Evidence map›Paper›PMID 33531474›Full record

SynthesisTranslational psychiatry2021

Genome-wide association study of pediatric obsessive-compulsive traits: shared genetic risk between traits and disorder.

Christie L Burton, Mathieu Lemire, Bowei Xiao, Elizabeth C Corfield, Lauren Erdman, Janita Bralten, Geert Poelmans, Dongmei Yu, S-M Shaheen, Tara Goodale and 12 more

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in Translational psychiatry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 6 pooled it
5.0field-weighted citation impact, top 4% 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

25 citing papers in PubMed, 6 syntheses or guidelines pooled it, 49 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Pooled it
  6. Genetic contributions to alcohol use disorder treatment outcomes: a genome-wide pharmacogenomics study.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2021
    Pooled it
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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

22 authors at 20 institutions in 13 countries.

Christie L BurtonNeurosciences and Mental Health, Toronto, Canada. christie.burton@sickkids.ca.ORCID 0000-0002-8955-6528
Mathieu LemireNeurosciences and Mental Health, Toronto, Canada.
Bowei XiaoGenetics and Genome Biology Hospital for Sick Children, Toronto, Canada.
Elizabeth C CorfieldNeurosciences and Mental Health, Toronto, Canada.ORCID 0000-0002-0119-157X
Lauren ErdmanGenetics and Genome Biology Hospital for Sick Children, Toronto, Canada.
Janita BraltenDepartment of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands.
Geert PoelmansDepartment of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands.
Dongmei YuThe Psychiatric and Neurodevelopmental Genetics Unit, Center for Genomic Medicine, Department of Psychiatry, Massachusetts General Hospital, Boston, MA, USA.
S-M ShaheenThe Mathison Centre for Mental Health Research and Education, Hotchkiss Brain Institute, Calgary, Canada.
Tara GoodaleNeurosciences and Mental Health, Toronto, Canada.
Vanessa M SinopoliGenetics and Genome Biology Hospital for Sick Children, Toronto, Canada.
OCD Working Group of the Psychiatric Genomics Consortium
Noam SoreniDepartment of Psychiatry and Behavioural Neurosciences, McMaster University, Ontario, Canada.
Gregory L HannaDepartment of Psychiatry, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0002-0742-6990
Kate D FitzgeraldDepartment of Psychiatry, University of Michigan, Ann Arbor, MI, USA.
David RosenbergDepartment of Psychiatry and Behavioural Neurosciences, Wayne State University, Detroit, MI, USA.
Gerald NestadtDepartment of Psychiatry and Behavioral Sciences, Johns Hopkins University, Baltimore, MD, USA.
Andrew D PatersonGenetics and Genome Biology Hospital for Sick Children, Toronto, Canada.
Lisa J StrugGenetics and Genome Biology Hospital for Sick Children, Toronto, Canada.
Russell J SchacharNeurosciences and Mental Health, Toronto, Canada.
Jennifer CrosbieNeurosciences and Mental Health, Toronto, Canada.
Paul D ArnoldGenetics and Genome Biology Hospital for Sick Children, Toronto, Canada.ORCID 0000-0003-2496-4624
Johns Hopkins University · USBroad Institute · USHarvard University · USHospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo · BRHospital for Sick Children · CAMental Health Research Canada · CAUniversity of Toronto · CAAmsterdam University Medical Centers · NLBrown University · USYale University · USCentre for Addiction and Mental Health · CAColumbia University Irving Medical Center · USNational Institute of Mental Health · USRadboud University Nijmegen · NLStellenbosch University · ZAUniversity of Calgary · CAUniversity of Illinois Chicago · USUniversity of Michigan · USUniversity of Milan · ITUniversity of Southern California · US

