IRIS
PASTORINO, LORENZA
 Distribuzione geografica
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Continente #
EU - Europa 13.240
AS - Asia 567
SA - Sud America 88
NA - Nord America 87
AF - Africa 4
Totale 13.986
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Nazione #
IT - Italia 13.215
SG - Singapore 227
CN - Cina 172
VN - Vietnam 126
US - Stati Uniti d'America 73
BR - Brasile 52
AR - Argentina 19
HK - Hong Kong 13
MX - Messico 9
ID - Indonesia 6
CL - Cile 5
EC - Ecuador 5
GB - Regno Unito 5
JP - Giappone 5
CO - Colombia 4
IQ - Iraq 4
RU - Federazione Russa 4
AT - Austria 3
BD - Bangladesh 3
NL - Olanda 3
CA - Canada 2
CR - Costa Rica 2
IE - Irlanda 2
PL - Polonia 2
UZ - Uzbekistan 2
AE - Emirati Arabi Uniti 1
AL - Albania 1
DE - Germania 1
FI - Finlandia 1
GY - Guiana 1
HR - Croazia 1
IL - Israele 1
IR - Iran 1
KW - Kuwait 1
LK - Sri Lanka 1
LT - Lituania 1
ME - Montenegro 1
PE - Perù 1
PK - Pakistan 1
PR - Porto Rico 1
PS - Palestinian Territory 1
PY - Paraguay 1
QA - Qatar 1
SN - Senegal 1
SO - Somalia 1
TG - Togo 1
TR - Turchia 1
ZA - Sudafrica 1
Totale 13.986
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Città #
Genova 7.156
Genoa 3.952
Rapallo 1.151
Vado Ligure 910
Singapore 76
Beijing 57
Ho Chi Minh City 55
Ashburn 36
Bordighera 27
Hanoi 26
Hong Kong 13
Tianjin 11
Mexico City 7
Haiphong 6
Milan 5
São Paulo 5
Tokyo 5
Buenos Aires 4
Hải Dương 4
New York 4
Orem 4
Quảng Ngãi 4
Rio de Janeiro 4
Biên Hòa 3
Brugherio 3
Bắc Ninh 3
Houston 3
Hưng Yên 3
London 3
Ninh Bình 3
Baghdad 2
Bari 2
Brasília 2
Colombo 2
Cuenca 2
Da Nang 2
Dallas 2
Denver 2
Guayaquil 2
Los Angeles 2
Montes Claros 2
Montreal 2
Santiago 2
Thái Nguyên 2
Tây Ninh 2
Vienna 2
Warsaw 2
Zhengzhou 2
Alagoinhas 1
Arecibo 1
Arequipa 1
Asunción 1
Bandung 1
Bekasi 1
Blumenau 1
Boa Esperança do Sul 1
Boardman 1
Buenaventura 1
Bukhara 1
Bắc Giang 1
Campos dos Goytacazes 1
Cartagena 1
Cartago 1
Central de Minas 1
Cipolletti 1
Cuauhtémoc 1
Curitiba 1
Dakar 1
Diamantina 1
Doha 1
Dongguan 1
Dublin 1
Elk Grove Village 1
Erzurum 1
Esmeraldas 1
Espumoso 1
Eṭ Ṭaiyiba 1
Fighiera 1
Filadélfia 1
Florencia 1
Floriano 1
Formosa 1
Georgetown 1
Goiânia 1
Graz 1
Guangzhou 1
Guernica 1
Gul'kevichi 1
Hargeisa 1
Hefei 1
Irecê 1
Itanhaém 1
Ituzaingó 1
Jacareí 1
Jackson 1
Jiujiang 1
Jizzakh 1
Johannesburg 1
Kizlyar 1
Kuwait City 1
Totale 13.631
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Nome #
Heterogeneity and frequency of BRAF mutations in primary melanoma: Comparison between molecular methods and immunohistochemistry 223
A combination of immunohistochemistry and molecular approaches improves highly sensitive detection of BRAF mutations in papillary thyroid cancer 204
Pathway-based analysis of a melanoma genome-wide association study: analysis of genes related to tumour-immunosuppression. 199
BRAF-mutant melanoma: treatment approaches, resistance mechanisms, and diagnostic strategies. 195
CDKN2A germline mutations are not associated with poor survival in an Italian cohort of melanoma patients 191
Contribution of germline mutations in the BRCA and PALB2 genes to pancreatic cancer in Italy. 187
CDKN2A is the main susceptibility gene in Italian pancreatic cancer families. 187
Combining molecular and immunohistochemical analyses of key drivers in primary melanomas: Interplay between germline and somatic variations 187
Ataxia-Telangiectasia Mutated Loss of Heterozygosity in Melanoma 183
A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma 180
Genome-wide association study identifies novel loci predisposing to cutaneous melanoma. 179
