Exome sequencing identifies germline mutations in African American families with hereditary prostate cancer

被引:0
|
作者
Wang, Zemin [1 ]
Qian, Chiping [1 ]
Eledet, Elisa M. [1 ]
Washington, George [1 ]
Zabaieta, Jovanny [1 ]
Hu, Jennifer J. [2 ]
Mandel, Diptasri [1 ]
Liu, Wanguo [1 ]
机构
[1] Louisiana State Univ Hlth Sci Ctr, Dept Genet, New Orleans, LA USA
[2] Univ Miami Leonard Miller Sch Med, Dept Epidemiol & Publ Hlth, Miami, FL USA
关键词
D O I
10.1158/1538-7755.DISP13-PR11
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PR11
引用
收藏
页数:1
相关论文
共 50 条
  • [21] Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer
    Barbieri, Christopher E.
    Baca, Sylvan C.
    Lawrence, Michael S.
    Demichelis, Francesca
    Blattner, Mirjam
    Theurillat, Jean-Philippe
    White, Thomas A.
    Stojanov, Petar
    Van Allen, Eliezer
    Stransky, Nicolas
    Nickerson, Elizabeth
    Chae, Sung-Suk
    Boysen, Gunther
    Auclair, Daniel
    Onofrio, Robert C.
    Park, Kyung
    Kitabayashi, Naoki
    MacDonald, Theresa Y.
    Sheikh, Karen
    Vuong, Terry
    Guiducci, Candace
    Cibulskis, Kristian
    Sivachenko, Andrey
    Carter, Scott L.
    Saksena, Gordon
    Voet, Douglas
    Hussain, Wasay M.
    Ramos, Alex H.
    Winckler, Wendy
    Redman, Michelle C.
    Ardlie, Kristin
    Tewari, Ashutosh K.
    Mosquera, Juan Miguel
    Rupp, Niels
    Wild, Peter J.
    Moch, Holger
    Morrissey, Colm
    Nelson, Peter S.
    Kantoff, Philip W.
    Gabriel, Stacey B.
    Golub, Todd R.
    Meyerson, Matthew
    Lander, Eric S.
    Getz, Gad
    Rubin, Mark A.
    Garraway, Levi A.
    NATURE GENETICS, 2012, 44 (06) : 685 - U107
  • [22] Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer
    Christopher E Barbieri
    Sylvan C Baca
    Michael S Lawrence
    Francesca Demichelis
    Mirjam Blattner
    Jean-Philippe Theurillat
    Thomas A White
    Petar Stojanov
    Eliezer Van Allen
    Nicolas Stransky
    Elizabeth Nickerson
    Sung-Suk Chae
    Gunther Boysen
    Daniel Auclair
    Robert C Onofrio
    Kyung Park
    Naoki Kitabayashi
    Theresa Y MacDonald
    Karen Sheikh
    Terry Vuong
    Candace Guiducci
    Kristian Cibulskis
    Andrey Sivachenko
    Scott L Carter
    Gordon Saksena
    Douglas Voet
    Wasay M Hussain
    Alex H Ramos
    Wendy Winckler
    Michelle C Redman
    Kristin Ardlie
    Ashutosh K Tewari
    Juan Miguel Mosquera
    Niels Rupp
    Peter J Wild
    Holger Moch
    Colm Morrissey
    Peter S Nelson
    Philip W Kantoff
    Stacey B Gabriel
    Todd R Golub
    Matthew Meyerson
    Eric S Lander
    Gad Getz
    Mark A Rubin
    Levi A Garraway
    Nature Genetics, 2012, 44 : 685 - 689
  • [23] Defining germline mutations of DNA damage repair genes in African American prostate cancer patients
    Babcock, Kevin
    Zhang, Xijun
    Wilkerson, Matthew
    Dalgard, Clifton L.
    Tan, Shyh-Han
    Ravindranath, Lakshmi
    Chen, Yongmei
    Cullen, Jennifer
    Srivastava, Shiv
    Rosner, Inger L.
    Petrovics, Gyorgy
    CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2020, 29 (06)
  • [24] Rare germline mutations in African American men diagnosed with early-onset prostate cancer
    Beebe-Dimmer, Jennifer L.
    Zuhlke, Kimberly A.
    Johnson, Anna M.
    Liesman, Daniel
    Cooney, Kathleen A.
    PROSTATE, 2018, 78 (05): : 321 - 326
  • [25] Whole exome sequencing identifies a germline MET mutation in two siblings with hereditary wild-type RET medullary thyroid cancer
    Sponziello, Marialuisa
    Benvenuti, Silvia
    Gentile, Alessandra
    Pecce, Valeria
    Rosignolo, Francesca
    Virzi, Anna Rita
    Milan, Melissa
    Comoglio, Paolo M.
    Londin, Eric
    Fortina, Paolo
    Barnabei, Agnese
    Appetecchia, Marialuisa
    Marandino, Ferdinando
    Russo, Diego
    Filetti, Sebastiano
    Durante, Cosimo
    Verrienti, Antonella
    HUMAN MUTATION, 2018, 39 (03) : 371 - 377
  • [26] African American exome sequencing identifies potential risk variants at Alzheimer disease loci
    N'Songo, Aurelie
    Carrasquillo, Minerva M.
    Wang, Xue
    Burgess, Jeremy D.
    Thuy Nguyen
    Asmann, Yan W.
    Serie, Daniel J.
    Younkin, Steven G.
    Allen, Mariet
    Pedraza, Otto
    Duara, Ranjan
    Custo, Maria T. Greig
    Graff-Radford, Neill R.
    Ertekin-Taner, Nilufer
    NEUROLOGY-GENETICS, 2017, 3 (02)
  • [27] RNASEL mutations are infrequent in hereditary prostate cancer families.
    Cooney, KA
    Zuhlke, KA
    Griffin, A
    Wu, YQ
    Tomsho, LP
    Gruber, SB
    Lange, E
    Chen, H
    AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 249 - 249
  • [28] Exome sequencing identifies MUTYH mutations in a family with colorectal cancer and an atypical phenotype
    Segui, Nuria
    Navarro, Matilde
    Pineda, Marta
    Koeger, Nicole
    Bellido, Fernando
    Gonzalez, Sara
    Campos, Olga
    Iglesias, Silvia
    Valdes-Mas, Rafael
    Lopez-Doriga, Adriana
    Gut, Marta
    Blanco, Ignacio
    Lazaro, Conxi
    Capella, Gabriel
    Puente, Xose S.
    Plotz, Guido
    Valle, Laura
    GUT, 2015, 64 (02) : 355 - U187
  • [29] Whole exome sequencing identifies novel variant underlying hereditary spastic paraplegia in consanguineous Pakistani families
    Zulfiqar, Shumaila
    Tariq, Muhammad
    Ali, Zafar
    Fatima, Ambrin
    Klar, Joakim
    Abdullah, Uzma
    Ali, Aamir
    Ramzan, Shafaq
    He, Sijie
    Zhang, Jianguo
    Khan, Ayaz
    Shah, Suleman
    Khan, Sheraz
    Makhdoom, Ehtishamul Haq
    Schuster, Jens
    Dahl, Niklas
    Baig, Shahid Mahmood
    JOURNAL OF CLINICAL NEUROSCIENCE, 2019, 67 : 19 - 23
  • [30] Characterization of germline copy number variation in high-risk African American families with prostate cancer
    Ledet, Elisa M.
    Hu, Xiaofeng
    Sartor, Oliver
    Rayford, Walter
    Li, Marilyn
    Mandal, Diptasri
    PROSTATE, 2013, 73 (06): : 614 - 623