IRIS
PASTORINO, LORENZA
 Distribuzione geografica
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Continente #
EU - Europa 1.135
Totale 1.135
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Nazione #
IT - Italia 1.135
Totale 1.135
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Città #
Genova 670
Rapallo 307
Genoa 149
Bordighera 9
Totale 1.135
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Nome #
MC1R variants as melanoma risk factors independent of at-risk phenotypic characteristics: A pooled analysis from the M-SKIP project, file e268c4ca-a1cc-a6b7-e053-3a05fe0adea1 117
Heterogeneity and frequency of BRAF mutations in primary melanoma: Comparison between molecular methods and immunohistochemistry, file e268c4c7-850d-a6b7-e053-3a05fe0adea1 110
BRAF-mutant melanoma: treatment approaches, resistance mechanisms, and diagnostic strategies., file e268c4ca-a329-a6b7-e053-3a05fe0adea1 102
Functional characterization of a multi-cancer risk locus on chr5p15.33 reveals regulation of TERT by ZNF148, file e268c4ca-c82b-a6b7-e053-3a05fe0adea1 100
Efficacy of novel immunotherapy regimens in patients with metastatic melanoma with germline CDKN2A mutations, file e268c4ca-c833-a6b7-e053-3a05fe0adea1 98
Functional analysis of a CDKN2A 5’UTR germline variant associated with pancreatic cancer development, file e268c4ca-e957-a6b7-e053-3a05fe0adea1 98
Novel PTCH1 Mutations in Patients with Keratocystic Odontogenic Tumors Screened for Nevoid Basal Cell Carcinoma (NBCC) Syndrome, file e268c4ca-90dd-a6b7-e053-3a05fe0adea1 87
A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma, file e268c4c6-b5c7-a6b7-e053-3a05fe0adea1 76
Cytogenetic/mutation profile of chronic lymphocytic leukemia/malignant melanoma collision tumors of the skin, file e268c4ca-94fb-a6b7-e053-3a05fe0adea1 73
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, file e268c4ca-e751-a6b7-e053-3a05fe0adea1 70
Combining molecular and immunohistochemical analyses of key drivers in primary melanomas: Interplay between germline and somatic variations, file e268c4c9-cdb3-a6b7-e053-3a05fe0adea1 63
MC1R variants increased the risk of sporadic cutaneous melanoma in darker-pigmented Caucasians: A pooled-analysis from the M-SKIP project., file e268c4ca-d1ba-a6b7-e053-3a05fe0adea1 48
CDKN2A is the main susceptibility gene in Italian pancreatic cancer families., file e268c4c6-0732-a6b7-e053-3a05fe0adea1 19
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, file e268c4c7-7169-a6b7-e053-3a05fe0adea1 12
Melanoma in children and adolescents: analysis of susceptibility genes in 123 Italian patients, file e268c4ce-41c7-a6b7-e053-3a05fe0adea1 12
Gene-Level Associations in Patients With and Without Pathogenic Germline Variants in CDKN2A and Pancreatic Cancer, file 254ea6ad-cff9-4e8d-bf19-331bd2a8fe1f 4
Pancreatic Cancer: From Genetic Mechanisms to Translational Challenges, file bae172b5-e719-4d80-93c1-949766d2d40a 4
Quality assessment of a clinical next-generation sequencing melanoma panel within the Italian Melanoma Intergroup (IMI), file e268c4cd-68f3-a6b7-e053-3a05fe0adea1 4
Molecular Assessment in Patients with Melanoma: When and Why?, file 0cac9e34-ffdc-42c4-b747-3f7c10db946e 3
MEDB-35. Relationship between genetic profile, histology, clinical features and long-term outcome in young children medulloblastoma (YCMB) treated with upfront high dose chemotherapy (HDCT) in Italy, file 7ce2efbd-8dca-4883-b972-e19fa887b67b 3
