Evidence map›Paper›PMID 30718465›Full record

ArticleTranslational psychiatry2019

The genomics of major psychiatric disorders in a large pedigree from Northern Sweden.

Jin Szatkiewicz, James J Crowley, Annelie Nordin Adolfsson, Karolina A Åberg, Maaike Alaerts, Giulio Genovese, Steven McCarroll, Jurgen Del-Favero, Rolf Adolfsson, Patrick F Sullivan

Abstract read
In one paragraph

Article in Translational psychiatry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

  1. Review
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  11. NicotinamideInternational journal of tryptophan research : IJTR · 2020
    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

10 authors.

Jin SzatkiewiczDepartment of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
James J CrowleyDepartment of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Annelie Nordin AdolfssonDepartment of Clinical Sciences and Psychiatry, University of Umeå, Umeå, Sweden.
Karolina A ÅbergCenter for Biomarker Research and Precision Medicine, Virginia Commonwealth University, Richmond, VA, USA.
Maaike AlaertsCenter of Medical Genetics, University of Antwerp and Antwerp University Hospital, Antwerp, Belgium.
Giulio GenoveseBroad Institute of MIT and Harvard, Cambridge, MA, USA.
Steven McCarrollBroad Institute of MIT and Harvard, Cambridge, MA, USA.
Jurgen Del-FaveroVIB Center for Molecular Neurology, Universiteitsplein 1, Antwerp, Belgium and Multiplicom N.V., Galileilaan 18, Niel, Belgium.
Rolf AdolfssonDepartment of Clinical Sciences and Psychiatry, University of Umeå, Umeå, Sweden. rolf.adolfsson@umu.se.
Patrick F SullivanDepartment of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA. pfsulliv@med.unc.edu.ORCID http://orcid.org/0000-0002-6619-873X

Funding

Finding causal variants within schizophrenia risk lociR01MH106611 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SZATKIEWICZ, JIN PENG · 2015 to 2019
$3.3M
OCD: Novel Comparative Genomic Approaches to Identify Disease and Treatment MechanismsR01MH110427 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CROWLEY, JAMES JOSEPH · 2016 to 2021
$3.0M
Finding single-gene copy number variants in schizophreniaR21MH104831 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CROWLEY, JAMES JOSEPH, SZATKIEWICZ, JIN PENG · 2014 to 2015
$418k
NIMH NIH HHS R01 MH106611NIMH NIH HHS R01 MH110427NIMH NIH HHS R21 MH104831
6 · The paper itself

Abstract

We searched for genetic causes of major psychiatric disorders (bipolar disorder, schizoaffective disorder, and schizophrenia) in a large, densely affected pedigree from Northern Sweden that originated with three pairs of founders born around 1650. We applied a systematic genomic approach to the pedigree via karyotyping (N = 9), genome-wide SNP arrays (N = 418), whole-exome sequencing (N = 26), and whole-genome sequencing (N = 10). Comprehensive analysis did not identify plausible variants of strong effect. Rather, pedigree cases had significantly higher genetic risk scores compared to pedigree and community controls.

Indexed as

AdultAgedBipolar DisorderCase-Control StudiesExome SequencingFemaleGenomicsHumansKaryotypingMaleMiddle AgedOligonucleotide Array Sequence AnalysisPedigreePolymorphism, Single NucleotidePsychotic DisordersSchizophrenia

Identifiers

PMID30718465
PMCPMC6362018

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Registered trials

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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.