IRIS
GIARDINA, EMILIANO
 Distribuzione geografica
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Continente #
NA - Nord America 36.962
AS - Asia 5.303
EU - Europa 4.404
SA - Sud America 760
AF - Africa 93
Continente sconosciuto - Info sul continente non disponibili 16
OC - Oceania 4
Totale 47.542
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Nazione #
US - Stati Uniti d'America 36.781
SG - Singapore 2.433
CN - Cina 1.055
IT - Italia 740
RU - Federazione Russa 637
BR - Brasile 626
DE - Germania 587
HK - Hong Kong 466
VN - Vietnam 461
IE - Irlanda 432
UA - Ucraina 409
FR - Francia 392
GB - Regno Unito 272
SE - Svezia 239
PL - Polonia 230
FI - Finlandia 178
BD - Bangladesh 171
JP - Giappone 162
CA - Canada 99
KR - Corea 97
IN - India 92
NL - Olanda 66
ID - Indonesia 61
AR - Argentina 51
AT - Austria 48
BE - Belgio 43
MX - Messico 43
TH - Thailandia 36
TR - Turchia 35
KG - Kirghizistan 34
ES - Italia 33
ZA - Sudafrica 33
CZ - Repubblica Ceca 32
UZ - Uzbekistan 32
PH - Filippine 27
IQ - Iraq 25
MY - Malesia 21
EC - Ecuador 17
RO - Romania 17
CL - Cile 16
MA - Marocco 16
PY - Paraguay 15
PK - Pakistan 14
CO - Colombia 13
EG - Egitto 12
EU - Europa 12
JM - Giamaica 11
IL - Israele 10
LT - Lituania 10
SA - Arabia Saudita 10
DZ - Algeria 9
VE - Venezuela 9
AE - Emirati Arabi Uniti 8
TN - Tunisia 8
IR - Iran 7
NP - Nepal 7
CH - Svizzera 6
CR - Costa Rica 6
KE - Kenya 6
AZ - Azerbaigian 5
GT - Guatemala 5
JO - Giordania 5
PE - Perù 5
TW - Taiwan 5
AL - Albania 4
BO - Bolivia 4
HN - Honduras 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
HR - Croazia 3
KW - Kuwait 3
PA - Panama 3
PS - Palestinian Territory 3
SV - El Salvador 3
AM - Armenia 2
DK - Danimarca 2
DM - Dominica 2
DO - Repubblica Dominicana 2
GE - Georgia 2
HU - Ungheria 2
KH - Cambogia 2
LB - Libano 2
NI - Nicaragua 2
NO - Norvegia 2
OM - Oman 2
QA - Qatar 2
SY - Repubblica araba siriana 2
BY - Bielorussia 1
CG - Congo 1
CM - Camerun 1
CW - ???statistics.table.value.countryCode.CW??? 1
DJ - Gibuti 1
GH - Ghana 1
KN - Saint Kitts e Nevis 1
Totale 47.530
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Città #
Woodbridge 9.259
Wilmington 9.115
Houston 8.045
Singapore 1.292
Fairfield 1.244
Ashburn 881
Chandler 761
Ann Arbor 729
San Jose 663
Beijing 475
Seattle 471
Hong Kong 460
Cambridge 411
Dublin 367
Jacksonville 351
Medford 293
New York 255
Dearborn 219
Los Angeles 218
Rome 210
Council Bluffs 207
The Dalles 200
Kraków 190
Santa Clara 177
Tokyo 143
Ho Chi Minh City 138
Lawrence 134
Hanoi 122
Buffalo 110
Dallas 108
Moscow 99
Chicago 98
Munich 94
Lauterbourg 92
San Diego 81
Menlo Park 68
Milan 65
São Paulo 65
Boardman 57
Helsinki 57
Zhengzhou 51
London 47
Redondo Beach 47
Jakarta 43
Nuremberg 42
Mülheim 41
North Bergen 38
Orem 37
Frankfurt am Main 36
Palo Alto 35
Montreal 34
Phoenix 34
Atlanta 33
Bangkok 32
Brussels 32
Salt Lake City 32
Chennai 31
Toronto 31
Nanjing 30
Warsaw 27
Da Nang 26
Johannesburg 26
Norwalk 26
Falls Church 25
Lappeenranta 23
Monte Vista 23
San Francisco 23
Brno 22
Guangzhou 22
Redwood City 22
Mexico City 21
Shanghai 21
Belo Horizonte 20
Brooklyn 20
Vienna 20
Stockholm 19
Elk Grove Village 18
Mountain View 18
Mumbai 18
Columbus 17
Manila 17
Tashkent 17
Turku 17
Ankara 16
Denver 16
Seoul 16
Boston 15
Haiphong 15
Amsterdam 14
Hefei 14
Paris 14
Poplar 14
Rio de Janeiro 14
University Park 14
Detroit 13
Tampa 13
Brasília 12
Lancaster 12
Baghdad 11
Campinas 11
Totale 39.472
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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 589
Application of precision medicine in neurodegenerative diseases 546
Gonadal mosaicism in hereditary angioedema 530
Review of nutrient actions on age-related macular degeneration 513
Mutational analysis of Peroxiredoxin IV: Exclusion of a positional candidate for multinodular goitre 512
Mannose-binding lectin polymorphisms and pulmonary outcome in premature neonates: a pilot study 507
Haplotypes in SLC24A5 Gene as Ancestry Informative Markers in Different Populations 497
Identification of multipotent cytotrophoblast cells from human first trimester chorionic villi 496
Age-related macular degeneration: insights into inflammatory genes 494
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 490
Absence of filaggrin mutation in a patient affected by pachyonychia congenita and mild atopic dermatitis 490
A Pharmacogenetics Study in Mozambican Patients Treated with Nevirapine: Full Resequencing of TRAF3IP2 Gene Shows a Novel Association with SJS/TEN Susceptibility 489
Forensic DNA challenges: replacing numbers with names of Fosse Ardeatine's victims 488
Exclusion of CARD15/NOD2 as a candidate susceptibility gene to psoriasis in the Italian population 485
