Whole-exome sequencing identifies a high frequency of germline deleterious variants in cancer predisposition genes in individuals with osteosarcoma

被引：0
|
作者：
Koster, Roelof
Zhu, Bin
Yeager, Meredith
Dean, Michael
Gianferante, Matthew
Song, Lei
Sampson, Joshua
Gastier-Foster, Julie
Gorlick, Richard
de Toledo, Silvia Regina Caminada
Petrilli, Antonio
Patino-Garcia, Ana
Lecanda, Fernando
Serra, Massimo
Hattinger, Claudia
Picci, Piero
Scotlandi, Katia
Flanagan, Adrienne
Tirabosco, Roberto
Amary, Maria
Kurucu, Nilgun
Ilhan, Inci Ergurhan
Sari, Neriman
Ballinger, Mandy
Thomas, David
Barkauskas, Donald
Hicks, Belynda
Tucker, Margaret
Caporaso, Neil
Hoover, Robert
Chanock, Stephen
Savage, Sharon
Mirabello, Lisa
机构：
来源：
CANCER RESEARCH | 2017年 / 77卷
关键词：
D O I：
10.1158/1538-7445.AM2017-4871
中图分类号：
R73 [肿瘤学];
学科分类号：
100214 ;
摘要：
4871
引用
收藏
页数：2
相关论文
共 50 条
  • [21] Whole-exome identifies RXRG and TH germline variants in familial isolated prolactinoma
    Melo, Flavia M.
    Couto, Patricia P.
    Bale, Allen E.
    Bastos-Rodrigues, Luciana
    Passos, Flavia M.
    Lisboa, Raony G. C.
    Ng, Jessica M. Y.
    Curran, Tom
    Dias, Eduardo P.
    Friedman, Eitan
    De Marco, Luiz
    CANCER GENETICS, 2016, 209 (06) : 251 - 257
  • [22] Unraveling genetic predisposition to familial or early onset gastric cancer using germline whole-exome sequencing
    Ingrid P Vogelaar
    Rachel S van der Post
    J Han JM van Krieken
    Liesbeth Spruijt
    Wendy AG van Zelst-Stams
    C Marleen Kets
    Jan Lubinski
    Anna Jakubowska
    Urszula Teodorczyk
    Cora M Aalfs
    Liselotte P van Hest
    Hugo Pinheiro
    Carla Oliveira
    Shalini N Jhangiani
    Donna M Muzny
    Richard A Gibbs
    James R Lupski
    Joep de Ligt
    Lisenka E L M Vissers
    Alexander Hoischen
    Christian Gilissen
    Maartje van de Vorst
    Jelle J Goeman
    Hans K Schackert
    Guglielmina N Ranzani
    Valeria Molinaro
    Encarna B Gómez García
    Frederik J Hes
    Elke Holinski-Feder
    Maurizio Genuardi
    Margreet G E M Ausems
    Rolf H Sijmons
    Anja Wagner
    Lizet E van der Kolk
    Inga Bjørnevoll
    Hildegunn Høberg-Vetti
    Ad Geurts van Kessel
    Roland P Kuiper
    Marjolijn J L Ligtenberg
    Nicoline Hoogerbrugge
    European Journal of Human Genetics, 2017, 25 : 1246 - 1252
  • [23] Unraveling genetic predisposition to familial or early onset gastric cancer using germline whole-exome sequencing
    Vogelaar, Ingrid P.
    van der Post, Rachel S.
    van Krieken, J. Han J. M.
    Spruijt, Liesbeth
    van Zelst-Stams, Wendy A. G.
    Kets, C. Marleen
    Lubinski, Jan
    Jakubowska, Anna
    Teodorczyk, Urszula
    Aalfs, Cora M.
    van Hest, Liselotte P.
    Pinheiro, Hugo
    Oliveira, Carla
    Jhangiani, Shalini N.
    Muzny, Donna M.
    Gibbs, Richard A.
    Lupski, James R.
    de Ligt, Joep
    Vissers, Lisenka E. L. M.
    Hoischen, Alexander
    Gilissen, Christian
    van de Vorst, Maartje
    Goeman, Jelle J.
    Schackert, Hans K.
    Ranzani, Guglielmina N.
    Molinaro, Valeria
    Garcia, Encarna B. Gomez
    Hes, Frederik J.
    Holinski-Feder, Elke
    Genuardi, Maurizio
    Ausems, Margreet G. E. M.
    Sijmons, Rolf H.
    Wagner, Anja
    van der Kolk, Lizet E.
