IRIS
D'ANDREA, GIOVANNA
 Distribuzione geografica
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Continente #
EU - Europa 2.936
NA - Nord America 2.830
AS - Asia 1.075
Continente sconosciuto - Info sul continente non disponibili 10
SA - Sud America 4
OC - Oceania 2
Totale 6.857
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Nazione #
US - Stati Uniti d'America 2.823
IE - Irlanda 1.088
CN - Cina 737
SE - Svezia 537
UA - Ucraina 525
IT - Italia 308
FR - Francia 140
IN - India 125
FI - Finlandia 121
TR - Turchia 109
SG - Singapore 82
DE - Germania 74
GB - Regno Unito 56
BE - Belgio 26
NL - Olanda 18
CZ - Repubblica Ceca 14
AT - Austria 10
RU - Federazione Russa 10
EU - Europa 9
IR - Iran 9
CA - Canada 6
AR - Argentina 3
IQ - Iraq 3
NO - Norvegia 3
JP - Giappone 2
MY - Malesia 2
PL - Polonia 2
VN - Vietnam 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AU - Australia 1
BA - Bosnia-Erzegovina 1
BD - Bangladesh 1
CH - Svizzera 1
CO - Colombia 1
ES - Italia 1
GT - Guatemala 1
HR - Croazia 1
IL - Israele 1
KR - Corea 1
NP - Nepal 1
NZ - Nuova Zelanda 1
Totale 6.857
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Città #
Dublin 1.087
Chandler 558
Jacksonville 371
Nyköping 349
Dearborn 315
Nanjing 197
Wilmington 125
Ann Arbor 118
Princeton 104
Ashburn 82
Beijing 75
Nanchang 75
San Mateo 68
Boardman 66
New York 66
Foggia 60
Woodbridge 58
Helsinki 55
Singapore 46
Changsha 43
Shenyang 43
Bari 37
Des Moines 34
Hebei 30
Jinan 28
Hilden 27
Kunming 27
Tianjin 26
Jiaxing 23
Brussels 22
Hangzhou 22
Los Angeles 21
Pune 19
Ningbo 16
Rome 16
San Severo 14
Brno 13
Munich 12
Guangzhou 11
Lanzhou 11
Auburn Hills 10
Orange 10
Vienna 10
Changchun 9
Zhengzhou 9
Milan 8
Norwalk 8
Shanghai 8
Florence 7
Fuzhou 7
London 7
Naples 7
Cutrofiano 6
Falls Church 6
Hefei 6
Stevenage 6
Haikou 5
Taizhou 5
Amsterdam 4
Borås 4
Cedar Knolls 4
Genoa 4
Redwood City 4
Taranto 4
Waanrode 4
Baghdad 3
Brescia 3
Buenos Aires 3
Chicago 3
Dongyang 3
Jinhua 3
Mola di Bari 3
Padova 3
Poli 3
Rui'an 3
Saint Petersburg 3
Seattle 3
Strasbourg 3
Taiyuan 3
Wuhan 3
Xuzhou 3
Augusta 2
Bologna 2
Cepagatti 2
Grottaglie 2
Hanoi 2
Kuala Lumpur 2
Leawood 2
Nutley 2
Palermo 2
Paris 2
Pietramontecorvino 2
Ravenna 2
San Cesario di Lecce 2
San Francisco 2
Tampa 2
Tokyo 2
Urmia 2
Vicenza 2
Walnut 2
Totale 4.618
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Nome #
Increased risk of venous thrombosis in carriers of the prothrombin A gene variant. 120
Detection of the factor V Leiden using SSCP 113
FV HR2 haplotype as additional inherited risk factor for deep vein thrombosis in individuals with a high-risk profile 107
ETEROGENEITA' FENOTIPICA NELLE IPERFENILALANINEMIE ALL'INTERNO DELLO STESSO NUCLEO FAMILIARE. 100
ADAMTS13 MUTATIONS AND POLYMORPHISMS IN CONGENITAL THROMBOTIC THROMBOCYTOPENIC PURPURA. 99
A polymorfism in VKORC1 gene is associated with an interindividual variability in the dose-anticoagulation effect of warfarin. 98
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 98
Role of tumour necrosis factor alpha and interleukin 1 beta in promoter effect induced by mercury in human keratinocytes 95
COESISTENZA DI DUE PATOLOGIE RARE: TROMBOASTENIA DI GLANZMANN E SINDROME DI KARTAGENER 94
Pharmacodynamic targets of psychotic patients treated with a long-acting therapy 94
An a priori prediction model of response to peginterferon plus ribavirin dual therapy in naïve patients with genotype 1 chronic hepatitis C. 92
Glanzmann's thrombasthenia: modulation of clinical phenotype by alpha2C807T gene polymorphism. 91
"Genetic modulation of oral anticoagulantion with warfarin " 89
ANALISI MOLECOLARE E CORRELAZIONE GENOTIPO-FENOTIPO IN FAMIGLIE CON IPERFENILALANINEMIE. 89
C0268 Higher risk of idiopathic small for gestational age newborns in Italian women carrying the annexin A5 M2 haplotype 88
Identification of six novel mutations in type I antithrombin deficient Italian families 88
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 88
Polymorphisms in factor II and factor VII genes modulate oral anticoagulation with warfarin 87
A beta3 Asp217-->Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin alphaIIBbeta3 functions. 87
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. 86
