IRIS
D'ANDREA, GIOVANNA
 Distribuzione geografica
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Continente #
NA - Nord America 4.484
EU - Europa 4.159
AS - Asia 3.095
SA - Sud America 449
AF - Africa 56
Continente sconosciuto - Info sul continente non disponibili 10
OC - Oceania 3
Totale 12.256
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Nazione #
US - Stati Uniti d'America 4.426
IE - Irlanda 1.142
SG - Singapore 1.100
CN - Cina 1.096
RU - Federazione Russa 589
SE - Svezia 551
UA - Ucraina 527
IT - Italia 448
BR - Brasile 359
FR - Francia 290
HK - Hong Kong 230
VN - Vietnam 209
DE - Germania 204
FI - Finlandia 166
IN - India 162
TR - Turchia 122
GB - Regno Unito 92
AR - Argentina 31
IQ - Iraq 31
NL - Olanda 31
CA - Canada 30
BD - Bangladesh 28
BE - Belgio 28
AT - Austria 23
PK - Pakistan 18
CZ - Repubblica Ceca 15
ID - Indonesia 14
JP - Giappone 14
PL - Polonia 14
TN - Tunisia 13
ZA - Sudafrica 13
VE - Venezuela 12
EC - Ecuador 11
MX - Messico 11
CO - Colombia 10
IR - Iran 10
CL - Cile 9
EU - Europa 9
JO - Giordania 9
AE - Emirati Arabi Uniti 8
BO - Bolivia 8
UZ - Uzbekistan 8
MA - Marocco 7
EG - Egitto 6
LT - Lituania 6
MY - Malesia 6
ES - Italia 5
KE - Kenya 5
AL - Albania 4
PY - Paraguay 4
SA - Arabia Saudita 4
BY - Bielorussia 3
CH - Svizzera 3
CR - Costa Rica 3
ET - Etiopia 3
HR - Croazia 3
IL - Israele 3
NO - Norvegia 3
PE - Perù 3
PS - Palestinian Territory 3
RO - Romania 3
RS - Serbia 3
AO - Angola 2
BG - Bulgaria 2
CY - Cipro 2
DO - Repubblica Dominicana 2
DZ - Algeria 2
GT - Guatemala 2
NI - Nicaragua 2
NP - Nepal 2
OM - Oman 2
PA - Panama 2
SV - El Salvador 2
SY - Repubblica araba siriana 2
UY - Uruguay 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AU - Australia 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BF - Burkina Faso 1
BH - Bahrain 1
BN - Brunei Darussalam 1
CU - Cuba 1
DK - Danimarca 1
GA - Gabon 1
GE - Georgia 1
HN - Honduras 1
JM - Giamaica 1
KG - Kirghizistan 1
KH - Cambogia 1
KR - Corea 1
KW - Kuwait 1
KZ - Kazakistan 1
LB - Libano 1
LV - Lettonia 1
MU - Mauritius 1
NZ - Nuova Zelanda 1
PH - Filippine 1
PR - Porto Rico 1
PT - Portogallo 1
Totale 12.252
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Città #
Dublin 1.141
San Jose 636
Chandler 558
Singapore 481
Jacksonville 372
Nyköping 358
Ashburn 326
Dearborn 315
Beijing 234
Hong Kong 230
Nanjing 197
Santa Clara 141
The Dalles 138
Wilmington 129
Ann Arbor 118
Lauterbourg 117
Princeton 110
Moscow 95
Dallas 93
Munich 93
New York 87
Ho Chi Minh City 75
Nanchang 75
Foggia 71
San Mateo 68
Boardman 67
Helsinki 67
Woodbridge 58
Bari 46
Los Angeles 46
Hanoi 45
Changsha 44
Shenyang 43
Des Moines 36
Hebei 30
Jinan 28
Tianjin 28
Hilden 27
Kunming 27
Rome 27
Turku 27
Jiaxing 26
Brussels 23
Hangzhou 23
Milan 22
São Paulo 22
Shanghai 21
Council Bluffs 20
Lanzhou 20
Nuremberg 20
Pune 20
Guangzhou 19
Frankfurt am Main 17
Hillsboro 16
Ningbo 16
Rio de Janeiro 16
Vienna 15
San Severo 14
Tokyo 14
Baghdad 13
Brno 13
London 13
San Francisco 13
Manfredonia 12
Porto Alegre 12
Warsaw 12
Modena 11
Naples 11
Amsterdam 10
Auburn Hills 10
Orange 10
Zhengzhou 10
Buenos Aires 9
Changchun 9
Norwalk 9
Paris 9
Amman 8
Atlanta 8
Brasília 8
Chennai 8
Florence 8
Fuzhou 8
Jakarta 8
Manchester 8
Biên Hòa 7
Chicago 7
Da Nang 7
Hefei 7
Orem 7
Tashkent 7
Toronto 7
Belo Horizonte 6
Charlotte 6
Cutrofiano 6
Espoo 6
Falls Church 6
Johannesburg 6
Montreal 6
Santiago 6
Seattle 6
Totale 7.601
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Nome #
Increased risk of venous thrombosis in carriers of the prothrombin A gene variant. 163
A polymorfism in VKORC1 gene is associated with an interindividual variability in the dose-anticoagulation effect of warfarin. 150
ADAMTS13 MUTATIONS AND POLYMORPHISMS IN CONGENITAL THROMBOTIC THROMBOCYTOPENIC PURPURA. 148
"Genetic modulation of oral anticoagulantion with warfarin " 144
FV HR2 haplotype as additional inherited risk factor for deep vein thrombosis in individuals with a high-risk profile 143
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. 142
Role of tumour necrosis factor alpha and interleukin 1 beta in promoter effect induced by mercury in human keratinocytes 141
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 141
Detection of the factor V Leiden using SSCP 140
A beta3 Asp217-->Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin alphaIIBbeta3 functions. 139
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 137
A Novel KCNN2 Variant in a Family with Essential Tremor Plus: Clinical Characteristics and In Silico Analysis 133
ANALISI MOLECOLARE E CORRELAZIONE GENOTIPO-FENOTIPO IN FAMIGLIE CON IPERFENILALANINEMIE. 132
A NOVEL NONSENSE TET2 MUTATION IN A PATIENT WITH PRIMARY MYELOFIBROSIS. 130