Transmission ratio distortion in the spinal muscular atrophy locus: Data from 314 prenatal tests 484
A New Splicing Mutation in the L1CAM Gene Responsible for X-Linked Hydrocephalus (HSAS) 479
Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis 478
A new CYP21A1P/CYP21A2 chimeric gene identified in an Italian woman suffering from classical congenital adrenal hyperplasia form 475
The 2011 GeFI collaborative exercise. Concordance study, proficiency testing and Italian population data on the new ENFSI/EDNAP loci D1S1656, D2S441, D10S1248, D12S391, D22S1045 474
R501X and 2282del4 filaggrin mutations do not confer susceptibility to psoriasis and atopic dermatitis in Italian patients [2] 473
Frequency assessment of 25 SNPs in five different populations 471
A multiplex molecular assay for the detection of uniparental disomy for human chromosome 15 470
Direct PCR: a new pharmacogenetic approach for the inexpensive testing of HLA-B*57:01 470
Transabdominal coelocentesis as early source of fetal DNA for chromosomal and molecular diagnosis 462
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 460
Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis 459
A fluorescence-based sequence-specific primer PCR for the screening of HLA-B(*)57:01 457
A long PCR-based molecular protocol for detecting normal and expanded ZNF9 alleles in myotonic dystrophy type 2 453
Comparative analysis between saliva and buccal swabs as source of DNA: Lesson from HLA-B∗57:01 testing 452
Evidence for differential S100 gene over-expression in psoriatic patients from genetically heterogeneous pedigrees 452
Stevens-Johnson syndrome and toxic epidermal necrolysis: an update on pharmacogenetics studies in drug-induced severe skin reaction 450
Role of genetics in prevention of coronary atherosclerosis 449
Prenatal diagnosis of spinal muscular atrophy with respiratory distress (SMARD1) in a twin pregnancy [5] 448
The long and winding road: Searching for non-MHC psoriasis susceptibility loci 447
Common sequence variants in the LOXL1 gene in pigment dispersion syndrome and pigmentary glaucoma 447
Typing of ARMS2 and CFH in age-related macular degeneration: case-control study and assessment of frequency in the Italian population 445
FLG (filaggrin) null mutations and sunlight exposure: Evidence of a correlation 444
"The Linosa Study": Epidemiological and heritability data of the metabolic syndrome in a Caucasian genetic isolate 443
Whole genome amplification and real-time PCR in forensic casework 442
Reliable and versatile immortal muscle cell models from healthy and myotonic dystrophy type 1 primary human myoblasts 442
Pharmacogenomics of multifactorial diseases: A focus on psoriatic arthritis 440
Association of single nucleotide polymorphisms in the oxidised LDL receptor 1 (OLR1) gene in patients with acute myocardial infarction. 439
Three-hour analysis of non-invasive foetal sex determination: application of Plexor chemistry 439
The molecular characterization of a depurinated trial DNA sample can be a model to understand the reliability of the results in forensic genetics. 438
Psoriatic arthritis and CARD15 gene polymorphisms: no evidence for association in the Italian population 437
May some HCV genotype 1 patients still benefit from dual therapy? The role of very early HCV kinetics 435
Familial Kaposi's Sarcoma in HHV8 infected subjects presenting the G-174C allele of the IL-6 promoter: a possible role for EBV? 432
TRAF3IP2 gene is associated with cutaneous extraintestinal manifestations in Inflammatory Bowel Disease 428
Deletion of Late Cornified Envelope 3B and 3C genes is not associated with atopic dermatitis 425
PSORS2 markers are not associated with psoriatic arthritis in the Italian population 425
A multiplex molecular assay for the detection of uniparental disomy for human chromosome 7 425
Population data for 17 Y-chromosome STRs in a sample from Apulia (Southern Italy) 423
Two molecular assays for the rapid and inexpensive detection of GJB2 and GJB6 mutations 423
Association of KIF3A, but not OVOL1 and ACTL9, with atopic eczema in Italian patients 422
Co-localization of susceptibility loci for psoriasis (PSORS4) and atopic dermatitis (ATOD2) on human chromosome 1q21 421
In silico and in vitro comparative analysis to select, validate and test SNPs for human identification 420
Characterization of the loricrin (LOR) gene as a positional candidate for the PSORS4 psoriasis susceptibility locus 419
Clinical trial sponsors' refusal to communicate genetic research results to subjects 418
Divergent phenotype of two siblings human leukocyte antigen identical, affected by nonclassical and classical congenital adrenal hyperplasia caused by 21-hydroxylase deficiency 416
