(Q34995233)

English

Chromosome 16q22 variants in a region associated with cardiovascular phenotypes correlate with ZFHX3 expression in a transcript-specific manner

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

Chromosome 16q22 variants in a region associated with cardiovascular phenotypes correlate with ZFHX3 expression in a transcript-specific manner (English)

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

4

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Bongani M Mayosi

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

Bernard Keavney

6

object named as

Bernard D Keavney

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

Michael S Cunnington

3

object named as

Michael S Cunnington

1 reference

Europe PubMed Central

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5 August 2017

author name string

Ruairidh I R Martin

1

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

W Andrew Owens

2

1 reference

Europe PubMed Central

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5 August 2017

Mauro Santibáñez Koref

5

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Europe PubMed Central

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5 August 2017

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publication date

24 December 2014

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Europe PubMed Central

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5 August 2017

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Europe PubMed Central

PubMed publication ID

5 August 2017

15

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

136

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

copyright license

Creative Commons Attribution 4.0 International

1 December 2014

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April 2022 Public Data File from Crossref

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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=4301889

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1 reference

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1 reference

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1 reference

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Patterns of cis regulatory variation in diverse human populations

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1 reference

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1 reference

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8 July 2018

Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry

1 reference

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8 July 2018

A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke

1 reference

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The MIQE guidelines: minimum information for publication of quantitative real-time PCR experiments

1 reference

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A genome-wide association study identifies novel and functionally related susceptibility Loci for Kawasaki disease

1 reference

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Validating discovered Cis-acting regulatory genetic variants: application of an allele specific expression approach to HapMap populations

1 reference

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Targeted screening of cis-regulatory variation in human haplotypes

1 reference

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Frequent somatic mutations of the transcription factor ATBF1 in human prostate cancer

1 reference

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1 reference

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8 July 2018

The structure of haplotype blocks in 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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21 January 2018

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1 reference

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12 December 2020

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Identifiers

10.1186/S12863-014-0136-1

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

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PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

ResearchGate publication ID

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