(Q37998941)

26 August 2017

title

Genomic microarrays: a technology overview (English)

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26 August 2017

2

Joris R Vermeesch

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26 August 2017

Paul D Brady

1

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26 August 2017

publication date

1 April 2012

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26 August 2017

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26 August 2017

volume

32

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26 August 2017

issue

4

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26 August 2017

page(s)

336-343

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Prenatal aneuploidy detection in interphase cells by fluorescence in situ hybridization (FISH).

26 August 2017

cites work

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Prenatal diagnosis using interphase fluorescence in situ hybridization (FISH): 2-year multi-center retrospective study and review of the literature

21 January 2018

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Development and implementation of a new rapid aneuploidy diagnostic service within the UK National Health Service and implications for the future of prenatal diagnosis.

21 January 2018

1 reference

MLPA for prenatal diagnosis of commonly occurring aneuploidies

21 January 2018

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Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

21 January 2018

1 reference

Molecular cytogenetic and rapid aneuploidy detection methods in prenatal diagnosis

21 January 2018

1 reference

Molecular karyotyping: array CGH quality criteria for constitutional genetic diagnosis.

21 January 2018

1 reference

Prenatal detection of unbalanced chromosomal rearrangements by array CGH.

21 January 2018

1 reference

Array-CGH analysis of cell-free fetal DNA in 10 mL of amniotic fluid supernatant.

21 January 2018

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Microarray analysis of cell-free fetal DNA in amniotic fluid: a prenatal molecular karyotype.

21 January 2018

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Whole-genome microarray analysis in prenatal specimens identifies clinically significant chromosome alterations without increase in results of unclear significance compared to targeted microarray

21 January 2018

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Identification of clinically significant, submicroscopic chromosome alterations and UPD in fetuses with ultrasound anomalies using genome-wide 250k SNP array analysis

21 January 2018

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Diagnostic utility of array-based comparative genomic hybridization (aCGH) in a prenatal setting.

21 January 2018

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Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flow

21 January 2018

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High resolution array analysis: diagnosing pregnancies with abnormal ultrasound findings.

21 January 2018

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Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases

21 January 2018

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Utilization of targeted array comparative genomic hybridization, MitoMet, in prenatal diagnosis of metabolic disorders

21 January 2018

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Genomic alterations that contribute to the development of isolated and non-isolated congenital diaphragmatic hernia

21 January 2018

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Complement factor H polymorphism in age-related macular degeneration

21 January 2018

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A genome-wide association study identifies novel risk loci for type 2 diabetes

21 January 2018

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Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

21 January 2018

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Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants

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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Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports

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 pitfalls of platform comparison: DNA copy number array technologies assessed

21 January 2018

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Genome-wide copy number profiling on high-density bacterial artificial chromosomes, single-nucleotide polymorphisms, and oligonucleotide microarrays: a platform comparison based on statistical power analysis

21 January 2018

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Comparison of genome-wide array genomic hybridization platforms for the detection of copy number variants in idiopathic mental retardation

21 January 2018

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Detection of submicroscopic constitutional chromosome aberrations in clinical diagnostics: a validation of the practical performance of different array platforms.

21 January 2018

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Copy number and SNP arrays in clinical diagnostics

21 January 2018

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Effects of ozone exposure during microarray posthybridization washes and scanning

21 January 2018

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Effects of atmospheric ozone on microarray data quality

21 January 2018

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Development of a novel ozone- and photo-stable HyPer5 red fluorescent dye for array CGH and microarray gene expression analysis with consistent performance irrespective of environmental conditions

21 January 2018

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Comparison of Alexa Fluor and CyDye for practical DNA microarray use.

21 January 2018

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Platinum(II)-based coordination compounds as nucleic acid labeling reagents: synthesis, reactivity, and applications in hybridization assays.

21 January 2018

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Universal Linkage System: versatile nucleic acid labeling technique

21 January 2018

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Single-cell copy number variation detection.

21 January 2018

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Chromosome instability is common in human cleavage-stage embryos.

21 January 2018

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Statistical issues in the analysis of DNA Copy Number Variations

21 January 2018

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Comparative analyses of seven algorithms for copy number variant identification from single nucleotide polymorphism arrays

21 January 2018

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Comparative analysis of algorithms for identifying amplifications and deletions in array CGH data

21 January 2018

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Comparing CNV detection methods for SNP arrays

21 January 2018

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Accurate and reliable high-throughput detection of copy number variation in the human genome

21 January 2018

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Guidelines for molecular karyotyping in constitutional genetic diagnosis

21 January 2018

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Ethical issues raised by common copy number variants and single nucleotide polymorphisms of certain and uncertain significance in general medical practice

21 January 2018

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The incidentalome: a threat to genomic medicine

21 January 2018

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Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis

21 January 2018

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Copy-number changes in prenatal diagnosis

21 January 2018

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Breakpoint mapping and array CGH in translocations: comparison of a phenotypically normal and an abnormal cohort

21 January 2018

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Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 patients.

21 January 2018

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Cryptic genomic imbalances in de novo and inherited apparently balanced chromosomal rearrangements: array CGH study of 47 unrelated cases

21 January 2018

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Detecting sex chromosome anomalies and common triploidies in products of conception by array-based comparative genomic hybridization

21 January 2018

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Detection of mosaicism for genome imbalance in a cohort of 3,042 clinical cases using an oligonucleotide array CGH platform

21 January 2018

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Detection of low-level mosaicism and placental mosaicism by oligonucleotide array comparative genomic hybridization.

21 January 2018

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Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells

21 January 2018

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Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

21 January 2018

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Targeted array comparative genomic hybridisation (array CGH) identifies genomic imbalances associated with isolated congenital diaphragmatic hernia (CDH)

21 January 2018

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Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization

21 January 2018

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Identification of submicroscopic chromosomal aberrations in fetuses with increased nuchal translucency and apparently normal karyotype

21 January 2018

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21 January 2018

Identifiers

DOI

10.1002/PD.2933

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26 August 2017

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