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L

Lorenza Pastorino

irccs azienda ospedaliera metropolitana - ospedale policlinico san martino
H指数:34
被引数:4,273

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Dissecting the Spectrum of Rare BRAF Mutations in Melanoma: A Nation-Wide Study by the Italian Melanoma Intergroup (IMI)

解析黑色素瘤中罕见BRAF突变的谱系：意大利黑色素瘤协作组（IMI）开展的一项全国性研究

Pigment Cell & Melanoma Research
IF2.6
2026-04-190
OAAI
Bruna Dalmasso; Maria Chiara Scaini; Laura Cendron; Monica Rodolfo; Ilaria Mattavelli; Elena Tamborini; Francesca Collina; Gerardo Ferrara; Gabriele Madonna; Carlo Cota; Elisa Melucci; Stefania Tommasi; Martina Ubaldi; Roberta Depenni; Andrea Carugno; Riccardo Marconcini; Laura Orgiano; Maurizio Lombardo; Simona Sola; Cristina Pellegrini; Francesca Castiglione; Matteo Gasparotto; Alireza Jorkesh; Stefania Pellegrini; Edoardo Raposio; Andrea Boutros; Enrica Teresa Tanda; Michele Guida; Pietro Quaglino; Giuseppe Palmieri; Daniela Massi; Paolo Antonio Ascierto; Francesco Spagnolo; Mario Mandalà; Chiara Menin; Paola Ghiorzo; Lorenza Pastorino; Italian Melanoma Intergroup
Combining germline, tissue and liquid biopsy analysis by comprehensive genomic profiling to improve the yield of actionable variants in a real-world cancer cohort
JOURNAL OF TRANSLATIONAL MEDICINE
IF7.5
2024-05-150
OAAI
Vanni, I.; Pastorino, L.; Andreotti, V.; Comandini, D.; Fornarini, G.; Grassi, M.; Puccini, A.; Tanda, E. T.; Pastorino, A.; Martelli, V.; Mastracci, L.; Grillo, F.; Cabiddu, F.; Guadagno, A.; Coco, S.; Allavena, E.; Barbero, F.; Bruno, W.; Dalmasso, B.; Bellomo, S. E.; Marchio, C.; Spagnolo, F.; Sciallero, S.; Berrino, E.; Ghiorzo, P.
High- and intermediate-risk susceptibility variants in melanoma families from the Mediterranean area: A multicentre cohort from the MelaNostrum Consortium
JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY
IF8
2023-09-054
OA
Pellegrini, C.; Cardelli, L.; Ghiorzo, P.; Pastorino, L.; Potrony, M.; Garcia-Casado, Z.; Elefanti, L.; Stefanaki, I.; Mastrangelo, M.; Necozione, S.; Aguilera, P.; Rodriguez-Hernandez, A.; Di Nardo, L.; Rocco, T.; Del Regno, L.; Badenas, C.; Carrera, C.; Malvehy, J.; Requena, C.; Banuls, J.; Stratigos, A. J.; Peris, K.; Menin, C.; Calista, D.; Nagore, E.; Puig, S.; Landi, M. T.; Fargnoli, M. C.
