CNR Institutional Research Information System

ANGIUS, ANDREA
 Distribuzione geografica
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Continente #
AS - Asia 4.939
NA - Nord America 2.070
EU - Europa 1.344
SA - Sud America 730
AF - Africa 76
OC - Oceania 11
Continente sconosciuto - Info sul continente non disponibili 4
Totale 9.174
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Nazione #
SG - Singapore 2.032
US - Stati Uniti d'America 1.934
CN - Cina 1.039
HK - Hong Kong 644
IT - Italia 626
BR - Brasile 586
VN - Vietnam 444
FR - Francia 224
KR - Corea 195
NL - Olanda 151
BD - Bangladesh 122
GB - Regno Unito 89
IN - India 84
JP - Giappone 72
ID - Indonesia 70
DE - Germania 58
AR - Argentina 51
CA - Canada 51
MX - Messico 51
TH - Thailandia 37
FI - Finlandia 35
EC - Ecuador 27
ZA - Sudafrica 27
IL - Israele 24
IQ - Iraq 23
ES - Italia 22
MY - Malesia 21
PH - Filippine 21
CO - Colombia 19
PL - Polonia 19
UA - Ucraina 18
PY - Paraguay 14
PK - Pakistan 13
SA - Arabia Saudita 13
TR - Turchia 13
UZ - Uzbekistan 13
CL - Cile 12
MA - Marocco 12
SE - Svezia 12
RU - Federazione Russa 11
KZ - Kazakistan 10
AT - Austria 9
EG - Egitto 9
IE - Irlanda 9
LT - Lituania 9
PE - Perù 9
CZ - Repubblica Ceca 8
TN - Tunisia 8
CR - Costa Rica 7
JM - Giamaica 7
PT - Portogallo 7
AU - Australia 6
AZ - Azerbaigian 6
KE - Kenya 6
HN - Honduras 5
NP - Nepal 5
VE - Venezuela 5
JO - Giordania 4
NZ - Nuova Zelanda 4
SN - Senegal 4
TT - Trinidad e Tobago 4
UY - Uruguay 4
BG - Bulgaria 3
CH - Svizzera 3
DK - Danimarca 3
DZ - Algeria 3
GE - Georgia 3
HR - Croazia 3
KG - Kirghizistan 3
LA - Repubblica Popolare Democratica del Laos 3
LB - Libano 3
LK - Sri Lanka 3
LV - Lettonia 3
MD - Moldavia 3
NO - Norvegia 3
XK - ???statistics.table.value.countryCode.XK??? 3
AE - Emirati Arabi Uniti 2
BB - Barbados 2
BE - Belgio 2
BH - Bahrain 2
BO - Bolivia 2
BS - Bahamas 2
HU - Ungheria 2
IR - Iran 2
MN - Mongolia 2
PS - Palestinian Territory 2
RO - Romania 2
SI - Slovenia 2
SV - El Salvador 2
VI - Stati Uniti Isole Vergini 2
AL - Albania 1
AM - Armenia 1
AO - Angola 1
BY - Bielorussia 1
CY - Cipro 1
EE - Estonia 1
GA - Gabon 1
GR - Grecia 1
GT - Guatemala 1
GU - Guam 1
Totale 9.154
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Città #
Singapore 1.158
Hong Kong 635
Santa Clara 485
Hefei 415
San Jose 295
Beijing 211
Assemini 208
Ashburn 196
Seoul 194
Lauterbourg 178
Ho Chi Minh City 151
Hanoi 103
Los Angeles 91
Cagliari 87
Dallas 79
New York 59
São Paulo 49
Jakarta 46
Tokyo 46
Orem 39
Bangkok 36
Rome 35
Buffalo 29
Milan 27
Frankfurt am Main 26
Helsinki 23
London 23
Minamishinagawa 23
Guangzhou 21
Rio de Janeiro 21
Chennai 18
Mexico City 18
Warsaw 18
Chicago 17
Curitiba 17
Manila 17
Montreal 17
Bengaluru 16
Haiphong 16
Phoenix 15
Amsterdam 14
Da Nang 14
Johannesburg 14
Paris 14
Atlanta 13
Düsseldorf 13
Baghdad 12
Biên Hòa 12
Brooklyn 12
Kuala Selangor 12
Tashkent 12
Hải Dương 11
Nuremberg 11
Stockholm 11
Belo Horizonte 10
Brasília 10
Catania 10
Goiânia 10
Lappeenranta 10
Manchester 10
Mumbai 10
Council Bluffs 9
Houston 9
Kyiv 9
Naples 9
Portsmouth 9
Toronto 9
Charlotte 8
Denver 8
Prague 8
Thái Bình 8
Dublin 7
Florence 7
Guarulhos 7
Kuala Lumpur 7
Newark 7
Piscataway 7
Poplar 7
Quito 7
Riyadh 7
Seattle 7
Baku 6
Bắc Giang 6
Dhaka 6
Genoa 6
Nairobi 6
Ninh Bình 6
Quận Một 6
San José 6
Shanghai 6
Thái Nguyên 6
Turin 6
Ankara 5
Betim 5
Boardman 5
Bogotá 5
Bologna 5
Bình Dương 5
Bắc Ninh 5
Campinas 5
Totale 5.665
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Nome #
An USH2A founder mutation is the cause of Usher syndrome type 2 in Sardinia 450
Identification of microRNA target sites: in-silico screening on NGS data 214
CAPRIN1-linked neurodevelopmental disorder: understanding the role of CAPRIN1 loss on neuronal differentiation, neurogenesis, and proliferation. 135
Vascular density normative data of radial peripapillary capillary plexus in healthy Caucasian subjects 133
Clinical relevance of immune microenvironment and gene-expression-based biomarkers in colorectal cancer 130
Intratumoral transcriptomic heterogeneity correlates with tumor location in colorectal cancer 129
A large-scale screening identified in USH2A gene the P3272L founder pathogenic variant explaining familial Usher syndrome in Sardinia, Italy 96
Mitogenome Diversity in Sardinians: A Genetic Window onto an Island's Past 84
Menke-Hennekam syndrome; delineation of domain-specific subtypes with distinct clinical and DNA methylation profiles 84
Overexpression of the Cytokine BAFF and Autoimmunity Risk 82