Association of MC1R Variants and Host Phenotypes With Melanoma Risk in CDKN2A Mutation Carriers: A GenoMEL Study 177
Germline MLH1 and MSH2 mutations in Italian pancreatic cancer patients with suspected Lynch syndrome. 176
CDKN2A and MC1R analysis in amelanotic and pigmented melanoma. 175
Multiple primary melanomas (MPMs) and criteria for genetic assessment: MultiMEL, a multicenter study of the Italian Melanoma Intergroup 175
Functional analysis of CDKN2A/p16INK4a 5'-UTR variants predisposing to melanoma 173
Ameloblastoma: a neglected criterion for nevoid basal cell carcinoma (Gorlin) syndrome. 170
Brooke-Spiegler syndrome tumor spectrum beyond the skin: a patient carrying germline R936X CYLD mutation and a somatic CYLDmutation in Brenner tumor 169
Clinical Significance of Germline Pathogenic Variants among 51 Cancer Predisposition Genes in an Unselected Cohort of Italian Pancreatic Cancer Patients 169
Association of Melanocortin-1 Receptor Variants with Pigmentary Traits in Humans: A Pooled Analysis from the M-Skip Project 168
A comparison of CDKN2A mutation detection within the Melanoma Genetics Consortium (GenoMEL) 167
Early onset may predict G101W CDKN2A founder mutation carrier status in Ligurian melanoma patients. 166
Functional characterization of a multi-cancer risk locus on chr5p15.33 reveals regulation of TERT by ZNF148 165
MC1R variants increased the risk of sporadic cutaneous melanoma in darker-pigmented Caucasians: A pooled-analysis from the M-SKIP project. 164
Gly101Trp germline mutation in the CDKN2A gene in familial and non familial Ligurian melanoma patients 157
Features associated with germline CDKN2A mutations: A GenoMEL study of melanoma-prone families from three continents 156
Brooke-Spiegler syndrome: report of two cases not associated with a mutation in the CYLD and PTCH tumor-suppressor genes 153
ANALISI GENOME-WIDE PER LA SUSCETTIBILITÀ AL MELANOMA: NUOVI LOCICHE CONFERMANO IL RUOLO DEI GENI DELLA PIGMENTAZIONE 149
Clinical genetic testing for familial melanoma in Italy: a cooperative study. 148
Comprehensive Study of the Clinical Phenotype of Germline BAP1 Variant-Carrying Families Worldwide 147
Clinical, pathological and dermoscopic phenotype of MITF p.E318K carrier cutaneous melanoma patients 145
Nevoid Basal Cell Carcinoma Syndrome in infants: improving diagnosis. 144
Novel PTCH1 Mutations in Patients with Keratocystic Odontogenic Tumors Screened for Nevoid Basal Cell Carcinoma (NBCC) Syndrome 144
Impact of E27X, a novel CDKN2A germ line mutation, on p16 and p14ARF expression in Italian melanoma families displaying pancreatic cancer and neuroblastoma. 143
Genome-wide association study identifies three new melanoma susceptibility loci 143
The CDKN2A/p16INK4a 5'UTR sequence and translational regulation: Impact of novel variants predisposing to melanoma 141
Prevalence of the E318K MITF germline mutation in Italian melanoma patients: associations with histological subtypes and family cancer history. 140
Correction: Combining molecular and immunohistochemical analyses of key drivers in primary melanomas: Interplay between germline and somatic variations [Oncotarget. 2018; 9:5691-5702]doi 10.18632/oncotarget.23204 137
Absence of high risk gene mutations in hereditary melanoma points to the interplay between somatic and low risk germline variants 134
Functional analysis of a CDKN2A 5’UTR germline variant associated with pancreatic cancer development 133
