IRIS
CUCCA, Francesco
 Distribuzione geografica
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Continente #
NA - Nord America 14.112
AS - Asia 8.346
SA - Sud America 4.700
EU - Europa 4.538
AF - Africa 323
OC - Oceania 31
Continente sconosciuto - Info sul continente non disponibili 18
Totale 32.068
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Nazione #
US - Stati Uniti d'America 13.778
BR - Brasile 4.162
SG - Singapore 3.545
CN - Cina 2.232
UA - Ucraina 1.457
DE - Germania 781
HK - Hong Kong 724
VN - Vietnam 591
IT - Italia 446
SE - Svezia 395
FR - Francia 353
FI - Finlandia 284
GB - Regno Unito 277
AR - Argentina 189
TR - Turchia 174
IN - India 159
BD - Bangladesh 142
CA - Canada 129
IQ - Iraq 124
MX - Messico 114
EC - Ecuador 96
RU - Federazione Russa 95
ZA - Sudafrica 93
UZ - Uzbekistan 91
JP - Giappone 76
PK - Pakistan 70
MA - Marocco 66
CZ - Repubblica Ceca 65
VE - Venezuela 64
AT - Austria 54
NL - Olanda 52
PL - Polonia 47
CO - Colombia 46
PY - Paraguay 46
AE - Emirati Arabi Uniti 39
TN - Tunisia 39
ID - Indonesia 37
AZ - Azerbaigian 36
BE - Belgio 36
LT - Lituania 36
PE - Perù 36
DZ - Algeria 33
ES - Italia 33
KR - Corea 28
AU - Australia 27
JO - Giordania 27
CL - Cile 25
NP - Nepal 25
EG - Egitto 23
IL - Israele 22
KZ - Kazakistan 22
AL - Albania 21
OM - Oman 21
JM - Giamaica 20
KE - Kenya 20
PH - Filippine 20
SA - Arabia Saudita 20
UY - Uruguay 19
IR - Iran 18
DO - Repubblica Dominicana 16
RO - Romania 16
BO - Bolivia 15
CR - Costa Rica 14
LB - Libano 14
MY - Malesia 13
SN - Senegal 13
PS - Palestinian Territory 12
CH - Svizzera 11
RS - Serbia 10
AO - Angola 9
BY - Bielorussia 9
EU - Europa 9
GE - Georgia 9
HN - Honduras 9
IE - Irlanda 9
KG - Kirghizistan 9
BN - Brunei Darussalam 8
NI - Nicaragua 8
PA - Panama 8
BG - Bulgaria 7
MN - Mongolia 7
A2 - ???statistics.table.value.countryCode.A2??? 5
GR - Grecia 5
QA - Qatar 5
TT - Trinidad e Tobago 5
BA - Bosnia-Erzegovina 4
BH - Bahrain 4
CI - Costa d'Avorio 4
ET - Etiopia 4
GT - Guatemala 4
KH - Cambogia 4
LU - Lussemburgo 4
PT - Portogallo 4
TH - Thailandia 4
XK - ???statistics.table.value.countryCode.XK??? 4
CG - Congo 3
DK - Danimarca 3
HR - Croazia 3
HU - Ungheria 3
MD - Moldavia 3
Totale 32.010
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Città #
Dallas 4.924
Singapore 1.978
Chandler 1.472
San Jose 1.079
Jacksonville 879
Hong Kong 713
Ashburn 617
Princeton 495
Beijing 402
Dearborn 368
Nanjing 341
São Paulo 279
Lauterbourg 259
Wilmington 253
Ho Chi Minh City 228
Shanghai 183
Ann Arbor 167
Rio de Janeiro 144
Santa Clara 139
Hanoi 135
Los Angeles 132
Boardman 130
Nanchang 128
Belo Horizonte 122
New York 112
The Dalles 101
Columbus 97
Munich 95
Sassari 88
Tianjin 87
Council Bluffs 82
Woodbridge 82
Tashkent 80
Nuremberg 79
Brasília 73
Tokyo 71
Orem 66
Helsinki 65
Hebei 63
Shenyang 61
Curitiba 59
Campinas 57
Frankfurt am Main 56
Salvador 55
Changsha 53
Toronto 53
Johannesburg 52
Brno 51
Falls Church 51
Guarulhos 51
San Francisco 51
Baghdad 50
Jiaxing 49
Chennai 45
Porto Alegre 44
Warsaw 41
Brooklyn 39
Izmir 39
Andover 38
Buffalo 37
Amsterdam 36
Brussels 36
Denver 36
Norwalk 36
Baku 34
London 34
Quito 32
Atlanta 31
Montreal 31
Ribeirão Preto 31
Santo André 31
Chicago 30
Dhaka 29
Houston 29
Cagliari 28
Fortaleza 28
Hangzhou 28
Seoul 28
Uberlândia 28
Da Nang 27
Istanbul 27
Kunming 27
Rome 27
Ankara 26
Jinan 26
Lahore 26
Mountain View 26
Asunción 25
Dubai 25
Guayaquil 25
Mexico City 25
Recife 25
Stockholm 25
Amman 24
Auburn Hills 24
Betim 24
Campo Grande 24
Guangzhou 24
Lima 24
Goiânia 23
Totale 18.965
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Nome #
Substituted 2-pyrrolinone compounds as inhibitors of B-cell activating factor (BAFF) for autoimmune diseases treatment 863
