IRIS
D'ANDREA, GIOVANNA
 Distribuzione geografica
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Continente #
NA - Nord America 5.709
EU - Europa 4.271
AS - Asia 3.147
SA - Sud America 463
Continente sconosciuto - Info sul continente non disponibili 420
AF - Africa 56
OC - Oceania 3
Totale 14.069
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Nazione #
US - Stati Uniti d'America 5.586
IE - Irlanda 1.142
CN - Cina 1.115
SG - Singapore 1.112
RU - Federazione Russa 590
SE - Svezia 552
UA - Ucraina 529
IT - Italia 525
BR - Brasile 371
FR - Francia 292
HK - Hong Kong 237
VN - Vietnam 210
DE - Germania 205
FI - Finlandia 166
IN - India 162
TR - Turchia 122
GB - Regno Unito 110
CA - Canada 63
BD - Bangladesh 37
NL - Olanda 32
AR - Argentina 31
IQ - Iraq 31
BE - Belgio 28
AT - Austria 24
PK - Pakistan 18
ID - Indonesia 16
CZ - Repubblica Ceca 15
JP - Giappone 14
PL - Polonia 14
TN - Tunisia 13
ZA - Sudafrica 13
CR - Costa Rica 12
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
HN - Honduras 6
LT - Lituania 6
MY - Malesia 6
KE - Kenya 5
AL - Albania 4
CH - Svizzera 4
GT - Guatemala 4
IL - Israele 4
JM - Giamaica 4
PR - Porto Rico 4
PY - Paraguay 4
SA - Arabia Saudita 4
SV - El Salvador 4
BY - Bielorussia 3
ET - Etiopia 3
HR - Croazia 3
NI - Nicaragua 3
NO - Norvegia 3
PE - Perù 3
PS - Palestinian Territory 3
RO - Romania 3
RS - Serbia 3
TT - Trinidad e Tobago 3
AO - Angola 2
BB - Barbados 2
BG - Bulgaria 2
CW - ???statistics.table.value.countryCode.CW??? 2
CY - Cipro 2
DK - Danimarca 2
DO - Repubblica Dominicana 2
DZ - Algeria 2
GR - Grecia 2
NP - Nepal 2
OM - Oman 2
PA - Panama 2
PH - Filippine 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
EE - Estonia 1
GA - Gabon 1
GD - Grenada 1
GE - Georgia 1
KG - Kirghizistan 1
KH - Cambogia 1
KR - Corea 1
KW - Kuwait 1
Totale 13.651
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Città #
Dublin 1.141
San Jose 936
Chandler 558
Singapore 486
Ashburn 381
Jacksonville 372
Nyköping 358
Dearborn 315
Beijing 243
Hong Kong 237
Nanjing 197
Santa Clara 167
Council Bluffs 160
The Dalles 138
Wilmington 129
Ann Arbor 118
Columbus 118
Lauterbourg 117
Princeton 113
Dallas 98
Moscow 95
New York 94
Munich 93
Ho Chi Minh City 76
Nanchang 75
Foggia 71
San Mateo 68
Boardman 67
Helsinki 67
Los Angeles 58
Woodbridge 58
Bari 47
Hanoi 45
Changsha 44
Shenyang 43
Phoenix 38
Des Moines 36
Rome 35
Hebei 30
Jinan 28
Milan 28
Tianjin 28
Hilden 27
Kunming 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 17
New Providence 17
Ningbo 16
Rio de Janeiro 16
Vienna 16
San Francisco 15
Atlanta 14
Fresno 14
Naples 14
San Severo 14
Tokyo 14
Baghdad 13
Brno 13
London 13
Buffalo 12
Manfredonia 12
Modena 12
Porto Alegre 12
Warsaw 12
Chicago 11
Montreal 11
San José 11
Amsterdam 10
Auburn Hills 10
Norwalk 10
Orange 10
Toronto 10
Zhengzhou 10
Agrolândia 9
Buenos Aires 9
Changchun 9
Manchester 9
Paris 9
Seattle 9
Amman 8
Brasília 8
Charlotte 8
Chennai 8
Florence 8
Fuzhou 8
Jakarta 8
Biên Hòa 7
Da Nang 7
Hefei 7
Orem 7
Totale 8.397
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Nome #
Increased risk of venous thrombosis in carriers of the prothrombin A gene variant. 173
A polymorfism in VKORC1 gene is associated with an interindividual variability in the dose-anticoagulation effect of warfarin. 162
Role of tumour necrosis factor alpha and interleukin 1 beta in promoter effect induced by mercury in human keratinocytes 161
ADAMTS13 MUTATIONS AND POLYMORPHISMS IN CONGENITAL THROMBOTIC THROMBOCYTOPENIC PURPURA. 160
"Genetic modulation of oral anticoagulantion with warfarin " 157
FV HR2 haplotype as additional inherited risk factor for deep vein thrombosis in individuals with a high-risk profile 156
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. 155
A beta3 Asp217-->Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin alphaIIBbeta3 functions. 151
ETEROGENEITA' FENOTIPICA NELLE IPERFENILALANINEMIE ALL'INTERNO DELLO STESSO NUCLEO FAMILIARE. 150
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 150
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 150
Detection of the factor V Leiden using SSCP 148
The Genetics of Hereditary Angioedema: A Review 148
COESISTENZA DI DUE PATOLOGIE RARE: TROMBOASTENIA DI GLANZMANN E SINDROME DI KARTAGENER 147
A Novel KCNN2 Variant in a Family with Essential Tremor Plus: Clinical Characteristics and In Silico Analysis 146
A NOVEL NONSENSE TET2 MUTATION IN A PATIENT WITH PRIMARY MYELOFIBROSIS. 140
A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin 140
ANALISI MOLECOLARE E CORRELAZIONE GENOTIPO-FENOTIPO IN FAMIGLIE CON IPERFENILALANINEMIE. 138
