Genetic and radiation hybrid mapping of the hyperekplexia region on chromosome 5q.

DNA sequencing with chain-terminating inhibitors

1977 • 69,181 citations

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1983 • 26,063 citations

Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction.

1989 • 3,458 citations

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination.

1985 • 1,207 citations

Radiation Hybrid Mapping: A Somatic Cell Genetic Method for Constructing High-Resolution Maps of Mammalian Chromosomes

1990 • 630 citations

Human dopamine D1 receptor encoded by an intronless gene on chromosome 5

1990 • 471 citations

Use of cyclosporin a in establishing epstein-barr virus-transformed human lymphoblastoid cell lines

1984 • 355 citations

Direct selection: a method for the isolation of cDNAs encoded by large genomic regions.

1991 • 271 citations

Evidence for the Involvement of GM-CSF and FMS in the Deletion (5q) in Myeloid Disorders

1986 • 233 citations

THE HYPEREKPLEXIAS AND THEIR RELATIONSHIP TO THE NORMAL STARTLE REFLEX

1991 • 223 citations

cDNA selection: efficient PCR approach for the selection of cDNAs encoded in large chromosomal DNA fragments.

1991 • 211 citations

Localization of the genetic defect in familial adenomatous polyposis within a small region of chromosome 5.

1988 • 196 citations

STARTLE DISEASE OR HYPEREKPLEXIA FURTHER DELINEATION OF THE SYNDROME

1980 • 185 citations

Chromosomal organization of adrenergic receptor genes.

1990 • 129 citations

Chromosomal localization of GABAA receptor subunit genes: relationship to human genetic disease

1989 • 121 citations

Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: linkage of an autosomal dominant form to chromosome 5q.

1992 • 115 citations

Startle disease, or hyperekplexia: Response to clonazepam and assignment of the gene (STHE) to chromosome 5q by linkage analysis

1992 • 115 citations

Physiological abnormalities in hereditary hyperekplexia

1992 • 99 citations

Chromosomal localization of the human c-fmsoncogene

1983 • 92 citations

A FAMILY WITH EMOTIONALLY PRECIPITATEED “DROP SEIZURES”

1958 • 87 citations

Structure of human osteonectin based upon analysis of cDNA and genomic sequences

1989 • 83 citations

A simple scheme for the analysis of HLA linkages in pedigrees

1978 • 82 citations

A radiation hybrid map of 18 growth factor, growth factor receptor, hormone receptor, or neurotransmitter receptor genes on the distal region of the long arm of chromosome 5

1992 • 81 citations

Mapping of human chromosome 5 microsatellite DNA polymorphisms

1991 • 75 citations

Complex patterns of linkage disequilibrium in the Huntington disease region.

1991 • 72 citations

Hyperekplexia and sudden neonatal death

1992 • 67 citations

Molecular cloning and chromosomal localization of one of the human glutamate receptor genes.

1991 • 64 citations

Hyperekplexia

1983 • 61 citations

Hereditary Stiff-Baby Syndrome

1981 • 59 citations

Radiation hybrid map of 13 loci on the long arm of chromosome 5

1991 • 48 citations

Hyperexplexia: an inherited disorder of the startle response

1982 • 47 citations

Familial Startle Disease (Hyperexplexia)

1984 • 46 citations

Characterization of recombinant GABAA receptors produced in transfected cells from murine α1, β1, and γ2 subunit cDNAs

1991 • 45 citations

Familial Congenital Disorder Resembling Stiff-Man Syndrome

1972 • 44 citations

Congenital stiff‐man syndrome

1980 • 41 citations

Startle disease or hyperekplexia: Adolescent onset and response to valproate

1989 • 41 citations

Hyperekplexia: Pedigree studies in two families

1991 • 36 citations

Epigene conversion: a proposal with implications for gene mapping in humans.

1992 • 19 citations

Dinucleotide repeat polymorphism at the human c-fms proto-oncogene for the CFS-1 receptor (CFS1R)

1991 • 15 citations

Synthesis and incorporation of human ribosomal protein S14 into functional ribosomes in human-Chinese hamster cell hybrids containing human chromosome 5: HumanRPS14 gene is the structural gene for ribosomal protein S14

1985 • 13 citations