Evidence map›Paper›PMID 24980794›Full record

ArticleAmerican journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics2014

Characterizing runs of homozygosity and their impact on risk for psychosis in a population isolate.

Nadine M Melhem, Cong Lu, Cara Dresbold, Frank A Middleton, Lambertus Klei, Shawn Wood, Stephen V Faraone, Sophia Vinogradov, Josepha Tiobech, Victor Yano and 4 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, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 21% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

14 authors at 7 institutions in 2 countries.

Nadine M MelhemDepartment of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Cong Lu
Cara Dresbold
Frank A Middleton
Lambertus Klei
Shawn Wood
Stephen V Faraone
Sophia Vinogradov
Josepha Tiobech
Victor Yano
Kathryn Roeder
William Byerley
Marina Myles-Worsley
Bernie Devlin
SUNY Upstate Medical University · USUniversity of Pittsburgh · USCarnegie Mellon University · USRepublic of Palau Ministry of Health · PWUniversity of Pittsburgh Medical Center · USUniversity of California, San Francisco · USUniversity of San Francisco · US

Funding

Genetics of Schizophrenia in Oceanic Palau.R01MH080373 · NIMH · UPSTATE MEDICAL UNIVERSITY · PI MYLES-WORSLEY, MARINA · 2007 to 2009
$1.3M
Genetic Linkage Study of Depression and Anxiety Disorders in an Arab KindredK01MH077930 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI MELHEM, NADINE M. · 2007 to 2011
$755k
Genetics of Schizophrenia in Oceanic Palau.R01MH080375 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DEVLIN, BERNIE · 2008 to 2010
$453k
Genetics of Schizophrenia in Oceanic PalauR01MH080299 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BYERLEY, WILLIAM · 2007 to 2009
$270k
NIMH NIH HHS K01 MH077930NIMH NIH HHS MH077930NIMH NIH HHS MH080299NIMH NIH HHS MH080373NIMH NIH HHS MH080375NIMH NIH HHS R01 MH080299NIMH NIH HHS R01 MH080373NIMH NIH HHS R01 MH080375
6 · The paper itself

Abstract

An increased abundance of runs of homozygosity (ROH) has been associated with risk for various diseases, including schizophrenia. Here we investigate the characteristics of ROH in Palau, an Oceanic population, evaluating whether these characteristics are related to risk for psychotic disorders and the nature of this association. To accomplish these aims we evaluate a sample of 203 cases with schizophrenia and related psychotic disorders-representing almost complete ascertainment of affected individuals in the population-and contrast their ROH to that of 125 subjects chosen to function as controls. While Palauan diagnosed with psychotic disorders tend to have slightly more ROH regions than controls, the distinguishing features are that they have longer ROH regions, greater total length of ROH, and their ROH tends to co-occur more often at the same locus. The nature of the sample allows us to investigate whether rare, highly penetrant recessive variants generate such case-control differences in ROH. Neither rare, highly penetrant recessive variants nor individual common variants of large effect account for a substantial proportion of risk for psychosis in Palau. These results suggest a more nuanced model for risk is required to explain patterns of ROH for this population.

Indexed as

Genetic Predisposition to DiseaseAllelesCase-Control StudiesGenome, HumanHaplotypesHomozygoteHumansPalauPolymorphism, Single NucleotidePsychotic DisordersRisk FactorshomozygosityPalaupsychosisROHschizophrenia

Identifiers

PMID24980794
PMCPMC5058445
OpenAlexW2160253429

What OpenQuestion holds

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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.