Combining common genetic variants and non-genetic risk factors to predict risk of cutaneous melanoma, file e268c4ca-aed5-a6b7-e053-3a05fe0adea1 3
Insights into genetic susceptibility to melanoma by gene panel testing: Potential pathogenic variants in acd, atm, bap1, and pot1, file e268c4cc-9aa1-a6b7-e053-3a05fe0adea1 3
Clinical, pathological and dermoscopic phenotype of MITF p.E318K carrier cutaneous melanoma patients, file e268c4cc-c04a-a6b7-e053-3a05fe0adea1 3
Contribution of germline mutations in the BRCA and PALB2 genes to pancreatic cancer in Italy., file e268c4c6-ceca-a6b7-e053-3a05fe0adea1 2
CDKN2A germline mutations are not associated with poor survival in an Italian cohort of melanoma patients, file e268c4c9-cdb7-a6b7-e053-3a05fe0adea1 2
Clinical utility gene card for: Gorlin syndrome - Update 2013, file e268c4ca-22c1-a6b7-e053-3a05fe0adea1 2
Multiple primary melanomas (MPMs) and criteria for genetic assessment: MultiMEL, a multicenter study of the Italian Melanoma Intergroup, file e268c4ca-aee7-a6b7-e053-3a05fe0adea1 2
Germline ATM variants predispose to melanoma: a joint analysis across the GenoMEL and MelaNostrum consortia, file e268c4ce-0b03-a6b7-e053-3a05fe0adea1 2
Insights into mechanisms of tumorigenesis in neuroendocrine neoplasms, file e268c4ce-41c9-a6b7-e053-3a05fe0adea1 2
High- and intermediate-risk susceptibility variants in melanoma families from the Mediterranean area: a multicenter cohort from the MelaNostrum Consortium, file b3c8c2c4-845f-4a0c-b56b-a46c9563a40c 1
Coping with formalin banning in pathology: under vacuum long-term tissue storage with no added formalin, file e268c4ca-7dbc-a6b7-e053-3a05fe0adea1 1
CDKN2A and MC1R analysis in amelanotic and pigmented melanoma., file e268c4ca-90d7-a6b7-e053-3a05fe0adea1 1
Identification of a SUFU germline mutation in a family with Gorlin syndrome, file e268c4ca-90db-a6b7-e053-3a05fe0adea1 1
A combination of immunohistochemistry and molecular approaches improves highly sensitive detection of BRAF mutations in papillary thyroid cancer, file e268c4ca-957f-a6b7-e053-3a05fe0adea1 1
MC1R gene variants and non-melanoma skin cancer: A pooled-analysis from the M-SKIP project, file e268c4ca-a1c9-a6b7-e053-3a05fe0adea1 1
MC1R variants in childhood and adolescent melanoma: a retrospective pooled analysis of a multicentre cohort, file e268c4ca-b201-a6b7-e053-3a05fe0adea1 1
Comprehensive Study of the Clinical Phenotype of Germline BAP1 Variant-Carrying Families Worldwide, file e268c4ca-c4fd-a6b7-e053-3a05fe0adea1 1
PTCH1 germline mutations and the basaloid follicular hamartoma values in the tumor spectrum of basal cell carcinoma syndrome (NBCCS), file e268c4ca-d945-a6b7-e053-3a05fe0adea1 1
Molecular characterisation of Italian Nevoid Basal Cell Carcinoma Syndrome patients, file e268c4ca-da41-a6b7-e053-3a05fe0adea1 1
Erratum: A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma (Nature (2011) 480:94-98 doi:10.1038/nature10539), file e268c4ca-e74d-a6b7-e053-3a05fe0adea1 1
Totale 1.135
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Categoria #
all - tutte 2.494
article - articoli 2.489
book - libri 0
conference - conferenze 2
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 3
Totale 4.988
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20191 0 0 0 0 0 0 0 0 0 0 0 1
2019/2020236 0 0 1 2 22 17 38 30 47 30 30 19
2020/2021209 13 19 22 15 16 18 20 19 16 17 17 17
2021/2022238 23 15 8 10 15 9 9 11 16 11 78 33
2022/2023337 10 22 73 47 33 81 14 35 2 3 16 1
2023/2024109 0 2 8 8 9 15 29 18 6 13 1 0
Totale 1.135