IRIS
D'ANDREA, GIOVANNA
 Distribuzione geografica
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Continente #
EU - Europa 3.091
NA - Nord America 3.007
AS - Asia 1.341
Continente sconosciuto - Info sul continente non disponibili 10
SA - Sud America 8
OC - Oceania 2
Totale 7.459
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Nazione #
US - Stati Uniti d'America 2.996
IE - Irlanda 1.141
CN - Cina 840
SE - Svezia 546
UA - Ucraina 525
IT - Italia 338
SG - Singapore 160
FR - Francia 140
FI - Finlandia 137
IN - India 127
DE - Germania 110
TR - Turchia 109
HK - Hong Kong 78
GB - Regno Unito 60
BE - Belgio 27
NL - Olanda 19
CZ - Repubblica Ceca 14
RU - Federazione Russa 11
AT - Austria 10
CA - Canada 9
EU - Europa 9
IR - Iran 9
AR - Argentina 4
ID - Indonesia 3
IQ - Iraq 3
LT - Lituania 3
NO - Norvegia 3
VN - Vietnam 3
BR - Brasile 2
JP - Giappone 2
MY - Malesia 2
PL - Polonia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AU - Australia 1
BA - Bosnia-Erzegovina 1
BD - Bangladesh 1
BO - Bolivia 1
CH - Svizzera 1
CO - Colombia 1
ES - Italia 1
GT - Guatemala 1
HR - Croazia 1
IL - Israele 1
KG - Kirghizistan 1
KR - Corea 1
NP - Nepal 1
NZ - Nuova Zelanda 1
PA - Panama 1
PT - Portogallo 1
Totale 7.459
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Città #
Dublin 1.140
Chandler 558
Jacksonville 371
Nyköping 358
Dearborn 315
Nanjing 197
Santa Clara 129
Wilmington 129
Ann Arbor 118
Princeton 110
Singapore 106
Ashburn 85
Beijing 78
Hong Kong 78
Nanchang 75
New York 70
Foggia 69
San Mateo 68
Boardman 66
Helsinki 65
Woodbridge 58
Changsha 44
Shenyang 43
Munich 40
Bari 39
Des Moines 35
Hebei 30
Jinan 28
Hilden 27
Kunming 27
Tianjin 27
Jiaxing 26
Los Angeles 25
Brussels 23
Hangzhou 22
Guangzhou 19
Lanzhou 19
Pune 19
Rome 18
Shanghai 18
Ningbo 16
San Severo 14
Brno 13
Auburn Hills 10
Orange 10
Vienna 10
Changchun 9
London 9
Milan 9
Norwalk 9
Zhengzhou 9
Fuzhou 8
Florence 7
Hefei 7
Naples 7
Cutrofiano 6
Espoo 6
Falls Church 6
Shenzhen 6
Stevenage 6
Taizhou 6
Frankfurt am Main 5
Haikou 5
Amsterdam 4
Borås 4
Cedar Knolls 4
Genoa 4
Manfredonia 4
Redwood City 4
Taranto 4
Waanrode 4
Wuhan 4
Baghdad 3
Brescia 3
Buenos Aires 3
Chicago 3
Dongyang 3
Foshan 3
Jakarta 3
Jinhua 3
Mola di Bari 3
Padova 3
Poli 3
Rui'an 3
Saint Petersburg 3
Seattle 3
Strasbourg 3
Taiyuan 3
Toronto 3
Xuzhou 3
Augusta 2
Bologna 2
Cepagatti 2
Grottaglie 2
Hanoi 2
Kuala Lumpur 2
Leawood 2
Nutley 2
Palermo 2
Palo del Colle 2
Totale 5.075
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Nome #
Increased risk of venous thrombosis in carriers of the prothrombin A gene variant. 121
Detection of the factor V Leiden using SSCP 117
FV HR2 haplotype as additional inherited risk factor for deep vein thrombosis in individuals with a high-risk profile 114
Role of tumour necrosis factor alpha and interleukin 1 beta in promoter effect induced by mercury in human keratinocytes 104
ETEROGENEITA' FENOTIPICA NELLE IPERFENILALANINEMIE ALL'INTERNO DELLO STESSO NUCLEO FAMILIARE. 102
ADAMTS13 MUTATIONS AND POLYMORPHISMS IN CONGENITAL THROMBOTIC THROMBOCYTOPENIC PURPURA. 102
A polymorfism in VKORC1 gene is associated with an interindividual variability in the dose-anticoagulation effect of warfarin. 101
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 101
Pharmacodynamic targets of psychotic patients treated with a long-acting therapy 98
"Genetic modulation of oral anticoagulantion with warfarin " 97
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 97
Detection of new deletions in a group of Italian patients with Hemophilia A by multiplex ligation-dependent probe amplification 96
An a priori prediction model of response to peginterferon plus ribavirin dual therapy in naïve patients with genotype 1 chronic hepatitis C. 96
Glanzmann's thrombasthenia: modulation of clinical phenotype by alpha2C807T gene polymorphism. 95
COESISTENZA DI DUE PATOLOGIE RARE: TROMBOASTENIA DI GLANZMANN E SINDROME DI KARTAGENER 95
Polymorphisms in factor II and factor VII genes modulate oral anticoagulation with warfarin 94
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. 93
A beta3 Asp217-->Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin alphaIIBbeta3 functions. 92
Identification of six novel mutations in type I antithrombin deficient Italian families 91
