(Q42228843)

19 October 2017

Analysis of copy number variation using quantitative interspecies competitive PCR (English)

1 reference

19 October 2017

8

1 reference

19 October 2017

Huw R Morris

6

0 references

Beate St Pourcain

object named as

Beate Glaser

5

0 references

author name string

Nigel M Williams

1

1 reference

19 October 2017

Hywel Williams

2

1 reference

19 October 2017

Elisa Majounie

3

1 reference

19 October 2017

Nadine Norton

4

1 reference

19 October 2017

Michael J Owen

7

1 reference

19 October 2017

12 August 2008

1 reference

19 October 2017

Nucleic Acids Research

1 reference

19 October 2017

36

1 reference

19 October 2017

17

1 reference

19 October 2017

e112

1 reference

Psoriasis is associated with increased beta-defensin genomic copy number

19 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553599

Copy-number variation and association studies of human disease

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553599

Methods and strategies for analyzing copy number variation using DNA microarrays

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553599

Strong association of de novo copy number mutations with autism

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553599

Relative impact of nucleotide and copy number variation on gene expression phenotypes

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553599

Accurate, high-throughput typing of copy number variation using paralogue ratios from dispersed repeats.

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553599

Global variation in copy number in the human genome

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553599

Understanding the recent evolution of the human genome: insights from human-chimpanzee genome comparisons

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553599

Effects of differential genotyping error rate on the type I error probability of case-control studies

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553599

Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553599

Structural variation in the human genome

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553599

Initial sequence of the chimpanzee genome and comparison with the human genome

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553599

Segmental duplications and copy-number variation in the human genome

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553599

Silhouette scores for assessment of SNP genotype clusters

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553599

The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553599

Large-scale copy number polymorphism in the human genome

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553599

Identification in 2 independent samples of a novel schizophrenia risk haplotype of the dystrobrevin binding protein gene (DTNBP1).

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553599

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

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553599

Measurement of locus copy number by hybridisation with amplifiable probes

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553599

Real time quantitative PCR

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553599

Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553599

Microdeletions involving the SCN1A gene may be common in SCN1A-mutation-negative SMEI patients.

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553599

Common deletion polymorphisms in the human genome.

17 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553599

DNA deletion associated with hereditary neuropathy with liability to pressure palsies

17 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553599

Statistical false positive or true disease pathway?

17 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553599

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

3 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553599

Enhancing linkage analysis of complex disorders: an evaluation of high-density genotyping

1 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2553599

Chromosome 22q11 deletions, velo-cardio-facial syndrome and early-onset psychosis

1 December 2018

1 reference

12 December 2020

Copy-number analysis goes more than skin deep

1 reference

12 December 2020

Copy-number variants in patients with a strong family history of pancreatic cancer

1 reference

12 December 2020

A high-resolution survey of deletion polymorphism in the human genome

1 reference

12 December 2020

Detection of exon deletions and duplications of the mismatch repair genes in hereditary nonpolyposis colorectal cancer families using multiplex polymerase chain reaction of short fluorescent fragments

1 reference

12 December 2020

Identifiers

DOI

10.1093/NAR/GKN495

1 reference

19 October 2017

1 reference

19 October 2017

PubMed publication ID

18697816

1 reference