Assessing individual risk for AMD with genetic counseling, family history, and genetic testing 416
Frequency assessment of SNPs for forensic identification in different populations 414
The Linosa Study: epidemiological and heritability data of the metabolic syndrome in a Caucasian genetic isolate 403
Rescue of murine silica-induced lung injury and fibrosis by human embryonic stem cells 401
Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. 400
The psoriasis genetics as a model of complex disease 399
Tumor necrosis factor promoter polymorphism TNF*-857 is a risk allele for psoriatic arthritis independent of the PSORS1 locus. 399
Haplotypes in IL-8 gene are associated to age-related macular degeneration: a case-control study 398
Deletion of LCE3C and LCE3B is a susceptibility factor for psoriatic arthritis: a study in Spanish and Italian populations and meta-analysis. 397
A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1 395
Generation of human induced pluripotent stem cells from extraembryonic tissues of fetuses affected by monogenic diseases 395
Expression and potential role of cellular retinol binding protein I in psoriasis 395
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 389
Variants in RUNX3 Contribute to Susceptibility to Psoriatic Arthritis, Exhibiting Further Common Ground with Ankylosing Spondylitis 383
Mapping the future of common diseases: lessons from psoriasis 382
Resequencing of FLG gene in atopic dermatitis: the American Society of human genetics 375
Fine mapping of the psoriasis susceptibility gene PSORS1: A reassessment of risk associated with a putative risk haplotype lacking HLA-Cw6 373
Polymorphisms in ARMS2 (LOC387715) and LOXL1 genes in the Japanese with age-related macular degeneration 373
Identification of Deletion Carriers in X-Linked Chronic Granulomatous Disease by Real-Time PCR. 369
Insight into genetics of atopic dermatitis: future approaches and directions 364
Meta-analysis confirms the LCE3C_LCE3B deletion as a risk factor for psoriasis in several ethnic groups and finds interaction with HLA-Cw6. 355
Digenic inheritance of shortened repeat units of the D4Z4 region and a loss-of-function variant in SMCHD1 in a Family with FSHD 348
Biomolecular index of therapeutic efficacy in psoriasis treated by anti-TNF alpha agents. 344
Mitochondrial Serine Protease HTRA2 p.G399S in a Female with Di George Syndrome and Parkinson's Disease 336
KIF3A and IL-4 are disease-specific biomarkers for psoriatic arthritis susceptibility 326
Towards the application of precision medicine in age-related macular degeneration 319
Atopic Eczema: Genetic Analysis of COL6A5, COL8A1, and COL10A1 in Mediterranean Populations. 309
Identification of Duchenne/Becker muscular dystrophy mosaic carriers through a combined DNA/RNA analysis 303
Facioscapulohumeral muscular dystrophy (FSHD) molecular diagnosis: from traditional technology to the NGS era. 293
The Interplay between miRNA-Related Variants and Age-Related Macular Degeneration: EVIDENCE of Association of MIR146A and MIR27A. 280
Uncovering genetic and non-genetic biomarkers specific for exudative age-related macular degeneration: Significant association of twelve variants 267
Defective proteasome biogenesis into skin fibroblasts isolated from Rett syndrome subjects with MeCP2 non-sense mutations 253
Doyne honeycomb retinal dystrophy - functional improvement following subthreshold nanopulse laser treatment: a case report. 249
Making progress in education: The EUROFORGEN master degree pilot project in forensic genetics. 248
Follicular occlusion tetrad in a male patient with pachyonychia congenita: clinical and genetic analysis 243
Limb-Girdle Muscular Dystrophies (LGMDs): The Clinical Application of NGS Analysis, a Family Case Report. 239
Heterozygous PLA2G6 Mutation Leads to Iron Accumulation Within Basal Ganglia and Parkinson's Disease. 236
Structural modeling of altered CLCN1 conformation following a novel mutation in a patient affected by autosomal dominant myotonia congenita (Thomsen disease) 228
The Variability of SMCHD1 Gene in FSHD Patients: Evidence of New Mutations 226
Next Generation Sequencing and ALS: known genes, different phenotyphes. 215
Migrainous Infarction in a Patient With Sporadic Hemiplegic Migraine and Cystic Fibrosis: A 99mTc-HMPAO Brain SPECT Study. 207
Totale 40.821
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Categoria #
all - tutte 120.131
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 120.131
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2025/20267.127 554 323 874 653 612 193 892 835 827 651 411 302
2026/2027175 175 0 0 0 0 0 0 0 0 0 0 0
Totale 48.223