Literature DB >> 22744653

Exome sequencing to find rare variants causing neurologic diseases.

Dan Doherty, Michael J Bamshad.   

Abstract

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Year:  2012        PMID： 22744653     DOI： 10.1212/WNL.0b013e3182617170

Source DB:  PubMed          Journal:  Neurology        ISSN： 0028-3878            Impact factor:   9.910


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  4 in total

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Authors:  Charles Y K Cheung; Elizabeth Marchani Blue; Ellen M Wijsman
Journal:  Am J Hum Genet       Date:  2014-02-06       Impact factor: 11.025

Review 2.  Using drug response data to identify molecular effectors, and molecular "omic" data to identify candidate drugs in cancer.

Authors:  William C Reinhold; Sudhir Varma; Vinodh N Rajapakse; Augustin Luna; Fabricio Garmus Sousa; Kurt W Kohn; Yves G Pommier
Journal:  Hum Genet       Date:  2014-09-12       Impact factor: 4.132

Review 3.  Sodium channel SCN8A (Nav1.6): properties and de novo mutations in epileptic encephalopathy and intellectual disability.

Authors:  Janelle E O'Brien; Miriam H Meisler
Journal:  Front Genet       Date:  2013-10-28       Impact factor: 4.599

4.  NCI-60 whole exome sequencing and pharmacological CellMiner analyses.

Authors:  William C Reinhold; Sudhir Varma; Fabricio Sousa; Margot Sunshine; Ogan D Abaan; Sean R Davis; Spencer W Reinhold; Kurt W Kohn; Joel Morris; Paul S Meltzer; James H Doroshow; Yves Pommier
Journal:  PLoS One       Date:  2014-07-17       Impact factor: 3.240
  4 in total

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