Genetic association analysis of copy-number variation (CNV) in human disease pathogenesis (Q37281239)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18822366%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

review article

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title

Genetic association analysis of copy-number variation (CNV) in human disease pathogenesis (English)

1 reference

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14 January 2020

0 references

2

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14 January 2020

1

Iuliana Ionita-Laza

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14 January 2020

author name string

Christoph Lange

series ordinal

3

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14 January 2020

Benjamin A Raby

series ordinal

4

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14 January 2020

Charles Lee

series ordinal

5

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14 January 2020

publication date

19 October 2008

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14 January 2020

number of pages

5

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based on heuristic

inferred from page(s)

published in

Genomics

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14 January 2020

volume

93

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14 January 2020

issue

1

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14 January 2020

page(s)

22-26

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18822366%20AND%20SRC:MED&resulttype=core&format=json

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

14 January 2020

cites work

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6 September 2017

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6 September 2017

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6 September 2017

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Diet and the evolution of human amylase gene copy number variation

6 September 2017

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Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma

6 September 2017

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6 September 2017

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Copy-number variation and association studies of human disease

6 September 2017

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6 September 2017

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Mutational and selective effects on copy-number variants in the human genome

6 September 2017

1 reference

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Methods and strategies for analyzing copy number variation using DNA microarrays

6 September 2017

1 reference

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

6 September 2017

1 reference

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

6 September 2017

1 reference

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A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer

6 September 2017

1 reference

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Genome-wide association study identifies novel breast cancer susceptibility loci

6 September 2017

1 reference

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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

6 September 2017

1 reference

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Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

6 September 2017

1 reference

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Strong association of de novo copy number mutations with autism

6 September 2017

1 reference

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2631358

Global variation in copy number in the human genome

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2631358

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2631358

Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays

6 September 2017

1 reference

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A genome-wide association study identifies IL23R as an inflammatory bowel disease gene

6 September 2017

1 reference

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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

6 September 2017

1 reference

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Principal components analysis corrects for stratification in genome-wide association studies

6 September 2017

1 reference

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Copy number variation: new insights in genome diversity

6 September 2017

1 reference

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Bias of selection on human copy-number variants

6 September 2017

1 reference

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

6 September 2017

1 reference

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Structural variation in the human genome

6 September 2017

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Fine-scale structural variation of the human genome

6 September 2017

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Complement factor H polymorphism in age-related macular degeneration

6 September 2017

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Complement factor H polymorphism and age-related macular degeneration

6 September 2017

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A common inversion under selection in Europeans

6 September 2017

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6 September 2017

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Detection of large-scale variation in the human genome

6 September 2017

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Large-scale copy number polymorphism in the human genome

6 September 2017

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6 September 2017

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6 September 2017

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Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

6 September 2017

1 reference

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Gene copy number regulates the production of the human chemokine CCL3-L1

6 September 2017

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Replication validity of genetic association studies

6 September 2017

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LD78beta, a non-allelic variant of human MIP-1alpha (LD78alpha), has enhanced receptor interactions and potent HIV suppressive activity

6 September 2017

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6 September 2017

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Psoriasis is associated with increased beta-defensin genomic copy number

7 January 2021

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On the analysis of copy-number variations in genome-wide association studies: a translation of the family-based association test

14 September 2017

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Possible gene dosage effect of glutathione-S-transferases on atopic asthma: using real-time PCR for quantification of GSTM1 and GSTT1 gene copy numbers

3 September 2018

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A New Powerful Non-Parametric Two-Stage Approach for Testing Multiple Phenotypes in Family-Based Association Studies

3 September 2018

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3 September 2018

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3 September 2018

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7 January 2021

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18822366

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12 December 2020

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Identifiers

DOI

10.1016/J.YGENO.2008.08.012

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18822366%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18822366%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

1 reference