Missense Mutations in the Rod Domain of the Lamin A/C Gene as Causes of Dilated Cardiomyopathy and Conduction-System Disease

Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

1987 • 2,353 citations

Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy

1999 • 1,318 citations

A Structural Scaffolding of Intermediate Filaments in Health and Disease

1998 • 1,003 citations

Idiopathic Dilated Cardiomyopathy

1994 • 976 citations

The nuclear envelope lamina is reversibly depolymerized during mitosis

1980 • 956 citations

Characterization of Dystrophin in Muscle-Biopsy Specimens from Patients with Duchenne's or Becker's Muscular Dystrophy

1988 • 910 citations

Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy

1994 • 874 citations

cDNA sequencing of nuclear lamins A and C reveals primary and secondary structural homology to intermediate filament proteins.

1986 • 711 citations

Nuclear Lamins: Their Structure, Assembly, and Interactions

1998 • 708 citations

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

1992 • 704 citations

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

1998 • 606 citations

X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus.

1993 • 513 citations

Frequency and Phenotypes of Familial Dilated Cardiomyopathy

1998 • 435 citations

Deletion of the Dystrophin Muscle-Promoter Region Associated with X-Linked Dilated Cardiomyopathy

1993 • 413 citations

Emerin deficiency at the nuclear membrane in patients with Emery-Dreif uss muscular dystrophy

1996 • 337 citations

The causes of dilated cardiomyopathy: A clinicopathologic review of 673 consecutive patients

1994 • 301 citations

Disruption of Nuclear Lamin Organization Alters the Distribution of Replication Factors and Inhibits DNA Synthesis

1997 • 281 citations

Report of the National Heart, Lung, and Blood Institute Special Emphasis Panel on Heart Failure Research

1997 • 221 citations

A- and B-type lamins are differentially expressed in normal human tissues

1997 • 211 citations

Mapping a cardiomyopathy locus to chromosome 3p22-p25.

1996 • 193 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

Intermediate filament assembly: fibrillogenesis is driven by decisive dimer-dimer interactions

1998 • 155 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

Nuclear lamina and organization of nuclear architecture

1986 • 138 citations

Familial Dilated Cardiomyopathy Locus Maps to Chromosome 2q31

1999 • 136 citations

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

1995 • 132 citations

Implications of intermediate filament protein phosphorylation

1996 • 106 citations

Distribution of emerin and lamins in the heart and implications for Emery-Dreifuss muscular dystrophy

1999 • 104 citations

Cardiac Features of an Unusual X-Linked Humeroperoneal Neuromuscular Disease

1975 • 99 citations

Chromosomal Assignment of Human Nuclear Envelope Protein Genes LMNA, LMNB1, and LBR by Fluorescencein SituHybridization

1996 • 99 citations

Emery-Dreifuss Muscular Dystrophy: Disease Spectrum and Differential Diagnosis

1988 • 86 citations

X‐linked muscular dystrophy with early contractures and cardiomyopathy (Emery‐Dreifuss type)

1987 • 82 citations

Scapuloperoneal Muscular Atrophy With Cardiopathy

1973 • 58 citations

Concomitant deficiency of β- and γ-sarcoglycans in 20 α-sarcoglycan (adhalin)-deficient patients: immunohistochemical analysis and clinical aspects

1997 • 43 citations

60th ENMC International Workshop: Non X-linked Emery–Dreifuss Muscular Dystrophy, 5–7 June 1998, Naarden, The Netherlands

1999 • 42 citations

Familial Congenital Sinus Rhythm Anomalies: Clinical and Pathological Correlations

1992 • 32 citations

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