IRIS
GIARDINA, EMILIANO
 Distribuzione geografica
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Continente #
NA - Nord America 32.973
EU - Europa 2.711
AS - Asia 693
SA - Sud America 18
Continente sconosciuto - Info sul continente non disponibili 15
AF - Africa 4
OC - Oceania 4
Totale 36.418
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Nazione #
US - Stati Uniti d'America 32.963
IE - Irlanda 424
DE - Germania 414
UA - Ucraina 401
CN - Cina 372
IT - Italia 347
FR - Francia 233
SE - Svezia 200
PL - Polonia 192
GB - Regno Unito 183
SG - Singapore 117
RU - Federazione Russa 111
FI - Finlandia 101
KR - Corea 89
BE - Belgio 35
KG - Kirghizistan 33
CZ - Repubblica Ceca 24
NL - Olanda 24
JP - Giappone 18
UZ - Uzbekistan 15
IN - India 14
VN - Vietnam 13
EU - Europa 12
BR - Brasile 11
CA - Canada 9
RO - Romania 8
TR - Turchia 6
AT - Austria 4
EG - Egitto 4
ES - Italia 4
A2 - ???statistics.table.value.countryCode.A2??? 3
AU - Australia 3
CL - Cile 3
IR - Iran 3
TW - Taiwan 3
HK - Hong Kong 2
IL - Israele 2
IQ - Iraq 2
AE - Emirati Arabi Uniti 1
AL - Albania 1
AR - Argentina 1
BD - Bangladesh 1
BG - Bulgaria 1
BO - Bolivia 1
DK - Danimarca 1
EC - Ecuador 1
GR - Grecia 1
GT - Guatemala 1
JO - Giordania 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
PE - Perù 1
PT - Portogallo 1
SA - Arabia Saudita 1
Totale 36.418
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Città #
Woodbridge 9.258
Wilmington 9.113
Houston 8.025
Fairfield 1.242
Chandler 761
Ann Arbor 729
Ashburn 579
Seattle 457
Cambridge 411
Dublin 359
Jacksonville 350
Medford 291
Dearborn 219
Kraków 190
New York 163
Beijing 155
Rome 140
Lawrence 133
San Diego 81
Singapore 74
Menlo Park 68
Boardman 54
Moscow 53
Zhengzhou 48
Mülheim 41
Palo Alto 34
Nanjing 28
Milan 27
Brussels 26
London 26
Falls Church 24
Norwalk 24
Brno 22
Redwood City 22
Mountain View 18
Shanghai 17
Guangzhou 16
Hefei 14
Seoul 14
University Park 14
Helsinki 13
Munich 12
Jinan 11
Lappeenranta 10
San Mateo 10
Detroit 9
Los Angeles 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
Indiana 6
Latiano 6
Toronto 6
Auburn Hills 5
Dong Ket 5
Leawood 5
Quzhou 5
Redmond 5
São Paulo 5
Cairo 4
Groningen 4
Hangzhou 4
Hebei 4
Istanbul 4
Nagold 4
Wuhan 4
Amsterdam 3
Augusta 3
Chicago 3
Chongqing 3
Colorado Springs 3
Esslingen am Neckar 3
Phoenix 3
Pisa 3
Prescot 3
Shenyang 3
Vienna 3
Ypsilanti 3
Baotou 2
Briosco 2
Capannori 2
Center 2
Changsha 2
Chennai 2
Chiari 2
Chikuma 2
Clearwater 2
Cologne 2
Totale 33.635
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Nome #
Gonadal mosaicism in hereditary angioedema 469
Mutational analysis of Peroxiredoxin IV: Exclusion of a positional candidate for multinodular goitre 469
Mannose-binding lectin polymorphisms and pulmonary outcome in premature neonates: a pilot study 440
Haplotypes in SLC24A5 Gene as Ancestry Informative Markers in Different Populations 439
Identification of multipotent cytotrophoblast cells from human first trimester chorionic villi 434
R501X and 2282del4 filaggrin mutations do not confer susceptibility to psoriasis and atopic dermatitis in Italian patients [2] 432
Review of nutrient actions on age-related macular degeneration 431
Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis 430
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 427
Forensic DNA challenges: replacing numbers with names of Fosse Ardeatine's victims 425
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 420
Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis 420
Absence of filaggrin mutation in a patient affected by pachyonychia congenita and mild atopic dermatitis 420
Transmission ratio distortion in the spinal muscular atrophy locus: Data from 314 prenatal tests 416
Frequency assessment of 25 SNPs in five different populations 415
Transabdominal coelocentesis as early source of fetal DNA for chromosomal and molecular diagnosis 415
Age-related macular degeneration: insights into inflammatory genes 414
A Pharmacogenetics Study in Mozambican Patients Treated with Nevirapine: Full Resequencing of TRAF3IP2 Gene Shows a Novel Association with SJS/TEN Susceptibility 414
Direct PCR: a new pharmacogenetic approach for the inexpensive testing of HLA-B*57:01 408
Exclusion of CARD15/NOD2 as a candidate susceptibility gene to psoriasis in the Italian population 407
A New Splicing Mutation in the L1CAM Gene Responsible for X-Linked Hydrocephalus (HSAS) 407
