المؤلفون: Giulia, Ongaro, Serena, Petrocchi, Mariarosaria, Calvello, Bernardo, Bonanni, Irene, Feroce, Gabriella, Pravettoni

المصدر: Current oncology (Toronto, Ont.). 29(4)

مصطلحات موضوعية: Male, Heterozygote, BRCA1 Protein, Humans, Mass Screening, Breast Neoplasms, Female, Genetic Testing, Germ-Line Mutation

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::4340566cacabe29e64770319e1298963
https://pubmed.ncbi.nlm.nih.gov/35448177

المؤلفون: Serena Petrocchi, Giulia Ongaro, Mariarosaria Calvello, Irene Feroce, Bernardo Bonanni, Gabriella Pravettoni

المصدر: PloS one. 17(4)

مصطلحات موضوعية: Male, Ovarian Neoplasms, Multidisciplinary, Germ Cells, BRCA1 Protein, Mutation, Humans, Breast Neoplasms, Female, Genetic Testing, Child, Referral and Consultation, Randomized Controlled Trials as Topic

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6e6f1eb0ed52fac00f84742b7952e8f
https://pubmed.ncbi.nlm.nih.gov/35395021

المؤلفون: Mariarosaria Calvello, Gianluca Tolva, Paola Rafaniello, Massimo Barberis, Sara Gandini, Matteo Dal Molin, Aliana Guerrieri-Gonzaga, Irene Feroce, Cristina Trovato, Monica Marabelli, Bernardo Bonanni, Lucio Bertario, Matteo Lazzeroni, Elena Marino, Wanda Petz

المصدر: Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver. 52(12)

مصطلحات موضوعية: Oncology, Adult, Male, Proto-Oncogene Proteins B-raf, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Colorectal cancer, medicine.disease_cause, MLH1, DNA Mismatch Repair, Germline, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, Medicine, Humans, Genetic Testing, Early Detection of Cancer, Aged, Aged, 80 and over, Mutation, Hepatology, business.industry, Rectal Neoplasms, Gastroenterology, DNA Methylation, Middle Aged, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, Immunohistochemistry, digestive system diseases, Lynch syndrome, MSH6, Logistic Models, 030220 oncology & carcinogenesis, Colonic Neoplasms, Multivariate Analysis, 030211 gastroenterology & hepatology, DNA mismatch repair, Female, Microsatellite Instability, business, MutL Protein Homolog 1

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::615c2350ee542f784f0eb7ae4694eb7a
https://pubmed.ncbi.nlm.nih.gov/32620519

المؤلفون: Luigi Mori, Maria Christina Sini, Michela Biancolella, Florentia Fostira, Andreas Hadjisavvas, Susan M. Domchek, Conxi Lázaro, Gabriele Lorenzo Capone, T. L. Chris Chan, Jeffrey N. Weitzel, Mark E. Robson, Diana Eccles, Inge Søkilde Pedersen, Gianluca Tedaldi, Sarah M. Nielsen, Iris L. Romero, Arcangela De Nicolo, Orland Diez, Arjen R. Mensenkamp, Jana Soukupova, Pietro Cavalli, Ros Eeles, Ana Vega, Kathleen Claes, Maria A. Loizidou, David E. Goldgar, Olufunmilayo I. Olopade, Amanda E. Toland, Yvonne Wallis, Mads Thomassen, Setareh Moghadasi, Fergus J. Couch, Mariarosaria Calvello, Judith Balmaña, Encarna B. Gomez-Garcia, Maria Rossing, Claude Houdayer, Erica Vaccari, April Morrow, Thomas Hansen, Maria Grazia Tibiletti, Sophie Krieger, Liliana Varesco, Nadia Naldi, Therese Törngren, Rien Blok, Fahd Al-Mulla, Henriette Roed Nielsen, Angela R. Solano, Amanda B. Spurdle, Akira Hirasawa, Laura Cortesi, Siranoush Manoukian, Maria A. Caligo, Barbara Wappenschmidt, Manuel R. Teixeira, Marianna Puzzo, Miguel de la Hoya, Alvaro N.A. Monteiro, Petra Kleiblova, Anna Efremidis, Edenir Inêz Palmero, Simona De Toffol, Nicholas Pachter, Maria Piane

