NASTI, SABINA
 Distribuzione geografica
Continente #
EU - Europa 2.934
Totale 2.934
Nazione #
IT - Italia 2.934
Totale 2.934
Città #
Genova 2.217
Rapallo 339
Genoa 302
Vado Ligure 68
Bordighera 8
Totale 2.934
Nome #
Pathway-based analysis of a melanoma genome-wide association study: analysis of genes related to tumour-immunosuppression. 157
Mutation Analysis of PRKAR1A Gene in a Patient with Atrial Myxoma 151
Contribution of germline mutations in the BRCA and PALB2 genes to pancreatic cancer in Italy. 144
C242T polymorphism in CYBA gene (p22phox) and risk of coronary artery disease in a population of Caucasian Italians 136
CDKN2A and MC1R analysis in amelanotic and pigmented melanoma. 135
CDKN2A is the main susceptibility gene in Italian pancreatic cancer families. 135
Increased Risk of Colorectal Adenomas in Italian Subjects Carrying the p53 PIN3 A2-Pro72 Haplotype. 134
Genome-wide association study identifies novel loci predisposing to cutaneous melanoma. 134
Brooke-Spiegler syndrome tumor spectrum beyond the skin: a patient carrying germline R936X CYLD mutation and a somatic CYLDmutation in Brenner tumor 133
Association of MC1R Variants and Host Phenotypes With Melanoma Risk in CDKN2A Mutation Carriers: A GenoMEL Study 127
Germline MLH1 and MSH2 mutations in Italian pancreatic cancer patients with suspected Lynch syndrome. 125
Nevoid Basal Cell Carcinoma Syndrome in infants: improving diagnosis. 121
Functional analysis of CDKN2A/p16INK4a 5'-UTR variants predisposing to melanoma 120
Carvedilol prevents doxorubicin-induced free radical release and apoptosis in cardiomyocytes in vitro. 119
Prevalence of the E318K MITF germline mutation in Italian melanoma patients: associations with histological subtypes and family cancer history. 116
A comparison of CDKN2A mutation detection within the Melanoma Genetics Consortium (GenoMEL) 112
Impact of E27X, a novel CDKN2A germ line mutation, on p16 and p14ARF expression in Italian melanoma families displaying pancreatic cancer and neuroblastoma. 105
Hereditary trichilemmal cysts: A proposal for the assessment of diagnostic clinical criteria 94
ANALISI GENOME-WIDE PER LA SUSCETTIBILITÀ AL MELANOMA: NUOVI LOCICHE CONFERMANO IL RUOLO DEI GENI DELLA PIGMENTAZIONE 93
MC1R variation and melanoma risk in relation to host/clinical and environmental factors in CDKN2A positive and negative melanoma patients. 88
CDKN2A mutations and MC1R variants in Italian patients with single or multiple primary melanoma 88
Identification of a SUFU germline mutation in a family with Gorlin syndrome 82
Five novel germline function-impairing mutations of CYLD in Italian patients with multiple cylindromas 81
Features associated with germline CDKN2A mutations: A GenoMEL study of melanoma-prone families from three continents 76
Predicting the risk of pancreatic cancer: on CDKN2A mutations in the melanoma-pancreatic cancer syndrome in Italy 76
CDKN2A/p16INK4a 5’UTR variants in melanoma and pancreatic cancer predisposition: lost in translation, somewhere 56
Molecular characterisation of Italian Nevoid Basal Cell Carcinoma Syndrome patients 48
Totale 2.986
Categoria #
all - tutte 8.880
article - articoli 8.342
book - libri 0
conference - conferenze 538
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 17.760


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020695 0 0 0 67 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
2024/202581 15 32 16 18 0 0 0 0 0 0 0 0
Totale 2.986