Age‐Associated Increase in Growth Differentiation Factor 15 Levels Correlates With Central Arterial Stiffness and Predicts All‐Cause Mortality in a Sardinian Population Cohort 469
A genome-wide association study by ImmunoChip reveals potential modifiers in myelodysplastic syndromes 246
A Comparison of Y-Chromosome Variation in Sardinia and Anatolia Is More Consistent with Cultural Rather than Demic Diffusion of Agriculture 241
A large-scale screening identified in USH2A gene the P3272L founder pathogenic variant explaining familial Usher syndrome in Sardinia, Italy 210
A Genome-wide association scan on the levels of markers of inflammation in Sardinians reveals associations that underpin its complex regulation 196
A correlation between the relative predisposition of MHC class II alleles to type 1 diabetes and the structure of their proteins 187
Genomic history of the Sardinian population 187
Overexpression of the Cytokine BAFF and Autoimmunity Risk 186
A genome-wide association scan on the levels of markers of inflammation in sardinians reveals associations that underpin its complex regulation 182
A gene dosage effect of the DQA1*0501/DQB1*0201 allelic combination influences the clinical heterogeneity of Celiac disease 179
A Likelihood-Based Framework for Variant Calling and De Novo Mutation Detection in Families 179
A male-female bias in type 1 diabetes and linkage to chromosome Xp in MHC HLA-DR3-positive patients 179
A HIGH-FREQUENCY OF THE A30, B18, DR3, DRW52, DQW2 EXTENDED HAPLOTYPE IN SARDINIAN CELIAC-DISEASE PATIENTS - FURTHER EVIDENCE THAT DISEASE SUSCEPTIBILITY IS CONFERRED BY DQ A1-STAR-0501, B1-STAR-0201 176
A genome-wide analysis of Sardinian population structure 173
A novel founder MYO15A frameshift duplication is the major cause of genetic hearing loss in Oman 173
A Genome-Wide Association Study of Depressive Symptoms 170
A Meta-Analysis of Thyroid-Related Traits Reveals Novel Loci and Gender-Specific Differences in the Regulation of Thyroid Function 167
Population structure of modern-day Italians reveals patterns of ancient and archaic ancestries in Southern Europe 165
A Comparison of Y-Chromosome variation in Sardinia and Anatolia is more consistent with cultural rather than demic diffusion of agriculture 161
Are personality traits associated with white-coat and masked hypertension? 159
Arterial stiffness and influences of the metabolic syndrome: A cross-countries study 159
Adipocytokine correlations with thyroid function and autoimmunity in euthyroid sardinians 157
A novel HLA-DQB1 allele: evidence for gene conversion event promoted by -like sequence at DQB1 locus 156
A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration 156
Y-chromosome based evidence for pre-neolithic origin of the genetically homogeneous but diverse sardinian population: inference for association scans 155
CXCR3 identifies human naive CD8+ T cells with enhanced effector differentiation potential 154
Keratitis-Ichthyosis-Deafness Syndrome, Atypical Connexin GJB2 Gene Mutation, and Peripheral T-Cell Lymphoma: More Than a Random Association? 152
An integrated map of genetic variation from 1,092 human genomes 150
Impulsivity is Associated with Uric Acid: Evidence from Humans and Mice 149
Potential and active functions in the gut microbiota of a healthy human cohort 149
analisi del ruolo dellla porzione non ricombinante del cromosoma Y nella predisposizione al diabete mellito di tipo 1 nella popolazione sarda. 149
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids 148
Arterial stiffness and multiple organ damage: a longitudinal study in population 144
Confirmation of a new phenotype in an individual with a variant in the last part of exon 30 of CREBBP 144
