X-linked borderline mental retardation with prominent behavioral disturbance: phenotype, genetic localization, and evidence for disturbed monoamine metabolism.

A simple salting out procedure for extracting DNA from human nucleated cells

1988 • 20,341 citations

Easy calculations of lod scores and genetic risks on small computers.

1984 • 1,526 citations

Aggression in humans correlates with cerebrospinal fluid amine metabolites

1979 • 1,126 citations

Cerebrospinal Fluid Monoamine Metabolites, Aggression, and Impulsivity in Disruptive Behavior Disorders of Children and Adolescents

1990 • 418 citations

Cerebrospinal Fluid Monoamine Metabolite Levels in Male Arsonists

1987 • 370 citations

Human monoamine oxidase A gene determines levels of enzyme activity.

1991 • 259 citations

A Behavioral Dimension of Constraint

1986 • 245 citations

Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphisms.

1991 • 220 citations

Isolation and characterization of a candidate gene for Norrie disease

1992 • 191 citations

Monoamines and Abnormal Behaviour a Multi-Aminergic Perspective

1990 • 175 citations

Dinucleotide repeat polymorphism at the MAOA locus

1991 • 124 citations

Monoamine oxidase deficiency in males with an X chromosome deletion

1989 • 110 citations

Norrie disease caused by a gene deletion allowing carrier detection and prenatal diagnosis

1985 • 80 citations

Clinical, biochemical, and neuropsychiatric evaluation of a patient with a contiguous gene syndrome due to a microdeletion Xp11.3 including the Norrie disease locus and monoamine oxidase (MAOA and MAOB) genes

1992 • 73 citations

Serotonergic dysfunction and aggression control

1991 • 73 citations

Norrie disease resulting from a gene deletion: clinical features and DNA studies.

1988 • 69 citations

Simultaneous determination of catecholamines and metanephrines in urine by HPLC with fluorometric detection

1984 • 68 citations

Structure of the human gene for monoamine oxidase type A

1991 • 68 citations

New X‐linked syndrome of mental retardation, gynecomastia, and obesity is linked to DXS255

1991 • 64 citations

Marked Amine and Amine Metabolite Changes in Norrie Disease Patients with an X‐Chromosomal Deletion Affecting Monoamine Oxidase

1990 • 55 citations

Microdeletion in the X-chromosome and prenatal diagnosis in a family with Norrie disease

1989 • 35 citations

XLMR genes: Update 1992

1992 • 32 citations

Assay of platelet monoamine oxidase in whole blood

1985 • 29 citations

Gene for non‐specific X‐linked mental retardation maps in the pericentromeric region

1991 • 28 citations

Simultaneous determination of acidic 3,4-dihydroxyphenylalanine metabolites and 5-hydroxyindole-3-acetic acid in urine by high-performance liquid chromatography

1990 • 22 citations

Norrie disease as part of a complex syndrome explained by a submicroscopic deletion of the X chromosome

1988 • 20 citations

High-density genetic and physical mapping of DNA markers near the X-linked Alport syndrome locus: definition and use of flanking polymorphic markers

1991 • 20 citations

Report of the committee on the genetic constitution of the X chromosome (Part 7 of 7)

1991 • 9 citations

Multipoint linkage analysis of DXS369 and DXS304 in fragile X families

1991 • 9 citations

Three dinucleotide repeat polymorphisms at the DXS178 locus

1992 • 9 citations

Use of linkage data obtained in single families: Prenatal diagnosis of a new X‐linked mental retardation syndrome

1992 • 5 citations

Norrie disease resulting fromagenedeletion: clinical features andDNA studies

1988 • 4 citations