Evidence map›Paper›PMID 15386212›Full record

ArticleAmerican journal of human genetics2004

Disrupted in schizophrenia 1 (DISC1): association with schizophrenia, schizoaffective disorder, and bipolar disorder.

Colin A Hodgkinson, David Goldman, Judith Jaeger, Shalini Persaud, John M Kane, Robert H Lipsky, Anil K Malhotra

Open access · bronzeAbstract read
In one paragraph

Article in American journal of human genetics, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 167 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
167citing papers in PubMed, 5 pooled it
16.0field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

167 citing papers in PubMed, 5 syntheses or guidelines pooled it, 444 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Pooled it
  6. Trial
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Excess Wnt in neurological disease.The Biochemical journal · 2025
    Review
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Mutations in DISC1 alter IPNeuronal signaling · 2021
    Review
  20. Review

107 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Colin A HodgkinsonSection of Human Neurogenetics and Laboratory of Neurogenetics, National Institute on Alcohol Abuse and Alcoholism, Rockville, MD, USA. chodg@mail.nih.gov
David Goldman
Judith Jaeger
Shalini Persaud
John M Kane
Robert H Lipsky
Anil K Malhotra
National Institute on Alcohol Abuse and Alcoholism · USZucker Hillside Hospital · US

Funding

CLINICAL TRIALS IN SCHIZOPHRENIA--MOLECULAR APPROACHESK23MH001760 · NIMH · LONG ISLAND JEWISH MEDICAL CENTER · PI MALHOTRA, ANIL K · 1999 to 2003
$621k
RELATIONSHIP OF CANDIDATE GENES AND ALLELES TO BEHAVIORZ01AA000302 · NIAAA · ALCOHOL ABUSE AND ALCOHOLISM · PI GOLDMAN, DAVID · 2000 to 2006
–
NIMH NIH HHS K23 MH001760
6 · The paper itself

Abstract

Schizophrenia, schizoaffective disorder, and bipolar disorder are common psychiatric disorders with high heritabilities and variable phenotypes. The Disrupted in Schizophrenia 1 (DISC1) gene, on chromosome 1q42, was originally discovered and linked to schizophrenia in a Scottish kindred carrying a balanced translocation that disrupts DISC1 and DISC2. More recently, DISC1 was linked to schizophrenia, broadly defined, in the general Finnish population, through the undertransmission to affected women of a common haplotype from the region of intron 1/exon 2. We present data from a case-control study of a North American white population, confirming the underrepresentation of a common haplotype of the intron 1/exon 2 region in individuals with schizoaffective disorder. Multiple haplotypes contained within four haplotype blocks extending between exon 1 and exon 9 are associated with schizophrenia, schizoaffective disorder, and bipolar disorder. We also find overrepresentation of the exon 9 missense allele Phe607 in schizoaffective disorder. These data support the idea that these apparently distinct disorders have at least a partially convergent etiology and that variation at the DISC1 locus predisposes individuals to a variety of psychiatric disorders.

Indexed as

AdultBipolar DisorderChromosomes, Human, Pair 1FemaleGenetic MarkersGenotypeHaplotypesHumansMaleNerve Tissue ProteinsNorth AmericaPolymorphism, Single NucleotidePsychotic DisordersSchizophreniaWhite PeopleDISC1 protein, humanGenetic MarkersNerve Tissue Proteins

Identifiers

PMID15386212
PMCPMC1182115
OpenAlexW2112007464

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.