Impact of Stiffer Arteries on the Response to Antihypertensive Treatment: A Longitudinal Study of the SardiNIA Cohort 143
Novel mutations in c2orf71 causing an early onset form of cone-rod dystrophy: A molecular diagnosis after 20 years of clinical follow-up 143
Novel NALCN biallelic truncating mutations in siblings with IHPRF1 syndrome 143
A genome-wide analysis of Sardinian population structure 142
Genetic history from the Middle Neolithic to present on the Mediterranean island of Sardinia 141
Complex genetic signatures in immune cells underlie autoimmunity and inform therapy 138
Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma 137
Y-chromosome phylogeny and haplotype sharing in Sardinians 135
High frequency of the TCRBV20S1 null allele in the Sardinian population 135
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits 135
Seventy-five genetic loci influencing the human red blood cell 134
Effect of Different Disease-Modifying Therapies on Humoral Response to BNT162b2 Vaccine in Sardinian Multiple Sclerosis Patients 134
Transmission of haplotypes of microsatellite markers rather than single marker alleles in the mapping of a putative type 1 diabetes susceptibility gene (IDDM6) 134
Serum free thyroxine levels are positively associated with arterial stiffness in the SardiNIA study 133
Meta-MultiSKAT: Multiple phenotype meta-analysis for region-based association test 133
The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis 132
Evolutionarily Selected Overexpression of the Cytokine BAFF Enhances Mucosal Immune Response Against P. falciparum 132
Number of autoantibodies and HLA genotype, more than high titers of glutamic acid decarboxylase autoantibodies, predict insulin dependence in latent autoimmune diabetes of adults 130
IDDM2-VNTR-encoded susceptibility to type 1 diabetes: Dominant protection and parental transmission of alleles of the insulin gene-linked minisatellite locus 130
Major factors influencing linkage disequilibrium by analysis of different chromosome regions in distinct populations: demography chromosome recombination frequency and selection 129
Systematic identification of NF90 target RNAs by iCLIP analysis 129
ANALISI DI LINKAGE SU FAMIGLIE DIABETICHE SARDE PER INDIVIDUARE GENI DI SUSCETTIBILITÀ AL DIABETE TIPO 1 129
A fast linkage method for population GWAS cohorts with related individuals 128
No evidence of association between subclinical thyroid disorders and common carotid intima medial thickness or atherosclerotic plaque 127
A Trans-Specific Polymorphism in ZC3HAV1 Is Maintained by Long-Standing Balancing Selection and May Confer Susceptibility to Multiple Sclerosis 126
Molecular Characterization of β-Thalassemia Mutations in Central Vietnam 126
Genetic Variation among Pharmacogenes in the Sardinian Population 124
HLA susceptibility to type 1 diabetes: methods and mechanisms 124
Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations 124
Detection of phylogenetically informative polymorphisms in the entire euchromatic portion of human Y chromosome from a Sardinian sample 124
Height-reducing variants and selection for short stature in Sardinia 123
Kidney size in relation to ageing, gender, renal function, birthweight and chronic kidney disease risk factors in a general population. 123
Y-Chromosome based evidence for pre-neolithic origin of the genetically homogeneous but diverse sardinian population: inference for association scans 122
Geographic population structure analysis of worldwide human populations infers their biogeographical origins 121
Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes 121
Assessing Mitochondrial DNA Variation and Copy Number in Lymphocytes of similar to 2,000 Sardinians Using Tailored Sequencing Analysis Tools 120
