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Paper · 24253340

Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder.

Lencz T and 25 others. Nat Commun, 2013. Cited by 90 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder. Papers, record 24253340. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/24253340

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Paper

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

Title
Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder.
PubMed
Journal
Nat Commun
PubMed
Year
2013
PubMed
Publication types
Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't
PubMed
Citations, by iCite
90
iCite
Relative citation ratio, by iCite
2.52
iCite
Revised in PubMed
2025-05-24
PubMed

Authors26

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

OrderAuthorForenameKindORCID iD
1Lencz TTodd
2Guha SSaurav
3Liu CChunyu
4Rosenfeld JJeffrey
5Mukherjee SSemanti
6DeRosse PPamela
7John MMajnu
8Cheng LLijun
9Zhang CChunling
10Badner JAJudith A

1 to 10 of 26Source PubMed

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Topics10

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

MeSH termMajor
Bipolar DisorderMajor topic
SchizophreniaMajor topic
SulfotransferasesMajor topic
Gene Expression Regulation
Genetic Predisposition to Disease
Genome, Human
Humans
Jews
Odds Ratio
Polymorphism, Single Nucleotide

Source PubMed

Grants8

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.

Grant, as the record writes itAgencyCountryNIH projectStated bySource
R01 MH095458NIMH NIH HHSUnited StatesR01MH095458PubMed and NIHNIH RePORTER
R01 MH084098NIMH NIH HHSUnited StatesR01MH084098PubMed and NIHNIH RePORTER
P50 MH080173NIMH NIH HHSUnited StatesP50MH080173PubMed and NIHNIH RePORTER
R01 MH080425NIMH NIH HHSUnited StatesR01MH080425PubMed and NIHNIH RePORTER
Wellcome TrustUnited KingdomPubMedPubMed
P30 MH090590NIMH NIH HHSUnited StatesP30MH090590PubMed and NIHNIH RePORTER
RC2 MH089964NIMH NIH HHSUnited StatesRC2MH089964PubMed and NIHNIH RePORTER
ZIAAA000301NIHNIH RePORTER

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.

References47

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

OrderPMIDTitleJournalYearIn PapersSource
116,632,515Adjusting batch effects in microarray expression data using empirical Bayes methods.Biostatistics2007https://conductscience.org/library/papers/16632515PubMed
221,926,972Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4.Nat Genet2011https://conductscience.org/library/papers/21926972PubMed
317,151,600Genome-wide atlas of gene expression in the adult mouse brain.Nature2007https://conductscience.org/library/papers/17151600PubMed
422,820,512Fast and accurate genotype imputation in genome-wide association studies through pre-phasing.Nat Genet2012https://conductscience.org/library/papers/22820512PubMed
523,104,006Genome-wide association meta-analysis identifies new endometriosis risk loci.Nat Genet2012https://conductscience.org/library/papers/23104006PubMed
619,543,373A flexible and accurate genotype imputation method for the next generation of genome-wide association studies.PLoS Genet2009https://conductscience.org/library/papers/19543373PubMed
720,616,382METAL: fast and efficient meta-analysis of genomewide association scans.Bioinformatics2010https://conductscience.org/library/papers/20616382PubMed
820,159,113Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene.Am J Hum Genet2010https://conductscience.org/library/papers/20159113PubMed
921,548,950Evaluation of 22 genetic variants with Crohn's disease risk in the Ashkenazi Jewish population: a case-control study.BMC Med Genet2011https://conductscience.org/library/papers/21548950PubMed
1010,025,441Heritability estimates for psychotic disorders: the Maudsley twin psychosis series.Arch Gen Psychiatry1999https://conductscience.org/library/papers/10025441PubMed

1 to 10 of 47

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Cited by59

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 90 citations.

PMIDTitleJournalYearIn PapersSource
42,585,021Pleiotrophin regulates presynaptic assembly and function through heparan sulfate-dependent binding to neurexin1.Cell Rep2026https://conductscience.org/library/papers/42585021PubMed
42,523,604PRANA: A Deep Learning Method for Adapting Polygenic Risk Scores to Diverse Ethnic Groups.medRxiv2026https://conductscience.org/library/papers/42523604PubMed
41,629,769Genomic signatures of environmental adaptation in Danzhou chickens.BMC Genomics2026https://conductscience.org/library/papers/41629769PubMed
39,630,030Genetic variability in proteoglycan biosynthetic genes reveals new facets of heparan sulfate diversity.Essays Biochem2024https://conductscience.org/library/papers/39630030PubMed
38,351,061Structural and mechanistic characterization of bifunctional heparan sulfate N-deacetylase-N-sulfotransferase 1.Nat Commun2024https://conductscience.org/library/papers/38351061PubMed
38,265,251The predictive capacity of polygenic risk scores for disease risk is only moderately influenced by imputation panels tailored to the target population.Bioinformatics2024https://conductscience.org/library/papers/38265251PubMed
38,015,989Knockout of the intellectual disability-linked gene Hs6st2 in mice decreases heparan sulfate 6-O-sulfation, impairs dendritic spines of hippocampal neurons, and affects memory.Glycobiology2024https://conductscience.org/library/papers/38015989PubMed
37,510,946Vascular Schizophrenia-like Psychosis in Older Adults.J Clin Med2023https://conductscience.org/library/papers/37510946PubMed
37,354,489Linking Polygenic Risk of Schizophrenia to Variation in Magnetic Resonance Imaging Brain Measures: A Comprehensive Systematic Review.Schizophr Bull2024https://conductscience.org/library/papers/37354489PubMed
36,980,855Integrating Whole-Genome Resequencing and RNA Sequencing Data Reveals Selective Sweeps and Differentially Expressed Genes Related to Nervous System Changes in Luxi Gamecocks.Genes (Basel)2023https://conductscience.org/library/papers/36980855PubMed

1 to 10 of 59

See all 59 cited by

Genes6

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
HLA-C3,107PubTator's text mininghttps://conductscience.org/library/genes/3107NCBI Gene
NDST39,348PubTator's text mininghttps://conductscience.org/library/genes/9348NCBI Gene
NOD264,127PubTator's text mininghttps://conductscience.org/library/genes/64127NCBI Gene
NT5C222,978PubTator's text mininghttps://conductscience.org/library/genes/22978NCBI Gene
PTGFR5,737PubTator's text mininghttps://conductscience.org/library/genes/5737NCBI Gene
RNF14681,847PubTator's text mininghttps://conductscience.org/library/genes/81847NCBI Gene

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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