IRIS
BORGIANI, PAOLA
 Distribuzione geografica
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Continente #
NA - Nord America 39.102
AS - Asia 4.208
EU - Europa 4.046
SA - Sud America 627
Continente sconosciuto - Info sul continente non disponibili 546
AF - Africa 72
OC - Oceania 9
Totale 48.610
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Nazione #
US - Stati Uniti d'America 38.854
SG - Singapore 1.939
CN - Cina 850
IT - Italia 707
DE - Germania 568
BR - Brasile 509
RU - Federazione Russa 470
UA - Ucraina 454
VN - Vietnam 375
IE - Irlanda 368
FR - Francia 349
HK - Hong Kong 309
GB - Regno Unito 268
PL - Polonia 259
SE - Svezia 213
FI - Finlandia 169
BD - Bangladesh 160
CA - Canada 136
JP - Giappone 135
KR - Corea 94
IN - India 60
NL - Olanda 56
TR - Turchia 46
AR - Argentina 37
ID - Indonesia 34
BE - Belgio 33
MX - Messico 33
ZA - Sudafrica 30
KG - Kirghizistan 29
IR - Iran 23
UZ - Uzbekistan 23
AT - Austria 22
ES - Italia 22
CZ - Repubblica Ceca 21
IQ - Iraq 21
CO - Colombia 18
EC - Ecuador 17
JM - Giamaica 17
PE - Perù 14
PK - Pakistan 14
MA - Marocco 13
CR - Costa Rica 12
MY - Malesia 12
EU - Europa 11
IL - Israele 11
LT - Lituania 11
VE - Venezuela 11
PR - Porto Rico 10
PH - Filippine 9
TH - Thailandia 9
CH - Svizzera 8
HN - Honduras 8
PY - Paraguay 8
RO - Romania 8
AU - Australia 7
CL - Cile 7
DZ - Algeria 7
NP - Nepal 7
SA - Arabia Saudita 7
A2 - ???statistics.table.value.countryCode.A2??? 6
AE - Emirati Arabi Uniti 5
EG - Egitto 5
KE - Kenya 5
LB - Libano 5
NI - Nicaragua 5
PT - Portogallo 5
SV - El Salvador 5
UY - Uruguay 5
AZ - Azerbaigian 4
DO - Repubblica Dominicana 4
EE - Estonia 4
GR - Grecia 4
KZ - Kazakistan 4
OM - Oman 4
TN - Tunisia 4
AL - Albania 3
GE - Georgia 3
GT - Guatemala 3
HU - Ungheria 3
IS - Islanda 3
JO - Giordania 3
PA - Panama 3
QA - Qatar 3
RS - Serbia 3
SC - Seychelles 3
TT - Trinidad e Tobago 3
BG - Bulgaria 2
BH - Bahrain 2
BY - Bielorussia 2
CG - Congo 2
DM - Dominica 2
GP - Guadalupe 2
NZ - Nuova Zelanda 2
SI - Slovenia 2
SK - Slovacchia (Repubblica Slovacca) 2
SY - Repubblica araba siriana 2
AG - Antigua e Barbuda 1
AM - Armenia 1
BA - Bosnia-Erzegovina 1
BB - Barbados 1
Totale 48.063
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Città #
Woodbridge 9.832
Wilmington 9.463
Houston 8.598
Fairfield 1.197
Singapore 1.122
Ashburn 1.061
Ann Arbor 737
Chandler 643
San Jose 590
Seattle 433
New York 411
Cambridge 392
Jacksonville 367
Beijing 354
Dublin 339
Hong Kong 304
Council Bluffs 282
Medford 258
Rome 229
Kraków 215
Santa Clara 198
The Dalles 183
Dallas 174
Los Angeles 167
Dearborn 160
Lawrence 119
Boardman 115
Ho Chi Minh City 107
Tokyo 107
Hanoi 101
Menlo Park 94
Lauterbourg 89
Buffalo 81
Moscow 71
Denver 68
São Paulo 66
Phoenix 63
Helsinki 61
San Diego 60
Munich 54
Milan 51
London 45
Atlanta 43
North Bergen 43
Toronto 42
Chicago 41
Zhengzhou 37
Montreal 36
Warsaw 34
Redwood City 33
Brooklyn 30
Palo Alto 30
Norwalk 28
Nuremberg 28
Orem 28
Shanghai 27
Brussels 26
Da Nang 26
Mülheim 26
Mountain View 23
Frankfurt am Main 22
Hefei 22
Redondo Beach 22
Chennai 21
Jakarta 21
Johannesburg 20
Stockholm 19
Queens 17
San Francisco 17
University Park 17
Seoul 16
Ankara 15
Columbus 15
Philadelphia 15
Poplar 15
Tashkent 15
Haiphong 14
Manchester 14
Nanjing 14
Naples 14
Amsterdam 13
Belo Horizonte 13
Detroit 13
Kunming 13
Lappeenranta 13
Monte Vista 13
Charlotte 12
Olomouc 12
Vienna 12
Boston 11
Brasília 11
Dhaka 11
Hangzhou 11
Hải Dương 11
Istanbul 11
Newark 11
Querétaro 11
Reading 11
Verona 11
Washington 11
Totale 40.222
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Nome #
ATG16L1 Ala197Thr Is Not Associated With Susceptibility to Crohn's Disease or With Phenotype in an Italian Population 548
High warfarin sensitivity in carriers of CYP2C9*35 is determined by the impaired interaction with P450 oxidoreductase 545
Common polymorphisms in MIR146a, MIR128a and MIR27a genes contribute to neuropathy susceptibility in type 2 diabetes 526
