(Q36943647)

17 August 2017

1 reference

title

Oligonucleotide arrays for high-resolution analysis of copy number alteration in mental retardation/multiple congenital anomalies (English)

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17 August 2017

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Tamim H Shaikh

1

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17 August 2017

language of work or name

English

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publication date

1 September 2007

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17 August 2017

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17 August 2017

volume

9

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17 August 2017

issue

9

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17 August 2017

page(s)

617-625

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https://scigraph.springernature.com/pub.10.1097/gim.0b013e318148bb81

17 August 2017

exact match

0 references

cites work

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Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints

21 January 2018

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Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13).

21 January 2018

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A physical map, including a BAC/PAC clone contig, of the Williams-Beuren syndrome--deletion region at 7q11.23

21 January 2018

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Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion syndrome

21 January 2018

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Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome.

21 January 2018

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Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis

21 January 2018

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The genetics of mental retardation

21 January 2018

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Subtelomeric rearrangements detected in patients with idiopathic mental retardation

21 January 2018

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Study of 250 children with idiopathic mental retardation reveals nine cryptic and diverse subtelomeric chromosome anomalies.

21 January 2018

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Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors

21 January 2018

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High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays

21 January 2018

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Assembly of microarrays for genome-wide measurement of DNA copy number

21 January 2018

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Genome-wide-array-based comparative genomic hybridization reveals genetic homogeneity and frequent copy number increases encompassing CCNE1 in fallopian tube carcinoma

21 January 2018

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High-resolution mapping of amplifications and deletions in pediatric osteosarcoma by use of CGH analysis of cDNA microarrays

21 January 2018

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Genomic profiling of gastric cancer predicts lymph node status and survival

21 January 2018

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Chromosome aberrations in solid tumors

21 January 2018

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Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities

21 January 2018

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The use of telomere probes to investigate submicroscopic rearrangements associated with mental retardation.

21 January 2018

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Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features

21 January 2018

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A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications

21 January 2018

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Additional patient with del(12)(q21.2q22): further evidence for a candidate region for cardio-facio-cutaneous syndrome?

21 January 2018

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Definition of a critical region on chromosome 18 for congenital aural atresia by arrayCGH

21 January 2018

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Chromosomal anomalies on 6p25 in iris hypoplasia and Axenfeld-Rieger syndrome patients defined on a purpose-built genomic microarray

21 January 2018

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BAC microarray analysis of 15q11-q13 rearrangements and the impact of segmental duplications

21 January 2018

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Use of targeted array-based CGH for the clinical diagnosis of chromosomal imbalance: is less more?

21 January 2018

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A 2.3 Mb duplication of chromosome 8q24.3 associated with severe mental retardation and epilepsy detected by standard karyotype.

21 January 2018

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Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome

21 January 2018

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A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism.

21 January 2018

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Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability

21 January 2018

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Targeted genomic microarray analysis for identification of chromosome abnormalities in 1500 consecutive clinical cases.

21 January 2018

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Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases

21 January 2018

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Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation

21 January 2018

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Large-scale copy number polymorphism in the human genome

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

Comparative genomic hybridization using oligonucleotide microarrays and total genomic DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

High-resolution analysis of DNA copy number using oligonucleotide microarrays

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

Molecular karyotyping using an SNP array for genomewide genotyping.

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

Whole genome DNA copy number changes identified by high density oligonucleotide arrays

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

High-resolution single-nucleotide polymorphism array and clustering analysis of loss of heterozygosity in human lung cancer cell lines

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

An integrated view of copy number and allelic alterations in the cancer genome using single nucleotide polymorphism arrays

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

Oligonucleotide microarray analysis of genomic imbalance in children with mental retardation

21 January 2018

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Detecting gene copy number fluctuations in tumor cells by microarray analysis of genomic representations

21 January 2018

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Strong association of de novo copy number mutations with autism

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

High density synthetic oligonucleotide arrays

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

Genome-wide detection of allelic imbalance using human SNPs and high-density DNA arrays

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

Parallel genotyping of over 10,000 SNPs using a one-primer assay on a high-density oligonucleotide array

21 January 2018

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Genotyping over 100,000 SNPs on a pair of oligonucleotide arrays.

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

High-resolution identification of chromosomal abnormalities using oligonucleotide arrays containing 116,204 SNPs

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.

21 January 2018

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Large-scale genotyping of complex DNA.

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

High resolution microarray comparative genomic hybridisation analysis using spotted oligonucleotides

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

High-resolution global profiling of genomic alterations with long oligonucleotide microarray

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

An oligonucleotide based array-CGH system for detection of genome wide copy number changes including subtelomeric regions for genetic evaluation of mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

Analysis of chromosome breakpoints in neuroblastoma at sub-kilobase resolution using fine-tiling oligonucleotide array CGH.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

Characterization of a recurrent 15q24 microdeletion syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

Recurrent 10q22-q23 deletions: a genomic disorder on 10q associated with cognitive and behavioral abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

Whole-genome genotyping with the single-base extension assay

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

Human and mouse oligonucleotide-based array CGH.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

BAC to the future! or oligonucleotides: a perspective for micro array comparative genomic hybridization (array CGH)

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

Light-directed, spatially addressable parallel chemical synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

Multiplexed biochemical assays with biological chips

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

Light-generated oligonucleotide arrays for rapid DNA sequence analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

dChipSNP: significance curve and clustering of SNP-array-based loss-of-heterozygosity data

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

Resolving the resolution of array CGH.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

Circular binary segmentation for the analysis of array-based DNA copy number data

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

Detection of large-scale variation in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

Segmental duplications and copy-number variation in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

Common deletion polymorphisms in the human genome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

Structural variation in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

Global variation in copy number in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

Microduplication and triplication of 22q11.2: a highly variable syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

Application of ROMA (representational oligonucleotide microarray analysis) to patients with cytogenetic rearrangements

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

Common deletions and SNPs are in linkage disequilibrium in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E318148BB81

10.1097/GIM.0B013E318148BB81

21 January 2018

Identifiers

DOI

1 reference

Dimensions Publication ID

17 August 2017

1023330210

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1 reference