"Gestione Melanoma" un "database" relazionale per lo studio e l’approfondimento della relazione genotipo/fenotipo e genotipo/ambiente nel melanoma familiare e sporadico 132
Coping with formalin banning in pathology: under vacuum long-term tissue storage with no added formalin 132
Varianti polimorfiche del gene MC1R (Melanocortin receptor 1) nella popolazione ligure ed associazione con il rischio di melanoma 131
Patched homolog 1 gene mutation (p.G1093R) induces nevoid basal cell carcinoma syndrome and non-syndromic keratocystic odontogenic tumors: A case report. 130
High prevalence of the G101W germline mutation in the CDKN2A (P16INK4A) gene in 62 Italian malignant melanoma families 130
CDKN2A mutations and MC1R variants in Italian patients with single or multiple primary melanoma 130
Identification of a SUFU germline mutation in a family with Gorlin syndrome 129
MC1R variation and melanoma risk in relation to host/clinical and environmental factors in CDKN2A positive and negative melanoma patients. 128
Hereditary trichilemmal cysts: A proposal for the assessment of diagnostic clinical criteria 128
Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma 127
CDKN2A germline mutation analysis in patients with pancreatic adenocarcinoma 126
3’UTR polymorphisms in the CDKN2A gene and age at onset of familial and sporadic melanoma 125
A novel PTCH1 gene mutation in a pediatric patient associated multiple keratocystic odontogenic tumors of the jaws and Gorlin-Goltz syndrome 123
The role of AIRE polymorphisms in melanoma. 122
Novel MC1R variants in Ligurian melanoma patients and controls 121
CDKN2A Unclassified Variants in Familial Malignant Melanoma: Combining Functional and Computational Approaches for Their Assessment 121
Combining common genetic variants and non-genetic risk factors to predict risk of cutaneous melanoma 121
Five novel germline function-impairing mutations of CYLD in Italian patients with multiple cylindromas 121
3’UTR polymorphisms in the CDKN2A gene and age at onset of familial and sporadic melanoma from Liguria 121
CDKN2A germline mutation analysis in patients with pancreatic adenocarcinoma from Liguria 120
Medulloblastoma variants: age-dependent occurrence and relation to Gorlin syndrome--a new clinical perspective. 120
Combining germline, tissue and liquid biopsy analysis by comprehensive genomic profiling to improve the yield of actionable variants in a real-world cancer cohort 117
Analysis of Cultured Human Melanocytes Based on Polymorphisms within the SLC45A2/MATP, SLC24A5/NCKX5, and OCA2/P Loci. 117
Analisi molecolare del gene PTCH nella Sindrome di Gorlin (Carcinoma Nevo Basocellulare NBCCS) 116
Ink4/ARF germline mutations and additional neoplasia in pancretic cancer patients and their families 116
Efficacy of novel immunotherapy regimens in patients with metastatic melanoma with germline CDKN2A mutations 116
Insights into genetic susceptibility to melanoma by gene panel testing: Potential pathogenic variants in acd, atm, bap1, and pot1 116
INK4/ARF germline alterations in pancreatic cancer patients 113
MC1R variants as melanoma risk factors independent of at-risk phenotypic characteristics: A pooled analysis from the M-SKIP project 112
Unicystic ameloblastoma associated with the novel K729M PTCH1 mutation in a patient with nevoid basal cell carcinoma (Gorlin) syndrome. 111
Quality assessment of a clinical next-generation sequencing melanoma panel within the Italian Melanoma Intergroup (IMI) 111
PTCH1 germline mutations and the basaloid follicular hamartoma values in the tumor spectrum of basal cell carcinoma syndrome (NBCCS) 109