Funding

Neurodevelopmental Genomics: Trajectories of Complex PhenotypesRC2MH089983 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI GUR, RAQUEL E · 2009 to 2011
$14.3M
2/2 Neurodevelopmental Genomics: Trajectories of Complex PhenotypesRC2MH089924 · NIMH · CHILDREN'S HOSP OF PHILADELPHIA · PI HAKONARSON, HAKON · 2009 to 2011
$10.7M
OCD Collaborative Genetics Association StudyR01MH071507 · NIMH · JOHNS HOPKINS UNIVERSITY · PI NESTADT, GERALD · 2007 to 2010
$6.5M
Obsessive-compulsive disorder (OCD) Collaborative Genetics Association StudyR01MH079489 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI GELLER, DANIEL A · 2007 to 2010
$3.4M
PsycheMERGE: Leveraging electronic health records and genomics for mental health researchR01MH118233 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI DAVIS, LEA K, SMOLLER, JORDAN W · 2019 to 2022
$3.1M
2/3 Brain Function and Genetics in Pediatric Obsessive-Compulsive BehaviorsR01MH085321 · NIMH · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HANNA, GREGORY L. · 2009 to 2019
$2.9M
Action Monitoring and Genomic Variants in Pediatric Obsessive-Compulsive BehaviorR01MH101493 · NIMH · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ARNOLD, PAUL DANIEL, GEHRING, WILLIAM J · 2013 to 2016
$2.3M
Mental health and chronic disease: A psycheMERGE investigation into the shared biology underlying psychiatric disorders and their physical comorbiditiesR56MH120736 · NIMH · VANDERBILT UNIVERSITY MEDICAL CENTER · PI DAVIS, LEA K · 2019 to 2020
$1.6M
Translational phenomics and genomics of Gilles de la Tourette SyndromeK23MH085057 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI SCHARF, JEREMIAH M · 2009 to 2013
$929k
OCD Collaborative Genetics Association StudyR01MH079488 · NIMH · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI FYER, ABBY J · 2007 to 2010
$906k
Obsessive-compulsive disorder (OCD) Collaborative Genetics Association StudyR01MH079494 · NIMH · UNIVERSITY OF SOUTHERN CALIFORNIA · PI KNOWLES, JAMES A · 2007 to 2011
$840k
OCD Collaborative Genetics Association StudyR01MH079487 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MCCRACKEN, JAMES T. · 2007 to 2010
$797k
NIMH NIH HHS K23 MH085057NIMH NIH HHS R01 MH071507NIMH NIH HHS R01 MH079487NIMH NIH HHS R01 MH079488NIMH NIH HHS R01 MH079489NIMH NIH HHS R01 MH079494NIMH NIH HHS R01 MH085321NIMH NIH HHS R01 MH101493NIMH NIH HHS R01 MH118233NIMH NIH HHS R13 MH073250NIMH NIH HHS R21 MH087748NIMH NIH HHS R56 MH120736NIMH NIH HHS RC2 MH089924NIMH NIH HHS RC2 MH089983
6 · The paper itself

Abstract

Using a novel trait-based measure, we examined genetic variants associated with obsessive-compulsive (OC) traits and tested whether OC traits and obsessive-compulsive disorder (OCD) shared genetic risk. We conducted a genome-wide association analysis (GWAS) of OC traits using the Toronto Obsessive-Compulsive Scale (TOCS) in 5018 unrelated Caucasian children and adolescents from the community (Spit for Science sample). We tested the hypothesis that genetic variants associated with OC traits from the community would be associated with clinical OCD using a meta-analysis of all currently available OCD cases. Shared genetic risk was examined between OC traits and OCD in the respective samples using polygenic risk score and genetic correlation analyses. A locus tagged by rs7856850 in an intron of PTPRD (protein tyrosine phosphatase δ) was significantly associated with OC traits at the genome-wide significance level (p = 2.48 × 10

Indexed as

Genome-Wide Association StudyObsessive-Compulsive DisorderAdolescentChildCompulsive BehaviorHumansPhenotypeRisk Factors

Identifiers

PMID33531474
PMCPMC7870035
OpenAlexW3128471417

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.