Dominant Hereditary Inclusion-Body Myopathy Gene (IBM3) Maps to Chromosome Region 17p13.1

A comprehensive genetic map of the human genome based on 5,264 microsatellites

1996 • 2,983 citations

Strategies for multilocus linkage analysis in humans.

1984 • 2,600 citations

Comprehensive Human Genetic Maps: Individual and Sex-Specific Variation in Recombination

1998 • 1,092 citations

Inclusion body myositis and myopathies

1995 • 806 citations

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

1998 • 606 citations

Three myosin heavy-chain isozymes appear sequentially in rat muscle development

1981 • 589 citations

Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle

1996 • 586 citations

INCLUSION BODY MYOSITIS

1989 • 570 citations

A Comprehensive Human Linkage Map with Centimorgan Density

1994 • 547 citations

A mutation in the α tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy

1995 • 358 citations

Co-expression of multiple myosin heavy chain genes, in addition to a tissue-specific one, in extraocular musculature.

1985 • 293 citations

Statistical methods for multipoint radiation hybrid mapping.

1991 • 288 citations

Familial distal myopathy with rimmed vacuole and lamellar (myeloid) body formation

1981 • 277 citations

The role of cytoskeletal proteins in cardiomyopathies

1998 • 275 citations

“Rimmed vacuole myopathy” sparing the quadriceps

1984 • 254 citations

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

1993 • 203 citations

Human cardiac myosin heavy chain genes and their linkage in the genome

1987 • 166 citations

Tibial Muscular Dystrophy

1993 • 144 citations

Multigene Family for Sarcomeric Myosin Heavy Chain in Mouse and Human DNA: Localization on a Single Chromosome

1983 • 141 citations

Sporadic inclusion-body myositis and hereditary inclusion-body myopathies: current concepts of diagnosis and pathogenesis

1998 • 117 citations

Hereditary Inclusion Body Myopathy Maps to Chromosome 9p1-q1

1996 • 102 citations

Autosomal dominant myopathy with congenital joint contractures, ophthalmoplegia, and rimmed vacuoles

1998 • 89 citations

Assignment of the Tibial Muscular Dystrophy Locus to Chromosome 2q31

1998 • 88 citations

Gene locus for autosomal recessive distal myopathy with rimmed vacuoles maps to chromosome 9

1997 • 83 citations

Rimmed vacuoles

1980 • 72 citations

The spectrum of familial inclusion body myopathies in 13 families and a description of a quadriceps-sparing phenotype in non-Iranian Jews

1996 • 64 citations

Sporadic Inclusion-body Myositis and Its Similarities to Alzheimer Disease Brain: Recent Approaches to Diagnosis and Pathogenesis, and Relation to Aging

1998 • 59 citations

Familial inclusion body myositis

1992 • 57 citations

Distal Myopathy Histochemical and Ultrastructural Studies

1982 • 52 citations

Organization of the human skeletal myosin heavy chain gene cluster.

1992 • 51 citations

Various types of herediary inclusion body myopathies map to chromosome 9p1‐q1

1997 • 49 citations

Inclusion body myositis and welander distal myopathy: a clinical, neurophysiological and morphological comparison

1991 • 35 citations

Oculopharyngeal muscular dystrophy and distal myopathy

1982 • 35 citations

Presence of inclusion body myositis‐like filaments in oculopharyngeal muscular dystrophy. Ultrastructural study of 10 cases

1990 • 32 citations

Tibial muscular dystrophy

1997 • 31 citations

Five skeletal myosin heavy chain genes are organized as a multigene complex in the human genome

1993 • 23 citations

Hereditary Inclusion Body Myopathy

1998 • 6 citations