IRIS
GIARDINA, EMILIANO
 Distribuzione geografica
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Continente #
NA - Nord America 39.091
AS - Asia 5.376
EU - Europa 4.498
SA - Sud America 798
Continente sconosciuto - Info sul continente non disponibili 697
AF - Africa 98
OC - Oceania 4
Totale 50.562
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Nazione #
US - Stati Uniti d'America 38.823
SG - Singapore 2.444
CN - Cina 1.061
IT - Italia 798
BR - Brasile 646
RU - Federazione Russa 637
DE - Germania 588
VN - Vietnam 469
HK - Hong Kong 466
IE - Irlanda 434
UA - Ucraina 409
FR - Francia 394
GB - Regno Unito 291
SE - Svezia 239
PL - Polonia 230
BD - Bangladesh 195
FI - Finlandia 178
JP - Giappone 167
CA - Canada 137
KR - Corea 97
IN - India 94
NL - Olanda 69
ID - Indonesia 67
AR - Argentina 53
AT - Austria 48
MX - Messico 45
BE - Belgio 43
TH - Thailandia 37
TR - Turchia 37
ES - Italia 34
KG - Kirghizistan 34
ZA - Sudafrica 33
CZ - Repubblica Ceca 32
UZ - Uzbekistan 32
PH - Filippine 29
IQ - Iraq 25
CO - Colombia 23
JM - Giamaica 22
EC - Ecuador 21
MY - Malesia 21
PK - Pakistan 17
RO - Romania 17
CL - Cile 16
MA - Marocco 16
PY - Paraguay 15
CR - Costa Rica 13
EG - Egitto 12
EU - Europa 12
SA - Arabia Saudita 12
VE - Venezuela 11
GT - Guatemala 10
IL - Israele 10
LT - Lituania 10
DZ - Algeria 9
HN - Honduras 9
NI - Nicaragua 9
AE - Emirati Arabi Uniti 8
TN - Tunisia 8
IR - Iran 7
NP - Nepal 7
CH - Svizzera 6
KE - Kenya 6
AZ - Azerbaigian 5
EE - Estonia 5
JO - Giordania 5
PE - Perù 5
SV - El Salvador 5
TW - Taiwan 5
AL - Albania 4
BO - Bolivia 4
DK - Danimarca 4
HR - Croazia 4
PT - Portogallo 4
RS - Serbia 4
UY - Uruguay 4
A2 - ???statistics.table.value.countryCode.A2??? 3
AU - Australia 3
BG - Bulgaria 3
BH - Bahrain 3
GR - Grecia 3
KW - Kuwait 3
PA - Panama 3
PS - Palestinian Territory 3
TT - Trinidad e Tobago 3
AM - Armenia 2
CG - Congo 2
DM - Dominica 2
DO - Repubblica Dominicana 2
GE - Georgia 2
GP - Guadalupe 2
HU - Ungheria 2
KH - Cambogia 2
KZ - Kazakistan 2
LB - Libano 2
LY - Libia 2
NG - Nigeria 2
NO - Norvegia 2
OM - Oman 2
PR - Porto Rico 2
QA - Qatar 2
Totale 49.859
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Città #
Woodbridge 9.259
Wilmington 9.117
Houston 8.046
Singapore 1.299
Fairfield 1.244
Ashburn 1.163
San Jose 830
Chandler 761
Ann Arbor 729
Beijing 478
Seattle 478
Hong Kong 460
Cambridge 413
Dublin 367
Jacksonville 354
Council Bluffs 343
Medford 293
New York 263
Los Angeles 241
Dearborn 219
Rome 216
Santa Clara 205
The Dalles 200
Kraków 190
Tokyo 148
Ho Chi Minh City 143
Lawrence 134
Hanoi 123
Dallas 120
Buffalo 116
Chicago 112
Moscow 99
Munich 94
Lauterbourg 92
San Diego 82
Milan 72
São Paulo 69
Menlo Park 68
Denver 65
Boardman 59
Helsinki 57
Zhengzhou 51
London 49
Phoenix 49
Atlanta 47
Redondo Beach 47
Jakarta 44
Montreal 42
Nuremberg 42
Mülheim 41
North Bergen 39
Toronto 39
Salt Lake City 38
Orem 37
Frankfurt am Main 36
Palo Alto 35
Bangkok 33
Brussels 32
Chennai 31
San Francisco 31
Nanjing 30
Brooklyn 28
Norwalk 27
Warsaw 27
Da Nang 26
Johannesburg 26
Falls Church 25
Lappeenranta 23
Monte Vista 23
Brno 22
Guangzhou 22
Mexico City 22
Redwood City 22
Shanghai 21
Belo Horizonte 20
Vienna 20
Elk Grove Village 19
Stockholm 19
Mountain View 18
Mumbai 18
Ankara 17
Charlotte 17
Columbus 17
Manila 17
Tashkent 17
Turku 17
Boston 16
Brasília 16
Detroit 16
Seoul 16
Amsterdam 15
Florence 15
Haiphong 15
Miami 15
Tampa 15
Hefei 14
Kingston 14
Lancaster 14
Paris 14
Philadelphia 14
Totale 40.353
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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 597