    Bjornevoll, Inga
    Hoberg-Vetti, Hildegunn
    van Kessel, Ad Geurts
    Kuiper, Roland P.
    Ligtenberg, Marjolijn J. L.
    Hoogerbrugge, Nicoline
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2017, 25 (11) : 1246 - 1252
  • [24] Whole-exome identifies germline variants in families with obstructive sleep apnea syndrome
    de Azevedo, Pedro Guimaraes
    Guimaraes, Maria de Lourdes Rabelo
    Albuquerque, Anna Luiza Braga
    Alves, Rayane Benfica
    Fernandes, Bianca Gomes
    de Melo, Flavia Marques
    Cardenas, Raony Guimaraes Correa Do Carmo Lisboa
    Friedman, Eitan
    De Marco, Luiz
    Bastos-Rodrigues, Luciana
    FRONTIERS IN GENETICS, 2023, 14
  • [25] Whole-Exome Sequencing of Germline Variants in Non-BRCA Families with Hereditary Breast Cancer
    Liu, Yaxuan
    Helgadottir, Hafdis T.
    Kharaziha, Pedram
    Choi, Jungmin
    Lopez-Giraldez, Francesc
    Mane, Shrikant M.
    Hoiom, Veronica
    Juhlin, Carl Christofer
    Larsson, Catharina
    Bajalica-Lagercrantz, Svetlana
    BIOMEDICINES, 2022, 10 (05)
  • [26] Detecting Germline Structure Variants in Cancer Predisposition Genes Using Whole Genome Sequencing
    Choate, L.
    Sellers, H.
    Stein, M.
    Tandale, P.
    Tan, J.
    Setlem, R.
    Sakai, Y.
    Sosa, C.
    Hoenig, M.
    Holdren, M.
    Urban, R.
    Gupta, S.
    Thorland, E.
    Boczek, N.
    Kearney, H.
    Shen, W.
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2022, 24 (10): : S76 - S76
  • [27] Germline Whole-Exome Sequencing in Non-Smoker Lung Cancer Patients Reveals Pathogenic Variants in Lung Cancer Driver Genes
    Carapezza, Giovanni
    Minardi, Simone Paolo
    Noci, Sara
    Pintarelli, Giulia
    Zanutto, Susanna
    Incarbone, Matteo
    Tosi, Davide
    Dragani, Tommaso Antonio
    Colombo, Francesca
    Pierotti, Marco Alessandro
    Gariboldi, Manuela
    GENES CHROMOSOMES & CANCER, 2025, 64 (03):
  • [28] Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol
    Lange, Leslie A.
    Hu, Youna
    Zhang, He
    Xue, Chenyi
    Schmidt, Ellen M.
    Tang, Zheng-Zheng
    Bizon, Chris
    Lange, Ethan M.
    Smith, Joshua D.
    Turner, Emily H.
    Jun, Goo
    Kang, Hyun Min
    Peloso, Gina
    Auer, Paul
    Li, Kuo-Ping
    Flannick, Jason
    Zhang, Ji
    Fuchsberger, Christian
    Gaulton, Kyle
    Lindgren, Cecilia
    Locke, Adam
    Manning, Alisa
    Sim, Xueling
    Rivas, Manuel A.
    Holmen, Oddgeir L.
    Gottesman, Omri
    Lu, Yingchang
    Ruderfer, Douglas
    Stah, Eli A.
    Duan, Qing
    Li, Yun
    Durda, Peter
    Jiao, Shuo
    Isaacs, Aaron
    Hofman, Albert
    Bis, Joshua C.
    Correa, Adolfo
    Griswold, Michael E.
    Jakobsdottir, Johanna
    Smith, Albert V.
    Schreiner, Pamela J.
    Feitosa, Mary E.
    Zhang, Qunyuan
    Huffman, Jennifer E.
    Crosby, Jacy
    Wasse, Christina L.
    Do, Ron
    Franceschini, Nora
    Martin, Lisa W.
    Robinson, Jennifer G.
    AMERICAN JOURNAL OF HUMAN GENETICS, 2014, 94 (02) : 233 - 245
  • [29] Whole-exome sequencing study identifies rare variants associated with intraocular pressure
    Lin, Yizi
    Williams, Kara
    Moroi, Sayoko E.
    Gao, Xiaoyi Raymond
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2021, 62 (08)
  • [30] Identification of novel variants in retinitis pigmentosa genes by whole-exome sequencing
    Kocaaga, Ayca
    Akoz, Irem Ozturk
    Demir, Nihal Ulus
    Paksoy, Baris
    REVISTA DA ASSOCIACAO MEDICA BRASILEIRA, 2023, 69 (05):
12345