Literature DB >> 16932541

Technology Insight: querying the genome with microarrays--progress and hope for neurological disease.

Giovanni Coppola1, Daniel H Geschwind.   

Abstract

The ability to perform large-scale analysis of the genome at the level of gene sequence, gene copy number and messenger RNA transcript expression characterizes the post-genomic era. In the past decade, the microarray-based approach has emerged as one of the major tools in this area of genome biology, contributing to advances in the understanding of Mendelian and complex neurological disorders. Despite technical issues regarding design, data analysis and validation that have to be addressed in the planning and interpretation of a microarray study, microarray-based approaches for studying transcript expression, single-nucleotide-polymorphism genotyping and gene resequencing are becoming more widely adopted. Genomic microarrays are providing an unprecedented opportunity to dissect the genetic risk for complex neurological disorders. Numerous clinical and preclinical applications are likely to dominate the ambitious microarray agenda within the next decade.

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Year:  2006        PMID: 16932541     DOI: 10.1038/ncpneuro0133

Source DB:  PubMed          Journal:  Nat Clin Pract Neurol        ISSN: 1745-834X


  5 in total

Review 1.  Microarrays and the microscope: balancing throughput with resolution.

Authors:  Giovanni Coppola; Daniel H Geschwind
Journal:  J Physiol       Date:  2006-06-29       Impact factor: 5.182

Review 2.  Preimplantation genetic diagnosis for inherited neurological disorders.

Authors:  Ilan Tur-Kaspa; Roohi Jeelani; P Murali Doraiswamy
Journal:  Nat Rev Neurol       Date:  2014-05-27       Impact factor: 42.937

Review 3.  Systems biology and gene networks in neurodevelopmental and neurodegenerative disorders.

Authors:  Neelroop N Parikshak; Michael J Gandal; Daniel H Geschwind
Journal:  Nat Rev Genet       Date:  2015-07-07       Impact factor: 53.242

4.  Polyamine pathway contributes to the pathogenesis of Parkinson disease.

Authors:  Nicole M Lewandowski; Shulin Ju; Miguel Verbitsky; Barbara Ross; Melissa L Geddie; Edward Rockenstein; Anthony Adame; Alim Muhammad; Jean Paul Vonsattel; Dagmar Ringe; Lucien Cote; Susan Lindquist; Eliezer Masliah; Gregory A Petsko; Karen Marder; Lorraine N Clark; Scott A Small
Journal:  Proc Natl Acad Sci U S A       Date:  2010-09-13       Impact factor: 11.205

5.  A clinical evaluation tool for SNP arrays, especially for autosomal recessive conditions in offspring of consanguineous parents.

Authors:  Klaas J Wierenga; Zhijie Jiang; Amy C Yang; John J Mulvihill; Nicholas F Tsinoremas
Journal:  Genet Med       Date:  2012-10-25       Impact factor: 8.822

  5 in total

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