(Q46809730)

25 December 2017

title

Genome-wide analysis of transcript isoform variation in humans (English)

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25 December 2017

author

Robert Sladek

8

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25 December 2017

author name string

Tony Kwan

1

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25 December 2017

David Benovoy

2

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25 December 2017

Christel Dias

3

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25 December 2017

Scott Gurd

4

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25 December 2017

Cathy Provencher

5

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25 December 2017

Patrick Beaulieu

6

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25 December 2017

Thomas J Hudson

7

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25 December 2017

Jacek Majewski

9

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25 December 2017

language of work or name

English

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publication date

13 January 2008

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25 December 2017

published in

Nature Genetics

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25 December 2017

volume

40

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25 December 2017

issue

2

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25 December 2017

page(s)

225-231

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25 December 2017

https://scigraph.springernature.com/pub.10.1038/ng.2007.57

exact match

0 references

cites work

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Pre-mRNA splicing and human disease

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The splicing machinery is a genetic modifier of disease severity

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OAS1 Splice Site Polymorphism Controlling Antiviral Enzyme Activity Influences Susceptibility to Type 1 Diabetes

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https://api.crossref.org/works/10.1038%2FNG.2007.57

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Genetic control of alternative splicing in the TAP2 gene: possible implication in the genetics of type 1 diabetes

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https://api.crossref.org/works/10.1038%2FNG.2007.57

7 January 2021

Association of IRF5 in UK SLE families identifies a variant involved in polyadenylation

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https://api.crossref.org/works/10.1038%2FNG.2007.57

7 January 2021

Three functional variants of IFN regulatory factor 5 (IRF5) define risk and protective haplotypes for human lupus

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7 January 2021

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

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https://api.crossref.org/works/10.1038%2FNG.2007.57

7 January 2021

Common genetic variants account for differences in gene expression among ethnic groups

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https://api.crossref.org/works/10.1038%2FNG.2007.57

7 January 2021

Genome-wide associations of gene expression variation in humans

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https://api.crossref.org/works/10.1038%2FNG.2007.57

7 January 2021

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

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https://api.crossref.org/works/10.1038%2FNG.2007.57

7 January 2021

Discovery of tissue-specific exons using comprehensive human exon microarrays

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7 January 2021

Alternative splicing and differential gene expression in colon cancer detected by a whole genome exon array.

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7 January 2021

Heritability of alternative splicing in the human genome

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7 January 2021

A haplotype map of the human genome

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https://api.crossref.org/works/10.1038%2FNG.2007.57

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Sequence polymorphisms cause many false cis eQTLs

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Allele-specific transcript isoforms in human

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Identification of common genetic variation that modulates alternative splicing

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7 January 2021

Large scale study of protein domain distribution in the context of alternative splicing

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7 January 2021

Evidence for the widespread coupling of alternative splicing and nonsense-mediated mRNA decay in humans

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7 January 2021

A large-scale analysis of mRNA polyadenylation of human and mouse genes

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7 January 2021

Computational analysis of 3'-ends of ESTs shows four classes of alternative polyadenylation in human, mouse, and rat

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7 January 2021

Control of translation and mRNA degradation by miRNAs and siRNAs

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MicroRNAs direct rapid deadenylation of mRNA

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Solving the riddle of the bright mismatches: labeling and effective binding in oligonucleotide arrays

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Identifiers

DOI

10.1038/NG.2007.57

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25 December 2017

PubMed ID

18193047

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25 December 2017