Inverse correlation between p16INK4A expression and NF-kappaB activation in melanoma progression 108
Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutations 107
Analisi della sequenza codificante e regolatrice del gene di suscettibilità al melanoma CDKN2A in 62 famiglie 106
Absence of melanocortin 1 receptor variants in Ligurian Gly101trp families 104
Correlation between NF-kB/GM-CSF expression and functional status of the p16 melanoma susceptibility gene 103
CDKN2A mutation distribution in ligurian sporadic melanoma according to age at diagnosis 101
Correlazione tra l’espressione di NF-KB e lo stato funzionale del gene di suscettibilità al melanoma familiare CDKN2A (p16ink4) 100
Analisi di mutazioni del gene PTCH nella sindrome di Gorlin 100
MC1R gene variants and non-melanoma skin cancer: A pooled-analysis from the M-SKIP project 98
Diagnostic and pathogenetic role of cafe-au-lait macules in nevoid basal cell carcinoma syndrome 98
Cytogenetic/mutation profile of chronic lymphocytic leukemia/malignant melanoma collision tumors of the skin 97
Clinical utility gene card for: Gorlin syndrome 97
Frequency of 3’UTR polymorphisms in the CDKN2A gene in familial and non-familial Ligurian melanoma patients 96
Varianti polimorfiche del gene MC1R (melanocortin receptor 1): Analisi in pazienti Liguri affetti da melanoma e negativi per mutazioni nei geni CDKN2A e CDK4 93
MC1R variants in childhood and adolescent melanoma: a retrospective pooled analysis of a multicentre cohort 93
Predicting the risk of pancreatic cancer: on CDKN2A mutations in the melanoma-pancreatic cancer syndrome in Italy 90
Erratum: A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma (Nature (2011) 480:94-98 doi:10.1038/nature10539) 90
INK4/ARF germline mutations and additional neoplasia in pancreatic cancer patients and their families 87
Germline ATM variants predispose to melanoma: a joint analysis across the GenoMEL and MelaNostrum consortia 86
Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility 85
Proteomic analysis of PTCH1 +/- Fibroblast lysate and conditioned culture media isolated from the skin of healthy subjects and nevoid basal cell carcinoma syndrome patients 83
Cutaneous phenotype and MC1R variants as modifying factors for the development of melanoma in CDKN2A G101W mutation carriers from 4 countries. 81
Melanoma prone families with CDK4 germline mutation: phenotypic profile and associations with MC1R variants 81
Germline mutations of the PTCH gene in Italian patients with Nevoid Basal Cell Carcinoma Syndrome 79
Prevalence of CDKN2A gene mutations in patients with early-onset sporadic melanoma 78
Clinical utility gene card for: Gorlin syndrome - Update 2013 78
Insights into mechanisms of tumorigenesis in neuroendocrine neoplasms 78
Multiple primary melanoma (MPM) as a valid criterion for genetic assessment : an Italian IMI multi-center study 77
Totale 13.109
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Categoria #
all - tutte 49.472
article - articoli 41.707
book - libri 0
conference - conferenze 7.473
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 292
Totale 98.944
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021497 0 0 0 0 0 53 55 74 78 103 69 65
2021/20221.312 30 103 83 178 53 85 94 308 70 111 50 147
2022/20231.399 154 117 11 156 260 193 10 97 201 12 167 21
2023/2024823 27 95 9 94 47 132 50 56 71 38 54 150
2024/20252.409 95 165 81 184 276 235 256 441 91 101 202 282
2025/20262.248 527 159 527 388 533 114 0 0 0 0 0 0
Totale 14.283