IRIS
D'ANDREA, GIOVANNA
 Distribuzione geografica
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Continente #
NA - Nord America 5.004
EU - Europa 4.222
AS - Asia 3.142
SA - Sud America 453
Continente sconosciuto - Info sul continente non disponibili 418
AF - Africa 56
OC - Oceania 3
Totale 13.298
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Nazione #
US - Stati Uniti d'America 4.926
IE - Irlanda 1.142
CN - Cina 1.115
SG - Singapore 1.112
RU - Federazione Russa 589
SE - Svezia 552
UA - Ucraina 528
IT - Italia 501
BR - Brasile 361
FR - Francia 291
HK - Hong Kong 237
VN - Vietnam 210
DE - Germania 204
FI - Finlandia 166
IN - India 162
TR - Turchia 122
GB - Regno Unito 93
CA - Canada 40
BD - Bangladesh 36
NL - Olanda 32
AR - Argentina 31
IQ - Iraq 31
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
MX - Messico 12
VE - Venezuela 12
CL - Cile 11
EC - Ecuador 11
CO - Colombia 10
IR - Iran 10
EU - Europa 9
JO - Giordania 9
AE - Emirati Arabi Uniti 8
BO - Bolivia 8
ES - Italia 8
UZ - Uzbekistan 8
MA - Marocco 7
EG - Egitto 6
LT - Lituania 6
MY - Malesia 6
CR - Costa Rica 5
KE - Kenya 5
AL - Albania 4
CH - Svizzera 4
JM - Giamaica 4
PY - Paraguay 4
SA - Arabia Saudita 4
BY - Bielorussia 3
ET - Etiopia 3
HN - Honduras 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
PR - Porto Rico 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
BB - Barbados 1
BF - Burkina Faso 1
BH - Bahrain 1
BN - Brunei Darussalam 1
CU - Cuba 1
DK - Danimarca 1
GA - Gabon 1
GE - Georgia 1
GR - Grecia 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
Totale 12.884
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Città #
Dublin 1.141
San Jose 846
Chandler 558
Singapore 486
Jacksonville 372
Nyköping 358
Ashburn 329
Dearborn 315
Beijing 243
Hong Kong 237
Nanjing 197
Santa Clara 152
Council Bluffs 142
The Dalles 138
Wilmington 129
Ann Arbor 118
Lauterbourg 117
Princeton 110
Dallas 95
Moscow 95
Munich 93
New York 88
Ho Chi Minh City 76
Nanchang 75
Foggia 71
San Mateo 68
Boardman 67
Helsinki 67
Columbus 60
Woodbridge 58
Bari 47
Los Angeles 47
Hanoi 45
Changsha 44
Shenyang 43
Des Moines 36
Rome 34
Hebei 30
Jinan 28
Tianjin 28
Hilden 27
Kunming 27
Milan 27
Turku 27
Jiaxing 26
Brussels 23
Hangzhou 23
Shanghai 23
São Paulo 22
Lanzhou 20
Nuremberg 20
Pune 20
Guangzhou 19
Frankfurt am Main 17
Hillsboro 16
Ningbo 16
Rio de Janeiro 16
Vienna 15
San Francisco 14
San Severo 14
Tokyo 14
Baghdad 13
Brno 13
London 13
Manfredonia 12
Naples 12
Porto Alegre 12
Warsaw 12
Modena 11
Amsterdam 10
Auburn Hills 10
Norwalk 10
Orange 10
Zhengzhou 10
Atlanta 9
Buenos Aires 9
Changchun 9
Paris 9
Toronto 9
Amman 8
Brasília 8
Charlotte 8
Chennai 8
Chicago 8
Florence 8
Fuzhou 8
Jakarta 8
Manchester 8
Phoenix 8
Biên Hòa 7
Da Nang 7
Hefei 7
Orem 7
Tashkent 7
Belo Horizonte 6
Blumenau 6
Cutrofiano 6
Espoo 6
Falls Church 6
Johannesburg 6
Totale 8.053
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Nome #
Increased risk of venous thrombosis in carriers of the prothrombin A gene variant. 168
A polymorfism in VKORC1 gene is associated with an interindividual variability in the dose-anticoagulation effect of warfarin. 157
ADAMTS13 MUTATIONS AND POLYMORPHISMS IN CONGENITAL THROMBOTIC THROMBOCYTOPENIC PURPURA. 153
"Genetic modulation of oral anticoagulantion with warfarin " 151
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. 148
Role of tumour necrosis factor alpha and interleukin 1 beta in promoter effect induced by mercury in human keratinocytes 147
FV HR2 haplotype as additional inherited risk factor for deep vein thrombosis in individuals with a high-risk profile 146
Detection of the factor V Leiden using SSCP 144
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 144
A beta3 Asp217-->Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin alphaIIBbeta3 functions. 143
COESISTENZA DI DUE PATOLOGIE RARE: TROMBOASTENIA DI GLANZMANN E SINDROME DI KARTAGENER 143
ETEROGENEITA' FENOTIPICA NELLE IPERFENILALANINEMIE ALL'INTERNO DELLO STESSO NUCLEO FAMILIARE. 142
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 142
A Novel KCNN2 Variant in a Family with Essential Tremor Plus: Clinical Characteristics and In Silico Analysis 142
The Genetics of Hereditary Angioedema: A Review 136
ANALISI MOLECOLARE E CORRELAZIONE GENOTIPO-FENOTIPO IN FAMIGLIE CON IPERFENILALANINEMIE. 135
A NOVEL NONSENSE TET2 MUTATION IN A PATIENT WITH PRIMARY MYELOFIBROSIS. 133
A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin 132