Association between a MIR499A polymorphism and diabetic neuropathy in type 2 diabetes 524
A family study of asymptomatic small bowel Crohn's disease 515
Allelic variants in the CYP2C9 and VKORC1 loci and interindividual variability in the anticoagulant dose effect of warfarin in Italians 514
Age-related macular degeneration: insights into inflammatory genes 512
Autophagy and inflammatory bowel disease: Association between variants of the autophagy-related IRGM gene and susceptibility to Crohn's disease 509
3020insC mutation within the NOD2 gene in Crohn's disease: frequency and association with clinical pattern in an Italian population 505
A Pharmacogenetics Study in Mozambican Patients Treated with Nevirapine: Full Resequencing of TRAF3IP2 Gene Shows a Novel Association with SJS/TEN Susceptibility 504
Exclusion of CARD15/NOD2 as a candidate susceptibility gene to psoriasis in the Italian population 501
Nevirapine-induced hepatotoxicity and pharmacogenetics: a retrospective study in a population from Mozambique 500
TCF7L2 gene polymorphisms and type 2 diabetes: Association with diabetic retinopathy and cardiovascular autonomic neuropathy 499
A multilocus genetic study in a cohort of Italian SLE patients confirms the association with STAT4 gene and describes a new association with HCP5 gene 495
CYP4F2 genetic variant (rs2108622) significantly contributes to warfarin dosing variability in the Italian population 492
Advances in exploring the role of micrornas in inflammatory bowel disease 492
Folic acid and methionine in the prevention of teratogen-induced congenital defects in mice 491
Intrauterine development and MNSs blood groups in repeated spontaneous abortion. 486
Direct PCR: a new pharmacogenetic approach for the inexpensive testing of HLA-B*57:01 482
Association between CYP2B6 polymorphisms and Nevirapine-induced SJS/TEN: a pharmacogenetics study 481
Type 2 diabetes and the genetics of signal transduction: a study of interaction between adenosine deaminase and acid phosphatase locus 1 polymorphisms 480
Biomarkers to predict drug efficacy and safety in neurodegenerative diseases 479
Recent advances in exploring the genetic susceptibility to diabetic neuropathy 477
Comparative analysis between saliva and buccal swabs as source of DNA: Lesson from HLA-B∗57:01 testing 474
Cannabinoid Poisoning by Hemp Seed Oil in a Child 474
Genetic factors in systemic lupus erythematosus: Contribution to disease phenotype 472
A study of three polymorphic sites of the ADA gene in children with type 1 diabetes mellitus 470
Polymorphisms in STAT4, PTPN2, PSORS1C1 and TRAF3IP2 genes are associated with the response to TNF inhibitors in patients with rheumatoid arthritis 470
HCP5 genetic variant (RS3099844) contributes to Nevirapine-induced Stevens Johnsons syndrome/toxic epidermal necrolysis susceptibility in a population from Mozambique 467
Foetal macrosomia and erythrocyte acid phosphatase (ACP1) polymorphism in diabetic and normal pregnancy. 467
Ala197Thr is not associated with susceptibility to Crohn’s Disease or with phenotype in an Italian population. 466
Characterization of a novel CYP2C9 gene mutation and structural bioinformatic protein analysis in a warfarin hypersensitive patient 465
Increased release and activity of matrix metalloproteinase-9 in patients with mandibuloacral dysplasia type A, a rare premature ageing syndrome 464
Crohn's disease, the mycobacterium paratuberculosis and the genetic bond: An unexpected trio 464
Stevens-Johnson syndrome and toxic epidermal necrolysis: an update on pharmacogenetics studies in drug-induced severe skin reaction 464
Role of genetics in prevention of coronary atherosclerosis 462
CARD15 mutation analysis in an Italian population: Leu1007fsinsC but neither Arg702Trp nor Gly908Arg mutations are associated with Crohn's disease 458
TRAF3IP2 gene and systemic lupus erythematosus: association with disease susceptibility and pericarditis development 458