Detection of new deletions in a group of Italian patients with Hemophilia A by multiplex ligation-dependent probe amplification 86
Thrombofilic genotypes in subjects with idiopathic antiphospholipid antibodies-prevalence and significance 85
The relationship between personality traits, the 5HTT polymorphisms, and the occurrence of anxiety and depressive symptoms in elite athletes 84
Methylenetetrahydrofolate reductase (MTHFR) 677T-> C mutation and unexplained early pregnancy loss 83
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 83
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A. 82
The methylenetetrahydrofolate reductase TT677 genotype is associated with venous thrombosis independently of the coexistence of the FV Leiden and the prothrombin A20210 mutation. 81
Increased risk for venous thrombosis in carriers of the prothrombin G-->A20210 gene variant. 79
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A 78
Inherited coagulation disorders in cirrhotic patients with portal vein thrombosis 77
A new vitamin K epoxide reductase complex subunit-1 (VKORC1) mutation in a patient with decreased stability of CYP2C9 enzyme 77
A NOVEL NONSENSE TET2 MUTATION IN A PATIENT WITH PRIMARY MYELOFIBROSIS. 77
Thrombophilic genotypes in subjects with idiopathic antiphospholipid antibodies--prevalence and significance 77
Compound heterozygosity (554-589 del, C-T transition) in the platelet glycoprotein iba gene in a patient with a severe bleeding tendency. 76
Molecular characterization of a factor Vii deficient patient supports the importance of the second epidermal growth factor-like domain. 76
Genetic susceptibility to pregnancy-related venous thromboembolism: roles of factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations 75
Chronic thromboembolic pulmonary hypertension. 75
A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin 75
The assessment of the relationship between personality, the presence of the 5htt polymorphism, and the occurrence of anxiety and depressive symptoms in elite athletes 75
Intra-familiar discordant PKU phenotype explained by mutation analysis in three pedigrees. 74
Molecular diversity and thrombotic risk in protein S deficiency: the PROSIT study. 74
Inherited prothrombotic conditions and premature ischemic stroke. Sex difference in the association with Factor V leiden 74
Variation in genes encoding for interferon λ-3 and λ-4 in the prediction of HCV-1 treatment-induced viral clearance. 74
The Genetics of Hereditary Angioedema: A Review 74
Mutation analysis in hyperphenylalaninemia patients from South Italy. 73
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 73
Coexistence of factor V Leiden and Factor II A20210 mutations and recurrent venous thromboembolism 72
Identification of naïve HCV-1 patients with chronic hepatitis who may benefit from dual therapy with peg-interferon and ribavirin. 72
Survival in primary antiphospholipid syndrome: A single-centre cohort study 72
A novel allele variant of the SERPINF2 gene responsible for severe plasmin inhibitor (α2-antiplasmin) deficiency in an Italian patient 72
RGD-containing peptides inhibit fibrinogen binding to platelet alpha(IIb)beta3 by inducing an allosteric change in the amino-terminal portion of alpha(IIb). 71
Inherited platelet disorders>thrombocytopenias and thrombocytopathies. 71
Outcome of patients with splanchnic venous thrombosis presenting without overt MPN: a role for the JAK2 V617F mutation re-evaluation. 71
A MODEL TO PREDICT SUCCESS FOLLOWING PEG-INTERFERON AND RIBAVIRIN THERAPY FOR PATIENTS WITH HCV-1 INFECTION 71
Identifying human platelet glycoproteins IIb and IIla by capillary electrophoresis 70
Hereditary protein C deficiency and thrombosis risk: genotype and phenotype relation in a large Italian family. 69
Homozygosity by descent of a 3Mb chromosome 17 haplotype causes coinheritance of Glanzmann thrombasthenia and primary ciliary dyskinesia 69
Pharmacogenetics of dabigatran etexilate interindividual variability 69
Molecular characterization of a factor VII deficient patient supports the importance of the second epidermal growth factor-like domain. 67
Oral anticoagulant: pharmacogenetics relationship between genetic and non-genetic factors 67
Maladaptive coping strategies and neuroticism mediate the relationship between 5HTT-LPR polymorphisms and symptoms of anxiety in elite athletes 67
