Dilated Cardiomyopathy and Sensorineural Hearing Loss

Genetic Epidemiology of Hearing Impairment

1991 • 941 citations

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

1997 • 878 citations

The Frequency of Familial Dilated Cardiomyopathy in a Series of Patients with Idiopathic Dilated Cardiomyopathy

1992 • 704 citations

Epidemiology of idiopathic dilated and hypertrophic cardiomyopathy. A population-based study in Olmsted County, Minnesota, 1975-1984.

1989 • 621 citations

Actin Mutations in Dilated Cardiomyopathy, a Heritable Form of Heart Failure

1998 • 606 citations

Hereditary Hearing Loss and its Syndromes

1995 • 502 citations

Desmin Mutation Responsible for Idiopathic Dilated Cardiomyopathy

1999 • 449 citations

Prevalence and etiology of idiopathic dilated cardiomyopathy (summary of a National Heart, Lung, and Blood Institute Workshop)

1992 • 443 citations

Frequency and Phenotypes of Familial Dilated Cardiomyopathy

1998 • 435 citations

Inner Ear Defects Induced by Null Mutationof the isk Gene

1996 • 395 citations

Genes responsible for human hereditary deafness: symphony of a thousand

1996 • 276 citations

Distribution and Categorization of Echocardiographic Measurements in Relation to Reference Limits

1997 • 239 citations

Mapping a cardiomyopathy locus to chromosome 3p22-p25.

1996 • 193 citations

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

1993 • 191 citations

Familial dilated cardiomyopathy in the United Kingdom.

1995 • 190 citations

A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1–1q1

1994 • 183 citations

Maternally inherited cardiomyopathy and hearing loss associated with a novel mutation in the mitochondrial tRNA(Lys) gene (G8363A).

1996 • 173 citations

Linkage of Familial Dilated Cardiomyopathy with Conduction Defect and Muscular Dystrophy to Chromosome 6q23

1997 • 171 citations

Pod-1, a mesoderm-specific basic-helix-loop-helix protein expressed in mesenchymal and glomerular epithelial cells in the developing kidney

1998 • 160 citations

Capsulin: a novel bHLH transcription factor expressed in epicardial progenitors and mesenchyme of visceral organs

1998 • 150 citations

Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23.

1996 • 149 citations

Localization of a Gene Responsible for Familial Dilated Cardiomyopathy to Chromosome 1q32

1995 • 148 citations

Familial Dilated Cardiomyopathy Locus Maps to Chromosome 2q31

1999 • 136 citations

Involvement of IsK-Associated K ⁺ Channel in Heart Rate Control of Repolarization in a Murine Engineered Model of Jervell and Lange-Nielsen Syndrome

1998 • 135 citations

Linkage of familial dilated cardiomyopathy to chromosome 9. Heart Muscle Disease Study Group.

1995 • 132 citations

External Ophthalmoplegia, Pigmentary Degeneration of the Retina, and Cardiomyopathy: A Newly Recognized Syndrome.

1965 • 113 citations

epicardin: A novel basic helix-loop-helix transcription factor gene expressed in epicardium, branchial arch myoblasts, and mesenchyme of developing lung, gut, kidney, and gonads

1998 • 111 citations

Cloning of capsulin, a basic helix-loop-helix factor expressed in progenitor cells of the pericardium and the coronary arteries

1998 • 105 citations

Natural history of Alström syndrome in early childhood: Onset with dilated cardiomyopathy

1996 • 102 citations

Homozygosity Mapping of Alstrom Syndrome to Chromosome 2p

1997 • 73 citations

A gene for autosomal dominant late-onset progressive non-syndromic hearing loss, DFNA10, maps to chromosome 6

1996 • 68 citations

The American College of Cardiology Evaluation of Preventive Therapeutics (ACCEPT) study: attainment of goals for comprehensive risk reduction in patients with coronary disease in the US

1998 • 57 citations

Genetic deafness.

1992 • 52 citations

Cardiac transplantation in an incomplete Kearns-Sayre syndrome with mitochondrial DNA deletion

1993 • 47 citations

Diagnosis, prevention and treatment of hereditary sensorineural hearing loss

1977 • 23 citations