Evidence map›Paper›PMID 16152575›Full record

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

Selection of eating-disorder phenotypes for linkage analysis.

Cynthia M Bulik, Silviu-Alin Bacanu, 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 · bronzeAbstract 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 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
4.3field-weighted citation impact, top 7% 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

10 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Genetic association of recovery from eating disorders: the role of GABA receptor SNPs.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2011
    Article
  5. 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
  6. Article
  7. Article
  8. Linkage analysis of anorexia and bulimia nervosa cohorts using selected behavioral phenotypes as quantitative traits or covariates.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2005
    Article
  9. Article
  10. Association of candidate genes with phenotypic traits relevant to anorexia nervosa.European eating disorders review : the journal of the Eating Disorders Association
    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

18 authors at 13 institutions in 5 countries.

Cynthia M BulikDepartment of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Silviu-Alin Bacanu
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 · CADivision of Cancer Epidemiology and GeneticsMichigan State University · 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

Vulnerability to anorexia nervosa (AN) and bulimia nervosa (BN) arise from the interplay of genetic and environmental factors. To explore the genetic contribution, we measured over 100 psychiatric, personality, and temperament phenotypes of individuals with eating disorders from 154 multiplex families accessed through an AN proband (AN cohort) and 244 multiplex families accessed through a BN proband (BN cohort). To select a parsimonious subset of these attributes for linkage analysis, we subjected the variables to a multilayer decision process based on expert evaluation and statistical analysis. Criteria for trait choice included relevance to eating disorders pathology, published evidence for heritability, and results from our data. Based on these criteria, we chose six traits to analyze for linkage. Obsessionality, Age-at-Menarche, and a composite Anxiety measure displayed features of heritable quantitative traits, such as normal distribution and familial correlation, and thus appeared ideal for quantitative trait locus (QTL) linkage analysis. By contrast, some families showed highly concordant and extreme values for three variables-lifetime minimum Body Mass Index (lowest BMI attained during the course of illness), concern over mistakes, and food-related obsessions-whereas others did not. These distributions are consistent with a mixture of populations, and thus the variables were matched with covariate linkage analysis. Linkage results appear in a subsequent report. Our report lays out a systematic roadmap for utilizing a rich set of phenotypes for genetic analyses, including the selection of linkage methods paired to those phenotypes.

Indexed as

Genetic LinkageAlgorithmsFeeding and Eating DisordersFemaleGenetic Predisposition to DiseaseHumansMaleMenarcheMultivariate AnalysisPhenotypeQuantitative Trait Loci

Identifiers

PMID16152575
PMCPMC2560991
OpenAlexW2102944757

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.