Evidence map›Paper›PMID 19526298›Full record

ArticleNeurotoxicity research2009

The ANKK1 kinase gene and psychiatric disorders.

Guillermo Ponce, Rocío Pérez-González, María Aragüés, Tomás Palomo, Roberto Rodríguez-Jiménez, Miguel Angel Jiménez-Arriero, Janet Hoenicka

Abstract read
PubMed Publisher
In one paragraph

Article in Neurotoxicity research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 11% 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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 91 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Influence of ANKK1 and DRD2 polymorphisms in response to haloperidol.European archives of psychiatry and clinical neuroscience · 2013
    Trial
  6. Article
  7. Article
  8. Investigating the impact of polymorphisms in theFrontiers in oral health · 2025
    Article
  9. ANKK1 Is a Wnt/PCP Scaffold Protein for Neural F-ACTIN Assembly.International journal of molecular sciences · 2024
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Frontiers in neuroscience · 2022
    Article
  16. Article
  17. Review
  18. Observational
  19. Article
  20. Review
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

7 authors at 3 institutions in 1 country.

Guillermo PonceUnidad de Alcoholismo y Patología Dual, Servicio de Psiquiatría, Hospital Universitario, 12 de Octubre, Av. de Córdoba s/n, Madrid, E-28041, Spain.
Rocío Pérez-González
María Aragüés
Tomás Palomo
Roberto Rodríguez-Jiménez
Miguel Angel Jiménez-Arriero
Janet Hoenicka
Hospital Universitario 12 De Octubre · ESCentro de Investigación Biomédica en Red de Salud Mental · ESInstituto de Salud Carlos III · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The TaqIA single nucleotide polymorphism (SNP, rs1800497), which is located in the gene that codes for the putative kinase ANKK1 (ANKK1) near the termination codon of the D2 dopamine receptor gene (DRD2; chromosome 11q22-q23), is the most studied genetic variation in a broad range of psychiatric disorders and personality traits. A large number of individual genetic association studies have found that the TaqIA SNP is linked to alcoholism and antisocial traits. In addition, it has also been related to other conditions such as schizophrenia, eating disorders, and some behavioral childhood disorders. The TaqIA A1 allele is mainly associated with addictions, antisocial disorders, eating disorders, and attention-deficit/hyperactivity disorders, while the A2 allele occurs more frequently in schizophrenic and obsessive-compulsive patients. Current data show that the TaqIA polymorphism may be a marker of both DRD2 and ANKK1 genetic variants. ANKK1 would belong to a family of kinases involved in signal transduction. This raises the question of whether signaling players intervene in the pathophysiology of psychiatric disorders. Basic research on the ANKK1 protein and its putative interaction with the D2 dopamine receptor could shed light on this issue.

Indexed as

Genetic Predisposition to DiseaseAnimalsChromosome MappingHumansMental DisordersPhylogenyPolymorphism, Single NucleotideProtein Serine-Threonine KinasesPsychiatric Status Rating ScalesReceptors, Dopamine D2ANKK1 protein, humanProtein Serine-Threonine KinasesReceptors, Dopamine D2

Identifiers

PMID19526298
OpenAlexW2018667373

What OpenQuestion 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 OpenQuestion graph.