Literature DB >> 21125684

Clinical cancer genomics: how soon is now?

Barry S Taylor1, Marc Ladanyi.   

Abstract

Germline and somatic alterations in DNA mediate the genesis and progression of human cancers. Not only do these events represent the molecular underpinnings of disease but many are of immense clinical importance as diagnostic markers and therapeutic targets. In fact, rapidly evolving sequencing technologies have empowered enormous growth in the breadth and depth of cancer genome characterization. Whether these will impact routine clinical practice and the treatment of disease is no longer debatable, but how precisely this will happen is a source of ongoing speculation and development.
Copyright © 2010 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.

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Year:  2010        PMID: 21125684     DOI: 10.1002/path.2794

Source DB:  PubMed          Journal:  J Pathol        ISSN: 0022-3417            Impact factor:   7.996


  16 in total

1.  The evolving role of the pathologist in the management of lung cancer.

Authors:  Adi F Gazdar
Journal:  Lung Cancer Manag       Date:  2012

2.  Deciphering intra-tumor heterogeneity of lung adenocarcinoma confirms that dominant, branching, and private gene mutations occur within individual tumor nodules.

Authors:  Giuseppe Pelosi; Alessio Pellegrinelli; Alessandra Fabbri; Elena Tamborini; Federica Perrone; Giulio Settanni; Adele Busico; Benedetta Picciani; Maria Adele Testi; Lucia Militti; Patrick Maisonneuve; Barbara Valeri; Angelica Sonzogni; Claudia Proto; Marina Garassino; Filippo De Braud; Ugo Pastorino
Journal:  Virchows Arch       Date:  2016-04-07       Impact factor: 4.064

3.  Pharmacogenomics in clinical practice: reality and expectations.

Authors:  C Lee Ventola
Journal:  P T       Date:  2011-07

Review 4.  Application of next generation sequencing to human gene fusion detection: computational tools, features and perspectives.

Authors:  Qingguo Wang; Junfeng Xia; Peilin Jia; William Pao; Zhongming Zhao
Journal:  Brief Bioinform       Date:  2012-08-09       Impact factor: 11.622

Review 5.  Identifying fusion transcripts using next generation sequencing.

Authors:  Shailesh Kumar; Sundus Khalid Razzaq; Angie Duy Vo; Mamta Gautam; Hui Li
Journal:  Wiley Interdiscip Rev RNA       Date:  2016-08-02       Impact factor: 9.957

Review 6.  Intergenically Spliced Chimeric RNAs in Cancer.

Authors:  Yuemeng Jia; Zhongqiu Xie; Hui Li
Journal:  Trends Cancer       Date:  2016-09

7.  RNA-seq analysis of prostate cancer in the Chinese population identifies recurrent gene fusions, cancer-associated long noncoding RNAs and aberrant alternative splicings.

Authors:  Shancheng Ren; Zhiyu Peng; Jian-Hua Mao; Yongwei Yu; Changjun Yin; Xin Gao; Zilian Cui; Jibin Zhang; Kang Yi; Weidong Xu; Chao Chen; Fubo Wang; Xinwu Guo; Ji Lu; Jun Yang; Min Wei; Zhijian Tian; Yinghui Guan; Liang Tang; Chuanliang Xu; Linhui Wang; Xu Gao; Wei Tian; Jian Wang; Huanming Yang; Jun Wang; Yinghao Sun
Journal:  Cell Res       Date:  2012-02-21       Impact factor: 25.617

8.  COLD-PCR enrichment of rare cancer mutations prior to targeted amplicon resequencing.

Authors:  Coren A Milbury; Mick Correll; John Quackenbush; Renee Rubio; G Mike Makrigiorgos
Journal:  Clin Chem       Date:  2011-12-21       Impact factor: 8.327

Review 9.  Population sciences, translational research, and the opportunities and challenges for genomics to reduce the burden of cancer in the 21st century.

Authors:  Muin J Khoury; Steven B Clauser; Andrew N Freedman; Elizabeth M Gillanders; Russ E Glasgow; William M P Klein; Sheri D Schully
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2011-07-27       Impact factor: 4.254

10.  Detecting somatic genetic alterations in tumor specimens by exon capture and massively parallel sequencing.

Authors:  Helen H Won; Sasinya N Scott; A Rose Brannon; Ronak H Shah; Michael F Berger
Journal:  J Vis Exp       Date:  2013-10-18       Impact factor: 1.355

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