Back to search

Genotype-phenotype correlations in hypertrophic cardiomyopathy. Insights provided by comparisons of kindreds with distinct and identical beta-myosin heavy chain gene mutations.

Data up to Jan 2025

Published1994
Citations223
References35
Clinical Trials (1)

Total Citations Per Year

Abstract

References (35)

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

1989 • 3,557 citations

A molecular basis for familial hypertrophic cardiomyopathy: A β cardiac myosin heavy chain gene missense mutation

1990 • 1,332 citations

Polymorphic DNA region adjacent to the 5' end of the human insulin gene.

1981 • 910 citations

Hypertrophic Cardiomyopathy

1987 • 907 citations

Enhanced Detection of Ischemic but Viable Myocardium by the Reinjection of Thallium after Stress-Redistribution Imaging

1990 • 801 citations

Intramural (“small vessel”) coronary artery disease in hypertrophic cardiomyopathy

1986 • 740 citations

Characteristics and Prognostic Implications of Myosin Missense Mutations in Familial Hypertrophic Cardiomyopathy

1992 • 732 citations

Prognosis in hypertrophic cardiomyopathy: Role of age and clinical, electrocardiographic and hemodynamic features

1981 • 631 citations

Patterns and significance of distribution of left ventricular hypertrophy in hypertrophic cardiomyopathy

1981 • 611 citations

Causes of sudden death in competitive athletes

1986 • 531 citations

Mapping a Gene for Familial Hypertrophic Cardiomyopathy to Chromosome 14q1

1989 • 526 citations

Prognostic significance of 24 hour ambulatory electrocardiographic monitoring in patients with hypertrophic cardiomyopathy: A prospective study

1981 • 491 citations

Arrhythmia in hypertrophic cardiomyopathy. I: Influence on prognosis.

1981 • 417 citations

Effects of verapamil on left ventricular systolic function and diastolic filling in patients with hypertrophic cardiomyopathy.

1981 • 401 citations

Myocardial ischemia detected by thallium scintigraphy is frequently related to cardiac arrest and syncope in young patients with hypertrophic cardiomyopathy

1993 • 276 citations

Skeletal muscle expression and abnormal function of beta-myosin in hypertrophic cardiomyopathy.

1993 • 239 citations

“Malignant” hypertrophic cardiomyopathy: Identification of a subgroup of families with unusually frequent premature death

1978 • 213 citations

Hypertrophic cardiomyopathy: an important cause of sudden death.

1984 • 204 citations

Missense mutations in the beta-myosin heavy-chain gene cause central core disease in hypertrophic cardiomyopathy.

1993 • 203 citations

Utility of continuous wave doppler echocardiography in the noninvasive assessment of left ventricular outflow tract pressure gradient in patients with hypertrophic cardiomyopathy

1992 • 197 citations

A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3

1993 • 191 citations

Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11

1993 • 186 citations

Preclinical Diagnosis of Familial Hypertrophic Cardiomyopathy by Genetic Analysis of Blood Lymphocytes

1991 • 186 citations

A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2.

1993 • 177 citations

Hypertrophic cardiomyopathy without hypertrophy: two families with myocardial disarray in the absence of increased myocardial mass.

1990 • 166 citations

Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease.

1990 • 153 citations

Complete sequence and organization of the human cardiac β-myosin heavy chain gene

1990 • 131 citations

Affinity generation of single-stranded DNA for dideoxy sequencing following the polymerase chain reaction

1989 • 113 citations

Detection of a new mutation in the beta-myosin heavy chain gene in an individual with hypertrophic cardiomyopathy.

1992 • 85 citations

Hemodynamic and electrophysiologic evaluation of patients with hypertrophic cardiomyopathy surviving cardiac arrest

1991 • 58 citations

Novel missense mutation in cardiac β myosin heavy chain gene found in a japanese patient with hypertrophic cardiomyopathy

1992 • 46 citations

Identification of a mutation in the beta cardiac myosin heavy chain gene in a family with hypertrophic cardiomyopathy.

1993 • 26 citations

Genetic evidence of dissociation (generational skips) of electrical from morphologic forms of hypertrophic cardiomyopathy

1990 • 23 citations

Ischemia, Coronary Blood Flow, and Coronary Reserve in Hypertrophic Cardiomyopathy

1990 • 7 citations

Left Ventricular Diastolic Function and Myocardial Ischemia in Hypertrophic Cardiomyopathy: Assessment by Radionuclide Methods

1990 • 2 citations

Cited By (0)

No citing papers found in database

Genotype-phenotype correlations in hypertrophic cardiomyopathy. Insights provided by… (1994) – Circulation | Metascience Observatory Explorer