Evidence map›Paper›PMID 15497111›Full record

ArticleAmerican journal of human genetics2004

Attention-deficit/hyperactivity disorder in a population isolate: linkage to loci at 4q13.2, 5q33.3, 11q22, and 17p11.

Mauricio Arcos-Burgos, F Xavier Castellanos, David Pineda, Francisco Lopera, Juan David Palacio, Luis Guillermo Palacio, Judith L Rapoport, Kate Berg, Joan E Bailey-Wilson, Maximilian Muenke

Open access · bronzeAbstract read
In one paragraph

Article in American journal of human genetics, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed, 3 pooled it
9.1field-weighted citation impact, top 1% 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

84 citing papers in PubMed, 3 syntheses or guidelines pooled it, 210 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2008
    Pooled it
  4. Trial
  5. Article
  6. Article
  7. Article
  8. Neuregulin 2 Is a Candidate Gene for Autism Spectrum Disorder.International journal of molecular sciences · 2024
    Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Brain sciences · 2021
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Proteolytic Processing of Neuregulin 2.Molecular neurobiology · 2020
    Article
  20. Article

24 more citing papers are in PubMed but not listed here.

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

10 authors at 4 institutions in 2 countries.

Mauricio Arcos-BurgosNational Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892-3717, USA.
F Xavier Castellanos
David Pineda
Francisco Lopera
Juan David Palacio
Luis Guillermo Palacio
Judith L Rapoport
Kate Berg
Joan E Bailey-Wilson
Maximilian Muenke
National Human Genome Research Institute · USUniversidad de Antioquia · CONational Institutes of Health · USThe Graduate Center, CUNY · US

Funding

Genetic Analysis of Attention Deficit Hyperactivity DisorderZIAHG000175 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI SHAW, PHILIP · 2009 to 2025
$13.4M
Genetic Epidemiology of Complex TraitsZIAHG200327 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI BAILEY-WILSON, JOAN ELLEN · 2009 to 2022
$10.5M
Neurobiology Of Disruptive Behavior DisordersZIAMH002240 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI RAPOPORT, JUDITH L. · 2009 to 2011
$4.1M
Genetics of Attention Deficit Hyperactivity DisorderZ01HG000175 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI MUENKE, MAXIMILIAN · 2000 to 2008
$2.6M
NEUROBIOLOGY OF DISRUPTIVE BEHAVIOR DISORDERSZ01MH002240 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI RAPOPORT, JUDITH L. · 1985 to 2008
$2.4M
Genetic Epidemiology of Complex TraitsZ01HG200327 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI BAILEY-WILSON, JOAN ELLEN · 2005 to 2008
$1.3M
6 · The paper itself

Abstract

Attention-deficit/hyperactivity disorder (ADHD [MIM 143465]) is the most common behavioral disorder of childhood. Twin, adoption, segregation, association, and linkage studies have confirmed that genetics plays a major role in conferring susceptibility to ADHD. We applied model-based and model-free linkage analyses, as well as the pedigree disequilibrium test, to the results of a genomewide scan of extended and multigenerational families with ADHD from a genetic isolate. In these families, ADHD is highly comorbid with conduct and oppositional defiant disorders, as well as with alcohol and tobacco dependence. We found evidence of linkage to markers at chromosomes 4q13.2, 5q33.3, 8q11.23, 11q22, and 17p11 in individual families. Fine mapping applied to these regions resulted in significant linkage in the combined families at chromosomes 4q13.2 (two-point allele-sharing LOD score from LODPAL = 4.44 at D4S3248), 5q33.3 (two-point allele-sharing LOD score from LODPAL = 8.22 at D5S490), 11q22 (two-point allele-sharing LOD score from LODPAL = 5.77 at D11S1998; multipoint nonparametric linkage [NPL]-log[P value] = 5.49 at approximately 128 cM), and 17p11 (multipoint NPL-log [P value] >12 at approximately 12 cM; multipoint maximum location score 2.48 [alpha = 0.10] at approximately 12 cM; two-point allele-sharing LOD score from LODPAL = 3.73 at D17S1159). Additionally, suggestive linkage was found at chromosome 8q11.23 (combined two-point NPL-log [P value] >3.0 at D8S2332). Several of these regions are novel (4q13.2, 5q33.3, and 8q11.23), whereas others replicate already-published loci (11q22 and 17p11). The concordance between results from different analytical methods of linkage and the replication of data between two independent studies suggest that these loci truly harbor ADHD susceptibility genes.

Indexed as

Genome, HumanAttention Deficit Disorder with HyperactivityChromosome MappingChromosomes, Human, Pair 11Chromosomes, Human, Pair 17Chromosomes, Human, Pair 4Chromosomes, Human, Pair 5ColombiaGenetic LinkageHaplotypesHumansLod ScorePedigree

Identifiers

PMID15497111
PMCPMC1182160
OpenAlexW2113241039

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.