Detection of new deletions in a group of Italian patients with Hemophilia A by multiplex ligation-dependent probe amplification 131
A MODEL TO PREDICT SUCCESS FOLLOWING PEG-INTERFERON AND RIBAVIRIN THERAPY FOR PATIENTS WITH HCV-1 INFECTION 131
Glanzmann's thrombasthenia: modulation of clinical phenotype by alpha2C807T gene polymorphism. 130
An a priori prediction model of response to peginterferon plus ribavirin dual therapy in naïve patients with genotype 1 chronic hepatitis C. 130
A myoferlin gain-of-function variant associates with a new type of hereditary angioedema 130
Polymorphisms in factor II and factor VII genes modulate oral anticoagulation with warfarin 128
C0268 Higher risk of idiopathic small for gestational age newborns in Italian women carrying the annexin A5 M2 haplotype 127
Increased risk for venous thrombosis in carriers of the prothrombin G-->A20210 gene variant. 127
Genetic susceptibility to pregnancy-related venous thromboembolism: roles of factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations 127
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 127
A new vitamin K epoxide reductase complex subunit-1 (VKORC1) mutation in a patient with decreased stability of CYP2C9 enzyme 126
Thrombofilic genotypes in subjects with idiopathic antiphospholipid antibodies-prevalence and significance 124
Inherited prothrombotic conditions and premature ischemic stroke. Sex difference in the association with Factor V leiden 124
Pharmacodynamic targets of psychotic patients treated with a long-acting therapy 124
A novel allele variant of the SERPINF2 gene responsible for severe plasmin inhibitor (α2-antiplasmin) deficiency in an Italian patient 124
Identification of six novel mutations in type I antithrombin deficient Italian families 123
THE MOLECULAR ORGANIZATION OF ENDOTHELIAL JUNCTIONS IN VASCULAR PERMEABILITY 123
Molecular diversity and thrombotic risk in protein S deficiency: the PROSIT study. 122
Compound heterozygosity (554-589 del, C-T transition) in the platelet glycoprotein iba gene in a patient with a severe bleeding tendency. 121
Mutation analysis in hyperphenylalaninemia patients from South Italy. 121
The relationship between personality traits, the 5HTT polymorphisms, and the occurrence of anxiety and depressive symptoms in elite athletes 121
Molecular characterization of a factor Vii deficient patient supports the importance of the second epidermal growth factor-like domain. 120
Identification of naïve HCV-1 patients with chronic hepatitis who may benefit from dual therapy with peg-interferon and ribavirin. 120
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 120
Methylenetetrahydrofolate reductase (MTHFR) 677T-> C mutation and unexplained early pregnancy loss 119
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A. 119
Phenylalanine hydroxylase deficiency in south Italy: Genotype-phenotype correlations, identification of a novel mutant PAH allele and prediction of BH4 responsiveness 119
The methylenetetrahydrofolate reductase TT677 genotype is associated with venous thrombosis independently of the coexistence of the FV Leiden and the prothrombin A20210 mutation. 118
Chronic thromboembolic pulmonary hypertension. 118
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A 118
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A 117
Thrombophilic genotypes in subjects with idiopathic antiphospholipid antibodies--prevalence and significance 117
Selection of HCV-1 patients with chronic hepatitis who might benefit from current standard of therapy with peg-interferon and ribavirin 116
Coexistence of factor V Leiden and Factor II A20210 mutations and recurrent venous thromboembolism 115
Inherited coagulation disorders in cirrhotic patients with portal vein thrombosis 115
Psychosomatic syndromes are associated with IL-6 pro-inflammatory cytokine in heart failure patients 115
Survival in primary antiphospholipid syndrome: A single-centre cohort study 113
RGD-containing peptides inhibit fibrinogen binding to platelet alpha(IIb)beta3 by inducing an allosteric change in the amino-terminal portion of alpha(IIb). 111
Deep intronic variations may cause mild hemophilia A. 111
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 111
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 110
Maladaptive coping strategies and neuroticism mediate the relationship between 5HTT-LPR polymorphisms and symptoms of anxiety in elite athletes 110
Intra-familiar discordant PKU phenotype explained by mutation analysis in three pedigrees. 109
