IRIS
GIARDINA, EMILIANO
 Distribuzione geografica
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Continente #
NA - Nord America 33.726
EU - Europa 3.075
AS - Asia 2.002
SA - Sud America 185
AF - Africa 19
Continente sconosciuto - Info sul continente non disponibili 15
OC - Oceania 4
Totale 39.026
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Nazione #
US - Stati Uniti d'America 33.705
SG - Singapore 1.015
DE - Germania 497
IE - Irlanda 428
CN - Cina 424
UA - Ucraina 401
IT - Italia 398
HK - Hong Kong 306
FR - Francia 237
RU - Federazione Russa 234
SE - Svezia 201
PL - Polonia 192
GB - Regno Unito 188
BR - Brasile 163
FI - Finlandia 130
KR - Corea 89
BE - Belgio 41
NL - Olanda 35
AT - Austria 33
KG - Kirghizistan 33
CZ - Repubblica Ceca 24
UZ - Uzbekistan 22
IN - India 18
JP - Giappone 18
CA - Canada 15
VN - Vietnam 14
EU - Europa 12
ID - Indonesia 12
RO - Romania 11
TR - Turchia 10
EG - Egitto 7
AR - Argentina 6
IQ - Iraq 6
MA - Marocco 6
CH - Svizzera 5
ES - Italia 5
IL - Israele 5
MX - Messico 5
AZ - Azerbaigian 4
EC - Ecuador 4
IR - Iran 4
A2 - ???statistics.table.value.countryCode.A2??? 3
AE - Emirati Arabi Uniti 3
AL - Albania 3
AU - Australia 3
BD - Bangladesh 3
CL - Cile 3
LT - Lituania 3
PK - Pakistan 3
TN - Tunisia 3
TW - Taiwan 3
BG - Bulgaria 2
BO - Bolivia 2
GR - Grecia 2
JO - Giordania 2
PE - Perù 2
PH - Filippine 2
PY - Paraguay 2
ZA - Sudafrica 2
AM - Armenia 1
CO - Colombia 1
DK - Danimarca 1
GE - Georgia 1
GT - Guatemala 1
HR - Croazia 1
KE - Kenya 1
KZ - Kazakistan 1
LV - Lettonia 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
OM - Oman 1
PS - Palestinian Territory 1
PT - Portogallo 1
SA - Arabia Saudita 1
UY - Uruguay 1
VE - Venezuela 1
Totale 39.026
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Città #
Woodbridge 9.259
Wilmington 9.113
Houston 8.025
Fairfield 1.244
Chandler 761
Ann Arbor 729
Singapore 687
Ashburn 587
Seattle 459
Cambridge 411
Dublin 363
Jacksonville 350
Hong Kong 306
Medford 293
Dearborn 219
Kraków 190
New York 163
Beijing 158
Rome 155
Santa Clara 135
Lawrence 134
San Diego 81
Council Bluffs 75
Menlo Park 68
Boardman 54
Moscow 54
Munich 51
Zhengzhou 50
The Dalles 47
Mülheim 41
Helsinki 38
Nuremberg 34
Palo Alto 34
Brussels 31
Milan 29
London 28
Nanjing 28
Falls Church 24
Norwalk 24
Brno 22
Guangzhou 22
Los Angeles 22
Redwood City 22
Shanghai 19
Mountain View 18
Vienna 17
Hefei 14
Seoul 14
University Park 14
Jakarta 11
Jinan 11
Lappeenranta 11
San Mateo 10
São Paulo 10
Toronto 10
Detroit 9
Nürnberg 9
Waanrode 9
Chicago 8
Engelhard 8
North Bergen 8
San Francisco 8
Chengdu 7
Hanoi 7
Kilburn 7
Kunming 7
Nanchang 7
Pune 7
Saint Petersburg 7
Shenzhen 7
Tashkent 7
Verona 7
Acton 6
Belo Horizonte 6
Cairo 6
Chiswick 6
Indiana 6
Latiano 6
Auburn Hills 5
Dong Ket 5
Frankfurt am Main 5
Istanbul 5
Leawood 5
Quzhou 5
Redmond 5
Baku 4
Bern 4
Campinas 4
Groningen 4
Hangzhou 4
Hebei 4
Nagold 4
Wuhan 4
Amsterdam 3
Augusta 3
Brasília 3
Buffalo 3
Cangzhou 3
Changsha 3
Chongqing 3
Totale 35.032
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Nome #
Gonadal mosaicism in hereditary angioedema 485
Mutational analysis of Peroxiredoxin IV: Exclusion of a positional candidate for multinodular goitre 475
Mannose-binding lectin polymorphisms and pulmonary outcome in premature neonates: a pilot study 466
Haplotypes in SLC24A5 Gene as Ancestry Informative Markers in Different Populations 462
Review of nutrient actions on age-related macular degeneration 457
Forensic DNA challenges: replacing numbers with names of Fosse Ardeatine's victims 454
Identification of multipotent cytotrophoblast cells from human first trimester chorionic villi 449
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 446
Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis 442
R501X and 2282del4 filaggrin mutations do not confer susceptibility to psoriasis and atopic dermatitis in Italian patients [2] 442
Transmission ratio distortion in the spinal muscular atrophy locus: Data from 314 prenatal tests 441
Exclusion of CARD15/NOD2 as a candidate susceptibility gene to psoriasis in the Italian population 438
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 437
Age-related macular degeneration: insights into inflammatory genes 437
Absence of filaggrin mutation in a patient affected by pachyonychia congenita and mild atopic dermatitis 431
A multiplex molecular assay for the detection of uniparental disomy for human chromosome 15 430
Transabdominal coelocentesis as early source of fetal DNA for chromosomal and molecular diagnosis 430
Frequency assessment of 25 SNPs in five different populations 429
