(Q38029978)

27 August 2017

title

Correlating multiallelic copy number polymorphisms with disease susceptibility (English)

1 reference

27 August 2017

Stuart Cantsilieris

1

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27 August 2017

Stefan J White

series ordinal

2

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27 August 2017

publication date

23 August 2012

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27 August 2017

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27 August 2017

volume

34

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27 August 2017

issue

1

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27 August 2017

page(s)

1-13

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CCL3L1-CCR5 genotype influences durability of immune recovery during antiretroviral therapy of HIV-1-infected individuals

27 August 2017

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Recent segmental duplications in the human genome

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Association of higher DEFB4 genomic copy number with Crohn's disease

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Genetically determined partial complement C4 deficiency states are not independent risk factors for SLE in UK and Spanish populations

21 January 2018

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Copy number variation of the activating FCGR2C gene predisposes to idiopathic thrombocytopenic purpura

21 January 2018

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Copy number variation at the FCGR locus includes FCGR3A, FCGR2C and FCGR3B but not FCGR2A and FCGR2B.

21 January 2018

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Genetic variations in the receptor-ligand pair CCR5 and CCL3L1 are important determinants of susceptibility to Kawasaki disease

21 January 2018

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Population-genetic properties of differentiated human copy-number polymorphisms

21 January 2018

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Accuracy and differential bias in copy number measurement of CCL3L1 in association studies with three auto-immune disorders

21 January 2018

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Population structure, differential bias and genomic control in a large-scale, case-control association study

21 January 2018

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Origins and functional impact of copy number variation in the human genome

21 January 2018

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A copy number variation morbidity map of developmental delay

21 January 2018

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Systematic assessment of copy number variant detection via genome-wide SNP genotyping

21 January 2018

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Sample degradation leads to false-positive copy number variation calls in multiplex real-time polymerase chain reaction assays.

21 January 2018

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Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis

21 January 2018

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CCL3L1 and CCR5 influence cell-mediated immunity and affect HIV-AIDS pathogenesis via viral entry-independent mechanisms

21 January 2018

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FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity

21 January 2018

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Copy number variation of Fc gamma receptor genes and disease predisposition

21 January 2018

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A chromosome 8 gene-cluster polymorphism with low human beta-defensin 2 gene copy number predisposes to Crohn disease of the colon

21 January 2018

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Assessment of complement C4 gene copy number using the paralog ratio test

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22172

Experimental aspects of copy number variant assays at CCL3L1

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22172

Determination of beta-defensin genomic copy number in different populations: A comparison of three methods

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22172

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22172

Human copy number variation and complex genetic disease.

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22172

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22172

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

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22172

CCL3L Copy number variation and the co-evolution of primate and viral genomes

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22172

Low copy number of the FCGR3B gene and rheumatoid arthritis: a case-control study and meta-analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

High-resolution mapping of the 8p23.1 beta-defensin cluster reveals strictly concordant copy number variation of all genes.

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22172

Reply to: "Experimental aspects of copy number variant assays at CCL3L1".

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Copy number variation of beta-defensins and relevance to disease

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22172

Extensive normal copy number variation of a beta-defensin antimicrobial-gene cluster

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22172

Beta-defensin genomic copy number is not a modifier locus for cystic fibrosis

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22172

An integrated approach for measuring copy number variation at the FCGR3 (CD16) locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Psoriasis is associated with increased beta-defensin genomic copy number

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

A common CFH haplotype, with deletion of CFHR1 and CFHR3, is associated with lower risk of age-related macular degeneration

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22172

MLPA analysis for the detection of deletions, duplications and complex rearrangements in the dystrophin gene: potential and pitfalls.

21 January 2018

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Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22172

Analysis of copy number variants and segmental duplications in the human genome: Evidence for a change in the process of formation in recent evolutionary history

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22172

Copy number variation detection and genotyping from exome sequence data

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22172

African infants' CCL3 gene copies influence perinatal HIV transmission in the absence of maternal nevirapine

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22172

Role of CCL3L1-CCR5 genotypes in the epidemic spread of HIV-1 and evaluation of vaccine efficacy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Copy number variation of CCL3L1 influences asthma risk by modulating IL-10 expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Copy number variation in CCL3L1 gene is associated with susceptibility to acute rejection in patients after liver transplantation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Human defensin gene copy number polymorphisms: comprehensive analysis of independent variation in alpha- and beta-defensin regions at 8p22-p23.

