Evidence map›Paper›PMID 22762300›Full record

ReviewCanadian journal of psychiatry. Revue canadienne de psychiatrie2012

Molecular genetics of the psychosis phenotype.

Pamela DeRosse, Anil K Malhotra, Todd Lencz

Abstract readReview
In one paragraph

Review in Canadian journal of psychiatry. Revue canadienne de psychiatrie, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. 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

3 authors.

Pamela DeRosseCenter for Psychiatric Neuroscience, Feinstein Institute for Medical Research, Manhasset, NY, USA. pderosse@lij.edu
Anil K Malhotra
Todd Lencz

Funding

The Genetics of Psychosis: Towards a Dimensional ApproachR00MH086756 · NIMH · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI DEROSSE, PAMELA · 2011 to 2013
$732k
The Genetics of Psychosis: Towards a Dimensional ApproachK99MH086756 · NIMH · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI DEROSSE, PAMELA · 2009 to 2010
$156k
NIMH NIH HHS K99 MH086756NIMH NIH HHS MH086756NIMH NIH HHS R00 MH086756
6 · The paper itself

Abstract

objectiveRelative to recent successes in elucidating the genetic mechanisms associated with complex diseases, including macular degeneration, diabetes mellitus, type 2, heart disease, and cancer, molecular genetic approaches to psychiatric illness have met with more limited success. While factors such as small allelic effects, allelic heterogeneity, and variation in population substructure have received considerable attention in attempt to explain the paucity of significant results in psychiatric genetics, significantly less focus has been directed toward phenotypic factors.

methodData derived from molecular genetic studies of the psychosis phenotype in patients with a range of psychiatric illnesses are reviewed.

resultsAvailable data suggest that genes do not respect the boundaries of the current diagnostic system but may confer risk for symptom-based phenotypic variation that traverses those boundaries.

conclusionsMolecular genetic studies offer convincing evidence for a relation between genetic variation and symptom-based phenotypic variation within psychiatric illness. These data may provide novel insights into the pathophysiology of schizophrenia and other related disorders. The exploration of relations between genetic variation and symptom variation that traverses traditional diagnostic boundaries may ultimately lead to more refined classification systems that more closely reflect the genetic etiology of psychiatric illness.

Indexed as

Genetic Association StudiesPhenotypeSchizophrenic PsychologyBipolar DisorderCarrier ProteinsCatechol O-MethyltransferaseDiagnosis, DifferentialDiagnostic and Statistical Manual of Mental DisordersDiseases in TwinsDysbindinDystrophin-Associated ProteinsGenetic LinkageGenetic Predisposition to DiseaseGenetic VariationGenotypeHumansCarrier ProteinsCatechol O-MethyltransferaseDAOA protein, humanDISC1 protein, humanDTNBP1 protein, humanDysbindinDystrophin-Associated ProteinsIntracellular Signaling Peptides and ProteinsNerve Tissue ProteinsNeuregulin-1NRG1 protein, human

Identifiers

PMID22762300
PMCPMC4211610

What OpenQuestion holds

Textmetadata
LicenceTDM
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.