GENSINI, FRANCESCA
 Distribuzione geografica
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Continente #
NA - Nord America 4.748
EU - Europa 3.984
AS - Asia 1.834
SA - Sud America 215
AF - Africa 66
Continente sconosciuto - Info sul continente non disponibili 56
OC - Oceania 32
Totale 10.935
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Nazione #
US - Stati Uniti d'America 4.674
PL - Polonia 1.507
RU - Federazione Russa 921
IT - Italia 589
SG - Singapore 488
CN - Cina 383
HK - Hong Kong 278
SE - Svezia 208
IE - Irlanda 205
VN - Vietnam 205
KR - Corea 170
BR - Brasile 169
DE - Germania 124
UA - Ucraina 99
FI - Finlandia 90
FR - Francia 88
GB - Regno Unito 63
BD - Bangladesh 61
IN - India 57
CA - Canada 48
JO - Giordania 47
JP - Giappone 41
AU - Australia 31
ES - Italia 26
ID - Indonesia 25
TR - Turchia 21
CH - Svizzera 18
NL - Olanda 18
AR - Argentina 13
MX - Messico 13
CI - Costa d'Avorio 11
IQ - Iraq 11
EC - Ecuador 10
ZA - Sudafrica 9
AT - Austria 8
SA - Arabia Saudita 8
MA - Marocco 7
NG - Nigeria 7
PY - Paraguay 7
PK - Pakistan 6
TN - Tunisia 6
DZ - Algeria 5
EG - Egitto 5
SC - Seychelles 5
AE - Emirati Arabi Uniti 4
CO - Colombia 4
MY - Malesia 4
PH - Filippine 4
VE - Venezuela 4
AL - Albania 3
CL - Cile 3
CR - Costa Rica 3
CZ - Repubblica Ceca 3
DK - Danimarca 3
HR - Croazia 3
LY - Libia 3
NP - Nepal 3
PE - Perù 3
UZ - Uzbekistan 3
BJ - Benin 2
DO - Repubblica Dominicana 2
GE - Georgia 2
HN - Honduras 2
KE - Kenya 2
LT - Lituania 2
OM - Oman 2
TT - Trinidad e Tobago 2
UY - Uruguay 2
AZ - Azerbaigian 1
BE - Belgio 1
BG - Bulgaria 1
CW - ???statistics.table.value.countryCode.CW??? 1
DM - Dominica 1
ET - Etiopia 1
GI - Gibilterra 1
GP - Guadalupe 1
GR - Grecia 1
IL - Israele 1
IR - Iran 1
KG - Kirghizistan 1
KW - Kuwait 1
KZ - Kazakistan 1
LK - Sri Lanka 1
MD - Moldavia 1
MN - Mongolia 1
MR - Mauritania 1
MU - Mauritius 1
NZ - Nuova Zelanda 1
PA - Panama 1
PS - Palestinian Territory 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
SV - El Salvador 1
SY - Repubblica araba siriana 1
TH - Thailandia 1
Totale 10.880
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Città #
Warsaw 1.507
Santa Clara 889
Ashburn 554
Fairfield 406
Singapore 330
Chandler 280
Hong Kong 231
Dublin 205
Woodbridge 175
Seattle 172
Seoul 169
San Jose 162
Cambridge 156
Jacksonville 151
Houston 135
Wilmington 118
Beijing 112
Dallas 103
Milan 101
Los Angeles 92
Buffalo 68
Ho Chi Minh City 64
Altamura 55
Lauterbourg 55
Ann Arbor 54
Florence 54
Princeton 54
Lawrence 51
The Dalles 48
Hefei 46
Boardman 42
New York 42
Tokyo 40
Munich 37
Boston 36
Hanoi 34
Council Bluffs 33
Rome 32
Medford 30
Moscow 30
Mumbai 30
Shanghai 29
San Diego 27
Helsinki 26
Melbourne 26
São Paulo 24
Dong Ket 22
Jakarta 20
Kent 17
Madrid 16
London 15
Turku 15
Bern 14
Naples 14
Norwalk 14
Reading 14
Paris 13
Turin 13
Phoenix 12
Toronto 12
Abidjan 11
Dearborn 10
Orem 10
Bologna 9
Brooklyn 9
Chicago 9
Haiphong 9
Izmir 9
Columbus 8
Bari 7
Falls Church 7
Figino 7
Lappeenranta 7
Abuja 6
Clifton 6
Pittsburgh 6
Redondo Beach 6
Vienna 6
Auburn Hills 5
Belo Horizonte 5
Can Tho 5
Chennai 5
Da Nang 5
Delhi 5
Dhaka 5
Goiânia 5
Guangzhou 5
Hillsboro 5
Hải Dương 5
Latina 5
Palermo 5
Redwood City 5
Reggio Emilia 5
Shenzhen 5
Tianjin 5
Verona 5
Amsterdam 4
Brasília 4
Cagliari 4
Cape Town 4
Totale 7.574
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Nome #