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22172

Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome

21 January 2018

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https://api.crossref.org/works/10.1002%2FHUMU.22172

Evolutionary history of copy-number-variable locus for the low-affinity Fcγ receptor: mutation rate, autoimmune disease, and the legacy of helminth infection

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Association of copy number variation in the FCGR3B gene with risk of autoimmune diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Influence of variations in CCL3L1 and CCR5 on tuberculosis in a northwestern Colombian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

CCL3L1 gene-containing segmental duplications and polymorphisms in CCR5 affect risk of systemic lupus erythaematosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Genetic variation of the Fc gamma receptor 3B gene and association with rheumatoid arthritis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Copy-number variation and association studies of human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Common deletion polymorphisms in the human genome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Integrated detection and population-genetic analysis of SNPs and copy number variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Association of variation in Fcgamma receptor 3B gene copy number with rheumatoid arthritis in Caucasian samples

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Reduced ability of newborns to produce CCL3 is associated with increased susceptibility to perinatal human immunodeficiency virus 1 transmission

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

The F158V polymorphism in FcgammaRIIIA shows disparate associations with rheumatoid arthritis in two genetically distinct populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Mapping copy number variation by population-scale genome sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

FCGR3B copy number variation is associated with systemic lupus erythematosus risk in Afro-Caribbeans.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Analysis of Fcgamma receptor haplotypes in rheumatoid arthritis: FCGR3A remains a major susceptibility gene at this locus, with an additional contribution from FCGR3B.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

FcgammaRIIIA-158V and rheumatoid arthritis: a confirmation study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Evidence for both copy number and allelic (NA1/NA2) risk at the FCGR3B locus in systemic lupus erythematosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Copy number variations of CCL3L1 and long-term prognosis of HIV-1 infection in asymptomatic HIV-infected Japanese with hemophilia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Copy number, linkage disequilibrium and disease association in the FCGR locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Copy number variation and mosaicism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Comparison of multiplex ligation-dependent probe amplification and real-time PCR accuracy for gene copy number quantification using the beta-defensin locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Diet and the evolution of human amylase gene copy number variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Association tests and software for copy number variant data

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Global variation in copy number in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Increased frequency of complement C4B deficiency in rheumatoid arthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Confirmation of association of FCGR3B but not FCGR3A copy number with susceptibility to autoantibody positive rheumatoid arthritis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Lower linkage disequilibrium at CNVs is due to both recurrent mutation and transposing duplications

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Host CCL3L1 gene copy number in relation to HIV-1-specific CD4+ and CD8+ T-cell responses and viral load in South African women

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

CCL3L1 and CCL4L1: variable gene copy number in adolescents with and without human immunodeficiency virus type 1 (HIV-1) infection

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Segmental duplications and copy-number variation in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Association of β-defensin copy number and psoriasis in three cohorts of European origin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Diversity of human copy number variation and multicopy genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Contribution of Fcgamma receptor IIIA gene 158V/F polymorphism and copy number variation to the risk of ACPA-positive rheumatoid arthritis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Fine-scale structural variation of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

CCL3L1 and HIV/AIDS susceptibility

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Low serum C4 concentrations: an inherited predisposition to insulin dependent diabetes?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Copy number of FCGR3B, which is associated with systemic lupus erythematosus, correlates with protein expression and immune complex uptake

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Six new loci associated with body mass index highlight a neuronal influence on body weight regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Molecular basis of complete complement C4 deficiency in two North-African families with systemic lupus erythematosus

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Strong association of de novo copy number mutations with sporadic schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Gene copy-number variation and associated polymorphisms of complement component C4 in human systemic lupus erythematosus (SLE): low copy number is a risk factor for and high copy number is a protective factor against SLE susceptibility in European A

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

CCL3L1 and HIV/AIDS susceptibility

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Meta-analysis confirms a role for deletion in FCGR3B in autoimmune phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Evidence for an influence of chemokine ligand 3-like 1 (CCL3L1) gene copy number on susceptibility to rheumatoid arthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

Detection of copy number variation using SNP genotyping

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

7 January 2021

Analysis of beta-defensin and Toll-like receptor gene copy number variation in celiac disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

7 January 2021

Lower copy numbers of the chemokine CCL3L1 gene in patients with chronic hepatitis C

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

7 January 2021

The 158V polymorphism of Fc gamma receptor type IIIA in early rheumatoid arthritis: increased susceptibility and severity in male patients (the Swedish TIRA project)

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

7 January 2021

FCGR3B copy number variation is not associated with lupus nephritis in a Chinese population

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

7 January 2021

Copy-number analysis goes more than skin deep

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

7 January 2021

Low serum C4 concentrations in insulin dependent diabetes mellitus.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22172

7 January 2021

Multiplex Paralogue Ratio Tests for accurate measurement of multiallelic CNVs

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https://api.crossref.org/works/10.1002%2FHUMU.22172

7 January 2021

Identifiers

DOI

10.1002/HUMU.22172

1 reference

27 August 2017

1 reference