IRIS
D'ANDREA, GIOVANNA
 Distribuzione geografica
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Continente #
EU - Europa 3.664
NA - Nord America 3.628
AS - Asia 2.798
SA - Sud America 422
AF - Africa 46
Continente sconosciuto - Info sul continente non disponibili 10
OC - Oceania 3
Totale 10.571
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Nazione #
US - Stati Uniti d'America 3.585
IE - Irlanda 1.142
CN - Cina 1.027
SG - Singapore 987
SE - Svezia 551
UA - Ucraina 527
IT - Italia 418
BR - Brasile 346
RU - Federazione Russa 301
HK - Hong Kong 213
DE - Germania 192
VN - Vietnam 176
FI - Finlandia 166
FR - Francia 149
IN - India 147
TR - Turchia 119
GB - Regno Unito 86
AR - Argentina 29
BE - Belgio 27
NL - Olanda 27
CA - Canada 25
BD - Bangladesh 23
IQ - Iraq 23
AT - Austria 22
CZ - Repubblica Ceca 15
PK - Pakistan 12
ZA - Sudafrica 12
ID - Indonesia 11
TN - Tunisia 11
EC - Ecuador 10
IR - Iran 10
JP - Giappone 10
VE - Venezuela 10
EU - Europa 9
AE - Emirati Arabi Uniti 7
CL - Cile 7
MX - Messico 7
BO - Bolivia 6
CO - Colombia 6
EG - Egitto 6
LT - Lituania 6
PL - Polonia 6
MA - Marocco 5
UZ - Uzbekistan 5
ES - Italia 4
JO - Giordania 4
KE - Kenya 4
AL - Albania 3
BY - Bielorussia 3
CH - Svizzera 3
CR - Costa Rica 3
IL - Israele 3
MY - Malesia 3
NO - Norvegia 3
PE - Perù 3
PY - Paraguay 3
RO - Romania 3
BG - Bulgaria 2
ET - Etiopia 2
GT - Guatemala 2
HR - Croazia 2
OM - Oman 2
PS - Palestinian Territory 2
RS - Serbia 2
SA - Arabia Saudita 2
SY - Repubblica araba siriana 2
UY - Uruguay 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AO - Angola 1
AU - Australia 1
BA - Bosnia-Erzegovina 1
BF - Burkina Faso 1
BH - Bahrain 1
BN - Brunei Darussalam 1
CU - Cuba 1
DK - Danimarca 1
DZ - Algeria 1
GA - Gabon 1
GE - Georgia 1
HN - Honduras 1
KG - Kirghizistan 1
KH - Cambogia 1
KR - Corea 1
KW - Kuwait 1
LB - Libano 1
LV - Lettonia 1
MU - Mauritius 1
NI - Nicaragua 1
NP - Nepal 1
NZ - Nuova Zelanda 1
PA - Panama 1
PH - Filippine 1
PR - Porto Rico 1
PT - Portogallo 1
SV - El Salvador 1
TV - Tuvalu 1
ZM - Zambia 1
Totale 10.571
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Città #
Dublin 1.141
Chandler 558
Singapore 419
Jacksonville 372
Nyköping 358
Dearborn 315
Ashburn 260
Beijing 216
Hong Kong 213
Nanjing 197
Santa Clara 137
Wilmington 129
Ann Arbor 118
Princeton 110
The Dalles 99
Munich 92
Dallas 90
New York 85
Moscow 75
Nanchang 75
Foggia 71
San Mateo 68
Boardman 67
Helsinki 67
Ho Chi Minh City 60
Woodbridge 58
Los Angeles 46
Changsha 44
Bari 43
Shenyang 43
Hanoi 40
Des Moines 35
Hebei 30
Jinan 28
Hilden 27
Kunming 27
Tianjin 27
Turku 27
Jiaxing 26
Rome 24
Brussels 23
Hangzhou 23
São Paulo 22
Milan 21
Shanghai 21
Lanzhou 20
Guangzhou 19
Nuremberg 19
Pune 19
Ningbo 16
Rio de Janeiro 16
Vienna 15
San Severo 14
Brno 13
Baghdad 12
Council Bluffs 12
Manfredonia 12
San Francisco 12
London 11
Porto Alegre 11
Auburn Hills 10
Orange 10
Tokyo 10
Zhengzhou 10
Buenos Aires 9
Changchun 9
Naples 9
Norwalk 9
Amsterdam 8
Florence 8
Frankfurt am Main 8
Fuzhou 8
Biên Hòa 7
Brasília 7
Hefei 7
Jakarta 7
Belo Horizonte 6
Charlotte 6
Chicago 6
Cutrofiano 6
Espoo 6
Falls Church 6
Montreal 6
Seattle 6
Shenzhen 6
Stevenage 6
Taizhou 6
Tunis 6
Atlanta 5
Chennai 5
Columbus 5
Haikou 5
Haiphong 5
Johannesburg 5
Manchester 5
Ninh Bình 5
Tashkent 5
Toronto 5
Amman 4
Ankara 4
Totale 6.514
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Nome #
Increased risk of venous thrombosis in carriers of the prothrombin A gene variant. 146
FV HR2 haplotype as additional inherited risk factor for deep vein thrombosis in individuals with a high-risk profile 135
A polymorfism in VKORC1 gene is associated with an interindividual variability in the dose-anticoagulation effect of warfarin. 131
ADAMTS13 MUTATIONS AND POLYMORPHISMS IN CONGENITAL THROMBOTIC THROMBOCYTOPENIC PURPURA. 131
