IRIS
GIARDINA, EMILIANO
 Distribuzione geografica
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Continente #
NA - Nord America 36.454
AS - Asia 5.100
EU - Europa 4.230
SA - Sud America 752
AF - Africa 93
Continente sconosciuto - Info sul continente non disponibili 15
OC - Oceania 4
Totale 46.648
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Nazione #
US - Stati Uniti d'America 36.306
SG - Singapore 2.422
CN - Cina 1.017
RU - Federazione Russa 637
BR - Brasile 622
IT - Italia 597
DE - Germania 587
HK - Hong Kong 462
VN - Vietnam 458
IE - Irlanda 432
UA - Ucraina 408
FR - Francia 390
GB - Regno Unito 270
PL - Polonia 229
SE - Svezia 221
FI - Finlandia 178
JP - Giappone 162
KR - Corea 96
IN - India 92
CA - Canada 83
NL - Olanda 64
ID - Indonesia 59
AR - Argentina 50
AT - Austria 48
BE - Belgio 43
MX - Messico 43
BD - Bangladesh 37
TH - Thailandia 35
TR - Turchia 35
KG - Kirghizistan 34
ZA - Sudafrica 33
ES - Italia 32
UZ - Uzbekistan 32
CZ - Repubblica Ceca 31
PH - Filippine 26
IQ - Iraq 25
EC - Ecuador 17
MY - Malesia 17
RO - Romania 17
CL - Cile 16
MA - Marocco 16
PY - Paraguay 15
PK - Pakistan 14
EG - Egitto 12
EU - Europa 12
CO - Colombia 10
IL - Israele 10
LT - Lituania 10
SA - Arabia Saudita 10
DZ - Algeria 9
VE - Venezuela 9
TN - Tunisia 8
AE - Emirati Arabi Uniti 7
CH - Svizzera 6
IR - Iran 6
KE - Kenya 6
AZ - Azerbaigian 5
JM - Giamaica 5
JO - Giordania 5
NP - Nepal 5
PE - Perù 5
TW - Taiwan 5
BO - Bolivia 4
RS - Serbia 4
UY - Uruguay 4
A2 - ???statistics.table.value.countryCode.A2??? 3
AL - Albania 3
AU - Australia 3
BG - Bulgaria 3
BH - Bahrain 3
CR - Costa Rica 3
GT - Guatemala 3
HN - Honduras 3
HR - Croazia 3
KW - Kuwait 3
PA - Panama 3
PS - Palestinian Territory 3
PT - Portogallo 3
AM - Armenia 2
DK - Danimarca 2
DM - Dominica 2
DO - Repubblica Dominicana 2
GE - Georgia 2
GR - Grecia 2
HU - Ungheria 2
KH - Cambogia 2
LB - Libano 2
NO - Norvegia 2
OM - Oman 2
QA - Qatar 2
SY - Repubblica araba siriana 2
BY - Bielorussia 1
CG - Congo 1
CM - Camerun 1
DJ - Gibuti 1
GH - Ghana 1
KZ - Kazakistan 1
LV - Lettonia 1
LY - Libia 1
MD - Moldavia 1
Totale 46.639
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Città #
Woodbridge 9.259
Wilmington 9.115
Houston 8.042
Singapore 1.287
Fairfield 1.244
Ashburn 846
Chandler 761
Ann Arbor 729
San Jose 609
Beijing 472
Seattle 467
Hong Kong 458
Cambridge 411
Dublin 367
Jacksonville 351
Medford 293
New York 228
Dearborn 219
Los Angeles 206
The Dalles 200
Rome 195
Kraków 190
Santa Clara 166
Council Bluffs 150
Tokyo 143
Ho Chi Minh City 136
Lawrence 134
Hanoi 121
Buffalo 102
Dallas 101
Moscow 99
Munich 94
Lauterbourg 92
Chicago 90
San Diego 81
Menlo Park 68
São Paulo 64
Boardman 57
Helsinki 57
Zhengzhou 51
London 47
Redondo Beach 47
Milan 44
Jakarta 43
Nuremberg 42
Mülheim 41
North Bergen 38
Frankfurt am Main 36
Orem 36
Palo Alto 35
Phoenix 33
Brussels 32
Montreal 32
Bangkok 31
Chennai 31
Salt Lake City 31
Atlanta 30
Nanjing 30
Warsaw 27
Da Nang 26
Johannesburg 26
Norwalk 25
Toronto 25
Falls Church 24
Lappeenranta 23
San Francisco 23
Brno 22
Guangzhou 22
Redwood City 22
Mexico City 21
Shanghai 21
Belo Horizonte 20
Vienna 20
Stockholm 19
Elk Grove Village 18
Mountain View 18
Mumbai 18
Brooklyn 17
Manila 17
Tashkent 17
Turku 17
Ankara 16
Columbus 16
Seoul 16
Boston 15
Denver 15
Haiphong 15
Amsterdam 14
Hefei 14
Paris 14
Poplar 14
Rio de Janeiro 14
University Park 14
Brasília 12
Lancaster 12
Tampa 12
Baghdad 11
Campinas 11
Curitiba 11
Jinan 11
Totale 39.159
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Nome #
Full sequencing of the FLG gene in Italian patients with atopic eczema: evidence of new mutations, but lack of an association 584
Application of precision medicine in neurodegenerative diseases 543
