Evidence map›Paper›PMID 18813210›Full record

ArticleMolecular psychiatry2009

Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2.

M C O'Donovan, N Norton, H Williams, T Peirce, V Moskvina, I Nikolov, M Hamshere, L Carroll, L Georgieva, S Dwyer and 43 more

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Molecular psychiatry, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00006418 (Molecular Genetics of Schizophrenia), which is not on this map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 5% 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.

NCT00006418 completednot on this map

Molecular Genetics of Schizophrenia

TypeobservationalSponsorEndeavor HealthRan2003 to 2007Enrolled10,800ConditionsSchizophreniaArmsDNA collection
3 · Its place in the literature

Who cites it

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 73 citations in OpenAlex.

  1. Pooled it
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  18. An Integrative Bayesian Modeling Approach to Imaging Genetics.Journal of the American Statistical Association · 2013
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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

53 authors at 19 institutions in 9 countries.

M C O'DonovanDepartment of Psychological Medicine, School of Medicine, Cardiff University, Cardiff, UK. odonovanmc@cf.ac.uk
N Norton
H Williams
T Peirce
V Moskvina
I Nikolov
M Hamshere
L Carroll
L Georgieva
S Dwyer
P Holmans
J L Marchini
C C A Spencer
B Howie
H-T Leung
I Giegling
A M Hartmann
H-J Möller
D W Morris
Y Shi
G Feng
P Hoffmann
P Propping
C Vasilescu
W Maier
M Rietschel
S Zammit
J Schumacher
E M Quinn
T G Schulze
N Iwata
M Ikeda
A Darvasi
S Shifman
L He
J Duan
A R Sanders
D F Levinson
R Adolfsson
U Osby
L Terenius
E G Jönsson
S Cichon
M M Nöthen
M Gill
A P Corvin
D Rujescu
P V Gejman
G Kirov
N Craddock
N M Williams
M J Owen
Molecular Genetics of Schizophrenia Collaboration
Cardiff University · GBTrinity College Dublin · IEUniversity of Bonn · DEKarolinska Institutet · SENorthShore University HealthSystem · USUniversity of Oxford · GBHebrew University of Jerusalem · ILInstitute of Neurobiology and Molecular Medicine · ITLife & Brain (Germany) · DELudwig-Maximilians-Universität München · DENational Institute of Mental Health · USShanghai Jiao Tong University · CNCentral Institute of Mental Health · DEFujita Health University · JPJapan Science and Technology Agency · JPShanghai Mental Health Center · CNStanford University · USUmeå University · SEUniversity of Cambridge · GB

Funding

White Matter Abnormalities in SchizophreniaP50MH066392 · NIMH · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI BUXBAUM, JOSEPH D. · 2002 to 2012
$18.6M
Medical Research Council G0800509Medical Research Council G0801418NIMH NIH HHS 2 P50 MH066392-05A1Wellcome TrustWellcome Trust 076113
6 · The paper itself

Abstract

We and others have previously reported linkage to schizophrenia on chromosome 10q25-q26 but, to date, a susceptibility gene in the region has not been identified. We examined data from 3606 single-nucleotide polymorphisms (SNPs) mapping to 10q25-q26 that had been typed in a genome-wide association study (GWAS) of schizophrenia (479 UK cases/2937 controls). SNPs with P<0.01 (n=40) were genotyped in an additional 163 UK cases and those markers that remained nominally significant at P<0.01 (n=22) were genotyped in replication samples from Ireland, Germany and Bulgaria consisting of a total of 1664 cases with schizophrenia and 3541 controls. Only one SNP, rs17101921, was nominally significant after meta-analyses across the replication samples and this was genotyped in an additional six samples from the United States/Australia, Germany, China, Japan, Israel and Sweden (n=5142 cases/6561 controls). Across all replication samples, the allele at rs17101921 that was associated in the GWAS showed evidence for association independent of the original data (OR 1.17 (95% CI 1.06-1.29), P=0.0009). The SNP maps 85 kb from the nearest gene encoding fibroblast growth factor receptor 2 (FGFR2) making this a potential susceptibility gene for schizophrenia.

Indexed as

Genetic Predisposition to DiseaseAdultAgedAged, 80 and overChromosomes, Human, Pair 10FemaleGene FrequencyGenome-Wide Association StudyGenotypeHumansLinkage DisequilibriumMaleMeta-Analysis as TopicMiddle AgedPolymorphism, Single NucleotideReceptor, Fibroblast Growth Factor, Type 2Receptor, Fibroblast Growth Factor, Type 2

Identifiers

PMID18813210
PMCPMC3016613
OpenAlexW2076544616

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.