(Q33778575)

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Digital genotyping of macrosatellites and multicopy genes reveals novel biological functions associated with copy number variation of large tandem repeats

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Europe PubMed Central

PubMed publication ID

29 July 2017

Digital genotyping of macrosatellites and multicopy genes reveals novel biological functions associated with copy number variation of large tandem repeats (English)

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

3

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Christelle Borel

5

object named as

Christelle Borel

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Europe PubMed Central

PubMed publication ID

29 July 2017

author name string

Manisha Brahmachary

1

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Audrey Guilmatre

2

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Dan Hasson

4

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Peter Warburton

6

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Andrew J Sharp

7

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

publication date

19 June 2014

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Europe PubMed Central

PubMed publication ID

29 July 2017

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

10

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

6

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

e1004418

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Europe PubMed Central

PubMed publication ID

29 July 2017

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Creative Commons Attribution 4.0 International

19 June 2014

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April 2022 Public Data File from Crossref

copyright status

0 references

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1 reference

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1 reference

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Differential evolution of MAGE genes based on expression pattern and selection pressure

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A direct characterization of human mutation based on microsatellites

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1 reference

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1 reference

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1 reference

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

1 reference

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Epigenetic regulation of the X-chromosomal macrosatellite repeat encoding for the cancer/testis gene CT47.

1 reference

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Facioscapulohumeral muscular dystrophy: molecular pathological advances and future directions

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Characterization of DXZ4 conservation in primates implies important functional roles for CTCF binding, array expression and tandem repeat organization on the X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4063668

4 July 2018

A worldwide analysis of beta-defensin copy number variation suggests recent selection of a high-expressing DEFB103 gene copy in East Asia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4063668

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4063668

4 July 2018

Diversity of human copy number variation and multicopy genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4063668

4 July 2018

Measurement methods and accuracy in copy number variation: failure to replicate associations of beta-defensin copy number with Crohn's disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4063668

4 July 2018

Variable tandem repeats accelerate evolution of coding and regulatory sequences.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4063668

4 July 2018

Missing heritability and strategies for finding the underlying causes of complex disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4063668

4 July 2018

Understanding mechanisms underlying human gene expression variation with RNA sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4063668

4 July 2018

Transcriptome genetics using second generation sequencing in a Caucasian population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4063668

4 July 2018

A paucity of heterochromatin at functional human neocentromeres

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4063668

4 July 2018

Repeat instability as the basis for human diseases and as a potential target for therapy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4063668

4 July 2018

Finding the missing heritability of complex diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4063668

4 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4063668

4 July 2018

Experimental aspects of copy number variant assays at CCL3L1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4063668

4 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4063668

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Personalized copy number and segmental duplication maps using next-generation sequencing.

1 reference

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Unstable tandem repeats in promoters confer transcriptional evolvability

1 reference

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Identification of common genetic variants that account for transcript isoform variation between human populations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4063668

4 July 2018

EnsemblCompara GeneTrees: Complete, duplication-aware phylogenetic trees in vertebrates

1 reference

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Analysis of the largest tandemly repeated DNA families in the human genome

1 reference

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lumi: a pipeline for processing Illumina microarray

1 reference

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1 reference

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1 reference

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An initial map of insertion and deletion (INDEL) variation in the human genome.

1 reference

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Intragenic tandem repeats generate functional variability

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4063668

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Microsatellite instability generates diversity in brain and sociobehavioral traits

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Molecular origins of rapid and continuous morphological evolution

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1 reference

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Inappropriate Gene Activation in FSHD

1 reference

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1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4063668

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Positive selection of a gene family during the emergence of humans and African apes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4063668

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1 reference

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Initial sequencing and analysis of the human genome

1 reference

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1 reference

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1 reference

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1 reference

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1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4063668

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1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4063668

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1 reference

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1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004418

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Haplotypic relationship between SNP and microsatellite markers at the NOS2A locus in two populations

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https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004418

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β-defensin genomic copy number is associated with HIV load and immune reconstitution in sub-saharan Africans

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004418

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004418

21 January 2018

CCL3L1 and HIV/AIDS susceptibility

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004418

21 January 2018

Beta-defensins and Crohn's disease: confusion from counting copies.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004418

21 January 2018

Gene copy number: learning to count past two.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004418

21 January 2018

CCL3L1 and HIV/AIDS susceptibility

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https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004418

21 January 2018

Expansions of transgene repeats cause heterochromatin formation and gene silencing in Drosophila.

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https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004418

21 January 2018

Repeat-induced gene silencing in mammals.

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https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004418

21 January 2018

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21 January 2018

In vitro secretion of anti-GOR protein and anti-hepatitis C virus antibodies in patients with chronic hepatitis C

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21 January 2018

Copy number variation of multiple genes at Rhg1 mediates nematode resistance in soybean

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21 January 2018

Color vision of ancestral organisms of higher primates.

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https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004418

21 January 2018

The molecular basis of dichromatic color vision in males with multiple red and green visual pigment genes

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21 January 2018

Formation of novel CENP-A domains on tandem repetitive DNA and across chromosome breakpoints on human chromosome 8q21 neocentromeres.

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https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004418

21 January 2018

Conspiracy of silence among repeated transgenes.

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4063668

30 October 2018

Visual pigment gene structure and the severity of color vision defects

1 reference

https://pubmed.ncbi.nlm.nih.gov/24945355

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Direct estimates of human per nucleotide mutation rates at 20 loci causing Mendelian diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/24945355

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heterogeneous mutation processes in human microsatellite DNA sequences

1 reference

https://pubmed.ncbi.nlm.nih.gov/24945355

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PGEN.1004418

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

ResearchGate publication ID

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