Paper · 39349682
Genome-wide association studies for pelvic organ prolapse in the Japanese population.
Matsunami M and 13 others. Commun Biol, 2024. Cited by 4 papers, by iCite.
11 sourcespapers-2026-11-12-0.1.0
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ConductScience Library. Genome-wide association studies for pelvic organ prolapse in the Japanese population. Papers, record 39349682. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/39349682
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Paper
PubMed's record of the paper, with iCite's citation figures. No abstract is shown.
Topics13
NLM's MeSH indexing of the paper, its major topics first.
| MeSH term | Major |
|---|---|
| Genetic Predisposition to Disease | Major topic |
| Pelvic Organ Prolapse | Major topic |
| Aged | |
| Female | |
| Humans | |
| Middle Aged | |
| Case-Control Studies | |
| East Asian People | |
| Genome-Wide Association Study | |
| Japan | |
| Polymorphism, Single Nucleotide | |
| Receptor, Fibroblast Growth Factor, Type 2 | |
| Japanese people |
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.
References54
The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.
| Order | PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|---|
| 1 | 28,892,062 | Genome-wide association study identifies 112 new loci for body mass index in the Japanese population. | Nat Genet | 2017 | https://conductscience.org/library/papers/28892062 | PubMed |
| 2 | 25,722,852 | Second-generation PLINK: rising to the challenge of larger and richer datasets. | Gigascience | 2015 | https://conductscience.org/library/papers/25722852 | PubMed |
| 3 | 23,012,258 | Empirical Bayes correction for the Winner's Curse in genetic association studies. | Genet Epidemiol | 2013 | https://conductscience.org/library/papers/23012258 | PubMed |
| 4 | 35,011,587 | WT1-AS/IGF2BP2 Axis Is a Potential Diagnostic and Prognostic Biomarker for Lung Adenocarcinoma According to ceRNA Network Comprehensive Analysis Combined with Experiments. | Cells | 2021 | https://conductscience.org/library/papers/35011587 | PubMed |
| 5 | 37,212,424 | Loss of Fgfr1 and Fgfr2 in Scleraxis-lineage cells leads to enlarged bone eminences and attachment cell death. | Dev Dyn | 2023 | https://conductscience.org/library/papers/37212424 | PubMed |
| 6 | 2,164,159 | The candidate Wilms' tumour gene is involved in genitourinary development. | Nature | 1990 | https://conductscience.org/library/papers/2164159 | PubMed |
| 7 | 16,501,574 | Mutations in different components of FGF signaling in LADD syndrome. | Nat Genet | 2006 | https://conductscience.org/library/papers/16501574 | PubMed |
| 8 | 8,544,844 | Wilms' tumor protein WT1 as an ovarian transcription factor: decreases in expression during follicle development and repression of inhibin-alpha gene promoter. | Mol Endocrinol | 1995 | https://conductscience.org/library/papers/8544844 | PubMed |
| 9 | 18,056,630 | Structural basis for reduced FGFR2 activity in LADD syndrome: Implications for FGFR autoinhibition and activation. | Proc Natl Acad Sci U S A | 2007 | https://conductscience.org/library/papers/18056630 | PubMed |
| 10 | 27,019,110 | Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets. | Nat Genet | 2016 | https://conductscience.org/library/papers/27019110 | PubMed |
1 to 10 of 54
See all 54 referencesCited by4
The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 4 citations.
| PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|
| 41,497,737 | Unraveling the Causal Linkages of RBP7 and SCGB3A1 on Pelvic Organ Prolapse: Multifaceted Insights From Genome-Wide Mendelian Randomization, Single-Cell RNA Analysis, and Network Pharmacology. | Biomed Res Int | 2026 | https://conductscience.org/library/papers/41497737 | PubMed |
| 39,987,337 | A variant in HMMR/HMMR-AS1 is associated with serum alanine aminotransferase levels in the Ryukyu population. | Sci Rep | 2025 | https://conductscience.org/library/papers/39987337 | PubMed |
| 39,858,552 | Genetic Etiology in Pelvic Organ Prolapse: Role of Connective Tissue Homeostasis, Hormone Metabolism, and Oxidative Stress. | Genes (Basel) | 2024 | https://conductscience.org/library/papers/39858552 | PubMed |
| 39,702,642 | Population-specific reference panel improves imputation quality for genome-wide association studies conducted on the Japanese population. | Commun Biol | 2024 | https://conductscience.org/library/papers/39702642 | PubMed |
Genes2
The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.
| Gene | NCBI Gene ID | Linked by | In Genes | Source |
|---|---|---|---|---|
| FGFR2 | 2,263 | PubTator's text mining | https://conductscience.org/library/genes/2263 | NCBI Gene |
| WT1 | 7,490 | PubTator's text mining | https://conductscience.org/library/genes/7490 | NCBI 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.
- 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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