Evidence map›Paper›PMID 15526234›Full record

ArticleAmerican journal of human genetics2005

Sex-specific genetic architecture of whole blood serotonin levels.

Lauren A Weiss, Mark Abney, Edwin H Cook, Carole Ober

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in American journal of human genetics, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00006512 (Characterizing a 5P-Linked BHR Susceptibility Locus), which is not on this map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
6.1field-weighted citation impact, top 3% 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.

NCT00006512 completednot on this map

Characterizing a 5P-Linked BHR Susceptibility Locus

TypeobservationalSponsorUniversity of ChicagoRan2000 to 2005ConditionsAsthma, Lung Diseases
3 · Its place in the literature

Who cites it

59 citing papers in PubMed, 135 citations in OpenAlex.

  1. Article
  2. Article
  3. Multivariate genetic architecture reveals testosterone-driven sexual antagonism in contemporary humans.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  4. Metabolomic changes in children with autism.World journal of clinical pediatrics · 2024
    Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Maternal Serotonin Levels Are Associated With Cognitive Ability and Core Symptoms in Autism Spectrum Disorder.Journal of the American Academy of Child and Adolescent Psychiatry · 2018
    Article
  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

4 authors at 1 institution in 1 country.

Lauren A WeissDepartment of Human Genetics, The University of Chicago, 920 East 58th Street, Chicago, IL 60637, USA.
Mark Abney
Edwin H Cook
Carole Ober
University of Chicago · US

Funding

T CELL CO-STIMULATION IN ALLERGIC ASTHMAP50HL056399 · NHLBI · UNIVERSITY OF CHICAGO · PI WHITE, STEVEN R · 1996 to 2005
$9.1M
NEUROIMAGING STUDIES OF AUTISM SPECTRUM CONDITIONSU19HD035482 · NICHD · YALE UNIVERSITY · PI VOLKMAR, FRED ROBERT · 2002 to 2006
$6.7M
NEUROIMAGING STUDIES OF AUTISM AND ASPERGER'S DISORDERP01HD035482 · NICHD · YALE UNIVERSITY · PI CICCHETTI, DOMINICK · 1997 to 2001
$3.9M
Methods for Complex Trait Mapping in Large PedigreesR01HG002899 · NHGRI · UNIVERSITY OF CHICAGO · PI ABNEY, MARK A · 2004 to 2015
$3.5M
CHARACTERIZING A 5P-LINKED BHR SUSCEPTIBILITY LOCUSR01HL066533 · NHLBI · UNIVERSITY OF CHICAGO · PI OBER, CAROLE · 2000 to 2004
$2.4M
Robust Methods for Indentifying Genes for Complex TraitsR01DK055889 · NIDDK · UNIVERSITY OF CHICAGO · PI COX, NANCY J. · 1998 to 2004
$1.3M
NHGRI NIH HHS HG 02899NHGRI NIH HHS R01 HG002899NHLBI NIH HHS HL 56399NHLBI NIH HHS HL 66533NHLBI NIH HHS P50 HL056399NHLBI NIH HHS R01 HL066533NICHD NIH HHS HD 35482NICHD NIH HHS P01 HD035482NICHD NIH HHS U19 HD035482NIDDK NIH HHS DK 55889NIDDK NIH HHS R01 DK055889
6 · The paper itself

Abstract

Recently, a quantitative-trait locus (QTL) for whole blood serotonin level was identified in a genomewide linkage and association study in a founder population. Because serotonin level is a sexually dimorphic trait, in the present study, we evaluated the sex-specific genetic architecture of whole blood serotonin level in the same population. Here, we use an extended homozygosity-by-descent linkage method that is suitable for large complex pedigrees. Although both males and females have high broad heritability (H2=0.99), females have a higher additive component (h2=0.63 in females; h2=0.27 in males). Furthermore, the serotonin QTL on 17q that was identified previously in this population, integrin beta 3 (ITGB3), and a novel locus on 2q influence serotonin levels only in males, whereas linkage to a region on chromosome 6q is specific to females. Both sexes contribute to linkage signals on 12q and 16p. There were, overall, more associations meeting criteria for suggestive significance in males than in females, including those of ITGB3 and the serotonin transporter gene (5HTT). This analysis is consistent with heritable sexual dimorphism in whole blood serotonin levels resulting from the effects of a combination of sex-specific and sex-independent loci.

Indexed as

Quantitative Trait, HeritableSex CharacteristicsAdolescentAdultAgedChildChild, PreschoolChromosome MappingFemaleFounder EffectGenetic LinkageHumansMaleMicrosatellite RepeatsMiddle AgedSerotoninSerotonin

Identifiers

PMID15526234
PMCPMC1196431
OpenAlexW2126589263

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.