Literature DB >> 21749364

Changing the game with whole exome sequencing.

Harry Ostrer1.   

Abstract

Mesh：

Year:  2011        PMID： 21749364     DOI： 10.1111/j.1399-0004.2011.01712.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  4 in total

Review 1.  The population genetics of the Jewish people.

Authors:  Harry Ostrer; Karl Skorecki
Journal:  Hum Genet       Date:  2012-10-10       Impact factor: 4.132

2.  Exome sequencing covers >98% of mutations identified on targeted next generation sequencing panels.

Authors:  Holly LaDuca; Kelly D Farwell; Huy Vuong; Hsiao-Mei Lu; Wenbo Mu; Layla Shahmirzadi; Sha Tang; Jefferey Chen; Shruti Bhide; Elizabeth C Chao
Journal:  PLoS One       Date:  2017-02-02       Impact factor: 3.240

Review 3.  Reflecting on earlier experiences with unsolicited findings: points to consider for next-generation sequencing and informed consent in diagnostics.

Authors:  Tessel Rigter; Lidewij Henneman; Ulf Kristoffersson; Alison Hall; Helger G Yntema; Pascal Borry; Holger Tönnies; Quinten Waisfisz; Mariet W Elting; Wybo J Dondorp; Martina C Cornel
Journal:  Hum Mutat       Date:  2013-07-16       Impact factor: 4.878

4.  Mutant-allele fraction heterogeneity is associated with non-small cell lung cancer patient survival.

Authors:  Sipeng Shen; Yongyue Wei; Ruyang Zhang; Mulong Du; Weiwei Duan; Sheng Yang; Yang Zhao; David C Christiani; Feng Chen
Journal:  Oncol Lett       Date:  2017-11-15       Impact factor: 2.967
  4 in total

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