Predictors of germline status for hereditary melanoma: 5 years of multi-gene panel testing within the Italian Melanoma Intergroup
ESMO OPEN
IF8.3
2022-08-0115
OAAI
Bruno, W.; Dalmasso, B.; Barile, M.; Andreotti, V; Elefanti, L.; Colombino, M.; Vanni, I; Allavena, E.; Barbero, F.; Passoni, E.; Merelli, B.; Pellegrini, S.; Morgese, F.; Danesi, R.; Calo, V; Bazan, V; D'Elia, A., V; Molica, C.; Gensini, F.; Sala, E.; Uliana, V; Soma, P. F.; Genuardi, M.; Ballestrero, A.; Spagnolo, F.; Tanda, E.; Queirolo, P.; Mandala, M.; Stanganelli, I; Palmieri, G.; Menin, C.; Pastorino, L.; Ghiorzo, P.
Cancer risk and tumour spectrum in 172 patients with a germline SUFU pathogenic variation: a collaborative study of the SIOPE Host Genome Working Group
JOURNAL OF MEDICAL GENETICS
IF3.7
2022-06-298
OAAI
Guerrini-Rousseau, Lea; Masliah-Planchon, Julien; Waszak, Sebastian M.; Alhopuro, Pia; Benusiglio, Patrick R.; Bourdeaut, Franck; Brecht, Ines B.; Del Baldo, Giada; Dhanda, Sandeep Kumar; Garre, Maria Luisa; Gidding, Corrie E. M.; Hirsch, Steffen; Hoarau, Pauline; Jorgensen, Mette; Kratz, Christian; Lafay-Cousin, Lucie; Mastronuzzi, Angela; Pastorino, Lorenza; Pfister, Stefan M.; Schroeder, Christopher; Smith, Miriam Jane; Vahteristo, Pia; Vibert, Roseline; Vilain, Catheline; Waespe, Nicolas; Winship, Ingrid M.; Evans, D. Gareth; Brugieres, Laurence
Germline ATM variants predispose to melanoma: a joint analysis across the GenoMEL and MelaNostrum consortia
GENETICS IN MEDICINE
IF6.2
2021-11-0123
OAAI
Dalmasso, B.; Pastorino, L.; Nathan, V; Shah, N. N.; Palmer, J. M.; Howlie, M.; Johansson, P. A.; Freedman, N. D.; Carter, B. D.; Beane-Freeman, L.; Hicks, B.; Molven, A.; Helgadottir, H.; Sankar, A.; Tsao, H.; Stratigos, A. J.; Helsing, P.; Van Doorn, R.; Gruis, N. A.; Visser, M.; Wadt, K. A. W.; Mann, G.; Holland, E. A.; Nagore, E.; Potrony, M.; Puig, S.; Menin, C.; Peris, K.; Fargnoli, M. C.; Calista, D.; Soufir, N.; Harland, M.; Bishop, T.; Kanetsky, P. A.; Elder, D. E.; Andreotti, V; Vanni, I; Bruno, W.; Hoiom, V; Tucker, M. A.; Yang, X. R.; Andresen, P. A.; Adams, D. J.; Landi, M. T.; Hayward, N. K.; Goldstein, A. M.; Ghiorzo, P.
MC1R variants in childhood and adolescent melanoma: a retrospective pooled analysis of a multicentre cohort

