Chromosomal Aberrations and Schizophrenia

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

1991 • 3,422 citations

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization.

1986 • 3,231 citations

Smith's Recognizable Patterns of Human Malformation

1998 • 1,959 citations

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

1983 • 1,952 citations

Smith's recognizable patterns of human malformation

1997 • 1,917 citations

Type 1 Neurofibromatosis Gene: Identification of a Large Transcript Disrupted in Three NF1 Patients

1990 • 1,471 citations

Linkage strategies for genetically complex traits. I. Multilocus models.

1990 • 1,335 citations

Schizophrenia: The epigenetic puzzle

1982 • 1,194 citations

The Genetic Defect Causing Familial Alzheimer's Disease Maps on Chromosome 21

1987 • 1,149 citations

Chromosome Abnormalities and Genetic Counseling

2011 • 852 citations

Catalogue of Unbalanced Chromosome Aberrations in Man

1983 • 759 citations

Association within a family of a balanced autosomal translocation with major mental illness

1990 • 730 citations

Localization of a susceptibility locus for schizophrenia on chromosome 5

1988 • 624 citations

Genomic imprinting: review and relevance to human diseases.

1990 • 621 citations

Deletions of Chromosome 15 as a Cause of the Prader–Willi Syndrome

1981 • 615 citations

Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.2–13.3

1990 • 579 citations

Angelman and Prader‐Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion

1989 • 575 citations

EVIDENCE THAT THE GENE FOR TUBEROUS SCLEROSIS IS ON CHROMOSOME 9

1987 • 516 citations

Retinoblastoma and Subband Deletion of Chromosome 13

1978 • 455 citations

The human dopamine D2 receptor gene is located on chromosome 11 at q22-q23 and identifies a TaqI RFLP.

1989 • 423 citations

Catalogue of Unbalanced Chromosome Aberrations in Man

1985 • 420 citations

Congenital anomalies in the newborninfant, including minor variations

1964 • 416 citations

Evidence against linkage of schizophrenia to markers on chromosome 5 in a northern Swedish pedigree

1988 • 394 citations

Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy

1985 • 368 citations

Down's Syndrome and Alzheimer's disease: a review

1986 • 316 citations

Mendelian inheritance in man

1991 • 304 citations

Psychiatric Illness in First-degree Relatives of Schizophrenic and Surgical Control Patients

1985 • 278 citations

PARTIAL TRISOMY CHROMOSOME 5 COSEGREGATING WITH SCHIZOPHRENIA

1988 • 247 citations

Minor Physical Anomalies in Schizophrenia

1989 • 220 citations

Congenital anomalies in the newborn infant, including minor variations

1964 • 182 citations

Human behavior and genetics

1982 • 168 citations

Pericentric inversions

1984 • 161 citations

Sex Chromosomes and Psychosis

1988 • 159 citations

The Incidence of Minor Physical Anomalies in Adult Male Schizophrenics

1983 • 152 citations

No linkage of chromosome 5q11-q13 markers to schizophrenia in Scottish families

1989 • 147 citations

Schizophrenia and mental handicap: an historical review, with implications for further research

1989 • 145 citations

The inheritance of schizophrenia spectrum disorders: a reanalysis of the Danish adoptee study data

1983 • 112 citations

Mapping of a gene determining tuberous sclerosis to human chromosome 11q1411q23

1990 • 105 citations

Chromosome 15 anomalies and the Prader-Willi syndrome: Cytogenetic analysis

1984 • 98 citations

Genetic disorders presenting as ?schizophrenia?. Karl bonhoeffer's early view of the psychoses in the light of medical genetics

1983 • 75 citations

A balanced chromosomal translocation partially co-segregating with psychotic illness in a family

1990 • 65 citations

Chromosomal Variation in Man

1982 • 58 citations

Analysis of the fragile-X chromosome: localization and detection of the fragile site in high resolution preparations

1985 • 57 citations

Chromosomal variation in man

1977 • 56 citations

Deletion mapping of DNA markers to a region of chromosome 5 that cosegregates with schizophrenia

1989 • 44 citations

Chromosome abnormalities and genetic counseling.

1990 • 43 citations

RING CHROMOSOME 18 IN MOTHER AND DAUGHTER

1970 • 39 citations

Mapping genes for manic-depression and schizophrenia with DNA markers

1989 • 38 citations

Chromosome aberrations in patients with paranoid psychosis

2008 • 36 citations

Trisomy 8

1980 • 30 citations

Fragile 19p13 in a family with mental illness

1987 • 30 citations

Mosaicism and the trisomy 8 syndrome

1978 • 27 citations

DEMENTIA IN AGEING MENTAL DEFECTIVES: A CLINIGAL AND NEUROPATHOLOGICAL STUDY

1978 • 24 citations

Familial 5q11.2→q13.3 segmental duplication cosegregating with multiple anomalies, including schizophrenia

1990 • 24 citations

Strategies for Linkage Studies of Schizophrenia: Pedigrees, DNA Markers, and Statistical Analyses

1989 • 23 citations

A new heritable fragile site on human chromosome 3

2008 • 23 citations

C3 and C6 Complement Types in Schizophrenia

1985 • 22 citations

Chromosome survey of new patients admitted to the four maximum security hospitals in the United Kingdom

1976 • 20 citations

Schizophrenia and organic brain syndrome with trisomy 8 (group-C trisomy 8 [47, XX, 8+]).

1975 • 20 citations

Down's Syndrome with Mania

1987 • 16 citations

Chromosome 5 and Schizophrenia: Implications for Genetic Linkage Studies

1989 • 16 citations

INTRACHROMOSOMAL INSERTION OF CHROMOSOME 13 IN A FAMILY WITH PSYCHOSIS AND MENTAL SUBNORMALITY

1986 • 16 citations

A folate sensitive heritable fragile site at 19p13

1985 • 15 citations

Human chromosome banding specific for electron microscopy

1988 • 14 citations

Familial Manic–Depressive Illness with Deleted Short Arm of Chromosome 21: Coincidental or Causal?

1989 • 12 citations

XXY syndrome XY XO mosaicism and acentric chromosomal fragments in male schizophrenics.

1973 • 12 citations

Chromosomal aberrations in 85 mentally retarded patients examined by high resolution banding.

1987 • 11 citations

Two pericentric inversions, inv(2)(p11q13) and inv(5)(p13q13), in a patient referred for psychiatric problems

1982 • 10 citations

Trisomy 8 syndrome

1977 • 10 citations

[18p- syndrome. A further case].

1969 • 8 citations

Chromosomal aberrations in 85 mentally retarded patients examined by high resolution banding

1987 • 7 citations

A cytogenetic study of children with psychiatric disorders

1976 • 6 citations

[Chromosomal translocation t(2;18)(q21;q23) in a schizophrenic individual and his daughter].

1976 • 5 citations

Paranoid Schizophrenia in a Mongoloid Defective: Some Theoretical Considerations Derived from an Unusual Case

1959 • 4 citations

Does it work efficiently?

1989 • 4 citations

D/D translocations in patients with mental illness

2009 • 4 citations

The Role of Molecular Genetics in Psychiatry: Unraveling the Etiology for Schizophrenia

1990 • 3 citations