Application of precision medicine in neurodegenerative diseases 558
Gonadal mosaicism in hereditary angioedema 538
Review of nutrient actions on age-related macular degeneration 525
Mannose-binding lectin polymorphisms and pulmonary outcome in premature neonates: a pilot study 524
Mutational analysis of Peroxiredoxin IV: Exclusion of a positional candidate for multinodular goitre 522
Age-related macular degeneration: insights into inflammatory genes 512
Haplotypes in SLC24A5 Gene as Ancestry Informative Markers in Different Populations 509
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 506
Identification of multipotent cytotrophoblast cells from human first trimester chorionic villi 506
Transmission ratio distortion in the spinal muscular atrophy locus: Data from 314 prenatal tests 504
A Pharmacogenetics Study in Mozambican Patients Treated with Nevirapine: Full Resequencing of TRAF3IP2 Gene Shows a Novel Association with SJS/TEN Susceptibility 503
Exclusion of CARD15/NOD2 as a candidate susceptibility gene to psoriasis in the Italian population 501
Absence of filaggrin mutation in a patient affected by pachyonychia congenita and mild atopic dermatitis 501
Forensic DNA challenges: replacing numbers with names of Fosse Ardeatine's victims 500
Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis 497
A New Splicing Mutation in the L1CAM Gene Responsible for X-Linked Hydrocephalus (HSAS) 491
A new CYP21A1P/CYP21A2 chimeric gene identified in an Italian woman suffering from classical congenital adrenal hyperplasia form 486
R501X and 2282del4 filaggrin mutations do not confer susceptibility to psoriasis and atopic dermatitis in Italian patients [2] 484
Direct PCR: a new pharmacogenetic approach for the inexpensive testing of HLA-B*57:01 482
The 2011 GeFI collaborative exercise. Concordance study, proficiency testing and Italian population data on the new ENFSI/EDNAP loci D1S1656, D2S441, D10S1248, D12S391, D22S1045 480
A multiplex molecular assay for the detection of uniparental disomy for human chromosome 15 479
Frequency assessment of 25 SNPs in five different populations 478
Transabdominal coelocentesis as early source of fetal DNA for chromosomal and molecular diagnosis 473
Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis 472
Comparative analysis between saliva and buccal swabs as source of DNA: Lesson from HLA-B∗57:01 testing 471
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 470
A fluorescence-based sequence-specific primer PCR for the screening of HLA-B(*)57:01 469
A long PCR-based molecular protocol for detecting normal and expanded ZNF9 alleles in myotonic dystrophy type 2 466
Evidence for differential S100 gene over-expression in psoriatic patients from genetically heterogeneous pedigrees 465
Role of genetics in prevention of coronary atherosclerosis 461
Stevens-Johnson syndrome and toxic epidermal necrolysis: an update on pharmacogenetics studies in drug-induced severe skin reaction 460
The long and winding road: Searching for non-MHC psoriasis susceptibility loci 457
Whole genome amplification and real-time PCR in forensic casework 456
Common sequence variants in the LOXL1 gene in pigment dispersion syndrome and pigmentary glaucoma 456
Prenatal diagnosis of spinal muscular atrophy with respiratory distress (SMARD1) in a twin pregnancy [5] 454
"The Linosa Study": Epidemiological and heritability data of the metabolic syndrome in a Caucasian genetic isolate 453
FLG (filaggrin) null mutations and sunlight exposure: Evidence of a correlation 453
