest City 2
Lecce 2
Benevento 1
Boardman 1
Cartagena 1
Dublin 1
Florence 1
Milan 1
Nanchang 1
Springfield 1
Totale 439
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Nome #
Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene. 31
A 24-bp duplication in exon 10 of human chitotriosidase gene from the sub-Saharan to the Mediterranean area: Role of parasitic diseases and environmental conditions 18
Low-pass DNA sequencing of 1200 Sardinians reconstructs European Y-chromosome phylogeny 16
Sequencing-based GWAS on peripheral blood monocyte counts in the SardiNIA cohort 14
A novel mutation in the GLC1A gene causes Juvenile Open Angle Glaucoma in four families from the Italian region of Puglia. 13
Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene. 13
Post GWAS analysis of the BCL11A intronic region to define its role in regulating HbF levels. 12
Post GWAS analysis of a BCL11A intronic region to define its role in regulating HbF levels 11
Striking differentiation of sub-populations within a genetically homogeneous isolate (Ogliastra) in Sardinia as revealed by mtDNA analysis. 8
Not all isolates are equal: Linkage disequilibrium analysis on Xq13.3 reveals different patterns in Sardinian sub-populations 8
The genetics of gene expression, splicing and transcriptional efficiency through Poly-A selection and ribosomal depletion RNA sequencing in humans. 7
Chitotriosidase, a prematurely orphan enzyme. 7
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Extent of linkage disequilibrium in a Sardinian sub-isolate: sampling and methodological considerations. 6
Novel action of FOXL2 as mediator of Col1a2 gene autoregulation 6
Synchronic macrophage response and Plasmodium falciparum malaria 6
Complete genome sequence of chloroplast DNA (cpDNA) of Chlorella sorokiniana. 6
Transcriptome organization of white blood cells through gene co-expression network analysis in a large RNA-seq dataset 6
Confirmation of a new phenotype in an individual with a variant in the last part of exon 30 of CREBBP 6
Microrna-425-5p expression affects BRAF/RAS/MAPK pathways in colorectal cancers 6
Methylenetetrahydrofolate reductase gene polymorphisms in Burkina Faso: Impact on plasma fasting homocysteine and after methionine loading test 6
Plasma chitotriosidase activity in patients with beta-thalassemia. 5
Critical comparison of colocalization algorithms on large datasets 5
Archival, demographic and genetic studies define a Sardinian sub-isolate as a suitable model for mapping complex traits 5
Biomarker dynamics affecting neoadjuvant therapy response and outcome of HER2-positive breast cancer subtype 5
Harnessing Minimal Residual Disease as a Predictor for Colorectal Cancer: Promising Horizons Amidst Challenges 5
Portrait of Cancer Stem Cells on Colorectal Cancer: Molecular Biomarkers, Signaling Pathways and miRNAome 5
High differentiation among eight villages in a secluded area of Sardinia revealed by genome-wide high density SNPs analysis. 5
Detection of phylogenetically informative polymorphisms in the entire euchromatic portion of human Y chromosome from a Sardinian sample Evolutionary Biology 5
Whole genome sequencing of 3,514 individuals from the isolated population of Sardinia 5
Polygenic risk score and biochemical/environmental variables predict a low-risk profile of age-related macular degeneration in Sardinia 5
Wilson disease mutations associated with uncommon haplotypes in Mediterranean patients 5
EDA2R Is Associated with Androgenetic Alopecia. 4
An integrated map of genetic variation from 1,092 human genomes 4
Rational design of new candidate compounds for multiple sclerosis treatment based on analysis of biological targets identified through genome wide association studies in Sardinia. 4
Genetic factors regulating the levels of immune system cells in health and disease 4
Epigenetics, stem cells, and autophagy: Exploring a path involving miRNA 4
Novel ANKRD11 gene mutation in an individual with a mild phenotype of KBG syndrome associated to a GEFS plus phenotypic spectrum: a case report 4
Integrated Analysis of miRNA and mRNA Endorses a Twenty miRNAs Signature for Colorectal Carcinoma 4
Large-scale transcriptome study in the Sardinian founder population. 4
A genome-wide association study for autoimmunity in Sardinia. 4
A New Essential Hypertension Susceptibility Locus on Chromosome 2p24-p25, Detected by Genomewide Search 4
A large-scale transcriptome study in the Sardinian population 4
Unravelling the genetic causes of syndromic Intellectual Disability in the era of exome sequencing. 4
Genetic studies on an isolate region of Sardinia unravels history and evolution of its population. 4
Haplotype and mutation analysis in Mediterranean patients with Wilson disease 3
Application of next generation sequencing to identify causative variant at the BCL11A locus 3
Molecular Basis of open-angle glaucoma in Italy 3
A genomewide search using an original pairwise sampling approach for large genealogies identifies a new locus for total and low-density lipoprotein cholesterol in two genetically differentiated isolates of Sardinia 3
Molecular pathology and haplotype analysis of Wilson disease in Mediterranean populations 3