Detection of the factor V Leiden using SSCP 130
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 129
A novel G-to-A mutation in the intron-N of the protein S gene leading to abnormal RNA splicing in a patient with protein S deficiency. 127
"Genetic modulation of oral anticoagulantion with warfarin " 126
A beta3 Asp217-->Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin alphaIIBbeta3 functions. 126
Role of tumour necrosis factor alpha and interleukin 1 beta in promoter effect induced by mercury in human keratinocytes 124
ANALISI MOLECOLARE E CORRELAZIONE GENOTIPO-FENOTIPO IN FAMIGLIE CON IPERFENILALANINEMIE. 123
ETEROGENEITA' FENOTIPICA NELLE IPERFENILALANINEMIE ALL'INTERNO DELLO STESSO NUCLEO FAMILIARE. 120
A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin 119
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 118
COESISTENZA DI DUE PATOLOGIE RARE: TROMBOASTENIA DI GLANZMANN E SINDROME DI KARTAGENER 116
The factor V (FV) gene ASP79HIS polymorphism modulates FV plasma levels and affects the activated protein C resistance phenotype in presence of the FV Leiden mutation 114
An a priori prediction model of response to peginterferon plus ribavirin dual therapy in naïve patients with genotype 1 chronic hepatitis C. 114
Pharmacodynamic targets of psychotic patients treated with a long-acting therapy 114
A Novel KCNN2 Variant in a Family with Essential Tremor Plus: Clinical Characteristics and In Silico Analysis 114
Glanzmann's thrombasthenia: modulation of clinical phenotype by alpha2C807T gene polymorphism. 113
Polymorphisms in factor II and factor VII genes modulate oral anticoagulation with warfarin 113
Detection of new deletions in a group of Italian patients with Hemophilia A by multiplex ligation-dependent probe amplification 113
A NOVEL NONSENSE TET2 MUTATION IN A PATIENT WITH PRIMARY MYELOFIBROSIS. 112
Increased risk for venous thrombosis in carriers of the prothrombin G-->A20210 gene variant. 110
C0268 Higher risk of idiopathic small for gestational age newborns in Italian women carrying the annexin A5 M2 haplotype 108
The Genetics of Hereditary Angioedema: A Review 108
Molecular diversity and thrombotic risk in protein S deficiency: the PROSIT study. 107
A MODEL TO PREDICT SUCCESS FOLLOWING PEG-INTERFERON AND RIBAVIRIN THERAPY FOR PATIENTS WITH HCV-1 INFECTION 107
Identification of naïve HCV-1 patients with chronic hepatitis who may benefit from dual therapy with peg-interferon and ribavirin. 106
The relationship between personality traits, the 5HTT polymorphisms, and the occurrence of anxiety and depressive symptoms in elite athletes 106
Inherited prothrombotic conditions and premature ischemic stroke. Sex difference in the association with Factor V leiden 105
Genetic susceptibility to pregnancy-related venous thromboembolism: roles of factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations 105
Selection of HCV-1 patients with chronic hepatitis who might benefit from current standard of therapy with peg-interferon and ribavirin 105
A myoferlin gain-of-function variant associates with a new type of hereditary angioedema 105
Identification of six novel mutations in type I antithrombin deficient Italian families 104
Molecular characterization of a factor Vii deficient patient supports the importance of the second epidermal growth factor-like domain. 104
Thrombofilic genotypes in subjects with idiopathic antiphospholipid antibodies-prevalence and significance 104
A new vitamin K epoxide reductase complex subunit-1 (VKORC1) mutation in a patient with decreased stability of CYP2C9 enzyme 104
Mutation analysis in hyperphenylalaninemia patients from South Italy. 104
preliminary Data From the Study of Coagulative Profile of HIV infected Individuals suggest a role for point mutations in the Gene in protein S deficiency in Individuals undergoing Higly Antiretroviral therapy 104