The 2011 GeFI collaborative exercise. Concordance study, proficiency testing and Italian population data on the new ENFSI/EDNAP loci D1S1656, D2S441, D10S1248, D12S391, D22S1045 406
A new CYP21A1P/CYP21A2 chimeric gene identified in an Italian woman suffering from classical congenital adrenal hyperplasia form 404
Prenatal diagnosis of spinal muscular atrophy with respiratory distress (SMARD1) in a twin pregnancy [5] 404
A multiplex molecular assay for the detection of uniparental disomy for human chromosome 15 403
Role of genetics in prevention of coronary atherosclerosis 400
Stevens-Johnson syndrome and toxic epidermal necrolysis: an update on pharmacogenetics studies in drug-induced severe skin reaction 399
Common sequence variants in the LOXL1 gene in pigment dispersion syndrome and pigmentary glaucoma 398
The molecular characterization of a depurinated trial DNA sample can be a model to understand the reliability of the results in forensic genetics. 397
A fluorescence-based sequence-specific primer PCR for the screening of HLA-B(*)57:01 396
FLG (filaggrin) null mutations and sunlight exposure: Evidence of a correlation 394
Whole genome amplification and real-time PCR in forensic casework 393
Deletion of Late Cornified Envelope 3B and 3C genes is not associated with atopic dermatitis 388
Psoriatic arthritis and CARD15 gene polymorphisms: no evidence for association in the Italian population 388
Evidence for differential S100 gene over-expression in psoriatic patients from genetically heterogeneous pedigrees 388
The long and winding road: Searching for non-MHC psoriasis susceptibility loci 387
Three-hour analysis of non-invasive foetal sex determination: application of Plexor chemistry 387
A long PCR-based molecular protocol for detecting normal and expanded ZNF9 alleles in myotonic dystrophy type 2 385
Pharmacogenomics of multifactorial diseases: A focus on psoriatic arthritis 385
Clinical trial sponsors' refusal to communicate genetic research results to subjects 384
Frequency assessment of SNPs for forensic identification in different populations 379
Comparative analysis between saliva and buccal swabs as source of DNA: Lesson from HLA-B∗57:01 testing 379
Reliable and versatile immortal muscle cell models from healthy and myotonic dystrophy type 1 primary human myoblasts 379
PSORS2 markers are not associated with psoriatic arthritis in the Italian population 378
In silico and in vitro comparative analysis to select, validate and test SNPs for human identification 378
Association of KIF3A, but not OVOL1 and ACTL9, with atopic eczema in Italian patients 378
Full sequencing of the FLG gene in Italian patients with atopic eczema: evidence of new mutations, but lack of an association 376
Familial Kaposi's Sarcoma in HHV8 infected subjects presenting the G-174C allele of the IL-6 promoter: a possible role for EBV? 375
Two molecular assays for the rapid and inexpensive detection of GJB2 and GJB6 mutations 375
TRAF3IP2 gene is associated with cutaneous extraintestinal manifestations in Inflammatory Bowel Disease 373
Divergent phenotype of two siblings human leukocyte antigen identical, affected by nonclassical and classical congenital adrenal hyperplasia caused by 21-hydroxylase deficiency 370
Association of single nucleotide polymorphisms in the oxidised LDL receptor 1 (OLR1) gene in patients with acute myocardial infarction. 368
Characterization of the loricrin (LOR) gene as a positional candidate for the PSORS4 psoriasis susceptibility locus 365
Population data for 17 Y-chromosome STRs in a sample from Apulia (Southern Italy) 365
The Linosa Study: epidemiological and heritability data of the metabolic syndrome in a Caucasian genetic isolate 363
Co-localization of susceptibility loci for psoriasis (PSORS4) and atopic dermatitis (ATOD2) on human chromosome 1q21 361
A multiplex molecular assay for the detection of uniparental disomy for human chromosome 7 360
May some HCV genotype 1 patients still benefit from dual therapy? The role of very early HCV kinetics 359
Deletion of LCE3C and LCE3B is a susceptibility factor for psoriatic arthritis: a study in Spanish and Italian populations and meta-analysis. 358
Generation of human induced pluripotent stem cells from extraembryonic tissues of fetuses affected by monogenic diseases 357
The psoriasis genetics as a model of complex disease 356
