Next-generation sequencing in BRCA1/2-negative breast and ovarian cancer families.

被引：0
|
作者：
Hauke, Jan
Heimbach, Andre
Richters, Lisa Katharina
Kroeber, Sandra
Altmuller, Janine
Thiele, Holger
Nuernberg, Peter
Wappenschmidt, Barbara
Neidhardt, Guido
Rhiem, Kerstin
Schmutzler, Rita K.
Hahnen, Eric
机构：
[1] Univ Cologne, Fac Med, Ctr Hereditary Breast & Ovarian Canc, Ctr Integrated Oncol CIO, Cologne, Germany
[2] Univ Cologne, Fac Med, Ctr Mol Med Cologne CMMC, Cologne, Germany
[3] Univ Cologne, Fac Med, Ctr Familial Breast & Ovarian Canc, Ctr Integrated Oncol CIO, Cologne, Germany
[4] Univ Hosp Cologne, Cologne, Germany
[5] Univ Cologne, Cologne Ctr Genom, Cologne, Germany
[6] Ctr Mol Med Cologne CMMC, Cologne, Germany
[7] Univ Cologne, Cologne, Germany
来源：
JOURNAL OF CLINICAL ONCOLOGY | 2016年 / 34卷 / 15期
关键词：
D O I：
10.1200/JCO.2016.34.15_suppl.1533
中图分类号：
R73 [肿瘤学];
学科分类号：
100214 ;
摘要：
1533
引用
收藏
页数：2
相关论文
共 50 条
  • [21] Detection of somatic BRCA1/2 mutations in ovarian cancer - next-generation sequencing analysis of 100 cases
    Koczkowska, Magdalena
    Zuk, Monika
    Gorczynski, Adam
    Ratajska, Magdalena
    Lewandowska, Marzena
    Biernat, Wojciech
    Limon, Janusz
    Wasag, Bartosz
    [J]. CANCER MEDICINE, 2016, 5 (07): : 1640 - 1646
  • [22] BRCA1 and BRCA2 mutations in Germany - indications for testing in hereditary breast and ovarian cancer families.
    Schwarz-Boeger, U
    Schmutzler, RK
    Bastert, G
    Bender, HG
    Beckmann, MW
    Caffier, H
    Crohns, C
    Deininger, J
    Dietl, J
    Ditsch, N
    Distler, W
    Estevez-Schwarz, L
    Hepp, H
    Herroeder, N
    Huebbel, V
    Huettner, C
    Jackisch, C
    Jonat, W
    Kandel, M
    Kast, K
    Kaufmann, M
    Krapfl-Gast, AS
    Kreienberg, R
    Kuschel, B
    Kuschel, B
    Luck, H
    Meindl, A
    von Minckwitz, G
    Nestle-Kraemling, C
    Paepke, S
    Prieshof, B
    Rensing, K
    Rhiem, KA
    Schaeffer, MA
    Straub, L
    Untch, M
    Kiechle, T
    [J]. BREAST CANCER RESEARCH AND TREATMENT, 2004, 88 : S154 - S155
  • [23] Detection of BRCA1/BRCA 2 gene mutations in ovarian cancer by next- generation sequencing
    Grahovac, B.
    Katunaric, M.
    Babarovic, E.
    Kraevic, M.
    [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 1012 - 1013
  • [24] BRCA1 analysis by DHPLC in 272 Austrian breast cancer only and breast and ovarian cancer families.
    Wagner, T
    Moeslinger, R
    Fleischmann, E
    Muhr, D
    Hareter, M
    Kofler, P
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (04) : A328 - A328
  • [25] NGS-based multi-gene panel analysis in BRCA1/2 negative breast and ovarian cancer families.
    Pohl, Esther
    Hauke, Jan
    Horvath, Judit
    Dworniczak, Bernd
    Gehrig, Andrea
    Niederacher, Dieter
    Arnold, Norbert
    Sutter, Christian
    Smogavec, Mateja
    Just, Walter
    Weber, Bernhard H. F.
    Hentschel, Julia
    Faust, Ulrike
    Hackmann, Karl
    Schmidt, Gunnar
    Gross, Eva
    Ramser, Juliane
    Rhiem, Kerstin
    Hahnen, Eric
    Schmutzler, Rita K.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2017, 35
  • [26] Risk of ovarian cancer in BRCA1 and BRCA2 mutation negative hereditary breast cancer families
    Kauff, ND
    Mitra, N
    Robson, ME
    Hurley, KE
    Chuai, S
    Goldfrank, D
    Wadsworth, E
    Lee, J
    Cigler, T
    Borgen, PI
    Norton, L
    Barakat, RR
    Offit, K
    [J]. JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2005, 97 (18) : 1382 - 1384
  • [27] BRCA1 and BRCA2 Next Generation Sequencingwith methodological improvements in HBOC Uruguayan families.
    Martin Marques, Juan
    Repetto, Leticia
    Guggeri, Lucia
    Garcia, Enrique
    Torres, Alejandra
    Cecilia Cardoso, Florencia
    Sapone, Marta
    Esperon, Patricia
    Della Valle, Adriana
    Acevedo, Carlos
    Azambuja, Carlos
    Neffa, Florencia
    Rosaria Solano, Angela
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2015, 33 (15)
  • [28] Copy Number Variation Analysis in Familial BRCA1/2-Negative Finnish Breast and Ovarian Cancer
    Kuusisto, Kirsi M.
    Akinrinade, Oyediran
    Vihinen, Mauno
    Kankuri-Tammilehto, Minna
    Laasanen, Satu-Leena
    Schleutker, Johanna
    [J]. PLOS ONE, 2013, 8 (08):
  • [29] BRCA1 and BRCA2 sequence variations detected with next-generation sequencing in patients with premature ovarian insufficiency
    Yilmaz, Nafiye Karakas
    Karagin, Peren Hatice
    Terzi, Yunus Kasim
    Kahyaoglu, Inci
    Yilmaz, Saynur
    Erkaya, Salim
    Sahin, Feride Iffet
    [J]. JOURNAL OF THE TURKISH-GERMAN GYNECOLOGICAL ASSOCIATION, 2016, 17 (02) : 77 - 82
  • [30] Incidence of ovarian cancer in BRCA-negative hereditary breast cancer families.
    Kauff, N
    Cigler, T
    Hurley, K
    Huang, H
    Rapaport, H
    Wadsworth, E
    Robson, M
    Norton, L
    Barakat, R
    Offit, K
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (14) : 843S - 843S
12345