Methylenetetrahydrofolate reductase (MTHFR) 677T-> C mutation and unexplained early pregnancy loss 103
Thrombophilic genotypes in subjects with idiopathic antiphospholipid antibodies--prevalence and significance 103
Compound heterozygosity (554-589 del, C-T transition) in the platelet glycoprotein iba gene in a patient with a severe bleeding tendency. 102
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A. 102
Coexistence of factor V Leiden and Factor II A20210 mutations and recurrent venous thromboembolism 101
A novel allele variant of the SERPINF2 gene responsible for severe plasmin inhibitor (α2-antiplasmin) deficiency in an Italian patient 101
The methylenetetrahydrofolate reductase TT677 genotype is associated with venous thrombosis independently of the coexistence of the FV Leiden and the prothrombin A20210 mutation. 100
Survival in primary antiphospholipid syndrome: A single-centre cohort study 100
Inherited coagulation disorders in cirrhotic patients with portal vein thrombosis 99
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A 99
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A 98
Chronic thromboembolic pulmonary hypertension. 97
Variation in genes encoding for interferon λ-3 and λ-4 in the prediction of HCV-1 treatment-induced viral clearance. 95
Intra-familiar discordant PKU phenotype explained by mutation analysis in three pedigrees. 94
Hereditary protein C deficiency and thrombosis risk: genotype and phenotype relation in a large Italian family. 94
Outcome of patients with splanchnic venous thrombosis presenting without overt MPN: a role for the JAK2 V617F mutation re-evaluation. 94
Phenylalanine hydroxylase deficiency in south Italy: Genotype-phenotype correlations, identification of a novel mutant PAH allele and prediction of BH4 responsiveness 94
Homozygosity by descent of a 3Mb chromosome 17 haplotype causes coinheritance of Glanzmann thrombasthenia and primary ciliary dyskinesia 93
Pharmacogenetics of dabigatran etexilate interindividual variability 93
Identifying human platelet glycoproteins IIb and IIla by capillary electrophoresis 92
RGD-containing peptides inhibit fibrinogen binding to platelet alpha(IIb)beta3 by inducing an allosteric change in the amino-terminal portion of alpha(IIb). 91
The assessment of the relationship between personality, the presence of the 5htt polymorphism, and the occurrence of anxiety and depressive symptoms in elite athletes 91
Maladaptive coping strategies and neuroticism mediate the relationship between 5HTT-LPR polymorphisms and symptoms of anxiety in elite athletes 91
Intra-familiar discordant PKU phenotype explained by mutation analysis in three pedigrees. 91
Inherited platelet disorders>thrombocytopenias and thrombocytopathies. 89
Molecular characterization of a factor VII deficient patient supports the importance of the second epidermal growth factor-like domain. 89
Deep intronic variations may cause mild hemophilia A. 87
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 87
Associations Between Personality Traits, Perceived Stress and Depressive Symptoms in Gynecological Cancer Patients Characterized by the Short and Long Allele Variant of the 5-HTTLPR Genotype: Preliminary Results 86
Clinical utility of screening for CALR gene exon 9 mutations in patients with splanchnic venous thrombosis 86
Psychosomatic syndromes are associated with IL-6 pro-inflammatory cytokine in heart failure patients 85
Pathogenic DNM1L variant (1085G>A) linked to infantile progressive neurological disorder: Evidence of maternal transmission by germline mosaicism and influence of a contemporary in cis variant (1535T>C) 83
Identification of the Novel G250R Variant Indicates a Role for Thrombomodulin in Modulating the Risk for Venous Thromboembolism 82