C0268 Higher risk of idiopathic small for gestational age newborns in Italian women carrying the annexin A5 M2 haplotype 90
ANALISI MOLECOLARE E CORRELAZIONE GENOTIPO-FENOTIPO IN FAMIGLIE CON IPERFENILALANINEMIE. 90
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 90
Thrombofilic genotypes in subjects with idiopathic antiphospholipid antibodies-prevalence and significance 87
The relationship between personality traits, the 5HTT polymorphisms, and the occurrence of anxiety and depressive symptoms in elite athletes 87
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A. 86
The methylenetetrahydrofolate reductase TT677 genotype is associated with venous thrombosis independently of the coexistence of the FV Leiden and the prothrombin A20210 mutation. 85
Methylenetetrahydrofolate reductase (MTHFR) 677T-> C mutation and unexplained early pregnancy loss 85
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A 85
A NOVEL NONSENSE TET2 MUTATION IN A PATIENT WITH PRIMARY MYELOFIBROSIS. 85
Compound heterozygosity (554-589 del, C-T transition) in the platelet glycoprotein iba gene in a patient with a severe bleeding tendency. 84
Molecular characterization of a factor Vii deficient patient supports the importance of the second epidermal growth factor-like domain. 84
Increased risk for venous thrombosis in carriers of the prothrombin G-->A20210 gene variant. 82
A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin 82
Inherited coagulation disorders in cirrhotic patients with portal vein thrombosis 80
A new vitamin K epoxide reductase complex subunit-1 (VKORC1) mutation in a patient with decreased stability of CYP2C9 enzyme 80
Intra-familiar discordant PKU phenotype explained by mutation analysis in three pedigrees. 79
Molecular diversity and thrombotic risk in protein S deficiency: the PROSIT study. 79
Coexistence of factor V Leiden and Factor II A20210 mutations and recurrent venous thromboembolism 79
Inherited prothrombotic conditions and premature ischemic stroke. Sex difference in the association with Factor V leiden 79
Genetic susceptibility to pregnancy-related venous thromboembolism: roles of factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations 79
Identification of naïve HCV-1 patients with chronic hepatitis who may benefit from dual therapy with peg-interferon and ribavirin. 78
Mutation analysis in hyperphenylalaninemia patients from South Italy. 78
Chronic thromboembolic pulmonary hypertension. 78
Thrombophilic genotypes in subjects with idiopathic antiphospholipid antibodies--prevalence and significance 78
Outcome of patients with splanchnic venous thrombosis presenting without overt MPN: a role for the JAK2 V617F mutation re-evaluation. 77
The assessment of the relationship between personality, the presence of the 5htt polymorphism, and the occurrence of anxiety and depressive symptoms in elite athletes 77
A novel allele variant of the SERPINF2 gene responsible for severe plasmin inhibitor (α2-antiplasmin) deficiency in an Italian patient 77
Inherited platelet disorders>thrombocytopenias and thrombocytopathies. 76
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 76
Variation in genes encoding for interferon λ-3 and λ-4 in the prediction of HCV-1 treatment-induced viral clearance. 75
The Genetics of Hereditary Angioedema: A Review 75
RGD-containing peptides inhibit fibrinogen binding to platelet alpha(IIb)beta3 by inducing an allosteric change in the amino-terminal portion of alpha(IIb). 74
A MODEL TO PREDICT SUCCESS FOLLOWING PEG-INTERFERON AND RIBAVIRIN THERAPY FOR PATIENTS WITH HCV-1 INFECTION 74
Survival in primary antiphospholipid syndrome: A single-centre cohort study 73
Identifying human platelet glycoproteins IIb and IIla by capillary electrophoresis 72
Homozygosity by descent of a 3Mb chromosome 17 haplotype causes coinheritance of Glanzmann thrombasthenia and primary ciliary dyskinesia 71
Pharmacogenetics of dabigatran etexilate interindividual variability 71
A Novel KCNN2 Variant in a Family with Essential Tremor Plus: Clinical Characteristics and In Silico Analysis 71
Oral anticoagulant: pharmacogenetics relationship between genetic and non-genetic factors 70
Hereditary protein C deficiency and thrombosis risk: genotype and phenotype relation in a large Italian family. 70