Gonadal mosaicism in hereditary angioedema 528
Mutational analysis of Peroxiredoxin IV: Exclusion of a positional candidate for multinodular goitre 509
Review of nutrient actions on age-related macular degeneration 504
Mannose-binding lectin polymorphisms and pulmonary outcome in premature neonates: a pilot study 495
Haplotypes in SLC24A5 Gene as Ancestry Informative Markers in Different Populations 495
Identification of multipotent cytotrophoblast cells from human first trimester chorionic villi 490
Age-related macular degeneration: insights into inflammatory genes 488
Absence of filaggrin mutation in a patient affected by pachyonychia congenita and mild atopic dermatitis 487
Effects of TNF-α and IL-1 β on the activation of genes related to inflammatory, immune responses and cell death in immortalized human HaCat keratinocytes 485
Forensic DNA challenges: replacing numbers with names of Fosse Ardeatine's victims 483
Exclusion of CARD15/NOD2 as a candidate susceptibility gene to psoriasis in the Italian population 483
A Pharmacogenetics Study in Mozambican Patients Treated with Nevirapine: Full Resequencing of TRAF3IP2 Gene Shows a Novel Association with SJS/TEN Susceptibility 483
Transmission ratio distortion in the spinal muscular atrophy locus: Data from 314 prenatal tests 479
Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis 477
A New Splicing Mutation in the L1CAM Gene Responsible for X-Linked Hydrocephalus (HSAS) 477
R501X and 2282del4 filaggrin mutations do not confer susceptibility to psoriasis and atopic dermatitis in Italian patients [2] 473
The 2011 GeFI collaborative exercise. Concordance study, proficiency testing and Italian population data on the new ENFSI/EDNAP loci D1S1656, D2S441, D10S1248, D12S391, D22S1045 470
A new CYP21A1P/CYP21A2 chimeric gene identified in an Italian woman suffering from classical congenital adrenal hyperplasia form 469
Frequency assessment of 25 SNPs in five different populations 469
A multiplex molecular assay for the detection of uniparental disomy for human chromosome 15 469
Direct PCR: a new pharmacogenetic approach for the inexpensive testing of HLA-B*57:01 464
Transabdominal coelocentesis as early source of fetal DNA for chromosomal and molecular diagnosis 460
Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis 456
A fluorescence-based sequence-specific primer PCR for the screening of HLA-B(*)57:01 455
Linkage between I172N mutation, a marker of 21-hydroxylase deficiency, and a single nucleotide polymorphism in Int6 of CYP21B gene: A genetic study of Sardinian family 453
Evidence for differential S100 gene over-expression in psoriatic patients from genetically heterogeneous pedigrees 450
Comparative analysis between saliva and buccal swabs as source of DNA: Lesson from HLA-B∗57:01 testing 449
Stevens-Johnson syndrome and toxic epidermal necrolysis: an update on pharmacogenetics studies in drug-induced severe skin reaction 449
A long PCR-based molecular protocol for detecting normal and expanded ZNF9 alleles in myotonic dystrophy type 2 448
Role of genetics in prevention of coronary atherosclerosis 447
The long and winding road: Searching for non-MHC psoriasis susceptibility loci 446
Prenatal diagnosis of spinal muscular atrophy with respiratory distress (SMARD1) in a twin pregnancy [5] 444
Typing of ARMS2 and CFH in age-related macular degeneration: case-control study and assessment of frequency in the Italian population 443
Common sequence variants in the LOXL1 gene in pigment dispersion syndrome and pigmentary glaucoma 443
FLG (filaggrin) null mutations and sunlight exposure: Evidence of a correlation 441