A MODEL TO PREDICT SUCCESS FOLLOWING PEG-INTERFERON AND RIBAVIRIN THERAPY FOR PATIENTS WITH HCV-1 INFECTION 136
A myoferlin gain-of-function variant associates with a new type of hereditary angioedema 136
Molecular diversity and thrombotic risk in protein S deficiency: the PROSIT study. 134
Glanzmann's thrombasthenia: modulation of clinical phenotype by alpha2C807T gene polymorphism. 134
Detection of new deletions in a group of Italian patients with Hemophilia A by multiplex ligation-dependent probe amplification 134
An a priori prediction model of response to peginterferon plus ribavirin dual therapy in naïve patients with genotype 1 chronic hepatitis C. 134
C0268 Higher risk of idiopathic small for gestational age newborns in Italian women carrying the annexin A5 M2 haplotype 132
Genetic susceptibility to pregnancy-related venous thromboembolism: roles of factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations 130
A new vitamin K epoxide reductase complex subunit-1 (VKORC1) mutation in a patient with decreased stability of CYP2C9 enzyme 130
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 130
Mutation analysis in hyperphenylalaninemia patients from South Italy. 130
The relationship between personality traits, the 5HTT polymorphisms, and the occurrence of anxiety and depressive symptoms in elite athletes 130
Pharmacodynamic targets of psychotic patients treated with a long-acting therapy 130
Increased risk for venous thrombosis in carriers of the prothrombin G-->A20210 gene variant. 129
Polymorphisms in factor II and factor VII genes modulate oral anticoagulation with warfarin 129
Inherited prothrombotic conditions and premature ischemic stroke. Sex difference in the association with Factor V leiden 128
THE MOLECULAR ORGANIZATION OF ENDOTHELIAL JUNCTIONS IN VASCULAR PERMEABILITY 128
A novel allele variant of the SERPINF2 gene responsible for severe plasmin inhibitor (α2-antiplasmin) deficiency in an Italian patient 127
Identification of six novel mutations in type I antithrombin deficient Italian families 126
Thrombofilic genotypes in subjects with idiopathic antiphospholipid antibodies-prevalence and significance 126
Identification of naïve HCV-1 patients with chronic hepatitis who may benefit from dual therapy with peg-interferon and ribavirin. 126
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 126
The methylenetetrahydrofolate reductase TT677 genotype is associated with venous thrombosis independently of the coexistence of the FV Leiden and the prothrombin A20210 mutation. 125
Chronic thromboembolic pulmonary hypertension. 125
Psychosomatic syndromes are associated with IL-6 pro-inflammatory cytokine in heart failure patients 125
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A. 124
Phenylalanine hydroxylase deficiency in south Italy: Genotype-phenotype correlations, identification of a novel mutant PAH allele and prediction of BH4 responsiveness 124
Compound heterozygosity (554-589 del, C-T transition) in the platelet glycoprotein iba gene in a patient with a severe bleeding tendency. 123
Molecular characterization of a factor Vii deficient patient supports the importance of the second epidermal growth factor-like domain. 123
Methylenetetrahydrofolate reductase (MTHFR) 677T-> C mutation and unexplained early pregnancy loss 123
Thrombophilic genotypes in subjects with idiopathic antiphospholipid antibodies--prevalence and significance 122
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A 121
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A 119
Survival in primary antiphospholipid syndrome: A single-centre cohort study 119
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 119
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 118
Inherited coagulation disorders in cirrhotic patients with portal vein thrombosis 118
Selection of HCV-1 patients with chronic hepatitis who might benefit from current standard of therapy with peg-interferon and ribavirin 118
Maladaptive coping strategies and neuroticism mediate the relationship between 5HTT-LPR polymorphisms and symptoms of anxiety in elite athletes 118
Coexistence of factor V Leiden and Factor II A20210 mutations and recurrent venous thromboembolism 117
Deep intronic variations may cause mild hemophilia A. 115
DAB2IP associates with hereditary angioedema: Insights into the role of VEGF signaling in HAE pathophysiology 114
RGD-containing peptides inhibit fibrinogen binding to platelet alpha(IIb)beta3 by inducing an allosteric change in the amino-terminal portion of alpha(IIb). 114
