IRIS
D'ANDREA, GIOVANNA
 Distribuzione geografica
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Continente #
EU - Europa 2.891
NA - Nord America 2.792
AS - Asia 931
Continente sconosciuto - Info sul continente non disponibili 10
SA - Sud America 4
OC - Oceania 2
Totale 6.630
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Nazione #
US - Stati Uniti d'America 2.785
IE - Irlanda 1.088
CN - Cina 676
SE - Svezia 537
UA - Ucraina 525
IT - Italia 300
FR - Francia 140
IN - India 125
FI - Finlandia 109
TR - Turchia 109
DE - Germania 63
GB - Regno Unito 56
BE - Belgio 26
NL - Olanda 18
AT - Austria 10
RU - Federazione Russa 10
EU - Europa 9
IR - Iran 7
CA - Canada 6
AR - Argentina 3
IQ - Iraq 3
NO - Norvegia 3
JP - Giappone 2
MY - Malesia 2
PL - Polonia 2
SG - Singapore 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
NZ - Nuova Zelanda 1
Totale 6.630
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Città #
Dublin 1.087
Chandler 558
Jacksonville 371
Nyköping 349
Dearborn 315
Nanjing 196
Wilmington 125
Ann Arbor 118
Princeton 104
Ashburn 82
Beijing 75
Nanchang 75
San Mateo 68
New York 66
Foggia 60
Woodbridge 58
Changsha 43
Helsinki 43
Shenyang 43
Boardman 38
Des Moines 34
Bari 30
Hebei 30
Jinan 28
Hilden 27
Kunming 27
Tianjin 26
Brussels 22
Hangzhou 22
Jiaxing 19
Pune 19
Ningbo 16
Rome 16
Los Angeles 15
San Severo 14
Lanzhou 11
Auburn Hills 10
Orange 10
Vienna 10
Changchun 9
Zhengzhou 9
Milan 8
Norwalk 8
Florence 7
Fuzhou 7
London 7
Naples 7
Cutrofiano 6
Falls Church 6
Hefei 6
Stevenage 6
Guangzhou 5
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
Mola di Bari 3
Padova 3
Poli 3
Saint Petersburg 3
Seattle 3
Strasbourg 3
Taiyuan 3
Augusta 2
Bologna 2
Cepagatti 2
Grottaglie 2
Hanoi 2
Jinhua 2
Kuala Lumpur 2
Leawood 2
Nutley 2
Palermo 2
Paris 2
Pietramontecorvino 2
Ravenna 2
San Cesario di Lecce 2
San Francisco 2
Shanghai 2
Tampa 2
Tokyo 2
Vicenza 2
Walnut 2
Acquaviva Delle Fonti 1
Acquaviva delle Fonti 1
Adelfia 1
Altamura 1
Apo 1
Arezzo 1
Arklow 1
Arzano 1
Totale 4.470
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Nome #
Increased risk of venous thrombosis in carriers of the prothrombin A gene variant. 119
Detection of the factor V Leiden using SSCP 111
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. 98
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 94
Role of tumour necrosis factor alpha and interleukin 1 beta in promoter effect induced by mercury in human keratinocytes 93
COESISTENZA DI DUE PATOLOGIE RARE: TROMBOASTENIA DI GLANZMANN E SINDROME DI KARTAGENER 93
A polymorfism in VKORC1 gene is associated with an interindividual variability in the dose-anticoagulation effect of warfarin. 92
Pharmacodynamic targets of psychotic patients treated with a long-acting therapy 92
Glanzmann's thrombasthenia: modulation of clinical phenotype by alpha2C807T gene polymorphism. 90
An a priori prediction model of response to peginterferon plus ribavirin dual therapy in naïve patients with genotype 1 chronic hepatitis C. 90
C0268 Higher risk of idiopathic small for gestational age newborns in Italian women carrying the annexin A5 M2 haplotype 88
ANALISI MOLECOLARE E CORRELAZIONE GENOTIPO-FENOTIPO IN FAMIGLIE CON IPERFENILALANINEMIE. 88
Identification of six novel mutations in type I antithrombin deficient Italian families 87
"Genetic modulation of oral anticoagulantion with warfarin " 87
Polymorphisms in factor II and factor VII genes modulate oral anticoagulation with warfarin 87
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 87
Thrombofilic genotypes in subjects with idiopathic antiphospholipid antibodies-prevalence and significance 84
Detection of new deletions in a group of Italian patients with Hemophilia A by multiplex ligation-dependent probe amplification 84
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. 83
A beta3 Asp217-->Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin alphaIIBbeta3 functions. 83
The relationship between personality traits, the 5HTT polymorphisms, and the occurrence of anxiety and depressive symptoms in elite athletes 83
Methylenetetrahydrofolate reductase (MTHFR) 677T-> C mutation and unexplained early pregnancy loss 81
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 81
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A. 80
The methylenetetrahydrofolate reductase TT677 genotype is associated with venous thrombosis independently of the coexistence of the FV Leiden and the prothrombin A20210 mutation. 79
Increased risk for venous thrombosis in carriers of the prothrombin G-->A20210 gene variant. 78
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A 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
A NOVEL NONSENSE TET2 MUTATION IN A PATIENT WITH PRIMARY MYELOFIBROSIS. 76
Inherited coagulation disorders in cirrhotic patients with portal vein thrombosis 75
A new vitamin K epoxide reductase complex subunit-1 (VKORC1) mutation in a patient with decreased stability of CYP2C9 enzyme 75
Thrombophilic genotypes in subjects with idiopathic antiphospholipid antibodies--prevalence and significance 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 74
Intra-familiar discordant PKU phenotype explained by mutation analysis in three pedigrees. 73
Inherited prothrombotic conditions and premature ischemic stroke. Sex difference in the association with Factor V leiden 73
Genetic susceptibility to pregnancy-related venous thromboembolism: roles of factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations 73
Variation in genes encoding for interferon λ-3 and λ-4 in the prediction of HCV-1 treatment-induced viral clearance. 73
Coexistence of factor V Leiden and Factor II A20210 mutations and recurrent venous thromboembolism 72
Mutation analysis in hyperphenylalaninemia patients from South Italy. 72
A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin 72
