Hereditary breast cancer gene variants- multigene panel testing outcome from Sri Lanka

被引：0
|
作者：
Padeniya, P. M. [1 ,2 ]
Abayasekara, M. [2 ]
Thanaseelan, C. [2 ]
Gnanam, V. [2 ]
机构：
[1] Fac Med, Ragama, Sri Lanka
[2] Credence Genom Private Ltd, Colombo, Sri Lanka
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2019年 / 27卷
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
P12.043C
引用
收藏
页码：407 / 408
页数：2
相关论文
共 50 条
  • [31] Increased Co-Occurrence of Pathogenic Variants in Hereditary Breast and Ovarian Cancer and Lynch Syndromes: A Consequence of Multigene Panel Genetic Testing?
    Infante, Mar
    Arranz-Ledo, Monica
    Lastra, Enrique
    Abella, Luis Enrique
    Ferreira, Raquel
    Orozco, Marta
    Hernandez, Lara
    Martinez, Noemi
    Duran, Mercedes
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (19)
  • [32] Hereditary gastric cancer: single gene or multigene panel testing? A mono-institutional experience
    Calvello, Mariarosaria
    Marabelli, Monica
    Gandini, Sara
    Marino, Elena
    Bernard, Loris
    Dal Molin, Matteo
    Di Cola, Giulia
    Zanzottera, Cristina
    Corso, Giovanni
    Fazio, Nicola
    Gervaso, Lorenzo
    Romario, Uberto Fumagalli
    Barberis, Massimo
    Guerrieri-Gonzaga, Aliana
    Bertario, Lucio
    Serrano, Davide
    Bonanni, Bernardo
    [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 258 - 258
  • [33] Impact of Panel Gene Testing for Hereditary Breast and Ovarian Cancer on Patients
    Lumish, Heidi S.
    Steinfeld, Hallie
    Koval, Carrie
    Russo, Donna
    Levinson, Elana
    Wynn, Julia
    Duong, James
    Chung, Wendy K.
    [J]. JOURNAL OF GENETIC COUNSELING, 2017, 26 (05) : 1116 - 1129
  • [34] Role of the multi-gene panel testing for detection of pathogenic variants in patients with hereditary bilateral breast cancer
    Filorizzo, C.
    Fanale, D.
    Incorvaia, L.
    Barraco, N.
    Bono, M.
    Brando, C.
    Calo, V.
    Cancelliere, D.
    Cucinella, A.
    Dimino, A.
    Fiorino, A.
    Magrin, L.
    Pedone, E.
    Perez, A.
    Pivetti, A.
    Sammataro, S.
    Sciacchitano, R.
    Vaccaro, G.
    Bazan, V.
    Russo, A.
    [J]. ANNALS OF ONCOLOGY, 2021, 32 : S432 - S433
  • [35] Recontacting patients for multigene panel testing in hereditary cancer: Efficacy and insights
    Sawyer, Lindsey
    Creswick, Heather
    Lewandowski, Raymond
    Quillin, John
    [J]. JOURNAL OF GENETIC COUNSELING, 2019, 28 (06) : 1198 - 1207
  • [36] Evaluation of criteria for genetic study of hereditary breast and ovarian cancer BRCAX families by multigene panel testing
    Castillo-Guardiola, V.
    Sarabia-Meseguer, M. D.
    Macias-Cerrolaza, J. A.
    Garcia-Aliaga, A.
    Rosado-Jimenez, L.
    Sanchez-Bermudez, A. I.
    Zafra-Poves, M.
    Moreno-Locubiche, M. A.
    Pascual-Gilabert, P.
    Aliaga-Bano, A.
    Noguera-Velasco, J. A.
    Ayala De La Pena, F.
    Ruiz-Espejo, F.
    [J]. CLINICA CHIMICA ACTA, 2019, 493 : S576 - S577
  • [37] Genetic Variation and the Role of Multigene Panel Testing for Hereditary Breast Cancer: A Single-Institution Experience
    Lu, Kit
    Smith, Meagan
    Kanderi, Tejaswi
    Verbiar, Julia
    Laspe, Jennifer
    Bair, Latesha
    Torp, Lisa
    [J]. CUREUS JOURNAL OF MEDICAL SCIENCE, 2021, 13 (04)
  • [38] Should all patients undergoing genetic testing for hereditary breast cancer syndromes be offered a multigene panel?
    Silver, Erica L.
    Niell-Swiller, Mariana
    [J]. CURRENT OPINION IN OBSTETRICS & GYNECOLOGY, 2022, 34 (01) : 36 - 40
  • [39] Identification of high and middle penetrance pathogenic variants in patients with hereditary breast/ovarian cancer by multigene panel analysis
    Ryu, Jin-Sun
    Cho, Eun Hae
    Yoon, Kyong-Ah
    Lee, Eun-Gyeong
    Lee, Eun-Sook
    Kong, Sun-Young
    [J]. CANCER RESEARCH, 2019, 79 (13)
  • [40] Multigene panel testing of triple negative breast cancer patients from Russia
    Abramov, I.
    Ikonnikova, A.
    Korneva, Y.
    Shisterova, O.
    Emelyanova, M.
    Nasedkina, T.
    [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2020, 28 (SUPPL 1) : 559 - 559
12345