Mapping of the serotonin 5‐HT_{1<scp>D</scp>β} autoreceptor gene on chromosome 6 and direct analysis for sequence variants

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

1987 • 6,762 citations

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

1989 • 3,557 citations

Strategies for multilocus linkage analysis in humans.

1984 • 2,600 citations

A second-generation linkage map of the human genome

1992 • 1,721 citations

Identity of inhibitory presynaptic 5-hydroxytryptamine (5-HT) autoreceptors in the rat brain cortex with 5-HT1B binding sites

1986 • 686 citations

CSF Biochemistries, Glucose Metabolism, and Diurnal Activity Rhythms in Alcoholic, Violent Offenders, Fire Setters, and Healthy Volunteers

1994 • 564 citations

A proposed new nomenclature for 5-HT receptors

1993 • 551 citations

Cerebrospinal Fluid Monoamine Metabolite Levels in Male Arsonists

1987 • 370 citations

A Comprehensive Genetic Linkage Map of the Human Genome

1992 • 355 citations

Multiple mutations in highly conserved residues are found in mildly affected cystic fibrosis patients

1990 • 353 citations

Human serotonin 1D receptor is encoded by a subfamily of two distinct genes: 5-HT1D alpha and 5-HT1D beta.

1992 • 293 citations

Population and Pedigree Studies Reveal a Lack of Association Between the Dopamine D2 Receptor Gene and Alcoholism

1990 • 280 citations

Optimization of the single-strand conformation polymorphism (SSCP) technique for detection of point mutations

1993 • 238 citations

Primary structure and functional characterization of a human 5-HT1D-type serotonin receptor.

1991 • 225 citations

Stereoselective blockade at [3H]5-HT binding sites and at the 5-HT autoreceptor by propranolol

1984 • 206 citations

North Carolina macular dystrophy is assigned to chromosome 6

1992 • 173 citations

Characterization of the human 5-hydroxytryptamine1B receptor.

1992 • 172 citations

Family History of Alcoholism in Violent Offenders and Impulsive Fire Setters

1989 • 146 citations

Expression of mRNA for the serotonin 5-hydroxytryptamine1D beta receptor subtype in human and bovine cerebral arteries.

1993 • 136 citations

Serotonin 1B receptors in the developing somatosensory and visual cortices are located on thalamocortical axons.

1993 • 115 citations

DRD2 Dopamine Receptor Genotype, Linkage Disequilibrium, and Alcoholism in American Indians and Other Populations

1993 • 114 citations

Opposing roles for 5‐HT_1B and 5‐HT₃ receptors in the control of 5‐HT release in rat hippocampus in vivo

1992 • 106 citations

A human serotonin 1D receptor variant (5HT1D beta) encoded by an intronless gene on chromosome 6.

1992 • 95 citations

Molecular cloning of a human serotonin receptor (S12) with a pharmacological profile resembling that of the 5-HT1D subtype.

1992 • 75 citations

Congenital anomalies including the VATER association in a patient with a del(6)q deletion

1977 • 66 citations

Chromosomal mapping of A1 and A2 adenosine receptors, VIP receptor, and a new subtype of serotonin receptor

1991 • 64 citations

Deletions of the long arm of chromosome 6: Two new cases and review of the literature

1985 • 52 citations

Detecting high-resolution polymorphisms in human coding loci by combining PCR and single-strand conformation polymorphism (SSCP) analysis.

1991 • 47 citations

New Polymorphism for the Human Serotonin 1D Receptor Variant (5-HT&lt;sub&gt;1D&amp;beta;&lt;/sub&gt;) not Linked to Schizophrenia in Five Canadian Pedigrees

1993 • 41 citations

5-HT1 receptor binding sites in the guinea pig superior colliculus are predominantly of the 5-HT1D class and are presynaptically located on primary retinal afferents

1990 • 36 citations

Deletion of proximal 6q: A clinical report and review of the literature

1986 • 27 citations

Ocular albinism in a male with del (6)(q13–q15): Candidate region for autosomal recessive ocular albinism?

1992 • 24 citations

Interstitial deletion (6) (q11----q15) in an infant with congenital abnormalities.

1988 • 18 citations

Partial trisomy 6q and bilateral retinal detachment

1986 • 18 citations

Single-stranded conformation polymorphism analysis of the CFTR gene in slovenian cystic fibrosis patients: Detection of mutations and sequence variations

1993 • 18 citations