(Q36481133)

14 August 2017

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title

Application of oligonucleotide arrays to high-content genetic analysis (English)

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14 August 2017

Neil J Gibson

1

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14 August 2017

publication date

1 May 2006

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Expert Review of Molecular Diagnostics: new diagnostic technologies are set to revolutionise healthcare

14 August 2017

published in

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14 August 2017

volume

6

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14 August 2017

issue

3

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14 August 2017

page(s)

451-464

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The use of real-time PCR methods in DNA sequence variation analysis

14 August 2017

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A high-resolution linkage-disequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphisms

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A whole-genome admixture scan finds a candidate locus for multiple sclerosis susceptibility

21 January 2018

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Physiogenomic analysis links serum creatine kinase activities during statin therapy to vascular smooth muscle homeostasis

21 January 2018

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A genome-wide scalable SNP genotyping assay using microarray technology

21 January 2018

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Large-scale genotyping of complex DNA.

21 January 2018

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Novel technology and the development of pharmacogenetics within the pharmaceutical industry

21 January 2018

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Whole-genome scan, in a complex disease, using 11,245 single-nucleotide polymorphisms: comparison with microsatellites

21 January 2018

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Comparison of microsatellites versus single-nucleotide polymorphisms in a genome linkage screen for prostate cancer-susceptibility Loci

21 January 2018

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Genomewide linkage analysis of bipolar disorder by use of a high-density single-nucleotide-polymorphism (SNP) genotyping assay: a comparison with microsatellite marker assays and finding of significant linkage to chromosome 6q22.

21 January 2018

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Genomewide linkage searches for Mendelian disease loci can be efficiently conducted using high-density SNP genotyping arrays

21 January 2018

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A HOX gene mutation in a family with isolated congenital vertical talus and Charcot-Marie-Tooth disease

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

A Novel Gene for Neonatal Diabetes Maps to Chromosome 10p12.1-p13

21 January 2018

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Mutations in VPS33B, encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome

21 January 2018

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Mutations in the gene encoding gap junction protein alpha 12 (connexin 46.6) cause Pelizaeus-Merzbacher-like disease

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

Mutations in PTF1A cause pancreatic and cerebellar agenesis

21 January 2018

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Microarray-based comparative genomic hybridization and its applications in human genetics

21 January 2018

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High-resolution analysis of DNA copy number using oligonucleotide microarrays

21 January 2018

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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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Molecular karyotyping using an SNP array for genomewide genotyping.

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

Genomewide single nucleotide polymorphism microarray mapping in basal cell carcinomas unveils uniparental disomy as a key somatic event.

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

A survey of homozygous deletions in human cancer genomes

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

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/10.1586%2F14737159.6.3.451

Concurrent analysis of loss of heterozygosity (LOH) and copy number abnormality (CNA) for oral premalignancy progression using the Affymetrix 10K SNP mapping array

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

Overexpression, amplification, and androgen regulation of TPD52 in prostate cancer

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

Genotyping pooled DNA on microarrays: a systematic genome screen of thousands of SNPs in large samples to detect QTLs for complex traits.

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

SNPs, microarrays and pooled DNA: identification of four loci associated with mild mental impairment in a sample of 6000 children.

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

Complement factor H polymorphism in age-related macular degeneration

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

Strong association of the Y402H variant in complement factor H at 1q32 with susceptibility to age-related macular degeneration

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

Complement factor H polymorphism and age-related macular degeneration

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

Complement factor H variant increases the risk of age-related macular degeneration

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

Integrative genomic analyses identify MITF as a lineage survival oncogene amplified in malignant melanoma

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

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

21 January 2018

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

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Use of a high-density DNA probe array for detecting mutations involved in rifampicin resistance in Mycobacterium tuberculosis.

21 January 2018

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The Human MitoChip: a high-throughput sequencing microarray for mitochondrial mutation detection.

21 January 2018

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Detection of human immunodeficiency virus type 1 antiretroviral resistance mutations by high-density DNA probe arrays

21 January 2018

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21 January 2018

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Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21.

21 January 2018

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Accessing genetic information with high-density DNA arrays.

21 January 2018

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Segmental phylogenetic relationships of inbred mouse strains revealed by fine-scale analysis of sequence variation across 4.6 mb of mouse genome

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

Genomic DNA insertions and deletions occur frequently between humans and nonhuman primates

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

Whole-genome patterns of common DNA variation in three human populations

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

High-resolution whole-genome association study of Parkinson disease.

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

Application of pooled genotyping to scan candidate regions for association with HDL cholesterol levels

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

Comparative genomic hybridization using oligonucleotide microarrays and total genomic DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.6.3.451

Gearing up for genome-wide gene-association studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.6.3.451

A comprehensive review of genetic association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.6.3.451

Multiplexed variation scanning for 1,000 amplicons in hundreds of patients using mismatch repair detection (MRD) on tag arrays

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

Examples of the complex architecture of the human transcriptome revealed by RACE and high-density tiling arrays

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

Transcriptional maps of 10 human chromosomes at 5-nucleotide resolution

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

Genomic maps and comparative analysis of histone modifications in human and mouse

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

Mapping determinants of human gene expression by regional and genome-wide association

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

Microarray-based DNA methylation profiling: technology and applications

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

High-throughput DNA methylation profiling using universal bead arrays

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

The elimination of primer-dimer accumulation in PCR

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.6.3.451

Reliable High-Throughput Genotyping and Loss-of-Heterozygosity Detection in Formalin-Fixed, Paraffin-Embedded Tumors Using Single Nucleotide Polymorphism Arrays

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.6.3.451

A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

Localisation of merosin-positive congenital muscular dystrophy to chromosome 4p16.3

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

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

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

An autosomal recessive cerebellar ataxia syndrome with upward gaze palsy, neuropathy, and seizures

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.6.3.451

Initial sequencing and analysis of the human genome

21 January 2018

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28 May 2022

https://opencitations.net/index/coci/api/v1/citations/10.1038/35057062

Identifiers

DOI

10.1586/14737159.6.3.451

1 reference

14 August 2017

1 reference