Evidence map›Paper›PMID 16152574›Full record

ArticleAmerican journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics2005

Linkage analysis of anorexia and bulimia nervosa cohorts using selected behavioral phenotypes as quantitative traits or covariates.

Silviu-Alin Bacanu, Cynthia M Bulik, Kelly L Klump, Manfred M Fichter, Katherine A Halmi, Pamela Keel, Allan S Kaplan, James E Mitchell, Alessandro Rotondo, Michael Strober and 8 more

Open access · greenAbstract read
In one paragraph

Article in American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
7.5field-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.

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

22 citing papers in PubMed, 68 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Genome-wide association analysis of eating disorder-related symptoms, behaviors, and personality traits.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2012
    Article
  7. Current status of functional imaging in eating disorders.The International journal of eating disorders · 2012
    Review
  8. Article
  9. Review
  10. Absence of association between specific common variants of the obesity-related FTO gene and psychological and behavioral eating disorder phenotypes.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2011
    Article
  11. Article
  12. Review
  13. Association study of 182 candidate genes in anorexia nervosa.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2010
    Article
  14. Eating disorders: the current status of molecular genetic research.European child & adolescent psychiatry · 2010
    Review
  15. The Genetics of Anorexia Nervosa: Current Findings and Future Perspectives.International journal of child and adolescent health · 2009
    Article
  16. Article
  17. Review
  18. Article
  19. Selection of eating-disorder phenotypes for linkage analysis.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2005
    Article
  20. Exploring the gene-environment nexus in eating disorders.Journal of psychiatry & neuroscience : JPN · 2005
    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

18 authors at 13 institutions in 5 countries.

Silviu-Alin BacanuDepartment of Psychiatry, University of Pittsburgh, Pittsburgh, PA 15213-2593, USA.
Cynthia M Bulik
Kelly L Klump
Manfred M Fichter
Katherine A Halmi
Pamela Keel
Allan S Kaplan
James E Mitchell
Alessandro Rotondo
Michael Strober
Janet Treasure
D Blake Woodside
Vibhor A Sonpar
Weiting Xie
Andrew W Bergen
Wade H Berrettini
Walter H Kaye
Bernie Devlin
University of Pittsburgh · USToronto General Hospital · CAMichigan State University · USNational Cancer Institute · USNational Health Service · GBNeuropsychiatric Research Institute · USNewYork–Presbyterian Hospital · USSchön Klinik Roseneck · DEUniversity of California, Los Angeles · USUniversity of Iowa · USUniversity of North Carolina at Chapel Hill · USUniversity of Pennsylvania · USUniversity of Pisa · IT

Funding

Genetics Association in Schizophrenia and Other DisordersR37MH057881 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DEVLIN, BERNIE · 2013 to 2022
$5.4M
GENETIC ASSOCIATION IN SCHIZOPHRENIA AND OTHER DISORDERSR01MH057881 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DEVLIN, BERNIE · 1998 to 2012
$4.8M
Genetics of Anorexia NervosaR01MH066117 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DEVLIN, BERNIE · 2002 to 2006
$1.0M
NIMH NIH HHS R01 MH057881NIMH NIH HHS R01 MH066117NIMH NIH HHS R37 MH057881
6 · The paper itself

Abstract

To increase the likelihood of finding genetic variation conferring liability to eating disorders, we measured over 100 attributes thought to be related to liability to eating disorders on affected individuals from multiplex families and two cohorts: one recruited through a proband with anorexia nervosa (AN; AN cohort); the other recruited through a proband with bulimia nervosa (BN; BN cohort). By a multilayer decision process based on expert evaluation and statistical analysis, six traits were selected for linkage analysis (1): obsessionality (OBS), age at menarche (MENAR), and anxiety (ANX) for quantitative trait locus (QTL) linkage analysis; and lifetime minimum body mass index (BMI), concern over mistakes (CM), and food-related obsessions (OBF) for covariate-based linkage analysis. The BN cohort produced the largest linkage signals: for QTL linkage analysis, four suggestive signals: (for MENAR, at 10p13; for ANX, at 1q31.1, 4q35.2, and 8q13.1); for covariate-based linkage analyses, both significant and suggestive linkages (for BMI, one significant [4q21.1] and three suggestive [3p23, 10p13, 5p15.3]; for CM, two significant [16p13.3, 14q21.1] and three suggestive [4p15.33, 8q11.23, 10p11.21]; and for OBF, one significant [14q21.1] and five suggestive [4p16.1, 10p13.1, 8q11.23, 16p13.3, 18p11.31]). Results from the AN cohort were far less compelling: for QTL linkage analysis, two suggestive signals (for OBS at 6q21 and for ANX at 9p21.3); for covariate-based linkage analysis, five suggestive signals (for BMI at 4q13.1, for CM at 11p11.2 and 17q25.1, and for OBF at 17q25.1 and 15q26.2). Overlap between the two cohorts was minimal for substantial linkage signals.

Indexed as

Genetic LinkagePhenotypeQuantitative Trait, HeritableQuantitative Trait LociAnorexia NervosaAnxietyBulimia NervosaFemaleHumansMenarche

Identifiers

PMID16152574
PMCPMC2590774
OpenAlexW2167884000

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.