Haplotype analysis of the COMT‐ARVCF gene region in Israeli anorexia nervosa family trios

Human catechol-O-methyltransferase pharmacogenetics: description of a functional polymorphism and its potential application to neuropsychiatric disorders

1996 • 1,780 citations

Functional Analysis of Genetic Variation in Catechol-O-Methyltransferase (COMT): Effects on mRNA, Protein, and Enzyme Activity in Postmortem Human Brain

2004 • 1,637 citations

Enzymatic O-Methylation of Epinephrine and Other Catechols

1958 • 1,291 citations

A Highly Significant Association between a COMT Haplotype and Schizophrenia

2002 • 701 citations

Training and quality assurance with the structured clinical interview for DSM-IV (SCID-I/P)

1998 • 596 citations

A Haplotype Implicated in Schizophrenia Susceptibility Is Associated with Reduced COMT Expression in Human Brain

2003 • 340 citations

Genomic organization of the human catechol O‐methyltransferase gene and its expression from two distinct promoters

1994 • 332 citations

Catechol-O-Methyltransferase Genotype and Dopamine Regulation in the Human Brain

2003 • 321 citations

Characterization and Implications of Estrogenic Down-Regulation of Human Catechol-O-Methyltransferase Gene Transcription

1999 • 297 citations

Transmission/Disequilibrium Tests for Extended Marker Haplotypes

1999 • 281 citations

Association of BDNF with anorexia, bulimia and age of onset of weight loss in six European populations

2004 • 228 citations

Anorexia and Bulimia Nervosa

2000 • 190 citations

COMT: A common susceptibility gene in bipolar disorder and schizophrenia

2004 • 165 citations

Strong evidence for association between the dystrobrevin binding protein 1 gene (DTNBP1) and schizophrenia in 488 parent-offspring trios from Bulgaria

2004 • 162 citations

Human catechol-O-methyltransferase down-regulation by estradiol

2003 • 158 citations

Identification of a novel neuregulin 1 at-risk haplotype in Han schizophrenia Chinese patients, but no association with the Icelandic/Scottish risk haplotype

2004 • 156 citations

Family-based linkage disequilibrium mapping using SNP marker haplotypes: application to a potential locus for schizophrenia at chromosome 22q11

2000 • 142 citations

Evidence for a susceptibility locus for panic disorder near the catechol-O-methyltransferase gene on chromosome 22

2002 • 111 citations

Identification of Sequence Variants and Analysis of the Role of the Catechol-O-Methyl-Transferase Gene in Schizophrenia Susceptibility

1998 • 109 citations

Association of anorexia nervosa with the high activity allele of the COMT gene: a family-based study in Israeli patients

2001 • 107 citations

Identification of a New Human Catenin Gene Family Member (ARVCF) from the Region Deleted in Velo–Cardio–Facial Syndrome

1997 • 104 citations

Association study of cannabinoid receptor gene (CNR1) alleles and anorexia nervosa: Differences between restricting and bingeing/purging subtypes

2003 • 103 citations

Contrasting patterns of Y chromosome variation in Ashkenazi Jewish and host non-Jewish European populations

2004 • 99 citations

THE EVOLVING GENETIC FOUNDATIONS OF EATING DISORDERS

2001 • 96 citations

Anorexia nervosa (restrictive subtype) is associated with a polymorphism in the novel norepinephrine transporter gene promoter polymorphic region

2002 • 77 citations

Combined family trio and case‐control analysis of the COMT Val158Met polymorphism in European patients with anorexia nervosa

2003 • 49 citations

Involvements of mitochondrial thioredoxin reductase (TrxR2) in cell proliferation

2003 • 39 citations

Randomization tests of disease‐marker associations

1997 • 34 citations

Maternal transmission disequilibrium of the glutamate receptor GRIK2 in schizophrenia

2004 • 33 citations

Haplotype analysis and identification of genes for a complex trait: examples from schizophrenia

2004 • 14 citations

Randomization tests of disease-marker associations

1997 • 4 citations

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