Direct PCR: a new pharmacogenetic approach for the inexpensive testing of HLA-B*57:01 426
A Pharmacogenetics Study in Mozambican Patients Treated with Nevirapine: Full Resequencing of TRAF3IP2 Gene Shows a Novel Association with SJS/TEN Susceptibility 426
Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis 425
The 2011 GeFI collaborative exercise. Concordance study, proficiency testing and Italian population data on the new ENFSI/EDNAP loci D1S1656, D2S441, D10S1248, D12S391, D22S1045 423
A New Splicing Mutation in the L1CAM Gene Responsible for X-Linked Hydrocephalus (HSAS) 421
A new CYP21A1P/CYP21A2 chimeric gene identified in an Italian woman suffering from classical congenital adrenal hyperplasia form 415
Common sequence variants in the LOXL1 gene in pigment dispersion syndrome and pigmentary glaucoma 415
Stevens-Johnson syndrome and toxic epidermal necrolysis: an update on pharmacogenetics studies in drug-induced severe skin reaction 414
Evidence for differential S100 gene over-expression in psoriatic patients from genetically heterogeneous pedigrees 413
Prenatal diagnosis of spinal muscular atrophy with respiratory distress (SMARD1) in a twin pregnancy [5] 413
A fluorescence-based sequence-specific primer PCR for the screening of HLA-B(*)57:01 411
Reliable and versatile immortal muscle cell models from healthy and myotonic dystrophy type 1 primary human myoblasts 410
Pharmacogenomics of multifactorial diseases: A focus on psoriatic arthritis 409
The molecular characterization of a depurinated trial DNA sample can be a model to understand the reliability of the results in forensic genetics. 408
Role of genetics in prevention of coronary atherosclerosis 407
FLG (filaggrin) null mutations and sunlight exposure: Evidence of a correlation 407
Psoriatic arthritis and CARD15 gene polymorphisms: no evidence for association in the Italian population 404
Comparative analysis between saliva and buccal swabs as source of DNA: Lesson from HLA-B∗57:01 testing 403
Whole genome amplification and real-time PCR in forensic casework 401
Deletion of Late Cornified Envelope 3B and 3C genes is not associated with atopic dermatitis 400
Three-hour analysis of non-invasive foetal sex determination: application of Plexor chemistry 399
A long PCR-based molecular protocol for detecting normal and expanded ZNF9 alleles in myotonic dystrophy type 2 398
Familial Kaposi's Sarcoma in HHV8 infected subjects presenting the G-174C allele of the IL-6 promoter: a possible role for EBV? 397
The long and winding road: Searching for non-MHC psoriasis susceptibility loci 396
Clinical trial sponsors' refusal to communicate genetic research results to subjects 395
Association of KIF3A, but not OVOL1 and ACTL9, with atopic eczema in Italian patients 394
In silico and in vitro comparative analysis to select, validate and test SNPs for human identification 393
Full sequencing of the FLG gene in Italian patients with atopic eczema: evidence of new mutations, but lack of an association 389
Association of single nucleotide polymorphisms in the oxidised LDL receptor 1 (OLR1) gene in patients with acute myocardial infarction. 389
Frequency assessment of SNPs for forensic identification in different populations 388
Co-localization of susceptibility loci for psoriasis (PSORS4) and atopic dermatitis (ATOD2) on human chromosome 1q21 385
PSORS2 markers are not associated with psoriatic arthritis in the Italian population 385
"The Linosa Study": Epidemiological and heritability data of the metabolic syndrome in a Caucasian genetic isolate 385
Two molecular assays for the rapid and inexpensive detection of GJB2 and GJB6 mutations 385
Characterization of the loricrin (LOR) gene as a positional candidate for the PSORS4 psoriasis susceptibility locus 381
TRAF3IP2 gene is associated with cutaneous extraintestinal manifestations in Inflammatory Bowel Disease 380
Population data for 17 Y-chromosome STRs in a sample from Apulia (Southern Italy) 380
Divergent phenotype of two siblings human leukocyte antigen identical, affected by nonclassical and classical congenital adrenal hyperplasia caused by 21-hydroxylase deficiency 379
May some HCV genotype 1 patients still benefit from dual therapy? The role of very early HCV kinetics 378
A multiplex molecular assay for the detection of uniparental disomy for human chromosome 7 377
Tumor necrosis factor promoter polymorphism TNF*-857 is a risk allele for psoriatic arthritis independent of the PSORS1 locus. 373
The psoriasis genetics as a model of complex disease 371
