Association between a catechol-o-methyltransferase polymorphism and obsessive–compulsive disorder in the Afrikaner population

The Yale-Brown Obsessive Compulsive Scale

1989 • 7,156 citations

The Yale-Brown Obsessive-Compulsive Scale: Measures of internal consistency

1994 • 2,415 citations

Large-Scale Identification, Mapping, and Genotyping of Single-Nucleotide Polymorphisms in the Human Genome

1998 • 2,163 citations

The Yale Global Tic Severity Scale: Initial Testing of a Clinician-Rated Scale of Tic Severity

1989 • 2,004 citations

Pediatric Autoimmune Neuropsychiatric Disorders Associated With Streptococcal Infections: Clinical Description of the First 50 Cases

1998 • 1,453 citations

Kinetics of Human Soluble and Membrane-Bound Catechol O-Methyltransferase: A Revised Mechanism and Description of the Thermolabile Variant of the Enzyme

1995 • 1,152 citations

A family study of obsessive-compulsive disorder

1995 • 1,036 citations

Gilles de la Tourette's Syndrome and Obsessive-Compulsive Disorder

1986 • 550 citations

Obsessive-compulsive disorder: psychobiological approaches to diagnosis, treatment, and pathophysiology

1987 • 421 citations

Bipolar spectrum disorders in patients diagnosed with velo-cardio- facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?

1996 • 368 citations

Genotype determining low catechol-O-methyltransferase activity as a risk factor for obsessive-compulsive disorder

1997 • 311 citations

Beyond the serotonin hypothesis: a role for dopamine in some forms of obsessive compulsive disorder?

1990 • 285 citations

Family-based association studies support a sexually dimorphic effect of COMT and MAOA on genetic susceptibility to obsessive-compulsive disorder

1999 • 270 citations

Neurobiology of the obsessive–compulsive spectrum disorders

2000 • 207 citations

Obsessive-compulsive disorder associated with brain lesions

1996 • 167 citations

Gene for Progressive Familial Heart Block Type I Maps to Chromosome 19q13

1995 • 134 citations

The Origins of Hypertrophic Cardiomyopathy–Causing Mutations in Two South African Subpopulations: A Unique Profile of Both Independent and Founder Events

1999 • 123 citations

No association between anxiety disorders and catechol-O-methyltransferase polymorphism

1998 • 108 citations

The molecular basis and diagnosis of familial hypercholesterolaemia in South African Afrikaners

1991 • 84 citations

Identification of Genetic Markers Associated with Gilles de la Tourette Syndrome in an Afrikaner Population

1998 • 83 citations

DRD2, DRD3 and 5HT2A receptor genes polymorphisms in obsessive-compulsive disorder.

1996 • 82 citations

Noradrenergic function in obsessive-compulsive disorder: Behavioral and neuroendocrine responses to clonidine and comparison to healthy controls

1991 • 71 citations

Erythrocyte catechol‐O‐methyltransferase activity in a Swedish population

1981 • 61 citations

Intact coding region of the serotonin transporter gene in obsessive-compulsive disorder

1996 • 58 citations

Exclusion of the 5-HT1A serotonin neuroreceptor and tryptophan oxygenase genes in a large British kindred multiply affected with Tourette's syndrome, chronic motor tics, and obsessive-compulsive behavior

1995 • 56 citations

Blood group gene frequencies. An indication of the genetic constitution of population samples in Cape Town.

1972 • 50 citations

Evidence of a long QT founder gene with varying phenotypic expression in South African families.

1996 • 49 citations

A study of the association of HLA DR, DQ, and complement C4 alleles with systemic lupus erythematosus in Iceland

1998 • 40 citations

A Molecular Investigation Suggests No Relationship between Obsessive-Compulsive Disorder and the Dopamine D<sub>2</sub> Receptor

1994 • 27 citations

Testing of human homologues of murine obesity genes as candidate regions in Finnish obese sib pairs

1999 • 17 citations

THE GALENIC VENOUS SYSTEM: A SELECTIVE RADIOGRAPHIC STUDY

1972 • 12 citations

Blood group gene frequencies.

1972 • 11 citations