GENSINI, FRANCESCA
 Distribuzione geografica
Continente #
EU - Europa 2.412
NA - Nord America 2.406
AS - Asia 277
AF - Africa 7
OC - Oceania 2
Totale 5.104
Nazione #
US - Stati Uniti d'America 2.401
PL - Polonia 1.498
IT - Italia 221
SE - Svezia 204
IE - Irlanda 203
HK - Hong Kong 127
UA - Ucraina 94
DE - Germania 74
CN - Cina 56
JO - Giordania 44
FI - Finlandia 43
GB - Regno Unito 33
VN - Vietnam 26
CH - Svizzera 15
FR - Francia 12
TR - Turchia 10
RU - Federazione Russa 7
SG - Singapore 7
IN - India 5
SC - Seychelles 5
CA - Canada 4
ES - Italia 3
NL - Olanda 2
AT - Austria 1
AU - Australia 1
BE - Belgio 1
GR - Grecia 1
IR - Iran 1
JP - Giappone 1
MA - Marocco 1
MU - Mauritius 1
MX - Messico 1
NZ - Nuova Zelanda 1
Totale 5.104
Città #
Warsaw 1.498
Fairfield 406
Chandler 280
Dublin 203
Ashburn 177
Woodbridge 174
Seattle 169
Cambridge 156
Jacksonville 151
Houston 132
Wilmington 118
Hong Kong 84
Altamura 55
Ann Arbor 54
Princeton 54
Lawrence 51
Florence 41
Boardman 38
Beijing 35
Boston 32
Buffalo 32
Medford 30
San Diego 25
Dong Ket 22
Shanghai 15
Bern 14
Norwalk 13
Dearborn 10
Milan 10
Phoenix 10
Izmir 8
Falls Church 7
London 7
Moscow 6
New York 6
Auburn Hills 5
Hillsboro 5
Latina 5
Los Angeles 5
Redwood City 5
Rome 5
Singapore 5
Bari 4
Fiesole 4
Frankfurt Am Main 4
Toronto 4
Verona 4
Barcelona 3
Bremen 3
Genoa 3
Helsinki 3
Laurel 3
Pune 3
Andover 2
Atessa 2
Catania 2
Porto 2
San Giovanni in Fiore 2
Acton 1
Almè 1
Arezzo 1
Auckland 1
Azcapotzalco 1
Brussels 1
Böblingen 1
Castel San Giorgio 1
Chengdu 1
Como 1
Delhi 1
Fremont 1
Grafing 1
Hefei 1
Islington 1
Kunming 1
Köln 1
Lausanne 1
Leawood 1
Meran 1
Nanjing 1
Napoli 1
Ospedaletto Euganeo 1
Padova 1
Palermo 1
Pisa 1
Polverigi 1
Portici 1
Prad am Stilfser Joch 1
Prescot 1
Putignano 1
Redmond 1
Rochester 1
Sant'ambrogio Di Torino 1
Sant'egidio Alla Vibrata 1
Siena 1
Southend 1
Tokyo 1
Torino 1
Tullamarine 1
Venezia 1
Vienna 1
Totale 4.248
Nome #
Role of C677T and A1298C MTHFR, A2756G MTR and -786 C/T eNOS gene polymorphisms in atrial fibrillation susceptibility 234
Clinical genetic testing for familial melanoma in Italy: a cooperative study 224
RAS genes influence exercise-induced left ventricular hypertrophy: an elite athletes study 218
High-speed detection of the G894T polymorphism in the exon 7 of the eNOS gene by real-time fluorescence PCR with the Light-Cycler 215
Lone and secondary nonvalvular atrial fibrillation: role of a genetic susceptibility 215
Homocysteine and tissue factor pathway inhibitor levels in patients with Fabry's disease 212
Multiple primary melanomas (MPMs) and criteria for genetic assessment: MultiMEL, a multicenter study of the Italian Melanoma Intergroup. 208
ACE I/D polymorphism and cardiac adaptations in adolescent athletes 205
High prevalence in ACE DD and genotype in patients with atrial fibrillation 202
Angiotensi-converting enzyme DD genotype, angiotensin type 1 receptor CC genotype, and hyperhomocysteinmeia increase first-trimester fetal-loss susceptibility 189
Novel human pathological mutations. Gene symbol: HBA1. Disease: haemoglobin variant 170
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification 137
ACE DD genotype: an independent predisposition factor to venous thromboembolism. 103
Application of COLD-PCR for improved detection of NF2 mosaic mutations 98
Analysis of minK and eNOS genes as candidate loci for predisposition to non-valvular atrial fibrillation. 93
Thrombophilias as risk factors for disorders of pregnancy and fetal damage 93
ACE DD genotype: a predisposing factor for abdominal aortic aneurysm 92
Evaluation of a Next-Generation Sequencing Assay for BRCA1 and BRCA2 Mutation Detection 90
A novel PAX1 null homozygous mutation in autosomal recessive otofaciocervical syndrome associated with severe combined immunodeficiency 88
Phenotype variability of neural crest-derived tumours in six Italian families segregating the same founder SDHD mutation Q109X. 87
