Evidence map›Paper›PMID 11122948›Full record

ReviewCurrent psychiatry reports2000

Genetics of bipolar affective disorder.

J I Nurnberger, T Foroud

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current psychiatry reports, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.3field-weighted citation impact, top 9% 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

9 citing papers in PubMed, 50 citations in OpenAlex.

  1. Multiple levels of impaired neural plasticity and cellular resilience in bipolar disorder: developing treatments using an integrated translational approach.The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry · 2014
    Review
  2. Article
  3. Gene-environment interaction and the genetics of depression.Journal of psychiatry & neuroscience : JPN · 2004
    Review
  4. Molecular genetics of schizophrenia: a critical review.Journal of psychiatry & neuroscience : JPN · 2003
    Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. 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

2 authors at 1 institution in 1 country.

J I NurnbergerDepartment of Psychiatry, The Institute of Psychiatric Research, 791 Union Drive, Indiana University Medical Center, Indianapolis, IN 46202, USA. jnurnber@iupui.edu
T Foroud
Indiana University – Purdue University Indianapolis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bipolar affective disorder is a highly heritable condition, as demonstrated in twin, family, and adoption studies. Morbid risk in first degree relatives is four to six times higher than the population prevalence of about 1%. However, the mode of inheritance is complex, and linkage findings have been difficult to replicate. Despite these limitations, consistent linkage findings have emerged on several chromosomes, notably 18p, 18q, 21q, 12q, 4p, and Xq. Two additional areas, 10p and 13q, have shown linkage in regions that appear to overlap with significant linkage findings in schizophrenia. Separate linkage studies in schizophrenia also have targeted the replicated bipolar linkages on 18p and 22q. New methods are being developed for fine mapping and candidate identification. Recent candidate gene studies include some positive results for the serotonin transporter gene on 17q and the catechol-o-methyltransferase gene on 22q. No other candidate gene studies are yet showing replicated results. A convincing demonstration for a susceptibility gene will probably require a mixture of case- control studies, family-based association methods, and pathophysiologic studies.

Indexed as

Bipolar DisorderCarrier ProteinsCatechol O-MethyltransferaseChromosome AberrationsChromosome DisordersChromosome MappingGene ExpressionGenetic LinkageGenetic MarkersHumansReceptors, DopamineSerotoninTrinucleotide Repeat ExpansionTryptophan HydroxylaseTyrosine 3-MonooxygenaseCarrier ProteinsCatechol O-MethyltransferaseGenetic MarkersReceptors, DopamineSerotoninTryptophan HydroxylaseTyrosine 3-Monooxygenase

Identifiers

PMID11122948
OpenAlexW1990955925

What Socratic 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 Socratic graph.