Abundant contribution of short tandem repeats to gene expression variation in humans (Q34504259)

2 August 2017

Abundant contribution of short tandem repeats to gene expression variation in humans (English)

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2 August 2017

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7

Mark J Daly

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2 August 2017

1

Melissa Gymrek

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2 August 2017

Jonathan K. Pritchard

9

object named as

Jonathan K Pritchard

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2 August 2017

8

Alkes L Price

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2 August 2017

Thomas Willems

2

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2 August 2017

Audrey Guilmatre

3

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2 August 2017

Haoyang Zeng

4

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2 August 2017

Barak Markus

5

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2 August 2017

Stoyan Georgiev

6

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2 August 2017

Andrew J Sharp

10

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Yaniv Erlich

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2 August 2017

language of work or name

English

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publication date

7 December 2015

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2 August 2017

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48

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22-29

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https://scigraph.springernature.com/pub.10.1038/ng.3461

2 August 2017

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The overdue promise of short tandem repeat variation for heritability.

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7 July 2018

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7 July 2018

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7 July 2018

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The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomes

7 July 2018

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Microsatellite tandem repeats are abundant in human promoters and are associated with regulatory elements

7 July 2018

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Aberrant splicing of HTT generates the pathogenic exon 1 protein in Huntington disease

7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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Tandem repeat sequence variation as causative cis-eQTLs for protein-coding gene expression variation: the case of CSTB.

7 July 2018

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Patterns of cis regulatory variation in diverse human populations

7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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Variable tandem repeats accelerate evolution of coding and regulatory sequences.

7 July 2018

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Common SNPs explain a large proportion of the heritability for human height

7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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7 July 2018

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Finding the missing heritability of complex diseases

7 July 2018

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Unstable tandem repeats in promoters confer transcriptional evolvability

7 July 2018

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TopHat: discovering splice junctions with RNA-Seq

7 July 2018

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Why Most Discovered True Associations Are Inflated

7 July 2018

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Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

7 July 2018

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Linkage disequilibrium between STRPs and SNPs across the human genome

7 July 2018

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SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout

7 July 2018

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SLC2A9 influences uric acid concentrations with pronounced sex-specific effects

7 July 2018

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Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia

7 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4909355

Population genomics of human gene expression

7 July 2018

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7 July 2018

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

7 July 2018

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Expandable DNA repeats and human disease.

7 July 2018

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

7 July 2018

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7 July 2018

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Microsatellite instability generates diversity in brain and sociobehavioral traits

7 July 2018

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7 July 2018

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Microsatellite instability regulates transcription factor binding and gene expression

7 July 2018

1 reference

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Microsatellites: simple sequences with complex evolution

7 July 2018

1 reference

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A variable dinucleotide repeat in the CFTR gene contributes to phenotype diversity by forming RNA secondary structures that alter splicing

7 July 2018

1 reference

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HnRNP L stimulates splicing of the eNOS gene by binding to variable-length CA repeats

7 July 2018

1 reference

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Abundant raw material for cis-regulatory evolution in humans

7 July 2018

1 reference

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The human genome browser at UCSC

7 July 2018

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A polymorphic microsatellite that mediates induction of PIG3 by p53.

7 July 2018

1 reference

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A polymorphic dinucleotide repeat in the rat nucleolin gene forms Z-DNA and inhibits promoter activity

7 July 2018

1 reference

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Genotyping for human whole-genome scans: past, present, and future

7 July 2018

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7 July 2018

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Trinucleotide repeat length instability and age of onset in Huntington's disease

7 July 2018

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Mutation of human short tandem repeats

7 July 2018

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The molecular mechanism of phase variation of H. influenzae lipopolysaccharide

7 July 2018

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Fimbrial phase variation in Bordetella pertussis: a novel mechanism for transcriptional regulation

7 July 2018

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Molecular basis of Mycoplasma surface antigenic variation: a novel set of divergent genes undergo spontaneous mutation of periodic coding regions and 5' regulatory sequences

7 July 2018

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Meiotic stability and genotype-phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophy

7 July 2018

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A genetic defect caused by a triplet repeat expansion in Arabidopsis thaliana

7 July 2018

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Shortened microsatellite d(CA)21 sequence down-regulates promoter activity of matrix metalloproteinase 9 gene

27 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26642241

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genotyping and functional analysis of a polymorphic (CCTTT)(n) repeat of NOS2A in diabetic retinopathy

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26642241

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The UK10K project identifies rare variants in health and disease

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.3461

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NG.3461

1 reference

2 August 2017

1 reference

2 August 2017

1 reference