IRIS
GIARDINA, EMILIANO
 Distribuzione geografica
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Continente #
NA - Nord America 33.454
EU - Europa 2.964
AS - Asia 1.343
SA - Sud America 19
Continente sconosciuto - Info sul continente non disponibili 15
AF - Africa 6
OC - Oceania 4
Totale 37.805
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Nazione #
US - Stati Uniti d'America 33.439
SG - Singapore 721
DE - Germania 458
IE - Irlanda 425
UA - Ucraina 401
CN - Cina 398
IT - Italia 380
FR - Francia 237
RU - Federazione Russa 227
SE - Svezia 200
PL - Polonia 192
GB - Regno Unito 187
FI - Finlandia 129
KR - Corea 89
BE - Belgio 41
KG - Kirghizistan 33
NL - Olanda 29
CZ - Repubblica Ceca 24
JP - Giappone 18
UZ - Uzbekistan 16
IN - India 15
CA - Canada 14
VN - Vietnam 14
EU - Europa 12
BR - Brasile 11
ID - Indonesia 11
RO - Romania 9
TR - Turchia 7
AT - Austria 5
EG - Egitto 5
ES - Italia 5
IR - Iran 4
A2 - ???statistics.table.value.countryCode.A2??? 3
AL - Albania 3
AU - Australia 3
CL - Cile 3
IL - Israele 3
LT - Lituania 3
TW - Taiwan 3
BO - Bolivia 2
GR - Grecia 2
HK - Hong Kong 2
IQ - Iraq 2
PH - Filippine 2
AE - Emirati Arabi Uniti 1
AR - Argentina 1
AZ - Azerbaigian 1
BD - Bangladesh 1
BG - Bulgaria 1
CH - Svizzera 1
DK - Danimarca 1
EC - Ecuador 1
GT - Guatemala 1
HR - Croazia 1
JO - Giordania 1
LV - Lettonia 1
MA - Marocco 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
PE - Perù 1
PT - Portogallo 1
SA - Arabia Saudita 1
Totale 37.805
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Città #
Woodbridge 9.258
Wilmington 9.113
Houston 8.025
Fairfield 1.242
Chandler 761
Ann Arbor 729
Singapore 641
Ashburn 584
Seattle 457
Cambridge 411
Dublin 360
Jacksonville 350
Medford 291
Dearborn 219
Kraków 190
New York 163
Beijing 158
Rome 150
Lawrence 133
Santa Clara 131
San Diego 81
Menlo Park 68
Boardman 54
Moscow 53
Munich 51
Zhengzhou 50
Mülheim 41
Helsinki 38
Palo Alto 34
Brussels 31
Milan 29
London 28
Nanjing 28
Falls Church 24
Norwalk 24
Brno 22
Redwood City 22
Los Angeles 19
Mountain View 18
Shanghai 18
Guangzhou 17
Hefei 14
Seoul 14
University Park 14
Jakarta 11
Jinan 11
Lappeenranta 10
San Mateo 10
Toronto 10
Detroit 9
Nürnberg 9
Waanrode 9
Engelhard 8
San Francisco 8
Chengdu 7
Hanoi 7
Kilburn 7
Kunming 7
Nanchang 7
Nuremberg 7
Pune 7
Saint Petersburg 7
Verona 7
Acton 6
Chiswick 6
Council Bluffs 6
Indiana 6
Latiano 6
Auburn Hills 5
Cairo 5
Dong Ket 5
Frankfurt am Main 5
Leawood 5
Quzhou 5
Redmond 5
São Paulo 5
Groningen 4
Hangzhou 4
Hebei 4
Istanbul 4
Nagold 4
Vienna 4
Wuhan 4
Amsterdam 3
Augusta 3
Changsha 3
Chicago 3
Chongqing 3
Colorado Springs 3
Espoo 3
Esslingen am Neckar 3
Paris 3
Phoenix 3
Pisa 3
Prescot 3
Shenyang 3
Ypsilanti 3
Ascoli Piceno 2
Baotou 2
Bengaluru 2
Totale 34.462
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Nome #
Gonadal mosaicism in hereditary angioedema 478
Mutational analysis of Peroxiredoxin IV: Exclusion of a positional candidate for multinodular goitre 474
Mannose-binding lectin polymorphisms and pulmonary outcome in premature neonates: a pilot study 457
Haplotypes in SLC24A5 Gene as Ancestry Informative Markers in Different Populations 457
Review of nutrient actions on age-related macular degeneration 451
Forensic DNA challenges: replacing numbers with names of Fosse Ardeatine's victims 445
Identification of multipotent cytotrophoblast cells from human first trimester chorionic villi 441
R501X and 2282del4 filaggrin mutations do not confer susceptibility to psoriasis and atopic dermatitis in Italian patients [2] 436
Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis 435
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 434
Transmission ratio distortion in the spinal muscular atrophy locus: Data from 314 prenatal tests 432
Transabdominal coelocentesis as early source of fetal DNA for chromosomal and molecular diagnosis 427
Absence of filaggrin mutation in a patient affected by pachyonychia congenita and mild atopic dermatitis 426
Frequency assessment of 25 SNPs in five different populations 424
Age-related macular degeneration: insights into inflammatory genes 424
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 423
Exclusion of CARD15/NOD2 as a candidate susceptibility gene to psoriasis in the Italian population 423
Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis 422
A multiplex molecular assay for the detection of uniparental disomy for human chromosome 15 422
The 2011 GeFI collaborative exercise. Concordance study, proficiency testing and Italian population data on the new ENFSI/EDNAP loci D1S1656, D2S441, D10S1248, D12S391, D22S1045 420