Deletion of LCE3C and LCE3B is a susceptibility factor for psoriatic arthritis: a study in Spanish and Italian populations and meta-analysis. 369
The Linosa Study: epidemiological and heritability data of the metabolic syndrome in a Caucasian genetic isolate 368
Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. 366
Rescue of murine silica-induced lung injury and fibrosis by human embryonic stem cells 365
Generation of human induced pluripotent stem cells from extraembryonic tissues of fetuses affected by monogenic diseases 365
Haplotypes in IL-8 gene are associated to age-related macular degeneration: a case-control study 362
Assessing individual risk for AMD with genetic counseling, family history, and genetic testing 361
Variants in RUNX3 Contribute to Susceptibility to Psoriatic Arthritis, Exhibiting Further Common Ground with Ankylosing Spondylitis 354
Mapping the future of common diseases: lessons from psoriasis 349
Resequencing of FLG gene in atopic dermatitis: the American Society of human genetics 348
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 346
Expression and potential role of cellular retinol binding protein I in psoriasis 341
Polymorphisms in ARMS2 (LOC387715) and LOXL1 genes in the Japanese with age-related macular degeneration 339
Identification of Deletion Carriers in X-Linked Chronic Granulomatous Disease by Real-Time PCR. 339
Fine mapping of the psoriasis susceptibility gene PSORS1: A reassessment of risk associated with a putative risk haplotype lacking HLA-Cw6 334
Insight into genetics of atopic dermatitis: future approaches and directions 330
Meta-analysis confirms the LCE3C_LCE3B deletion as a risk factor for psoriasis in several ethnic groups and finds interaction with HLA-Cw6. 326
A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1 321
Application of precision medicine in neurodegenerative diseases 312
Typing of ARMS2 and CFH in age-related macular degeneration: case-control study and assessment of frequency in the Italian population 300
Mitochondrial Serine Protease HTRA2 p.G399S in a Female with Di George Syndrome and Parkinson's Disease 299
Digenic inheritance of shortened repeat units of the D4Z4 region and a loss-of-function variant in SMCHD1 in a Family with FSHD 298
KIF3A and IL-4 are disease-specific biomarkers for psoriatic arthritis susceptibility 294
Biomolecular index of therapeutic efficacy in psoriasis treated by anti-TNF alpha agents. 285
Towards the application of precision medicine in age-related macular degeneration 280
Identification of Duchenne/Becker muscular dystrophy mosaic carriers through a combined DNA/RNA analysis 267
Atopic Eczema: Genetic Analysis of COL6A5, COL8A1, and COL10A1 in Mediterranean Populations. 255
Facioscapulohumeral muscular dystrophy (FSHD) molecular diagnosis: from traditional technology to the NGS era. 240
The Interplay between miRNA-Related Variants and Age-Related Macular Degeneration: EVIDENCE of Association of MIR146A and MIR27A. 238
Uncovering genetic and non-genetic biomarkers specific for exudative age-related macular degeneration: Significant association of twelve variants 222
Doyne honeycomb retinal dystrophy - functional improvement following subthreshold nanopulse laser treatment: a case report. 220
Heterozygous PLA2G6 Mutation Leads to Iron Accumulation Within Basal Ganglia and Parkinson's Disease. 212
Limb-Girdle Muscular Dystrophies (LGMDs): The Clinical Application of NGS Analysis, a Family Case Report. 212
Making progress in education: The EUROFORGEN master degree pilot project in forensic genetics. 209
Defective proteasome biogenesis into skin fibroblasts isolated from Rett syndrome subjects with MeCP2 non-sense mutations 197
The Variability of SMCHD1 Gene in FSHD Patients: Evidence of New Mutations 194
Next Generation Sequencing and ALS: known genes, different phenotyphes. 190
Follicular occlusion tetrad in a male patient with pachyonychia congenita: clinical and genetic analysis 189
PCR-based approach for qualitative molecular analysis of six neurotropic pathogens 179
Migrainous Infarction in a Patient With Sporadic Hemiplegic Migraine and Cystic Fibrosis: A 99mTc-HMPAO Brain SPECT Study. 176
Totale 36.350
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Categoria #
all - tutte 88.267
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 88.267
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20202.229 0 0 0 0 0 0 0 0 0 894 605 730
2020/20216.213 671 746 675 806 615 606 805 637 172 186 224 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
2024/20252.894 127 697 308 217 77 190 383 197 615 83 0 0
Totale 39.679