NASTI, SABINA
 Distribuzione geografica
Continente #
EU - Europa 3.015
Totale 3.015
Nazione #
IT - Italia 3.015
Totale 3.015
Città #
Genova 2.217
Rapallo 339
Genoa 302
Vado Ligure 149
Bordighera 8
Totale 3.015
Nome #
Pathway-based analysis of a melanoma genome-wide association study: analysis of genes related to tumour-immunosuppression. 161
Mutation Analysis of PRKAR1A Gene in a Patient with Atrial Myxoma 153
Contribution of germline mutations in the BRCA and PALB2 genes to pancreatic cancer in Italy. 148
CDKN2A is the main susceptibility gene in Italian pancreatic cancer families. 140
C242T polymorphism in CYBA gene (p22phox) and risk of coronary artery disease in a population of Caucasian Italians 138
Genome-wide association study identifies novel loci predisposing to cutaneous melanoma. 138
CDKN2A and MC1R analysis in amelanotic and pigmented melanoma. 137
Brooke-Spiegler syndrome tumor spectrum beyond the skin: a patient carrying germline R936X CYLD mutation and a somatic CYLDmutation in Brenner tumor 137
Increased Risk of Colorectal Adenomas in Italian Subjects Carrying the p53 PIN3 A2-Pro72 Haplotype. 136
Germline MLH1 and MSH2 mutations in Italian pancreatic cancer patients with suspected Lynch syndrome. 130
Association of MC1R Variants and Host Phenotypes With Melanoma Risk in CDKN2A Mutation Carriers: A GenoMEL Study 129
Nevoid Basal Cell Carcinoma Syndrome in infants: improving diagnosis. 124
Functional analysis of CDKN2A/p16INK4a 5'-UTR variants predisposing to melanoma 124
Carvedilol prevents doxorubicin-induced free radical release and apoptosis in cardiomyocytes in vitro. 122
Prevalence of the E318K MITF germline mutation in Italian melanoma patients: associations with histological subtypes and family cancer history. 117
A comparison of CDKN2A mutation detection within the Melanoma Genetics Consortium (GenoMEL) 115
Impact of E27X, a novel CDKN2A germ line mutation, on p16 and p14ARF expression in Italian melanoma families displaying pancreatic cancer and neuroblastoma. 108
Hereditary trichilemmal cysts: A proposal for the assessment of diagnostic clinical criteria 99
ANALISI GENOME-WIDE PER LA SUSCETTIBILITÀ AL MELANOMA: NUOVI LOCICHE CONFERMANO IL RUOLO DEI GENI DELLA PIGMENTAZIONE 94
CDKN2A mutations and MC1R variants in Italian patients with single or multiple primary melanoma 91
MC1R variation and melanoma risk in relation to host/clinical and environmental factors in CDKN2A positive and negative melanoma patients. 90
Identification of a SUFU germline mutation in a family with Gorlin syndrome 86
Five novel germline function-impairing mutations of CYLD in Italian patients with multiple cylindromas 84
Features associated with germline CDKN2A mutations: A GenoMEL study of melanoma-prone families from three continents 79
Predicting the risk of pancreatic cancer: on CDKN2A mutations in the melanoma-pancreatic cancer syndrome in Italy 77
CDKN2A/p16INK4a 5’UTR variants in melanoma and pancreatic cancer predisposition: lost in translation, somewhere 59
Molecular characterisation of Italian Nevoid Basal Cell Carcinoma Syndrome patients 51
Totale 3.067
Categoria #
all - tutte 9.195
article - articoli 8.630
book - libri 0
conference - conferenze 565
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 18.390


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020628 0 0 0 0 83 78 119 55 65 124 75 29
2020/2021189 11 36 12 21 15 9 5 21 12 23 11 13
2021/2022383 11 32 28 58 22 24 30 79 16 32 15 36
2022/2023391 31 41 2 50 77 45 2 31 42 3 63 4
2023/2024244 7 27 2 24 15 53 16 10 31 5 13 41
2024/2025162 15 32 16 64 35 0 0 0 0 0 0 0
Totale 3.067