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Article

Transthyretin V142I Genetic Variant and Cardiac Remodeling, Injury, and Heart Failure Risk in Black Adults

8 Dec 2021

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 35115086
DOI: 10.1016/j.jchf.2021.09.006

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Transthyretin V142I Genetic Variant and Cardiac Remodeling, Injury, and Heart Failure Risk in Black AdultsPMID 35115086Read ↗

Cardiovascular Risk Factors and Genetic Risk in Transthyretin V142I Carriers.Semantic proximity Read ↗

The amyloidogenic V122I transthyretin variant in elderly black Americans.Semantic proximity Read ↗

Clinical Implications of the Amyloidogenic V122I Transthyretin Variant in the General Population.Semantic proximity Read ↗

Hereditary Transthyretin Cardiac Amyloidosis With the p.V142I Variant: Mechanistic Insights and Diagnostic Challenges.Semantic proximity Read ↗

Genomic Screening for Pathogenic Transthyretin Variants Finds Evidence of Underdiagnosed Amyloid Cardiomyopathy From Health RecordsSemantic proximity Read ↗

V122I Transthyretin Cardiomyopathy: An Opportunity to Build Trust and Resolve Disparities.Semantic proximity Read ↗

Left ventricular strain does not differentiate amyloidogenic profiles in at-risk individuals with<i>TTR</i>Val142IleSemantic proximity Read ↗

Enrichment for Cases of African-American Patients with Pathogenic <i>TTR</i> V142I Variant in the TOPCAT TrialSemantic proximity Read ↗

Prevalence, Cardiac Phenotype, and Outcomes of Transthyretin Variants in the UK Biobank Population.Semantic proximity Read ↗

Association of the V122I Hereditary Transthyretin Amyloidosis Genetic Variant With Heart Failure Among Individuals of African or Hispanic/Latino Ancestry.Semantic proximity Read ↗

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Genome-wide association analysis reveals insights into the genetic architecture of right ventricular structure and functionSemantic proximity Read ↗

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