Identification of Japanese Familial Breast Cancer Susceptibility Genes Through Whole-Exome Sequencing

被引：0
|
作者：
Abdullah, Ili S. [1 ]
Matsushita, Yosuke [1 ]
Miyoshi, Yasuo [2 ]
Ohsumi, Shozo [3 ]
Sasa, Mitsunori [4 ]
Katagiri, Toyomasa [1 ]
机构：
[1] Natl Inst Biomed Innovat, Lab Biofunct Mol Med, Ibaraki, Japan
[2] Hyogo Coll Med, Dept Breast & Endocrine Surg, Nishinomiya, Hyogo, Japan
[3] Natl Hosp Org, Shikoku Canc Ctr, Dept Breast Surg, Matsuyama, Ehime, Japan
[4] Tokushima Breast Care Clin, Dept Surg, Tokushima, Japan
来源：
CANCER SCIENCE | 2025年 / 116卷
关键词：
D O I：
暂无
中图分类号：
R73 [肿瘤学];
学科分类号：
100214 ;
摘要：
P-1063
引用
收藏
页码：253 / 253
页数：1
相关论文
共 50 条
  • [31] Uncovering the Contribution of Moderate-Penetrance Susceptibility Genes to Breast Cancer by Whole-Exome Sequencing and Targeted Enrichment Sequencing of Candidate Genes in Women of European Ancestry
    Dumont, Martine
    Weber-Lassalle, Nana
    Joly-Beauparlant, Charles
    Ernst, Corinna
    Droit, Arnaud
    Feng, Bing-Jian
    Dubois, Stephane
    Collin-Deschesnes, Annie-Claude
    Soucy, Penny
    Vallee, Maxime
    Fournier, Frederic
    Lemacon, Audrey
    Adank, Muriel A.
    Allen, Jamie
    Altmueller, Janine
    Arnold, Norbert
    Ausems, Margreet G. E. M.
    Berutti, Riccardo
    Bolla, Manjeet K.
    Bull, Shelley
    Carvalho, Sara
    Cornelissen, Sten
    Dufault, Michael R.
    Dunning, Alison M.
    Engel, Christoph
    Gehrig, Andrea
    Geurts-Giele, Willemina R. R.
    Gieger, Christian
    Green, Jessica
    Hackmann, Karl
    Helmy, Mohamed
    Hentschel, Julia
    Hogervorst, Frans B. L.
    Hollestelle, Antoinette
    Hooning, Maartje J.
    Horvath, Judit
    Ikram, M. Arf An
    Kaulfuss, Silke
    Keeman, Renske
    Kuang, Da
    Luccarini, Craig
    Maier, Wolfgang
    Martens, John W. M.
    Niederacher, Dieter
    Nurnberg, Peter
    Ott, Claus-Eric
    Peters, Annette
    Pharoah, Paul D. P.
    Ramirez, Alfredo
    Ramser, Juliane
    CANCERS, 2022, 14 (14)
  • [32] Whole-exome sequencing identifies novel candidate predisposition genes for familial polycythemia vera
    Elina A. M. Hirvonen
    Esa Pitkänen
    Kari Hemminki
    Lauri A. Aaltonen
    Outi Kilpivaara
    Human Genomics, 11
  • [33] Whole-exome sequencing identifies novel candidate predisposition genes for familial polycythemia vera
    Hirvonen, Elina A. M.
    Pitkanen, Esa
    Hemminki, Kari
    Aaltonen, Lauri A.
    Kilpivaara, Outi
    HUMAN GENOMICS, 2017, 11
  • [34] Identification of Novel Genes Contributing to Autosomal Dominant Diabetes by Whole-Exome Sequencing
    Jungtrakoon, Prapaporn
    Buranasupkajorn, Patinut
    Hastings, Timothy
    Shirakawa, Jun
    Pezzolesi, Marcus
    Mendonca, Christine
    Kulkarni, Rohit N.
    Doria, Alessandro
    DIABETES, 2015, 64 : A460 - A461
  • [35] Identification of potential pathogenic genes for severe aplastic anemia by whole-exome sequencing
    Zhang, Yang
    Zhang, Yu
    Ge, Hongyu
    Li, Nianbin
    Liu, Chunyan
    Wang, Ting
    Fu, Rong
    Shao, Zonghong
    JOURNAL OF CLINICAL LABORATORY ANALYSIS, 2022, 36 (05)
  • [36] Identification of novel mutations in endometrial cancer patients by whole-exome sequencing
    Chang, Ya-Sian
    Huang, Hsien-Da
    Yeh, Kun-Tu
    Chang, Jan-Gowth
    INTERNATIONAL JOURNAL OF ONCOLOGY, 2017, 50 (05) : 1778 - 1784
  • [37] Whole-exome sequencing reveals candidate high-risk susceptibility genes for endometriosis
    Nousiainen, Susanna
    Kuismin, Outi
    Reinikka, Siiri
    Manninen, Roosa
    Khamaiseh, Sara
    Kuivalainen, Mari
    Terho, Anna
    Koivurova, Sari
    Niinimaki, Maarit
    Salokas, Kari
    Varjosalo, Markku
    Ahtikoski, Anne
    Butzow, Ralf
    Lindgren, Outi
    Uimari, Outi
    Vahteristo, Pia
    HUMAN GENOMICS, 2023, 17 (01)
  • [38] Whole-exome sequencing reveals candidate high-risk susceptibility genes for endometriosis
    Susanna Nousiainen
    Outi Kuismin
    Siiri Reinikka
    Roosa Manninen
    Sara Khamaiseh
    Mari Kuivalainen
    Anna Terho
    Sari Koivurova
    Maarit Niinimäki
    Kari Salokas
    Markku Varjosalo
    Anne Ahtikoski
    Ralf Bützow
    Outi Lindgren
    Outi Uimari
    Pia Vahteristo
    Human Genomics, 17
  • [39] Whole-exome sequencing for screening noise-induced hearing loss susceptibility genes
    Fan, Boya
    Wang, Gang
    Liu, Gang
    Zhang, Xiaoli
    Wu, Wei
    ACTA OTO-LARYNGOLOGICA, 2023, 143 (05) : 408 - 415
  • [40] Candidate genes and sequence variants for susceptibility to mycobacterial infection identified by whole-exome sequencing
    Varzari, Alexander
    Deyneko, Igor V.
    Bruun, Gitte Hoffmann
    Dembic, Maja
    Hofmann, Winfried
    Cebotari, Victor M.
    Ginda, Sergei S.
    Andresen, Brage S.
    Illig, Thomas
    FRONTIERS IN GENETICS, 2022, 13
12345