High prevalence of thrombophilic genotypes in patients with acute mesenteric vein thrombosis. 82
Oral anticoagulant: pharmacogenetics relationship between genetic and non-genetic factors 82
Selection of HCV-1 patients with chronic hepatitis who might benefit from current standard of therapy with peg-interferon and ribavirin. 19th International Symposium on Hepatitis C Virus and Related Viruses 82
Lack of genotypephenotype correlation in congenital adrenal hyperplasia due to a CYP21A2-like gene. 82
THE MOLECULAR ORGANIZATION OF ENDOTHELIAL JUNCTIONS IN VASCULAR PERMEABILITY 81
The Genetics of Hereditary Angioedema: A Review 80
Identification of the Novel G250R Variant Indicates a Role for Thrombomodulin in Modulating the Risk for Venous Thromboembolism 78
Lack of genotypephenotype correlation in congenital adrenal hyperplasia due to a CYP21A2-like gene 78
Factor XI gene variants in factor XI-deficient patients of Southern Italy: identification of a novel mutation and genotype-phenotype relationship 78
A beta3 Asp217-->Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin alphaIIBbeta3 functions 78
. The Methylenetetrahydrofolate reductase TT677 genotype is associated with venous thrombosis independently of the coexistence of the FV Leiden and the prothrombin A20210 mutations. Thromb Haemost 1998; 79:907-911 78
Venous thrombosis in afibrinogenemia: a successful use of rivaroxaban 77
Glanzmann's thrombasthenia: identification of 19 new mutations in 30 patients 75
Harm Avoidance as a possible mediator in the relationship between the 5-HTTLPR and Cognitive Anxiety in High Level Athletes 74
.A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin. Blood. 105(2):645-9; 2005 74
Validation of PLASMIC score and follow-up data in a cohort of patients with suspected microangiopathies from Southern Italy 74
Factor XI gene variants in factor XI-deficient patients of Southern Italy: identification of a novel mutation and genotype-phenotype relationship 73
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 72
. Compound heterozygosity (554-589 del, C515-T transition) in the platelet glycoprotein Ib gene in a patient with a severe bleeding tendency. Thromb Haemost 1999, 81(4): 486-92 69
Validation of PLASMIC score and follow-up data in a cohort of patients with suspected microangiopathies from Southern Italy 66
Anticoagulation in Italian patients with venous thromboembolism and thrombophilic alterations: findings from START2 register study 66
An a priori prediction model of response to peginterferon plus ribavirin dual therapy in naïve patients with genotype 1 chronic hepatitis C. (2014) Digestive and Liver Disease, 46 (9), pp. 818-825. 65
DAB2IP associates with hereditary angioedema: Insights into the role of VEGF signaling in HAE pathophysiology 64
Predictive Value of Oxidized Low-Density Lipoprotein/β2-Glycoprotein-I Complexes (oxLDL/β2GPI) in Nonautoimmune Atherothrombosis 63
Interleukin 28B Gene Polymorphisms in Hepatitis C Virus-related Cryoglobulinemic Vasculitis 62
Genetic modulation of oral anticoagulation with warfarin. Thromb Haemost. 2000; 84(5):775-8 61
De Novo p.Asp3368Gly Variant of Dystrophin Gene Associated with X-Linked Dilated Cardiomyopathy and Skeletal Myopathy: Clinical Features and In Silico Analysis 60
Totale 9.670
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Categoria #
all - tutte 61.409
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 61.409
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021434 0 0 0 0 0 49 98 40 135 96 3 13
2021/2022781 79 0 29 20 140 14 25 55 84 136 30 169
2022/20232.680 245 92 123 165 167 234 17 216 1.301 19 45 56
2023/2024486 81 22 24 15 34 130 44 20 3 9 9 95
2024/20251.994 105 35 49 106 95 245 224 114 469 80 251 221
2025/20261.793 287 273 416 545 174 98 0 0 0 0 0 0
Totale 10.973