Typing of ARMS2 and CFH in age-related macular degeneration: case-control study and assessment of frequency in the Italian population 452
Three-hour analysis of non-invasive foetal sex determination: application of Plexor chemistry 451
Reliable and versatile immortal muscle cell models from healthy and myotonic dystrophy type 1 primary human myoblasts 451
Pharmacogenomics of multifactorial diseases: A focus on psoriatic arthritis 450
May some HCV genotype 1 patients still benefit from dual therapy? The role of very early HCV kinetics 449
Psoriatic arthritis and CARD15 gene polymorphisms: no evidence for association in the Italian population 446
Association of single nucleotide polymorphisms in the oxidised LDL receptor 1 (OLR1) gene in patients with acute myocardial infarction. 446
TRAF3IP2 gene is associated with cutaneous extraintestinal manifestations in Inflammatory Bowel Disease 445
The molecular characterization of a depurinated trial DNA sample can be a model to understand the reliability of the results in forensic genetics. 445
Familial Kaposi's Sarcoma in HHV8 infected subjects presenting the G-174C allele of the IL-6 promoter: a possible role for EBV? 442
A multiplex molecular assay for the detection of uniparental disomy for human chromosome 7 441
PSORS2 markers are not associated with psoriatic arthritis in the Italian population 438
Characterization of the loricrin (LOR) gene as a positional candidate for the PSORS4 psoriasis susceptibility locus 436
Deletion of Late Cornified Envelope 3B and 3C genes is not associated with atopic dermatitis 435
Two molecular assays for the rapid and inexpensive detection of GJB2 and GJB6 mutations 433
Assessing individual risk for AMD with genetic counseling, family history, and genetic testing 432
In silico and in vitro comparative analysis to select, validate and test SNPs for human identification 430
Population data for 17 Y-chromosome STRs in a sample from Apulia (Southern Italy) 430
Co-localization of susceptibility loci for psoriasis (PSORS4) and atopic dermatitis (ATOD2) on human chromosome 1q21 429
Association of KIF3A, but not OVOL1 and ACTL9, with atopic eczema in Italian patients 429
Clinical trial sponsors' refusal to communicate genetic research results to subjects 426
Divergent phenotype of two siblings human leukocyte antigen identical, affected by nonclassical and classical congenital adrenal hyperplasia caused by 21-hydroxylase deficiency 425
Frequency assessment of SNPs for forensic identification in different populations 423
A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1 419
The Linosa Study: epidemiological and heritability data of the metabolic syndrome in a Caucasian genetic isolate 417
Rescue of murine silica-induced lung injury and fibrosis by human embryonic stem cells 417
Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. 412
Tumor necrosis factor promoter polymorphism TNF*-857 is a risk allele for psoriatic arthritis independent of the PSORS1 locus. 411
Deletion of LCE3C and LCE3B is a susceptibility factor for psoriatic arthritis: a study in Spanish and Italian populations and meta-analysis. 410
Haplotypes in IL-8 gene are associated to age-related macular degeneration: a case-control study 410
The psoriasis genetics as a model of complex disease 409
Expression and potential role of cellular retinol binding protein I in psoriasis 408
Generation of human induced pluripotent stem cells from extraembryonic tissues of fetuses affected by monogenic diseases 405
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 396