HLA-DQB1*0201 homozygosis predisposes to severe intestinal damage in celiac disease 119
GENE-FREQUENCY AND MECHANISM OF GENERATION OF A NOVEL HLA-DQB1 ALLELE 118
Integrative Annotation of Variants from 1092 Humans: Application to Cancer Genomics 118
Low pass DNA sequencing of 1,200 Sardinians reconstructs European Y chromosome phylogeny 118
Cross-sectional analysis of the humoral response after SARS-CoV-2 vaccination in Sardinian multiple sclerosis patients, a follow-up study 116
Polygenic risk score and biochemical/environmental variables predict a low-risk profile of age-related macular degeneration in Sardinia 116
The distribution of HLA class II haplotypes reveals that the Sardinian population is genetically differentiated from the other Caucasian populations 115
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci 115
PRF1 mutation alters immune system activation, inflammation, and risk of autoimmunity 115
Methods for Association Analysis and Meta-Analysis of Rare Variants in Families 114
A saturated map of common genetic variants associated with human height 113
Nutritional factors and worldwide incidence of childhood type 1 diabetes 113
DIFFERENT HLA DR2-DQWL HAPLOTYPES IN SARDINIAN AND NORTHERN ITALIAN POPULATIONS - IMPLICATIONS FOR MULTIPLE-SCLEROSIS SUSCEPTIBILITY 113
Genetic loci linked to type 1 diabetes and multiple sclerosis families in Sardinia 113
GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment 113
Human chromosome 18q12-q21 and distal rodent chromosome 18 are associated with multiple autoimmune phenotypes. 113
Predicting physiological aging rates from a range of quantitative traits using machine learning 112
Insulin Dependent Diabetes Mellitus and the mayor histocompatibility complex peptide transporters TAP1 and TAP2: no association in a population with a high disease incidence 112
Genome-Wide Association Study of Multiple Sclerosis Confirms a Novel Locus at 5p13.1 112
Keratitis-ichthyosis-deafness syndrome, atypical connexin GJB2 genemutation, and peripheral T-cell lymphoma: more than a random association? 112
Suggestive evidence for association of human chromosome 18q12-q21 and its orthologue on rat and mouse chromosome 18 with several autoimmune diseases 112
Vascular density normative data of radial peripapillary capillary plexus in healthy Caucasian subjects 111
Echocardiographic heart ageing patterns predict cardiovascular and non-cardiovascular events and reflect biological age: the SardiNIA study 109
Conditional ETDT analysis of the Human Leukocyte Antigen region in type 1 diabetes 109
Evaluation of IgA deficiency in Sardinians indicates a susceptibility gene is encoded within the HLA class III region 109
Fine mapping of the diabetes-susceptibility locus, IDDM4, on chromosome 11q13 109
Investigation of linkage of chromosome 8 to type 1 diabetes - Multipoint analysis and exclusion mapping of human chromosome 8 in 593 affected sib-pair families from the UK and US 109
The Molecular Genetic Architecture of Self-Employment 108
Novel ANKRD11 gene mutation in an individual with a mild phenotype of KBG syndrome associated to a GEFS+ phenotypic spectrum: A case report 108
Totale 14.948
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Categoria #
all - tutte 132.606
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 132.606
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202138 0 0 0 0 0 0 0 0 0 0 0 38
2021/20221.216 162 5 13 17 25 37 61 99 114 43 122 518
2022/20232.729 269 142 84 484 289 467 5 304 470 19 107 89
2023/2024630 138 63 26 20 82 35 2 48 10 14 60 132
2024/20258.987 71 94 518 317 374 360 516 1.576 3.237 1.256 452 216
2025/202613.300 455 3.017 2.758 1.611 1.082 817 1.739 397 559 559 206 100
Totale 32.305