Evidence map›Paper›PMID 19073419›Full record

ReviewNeurotoxicity research2008

Chromosome abnormalities, mental retardation and the search for genes in bipolar disorder and schizophrenia.

D H R Blackwood, T Thiagarajah, P Malloy, B S Pickard, W J Muir

Abstract readReview
PubMed Publisher
In one paragraph

Review in Neurotoxicity research, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.1field-weighted citation impact, top 19% 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

8 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Genetics in schizophrenia: where are we and what next?Dialogues in clinical neuroscience · 2010
    Review
  7. Article
  8. Review
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

5 authors at 2 institutions in 1 country.

D H R BlackwoodDivision of Psychiatry, School of Molecular and Clinical Medicine, University of Edinburgh, Royal Edinburgh Hospital, Edinburgh EH10 5HF, UK. d.blackwood@ed.ac.uk
T Thiagarajah
P Malloy
B S Pickard
W J Muir
Royal Edinburgh Hospital · GBUniversity of Edinburgh · GB

Funding

Chief Scientist OfficeWellcome Trust 066717
6 · The paper itself

Abstract

Genetic factors contribute to schizophrenia and bipolar disorder, and linkage and association studies have been successful in identifying several candidate genes. However these genes explain only a very small part of the total population risk and the psychoses appear to be very heterogeneous with several models of genetic inheritance relevant to different groups of patients, including some cases caused by multiple common genetic variants, while others are single gene disorders. Studying chromosomal abnormalities is a useful strategy for identifying genes in illness, and patients with both mental retardation and psychosis form a special group where large chromosomal abnormalities detected by routine cytogenetic analysis are more prevalent than in patients with schizophrenia or bipolar disorder alone, or in the general population. Studying these patients provides valuable opportunities to identify genes contributing to psychoses. This review of the literature on large chromosomal rearrangements in patients with mental retardation and psychotic illness illustrates how schizophrenia and bipolar phenotypes are associated with a large number of different chromosomal disruptions. Recent genome wide association studies have identified an excess of small chromosomal deletions and duplications in schizophrenia, adding further support to the importance of chromosomal structural variation in psychotic illness. The genes GRIK4 and NPAS3, each associated with psychosis in patients with mental retardation are discussed to illustrate the value of rare cytogenetic events as a means to signpost neurobiological pathways of general importance for illness in the wider population.

Indexed as

Chromosome AberrationsAnimalsBasic Helix-Loop-Helix ProteinsBipolar DisorderComorbidityGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansIntellectual DisabilityKainic Acid ReceptorsNerve Tissue ProteinsPsychotic DisordersSchizophreniaTranscription FactorsBasic Helix-Loop-Helix ProteinsGRIK4 protein, humanKainic Acid ReceptorsNerve Tissue ProteinsNPAS3 protein, humanTranscription Factors

Identifiers

PMID19073419
OpenAlexW2144726353

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.