Quantitative Metabolomics to Explore the Role of Plasma Polyamines in Colorectal Cancer 82
A Novel Affordable and Reliable Framework for Accurate Detection and Comprehensive Analysis of Somatic Mutations in Cancer 79
Haplotype and mutation analysis in Mediterranean patients with Wilson disease 78
Transcriptome organization of white blood cells through gene co-expression network analysis in a large RNA-seq dataset 77
Novel NALCN biallelic truncating mutations in siblings with IHPRF1 syndrome 74
Insulin-like growth factor 1 (IGF-1) expression is up-regulated in lymphoblastoid cell lines of lithium responsive bipolar disorder patients 72
Identification of diagnostic biomarkers through analysis of peripheral blood mononuclear cells from amyotrophic lateral sclerosis patients 68
Whole-Genome Sequence of Listeria monocytogenes Serovar 4b Strain IZSAM_Lm_hs2008, Isolated from a Human Infection in Italy. 67
A GWAS in Sardinians revelas a novel gene associated with Multiple Sclerosis 67
Novel action of FOXL2 as mediator of Col1a2 gene autoregulation 66
A novel mutation in the GLC1A gene causes Juvenile Open Angle Glaucoma in four families from the Italian region of Puglia. 65
Mutation analysis in patients of Mediterranean descent with Wilson disease: Identification of 19 novel mutations 64
Molecular Basis of open-angle glaucoma in Italy 64
Whole genome sequencing increase the power to detect trait-associated rare variants shifted towards high frequencies in the Sardinian island population. 64
Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene. 63
Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa 63
Genomic history of the Sardinian population 63
A New Essential Hypertension Susceptibility Locus on Chromosome 2p24-p25, Detected by Genomewide Search 63
Novel ANKRD11 gene mutation in an individual with a mild phenotype of KBG syndrome associated to a GEFS plus phenotypic spectrum: a case report 62
Heritability of the Variation in Aging in Two Longitudinal Family Cohort Studies: SardiNIA/Progenia Study and Framingham Heart Study. 60
Global microRNA profiling of peripheral blood mononuclear cells in patients with Behcet's disease 59
miRNA-135b in molecular characterization of triple-negative breast cancer (TNBC). 59
Population structure of modern-day Italians reveals patterns of ancient and archaic ancestries in Southern Europe 59
Genetic variants regulating immune cell levels in health and disease. 59
Mutation analysis in patients of Mediterranean descent with Wilson disease. Identification of 19 novel mutations. 58
Rational design of new candidate compounds for multiple sclerosis treatment based on analysis of biological targets identified through genome wide association studies in Sardinia. 58
Deciphering clinical significance of BCL11A isoforms and protein expression roles in triple-negative breast cancer subtype 58
Varianti del gene DCP1 influenzano in maniera diversa i livelli sierologici di Angiotensin Convertine Enzyme (ACE). 57
DNA hydroxymethylation controls cardiomyocyte gene expression in development and hypertrophy. 57
Biomarker dynamics affecting neoadjuvant therapy response and outcome of HER2-positive breast cancer subtype 57
Application of next generation sequencing to identify causative variant at the BCL11A locus 56
Population- and individual-specific regulatory variation in Sardinia. 56
Involvement of core clock genes in lithium response 55
Mandibular hypoplasia, deafness, progeroid features and lipodystrophy (MDPL) syndrome in the context of inherited lipodystrophies 55
Rare variant genotype imputation with thousands of study-specific whole-genome sequences: implications for cost-effective study designs 55
Critical comparison of colocalization algorithms on large datasets 54
Epidemiology and Genetics of Obesity in three Sardinian Genetic Isolates 54
Post GWAS analysis of a BCL11A intronic region to define its role in regulating HbF levels 54
Polygenic risk score and biochemical/environmental variables predict a low-risk profile of age-related macular degeneration in Sardinia 54
Patterns of linkage disequilibrium between SNPs in a Sardinian population isolate 53
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)) 53
Sequencing-based GWAS on peripheral blood monocyte counts in the SardiNIA cohort 52
Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers 52
A reference panel of 64,976 haplotypes for genotype imputation 52
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 51
