ArticleMolecular psychiatry2013
Identifying bipolar disorder susceptibility loci in a densely affected pedigree.
Article in Molecular psychiatry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled 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.
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.
Who cites it
16 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Exome Sequencing of Familial Bipolar Disorder.JAMA psychiatry · 2016Pooled it
- Elevated common variant genetic risk for tourette syndrome in a densely-affected pedigree.Molecular psychiatry · 2021Article
- Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders.Molecular psychiatry · 2021Article
- Positional cloning and comprehensive mutation analysis of a Japanese family with lithium-responsive bipolar disorder identifies a novel DOCK5 mutation.Journal of human genetics · 2021Article
- Clinical and genetic differences between bipolar disorder type 1 and 2 in multiplex families.Translational psychiatry · 2021Article
- Multiplex melanoma families are enriched for polygenic risk.Human molecular genetics · 2020Article
- Polygenic risk for anxiety influences anxiety comorbidity and suicidal behavior in bipolar disorder.Translational psychiatry · 2020Article
- Contribution of common and rare damaging variants in familial forms of bipolar disorder and phenotypic outcome.Translational psychiatry · 2020Article
- Whole-exome sequencing of 81 individuals from 27 multiply affected bipolar disorder families.Translational psychiatry · 2020Article
- The genomics of major psychiatric disorders in a large pedigree from Northern Sweden.Translational psychiatry · 2019Article
- Whole Exome Sequencing Identifies a Novel Predisposing Gene, MAPKAP1, for Familial Mixed Mood Disorder.Frontiers in genetics · 2019Article
- Article
- Psychiatric Genomics: An Update and an Agenda.The American journal of psychiatry · 2018Review
- Genetic Studies on the Tripartite Glutamate Synapse in the Pathophysiology and Therapeutics of Mood Disorders.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2017Review
- Patterns of Nonrandom Mating Within and Across 11 Major Psychiatric Disorders.JAMA psychiatry · 2016Article
- Genetics of Bipolar Disorder: Recent Update and Future Directions.The Psychiatric clinics of North America · 2016Review
Corrections and comments
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Authors and funding
13 authors.
Funding
Abstract
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What OpenQuestion holds
Registered trials
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.