Direct PCR: a new pharmacogenetic approach for the inexpensive testing of HLA-B*57:01 419
A Pharmacogenetics Study in Mozambican Patients Treated with Nevirapine: Full Resequencing of TRAF3IP2 Gene Shows a Novel Association with SJS/TEN Susceptibility 419
A New Splicing Mutation in the L1CAM Gene Responsible for X-Linked Hydrocephalus (HSAS) 416
Evidence for differential S100 gene over-expression in psoriatic patients from genetically heterogeneous pedigrees 411
A new CYP21A1P/CYP21A2 chimeric gene identified in an Italian woman suffering from classical congenital adrenal hyperplasia form 410
Prenatal diagnosis of spinal muscular atrophy with respiratory distress (SMARD1) in a twin pregnancy [5] 410
Common sequence variants in the LOXL1 gene in pigment dispersion syndrome and pigmentary glaucoma 407
A fluorescence-based sequence-specific primer PCR for the screening of HLA-B(*)57:01 406
Role of genetics in prevention of coronary atherosclerosis 404
Stevens-Johnson syndrome and toxic epidermal necrolysis: an update on pharmacogenetics studies in drug-induced severe skin reaction 403
The molecular characterization of a depurinated trial DNA sample can be a model to understand the reliability of the results in forensic genetics. 402
FLG (filaggrin) null mutations and sunlight exposure: Evidence of a correlation 400
Pharmacogenomics of multifactorial diseases: A focus on psoriatic arthritis 399
Reliable and versatile immortal muscle cell models from healthy and myotonic dystrophy type 1 primary human myoblasts 398
Whole genome amplification and real-time PCR in forensic casework 396
Comparative analysis between saliva and buccal swabs as source of DNA: Lesson from HLA-B∗57:01 testing 396
Psoriatic arthritis and CARD15 gene polymorphisms: no evidence for association in the Italian population 395
Three-hour analysis of non-invasive foetal sex determination: application of Plexor chemistry 395
Deletion of Late Cornified Envelope 3B and 3C genes is not associated with atopic dermatitis 394
The long and winding road: Searching for non-MHC psoriasis susceptibility loci 392
A long PCR-based molecular protocol for detecting normal and expanded ZNF9 alleles in myotonic dystrophy type 2 391
In silico and in vitro comparative analysis to select, validate and test SNPs for human identification 391
Clinical trial sponsors' refusal to communicate genetic research results to subjects 389
Familial Kaposi's Sarcoma in HHV8 infected subjects presenting the G-174C allele of the IL-6 promoter: a possible role for EBV? 386
Association of KIF3A, but not OVOL1 and ACTL9, with atopic eczema in Italian patients 386
Frequency assessment of SNPs for forensic identification in different populations 385
Association of single nucleotide polymorphisms in the oxidised LDL receptor 1 (OLR1) gene in patients with acute myocardial infarction. 383
PSORS2 markers are not associated with psoriatic arthritis in the Italian population 382
Full sequencing of the FLG gene in Italian patients with atopic eczema: evidence of new mutations, but lack of an association 381
Two molecular assays for the rapid and inexpensive detection of GJB2 and GJB6 mutations 381
Co-localization of susceptibility loci for psoriasis (PSORS4) and atopic dermatitis (ATOD2) on human chromosome 1q21 377
TRAF3IP2 gene is associated with cutaneous extraintestinal manifestations in Inflammatory Bowel Disease 376
Divergent phenotype of two siblings human leukocyte antigen identical, affected by nonclassical and classical congenital adrenal hyperplasia caused by 21-hydroxylase deficiency 375
"The Linosa Study": Epidemiological and heritability data of the metabolic syndrome in a Caucasian genetic isolate 375
Characterization of the loricrin (LOR) gene as a positional candidate for the PSORS4 psoriasis susceptibility locus 374
Population data for 17 Y-chromosome STRs in a sample from Apulia (Southern Italy) 373
A multiplex molecular assay for the detection of uniparental disomy for human chromosome 7 370
May some HCV genotype 1 patients still benefit from dual therapy? The role of very early HCV kinetics 370
Tumor necrosis factor promoter polymorphism TNF*-857 is a risk allele for psoriatic arthritis independent of the PSORS1 locus. 369
The Linosa Study: epidemiological and heritability data of the metabolic syndrome in a Caucasian genetic isolate 367
Generation of human induced pluripotent stem cells from extraembryonic tissues of fetuses affected by monogenic diseases 364
