CNR Institutional Research Information System

ANGIUS, ANDREA
 Distribuzione geografica
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Continente #
NA - Nord America 528
EU - Europa 374
AS - Asia 320
AF - Africa 1
Totale 1.223
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Nazione #
US - Stati Uniti d'America 528
IT - Italia 332
SG - Singapore 272
KR - Corea 30
FI - Finlandia 17
CN - Cina 15
ES - Italia 7
NL - Olanda 6
IE - Irlanda 4
AT - Austria 3
DE - Germania 3
HK - Hong Kong 3
EG - Egitto 1
LT - Lituania 1
SE - Svezia 1
Totale 1.223
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Città #
Santa Clara 467
Assemini 203
Singapore 187
Cagliari 61
Seoul 30
Helsinki 17
Guangzhou 14
Dublin 4
Rome 4
Amsterdam 3
Catania 3
Falkenstein 3
Hong Kong 3
Oristano 3
Vienna 3
Decimomannu 2
Forest City 2
Lecce 2
Al Qāhirah al Jadīdah 1
Benevento 1
Boardman 1
Borore 1
Cartagena 1
Florence 1
Milan 1
Nanchang 1
Phoenix 1
Pittsburgh 1
San Marcellino 1
Sassari 1
Seattle 1
Springfield 1
White Plains 1
Totale 1.026
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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. 35
Vascular density normative data of radial peripapillary capillary plexus in healthy Caucasian subjects 31
Overexpression of the Cytokine BAFF and Autoimmunity Risk 29
Quantitative Metabolomics to Explore the Role of Plasma Polyamines in Colorectal Cancer 25
Quantitative Metabolomics to Explore the Role of Plasma Polyamines in Colorectal Cancer 23
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 20
DNA hydroxymethylation controls cardiomyocyte gene expression in development and hypertrophy. 19
Sequencing-based GWAS on peripheral blood monocyte counts in the SardiNIA cohort 17
A novel mutation in the GLC1A gene causes Juvenile Open Angle Glaucoma in four families from the Italian region of Puglia. 16
Post GWAS analysis of a BCL11A intronic region to define its role in regulating HbF levels 16
A large-scale screening identified in USH2A gene the P3272L founder pathogenic variant explaining familial Usher syndrome in Sardinia, Italy 16
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. 14
Post GWAS analysis of the BCL11A intronic region to define its role in regulating HbF levels. 14
Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene. 14
Chitotriosidase, a prematurely orphan enzyme 13
Identification of a founder BRCA2 mutation in Sardinia 12
Whole genome sequencing of 3,514 individuals from the isolated population of Sardinia 12
Novel action of FOXL2 as mediator of Col1a2 gene autoregulation 11
Not all isolates are equal: Linkage disequilibrium analysis on Xq13.3 reveals different patterns in Sardinian sub-populations 11
Transcriptome organization of white blood cells through gene co-expression network analysis in a large RNA-seq dataset 11
Confirmation of a new phenotype in an individual with a variant in the last part of exon 30 of CREBBP 11
Chitotriosidase, a prematurely orphan enzyme. 11
Genomic history of the Sardinian population 11
Extent of linkage disequilibrium in a Sardinian sub-isolate: sampling and methodological considerations. 10
High differentiation among eight villages in a secluded area of Sardinia revealed by genome-wide high density SNPs analysis. 10
The genetics of gene expression, splicing and transcriptional efficiency through Poly-A selection and ribosomal depletion RNA sequencing in humans. 10
Demographic, genealogical and genetic characterization of an isolated Sardinian micropopulation suitable for the study of complex traits. 10
Menke-Hennekam syndrome; delineation of domain-specific subtypes with distinct clinical and DNA methylation profiles 10
Novel NALCN biallelic truncating mutations in siblings with IHPRF1 syndrome 9
Epileptic phenotypes related to the UNC79-UNC80-NALCN protein complex. 9
Assessing the Predictive Power of the Hemoglobin/Red Cell Distribution Width Ratio in Cancer: A Systematic Review and Future Directions 9
A reference panel of 64,976 haplotypes for genotype imputation 9
Novel ANKRD11 gene mutation in an individual with a mild phenotype of KBG syndrome associated to a GEFS plus phenotypic spectrum: a case report 9
Portrait of Cancer Stem Cells on Colorectal Cancer: Molecular Biomarkers, Signaling Pathways and miRNAome 9
Extent and distribuition of linkage disequilibrium on Xq13.3 in nested Sardinian subpopulations 9
Improvement of prenatal diagnosis of Wilson disease using microsatellite markers. 9
Methylenetetrahydrofolate reductase gene polymorphisms in Burkina Faso: Impact on plasma fasting homocysteine and after methionine loading test 9
Detection of phylogenetically informative polymorphisms in the entire euchromatic portion of human Y chromosome from a Sardinian sample Evolutionary Biology 9
A GWAS in Sardinians revelas a novel gene associated with Multiple Sclerosis 8
Haplotype and mutation analysis in Mediterranean patients with Wilson disease 8
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 8
Molecular pathology and haplotype analysis of Wilson disease in Mediterranean populations 8
EDA2R Is Associated with Androgenetic Alopecia. 8
Rational design of new candidate compounds for multiple sclerosis treatment based on analysis of biological targets identified through genome wide association studies in Sardinia. 8
Exome sequencing in Crisponi/cold-induced sweating syndrome-like individuals reveals unpredicted alternative diagnoses 8
Genome-wide screen for essential hypertension genes in a deep rooted Sardinian pedigree 8
Integrated Analysis of miRNA and mRNA Endorses a Twenty miRNAs Signature for Colorectal Carcinoma 8