Deep intronic variations may cause mild hemophilia A. 70
Maladaptive coping strategies and neuroticism mediate the relationship between 5HTT-LPR polymorphisms and symptoms of anxiety in elite athletes 70
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A 70
Molecular characterization of a factor VII deficient patient supports the importance of the second epidermal growth factor-like domain. 68
Selection of HCV-1 patients with chronic hepatitis who might benefit from current standard of therapy with peg-interferon and ribavirin 67
Phenylalanine hydroxylase deficiency in south Italy: Genotype-phenotype correlations, identification of a novel mutant PAH allele and prediction of BH4 responsiveness 67
Clinical utility of screening for CALR gene exon 9 mutations in patients with splanchnic venous thrombosis 67
A myoferlin gain-of-function variant associates with a new type of hereditary angioedema 66
Venous thrombosis in afibrinogenemia: a successful use of rivaroxaban 66
High prevalence of thrombophilic genotypes in patients with acute mesenteric vein thrombosis. 65
Intra-familiar discordant PKU phenotype explained by mutation analysis in three pedigrees. 65
Glanzmann's thrombasthenia: identification of 19 new mutations in 30 patients 62
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 62
The Genetics of Hereditary Angioedema: A Review 62
Lack of genotypephenotype correlation in congenital adrenal hyperplasia due to a CYP21A2-like gene 59
Factor XI gene variants in factor XI-deficient patients of Southern Italy: identification of a novel mutation and genotype-phenotype relationship 57
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) 57
null 55
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 53
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 52
A beta3 Asp217-->Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin alphaIIBbeta3 functions 52
Validation of PLASMIC score and follow-up data in a cohort of patients with suspected microangiopathies from Southern Italy 52
Identification of the Novel G250R Variant Indicates a Role for Thrombomodulin in Modulating the Risk for Venous Thromboembolism 50
Harm Avoidance as a possible mediator in the relationship between the 5-HTTLPR and Cognitive Anxiety in High Level Athletes 50
Interleukin 28B Gene Polymorphisms in Hepatitis C Virus-related Cryoglobulinemic Vasculitis 49
.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 49
Anticoagulation in Italian patients with venous thromboembolism and thrombophilic alterations: findings from START2 register study 48
Identification of the Novel G250R Variant Indicates a Role for Thrombomodulin in Modulating the Risk for Venous Thromboembolism 45
Lack of genotypephenotype correlation in congenital adrenal hyperplasia due to a CYP21A2-like gene. 45
Validation of PLASMIC score and follow-up data in a cohort of patients with suspected microangiopathies from Southern Italy 44
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 44
Psychosomatic syndromes are associated with IL-6 pro-inflammatory cytokine in heart failure patients 42
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. 40
Clinical utility of screening for CALR gene exon 9 mutations in patients with splanchnic venous thrombosis. 36
. 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 36
. 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 34
. 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. 32
Factor XI gene variants in factor XI-deficient patients of Southern Italy: identification of a novel mutation and genotype-phenotype relationship 31
Juvenile patients with the homozygous MTHFR C677T genotype develop ischemic stroke 5 years earlier than wild type 28
. Polymorphisms in factor II and factor VII genes modulate oral anticoagulation with warfarin. Haematologica 2004; 89(12):1510-6. 28
Totale 7.249
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Categoria #
all - tutte 43.703
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 43.703
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020488 0 0 0 0 0 0 231 13 105 23 96 20
2020/2021704 90 6 83 11 80 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
2024/2025640 105 35 49 106 95 247 3 0 0 0 0 0
Totale 7.826