Deletion of LCE3C and LCE3B is a susceptibility factor for psoriatic arthritis: a study in Spanish and Italian populations and meta-analysis. 364
The psoriasis genetics as a model of complex disease 363
Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. 361
Rescue of murine silica-induced lung injury and fibrosis by human embryonic stem cells 360
Haplotypes in IL-8 gene are associated to age-related macular degeneration: a case-control study 357
Assessing individual risk for AMD with genetic counseling, family history, and genetic testing 355
Variants in RUNX3 Contribute to Susceptibility to Psoriatic Arthritis, Exhibiting Further Common Ground with Ankylosing Spondylitis 346
Mapping the future of common diseases: lessons from psoriasis 343
Resequencing of FLG gene in atopic dermatitis: the American Society of human genetics 341
Expression and potential role of cellular retinol binding protein I in psoriasis 340
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 339
Polymorphisms in ARMS2 (LOC387715) and LOXL1 genes in the Japanese with age-related macular degeneration 336
Identification of Deletion Carriers in X-Linked Chronic Granulomatous Disease by Real-Time PCR. 332
Fine mapping of the psoriasis susceptibility gene PSORS1: A reassessment of risk associated with a putative risk haplotype lacking HLA-Cw6 329
Insight into genetics of atopic dermatitis: future approaches and directions 328
A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1 318
Meta-analysis confirms the LCE3C_LCE3B deletion as a risk factor for psoriasis in several ethnic groups and finds interaction with HLA-Cw6. 316
Application of precision medicine in neurodegenerative diseases 301
Typing of ARMS2 and CFH in age-related macular degeneration: case-control study and assessment of frequency in the Italian population 299
Digenic inheritance of shortened repeat units of the D4Z4 region and a loss-of-function variant in SMCHD1 in a Family with FSHD 295
Mitochondrial Serine Protease HTRA2 p.G399S in a Female with Di George Syndrome and Parkinson's Disease 293
KIF3A and IL-4 are disease-specific biomarkers for psoriatic arthritis susceptibility 283
Biomolecular index of therapeutic efficacy in psoriasis treated by anti-TNF alpha agents. 278
Towards the application of precision medicine in age-related macular degeneration 277
Identification of Duchenne/Becker muscular dystrophy mosaic carriers through a combined DNA/RNA analysis 262
Atopic Eczema: Genetic Analysis of COL6A5, COL8A1, and COL10A1 in Mediterranean Populations. 251
Facioscapulohumeral muscular dystrophy (FSHD) molecular diagnosis: from traditional technology to the NGS era. 236
The Interplay between miRNA-Related Variants and Age-Related Macular Degeneration: EVIDENCE of Association of MIR146A and MIR27A. 233
Uncovering genetic and non-genetic biomarkers specific for exudative age-related macular degeneration: Significant association of twelve variants 218
Doyne honeycomb retinal dystrophy - functional improvement following subthreshold nanopulse laser treatment: a case report. 212
Heterozygous PLA2G6 Mutation Leads to Iron Accumulation Within Basal Ganglia and Parkinson's Disease. 206
Making progress in education: The EUROFORGEN master degree pilot project in forensic genetics. 204
Limb-Girdle Muscular Dystrophies (LGMDs): The Clinical Application of NGS Analysis, a Family Case Report. 204
The Variability of SMCHD1 Gene in FSHD Patients: Evidence of New Mutations 189
Follicular occlusion tetrad in a male patient with pachyonychia congenita: clinical and genetic analysis 186
Defective proteasome biogenesis into skin fibroblasts isolated from Rett syndrome subjects with MeCP2 non-sense mutations 182
Next Generation Sequencing and ALS: known genes, different phenotyphes. 181
PCR-based approach for qualitative molecular analysis of six neurotropic pathogens 175
Bilateral Retinal Angiomatous Proliferation in a Variant of Retinitis Pigmentosa 171
Totale 35.732
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Categoria #
all - tutte 81.234
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 81.234
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20206.235 0 0 0 0 0 1.081 1.035 968 922 894 605 730
2020/20216.210 671 746 675 806 615 606 805 637 170 186 223 70
2021/20221.637 53 140 206 115 88 185 74 76 101 114 109 376
2022/20231.842 167 177 44 256 170 432 152 113 168 11 101 51
2023/2024720 94 24 60 28 63 200 31 13 10 27 9 161
2024/20251.510 127 691 307 216 77 92 0 0 0 0 0 0
Totale 38.279