Whole genome amplification and real-time PCR in forensic casework 440
"The Linosa Study": Epidemiological and heritability data of the metabolic syndrome in a Caucasian genetic isolate 440
Association of single nucleotide polymorphisms in the oxidised LDL receptor 1 (OLR1) gene in patients with acute myocardial infarction. 438
Pharmacogenomics of multifactorial diseases: A focus on psoriatic arthritis 437
Reliable and versatile immortal muscle cell models from healthy and myotonic dystrophy type 1 primary human myoblasts 437
The molecular characterization of a depurinated trial DNA sample can be a model to understand the reliability of the results in forensic genetics. 436
Familial Kaposi's Sarcoma in HHV8 infected subjects presenting the G-174C allele of the IL-6 promoter: a possible role for EBV? 431
Three-hour analysis of non-invasive foetal sex determination: application of Plexor chemistry 431
Psoriatic arthritis and CARD15 gene polymorphisms: no evidence for association in the Italian population 429
Deletion of Late Cornified Envelope 3B and 3C genes is not associated with atopic dermatitis 425
Population data for 17 Y-chromosome STRs in a sample from Apulia (Southern Italy) 422
A multiplex molecular assay for the detection of uniparental disomy for human chromosome 7 421
Association of KIF3A, but not OVOL1 and ACTL9, with atopic eczema in Italian patients 421
May some HCV genotype 1 patients still benefit from dual therapy? The role of very early HCV kinetics 421
In silico and in vitro comparative analysis to select, validate and test SNPs for human identification 420
Two molecular assays for the rapid and inexpensive detection of GJB2 and GJB6 mutations 419
TRAF3IP2 gene is associated with cutaneous extraintestinal manifestations in Inflammatory Bowel Disease 418
Co-localization of susceptibility loci for psoriasis (PSORS4) and atopic dermatitis (ATOD2) on human chromosome 1q21 417
Clinical trial sponsors' refusal to communicate genetic research results to subjects 417
Characterization of the loricrin (LOR) gene as a positional candidate for the PSORS4 psoriasis susceptibility locus 416
Assessing individual risk for AMD with genetic counseling, family history, and genetic testing 415
PSORS2 markers are not associated with psoriatic arthritis in the Italian population 414
Frequency assessment of SNPs for forensic identification in different populations 413
Divergent phenotype of two siblings human leukocyte antigen identical, affected by nonclassical and classical congenital adrenal hyperplasia caused by 21-hydroxylase deficiency 409
The Linosa Study: epidemiological and heritability data of the metabolic syndrome in a Caucasian genetic isolate 399
Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. 399
Rescue of murine silica-induced lung injury and fibrosis by human embryonic stem cells 398
Tumor necrosis factor promoter polymorphism TNF*-857 is a risk allele for psoriatic arthritis independent of the PSORS1 locus. 398
Haplotypes in IL-8 gene are associated to age-related macular degeneration: a case-control study 397
Deletion of LCE3C and LCE3B is a susceptibility factor for psoriatic arthritis: a study in Spanish and Italian populations and meta-analysis. 395
The psoriasis genetics as a model of complex disease 394
Expression and potential role of cellular retinol binding protein I in psoriasis 394
Generation of human induced pluripotent stem cells from extraembryonic tissues of fetuses affected by monogenic diseases 392
Next generation sequencing and linkage analysis for the molecular diagnosis of a novel overlapping syndrome characterized by hypertrophic cardiomyopathy and typical electrical instability of brugada syndrome 385