المساهمون: RS: GROW - R4 - Reproductive and Perinatal Medicine, MUMC+: DA KG Lab Centraal Lab (9), MUMC+: DA KG Polikliniek (9), Klinische Genetica

المصدر: Nielsen, S M, Eccles, D M, Romero, I L, Al-Mulla, F, Balmaña, J, Biancolella, M, Blok, R, Caligo, M A, Calvello, M, Capone, G L, Cavalli, P, Chan, T L C, Claes, K B M, Cortesi, L, Couch, F J, de la Hoya, M, De Toffol, S, Diez, O, Domchek, S M, Eeles, R, Efremidis, A, Fostira, F, Goldgar, D, Hadjisavvas, A, Hansen, T V O, Hirasawa, A, Houdayer, C, Kleiblova, P, Krieger, S, Lázaro, C, Loizidou, M, Manoukian, S, Mensenkamp, A R, Moghadasi, S, Monteiro, A N, Mori, L, Morrow, A, Naldi, N, Nielsen, H R, Olopade, O I, Pachter, N S, Palmero, E I, Pedersen, I S, Piane, M, Puzzo, M, Robson, M, Rossing, M, Sini, M C, Solano, A & Thomassen, M 2018, ' Genetic testing and clinical management practices for variants in non-BRCA1/2 breast (and breast/ovarian) cancer susceptibility genes : An international survey by the Evidence-based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) clinical working group ', JCO Precision Oncology, vol. 2 . https://doi.org/10.1200/PO.18.00091
Nielsen, S M, Eccles, D M, Romero, I L, Al-Mulla, F, Balmaña, J, Biancolella, M, Blok, R, Caligo, M A, Calvello, M, Capone, G L, Cavalli, P, Chan, T L C, Claes, K B M, Cortesi, L, Couch, F J, de la Hoya, M, De Toffol, S, Diez, O, Domchek, S M, Eeles, R, Efremidis, A, Fostira, F, Goldgar, D, Hadjisavvas, A, Hansen, T V O, Hirasawa, A, Houdayer, C, Kleiblova, P, Krieger, S, Lázaro, C, Loizidou, M, Manoukian, S, Mensenkamp, A R, Moghadasi, S, Monteiro, A N, Mori, L, Morrow, A, Naldi, N, Nielsen, H R, Olopade, O I, Pachter, N S, Palmero, E I, Pedersen, I S, Piane, M, Puzzo, M, Robson, M, Rossing, M, Sini, M C, Solano, A, Soukupova, J, Tedaldi, G, Teixeira, M, Thomassen, M, Tibiletti, M G, Toland, A, Törngren, T, Vaccari, E, Varesco, L, Vega, A, Wallis, Y, Wappenschmidt, B, Weitzel, J, Spurdle, A B, De Nicolo, A & Gómez-García, E B 2018, ' Genetic Testing and Clinical Management Practices for Variants in Non-BRCA1/2 Breast (and Breast/Ovarian) Cancer Susceptibility Genes : An International Survey by the Evidence-Based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) Clinical Working Group ', JCO Precision Oncology, vol. 2 . https://doi.org/10.1200/PO.18.00091
JCO Precision Oncology, 2, 1-43. American Society of Clinical Oncology
Journal of clinical oncology 2 (2018). doi:10.1200/PO.18.00091
info:cnr-pdr/source/autori:Nielsen, Sarah M.; Eccles, Diana M.; Romero, Iris L.; Al-Mulla, Fand; Balmana, Judith; Biancolella, Michela; Blok, Rien; Caligo, Maria Adelaide; Calvello, Mariarosaria; Capone, Gabriele Lorenzo; Cavalli, Pietro; Chan, T. L. Chris; Claes, Kathleen B. M.; Cortesi, Laura; Couch, Fergus J.; de la Hoya, Miguel; de Toffol, Simona; Diez, Orland; Domchek, Susan M.; Eeles, Ros; Efremidis, Anna; Fostira, Florentia; Goldgar, David; Hadjisavvas, Andreas; Hansen, Thomas v O.; Hirasawa, Akira; Houdayer, Claude; Kleiblova, Petra; Krieger, Sophie; Lazaro, Conxi; Loizidou, Maria; Manoukian, Siranoush; Mensenkamp, Arjen R.; Moghadasi, Setareh; Monteiro, Alvaro N.; Mori, Luigi; Morrow, April; Naldi, Nadia; Nielsen, Henriette R.; Olopade, Olufunmilayo, I; Pachter, Nicholas S.; Palrnero, Edenir, I; Pedersen, Inge S.; Piane, Maria; Puzzo, Marianna; Robson, Mark; Rossing, Maria; Sini, Maria Christina; Solano, Angela; Soukupova, Jana; Tedaldi, Gianluca; Teixeira, Manuel; Thomassen, Mads; Tibiletti, Maria Grazia; Toland, Amanda; Torngren, Therese; Vaccari, Erica; Varesco, Liliana; Vega, Ana; Wallis, Yvonne; Wappenschmidt, Barbara; Weitzel, Jeffrey; Spurdle, Amanda B.; De Nicolo, Arcangela; Gomez-Garcia, Encarna B./titolo:Genetic Testing and Clinical Management Practices for Variants in Non-BRCA1%2F2 Breast (and Breast%2FOvarian) Cancer Susceptibility Genes: An International Survey by the Evidence-Based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) Clinical Working Group/doi:10.1200%2FPO.18.00091/rivista:Journal of clinical oncology/anno:2018/pagina_da:/pagina_a:/intervallo_pagine:/volume:2
JCO Precision Oncology

