Exome-sequencing in a large population-based study reveals a rare Asn396Ser variant in the LIPG gene associated with depressive symptoms.

What it found

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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

7 citing papers in PubMed.

1. Investigating the shared genetic architecture between depression and subcortical volumes.Nature communications · 2024
   Article
2. Weighted Gene Coexpression Network Analysis Identifies Specific Modules and Hub Genes Related to Major Depression.Neuropsychiatric disease and treatment · 2020
   Article
3. A single-nucleotide polymorphism influences brain morphology in drug-naïve patients with major depressive disorder.Neuropsychiatric disease and treatment · 2019
   Article
4. Variants in TTC25 affect autistic trait in patients with autism spectrum disorder and general population.European journal of human genetics : EJHG · 2017
   Article
5. The PHF21B gene is associated with major depression and modulates the stress response.Molecular psychiatry · 2017
   Article
6. Whole-genome single nucleotide variant distribution on genomic regions and its relationship to major depression.Psychiatry research · 2017
   Article
7. A novel strategy for clustering major depression individuals using whole-genome sequencing variant data.Scientific reports · 2017
   Article

Corrections and comments

• Erratum for
  Exome-sequencing in a large population-based study reveals a rare Asn396Ser variant in the LIPG gene associated with depressive symptoms.2017

Authors and funding

26 authors.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.