A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1 383
Variants in RUNX3 Contribute to Susceptibility to Psoriatic Arthritis, Exhibiting Further Common Ground with Ankylosing Spondylitis 382
Mapping the future of common diseases: lessons from psoriasis 381
Resequencing of FLG gene in atopic dermatitis: the American Society of human genetics 374
Polymorphisms in ARMS2 (LOC387715) and LOXL1 genes in the Japanese with age-related macular degeneration 372
Fine mapping of the psoriasis susceptibility gene PSORS1: A reassessment of risk associated with a putative risk haplotype lacking HLA-Cw6 370
Identification of Deletion Carriers in X-Linked Chronic Granulomatous Disease by Real-Time PCR. 368
Insight into genetics of atopic dermatitis: future approaches and directions 359
Meta-analysis confirms the LCE3C_LCE3B deletion as a risk factor for psoriasis in several ethnic groups and finds interaction with HLA-Cw6. 353
Digenic inheritance of shortened repeat units of the D4Z4 region and a loss-of-function variant in SMCHD1 in a Family with FSHD 345
Mitochondrial Serine Protease HTRA2 p.G399S in a Female with Di George Syndrome and Parkinson's Disease 336
Biomolecular index of therapeutic efficacy in psoriasis treated by anti-TNF alpha agents. 334
KIF3A and IL-4 are disease-specific biomarkers for psoriatic arthritis susceptibility 322
Towards the application of precision medicine in age-related macular degeneration 313
Atopic Eczema: Genetic Analysis of COL6A5, COL8A1, and COL10A1 in Mediterranean Populations. 305
Identification of Duchenne/Becker muscular dystrophy mosaic carriers through a combined DNA/RNA analysis 300
Facioscapulohumeral muscular dystrophy (FSHD) molecular diagnosis: from traditional technology to the NGS era. 290
The Interplay between miRNA-Related Variants and Age-Related Macular Degeneration: EVIDENCE of Association of MIR146A and MIR27A. 274
Uncovering genetic and non-genetic biomarkers specific for exudative age-related macular degeneration: Significant association of twelve variants 260
Doyne honeycomb retinal dystrophy - functional improvement following subthreshold nanopulse laser treatment: a case report. 249
Defective proteasome biogenesis into skin fibroblasts isolated from Rett syndrome subjects with MeCP2 non-sense mutations 247
Making progress in education: The EUROFORGEN master degree pilot project in forensic genetics. 246
Limb-Girdle Muscular Dystrophies (LGMDs): The Clinical Application of NGS Analysis, a Family Case Report. 238
Heterozygous PLA2G6 Mutation Leads to Iron Accumulation Within Basal Ganglia and Parkinson's Disease. 236
Follicular occlusion tetrad in a male patient with pachyonychia congenita: clinical and genetic analysis 236
The Variability of SMCHD1 Gene in FSHD Patients: Evidence of New Mutations 225
Structural modeling of altered CLCN1 conformation following a novel mutation in a patient affected by autosomal dominant myotonia congenita (Thomsen disease) 223
Next Generation Sequencing and ALS: known genes, different phenotyphes. 210
Migrainous Infarction in a Patient With Sporadic Hemiplegic Migraine and Cystic Fibrosis: A 99mTc-HMPAO Brain SPECT Study. 206
Totale 40.463
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Categoria #
all - tutte 113.112
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 113.112
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021480 0 0 0 0 0 0 0 0 0 186 224 70
2021/20221.642 53 140 206 115 89 185 74 76 102 114 109 379
2022/20231.846 168 177 44 256 170 434 153 113 168 11 101 51
2023/2024722 94 24 60 28 64 200 31 13 10 27 9 162
2024/20254.136 127 697 308 217 77 189 381 197 605 505 426 407
2025/20266.378 554 323 874 653 612 193 892 835 827 615 0 0
Totale 47.299