Viassolo相关文献与解析，生知库 | 链接生命科学的每一步

Costanzo, Silvia; Godino, Lea; De Summa, Simona; Marvulli, Tommaso Maria; Genuardi, Maurizio; Di Pietro, Maria Luisa; Cordisco, Emanuela Lucci; Turchetti, Daniela; Miccoli, Sara; Deledda, Giuseppe; Fantoni, Giovanna; Viassolo, Valeria; Brunetti, Oronzo; De Luca, Raffaele; Digennaro, Maria; Romito, Francesca; Campanella, Maria; Patruno, Margherita

发表日期：2025

文献求助收藏

Deep Neural Network Integrated into Network-Based Stratification (D3NS): A Method to Uncover Cancer Subtypes from Somatic Mutations

深度神经网络与基于网络的分层（D3NS）：一种从体细胞突变中揭示癌症亚型的方法

期刊:Cancers

影响因子:4.4

doi:10.3390/cancers16162845

Valerio, Matteo; Inno, Alessandro; Zambelli, Alberto; Cortesi, Laura; Lorusso, Domenica; Viassolo, Valeria; Verzè, Matteo; Nicolis, Fabrizio; Gori, Stefania

Prevalence of CDKN2A, CDK4, POT1, BAP1, MITF, ATM, and TERT Pathogenic Variants in a Single-Center Retrospective Series of Patients With Melanoma and Personal or Family History Suggestive of Genetic Predisposition

在单中心回顾性研究中，黑色素瘤患者（具有提示遗传易感性的个人或家族史）中 CDKN2A、CDK4、POT1、BAP1、MITF、ATM 和 TERT 致病性变异的患病率

期刊:Dermatology Practical & Conceptual

影响因子:2.3

doi:10.5826/dpc.1403a120

Ferrara, Giada; Paiella, Salvatore; Settanni, Giulio; Frizziero, Melissa; Rosina, Paolo; Viassolo, Valeria

Hematologic toxicities of chemotherapy in breast and ovarian cancer patients carrying BRCA1/BRCA2 germline pathogenic variants. A single center experience and review of the literature

携带 BRCA1/BRCA2 生殖系致病变异的乳腺癌和卵巢癌患者化疗的血液学毒性：单中心经验及文献回顾

期刊:Familial Cancer

影响因子:2

doi:10.1007/s10689-023-00331-6

Hu-Heimgartner, Ketty; Lang, Noémie; Ayme, Aurélie; Ming, Chang; Combes, Jean-Damien; Chappuis, Victor N; Vazquez, Carla; Friedlaender, Alex; Vuilleumier, Aurélie; Bodmer, Alexandre; Viassolo, Valeria; Sandoval, José L; Chappuis, Pierre O; Labidi-Galy, S Intidhar

Cohort profile: population-based cohorts of patients with colorectal cancer and of their relatives in Geneva, Switzerland

队列概况：瑞士日内瓦结直肠癌患者及其亲属的基于人群的队列研究

期刊:BMJ Open

影响因子:2.3

doi:10.1136/bmjopen-2022-063914

Benhamou, Simone; Fournier, Evelyne; Puppa, Giacomo; McKee, Thomas; Ris, Frédéric; Rubbia-Brandt, Laura; Viassolo, Valeria; Zilli, Thomas; Zlobec, Inti; Chappuis, Pierre Olivier; Rapiti, Elisabetta

Machine learning-based lifetime breast cancer risk reclassification compared with the BOADICEA model: impact on screening recommendations

基于机器学习的终生乳腺癌风险重新分类与BOADICEA模型的比较：对筛查建议的影响

期刊:British Journal of Cancer

影响因子:6.8

doi:10.1038/s41416-020-0937-0

Ming, Chang; Viassolo, Valeria; Probst-Hensch, Nicole; Dinov, Ivo D; Chappuis, Pierre O; Katapodi, Maria C

Publisher Correction: Clinical outcome of breast cancer in carriers of BRCA1 and BRCA2 mutations according to molecular subtypes

出版商更正：根据分子亚型划分的BRCA1和BRCA2突变携带者乳腺癌的临床结果

期刊:Scientific Reports

影响因子:3.9

doi:10.1038/s41598-020-76385-8

De Talhouet, Solene; Peron, Julien; Vuilleumier, Aurelie; Friedlaender, Alex; Viassolo, Valeria; Ayme, Aurélie; Bodmer, Alexandre; Treilleux, Isabelle; Lang, Noemie; Tille, Jean-Christophe; Chappuis, Pierre O; Buisson, Adrien; Giraud, Sophie; Lasset, Christine; Bonadona, Valerie; Trédan, Olivier; Labidi-Galy, S Intidhar