Homozygosity by descent of a 3Mb chromosome 17 haplotype causes coinheritance of Glanzmann thrombasthenia and primary ciliary dyskinesia 109
Outcome of patients with splanchnic venous thrombosis presenting without overt MPN: a role for the JAK2 V617F mutation re-evaluation. 108
DAB2IP associates with hereditary angioedema: Insights into the role of VEGF signaling in HAE pathophysiology 107
Hereditary protein C deficiency and thrombosis risk: genotype and phenotype relation in a large Italian family. 107
Intra-familiar discordant PKU phenotype explained by mutation analysis in three pedigrees. 107
Variation in genes encoding for interferon λ-3 and λ-4 in the prediction of HCV-1 treatment-induced viral clearance. 104
The assessment of the relationship between personality, the presence of the 5htt polymorphism, and the occurrence of anxiety and depressive symptoms in elite athletes 104
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) 103
Inherited platelet disorders>thrombocytopenias and thrombocytopathies. 102
Molecular characterization of a factor VII deficient patient supports the importance of the second epidermal growth factor-like domain. 102
Identification of the Novel G250R Variant Indicates a Role for Thrombomodulin in Modulating the Risk for Venous Thromboembolism 101
Pharmacogenetics of dabigatran etexilate interindividual variability 101
Identifying human platelet glycoproteins IIb and IIla by capillary electrophoresis 101
High prevalence of thrombophilic genotypes in patients with acute mesenteric vein thrombosis. 99
Factor XI gene variants in factor XI-deficient patients of Southern Italy: identification of a novel mutation and genotype-phenotype relationship 99
Anticoagulation in Italian patients with venous thromboembolism and thrombophilic alterations: findings from START2 register study 99
Identification of the Novel G250R Variant Indicates a Role for Thrombomodulin in Modulating the Risk for Venous Thromboembolism 98
Clinical utility of screening for CALR gene exon 9 mutations in patients with splanchnic venous thrombosis 98
A beta3 Asp217-->Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin alphaIIBbeta3 functions 98
.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 97
Caveolin 3 Variant T78M in a Large Family With Brugada Syndrome: Clinical Features and Coexistence of ADRB1 and GRK5 Gene Mutation 96
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 95
Oral anticoagulant: pharmacogenetics relationship between genetic and non-genetic factors 94
. 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 94
The Genetics of Hereditary Angioedema: A Review 93
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 93
Lack of genotypephenotype correlation in congenital adrenal hyperplasia due to a CYP21A2-like gene. 92
Factor XI gene variants in factor XI-deficient patients of Southern Italy: identification of a novel mutation and genotype-phenotype relationship 92
Glanzmann's thrombasthenia: identification of 19 new mutations in 30 patients 90
Validation of PLASMIC score and follow-up data in a cohort of patients with suspected microangiopathies from Southern Italy 90
Lack of genotypephenotype correlation in congenital adrenal hyperplasia due to a CYP21A2-like gene 87
Venous thrombosis in afibrinogenemia: a successful use of rivaroxaban 87
Uncovering a Genetic Diagnosis in a Pediatric Patient by Whole Exome Sequencing: A Modeling Investigation in Wiedemann–Steiner Syndrome 86
Validation of PLASMIC score and follow-up data in a cohort of patients with suspected microangiopathies from Southern Italy 84
De Novo p.Asp3368Gly Variant of Dystrophin Gene Associated with X-Linked Dilated Cardiomyopathy and Skeletal Myopathy: Clinical Features and In Silico Analysis 83
Harm Avoidance as a possible mediator in the relationship between the 5-HTTLPR and Cognitive Anxiety in High Level Athletes 83
. 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 83
. 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 80
Genetic Background and Clinical Phenotype in an Italian Cohort with Inherited Arrhythmia Syndromes and Arrhythmogenic Cardiomyopathy (ACM): A Whole-Exome Sequencing Study 79
Totale 11.513
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Categoria #
all - tutte 70.045
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 70.045
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022702 0 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
2025/20263.815 287 273 416 545 174 173 761 438 260 232 89 167
2026/2027303 87 216 0 0 0 0 0 0 0 0 0 0
Totale 13.298