Evidence map›Paper›PMID 12687500›Full record

ArticleAmerican journal of human genetics2003

A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11.

Matthew N Ogdie, I Laurence Macphie, Sonia L Minassian, May Yang, Simon E Fisher, Clyde Francks, Rita M Cantor, James T McCracken, James J McGough, Stanley F Nelson and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in American journal of human genetics, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed, 2 pooled it
11.7field-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

64 citing papers in PubMed, 2 syntheses or guidelines pooled it, 218 citations in OpenAlex.

  1. Pooled it
  2. 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
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. The neurobiological link between OCD and ADHD.Attention deficit and hyperactivity disorders · 2014
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Genome-Wide Studies of Specific Language Impairment.Current behavioral neuroscience reports · 2014
    Review
  15. Article
  16. Attention deficit hyperactivity disorder.Current topics in behavioral neurosciences · 2014
    Review
  17. Review
  18. Article
  19. Article
  20. Article

4 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

12 authors at 3 institutions in 2 countries.

Matthew N OgdieDepartment of Human Genetics, University of California, Los Angeles, Los Angeles, CA, USA.
I Laurence Macphie
Sonia L Minassian
May Yang
Simon E Fisher
Clyde Francks
Rita M Cantor
James T McCracken
James J McGough
Stanley F Nelson
Anthony P Monaco
Susan L Smalley
University of California, Los Angeles · USCentre for Human Genetics · GBUniversity of Oxford · GB

Funding

DETECTION OF SUSCEPTIBILITY GENES IN ADHDR01MH058277 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SMALLEY, SUSAN L · 1998 to 2008
$4.6M
PREDOCTORAL TRAINING PROGRAM IN GENETIC MECHANISMS AT UCT32GM007104 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI GOBER, JAMES W · 1985 to 2011
$3.6M
Drug Response in Pediatric PsychopharmacologyK24MH001805 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MCCRACKEN, JAMES T. · 2001 to 2005
$662k
NIGMS NIH HHS GM07104NIGMS NIH HHS T32 GM007104NIMH NIH HHS K24 MH001805NIMH NIH HHS MH01805NIMH NIH HHS MH01969NIMH NIH HHS MH58277NIMH NIH HHS R01 MH058277Wellcome Trust
6 · The paper itself

Abstract

Attention-deficit/hyperactivity disorder (ADHD [MIM 143465]) is a common, highly heritable neurobehavioral disorder of childhood onset, characterized by hyperactivity, impulsivity, and/or inattention. As part of an ongoing study of the genetic etiology of ADHD, we have performed a genomewide linkage scan in 204 nuclear families comprising 853 individuals and 270 affected sibling pairs (ASPs). Previously, we reported genomewide linkage analysis of a "first wave" of these families composed of 126 ASPs. A follow-up investigation of one region on 16p yielded significant linkage in an extended sample. The current study extends the original sample of 126 ASPs to 270 ASPs and provides linkage analyses of the entire sample, using polymorphic microsatellite markers that define an approximately 10-cM map across the genome. Maximum LOD score (MLS) analysis identified suggestive linkage for 17p11 (MLS=2.98) and four nominal regions with MLS values >1.0, including 5p13, 6q14, 11q25, and 20q13. These data, taken together with the fine mapping on 16p13, suggest two regions as highly likely to harbor risk genes for ADHD: 16p13 and 17p11. Interestingly, both regions, as well as 5p13, have been highlighted in genomewide scans for autism.

Indexed as

Genetic LinkageAdolescentAttention Deficit Disorder with HyperactivityChildChild, PreschoolChromosome MappingChromosomes, HumanChromosomes, Human, Pair 17Cohort StudiesFemaleGenomeHumansLos AngelesMaleSample SizeSiblings

Identifiers

PMID12687500
PMCPMC1180278
OpenAlexW2109068683

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.