Personalised care and the genome

被引:9
作者
Doerr, Megan [1 ]
Eng, Charis [1 ]
机构
[1] Cleveland Clin, Genom Med Inst, Cleveland, OH 44195 USA
来源
BRITISH MEDICAL JOURNAL | 2012年 / 344卷
关键词
RISK-ASSESSMENT; DISEASES; HISTORY;
D O I
10.1136/bmj.e3174
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页数:2
相关论文
共 15 条
  • [1] Borry P, 2012, EUR J HUM GENET
  • [2] Euhus D, 2012, ANN SURG ONCOL
  • [3] Prospective comparison of family medical history with personal genome screening for risk assessment of common cancers
    Heald, Brandie
    Edelman, Emily
    Eng, Charis
    [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2012, 20 (05) : 547 - 551
  • [4] Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
    Hindorff, Lucia A.
    Sethupathy, Praveen
    Junkins, Heather A.
    Ramos, Erin M.
    Mehta, Jayashri P.
    Collins, Francis S.
    Manolio, Teri A.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (23) : 9362 - 9367
  • [5] International network of cancer genome projects
    Hudson, Thomas J.
    Anderson, Warwick
    Aretz, Axel
    Barker, Anna D.
    Bell, Cindy
    Bernabe, Rosa R.
    Bhan, M. K.
    Calvo, Fabien
    Eerola, Iiro
    Gerhard, Daniela S.
    Guttmacher, Alan
    Guyer, Mark
    Hemsley, Fiona M.
    Jennings, Jennifer L.
    Kerr, David
    Klatt, Peter
    Kolar, Patrik
    Kusuda, Jun
    Lane, David P.
    Laplace, Frank
    Lu, Youyong
    Nettekoven, Gerd
    Ozenberger, Brad
    Peterson, Jane
    Rao, T. S.
    Remacle, Jacques
    Schafer, Alan J.
    Shibata, Tatsuhiro
    Stratton, Michael R.
    Vockley, Joseph G.
    Watanabe, Koichi
    Yang, Huanming
    Yuen, Matthew M. F.
    Knoppers, M.
    Bobrow, Martin
    Cambon-Thomsen, Anne
    Dressler, Lynn G.
    Dyke, Stephanie O. M.
    Joly, Yann
    Kato, Kazuto
    Kennedy, Karen L.
    Nicolas, Pilar
    Parker, Michael J.
    Rial-Sebbag, Emmanuelle
    Romeo-Casabona, Carlos M.
    Shaw, Kenna M.
    Wallace, Susan
    Wiesner, Georgia L.
    Zeps, Nikolajs
    Lichter, Peter
    [J]. NATURE, 2010, 464 (7291) : 993 - 998
  • [6] A critical appraisal of the scientific basis of commercial genomic profiles used to assess health risks and personalize health interventions
    Janssens, A. Cecile J. W.
    Gwinn, Marta
    Bradley, Linda A.
    Oostra, Ben A.
    van Duijn, Cornelia M.
    Khoury, Muin J.
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2008, 82 (03) : 593 - 599
  • [7] Who should be sent for genetic testing in hereditary colorectal cancer syndromes?
    Lynch, Henry T.
    Boland, C. Richard
    Rodriguez-Bigas, Miguel A.
    Amos, Christopher
    Lynch, Jane F.
    Lynch, Patrick M.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2007, 25 (23) : 3534 - 3542
  • [8] Whole genome sequencing fails to predict risk of most common diseases
    Mayor, Susan
    [J]. BRITISH MEDICAL JOURNAL, 2012, 344
  • [9] Health Behavior Change: Can Genomics Improve Behavioral Adherence?
    McBride, Colleen M.
    Bryan, Angela D.
    Bray, Molly S.
    Swan, Gary E.
    Green, Eric D.
    [J]. AMERICAN JOURNAL OF PUBLIC HEALTH, 2012, 102 (03) : 401 - 405
  • [10] Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome
    Ng, Sarah B.
    Bigham, Abigail W.
    Buckingham, Kati J.
    Hannibal, Mark C.
    McMillin, Margaret J.
    Gildersleeve, Heidi I.
    Beck, Anita E.
    Tabor, Holly K.
    Cooper, Gregory M.
    Mefford, Heather C.
    Lee, Choli
    Turner, Emily H.
    Smith, Joshua D.
    Rieder, Mark J.
    Yoshiura, Koh-ichiro
    Matsumoto, Naomichi
    Ohta, Tohru
    Niikawa, Norio
    Nickerson, Deborah A.
    Bamshad, Michael J.
    Shendure, Jay
    [J]. NATURE GENETICS, 2010, 42 (09) : 790 - U85