Evidence map›Paper›PMID 9758604›Full record

ArticleAmerican journal of human genetics1998

Support for a chromosome 18p locus conferring susceptibility to functional psychoses in families with schizophrenia, by association and linkage analysis.

S G Schwab, J Hallmayer, B Lerer, M Albus, M Borrmann, S Hönig, M Strauss, R Segman, D Lichtermann, M Knapp and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in American journal of human genetics, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
11.7field-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

48 citing papers in PubMed, 143 citations in OpenAlex.

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  17. The psychopathology and treatment of bipolar disorder.Annual review of clinical psychology · 2006
    Review
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  19. Article
  20. Genetics of major mood disorders.Psychiatry (Edgmont (Pa. : Township)) · 2004
    Article
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

13 authors at 5 institutions in 5 countries.

S G SchwabMolecular Genetics Laboratory, Department of Psychiatry, University of Bon, Germany.
J Hallmayer
B Lerer
M Albus
M Borrmann
S Hönig
M Strauss
R Segman
D Lichtermann
M Knapp
M Trixler
W Maier
D B Wildenauer
University of Bonn · DEHadassah Medical Center · ILLudwig-Maximilians-Universität München · DEUniversity of Pecs · HUUniversity of Western Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The action of antipsychotic drugs on dopamine receptors suggests that dopaminergic signal transmission may play a role in the development of schizophrenia. We tested eight candidate genes (coding for dopamine receptors, the dopamine transporter, and G-proteins) in 59 families from Germany and Israel, for association. A P value of .00055 (.0044 when corrected for the no. of markers tested) was obtained for the intronic CA-repeat marker G-olfalpha on chromosome 18p. The value decreased to .000088 (.0007) when nine sibs with recurrent unipolar depressive disorder were included. Linkage analysis using SSLP markers densely spaced around G-olfalpha yielded a maximum two-point LOD score of 3.1 for a marker 0.5 cM distal to G-olfalpha. Multipoint analysis under the assumption of heterogeneity supported this linkage-whether the affected pheotype was defined narrowly or broadly-as did nonparametric linkage (NPL). In 12 families with exclusively maternal transmission of the disease, the NPL value also supported linkage to this marker. In order to test for association/linkage disequilibrium in the presence of linkage, the sample was restricted to independent offspring. When this sample was combined with 65 additional simplex families (each of them comprising one schizophrenic offspring and his or her parents), the 124-bp allele of G-olfalpha was transmitted 47 times and was not transmitted 21 times (P=.009). These results suggest the existence, on chromosome 18p, of a potential susceptibility locus for functional psychoses.

Indexed as

Heterotrimeric GTP-Binding ProteinsChromosomes, Human, Pair 18FemaleGenetic MarkersGenetic Predisposition to DiseaseGenotypeGermanyGTP-Binding Protein alpha SubunitsGTP-Binding ProteinsHumansIsraelLinkage DisequilibriumLod ScoreMaleMultivariate AnalysisPsychotic DisordersGenetic MarkersGTP-Binding Protein alpha SubunitsGTP-Binding ProteinsHeterotrimeric GTP-Binding Proteinsolfactory G protein subunit alpha olf

Identifiers

PMID9758604
PMCPMC1377479
OpenAlexW1992321119

What OpenQuestion holds

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Registered trials

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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.