(Q28652887)

25 June 2017

title

Prioritizing causal disease genes using unbiased genomic features (English)

1 reference

25 June 2017

1 reference

1 reference

Janine F Felix

7

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Frederick P. Roth

object named as

Frederick P Roth

13

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Ramachandran S. Vasan

object named as

Ramachandran S Vasan

8

0 references

Rameen Beroukhim

9

object named as

Rameen Beroukhim

1 reference

25 June 2017

Rahul C Deo

1

1 reference

25 June 2017

Gabriel Musso

2

1 reference

25 June 2017

Murat Tasan

3

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25 June 2017

Paul Tang

4

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25 June 2017

Annie Poon

5

1 reference

25 June 2017

Christiana Yuan

6

1 reference

25 June 2017

Teresa De Marco

10

1 reference

25 June 2017

Pui-Yan Kwok

11

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25 June 2017

Calum A MacRae

12

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25 June 2017

language of work or name

English

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publication date

3 December 2014

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25 June 2017

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25 June 2017

volume

15

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25 June 2017

issue

12

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25 June 2017

page(s)

534

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Creative Commons Attribution 4.0 International

25 June 2017

copyright license

start time

1 December 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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HSPB1, HSPB6, HSPB7 and HSPB8 protect against RhoA GTPase-induced remodeling in tachypaced atrial myocytes

17 March 2017

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A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy

17 March 2017

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17 March 2017

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Wnt11 patterns a myocardial electrical gradient through regulation of the L-type Ca(2+) channel

17 March 2017

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Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data

17 March 2017

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17 March 2017

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17 March 2017

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Most mammalian mRNAs are conserved targets of microRNAs

17 March 2017

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Mapping the genetic architecture of gene expression in human liver

17 March 2017

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Evolving gene/transcript definitions significantly alter the interpretation of GeneChip data

17 March 2017

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Complement factor H polymorphism in age-related macular degeneration

17 March 2017

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17 March 2017

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A gene atlas of the mouse and human protein-encoding transcriptomes

17 March 2017

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A comparison of normalization methods for high density oligonucleotide array data based on variance and bias

17 March 2017

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The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms

17 March 2017

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17 March 2017

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TRANSFAC: a database on transcription factors and their DNA binding sites

17 March 2017

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17 March 2017

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A framework for variation discovery and genotyping using next-generation DNA sequencing data

17 March 2017

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Genetic mapping in human disease

7 April 2017

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A human phenome-interactome network of protein complexes implicated in genetic disorders

7 April 2017

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7 April 2017

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Evolution and functional impact of rare coding variation from deep sequencing of human exomes

7 April 2017

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7 April 2017

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Novel cardiovascular gene functions revealed via systematic phenotype prediction in zebrafish

7 April 2017

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Identifying multiple causative genes at a single GWAS locus

3 June 2018

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Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

3 June 2018

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Where genome meets phenome: rationale for integrating genetic and protein biomarkers in the diagnosis and management of dilated cardiomyopathy and heart failure.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4279789

Genetics of hypertrophic cardiomyopathy after 20 years: clinical perspectives

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4279789

Meta-analysis identifies six new susceptibility loci for atrial fibrillation

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4279789

A Resource of Quantitative Functional Annotation for Homo sapiens Genes

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4279789

Assessing fracture risk using gradient boosting machine (GBM) models

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4279789

Truncations of titin causing dilated cardiomyopathy.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4279789

Needles in stacks of needles: finding disease-causal variants in a wealth of genomic data

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4279789

Haploinsufficiency of target of rapamycin attenuates cardiomyopathies in adult zebrafish

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4279789

Prioritizing candidate disease genes by network-based boosting of genome-wide association data.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4279789

Quantitative proteomic analysis of PCSK9 gain of function in human hepatic HuH7 cells

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4279789

Proteins encoded in genomic regions associated with immune-mediated disease physically interact and suggest underlying biology

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4279789

Analysing biological pathways in genome-wide association studies

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4279789

Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4279789

Deciphering the splicing code

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4279789

A quantitative model of transcriptional regulation reveals the influence of binding location on expression

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4279789

Lack of Apobec2-related proteins causes a dystrophic muscle phenotype in zebrafish embryos

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4279789

Genome-wide association study of PR interval

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4279789

Next generation software for functional trend analysis

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4279789

Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4279789

Validating, augmenting and refining genome-wide association signals

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4279789

Common variants at ten loci influence QT interval duration in the QTGEN Study

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4279789

The Human Phenotype Ontology: a tool for annotating and analyzing human hereditary disease

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4279789

Molecular etiology and pathogenesis of hereditary cardiomyopathy

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4279789

Complement-targeted therapeutics

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4279789

ECRbase: database of evolutionary conserved regions, promoters, and transcription factor binding sites in vertebrate genomes

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4279789

Gene prioritization through genomic data fusion

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4279789

A mutation in the dimerization domain of filamin c causes a novel type of autosomal dominant myofibrillar myopathy.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4279789

Dilated cardiomyopathy and heart failure caused by a mutation in phospholamban

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4279789

The Genetic Basis for Cardiomyopathy

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4279789

Left ventricular dilatation and the risk of congestive heart failure in people without myocardial infarction.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4279789

Glycogen-branching enzyme deficiency leads to abnormal cardiac development: novel insights into glycogen storage disease IV.

3 June 2018

1 reference

https://api.crossref.org/works/10.1186%2FS13059-014-0534-8

Characterization and investigation of zebrafish models of filamin-related myofibrillar myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS13059-014-0534-8

Gene expression analyses reveal molecular relationships among 20 regions of the human CNS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS13059-014-0534-8

Inherited Cardiomyopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS13059-014-0534-8

Greedy function approximation: A gradient boosting machine

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS13059-014-0534-8

10.1186/S13059-014-0534-8

21 January 2018

Identifiers

DOI

1 reference

Dimensions Publication ID

25 June 2017

1010160022

0 references

OpenCitations bibliographic resource ID

2487884

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2487884

1 reference