Harnessing Minimal Residual Disease as a Predictor for Colorectal Cancer: Promising Horizons Amidst Challenges 8
Large-scale transcriptome study in the Sardinian founder population. 8
Whole genome sequencing increase the power to detect trait-associated rare variants shifted towards high frequencies in the Sardinian island population. 8
A genome-wide association study for autoimmunity in Sardinia. 8
Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa 8
A refined physical and EST map spanning 7.4 Mb of 10q24, a region involved in neurological disorders 8
A large-scale transcriptome study in the Sardinian population 8
Unravelling the genetic causes of syndromic Intellectual Disability in the era of exome sequencing. 8
Complete genome sequence of mitochondrial DNA (mtDNA) of chlorella sorokiniana 8
Polygenic risk score and biochemical/environmental variables predict a low-risk profile of age-related macular degeneration in Sardinia 8
Wilson disease mutations associated with uncommon haplotypes in Mediterranean patients 8
Mitogenome Diversity in Sardinians: A Genetic Window onto an Island's Past 7
Varianti del gene DCP1 influenzano in maniera diversa i livelli sierologici di Angiotensin Convertine Enzyme (ACE). 7
Application of next generation sequencing to identify causative variant at the BCL11A locus 7
Molecular Basis of open-angle glaucoma in Italy 7
Plasma chitotriosidase activity in patients with beta-thalassemia. 7
Novel mutations in c2orf71 causing an early onset form of cone-rod dystrophy: A molecular diagnosis after 20 years of clinical follow-up 7
Population structure of modern-day Italians reveals patterns of ancient and archaic ancestries in Southern Europe 7
Multiple bilateral retinal astrocytic hamartomas in Usher syndrome 7
Critical comparison of colocalization algorithms on large datasets 7
Whole Genome Sequencing of 2100 Individuals in the founder Sardinian Population. 7
Identificazione di loci candidati per l'ipertensione arteriosa essenziale tramite genome-wide search in un isolato genetico della Sardegna. 7
Identification of a new candidate locus for uric acid nephrolithiasis. 7
Synchronic macrophage response and Plasmodium falciparum malaria 7
Environmental and Genetic Contribution to Hypertension Prevalence: Data from an Epidemiological Survey on Sardinian Genetic Isolates 7
Archival, demographic and genetic studies define a Sardinian sub-isolate as a suitable model for mapping complex traits 7
Ogliastra Project: Population, Methodology and Results. 7
Microsatellites and SNPs linkage analysis in a Sardinian genetic isolate confirms several essential hypertension loci previously identified in different populations. 7
Genetic factors regulating the levels of immune system cells in health and disease 7
Complete genome sequence of chloroplast DNA (cpDNA) of Chlorella sorokiniana. 7
Landscape of transcriptome variations uncovering known and novel driver events in colorectal carcinoma 7
hole Genome Sequencing of 1000 Individuals in an Isolated Population. 7
Genome-wide screen for essential hypertension in a deep rooted pedigree from an isolated Sardinian subpopulation. 7
Haplotype and mutation analysis in Greek patients with Wilson disease 7
Identification of candidate loci for essential hypertension by genome-wide search in a genetic isolate from Sardinia. 7
Modulatory role of microRNAs in triple negative breast cancer with basal-like phenotype 7
A Portrait of Intratumoral Genomic and Transcriptomic Heterogeneity at Single-Cell Level in Colorectal Cancer 7
High resolution genetic maps and complete genealogy of an isolated Sardinian sub-population as prerequisite for the study of complex traits. 7
Genetic studies on an isolate region of Sardinia unravels history and evolution of its population. 7
Heritability of the Variation in Aging in Two Longitudinal Family Cohort Studies: SardiNIA/Progenia Study and Framingham Heart Study. 6
A Novel Affordable and Reliable Framework for Accurate Detection and Comprehensive Analysis of Somatic Mutations in Cancer 6
Haplotype and mutation analysis in Greek patients with Wilson disease 6
Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels 6
Extent of linkage disequilibrium in a Sardinian sub-isolate: Sampling and methodological considerations 6
An integrated map of genetic variation from 1,092 human genomes 6
Striking differentiation of sub-populations within a genetically homogeneous isolate (Ogliastra) in Sardinia as revealed by mtDNA analysis 6
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)) 6
Rare variant genotype imputation with thousands of study-specific whole-genome sequences: implications for cost-effective study designs 6
Essential Hypertension is associated to several worldwide genetic factors in a Sardinian genetic isolate 6
Genetic of bitter taste: identification of a Ch 7q35 locus in a Sardinian genetic isolate. 6
Biomarker dynamics affecting neoadjuvant therapy response and outcome of HER2-positive breast cancer subtype 6
Likelihood Based Deletion Analysis in a Sample of Sequenced Sardinian Individuals. 6
An integrated framework for evaluating the pathogenicity of rare, population-specific non-coding variation. 6
Totale 972
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Categoria #
all - tutte 5.703
article - articoli 4.168
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 43
Totale 9.914
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/2024239 0 0 0 0 0 0 0 0 9 6 44 180
2024/20251.133 13 27 218 111 523 241 0 0 0 0 0 0
Totale 1.372