Francesca Gensini
Francesca Gensini
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Low-molecular-weight heparin lowers the recurrence rate of preeclampsia and restores the physiological vascular changes in angiotensin-converting enzyme DD women
G Mello, E Parretti, C Fatini, C Riviello, F Gensini, M Marchionni, ...
Hypertension 45 (1), 86-91, 2005
Searching for a better assessment of the individual coronary risk profile. The role of angiotensin-converting enzyme, angiotensin II type 1 receptor and angiotensinogen geneá…
C Fatini, R Abbate, G Pepe, B Battaglini, F Gensini, G Ruggiano, ...
European heart journal 21 (8), 633-638, 2000
Maternal-fetal flow, negative events, and preeclampsia: role of ACE I/D polymorphism
G Mello, E Parretti, F Gensini, E Sticchi, F Mecacci, G Scarselli, ...
Hypertension 41 (4), 932-937, 2003
Influence of endothelial nitric oxide synthase gene polymorphisms (G894T, 4a4b, T-786C) and hyperhomocysteinemia on the predisposition to acute coronary syndromes
C Fatini, F Sofi, E Sticchi, F Gensini, AM Gori, S Fedi, I Lapini, C Rostagno, ...
American heart journal 147 (3), 516-521, 2004
Hereditary nonpolyposis colorectal cancer and related conditions
E Lucci‐Cordisco, I Zito, F Gensini, M Genuardi
American journal of medical genetics Part A 122 (4), 325-334, 2003
RAS genes influence exercise-induced left ventricular hypertrophy: an elite athletes study
C Fatini, R Guazzelli, P Manetti, B Battaglini, F Gensini, R Vono, L Toncelli, ...
Medicine and science in sports and exercise 32 (11), 1868-1872, 2000
Analysis of minK and eNOS genes as candidate loci for predisposition to non-valvular atrial fibrillation
C Fatini, E Sticchi, M Genuardi, F Sofi, F Gensini, AM Gori, M Lenti, ...
European heart journal 27 (14), 1712-1718, 2006
Angiotensin-converting enzyme DD genotype, angiotensin type 1 receptor CC genotype, and hyperhomocysteinemia increase first-trimester fetal-loss susceptibility
C Fatini, F Gensini, B Battaglini, D Prisco, AP Cellai, S Fedi, R Marcucci, ...
Blood coagulation & fibrinolysis 11 (7), 657-662, 2000
Angiotensin‐converting enzyme and endothelial nitric oxide synthase polymorphisms in patients with atrial fibrillation
F Gensini, L Padeletti, C Fatini, E Sticchi, G Franco Gensini, A Michelucci
Pacing and clinical electrophysiology 26 (1p2), 295-298, 2003
High prevalence of polymorphisms of angiotensin-converting enzyme (I/D) and endothelial nitric oxide synthase (Glu298Asp) in patients with systemic sclerosis
C Fatini, F Gensini, E Sticchi, B Battaglini, C Angotti, ML Conforti, ...
The American journal of medicine 112 (7), 540-544, 2002
ACE DD genotype: a predisposing factor for abdominal aortic aneurysm
C Fatini, G Pratesi, F Sofi, F Gensini, E Sticchi, B Lari, R Pulli, W Dorigo, ...
European journal of vascular and endovascular surgery 29 (3), 227-232, 2005
A kindred with MYH‐associated polyposis and pilomatricomas
S Baglioni, G Melean, F Gensini, M Santucci, M Scatizzi, L Papi, ...
American Journal of Medical Genetics Part A 134 (2), 212-214, 2005
ACE DD genotype: an independent predisposition factor to venous thromboembolism
C Fatini, F Gensini, E Sticchi, B Battaglini, D Prisco, S Fedi, T Brunelli, ...
European journal of clinical investigation 33 (8), 642-647, 2003
Influence of eNOS gene polymorphisms on carotid atherosclerosis
C Fatini, F Sofi, F Gensini, E Sticchi, B Lari, G Pratesi, R Pulli, W Dorigo, ...
European journal of vascular and endovascular surgery 27 (5), 540-544, 2004
Endothelial nitric oxide synthase gene influences the risk of pre-eclampsia, the recurrence of negative pregnancy events, and the maternal–fetal flow
C Fatini, E Sticchi, F Gensini, M Genuardi, F Tondi, GF Gensini, C Riviello, ...
Journal of hypertension 24 (9), 1823-1829, 2006
Lone and secondary nonvalvular atrial fibrillation: role of a genetic susceptibility
C Fatini, E Sticchi, F Gensini, AM Gori, R Marcucci, M Lenti, A Michelucci, ...
International journal of cardiology 120 (1), 59-65, 2007
Phenotype variability of neural crest derived tumours in six Italian families segregating the same founder SDHD mutation Q109X
L Simi, R Sestini, P Ferruzzi, MS Gagliano, F Gensini, M Mascalchi, ...
Journal of medical genetics 42 (8), e52-e52, 2005
Impaired fibrinolysis in retinal vein occlusion: a role for genetic determinants of PAI-1 levels
AM Gori, R Marcucci, C Fatini, F Gensini, E Sticchi, A Sodi, S Cappelli, ...
Thrombosis and haemostasis 92 (07), 54-60, 2004
Clinical genetic testing for familial melanoma in Italy: a cooperative study
W Bruno, P Ghiorzo, L Battistuzzi, PA Ascierto, M Barile, S Gargiulo, ...
Journal of the American Academy of Dermatology 61 (5), 775-782, 2009
Impact of E27X, a novel CDKN2A germ line mutation, on p16 and p14ARF expression in Italian melanoma families displaying pancreatic cancer and neuroblastoma
P Ghiorzo, S Gargiulo, L Pastorino, S Nasti, R Cusano, W Bruno, S Gliori, ...
Human molecular genetics 15 (18), 2682-2689, 2006
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