Variants in RUNX3 Contribute to Susceptibility to Psoriatic Arthritis, Exhibiting Further Common Ground with Ankylosing Spondylitis 390
Mapping the future of common diseases: lessons from psoriasis 389
Resequencing of FLG gene in atopic dermatitis: the American Society of human genetics 385
Insight into genetics of atopic dermatitis: future approaches and directions 384
Fine mapping of the psoriasis susceptibility gene PSORS1: A reassessment of risk associated with a putative risk haplotype lacking HLA-Cw6 383
Polymorphisms in ARMS2 (LOC387715) and LOXL1 genes in the Japanese with age-related macular degeneration 382
Identification of Deletion Carriers in X-Linked Chronic Granulomatous Disease by Real-Time PCR. 378
Meta-analysis confirms the LCE3C_LCE3B deletion as a risk factor for psoriasis in several ethnic groups and finds interaction with HLA-Cw6. 363
Digenic inheritance of shortened repeat units of the D4Z4 region and a loss-of-function variant in SMCHD1 in a Family with FSHD 361
Biomolecular index of therapeutic efficacy in psoriasis treated by anti-TNF alpha agents. 354
Mitochondrial Serine Protease HTRA2 p.G399S in a Female with Di George Syndrome and Parkinson's Disease 346
KIF3A and IL-4 are disease-specific biomarkers for psoriatic arthritis susceptibility 334
Towards the application of precision medicine in age-related macular degeneration 328
Atopic Eczema: Genetic Analysis of COL6A5, COL8A1, and COL10A1 in Mediterranean Populations. 325
Identification of Duchenne/Becker muscular dystrophy mosaic carriers through a combined DNA/RNA analysis 309
Facioscapulohumeral muscular dystrophy (FSHD) molecular diagnosis: from traditional technology to the NGS era. 306
The Interplay between miRNA-Related Variants and Age-Related Macular Degeneration: EVIDENCE of Association of MIR146A and MIR27A. 290
Uncovering genetic and non-genetic biomarkers specific for exudative age-related macular degeneration: Significant association of twelve variants 278
Defective proteasome biogenesis into skin fibroblasts isolated from Rett syndrome subjects with MeCP2 non-sense mutations 276
Doyne honeycomb retinal dystrophy - functional improvement following subthreshold nanopulse laser treatment: a case report. 260
Making progress in education: The EUROFORGEN master degree pilot project in forensic genetics. 259
Limb-Girdle Muscular Dystrophies (LGMDs): The Clinical Application of NGS Analysis, a Family Case Report. 251
Follicular occlusion tetrad in a male patient with pachyonychia congenita: clinical and genetic analysis 249
Heterozygous PLA2G6 Mutation Leads to Iron Accumulation Within Basal Ganglia and Parkinson's Disease. 247
Structural modeling of altered CLCN1 conformation following a novel mutation in a patient affected by autosomal dominant myotonia congenita (Thomsen disease) 237
The Variability of SMCHD1 Gene in FSHD Patients: Evidence of New Mutations 235
Next Generation Sequencing and ALS: known genes, different phenotyphes. 221
A Novel Homozygous Variant in the Fork-Head-Associated Domain of Polynucleotide Kinase Phosphatase in a Patient Affected by Late-Onset Ataxia With Oculomotor Apraxia Type 4 218
Totale 41.955
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Categoria #
all - tutte 129.086
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 129.086
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.243 0 0 0 115 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
2025/20267.127 554 323 874 653 612 193 892 835 827 651 411 302
2026/20272.514 332 371 1.362 449 0 0 0 0 0 0 0 0
Totale 50.562