Human gene for torsion dystonia located on chromosome 9q32-q34

MAPMAKER: An interactive computer package for constructing primary genetic linkage maps of experimental and natural populations

1987 • 6,762 citations

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

1984 • 4,899 citations

Dystrophin: The protein product of the duchenne muscular dystrophy locus

1987 • 4,477 citations

Hypervariable ‘minisatellite’ regions in human DNA

1985 • 3,789 citations

Variable Number of Tandem Repeat (VNTR) Markers for Human Gene Mapping

1987 • 1,683 citations

A genetic linkage map of the human genome

1987 • 913 citations

Actions of cytochalasins on the organization of actin filaments and microtubules in a neuronal growth cone.

1988 • 851 citations

Control of cytoplasmic actin gel–sol transformation by gelsolin, a calcium-dependent regulatory protein

1979 • 782 citations

[9] Gel electrophoresis of restriction fragments

1979 • 653 citations

The retinoblastoma susceptibility gene encodes a nuclear phosphoprotein associated with DNA binding activity

1987 • 649 citations

THE ANATOMICAL BASIS OF SYMPTOMATIC HEMIDYSTONIA

1985 • 587 citations

Hereditary progressive dystonia with marked diurnal fluctuation

1991 • 459 citations

The Varied Clinical Expressions of Dystonia

1984 • 401 citations

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

1984 • 355 citations

Construction of linkage maps with DNA markers for human chromosomes

1985 • 325 citations

Familial paroxysmal dystonic choreoathetosis and its differentiation from related syndromes

1977 • 290 citations

Hereditary progressive dystonia with marked diurnal fluctuation

2000 • 270 citations

Gelsolin: Calcium‐ and polyphosphoinositide‐regulated actin‐ modulating protein

1987 • 228 citations

Familial aggregation in Alzheimer's disease

1988 • 195 citations

Dopa-responsive dystonia

2012 • 192 citations

Isolated Failure of Autonomic Noradrenergic Neurotransmission

1986 • 181 citations

Precise localization of human beta-globin gene complex on chromosome 11.

1979 • 175 citations

Genomic organization and biosynthesis of secreted and cytoplasmic forms of gelsolin

1988 • 165 citations

The torsion dystonias

1970 • 165 citations

CONGENITAL DOPAMINE-BETA-HYDROXYLASE DEFICIENCY

1987 • 164 citations

Muscle is the major source of plasma gelsolin.

1988 • 154 citations

Leber's disease and dystonia

1986 • 153 citations

Torsion dystonia in Panay, Philippines.

1976 • 144 citations

The primary structure of human dopamine-beta-hydroxylase: insights into the relationship between the soluble and the membrane-bound forms of the enzyme.

1987 • 125 citations

Efficient computations in multilocus linkage analysis.

1988 • 117 citations

Pieces in the actin-severing protein puzzle

1988 • 112 citations

Dopa responsive dystonia.

1989 • 103 citations

Hereditary myoclonic dystonia, hereditary torsion dystonia and hereditary essential myoclonus: an area of confusion.

1988 • 99 citations

Localization of the human dopamine beta hydroxylase (DBH) gene to chromosome 9q34

1988 • 91 citations

The ‘singles’ method for segregation analysis under incomplete ascertainment

1979 • 85 citations

Inheritance of idiopathic torsion dystonia among Jews.

1984 • 82 citations

Primary dystonias: a review of the pathology and suggestions for new directions of study.

1988 • 81 citations

Elevated Plasma Dopamine-β-Hydroxylase Activity in Autosomal Dominant Torsion Dystonia

1973 • 78 citations

Paroxysmal non-kinesigenic dystonia.

1988 • 74 citations

Linkage of a gene regulating dopamine-beta-hydroxylase activity and the ABO blood group locus.

1988 • 71 citations

Localization of gelsolin proximal to ABL on chromosome 9.

1988 • 69 citations

Pathology of the torsion dystonias (dystonia musculorum deformans)

1970 • 66 citations

A mapped set of genetic markers for human chromosome 9

1988 • 65 citations

Dystonia musculorum--an inherited disease of the nervous system in the mouse.

1976 • 60 citations

Dispersion of argininosuccinate synthetase-like human genes to multiple autosomes and the X chromosome

1982 • 56 citations

Postural Asymmetry and Movement Disorder After Unilateral Microinjection of Adrenocorticotropin 1-24 in Rat Brainstem

1982 • 44 citations

The Human as an Experimental System in Molecular Genetics

1988 • 42 citations

Myoclonus and dystonia: a family study.

1988 • 39 citations

Studies on Dystonia Musculorum Deformans

1962 • 38 citations

Neuropharmacological correlates of the motor syndrome of the genetically dystonic (dt) rat.

1988 • 37 citations

Multilocus linkage analysis with the human argininosuccinate synthetase gene

1989 • 33 citations

Generalized Dystonia

1986 • 31 citations

Biochemical findings in symptomatic dystonias.

1988 • 31 citations

Generalized Dystonia

1986 • 29 citations

Analysis of the clinical course of non‐Jewish, autosomal dominant torsion dystonia

1986 • 25 citations

Autosomal dominant torsion dystonia in a Swedish family.

1988 • 25 citations

Plasma norepinephrine and dopamine-beta-hydroxylase in dystonia.

1976 • 24 citations

Isolation and mapping of a polymorphic DNA sequence pMCT112 on chromosome 9q (D9S15)

1987 • 21 citations

Linkage Analysis in a Family with Dominantly Inherited Torsion Dystonia: Exclusion of the Pro-Opiomelanocortin and Glutamic Acid Decarboxylase Genes and Other Chromosomal Regions Using DNA Polymorphisms

1986 • 21 citations

Biochemical evidence for brain neurotransmitter changes in idiopathic torsion dystonia (dystonia musculorum deformans).

1988 • 19 citations

Inheritance of idiopathic torsion dystonia among Ashkenazi Jews.

1988 • 17 citations

Possible involvement of brain noradrenergic neurons in dystonia.

1988 • 13 citations

The gelsolin (GSN) cDNA clone, from 9q32-34, identifies Bell and StuI RFLPs

1989 • 10 citations

Isolation and mapping of a polymorphic DNA sequence pMCT112 on chromosome 9q (D9S10)

1987 • 9 citations

Molecular genetics of an autosomal dominant form of torsion dystonia.

1988 • 8 citations

Isolation and mapping of a polymorphic DNA sequence pEKZ19.3 on chromosome 9q (D9S17)

1987 • 4 citations

Exclusion of autosomal dominant dystonia gene from large regions of chromosomes 11p, 13q, and 21q by multi‐point linkage analysis

1987 • 2 citations

Linkage studies in families with dystonia: linkage analysis as a tool to locate and characterize the gene(s) for dystonia.

1988 • 1 citations

Deleted Work

1955 • 0 citations