Evidence map›Paper›PMID 21611732›Full record

ArticleJournal of abnormal child psychology2011

Association of ADAM10 and CAMK2A polymorphisms with conduct disorder: evidence from family-based studies.

Xue-Qiu Jian, Ke-Sheng Wang, Tie-Jian Wu, Joel J Hillhouse, Jerald E Mullersman

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of abnormal child psychology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.4field-weighted citation impact, top 38% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Regulation of Alpha-Secretase ADAM10Frontiers in molecular neuroscience · 2017
    Review
  7. Article
  8. 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

5 authors at 1 institution in 1 country.

Xue-Qiu JianDepartment of Biostatistics and Epidemiology, College of Public Health, East Tennessee State University, PO BOX 70259, Lamb Hall, Johnson City, TN 37614-1700, USA.
Ke-Sheng Wang
Tie-Jian Wu
Joel J Hillhouse
Jerald E Mullersman
East Tennessee State University · US

Funding

Subject CollectionU10AA008401 · NIAAA · SUNY DOWNSTATE MEDICAL CENTER · PI JESSICA E SALVATORE · 1989 to 2026
$162.7M
PSYCHOPHARMACOLOGY--ORAL ALCOHOL CHALLENGE/ALCOHOL CLAMPINGU10AA008403 · NIAAA · SUNY DOWNSTATE MEDICAL CENTER · PI BEGLEITER, HENRI · 1989 to 2003
$23.7M
GENETIC ANALYSIS OF COMMON DISEASES: AN EVALUATIONR01GM031575 · NIGMS · UNIVERSITY OF TEXAS RIO GRANDE VALLEY · PI ALMASY, LAURA A. · 1985 to 2016
$7.8M
International Multi-Center ADHD Genetics ProjectR01MH062873 · NIMH · UPSTATE MEDICAL UNIVERSITY · PI FARAONE, STEPHEN V · 2002 to 2007
$7.2M
Analysis of an ADHD Whole Genome Association ScanR01MH081803 · NIMH · UPSTATE MEDICAL UNIVERSITY · PI FARAONE, STEPHEN V · 2007 to 2007
$157k
NIAAA NIH HHS U10AA08401NIAAA NIH HHS U10AA08403NIGMS NIH HHS R01 GM31575NIMH NIH HHS R01MH081803NIMH NIH HHS R01MH62873
6 · The paper itself

Abstract

Twin and family studies have shown that genetic factors play a role in the development of conduct disorder (CD). The purpose of this study was to identify genetic variants associated with CD using a family-based association study. We used 4,720 single nucleotide polymorphisms (SNPs) from the Illumina Panel and 11,120 SNPs from the Affymetrix 10K GeneChips genotyped in 155 Caucasian nuclear families from Genetic Analysis Workshop (GAW) 14, a subset from the Collaborative Study on the Genetics of Alcoholism (COGA). 20 SNPs had suggestive associations with CD (p<10(-3)), nine of which were located in known genes, including ADAM10 (rs383902, p=0.00036) and CAMK2A (rs2053053, p=0.00098). Our results were verified using the International Multi-Center ADHD Genetics Project (IMAGE) dataset. In conclusion, we identified several loci associated with CD. Especially, the two genes (ADAM10 and CAMK2A) have been reported to be associated with Alzheimer's disease, bipolar disorder and depression. These findings may serve as a resource for replication in other populations.

Indexed as

Genetic Predisposition to DiseasePolymorphism, Single NucleotideADAM10 ProteinADAM ProteinsAdolescentAdultAgedAged, 80 and overAmyloid Precursor Protein SecretasesCalcium-Calmodulin-Dependent Protein Kinase Type 2ChildChild, PreschoolConduct DisorderDatabases, GeneticFemaleGenetic Association StudiesADAM10 ProteinADAM10 protein, humanADAM ProteinsAmyloid Precursor Protein SecretasesCalcium-Calmodulin-Dependent Protein Kinase Type 2CAMK2A protein, humanMembrane Proteins

Identifiers

PMID21611732
OpenAlexW2031955029

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.