(Q47650845)

4 February 2018

title

A Comparison of Whole Genome Sequencing to Multigene Panel Testing in Hypertrophic Cardiomyopathy Patients. (English)

1 reference

4 February 2018

hypertrophic cardiomyopathy

main subject

whole genome sequencing

1 reference

based on heuristic

inferred from title

1 reference

Matthew Lebo

10

0 references

Robert C. Green

12

Robert C Green

1 reference

4 February 2018

3

Barbara McDonough

1 reference

4 February 2018

Christine E. Seidman

14

Christine E Seidman

1 reference

4 February 2018

Heidi L. Rehm

8

Heidi L Rehm

1 reference

4 February 2018

Lauren Conner

4

Lauren Conner

1 reference

4 February 2018

Allison L Cirino

1

Allison L Cirino

1 reference

4 February 2018

Neal K Lakdawala

2

Neal K Lakdawala

1 reference

4 February 2018

Calum MacRae

13

Calum A MacRae

1 reference

4 February 2018

author name string

Dale Adler

5

1 reference

4 February 2018

Mark Weinfeld

6

1 reference

4 February 2018

Patrick O'Gara

7

1 reference

4 February 2018

Kalotina Machini

9

1 reference

4 February 2018

Carrie Blout

11

1 reference

4 February 2018

Carolyn Y Ho

15

1 reference

4 February 2018

MedSeq Project*

16

1 reference

4 February 2018

publication date

1 October 2017

1 reference

4 February 2018

Circulation: Cardiovascular Genetics

published in

1 reference

4 February 2018

volume

10

1 reference

4 February 2018

issue

5

1 reference

4 February 2018

Preferences for the Return of Individual Results From Research on Pediatric Biobank Samples

cites work

1 reference

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Screening of the Filamin C Gene in a Large Cohort of Hypertrophic Cardiomyopathy Patients.

26 August 2018

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26 August 2018

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Evaluation of the Mayo Clinic Phenotype-Based Genotype Predictor Score in Patients with Clinically Diagnosed Hypertrophic Cardiomyopathy

26 August 2018

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Biallelic Truncating Mutations in ALPK3 Cause Severe Pediatric Cardiomyopathy.

26 August 2018

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26 August 2018

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Mutations in FLNC are Associated with Familial Restrictive Cardiomyopathy.

26 August 2018

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Exome Sequencing Identifies Pathogenic and Modifier Mutations in a Child With Sporadic Dilated Cardiomyopathy

26 August 2018

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Comprehensive red blood cell and platelet antigen prediction from whole genome sequencing: proof of principle

26 August 2018

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Genetic risk assessment and prevention: the role of genetic testing panels in breast cancer

26 August 2018

1 reference

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26 August 2018

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Cardiomyopathies in Noonan syndrome and the other RASopathies

26 August 2018

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26 August 2018

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26 August 2018

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26 August 2018

1 reference

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Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity.

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5683423

Genetics of breast cancer: a topic in evolution

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5683423

Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy

26 August 2018

1 reference

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26 August 2018

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Targeted analysis of whole genome sequence data to diagnose genetic cardiomyopathy

26 August 2018

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26 August 2018

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26 August 2018

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26 August 2018

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26 August 2018

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26 August 2018

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26 August 2018

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26 August 2018

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26 August 2018

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Toronto hypertrophic cardiomyopathy genotype score for prediction of a positive genotype in hypertrophic cardiomyopathy.

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5683423

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26 August 2018

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26 August 2018

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A novel splice site mutation in EYA4 causes DFNA10 hearing loss.

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5683423

Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domain.

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5683423

Integrin-linked kinase at the heart of cardiac contractility, repair, and disease.

26 August 2018

1 reference

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Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing loss

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5683423

2011 ACCF/AHA Guideline for the Diagnosis and Treatment of Hypertrophic Cardiomyopathy: A Report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines

26 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5683423

Diagnostic clinical genome and exome sequencing

1 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/29030401

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Prevalence of C282Y and H63D mutations in the hemochromatosis (HFE) gene in the United States

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/29030401

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1161/CIRCGENETICS.117.001768

1 reference

4 February 2018

0 references

1 reference

4 February 2018