Fine-Structure Mapping of the Hereditary Inclusion Body Myopathy Locus

Strategies for multilocus linkage analysis in humans.

1984 • 2,600 citations

α-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere

1994 • 1,008 citations

Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A

1995 • 976 citations

The diastrophic dysplasia gene encodes a novel sulfate transporter: Positional cloning by fine-structure linkage disequilibrium mapping

1994 • 751 citations

A powerful likelihood method for the analysis of linkage disequilibrium between trait loci and one or more polymorphic marker loci.

1995 • 460 citations

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

1995 • 358 citations

The molecular basis for tropomyosin isoform diversity

1991 • 350 citations

A metric map of humans: 23,500 loci in 850 bands

1996 • 265 citations

“Rimmed vacuole myopathy” sparing the quadriceps

1984 • 254 citations

Linkage disequilibrium predicts physical distance in the adenomatous polyposis coli region.

1994 • 129 citations

Hereditary Inclusion Body Myopathy Maps to Chromosome 9p1-q1

1996 • 102 citations

New advances in the understanding of sporadic inclusion-body myositis and hereditary inclusion-body myopathies

1995 • 98 citations

Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA marker.

1991 • 93 citations

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

1997 • 83 citations

Vacuolar myopathy sparing the quadriceps

1993 • 63 citations

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

1997 • 49 citations

Construction and characterization of radiation hybrids for chromosome 9, and their use in mapping cosmid probes on the chromosome

1992 • 12 citations