Academic literature on the topic 'Multigene mutational panels'
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Journal articles on the topic "Multigene mutational panels"
Zagorodnev, Kirill, Yevgeniy Suspitsyn, Anna Sokolenko, A. Romanko, M. Anisimova, Ilya Bizin, Ye Kuligina, and Yevgeniy Imyanitov. "APPLICATION OF THE TARGETED MULTIGENE SEQUENCING FOR THE SEARCH OF HEREDITARY BREAST CANCER MUTATIONS IN RUSSIAN PATIENTS." Problems in oncology 65, no. 3 (March 1, 2019): 349–56. http://dx.doi.org/10.37469/0507-3758-2019-65-3-349-356.
Full textStadler, Zsofia K., Francesca Battaglin, Sumit Middha, Jaclyn F. Hechtman, Christina Tran, Andrea Cercek, Rona Yaeger, et al. "Reliable Detection of Mismatch Repair Deficiency in Colorectal Cancers Using Mutational Load in Next-Generation Sequencing Panels." Journal of Clinical Oncology 34, no. 18 (June 20, 2016): 2141–47. http://dx.doi.org/10.1200/jco.2015.65.1067.
Full textAlemar, Barbara, Cristina Netto, Camila Bittar, Osvaldo Artigalas, Cleandra Gregorio, Marina Roberta Scheid, and Patricia Ashton-Prolla. "Germline mutational spectrum of Brazilian HBOC patients tested with hereditary cancer multigene panels." Journal of Clinical Oncology 34, no. 15_suppl (May 20, 2016): e13113-e13113. http://dx.doi.org/10.1200/jco.2016.34.15_suppl.e13113.
Full textPajares, Bella, Marcos Iglesias Campos, Tamara Díaz, Rafael Jesus Peralta, Emilio Alba, and Antonia Marquez. "Genetic and clinical characterization of multigene hereditary breast and ovarian cancer (HBOC) panels in Málaga (Spain)." Journal of Clinical Oncology 39, no. 15_suppl (May 20, 2021): e22530-e22530. http://dx.doi.org/10.1200/jco.2021.39.15_suppl.e22530.
Full textfontana, sabrina K. kahler ribeiro, emanuele bonetti, loris bernard, mariarosaria calvello, Bernardo Bonanni, ppina Bonizzi, Paolo Veronesi, Luca Mazzarella, Viviana Galimberti, and claudia sangalli. "Abstract P6-02-11: Implementation of multigene panel testing in triple-negative breast cancer. The PERSONA-breast trial." Cancer Research 83, no. 5_Supplement (March 1, 2023): P6–02–11—P6–02–11. http://dx.doi.org/10.1158/1538-7445.sabcs22-p6-02-11.
Full textBapat, Bela, Connor Sweetnam, Ashleigh McBratney, Monika A. Izano, Brock Schroeder, Sheetal Walters, William Chen, Phillip G. Febbo, and Anna B. Berry. "Actionability of comprehensive genomic profiling (CGP) compared to single-gene and small panels in patients with advanced/metastatic non-small cell lung cancer (aNSCLC): A real-world study." Journal of Clinical Oncology 40, no. 16_suppl (June 1, 2022): e21114-e21114. http://dx.doi.org/10.1200/jco.2022.40.16_suppl.e21114.
Full textBapat, Bela, Connor Sweetnam, Ashleigh McBratney, Monika A. Izano, Brock Schroeder, Sheetal Walters, William Chen, Phillip G. Febbo, and Anna B. Berry. "Actionability of comprehensive genomic profiling (CGP) compared to single-gene and small panels in patients with advanced/metastatic non-small cell lung cancer (aNSCLC): A real-world study." Journal of Clinical Oncology 40, no. 16_suppl (June 1, 2022): e21114-e21114. http://dx.doi.org/10.1200/jco.2022.40.16_suppl.e21114.
Full textFields, Jessica, Dimitrios Nasioudis, Zhen Ni Zhou, Ann Carlson, Melissa Kristen Frey, Kevin Holcomb, and Eloise Chapman-Davis. "Underutilization of multigene panels among Ashkenazi Jewish patients." Journal of Clinical Oncology 35, no. 15_suppl (May 20, 2017): 1533. http://dx.doi.org/10.1200/jco.2017.35.15_suppl.1533.
Full textKapoor, Nimmi S., Jennifer Swisher, Rachel E. McFarland, Mychael Patrick, and Lisa D. Curcio. "Impact of hereditary multigene panel testing for cancer survivors." Journal of Clinical Oncology 34, no. 3_suppl (January 20, 2016): 261. http://dx.doi.org/10.1200/jco.2016.34.3_suppl.261.
Full textYadav, Siddhartha, Jennifer Fulbright, Heidi Dreyfuss, Ashley Reeves, Sarah Campian, Vicky Thomas, and Dana Zakalik. "Outcomes of retesting BRCA-negative patients using multigene panels." Journal of Clinical Oncology 33, no. 28_suppl (October 1, 2015): 23. http://dx.doi.org/10.1200/jco.2015.33.28_suppl.23.
Full textDissertations / Theses on the topic "Multigene mutational panels"
BONO, Marco. "Multigene panel testing in Hereditary Breast and Ovarian Cancer: an effective liquid biopsy approach to identify mutations in genes involved in the Homologous Recombination pathway." Doctoral thesis, Università degli Studi di Palermo, 2021. http://hdl.handle.net/10447/479959.
Full textConference papers on the topic "Multigene mutational panels"
Heinzen, Rebeca Neves, Maria Eduarda Meyer, Liliane Raupp Gomes Pizatto, and Adriana Magalhães de Oliveira Freitas. "PREVALENCE OF VARIANTS OF UNCERTAIN SIGNIFICANCE IN TESTS REQUESTED FOR BREAST CANCER PATIENTS IN A PRIVATE SERVICE." In Scientifc papers of XXIII Brazilian Breast Congress - 2021. Mastology, 2021. http://dx.doi.org/10.29289/259453942021v31s1049.
Full textGau, Chia-Ling, Holly LaDuca, Hong Lu, AJ Stuenkel, Tina Pesaran, Elaine Chen, Jill Siegfried, et al. "Abstract 14: Identification of probands with multiple mutations in cancer susceptibility genes using a multigene panel approach." In Abstracts: AACR Special Conference: Cancer Susceptibility and Cancer Susceptibility Syndromes; January 29-February 1, 2014; San Diego, CA. American Association for Cancer Research, 2014. http://dx.doi.org/10.1158/1538-7445.cansusc14-14.
Full textCouch, Fergus J., David E. Goldgar, Steven N. Hart, Emily Hallberg, Raymond Moore, Huong Meeks, Robert Huether, Holly LaDuca, Elizabeth Chao, and Jill Dolinsky. "Abstract 2597: Breast and ovarian cancer risks associated with cancer predisposition gene mutations identified by multigene panel testing." In Proceedings: AACR 107th Annual Meeting 2016; April 16-20, 2016; New Orleans, LA. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7445.am2016-2597.
Full textKwong, A., V. Shin, CH Au, C. Ho, T. Slavin, J. Weitzel, TL Chan, and E. Ma. "Abstract P5-09-12: Germline mutation inTP53gene in a cohort of 2,561 Chinese high-risk breast cancer patients using multigene panel testing." In Abstracts: 2018 San Antonio Breast Cancer Symposium; December 4-8, 2018; San Antonio, Texas. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.sabcs18-p5-09-12.
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