Polymorphisms in MIR122, MIR196A2, and MIR124A genes are associated with clinical phenotypes in inflammatory bowel diseases 458
Interleukin-23R Arg381Gln Is Associated With Susceptibility to Crohn's Disease But Not With Phenotype in an Italian Population 456
FLG (filaggrin) null mutations and sunlight exposure: Evidence of a correlation 453
Pharmacogenomics of multifactorial diseases: A focus on psoriatic arthritis 450
Association of the ACP1 genotype with metabolic parameters upon initial diagnosis of type 1 diabetes. 449
Association of single nucleotide polymorphisms in the oxidised LDL receptor 1 (OLR1) gene in patients with acute myocardial infarction. 447
Psoriatic arthritis and CARD15 gene polymorphisms: no evidence for association in the Italian population 446
TRAF3IP2 gene is associated with cutaneous extraintestinal manifestations in Inflammatory Bowel Disease 446
Association between ACP(1) and favism: A possible biochemical mechanism 446
Recent advances in the genetic susceptibility to osteoarthritis 445
Characterization of a single nucleotide polymorphism in the ZNF9 gene and analysis of association with myotonic dystrophy type II (DM2) in the Italian population 442
Impact of the CYP4F2 p.V433M polymorphism on coumarin dose requirement: systematic review and meta-analysis 441
Enzyme variability and neonatal jaundice. The role of adenosine deaminase and acid phosphatase 440
Diabetic complications and the genetics of signal transduction. A study of retinopathy in NIDDM 437
Pharmacogenomics in cardiovascular disease: the role of single nucleotide polymorphisms in improving drug therapy 436
Acid phosphatase locus 1 (ACP1): Possible relationship of allelic variation to body size and human population adaptation to thermal stress - A theoretical perspective 435
Two molecular assays for the rapid and inexpensive detection of GJB2 and GJB6 mutations 434
Assessing individual risk for AMD with genetic counseling, family history, and genetic testing 432
IL-4 receptor alpha chain genetic polymorphism and total IgE levels in the English population: two-locus haplotypes are more informative than individual SNPs 431
Phosphotyrosine-protein-phosphatase and diabetic disorders. Further studies on the relationship between low molecular weight acid phosphatase genotype and degree of glycemic control 431
A European spectrum of pharmacogenomic biomarkers: Implications for clinical pharmacogenomics 431
Neonatal screening, clinical features and genetic testing for galactosemia [3] 430
MicroRNA genetic variations: association with type 2 diabetes 430
Genetic control of serum IgE levels: a study of low molecular weight protein tyrosine phosphatase. 430
Identification of two SNPs in the 5' flanking region of the ACP1 gene and evaluation of disequilibrium among polymorphic sites. 429
EPHX1 Polymorphisms Are Not Associated With Warfarin Response in an Italian Population 422
ABCC10 rs2125739 polymorphism and nevirapine-induced hepatotoxicity: lack of association in a population from Mozambique 422
RH blood groups and diabetic disorders: Is there an effect on glycosylated hemoglobin level? 421
New insights in atherosclerosis research: LOX-1, leading actor of cardiovascular diseases [Nuovi approfondimenti nella ricerca su l'ateroslerosi: LOX-1, un primo attore nelle malattie cardiovascolari] 418
Rh blood groups and diabetic disorders 418
Phosphoglucomutase genetic polymorphism of newborns 417
Resequencing of VKORC1, CYP2C9 and CYP4F2 genes in Italian patients requiring extreme low and high warfarin doses 416
Correction: A European spectrum of pharmacogenomic biomarkers: implications for clinical pharmacogenomics 414
Genotyping OLR1 gene: A genomic biomarker for cardiovascular diseases 413
L’impatto sulla salute umana dell’arsenico presente in basse concentrazioni nelle acque. Proposta di uno studio caso controllo Nested nell’area del viterbese 413