A new bioinformatics tool to help assess the significance of BRCA1 variants

一种用于评估BRCA1变异意义的新型生物信息学工具

期刊:Human Genomics

影响因子:4.3

doi:10.1186/s40246-018-0168-0

Cusin, Isabelle; Teixeira, Daniel; Zahn-Zabal, Monique; Rech de Laval, Valentine; Gleizes, Anne; Viassolo, Valeria; Chappuis, Pierre O; Hutter, Pierre; Bairoch, Amos; Gaudet, Pascale

BRCA1

发表日期：2018

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Cancer Predisposition Cascade Screening for Hereditary Breast/Ovarian Cancer and Lynch Syndromes in Switzerland: Study Protocol

瑞士遗传性乳腺癌/卵巢癌和林奇综合征的癌症易感性级联筛查：研究方案

期刊:JMIR Research Protocols

影响因子:1.5

doi:10.2196/resprot.8138

Katapodi, Maria C; Viassolo, Valeria; Caiata-Zufferey, Maria; Nikolaidis, Christos; Bührer-Landolt, Rosmarie; Buerki, Nicole; Graffeo, Rossella; Horváth, Henrik Csaba; Kurzeder, Christian; Rabaglio, Manuela; Scharfe, Michael; Urech, Corinne; Erlanger, Tobias E; Probst-Hensch, Nicole; Heinimann, Karl; Heinzelmann-Schwarz, Viola; Pagani, Olivia; Chappuis, Pierre O

Side effects of antituberculosis treatment

抗结核治疗的副作用

期刊:Thorax

影响因子:7.7

doi:10.1136/thorax.56.12.983

de Maria, A; Berardi, M; Dignetti, P; Ferrera, L; Viassolo, L; Canonica, G W

发表日期：2001

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BRCA cascade counselling and testing in Italy: current position and future directions

意大利BRCA级联咨询和检测：现状与未来方向

Deep Neural Network Integrated into Network-Based Stratification (D3NS): A Method to Uncover Cancer Subtypes from Somatic Mutations

深度神经网络与基于网络的分层（D3NS）：一种从体细胞突变中揭示癌症亚型的方法

Prevalence of CDKN2A, CDK4, POT1, BAP1, MITF, ATM, and TERT Pathogenic Variants in a Single-Center Retrospective Series of Patients With Melanoma and Personal or Family History Suggestive of Genetic Predisposition

在单中心回顾性研究中，黑色素瘤患者（具有提示遗传易感性的个人或家族史）中 CDKN2A、CDK4、POT1、BAP1、MITF、ATM 和 TERT 致病性变异的患病率

Hematologic toxicities of chemotherapy in breast and ovarian cancer patients carrying BRCA1/BRCA2 germline pathogenic variants. A single center experience and review of the literature

携带 BRCA1/BRCA2 生殖系致病变异的乳腺癌和卵巢癌患者化疗的血液学毒性：单中心经验及文献回顾

Cohort profile: population-based cohorts of patients with colorectal cancer and of their relatives in Geneva, Switzerland

队列概况：瑞士日内瓦结直肠癌患者及其亲属的基于人群的队列研究

Machine learning-based lifetime breast cancer risk reclassification compared with the BOADICEA model: impact on screening recommendations

基于机器学习的终生乳腺癌风险重新分类与BOADICEA模型的比较：对筛查建议的影响

Publisher Correction: Clinical outcome of breast cancer in carriers of BRCA1 and BRCA2 mutations according to molecular subtypes

出版商更正：根据分子亚型划分的BRCA1和BRCA2突变携带者乳腺癌的临床结果

A new bioinformatics tool to help assess the significance of BRCA1 variants

一种用于评估BRCA1变异意义的新型生物信息学工具

Cancer Predisposition Cascade Screening for Hereditary Breast/Ovarian Cancer and Lynch Syndromes in Switzerland: Study Protocol

瑞士遗传性乳腺癌/卵巢癌和林奇综合征的癌症易感性级联筛查：研究方案

Side effects of antituberculosis treatment

抗结核治疗的副作用