儿童和青少年黑色素瘤中的MC1R变异: 多中心队列的回顾性汇总分析

LANCET CHILD & ADOLESCENT HEALTH
IF15.5
2019-05-0117
OAAI
Pellegrini, Cristina; Botta, Francesca; Massi, Daniela; Martorelli, Claudia; Facchetti, Fabio; Gandini, Sara; Maisonneuve, Patrick; Avril, Marie-Francoise; Demenais, Florence; Bressac-de Paillerets, Brigitte; Hoiom, Veronica; Cust, Anne E.; Anton-Culver, Hoda; Gruber, Stephen B.; Gallagher, Richard P.; Marrett, Loraine; Zanetti, Roberto; Dwyer, Terence; Thomas, Nancy E.; Begg, Colin B.; Berwick, Marianne; Puig, Susana; Potrony, Miriam; Nagore, Eduardo; Ghiorzo, Paola; Menin, Chiara; Manganoni, Ausilia Maria; Rodolfo, Monica; Brugnara, Sonia; Passoni, Emanuela; Sekulovic, Lidija Kandolf; Baldini, Federica; Guida, Gabriella; Stratigos, Alexandros; Ozdemir, Fezal; Ayala, Fabrizio; Fernandez-de-Misa, Ricardo; Quaglino, Pietro; Ribas, Gloria; Romanini, Antonella; Migliano, Emilia; Stanganelli, Ignazio; Kanetsky, Peter A.; Antonietta Pizzichetta, Maria; Garcia-Borron, Jose Carlos; Nan, Hongmei; Landi, Maria Teresa; Little, Julian; Newton-Bishop, Julia; Sera, Francesco; Fargnoli, Maria Concetta; Raimondi, Sara; Massi, Daniela; Pastorino, Lorenza; Menin, Chiara; Alaibac, Mauro; Manganoni, Ausilia Maria; Facchetti, Fabio; Rodolfo, Monica; Ferrari, Andrea; Valeri, Barbara; Fargnoli, Maria Concetta; Pellegrini, Cristina; Brugnara, Sonia; Sicher, Mariacristina; Mangiola, Daniela; Passoni, Emanuela; Nazzaro, Gianluca; Baldini, Federica; Tosti, Giulio; Gandini, Sara; Mazzarol, Giovanni; Guida, Gabriella; Guida, Stefania; Giudice, Giuseppe; Ayala, Fabrizio; Quaglino, Pietro; Ribero, Simone; Astrua, Chiara; Romanini, Antonella; Migliano, Emilia; Stanganelli, Ignazio; Mazzoni, Laura; Pizzichetta, Maria Antonietta; Berwick, Marianne; Begg, Colin; Orlow, Irene; Mujumdar, Urvi; Hummer, Amanda; Busam, Klaus; Roy, Pampa; Cotignola, Javiar; Monroe, Yvette; Armstrong, Bruce; Kricker, Anne; Litchfield, Melisa; Tucker, Paul; Stephens, Nicola; Gallagher, Richard; Switzer, Teresa; Marrett, Loraine; Theis, Beth; From, Lynn; Chowdhury, Noori; Vanasse, Louise; Purdue, Mark; Northrup, David; Zanetti, Roberto; Rosso, Stefano; Sacerdote, Carlotta; Anton-Culver, Hoda; Leighton, Nancy; Gildea, Maureen; Gruber, Stephen; Bonner, Joe; Jeter, Joanne; Klotz, Judith; Wilcox, Homer; Weiss, Helen; Millikan, Robert; Thomas, Nancy; Mattingly, Dianne; Player, Jon; Tse, Chiu-Kit; Rebbeck, Timothy; Kanetsky, Peter; Walker, Amy; Panossian, Saarene; Mohrenweiser, Harvey; Setlow, Richard; Raimondi, Sara; Autier, Philippe; Fargnoli, Maria Concetta; Kanetsky, Peter A.; Landi, Maria Teresa; Little, Julian; Newton-Bishop, Julia; Sera, Francesco; Caini, Saverio; Gandini, Sara; Maisonneuve, Patrick; Hofman, Albert; Kayser, Manfred; Liu, Fan; Nijsten, Tamar; Uitterlinden, Andre G.; Kumar, Rajiv; Bishop, Tim; Elliott, Faye; Nagore, Eduardo; Lazovich, DeAnn; Polsky, David; Hansson, Johan; Hoiom, Veronica; Ghiorzo, Paola; Pastorino, Lorenza; Gruis, Nelleke A.; Bavinck, Jan Nico Bouwes; Aguilera, Paula; Badenas, Celia; Carrera, Cristina; Gimenez-Xavier, Pol; Tell-Marti, Gemma; Dwyer, Terence; Blizzard, Leigh; Cochrane, Jennifer; Branicki, Wojciech; Debniak, Tadeusz; Morling, Niels; Johansen, Peter; Mayne, Susan; Bale, Allen; Cartmel, Brenda; Ferrucci, Leah; Pfeiffer, Ruth; Palmieri, Giuseppe; Ribas, Gloria; Menin, Chiara; Stratigos, Alexandros; Kypreou, Katerina; Bowcock, Anne; Cornelius, Lynn; Council, M. Laurin; Motokawa, Tomonori; Anno, Sumiko; Helsing, Per; Andresen, Per Arne; Guida, Gabriella; Guida, Stefania; Wong, Terence H.