Novel mutations in c2orf71 causing an early onset form of cone-rod dystrophy: A molecular diagnosis after 20 years of clinical follow-up 3
Identification of a founder BRCA2 mutation in Sardinia 3
A reference panel of 64,976 haplotypes for genotype imputation 3
Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels 3
Identification of a new candidate locus for uric acid nephrolithiasis. 3
Environmental and Genetic Contribution to Hypertension Prevalence: Data from an Epidemiological Survey on Sardinian Genetic Isolates 3
Myocilin Gln368stop mutation and advanced age as risk factors for late- onset primary open-angle glaucoma 3
Erratum: Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa (The American Journal of Human Genetics (2016) 99(1) (236-245) (S0002929716301616) (10.1016/j.ajhg.2016.05.026)) 3
Genetic factors associated with levels of immune cell types. 3
Epidemiology and Genetics of Obesity in three Sardinian Genetic Isolates 3
Genome-wide screen for essential hypertension genes in a deep rooted Sardinian pedigree. 3
Genetic of bitter taste: identification of a Ch 7q35 locus in a Sardinian genetic isolate. 3
Likelihood Based Deletion Analysis in a Sample of Sequenced Sardinian Individuals. 3
An integrated framework for evaluating the pathogenicity of rare, population-specific non-coding variation. 3
Exome sequencing in Crisponi/cold-induced sweating syndrome-like individuals reveals unpredicted alternative diagnoses 3
hole Genome Sequencing of 1000 Individuals in an Isolated Population. 3
Synchronic macrophage response and Plasmodium falciparum malaria. 3
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. 3
Identification of candidate loci for essential hypertension by genome-wide search in a genetic isolate from Sardinia. 3
Whole genome sequencing increase the power to detect trait-associated rare variants shifted towards high frequencies in the Sardinian island population. 3
EPIDEMIOLOGICAL SURVEY OF OSTEOPOROSIS IN A GENETIC ISOLATE OF OGLIASTRA AS A PREREQUISITE FOR IDENTIFICATION OF PREDISPOSING RISK FACTORS 3
Imputation quality thresholds for rare and common variants. 3
Expanding the Mutational Spectrum of CRLF1 in Crisponi/CISS1 Syndrome 3
A Genomic Map of Positive Selection in Sardinia 3
Improvement of prenatal diagnosis of Wilson disease using microsatellite markers. 3
Gut Microbiota Functional Dysbiosis Relates to Individual Diet in Subclinical Carotid Atherosclerosis 3
Deciphering clinical significance of BCL11A isoforms and protein expression roles in triple-negative breast cancer subtype 3
Modulatory role of microRNAs in triple negative breast cancer with basal-like phenotype 3
Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa 3
A refined physical and EST map spanning 7.4 Mb of 10q24, a region involved in neurological disorders 3
Gut Microbiota Functional Dysbiosis Relates to Individual Diet in Subclinical Carotid Atherosclerosis 3
Genomic history of the Sardinian population 3
Genetic variants regulating immune cell levels in health and disease. 3
lincRNA-mRNA transcriptional regulatory co-expression network from RNA-seq data in 624 Sardinian individuals 3
Bitter taste study in a sardinian genetic isolate supports the association of phenylthiocarbamide sensitivity to the TAS2R38 bitter receptor gene. 3
Synchronic macrophage response and Plasmodium falciparum malaria. 3
Whole-Genome Sequence of Listeria monocytogenes Serovar 4b Strain IZSAM_Lm_hs2008, Isolated from a Human Infection in Italy. 2
Insulin-like growth factor 1 (IGF-1) expression is up-regulated in lymphoblastoid cell lines of lithium responsive bipolar disorder patients 2
Global microRNA profiling of peripheral blood mononuclear cells in patients with Behcet's disease 2
Mitogenome Diversity in Sardinians: A Genetic Window onto an Island's Past 2
Heritability of the Variation in Aging in Two Longitudinal Family Cohort Studies: SardiNIA/Progenia Study and Framingham Heart Study. 2
Novel NALCN biallelic truncating mutations in siblings with IHPRF1 syndrome 2
Haplotype and mutation analysis in Greek patients with Wilson disease 2
A novel spontaneous missense mutation in VMD2 gene is a cause of a Best macular distrophy sporadic case 2
Landmark study of LD in a genetic Sardinian isolate using 500k SNP: prerequisite for GW association approach. 2
Novel X-Linked mental retardation syndrome with short stature maps to Xq24. 2
QCTool: an efficient toolkit to automatically generate quality metrics of next-generation sequencing data 2
High resolution analysis and phylogenetic network construction using complete mtDNA sequences in sardinian genetic isolates. 2
Population structure of modern-day Italians reveals patterns of ancient and archaic ancestries in Southern Europe 2
Multiple bilateral retinal astrocytic hamartomas in Usher syndrome 2
Totale 471
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Categoria #
all - tutte 3.677
article - articoli 2.763
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 29
Totale 6.469
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/2024240 0 0 0 0 0 0 0 0 9 6 40 185
2024/2025359 12 26 209 110 2 0 0 0 0 0 0 0
Totale 599