Genomic microarrays: a technology overview

Copy Number and SNP Arrays in Clinical Diagnostics

(2011) Christian P. Schaaf et al.   Annual Review of Genomics and Human Genetics

Genomic imbalances detected through array CGH in fetuses with holoprosencephaly

(2011) Isabela Nelly Machado et al.   ARQUIVOS DE NEURO-PSIQUIATRIA

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

(2011) Tracy Tucker et al.   BMC Medical Genomics

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

(2011) Malgorzata Srebniak et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Copy-number changes in prenatal diagnosis

(2011) Melissa Strassberg et al.   EXPERT REVIEW OF MOLECULAR DIAGNOSTICS

Copy number imbalances detected with a BAC-based array comparative genomic hybridization platform in congenital diaphragmatic hernia fetuses

(2011) I.N. Machado et al.   GENETICS AND MOLECULAR RESEARCH

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

(2011) M. J. Wat et al.   JOURNAL OF MEDICAL GENETICS

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

(2011) Megan L. Landsverk et al.   MOLECULAR GENETICS AND METABOLISM

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

(2011) Dalila Pinto et al.   NATURE BIOTECHNOLOGY

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

(2011) T. Y. Leung et al.   ULTRASOUND IN OBSTETRICS & GYNECOLOGY

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

(2011) Roberto Valli et al.   Molecular Cytogenetics

Single-cell copy number variation detection

(2011) Jiqiu Cheng et al.   GENOME BIOLOGY

Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies

(2010) David T. Miller et al.   AMERICAN JOURNAL OF HUMAN GENETICS

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

(2010) Sarah Hoang et al.   European Journal of Medical Genetics

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

(2010) Stuart A Scott et al.   GENETICS IN MEDICINE

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

(2010) B. H. W. Faas et al.   JOURNAL OF MEDICAL GENETICS

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

(2010) Andrew E. Dellinger et al.   NUCLEIC ACIDS RESEARCH

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

(2010) Idit Maya et al.   PRENATAL DIAGNOSIS

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

(2010) Kasemsri Srisupundit et al.   PRENATAL DIAGNOSIS

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

(2010) S. C. Hillman et al.   ULTRASOUND IN OBSTETRICS & GYNECOLOGY

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

(2010) Arthur L Beaudet   Genome Medicine

The pitfalls of platform comparison: DNA copy number array technologies assessed

(2009) Christina Curtis et al.   BMC GENOMICS

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

(2009) Caroline Schluth-Bolard et al.   European Journal of Medical Genetics

High resolution array analysis: diagnosing pregnancies with abnormal ultrasound findings

(2009) M Tyreman et al.   JOURNAL OF MEDICAL GENETICS

Effects of Ozone Exposure during Microarray Posthybridization Washes and Scanning

(2009) Steve Byerly et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

Chromosome instability is common in human cleavage-stage embryos

(2009) Evelyne Vanneste et al.   NATURE MEDICINE

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

(2009) Justine Coppinger et al.   PRENATAL DIAGNOSIS

De novobalanced chromosome rearrangements in prenatal diagnosis

(2009) Daniela Giardino et al.   PRENATAL DIAGNOSIS

Breakpoint Mapping and Array CGH in Translocations: Comparison of a Phenotypically Normal and an Abnormal Cohort

(2008) Julia Baptista et al.   AMERICAN JOURNAL OF HUMAN GENETICS

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

(2008) Mubasher Dar et al.   BMC BIOTECHNOLOGY

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

(2008) Zhong-Fa Zhang et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Comparison of microarray-based detection rates for cytogenetic abnormalities in prenatal and neonatal specimens

(2008) Lisa G. Shaffer et al.   PRENATAL DIAGNOSIS

Rapid prenatal diagnosis using uncultured amniocytes and oligonucleotide array CGH

(2008) Weimin Bi et al.   PRENATAL DIAGNOSIS

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

(2008) Ignatia B. Van den Veyver et al.   PRENATAL DIAGNOSIS