Angiotensi-converting enzyme DD genotype, angiotensin type 1 receptor CC genotype, and hyperhomocysteinmeia increase first-trimester fetal-loss susceptibility 342
Clinical genetic testing for familial melanoma in Italy: a cooperative study 334
Role of C677T and A1298C MTHFR, A2756G MTR and -786 C/T eNOS gene polymorphisms in atrial fibrillation susceptibility 311
RAS genes influence exercise-induced left ventricular hypertrophy: an elite athletes study 311
ACE I/D polymorphism and cardiac adaptations in adolescent athletes 310
Multiple primary melanomas (MPMs) and criteria for genetic assessment: MultiMEL, a multicenter study of the Italian Melanoma Intergroup. 294
Lone and secondary nonvalvular atrial fibrillation: role of a genetic susceptibility 289
High-speed detection of the G894T polymorphism in the exon 7 of the eNOS gene by real-time fluorescence PCR with the Light-Cycler 282
Homocysteine and tissue factor pathway inhibitor levels in patients with Fabry's disease 276
High prevalence in ACE DD and genotype in patients with atrial fibrillation 274
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification 251
Evaluation of a Next-Generation Sequencing Assay for BRCA1 and BRCA2 Mutation Detection 232
Novel human pathological mutations. Gene symbol: HBA1. Disease: haemoglobin variant 227
Analysis of minK and eNOS genes as candidate loci for predisposition to non-valvular atrial fibrillation. 213
A novel PAX1 null homozygous mutation in autosomal recessive otofaciocervical syndrome associated with severe combined immunodeficiency 209
ACE DD genotype: an independent predisposition factor to venous thromboembolism. 207
Breast cancer: the first comparative evaluation of oncobiome composition between males and females 203
ACE DD genotype: a predisposing factor for abdominal aortic aneurysm 201
The genes that codify angiotensin converting enzyme and type 1 receptor for angiotensin II have a different effect on longevity 200
Application of COLD-PCR for improved detection of NF2 mosaic mutations 194
Angiotensin converting enzyme and endothelial nitric oxide synthase polymorphisms in patients with atrial fibrillation 189
A kindred with MYH-associated polyposis and pilomatricomas. 186
Endothelial nitric oxide synthase gene influences the risk of preeclampsia, the recurrence of negative pregnancy events, and the maternal-fetal flow 185
SDH mutations in patients affected by paraganglioma syndromes: a personal experience. 183
Emoglobinopatie 182
Retrospective analysis of 77 patients with ovarian cancer undergoing genetic testing for BRCA1 and BRCA2 mutations 182
The p.G23S CDKN2A founder mutation in high-risk melanoma families from Central Italy. 180
Germline mutations in MSH2 and ATM gene in patients with GIST (gastrointestinal stromal tumor) and second epitelial tumors 180
Phenotype variability of neural crest-derived tumours in six Italian families segregating the same founder SDHD mutation Q109X. 179
Detection of BRCA1 and BRCA2 variants in circulating free DNA by using a commercial kit 178
Epigenomic, genomic, and transcriptomic landscape of schwannomatosis 173
Impaired fibrinolysis in retinal vein occlusion: a role for genetic determinants of PAI-1 levels. 165
Angiotensin converting enzyme DD genotype affects the changes of plasma plasminogen activator inhibitor-1 activity after primary percutaneous transluminal coronary angioplasty in acute myocardial infarction patients 164