مصطلحات موضوعية: 0301 basic medicine, HEREDITARY BREAST, Cancer Research, endocrine system, Evidence-based practice, PALB2, Biology, GUIDELINES, Germline, Article, CLASSIFICATION, FAMILIES, PANEL, GENOMIC CAPTURE, 03 medical and health sciences, 0302 clinical medicine, medicine, Allele, CHEK2, Gene, INHERITED MUTATIONS, Genetic testing, Genetics, RISK, medicine.diagnostic_test, BRIP1, ENIGMA, 16. Peace & justice, OVARIAN, PREDISPOSITION, 3. Good health, 030104 developmental biology, Settore MED/03 - Genetica Medica, Oncology, 030220 oncology & carcinogenesis, hereditary breast, inherited mutations, genomic capture, ovarian, panel, risk, predisposition, classification, guidelines, families

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e18cc8c44cbb31dff032d04c5f92d254
https://pubmed.ncbi.nlm.nih.gov/31517176

المؤلفون: Paolo Radice, Jacopo Azzollini, Daniela Zaffaroni, Mariarosaria Calvello, Mara Colombo, Eleonora Bruno, Giulietta Scuvera, Barbara Pasini, Valeria Pensotti, Bernard Peissel, Patrizia Pasanisi, Carla B. Ripamonti, Siranoush Manoukian

المصدر: European journal of internal medicine. 32

مصطلحات موضوعية: 0301 basic medicine, Proband, Oncology, Adult, Male, medicine.medical_specialty, endocrine system diseases, Genetic counseling, BRCA2 gene, DNA Mutational Analysis, Genes, BRCA2, Genes, BRCA1, Risk Assessment, 03 medical and health sciences, symbols.namesake, BRCA1 gene, 0302 clinical medicine, Internal medicine, medicine, Genetic predisposition, Internal Medicine, Humans, Selection criteria, Genetic Testing, Fisher's exact test, Genetic testing, Gynecology, medicine.diagnostic_test, business.industry, Patient Selection, BRCA mutation, Odds ratio, Middle Aged, BRCA1, BRCA2, female genital diseases and pregnancy complications, 030104 developmental biology, Genes, Italy, 030220 oncology & carcinogenesis, Mutation (genetic algorithm), Mutation, symbols, Hereditary Breast and Ovarian Cancer Syndrome, Female, business, Hereditary breast and ovarian cancer syndrome

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b67b839186e35b2fab5a71c46476091
https://pubmed.ncbi.nlm.nih.gov/27062684