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Array-Based Comparative Genomic Hybridization

Known as: Array Based Comparative Genomic Hybridization, Array Comparative Genomic Hybridization 
 
National Institutes of Health

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Broader (1)

comparative genomic analysis

Papers overview

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Highly Cited
2015
Highly Cited
2015
Androgen Receptor Gene Aberrations in Circulating Cell-Free DNA: Biomarkers of Therapeutic Resistance in Castration-Resistant Prostate Cancer
Purpose: Although novel agents targeting the androgen–androgen receptor (AR) axis have altered the treatment paradigm of… Expand
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Review
2009
Review
2009
Copy number variation in human health, disease, and evolution.
Copy number variation (CNV) is a source of genetic diversity in humans. Numerous CNVs are being identified with various genome… Expand
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Highly Cited
2009
Highly Cited
2009
Alterations in Genes of the EGFR Signaling Pathway and Their Relationship to EGFR Tyrosine Kinase Inhibitor Sensitivity in Lung Cancer Cell Lines
Background Deregulation of EGFR signaling is common in non-small cell lung cancers (NSCLC) and this finding led to the… Expand
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Highly Cited
2009
Highly Cited
2009
Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases
To evaluate the use of array comparative genomic hybridization (aCGH) for prenatal diagnosis, including assessment of variants of… Expand
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Highly Cited
2008
Highly Cited
2008
Recurrent 16p11.2 microdeletions in autism.
Autism is a childhood neurodevelopmental disorder with a strong genetic component, yet the identification of autism… Expand
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Highly Cited
2008
Highly Cited
2008
Novel Submicroscopic Chromosomal Abnormalities Detected in Autism Spectrum Disorder
BACKGROUND One genetic mechanism known to be associated with autism spectrum disorders (ASD) is chromosomal abnormalities. The… Expand
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Highly Cited
2008
Highly Cited
2008
CNV-seq, a new method to detect copy number variation using high-throughput sequencing
BackgroundDNA copy number variation (CNV) has been recognized as an important source of genetic variation. Array comparative… Expand
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Review
2008
Review
2008
The array CGH and its clinical applications.
Array comparative genomic hybridization (aCGH) is a technique enabling high-resolution, genome-wide screening of segmental… Expand
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Highly Cited
2007
Highly Cited
2007
Gene dosage alterations revealed by cDNA microarray analysis in cervical cancer: Identification of candidate amplified and overexpressed genes
Cervical cancer (CC) cells exhibit complex karyotypic alterations, which is consistent with deregulation of numerous critical… Expand
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Highly Cited
2006
Highly Cited
2006
High-resolution genomic profiles define distinct clinico-pathogenetic subgroups of multiple myeloma patients.
To identify genetic events underlying the genesis and progression of multiple myeloma (MM), we conducted a high-resolution… Expand
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