Comprehensive Study of the Clinical Phenotype of Germline BAP1 Variant-Carrying Families Worldwide
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE
IF7.2
2018-12-04170
OAAI
Walpole, Sebastian; Pritchard, Antonia L.; Cebulla, Colleen M.; Pilarski, Robert; Stautberg, Meredith; Davidorf, Frederick H.; de la Fouchardiere, Arnaud; Cabaret, Odile; Golmard, Lisa; Stoppa-Lyonnet, Dominique; Garfield, Erin; Njauw, Ching-Ni; Cheung, Mitchell; Turunen, Joni A.; Repo, Pauliina; Jarvinen, Reetta-Stiina; van Doorn, Remco; Jager, Martine J.; Luyten, Gregorius P. M.; Marinkovic, Marina; Chau, Cindy; Potrony, Miriam; Hoiom, Veronica; Helgadottir, Hildur; Pastorino, Lorenza; Bruno, William; Andreotti, Virginia; Dalmasso, Bruna; Ciccarese, Giulia; Queirolo, Paola; Mastracci, Luca; Wadt, Karin; Kiilgaard, Jens Folke; Speicher, Michael R.; van Poppelen, Natasha; Kilic, Emine; Al-Jamal, Rana'a T.; Dianzani, Irma; Betti, Marta; Bergmann, Carsten; Santagata, Sandro; Dahiya, Sonika; Taibjee, Saleem; Burke, Jo; Poplawski, Nicola; O'Shea, Sally J.; Newton-Bishop, Julia; Adlard, Julian; Adams, David J.; Lane, Anne-Marie; Kim, Ivana; Klebe, Sonja; Racher, Hilary; Harbour, J. William; Nickerson, Michael L.; Murali, Rajmohan; Palmer, Jane M.; Howlie, Madeleine; Symmons, Judith; Hamilton, Hayley; Warrier, Sunil; Glasson, William; Johansson, Peter; Robles-Espinoza, Carla Daniela; Ossio, Raul; de Klein, Annelies; Puig, Susana; Ghiorzo, Paola; Nielsen, Maartje; Kivela, Tero T.; Tsao, Hensin; Testa, Joseph R.; Gerami, Pedram; Stern, Marc-Henri; Bressac-de Paillerets, Brigitte; Abdel-Rahman, Mohamed H.; Hayward, Nicholas K.
Combining common genetic variants and non-genetic risk factors to predict risk of cutaneous melanoma
HUMAN MOLECULAR GENETICS
IF3.2
2018-08-3133
OAAI
Gu, Fangyi; Chen, Ting-Huei; Pfeiffer, Ruth M.; Fargnoli, Maria Concetta; Calista, Donato; Ghiorzo, Paola; Peris, Ketty; Puig, Susana; Menin, Chiara; De Nicolo, Arcangela; Rodolfo, Monica; Pellegrini, Cristina; Pastorino, Lorenza; Evangelou, Evangelos; Zhang, Tongwu; Hua, Xing; Dellavalle, Curt T.; Bishop, D. Timothy; MacGregor, Stuart; Iles, Mark I.; Law, Matthew H.; Cust, Anne; Brown, Kevin M.; Stratigos, Alexander J.; Nagore, Eduardo; Chanock, Stephen; Shi, Jianxin; Landi, Maria Teresa
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
HUMAN GENETICS
IF3.6
2016-07-2322
OAAI
Yang, Xiaohong R.; Rotunno, Melissa; Xiao, Yanzi; Ingvar, Christian; Helgadottir, Hildur; Pastorino, Lorenza; van Doorn, Remco; Bennett, Hunter; Graham, Cole; Sampson, Joshua N.; Malasky, Michael; Vogt, Aurelie; Zhu, Bin; Bianchi-Scarra, Giovanna; Bruno, William; Queirolo, Paola; Fornarini, Giuseppe; Hansson, Johan; Tuominen, Rainer; Burdett, Laurie; Hicks, Belynda; Hutchinson, Amy; Jones, Kristine; Yeager, Meredith; Chanock, Stephen J.; Landi, Maria Teresa; Hoiom, Veronica; Olsson, Hakan; Gruis, Nelleke; Ghiorzo, Paola; Tucker, Margaret A.; Goldstein, Alisa M.

研究方向

暂未获取到该数据
P
Paola Ghiorzo
H 指数:46论文数:200被引数:8,057
G
Giovanna Bianchi‐Scarrà
H 指数:38论文数:130被引数:5,569
W
William Bruno
H 指数:43论文数:153被引数:7,015
P
Paola Queirolo
H 指数:68论文数:600被引数:1.8万
M
Menin, Chiara
H 指数:0论文数:2被引数:10
S
Susana Puig
H 指数:102论文数:1,006被引数:4.9万
B
Bruna Dalmasso
H 指数:18论文数:56被引数:1,180
V
Virginia Andreotti
H 指数:19论文数:55被引数:1,211
B
Brigitte Bressac–de Paillerets
H 指数:69论文数:265被引数:1.8万
S
Sabina Nasti
H 指数:19论文数:52被引数:1,269