Angiotensin converting enzyme and endothelial nitric oxide synthase polymorphisms in patients with atrial fibrillation 85
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 85
The p.G23S CDKN2A founder mutation in high-risk melanoma families from Central Italy. 85
High prevalence of polymorphisms of angiotensin-converting enzyme (I/D) and endothelial nitric oxide synthase (Glu298Asp) in patients with systemic sclerosis. 83
Hereditary nonpolyposis colorectal cancer and related conditions 82
Influence of endothelial nitric oxide synthase gene polymorphisms (G894T, 4a4b, T-786C) and hyperhomocysteinemia on the predisposition to acute coronary syndromes 79
Endothelial nitric oxide synthase gene influences the risk of preeclampsia, the recurrence of negative pregnancy events, and the maternal-fetal flow 78
Emoglobinopatie 77
A kindred with MYH-associated polyposis and pilomatricomas. 75
Impact of E27X, a novel CDKN2A germ line mutation, on p16 and p14ARF expression in Italian melanoma families displaying pancreatic cancer and neuroblastoma. 74
SDH mutations in patients affected by paraganglioma syndromes: a personal experience. 73
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 72
Impaired fibrinolysis in retinal vein occlusion: a role for genetic determinants of PAI-1 levels. 68
Influence of eNOS gene polymorphisms on carotid atherosclerosis 66
The Spectrum of FANCM Protein Truncating Variants in European Breast Cancer Cases 63
Epigenomic, genomic, and transcriptomic landscape of schwannomatosis 63
Retrospective analysis of 77 patients with ovarian cancer undergoing genetic testing for BRCA1 and BRCA2 mutations 62
Genomic rearrangements of the CDKN2A locus are infrequent in Italian malignant melanoma families without evidence of CDKN2A/CDK4 point mutations. 61
MLH1 constitutional and somatic methylation in patients with MLH1 negative tumors fulfilling the revised Bethesda criteria. 60
Germline mutations in MSH2 and ATM gene in patients with GIST (gastrointestinal stromal tumor) and second epitelial tumors 57
Caratteri multifattoriali 55
I/D polymorphism of the ACE gene and A1166C of the AT1R gene as risk factors for restenosis after coronary angioplasty 53
Detection of BRCA1 and BRCA2 variants in circulating free DNA by using a commercial kit 50
Early-onset malignant phyllodes breast tumor in a patient with germline pathogenic variants in NF1 and BRCA1 genes 44
Caratteri multifattoriali 41
The genes that codify angiotensin converting enzyme and type 1 receptor for angiotensin II have a different effect on longevity 40
Capitolo 10 - Caratteri multifattoriali 38
Maternal-fetal flow, negative events, and preeclampsia: Role of ACE I/D polymorphism 37
Schwannomatosis associated schwannomas show a different NF2 mutational spectrum compared to Neurofibromatosis type 2 patients 35
The C1166 allele of the AT1R gene associated with ACE DD phenotype increase the risk for deep venous thrombosis 34
Low-molecular-weight heparin lowers the recurrence rate of preclampsia and restores the physiological vascular changes in a ngiotensin-converting enzyme DD women 33
Caratteri Multifattoriali 31
Breast cancer: the first comparative evaluation of oncobiome composition between males and females 21
Polygenic risk modeling for prediction of epithelial ovarian cancer risk 11
Predictors of germline status for hereditary melanoma: 5 years of multi-gene panel testing within the Italian Melanoma Intergroup 7
Totale 5.151
Categoria #
all - tutte 12.362
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 12.362


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019398 0 0 0 0 0 0 0 0 0 82 172 144
2019/20201.178 83 109 38 99 141 145 121 146 99 67 119 11
2020/2021797 66 67 52 124 32 75 38 64 61 121 34 63
2021/2022394 22 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
2023/2024325 17 43 56 23 18 25 34 95 9 5 0 0
Totale 5.151