Peroxisome Biogenesis Disorder, Complementation Group H

Known as: CGH 
 
National Institutes of Health

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Peroxisomal Disorders

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Highly Cited
2012
Highly Cited
2012
Selection of single blastocysts for fresh transfer via standard morphology assessment alone and with array CGH for good prognosis IVF patients: results from a randomized pilot study
Single embryo transfer (SET) remains underutilized as a strategy to reduce multiple gestation risk in IVF, and its overall lower… (More)
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Highly Cited
2007
Highly Cited
2007
A faster circular binary segmentation algorithm for the analysis of array CGH data
MOTIVATION Array CGH technologies enable the simultaneous measurement of DNA copy number for thousands of sites on a genome. We… (More)
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Highly Cited
2007
Highly Cited
2007
CGHcall: calling aberrations for array CGH tumor profiles
UNLABELLED CGHcall achieves high calling accuracy for array CGH data by effective use of breakpoint information from segmentation… (More)
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Highly Cited
2007
Highly Cited
2007
Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation.
Autism and mental retardation (MR) are often associated, suggesting that these conditions are etiologically related. Recently… (More)
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Highly Cited
2005
Highly Cited
2005
Diagnostic genome profiling in mental retardation.
Mental retardation (MR) occurs in 2%-3% of the general population. Conventional karyotyping has a resolution of 5-10 million… (More)
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Highly Cited
2005
Highly Cited
2005
A method for calling gains and losses in array CGH data.
Array CGH is a powerful technique for genomic studies of cancer. It enables one to carry out genome-wide screening for regions of… (More)
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Highly Cited
2004
Highly Cited
2004
Analysis of array CGH data: from signal ratio to gain and loss of DNA regions
MOTIVATION Genomic DNA regions are frequently lost or gained during tumor progression. Array Comparative Genomic Hybridization… (More)
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Highly Cited
2004
Highly Cited
2004
Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic…
The underlying causes of learning disability and dysmorphic features in many patients remain unidentified despite extensive… (More)
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Highly Cited
2004
Highly Cited
2004
Hidden Markov models approach to the analysis of array CGH data
The development of solid tumors is associated with acquisition of complex genetic alterations, indicating that failures in the… (More)
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Highly Cited
2004
Highly Cited
2004
A statistical approach for array CGH data analysis
Microarray-CGH experiments are used to detect and map chromosomal imbalances, by hybridizing targets of genomic DNA from a test… (More)
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