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Paper · 27028512

Genetic Evaluation of Schizophrenia Using the Illumina HumanExome Chip.

Moons T and 8 others. PLoS One, 2016. Cited by 12 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Genetic Evaluation of Schizophrenia Using the Illumina HumanExome Chip. Papers, record 27028512. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/27028512

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Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title
Genetic Evaluation of Schizophrenia Using the Illumina HumanExome Chip.
PubMed
Journal
PLoS One
PubMed
Year
2016
PubMed
Publication types
Journal Article
PubMed
Citations, by iCite
12
iCite
Relative citation ratio, by iCite
0.4
iCite
Revised in PubMed
2023-11-11
PubMed

Authors9

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

OrderAuthorForenameKindORCID iD
1Moons TTim
2De Hert MMarc
3Gellens EEdith
4Gielen LLeen
5Sweers KKim
6Jacqmaert SSigrun
7van Winkel RRuud
8Vandekerckhove PPhilippe
9Claes SStephan

Source PubMed

Topics14

NLM's MeSH indexing of the paper, its major topics first.

MeSH termMajor
SchizophreniaMajor topic
Adult
Case-Control Studies
Exome
Female
Gene Frequency
Genetic Predisposition to Disease
Genome-Wide Association Study
Humans
Male
Oligonucleotide Array Sequence Analysis
Polymorphism, Single Nucleotide
Sequence Analysis, RNA
Transcriptome

Source PubMed

Grants0

Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.

None in this release.

Trials0

The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.

None in this release.

Comments and corrections0

PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.

None in this release.

References71

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

OrderPMIDTitleJournalYearIn PapersSource
124,253,340Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder.Nat Commun2013https://conductscience.org/library/papers/24253340PubMed
224,463,508A polygenic burden of rare disruptive mutations in schizophrenia.Nature2014https://conductscience.org/library/papers/24463508PubMed
311,121,167Mutation and association analysis of the Fyn kinase gene with alcoholism and schizophrenia.Am J Med Genet2000https://conductscience.org/library/papers/11121167PubMed
410,402,499Follow-up study on a susceptibility locus for schizophrenia on chromosome 6q.Am J Med Genet1999https://conductscience.org/library/papers/10402499PubMed
515,908,096Apoptotic mechanisms in the pathophysiology of schizophrenia.Prog Neuropsychopharmacol Biol Psychiatry2005https://conductscience.org/library/papers/15908096PubMed
622,277,805Genome-wide association studies of schizophrenia: does bigger lead to better results?Curr Opin Psychiatry2012https://conductscience.org/library/papers/22277805PubMed
722,614,287Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC.Mol Psychiatry2013https://conductscience.org/library/papers/22614287PubMed
819,886,379Declaration of Helsinki. Ethical principles for medical research involving human subjects.J Indian Med Assoc2009https://conductscience.org/library/papers/19886379PubMed
923,732,877708 Common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits.Mol Psychiatry2014https://conductscience.org/library/papers/23732877PubMed
101,615,098Will schizophrenia become a graveyard for molecular geneticists?Psychol Med1992https://conductscience.org/library/papers/1615098PubMed

Cited by6

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 12 citations.

PMIDTitleJournalYearIn PapersSource
41,333,154Alpha-neurexins in health and disease.Front Mol Neurosci2025https://conductscience.org/library/papers/41333154PubMed
36,598,609Pathophysiological Roles of Auxiliary Calcium Channel α2δ Subunits.Handb Exp Pharmacol2023https://conductscience.org/library/papers/36598609PubMed
34,584,171Common and disorder-specific upregulation of the inflammatory markers TRAIL and CCL20 in depression and schizophrenia.Sci Rep2021https://conductscience.org/library/papers/34584171PubMed
33,679,366Phenotypic Characterization and Brain Structure Analysis of Calcium Channel Subunit α2δ-2 Mutant (Ducky) and α2δ Double Knockout Mice.Front Synaptic Neurosci2021https://conductscience.org/library/papers/33679366PubMed
32,607,809Neuronal α2δ proteins and brain disorders.Pflugers Arch2020https://conductscience.org/library/papers/32607809PubMed
30,683,685Presynaptic α2δ-2 Calcium Channel Subunits Regulate Postsynaptic GABAA Receptor Abundance and Axonal Wiring.J Neurosci2019https://conductscience.org/library/papers/30683685PubMed

Genes22

The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.

GeneNCBI Gene IDLinked byIn GenesSource
ADGRE5976PubTator's text mininghttps://conductscience.org/library/genes/976NCBI Gene
CACNA1C775PubTator's text mininghttps://conductscience.org/library/genes/775NCBI Gene
CACNA2D355,799PubTator's text mininghttps://conductscience.org/library/genes/55799NCBI Gene
CCDC60160,777PubTator's text mininghttps://conductscience.org/library/genes/160777NCBI Gene
CCN68,838PubTator's text mininghttps://conductscience.org/library/genes/8838NCBI Gene
CHRNA31,136PubTator's text mininghttps://conductscience.org/library/genes/1136NCBI Gene
CNNM254,805PubTator's text mininghttps://conductscience.org/library/genes/54805NCBI Gene
EBLN1340,900PubTator's text mininghttps://conductscience.org/library/genes/340900NCBI Gene
FYN2,534PubTator's text mininghttps://conductscience.org/library/genes/2534NCBI Gene
LAMA43,910PubTator's text mininghttps://conductscience.org/library/genes/3910NCBI Gene

1 to 10 of 22

See all 22 genes

Drugs0

The drugs whose trials, in the Pipelines release, list the paper.

None in this release.

Data0

The data bank entries PubMed's record names. Trial numbers are under Trials.

None in this release.

Data dates

The date of each source this release read.

PubMed
2026-11-06
PubMed
iCite
2026-11-05
iCite
PMC's ID file
2026-11-05
PMC's ID file
NIH RePORTER's grant and paper links
2026-11-01
NIH RePORTER's grant and paper links
Trials
2026-11-12
Gene search
2026-11-11
Pipelines
2026-09-18

Sources 11

  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ClinicalTrials.govNo license stated
  • HGNCCC0
  • iCiteCC BY 4.0
  • NCBI GenePublic domain (US government)
  • NIH RePORTER's grant and paper linksPublic domain
  • Open TargetsCC0 1.0
  • PMC's ID filePublic domain (US government)
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0
Each source's terms
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ClinicalTrials.govnone stated
  • HGNCCC0: https://www.genenames.org/about/license/
  • iCiteCC BY 4.0
  • NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
  • Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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