Evidence for a genetic association between alleles of monoamine oxidase a gene and bipolar affective disorder

Primer-Directed Enzymatic Amplification of DNA with a Thermostable DNA Polymerase

1988 • 17,059 citations

Diagnostic and Statistical Manual of Mental Disorders

1988 • 12,705 citations

Research Diagnostic Criteria

1978 • 6,988 citations

A Diagnostic Interview

1978 • 5,735 citations

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

1988 • 4,259 citations

Abnormal Behavior Associated with a Point Mutation in the Structural Gene for Monoamine Oxidase A

1993 • 1,620 citations

cDNA cloning of human liver monoamine oxidase A and B: molecular basis of differences in enzymatic properties.

1988 • 713 citations

Mapping Human Brain Monoamine Oxidase A and B with ¹¹ C-Labeled Suicide Inactivators and PET

1987 • 388 citations

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

1993 • 363 citations

Platelet and plasma amine oxidase activity in 680 normals: Sex and age differences and stability over time

1976 • 346 citations

Juvenile myoclonic epilepsy (JME) may be linked to the BF and HLA loci on human chromosome 6

1988 • 317 citations

Biochemistry and genetics of monoamine oxidase

1990 • 306 citations

Human monoamine oxidase A and B genes exhibit identical exon-intron organization.

1991 • 265 citations

Human monoamine oxidase A gene determines levels of enzyme activity.

1991 • 259 citations

Depressive Disease

1971 • 252 citations

Substrate- and inhibitor-related characteristics of human platelet monoamine oxidase

1977 • 237 citations

Linkage analysis of "necessary" disease loci versus "susceptibility" loci.

1993 • 218 citations

Genetic Control of Platelet and Plasma Monoamine Oxidase Activity

1973 • 204 citations

Human monoamine oxidase A and B genes map to xp11.23 and are deleted in a patient with norrie disease

1989 • 199 citations

Isolation and characterization of a candidate gene for Norrie disease

1992 • 191 citations

Immunocytochemical localization of monoamine oxidases A and B in human peripheral tissues and brain.

1987 • 170 citations

Personality traits related to monoamine oxidase activity in platelets

1984 • 168 citations

Association of a monoamine oxidase B allele with Parkinson's disease

1993 • 163 citations

Dinucleotide repeat polymorphism at the MAOA locus

1991 • 124 citations

Platelet monoamine oxidase activity in sensation seekers

1980 • 111 citations

Structural Features of Human Monoamine Oxidase A Elucidated from cDNA and Peptide Sequences

1988 • 110 citations

Monoamine oxidase deficiency in males with an X chromosome deletion

1989 • 110 citations

Human monoamine oxidase gene (MAOA): Chromosome position (Xp21-p11) and DNA polymorphism

1988 • 101 citations

Regulation of neurotransmitter receptors by desipramine and other antidepressant drugs: the neurotransmitter receptor hypothesis of antidepressant action.

1984 • 84 citations

Monoamine oxidase type a: differences in selectivity towards l-norepinephrine compared to serotonin

1982 • 82 citations

CAUSES OF BLINDNESS IN CHILDREN

1927 • 81 citations

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

1985 • 80 citations

Importance of genetic effects for monoamine oxidase activity in thrombocytes in twins reared apart and twins reared together

1993 • 80 citations

REM sleep and central monoamine oxidase inhibition

1972 • 76 citations

Submicroscopic interstitial deletion of the X chromosome explains a complex genetic syndrome dominated by Norrie disease

1986 • 75 citations

Personality Correlates of Platelet Monoamine Oxidase (MAO) Activity in Female and Male Subjects

1987 • 75 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

Characterization of a highly polymorphic region near the first exon of the human MAOA gene containing a GT dinucleotide and a novel VNTR motif

1992 • 69 citations

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

1988 • 69 citations

Structure of the human gene for monoamine oxidase type A

1991 • 68 citations

Organization of the human monoamine oxidase genes and long-range physical mapping around them

1992 • 64 citations

Defining the Schizophrenia Spectrum: Issues for Genetic Linkage Studies

1991 • 59 citations

Genetics of Platelet MAO Activity in Discordant Schizophrenic and Normal Twins

1983 • 59 citations

Monoamine Oxidase Activity Decreased in Cells Lacking Hypoxanthine Phosphoribosyltransferase Activity

1976 • 58 citations

Highly polymorphic (GT)n repeat sequence in intron II of the human MAOB gene

1992 • 49 citations

A chi‐square test to distinguish allelic association from other causes of phenotypic association between two loci

1985 • 46 citations

Monoamine oxidase type a in fibroblasts from patients with bipolar depressive illness

1980 • 43 citations

Elevated platelet monoamine oxidase activity in patients wth nonendogenous depression

1980 • 40 citations

Reduced platelet MAO activity and vulnerability to psychiatric disorders

1980 • 35 citations

Biological and Behavioral Consequences of Alterations in Monoamine Oxidase Activity

1980 • 35 citations

Bipolar Illness

1983 • 31 citations

Psychological characteristics corresponding to low versus high platelet monoamine oxidase activity.

1979 • 28 citations

Toward a biochemical classification of depressive disorders—VIII. Platelet monoamine oxidase activity in subtypes of depressions

1985 • 23 citations

Morbidity risk for psychiatric disorders in families of probands with affective disorders divided according to levels of platelet MAO activity

1985 • 22 citations

Platelet monoamine oxidase (MAO) activity and genetic vulnerability to bipolar (BP) affective illness.

1979 • 20 citations

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

1988 • 20 citations

GABAA receptor subunit genes as candidate genes for bipolar affective disorder—an association analysis

1992 • 19 citations

Deleted Work

1955 • 0 citations