"The Linosa Study": Epidemiological and heritability data of the metabolic syndrome in a Caucasian genetic isolate 356
Rescue of murine silica-induced lung injury and fibrosis by human embryonic stem cells 354
Tumor necrosis factor promoter polymorphism TNF*-857 is a risk allele for psoriatic arthritis independent of the PSORS1 locus. 354
Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. 351
Haplotypes in IL-8 gene are associated to age-related macular degeneration: a case-control study 351
Assessing individual risk for AMD with genetic counseling, family history, and genetic testing 345
Variants in RUNX3 Contribute to Susceptibility to Psoriatic Arthritis, Exhibiting Further Common Ground with Ankylosing Spondylitis 337
Mapping the future of common diseases: lessons from psoriasis 336
Resequencing of FLG gene in atopic dermatitis: the American Society of human genetics 334
Expression and potential role of cellular retinol binding protein I in psoriasis 333
Polymorphisms in ARMS2 (LOC387715) and LOXL1 genes in the Japanese with age-related macular degeneration 329
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 329
Identification of Deletion Carriers in X-Linked Chronic Granulomatous Disease by Real-Time PCR. 328
Insight into genetics of atopic dermatitis: future approaches and directions 321
A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1 311
Fine mapping of the psoriasis susceptibility gene PSORS1: A reassessment of risk associated with a putative risk haplotype lacking HLA-Cw6 310
Meta-analysis confirms the LCE3C_LCE3B deletion as a risk factor for psoriasis in several ethnic groups and finds interaction with HLA-Cw6. 304
Typing of ARMS2 and CFH in age-related macular degeneration: case-control study and assessment of frequency in the Italian population 291
Digenic inheritance of shortened repeat units of the D4Z4 region and a loss-of-function variant in SMCHD1 in a Family with FSHD 291
Application of precision medicine in neurodegenerative diseases 285
Mitochondrial Serine Protease HTRA2 p.G399S in a Female with Di George Syndrome and Parkinson's Disease 278
KIF3A and IL-4 are disease-specific biomarkers for psoriatic arthritis susceptibility 277
Biomolecular index of therapeutic efficacy in psoriasis treated by anti-TNF alpha agents. 268
Towards the application of precision medicine in age-related macular degeneration 261
Identification of Duchenne/Becker muscular dystrophy mosaic carriers through a combined DNA/RNA analysis 256
Atopic Eczema: Genetic Analysis of COL6A5, COL8A1, and COL10A1 in Mediterranean Populations. 231
Facioscapulohumeral muscular dystrophy (FSHD) molecular diagnosis: from traditional technology to the NGS era. 223
The Interplay between miRNA-Related Variants and Age-Related Macular Degeneration: EVIDENCE of Association of MIR146A and MIR27A. 211
Uncovering genetic and non-genetic biomarkers specific for exudative age-related macular degeneration: Significant association of twelve variants 211
Doyne honeycomb retinal dystrophy - functional improvement following subthreshold nanopulse laser treatment: a case report. 209
Heterozygous PLA2G6 Mutation Leads to Iron Accumulation Within Basal Ganglia and Parkinson's Disease. 201
Making progress in education: The EUROFORGEN master degree pilot project in forensic genetics. 200
Limb-Girdle Muscular Dystrophies (LGMDs): The Clinical Application of NGS Analysis, a Family Case Report. 195
The Variability of SMCHD1 Gene in FSHD Patients: Evidence of New Mutations 183
Follicular occlusion tetrad in a male patient with pachyonychia congenita: clinical and genetic analysis 177
Next Generation Sequencing and ALS: known genes, different phenotyphes. 170
Bilateral Retinal Angiomatous Proliferation in a Variant of Retinitis Pigmentosa 167
Migrainous Infarction in a Patient With Sporadic Hemiplegic Migraine and Cystic Fibrosis: A 99mTc-HMPAO Brain SPECT Study. 162
Ngs analysis for molecular diagnosis of Retinitis Pigmentosa (RP): Detection of a novel variant in PRPH2 gene 162
Totale 34.782
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Categoria #
all - tutte 72.758
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 72.758
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202010.493 832 873 687 1.011 855 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
2024/2025111 111 0 0 0 0 0 0 0 0 0 0 0
Totale 36.880