Selection of HCV-1 patients with chronic hepatitis who might benefit from current standard of therapy with peg-interferon and ribavirin 66
Clinical utility of screening for CALR gene exon 9 mutations in patients with splanchnic venous thrombosis 66
Deep intronic variations may cause mild hemophilia A. 64
Phenylalanine hydroxylase deficiency in south Italy: Genotype-phenotype correlations, identification of a novel mutant PAH allele and prediction of BH4 responsiveness 64
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A 64
Venous thrombosis in afibrinogenemia: a successful use of rivaroxaban 64
High prevalence of thrombophilic genotypes in patients with acute mesenteric vein thrombosis. 62
A myoferlin gain-of-function variant associates with a new type of hereditary angioedema 61
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 60
Intra-familiar discordant PKU phenotype explained by mutation analysis in three pedigrees. 59
The Genetics of Hereditary Angioedema: A Review 59
Glanzmann's thrombasthenia: identification of 19 new mutations in 30 patients 58
Lack of genotypephenotype correlation in congenital adrenal hyperplasia due to a CYP21A2-like gene 58
Factor XI gene variants in factor XI-deficient patients of Southern Italy: identification of a novel mutation and genotype-phenotype relationship 55
A Novel KCNN2 Variant in a Family with Essential Tremor Plus: Clinical Characteristics and In Silico Analysis 52
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) 51
THE MOLECULAR ORGANIZATION OF ENDOTHELIAL JUNCTIONS IN VASCULAR PERMEABILITY 51
A beta3 Asp217-->Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin alphaIIBbeta3 functions 51
Interleukin 28B Gene Polymorphisms in Hepatitis C Virus-related Cryoglobulinemic Vasculitis 47
Validation of PLASMIC score and follow-up data in a cohort of patients with suspected microangiopathies from Southern Italy 47
Identification of the Novel G250R Variant Indicates a Role for Thrombomodulin in Modulating the Risk for Venous Thromboembolism 46
Harm Avoidance as a possible mediator in the relationship between the 5-HTTLPR and Cognitive Anxiety in High Level Athletes 46
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 46
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 45
.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 43
Identification of the Novel G250R Variant Indicates a Role for Thrombomodulin in Modulating the Risk for Venous Thromboembolism 42
Anticoagulation in Italian patients with venous thromboembolism and thrombophilic alterations: findings from START2 register study 42
Lack of genotypephenotype correlation in congenital adrenal hyperplasia due to a CYP21A2-like gene. 42
Validation of PLASMIC score and follow-up data in a cohort of patients with suspected microangiopathies from Southern Italy 40
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 39
Psychosomatic syndromes are associated with IL-6 pro-inflammatory cytokine in heart failure patients 38
Clinical utility of screening for CALR gene exon 9 mutations in patients with splanchnic venous thrombosis. 35
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. 33
. 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 33
. FV HR2 haplotype as additional inherited risk factor for deep vein thrombosis in individuals with a high-risk profile. Thromb Haemost. 2002; 87(1):32-6. 30
Factor XI gene variants in factor XI-deficient patients of Southern Italy: identification of a novel mutation and genotype-phenotype relationship 30
. 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 30
. 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. Haematologica 2003; .88(3):286-9. 25
null 24
Totale 6.838
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Categoria #
all - tutte 35.692
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 35.692
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.053 0 149 58 22 154 182 231 13 105 23 96 20
2020/2021704 90 6 83 11 80 49 98 40 135 96 3 13
2021/2022741 79 0 29 20 122 14 16 51 82 136 30 162
2022/20232.611 236 92 119 165 167 231 17 214 1.250 19 45 56
2023/2024467 81 21 23 15 34 124 36 20 3 9 8 93
2024/2025128 100 28 0 0 0 0 0 0 0 0 0 0
Totale 7.186