ETEROGENEITA' FENOTIPICA NELLE IPERFENILALANINEMIE ALL'INTERNO DELLO STESSO NUCLEO FAMILIARE. 129
A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin 129
COESISTENZA DI DUE PATOLOGIE RARE: TROMBOASTENIA DI GLANZMANN E SINDROME DI KARTAGENER 128
A MODEL TO PREDICT SUCCESS FOLLOWING PEG-INTERFERON AND RIBAVIRIN THERAPY FOR PATIENTS WITH HCV-1 INFECTION 127
Glanzmann's thrombasthenia: modulation of clinical phenotype by alpha2C807T gene polymorphism. 125
Polymorphisms in factor II and factor VII genes modulate oral anticoagulation with warfarin 125
Detection of new deletions in a group of Italian patients with Hemophilia A by multiplex ligation-dependent probe amplification 125
An a priori prediction model of response to peginterferon plus ribavirin dual therapy in naïve patients with genotype 1 chronic hepatitis C. 125
Genetic susceptibility to pregnancy-related venous thromboembolism: roles of factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations 124
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 124
A myoferlin gain-of-function variant associates with a new type of hereditary angioedema 124
The Genetics of Hereditary Angioedema: A Review 123
C0268 Higher risk of idiopathic small for gestational age newborns in Italian women carrying the annexin A5 M2 haplotype 122
Increased risk for venous thrombosis in carriers of the prothrombin G-->A20210 gene variant. 122
Pharmacodynamic targets of psychotic patients treated with a long-acting therapy 121
Inherited prothrombotic conditions and premature ischemic stroke. Sex difference in the association with Factor V leiden 120
A new vitamin K epoxide reductase complex subunit-1 (VKORC1) mutation in a patient with decreased stability of CYP2C9 enzyme 120
A novel allele variant of the SERPINF2 gene responsible for severe plasmin inhibitor (α2-antiplasmin) deficiency in an Italian patient 120
Identification of six novel mutations in type I antithrombin deficient Italian families 119
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 119
Thrombofilic genotypes in subjects with idiopathic antiphospholipid antibodies-prevalence and significance 118
Molecular diversity and thrombotic risk in protein S deficiency: the PROSIT study. 116
Identification of naïve HCV-1 patients with chronic hepatitis who may benefit from dual therapy with peg-interferon and ribavirin. 116
Mutation analysis in hyperphenylalaninemia patients from South Italy. 116
Compound heterozygosity (554-589 del, C-T transition) in the platelet glycoprotein iba gene in a patient with a severe bleeding tendency. 115
Molecular characterization of a factor Vii deficient patient supports the importance of the second epidermal growth factor-like domain. 115
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A. 115
The relationship between personality traits, the 5HTT polymorphisms, and the occurrence of anxiety and depressive symptoms in elite athletes 115
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A 115
Methylenetetrahydrofolate reductase (MTHFR) 677T-> C mutation and unexplained early pregnancy loss 114
Thrombophilic genotypes in subjects with idiopathic antiphospholipid antibodies--prevalence and significance 113
The methylenetetrahydrofolate reductase TT677 genotype is associated with venous thrombosis independently of the coexistence of the FV Leiden and the prothrombin A20210 mutation. 112
Chronic thromboembolic pulmonary hypertension. 112
Selection of HCV-1 patients with chronic hepatitis who might benefit from current standard of therapy with peg-interferon and ribavirin 112
Phenylalanine hydroxylase deficiency in south Italy: Genotype-phenotype correlations, identification of a novel mutant PAH allele and prediction of BH4 responsiveness 112
Inherited coagulation disorders in cirrhotic patients with portal vein thrombosis 111
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A 111
Coexistence of factor V Leiden and Factor II A20210 mutations and recurrent venous thromboembolism 110
Deep intronic variations may cause mild hemophilia A. 108
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 108
Psychosomatic syndromes are associated with IL-6 pro-inflammatory cytokine in heart failure patients 107
Survival in primary antiphospholipid syndrome: A single-centre cohort study 106
Maladaptive coping strategies and neuroticism mediate the relationship between 5HTT-LPR polymorphisms and symptoms of anxiety in elite athletes 106
RGD-containing peptides inhibit fibrinogen binding to platelet alpha(IIb)beta3 by inducing an allosteric change in the amino-terminal portion of alpha(IIb). 105
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 104