Confirmation of a new phenotype in an individual with a variant in the last part of exon 30 of CREBBP 51
Systematic assessment of the immune system by genetic mapping of its quantitative dimensions 51
Haplotype and mutation analysis in Greek patients with Wilson disease 50
A reference panel of 64,976 haplotypes for genotype imputation 50
Harnessing Minimal Residual Disease as a Predictor for Colorectal Cancer: Promising Horizons Amidst Challenges 50
Genetic factors regulating the levels of immune system cells in health and disease 49
Post GWAS analysis of the BCL11A intronic region to define its role in regulating HbF levels. 49
Portrait of Cancer Stem Cells on Colorectal Cancer: Molecular Biomarkers, Signaling Pathways and miRNAome 49
Identification of a new candidate locus for uric acid nephrolithiasis. 48
Height-reducing variants and selection for short stature in Sardinia 48
Environmental and Genetic Contribution to Hypertension Prevalence: Data from an Epidemiological Survey on Sardinian Genetic Isolates 47
Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels 46
Exome sequencing in Crisponi/cold-induced sweating syndrome-like individuals reveals unpredicted alternative diagnoses 46
Genome wide screen in Sardinian genetic isolates identifies two genomic regions linked to androgenetic alopecia 46
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 46
hole Genome Sequencing of 1000 Individuals in an Isolated Population. 45
Improvement of prenatal diagnosis of Wilson disease using microsatellite markers. 45
Molecular pathology and haplotype analysis of Wilson disease in Mediterranean populations 44
Epigenetics, stem cells, and autophagy: Exploring a path involving miRNA 44
High differentiation among eight villages in a secluded area of Sardinia revealed by genome-wide high density SNPs analysis. 44
Modulatory role of microRNAs in triple negative breast cancer with basal-like phenotype 44
Complete genome sequence of mitochondrial DNA (mtDNA) of chlorella sorokiniana 44
Epileptic phenotypes related to the UNC79-UNC80-NALCN protein complex. 43
Ogliastra Project: Population, Methodology and Results. 43
Genetic factors associated with levels of immune cell types. 43
Esiste una predisposizione genetica per l'espansione infartuale? Valutazione dei polimorfismi genetici del sistema renina-angiotensina 43
Chitotriosidase, a prematurely orphan enzyme 43
Variants within the immunoregulatory CBLB gene are associated with multiple sclerosis 43
lincRNA-mRNA transcriptional regulatory co-expression network from RNA-seq data in 624 Sardinian individuals 43
A large-scale transcriptome study in the Sardinian population 43
Whole genome sequencing of 3,514 individuals from the isolated population of Sardinia 43
Extent of linkage disequilibrium in a Sardinian sub-isolate: sampling and methodological considerations. 42
A novel spontaneous missense mutation in VMD2 gene is a cause of a Best macular distrophy sporadic case 42
Multiple bilateral retinal astrocytic hamartomas in Usher syndrome 42
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. 42
Extent of linkage disequilibrium in a Sardinian sub-isolate: Sampling and methodological considerations 41
Identification of a new candidate locus for uric acid nephrolithiasis 41
Likelihood Based Deletion Analysis in a Sample of Sequenced Sardinian Individuals. 41
First evidence of candidate loci for uric acid nephrolithiasis using an ideal genetic-isolate. 41
A Genomic Map of Positive Selection in Sardinia 41
Detection of phylogenetically informative polymorphisms in the entire euchromatic portion of human Y chromosome from a Sardinian sample Evolutionary Biology 41
Wilson disease mutations associated with uncommon haplotypes in Mediterranean patients 41
A new Androgenetic Alopecia genetic predisposing factor 40
The genetics of gene expression, splicing and transcriptional efficiency through Poly-A selection and ribosomal depletion RNA sequencing in humans. 40
A Portrait of Intratumoral Genomic and Transcriptomic Heterogeneity at Single-Cell Level in Colorectal Cancer 40
Totale 6.283
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Categoria #
all - tutte 29.531
article - articoli 21.541
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 189
Totale 51.261
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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
2024/20253.128 12 27 214 110 516 221 64 201 168 180 784 631
2025/20266.036 313 517 691 857 1.264 263 742 236 293 370 305 185
Totale 9.403