Literature DB >> 20816574

Inherited predisposition to cancer: introduction and overview.

Mark Robson1, Kenneth Offit.   

Abstract

The past three decades have witnessed an explosion in information regarding the genetic mutations underlying predisposition to common malignancies. Discoveries are now being made regarding genomic variants associated with disease risk for, and outcome following, treatment for cancer. Responsible translation of these discoveries to medical practice requires attention to principles of clinical utility as well as social and ethical aspects. Copyright 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID： 20816574     DOI： 10.1016/j.hoc.2010.06.005

Source DB:  PubMed          Journal:  Hematol Oncol Clin North Am        ISSN： 0889-8588            Impact factor:   3.722


  2 in total

1.  Value of bilateral breast cancer for identification of rare recessive at-risk alleles: evidence for the role of homozygous GEN1 c.2515_2519delAAGTT mutation.

Authors:  Ekatherina Sh Kuligina; Anna P Sokolenko; Nathalia V Mitiushkina; Svetlana N Abysheva; Elena V Preobrazhenskaya; Tatiana V Gorodnova; Grigoriy A Yanus; Alexandr V Togo; Nadezhda V Cherdyntseva; Svetlana A Bekhtereva; J Michael Dixon; Alexey A Larionov; Sergey G Kuznetsov; Evgeny N Imyanitov
Journal:  Fam Cancer       Date:  2013-03       Impact factor: 2.375

Review 2.  Ethnic background and genetic variation in the evaluation of cancer risk: a systematic review.

Authors:  Lijun Jing; Li Su; Brian Z Ring
Journal:  PLoS One       Date:  2014-06-05       Impact factor: 3.240
  2 in total

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