Hereditary protein C deficiency and thrombosis risk: genotype and phenotype relation in a large Italian family. 104
Intra-familiar discordant PKU phenotype explained by mutation analysis in three pedigrees. 104
Homozygosity by descent of a 3Mb chromosome 17 haplotype causes coinheritance of Glanzmann thrombasthenia and primary ciliary dyskinesia 103
Outcome of patients with splanchnic venous thrombosis presenting without overt MPN: a role for the JAK2 V617F mutation re-evaluation. 103
Intra-familiar discordant PKU phenotype explained by mutation analysis in three pedigrees. 102
Variation in genes encoding for interferon λ-3 and λ-4 in the prediction of HCV-1 treatment-induced viral clearance. 102
DAB2IP associates with hereditary angioedema: Insights into the role of VEGF signaling in HAE pathophysiology 101
The assessment of the relationship between personality, the presence of the 5htt polymorphism, and the occurrence of anxiety and depressive symptoms in elite athletes 101
THE MOLECULAR ORGANIZATION OF ENDOTHELIAL JUNCTIONS IN VASCULAR PERMEABILITY 101
Inherited platelet disorders>thrombocytopenias and thrombocytopathies. 99
Identifying human platelet glycoproteins IIb and IIla by capillary electrophoresis 99
Pharmacogenetics of dabigatran etexilate interindividual variability 98
Identification of the Novel G250R Variant Indicates a Role for Thrombomodulin in Modulating the Risk for Venous Thromboembolism 97
Molecular characterization of a factor VII deficient patient supports the importance of the second epidermal growth factor-like domain. 96
Anticoagulation in Italian patients with venous thromboembolism and thrombophilic alterations: findings from START2 register study 96
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) 96
Clinical utility of screening for CALR gene exon 9 mutations in patients with splanchnic venous thrombosis 94
A beta3 Asp217-->Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin alphaIIBbeta3 functions 94
Identification of the Novel G250R Variant Indicates a Role for Thrombomodulin in Modulating the Risk for Venous Thromboembolism 93
High prevalence of thrombophilic genotypes in patients with acute mesenteric vein thrombosis. 93
.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 93
Factor XI gene variants in factor XI-deficient patients of Southern Italy: identification of a novel mutation and genotype-phenotype relationship 91
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 90
Lack of genotypephenotype correlation in congenital adrenal hyperplasia due to a CYP21A2-like gene. 90
The Genetics of Hereditary Angioedema: A Review 90
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 90
Oral anticoagulant: pharmacogenetics relationship between genetic and non-genetic factors 89
. 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 88
Glanzmann's thrombasthenia: identification of 19 new mutations in 30 patients 87
Factor XI gene variants in factor XI-deficient patients of Southern Italy: identification of a novel mutation and genotype-phenotype relationship 86
Caveolin 3 Variant T78M in a Large Family With Brugada Syndrome: Clinical Features and Coexistence of ADRB1 and GRK5 Gene Mutation 85
Venous thrombosis in afibrinogenemia: a successful use of rivaroxaban 85
Validation of PLASMIC score and follow-up data in a cohort of patients with suspected microangiopathies from Southern Italy 85
Lack of genotypephenotype correlation in congenital adrenal hyperplasia due to a CYP21A2-like gene 84
Harm Avoidance as a possible mediator in the relationship between the 5-HTTLPR and Cognitive Anxiety in High Level Athletes 81
Validation of PLASMIC score and follow-up data in a cohort of patients with suspected microangiopathies from Southern Italy 80
. 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 80
De Novo p.Asp3368Gly Variant of Dystrophin Gene Associated with X-Linked Dilated Cardiomyopathy and Skeletal Myopathy: Clinical Features and In Silico Analysis 79
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. 75
. Molecular characterization of a factor VII deficient patient supports the importance of the second epidermal growth factor-like domain. Haematologica. 89(8):979-84; 2004 74
Uncovering a Genetic Diagnosis in a Pediatric Patient by Whole Exome Sequencing: A Modeling Investigation in Wiedemann–Steiner Syndrome 73
Totale 10.997
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Categoria #
all - tutte 64.433
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 64.433
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021112 0 0 0 0 0 0 0 0 0 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
2025/20263.478 287 273 416 545 174 173 761 438 260 151 0 0
Totale 12.658