Homozygosity by descent of a 3Mb chromosome 17 haplotype causes coinheritance of Glanzmann thrombasthenia and primary ciliary dyskinesia 114
Intra-familiar discordant PKU phenotype explained by mutation analysis in three pedigrees. 114
Intra-familiar discordant PKU phenotype explained by mutation analysis in three pedigrees. 113
Caveolin 3 Variant T78M in a Large Family With Brugada Syndrome: Clinical Features and Coexistence of ADRB1 and GRK5 Gene Mutation 112
Outcome of patients with splanchnic venous thrombosis presenting without overt MPN: a role for the JAK2 V617F mutation re-evaluation. 111
Pharmacogenetics of dabigatran etexilate interindividual variability 110
The assessment of the relationship between personality, the presence of the 5htt polymorphism, and the occurrence of anxiety and depressive symptoms in elite athletes 110
Inherited platelet disorders>thrombocytopenias and thrombocytopathies. 109
Hereditary protein C deficiency and thrombosis risk: genotype and phenotype relation in a large Italian family. 109
Variation in genes encoding for interferon λ-3 and λ-4 in the prediction of HCV-1 treatment-induced viral clearance. 109
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) 109
Validation of PLASMIC score and follow-up data in a cohort of patients with suspected microangiopathies from Southern Italy 108
Identification of the Novel G250R Variant Indicates a Role for Thrombomodulin in Modulating the Risk for Venous Thromboembolism 107
Factor XI gene variants in factor XI-deficient patients of Southern Italy: identification of a novel mutation and genotype-phenotype relationship 107
Anticoagulation in Italian patients with venous thromboembolism and thrombophilic alterations: findings from START2 register study 107
Identifying human platelet glycoproteins IIb and IIla by capillary electrophoresis 107
Molecular characterization of a factor VII deficient patient supports the importance of the second epidermal growth factor-like domain. 105
A beta3 Asp217-->Val substitution in a patient with variant Glanzmann Thrombasthenia severely affects integrin alphaIIBbeta3 functions 104
Identification of the Novel G250R Variant Indicates a Role for Thrombomodulin in Modulating the Risk for Venous Thromboembolism 103
High prevalence of thrombophilic genotypes in patients with acute mesenteric vein thrombosis. 103
Oral anticoagulant: pharmacogenetics relationship between genetic and non-genetic factors 103
.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 103
Clinical utility of screening for CALR gene exon 9 mutations in patients with splanchnic venous thrombosis 101
Lack of genotypephenotype correlation in congenital adrenal hyperplasia due to a CYP21A2-like gene. 101
ABCB1 SNP rs4148738 modulation of apixaban interindividual variability 100
Uncovering a Genetic Diagnosis in a Pediatric Patient by Whole Exome Sequencing: A Modeling Investigation in Wiedemann–Steiner Syndrome 99
Factor XI gene variants in factor XI-deficient patients of Southern Italy: identification of a novel mutation and genotype-phenotype relationship 99
. 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 99
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 98
The Genetics of Hereditary Angioedema: A Review 97
De Novo p.Asp3368Gly Variant of Dystrophin Gene Associated with X-Linked Dilated Cardiomyopathy and Skeletal Myopathy: Clinical Features and In Silico Analysis 95
Lack of genotypephenotype correlation in congenital adrenal hyperplasia due to a CYP21A2-like gene 95
Venous thrombosis in afibrinogenemia: a successful use of rivaroxaban 95
Glanzmann's thrombasthenia: identification of 19 new mutations in 30 patients 93
Harm Avoidance as a possible mediator in the relationship between the 5-HTTLPR and Cognitive Anxiety in High Level Athletes 93
Validation of PLASMIC score and follow-up data in a cohort of patients with suspected microangiopathies from Southern Italy 91
. 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 88
. 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 88
Genetic Background and Clinical Phenotype in an Italian Cohort with Inherited Arrhythmia Syndromes and Arrhythmogenic Cardiomyopathy (ACM): A Whole-Exome Sequencing Study 84
Totale 12.114
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Categoria #
all - tutte 73.318
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 73.318
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022673 0 0 0 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
2026/20271.074 87 313 272 402 0 0 0 0 0 0 0 0
Totale 14.069