A study of human growth hormone and insulin gene regions in relation to metabolic control of non-insulin-dependent diabetes mellitus 412
Haplotypes in IL-8 gene are associated to age-related macular degeneration: a case-control study 410
Further evidence that polymorphisms of the OLR1 gene are associated with susceptibility to coronary artery disease and myocardial infarction 408
Could MicroRNA polymorphisms influence warfarin dosing? A pharmacogenetics study on mir133 genes 408
Polymorphisms in STAT-4, IL-10, PSORS1C1, PTPN2 and MIR146A genes are associated differently with prognostic factors in Italian patients affected by rheumatoid arthritis 406
OLR1 gene and coronary artery disease/acute myocardial infarction: Replication in an independently collected sample [1] 404
Pharmacogenomics: role in medicines approval and clinical use 404
Low molecular weight PTP-IL-4RA interaction in atopy predisposition 403
Genetic tests and genomic biomarkers: regulation, qualification and validation 399
A polymorphism upstream MIR1279 gene is associated with pericarditis development in Systemic Lupus Erythematosus and contributes to definition of a genetic risk profile for this complication 398
Foetal macrosomia in diabetic pregnancy. Further data on the association with maternal PGM1 genotype 386
A common polymorphism in MIR155 gene promoter region is associated with a lower risk to develop type 2 diabetes 379
Genetics and Treatment Response in Parkinson’s Disease: An Update on Pharmacogenetic Studies 378
Pharmacogenetics of inflammatory bowel disease: A focus on Crohn's disease 378
Impact of glutathione transferases genes polymorphisms in nevirapine adverse reactions: a possible role for GSTM1 in SJS/TEN susceptibility 376
Genotypes of cytosolic low-molecular-weight protein-tyrosine-phosphatase correlate with age at onset of type 1 diabetes in a sex-specific manner. 358
TNFAIP3 gene polymorphisms in three common autoimmune diseases: Systemic lupus erythematosus, rheumatoid arthritis, and primary sjogren syndrome - association with disease susceptibility and clinical phenotypes in Italian patients 353
Genome-wide association study of nevirapine hypersensitivity in a sub-Saharan African HIV-infected population 350
A multivariate genetic analysis confirms rs5010528 in the human leucocyte antigen-C locus as a significant contributor to Stevens-Johnson syndrome/toxic epidermal necrolysis susceptibility in a Mozambique HIV population treated with nevirapine 338
Polymorphisms in miRNA genes and their involvement in autoimmune diseases susceptibility 324
Interaction between microbiome and host genetics in psoriatic arthritis 314
STAT4, TRAF3IP2, IL10, and HCP5 Polymorphisms in Sjögren's Syndrome: Association with Disease Susceptibility and Clinical Aspects 307
Evaluation of ATG5 polymorphisms in Italian patients with systemic lupus erythematosus: contribution to disease susceptibility and clinical phenotypes 285
Uncovering genetic and non-genetic biomarkers specific for exudative age-related macular degeneration: Significant association of twelve variants 278
Pharmacogenomics in Parkinson's disease: which perspective for developing a personalized medicine? 273
Effect of CYP4F2, VKORC1, and CYP2C9 in Influencing Coumarin Dose: A Single-Patient Data Meta-Analysis in More Than 15,000 Individuals 269
COVID-19 and genetic variants of protein involved in the SARS-CoV-2 entry into the host cells 237
Totale 43.366
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Categoria #
all - tutte 116.679
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 116.679
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.081 0 0 0 83 52 145 67 55 121 120 104 334
2022/20231.635 170 142 47 232 158 373 135 91 137 20 85 45
2023/2024840 84 19 40 24 47 325 34 41 12 8 16 190
2024/20252.976 91 669 304 225 59 123 221 180 336 275 225 268
2025/20265.471 496 202 638 537 523 207 688 561 578 535 251 255
2026/20272.243 349 396 945 553 0 0 0 0 0 0 0 0
Totale 48.610