Influence of eNOS gene polymorphisms on carotid atherosclerosis 164
Thrombophilias as risk factors for disorders of pregnancy and fetal damage 163
Searching for a better assessment of the individual coronary risk profile. The role of angiotensin-converting-enzyme, angiotensin II type 1 receptor and angiotensinogen gene polymorphisms 160
MLH1 constitutional and somatic methylation in patients with MLH1 negative tumors fulfilling the revised Bethesda criteria. 158
Influence of endothelial nitric oxide synthase gene polymorphisms (G894T, 4a4b, T-786C) and hyperhomocysteinemia on the predisposition to acute coronary syndromes 156
High prevalence of polymorphisms of angiotensin-converting enzyme (I/D) and endothelial nitric oxide synthase (Glu298Asp) in patients with systemic sclerosis. 154
Schwannomatosis associated schwannomas show a different NF2 mutational spectrum compared to Neurofibromatosis type 2 patients 154
Alu–Mediated Duplication and Deletion of Exon 11 Are Frequent Mechanisms of PALB2 Inactivation, Predisposing Individuals to Hereditary Breast–Ovarian Cancer Syndrome 149
The Spectrum of FANCM Protein Truncating Variants in European Breast Cancer Cases 148
Maternal-fetal flow, negative events, and preeclampsia: Role of ACE I/D polymorphism 147
Genetic signatures of ERCC1 and ERCC2 expression, along with SNPs variants, unveil favorable prognosis in SCLC patients undergoing platinum-based chemotherapy 144
Capitolo 10 - Caratteri multifattoriali 142
I/D polymorphism of the ACE gene and A1166C of the AT1R gene as risk factors for restenosis after coronary angioplasty 141
Genomic rearrangements of the CDKN2A locus are infrequent in Italian malignant melanoma families without evidence of CDKN2A/CDK4 point mutations. 141
Hereditary nonpolyposis colorectal cancer and related conditions 138
Caratteri multifattoriali 137
Impact of E27X, a novel CDKN2A germ line mutation, on p16 and p14ARF expression in Italian melanoma families displaying pancreatic cancer and neuroblastoma. 133
Early-onset malignant phyllodes breast tumor in a patient with germline pathogenic variants in NF1 and BRCA1 genes 131
Polygenic risk modeling for prediction of epithelial ovarian cancer risk 118
Caratteri Multifattoriali 116
Predictors of germline status for hereditary melanoma: 5 years of multi-gene panel testing within the Italian Melanoma Intergroup 114
Caratteri multifattoriali 114
Low-molecular-weight heparin lowers the recurrence rate of preclampsia and restores the physiological vascular changes in a ngiotensin-converting enzyme DD women 108
The C1166 allele of the AT1R gene associated with ACE DD phenotype increase the risk for deep venous thrombosis 82
Foetal cardiac rhabdomyoma due to paternal TSC1 Mutation: a case report and literature review 81
Bicuspid Aortic Valve: Old and Novel Gene Contribution to Disease Onset and Complications 56
Totale 10.935
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Categoria #
all - tutte 28.600
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 28.600
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022372 0 30 34 15 14 15 13 23 21 23 76 108
2022/20231.032 87 187 38 77 87 178 128 62 124 8 21 35
2023/2024370 17 43 56 23 18 25 34 95 9 12 29 9
2024/20252.564 71 253 146 419 741 374 51 156 110 59 104 80
2025/20263.024 351 407 208 256 354 121 348 140 179 188 124 348
2026/2027151 116 35 0 0 0 0 0 0 0 0 0 0
Totale 10.935