Molecular diversity and thrombotic risk in protein S deficiency: the PROSIT study. 71
Identification of naïve HCV-1 patients with chronic hepatitis who may benefit from dual therapy with peg-interferon and ribavirin. 71
Outcome of patients with splanchnic venous thrombosis presenting without overt MPN: a role for the JAK2 V617F mutation re-evaluation. 71
Chronic thromboembolic pulmonary hypertension. 71
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 71
The Genetics of Hereditary Angioedema: A Review 71
RGD-containing peptides inhibit fibrinogen binding to platelet alpha(IIb)beta3 by inducing an allosteric change in the amino-terminal portion of alpha(IIb). 70
Inherited platelet disorders>thrombocytopenias and thrombocytopathies. 70
Survival in primary antiphospholipid syndrome: A single-centre cohort study 70
Identifying human platelet glycoproteins IIb and IIla by capillary electrophoresis 70
Pharmacogenetics of dabigatran etexilate interindividual variability 69
Hereditary protein C deficiency and thrombosis risk: genotype and phenotype relation in a large Italian family. 68
Homozygosity by descent of a 3Mb chromosome 17 haplotype causes coinheritance of Glanzmann thrombasthenia and primary ciliary dyskinesia 68
A novel allele variant of the SERPINF2 gene responsible for severe plasmin inhibitor (α2-antiplasmin) deficiency in an Italian patient 67
Oral anticoagulant: pharmacogenetics relationship between genetic and non-genetic factors 66
A MODEL TO PREDICT SUCCESS FOLLOWING PEG-INTERFERON AND RIBAVIRIN THERAPY FOR PATIENTS WITH HCV-1 INFECTION 66
Clinical utility of screening for CALR gene exon 9 mutations in patients with splanchnic venous thrombosis 66
Maladaptive coping strategies and neuroticism mediate the relationship between 5HTT-LPR polymorphisms and symptoms of anxiety in elite athletes 66
Molecular characterization of a factor VII deficient patient supports the importance of the second epidermal growth factor-like domain. 65
Selection of HCV-1 patients with chronic hepatitis who might benefit from current standard of therapy with peg-interferon and ribavirin 64
Deep intronic variations may cause mild hemophilia A. 63
Venous thrombosis in afibrinogenemia: a successful use of rivaroxaban 63
High prevalence of thrombophilic genotypes in patients with acute mesenteric vein thrombosis. 62
Phenylalanine hydroxylase deficiency in south Italy: Genotype-phenotype correlations, identification of a novel mutant PAH allele and prediction of BH4 responsiveness 62
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A 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 59
Intra-familiar discordant PKU phenotype explained by mutation analysis in three pedigrees. 58
Glanzmann's thrombasthenia: identification of 19 new mutations in 30 patients 57
Lack of genotypephenotype correlation in congenital adrenal hyperplasia due to a CYP21A2-like gene 57
The Genetics of Hereditary Angioedema: A Review 57
A myoferlin gain-of-function variant associates with a new type of hereditary angioedema 56
Factor XI gene variants in factor XI-deficient patients of Southern Italy: identification of a novel mutation and genotype-phenotype relationship 53
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) 50
THE MOLECULAR ORGANIZATION OF ENDOTHELIAL JUNCTIONS IN VASCULAR PERMEABILITY 50
Interleukin 28B Gene Polymorphisms in Hepatitis C Virus-related Cryoglobulinemic Vasculitis 46
A beta3 Asp217-->Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin alphaIIBbeta3 functions 45
Validation of PLASMIC score and follow-up data in a cohort of patients with suspected microangiopathies from Southern Italy 45
Identification of the Novel G250R Variant Indicates a Role for Thrombomodulin in Modulating the Risk for Venous Thromboembolism 44
Harm Avoidance as a possible mediator in the relationship between the 5-HTTLPR and Cognitive Anxiety in High Level Athletes 42
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 42
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 41
.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 41
A Novel KCNN2 Variant in a Family with Essential Tremor Plus: Clinical Characteristics and In Silico Analysis 41
Anticoagulation in Italian patients with venous thromboembolism and thrombophilic alterations: findings from START2 register study 40
Lack of genotypephenotype correlation in congenital adrenal hyperplasia due to a CYP21A2-like gene. 40
Identification of the Novel G250R Variant Indicates a Role for Thrombomodulin in Modulating the Risk for Venous Thromboembolism 39
Validation of PLASMIC score and follow-up data in a cohort of patients with suspected microangiopathies from Southern Italy 39
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 34
Psychosomatic syndromes are associated with IL-6 pro-inflammatory cytokine in heart failure patients 34
Clinical utility of screening for CALR gene exon 9 mutations in patients with splanchnic venous thrombosis. 33
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. 31
. 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 30
Factor XI gene variants in factor XI-deficient patients of Southern Italy: identification of a novel mutation and genotype-phenotype relationship 28
. 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. 27
. 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 26
null 24
Juvenile patients with the homozygous MTHFR C677T genotype develop ischemic stroke 5 years earlier than wild type 22
Totale 6.644
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Categoria #
all - tutte 31.275
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 31.275
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019135 0 0 0 0 0 0 0 0 0 0 41 94
2019/20201.332 279 149 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
2023/2024366 81 21 23 15 34 124 36 20 3 9 0 0
Totale 6.957