Paper · 42988826

Integrated genomic and transcriptomic profiling across the clinical spectrum of Lynch syndrome-associated endometrial disease.

Kim YN and 14 others. NPJ Precis Oncol, 2026.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Integrated genomic and transcriptomic profiling across the clinical spectrum of Lynch syndrome-associated endometrial disease. Papers, record 42988826. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/42988826

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Paper

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Title: Integrated genomic and transcriptomic profiling across the clinical spectrum of Lynch syndrome-associated endometrial disease.
Journal: NPJ Precis Oncol
Year: 2026
Publication types: Journal Article
PubMed: https://pubmed.ncbi.nlm.nih.gov/42988826/
DOI: https://doi.org/10.1038/s41698-026-01676-8
The journal: https://conductscience.org/library/journal-index/101708166
Revised in PubMed: 2026-11-05

Source PubMed

Authors15

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

Order	Author	Forename	ORCID iD
1	Kim YN	Yoo-Na
2	Moon Y	Youngbeen	https://orcid.org/0009-0008-9046-076X
3	Lee SY	Seo-Young
4	Choi EH	Eun Hye
5	Han DJ	Dong-Jin
6	Kim S	Sunmin
7	Lee YJ	Yong Jae	https://orcid.org/0000-0003-0297-3116
8	Lee JY	Jung-Yun
9	Kim S	Sunghoon
10	Kim SW	Sang Wun

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Topics0

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Grants2

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Grant, as the record writes it	Agency	Country	NIH project	Stated by
RS-2023-NR076625	National Research Foundation of Korea (NRF) grant funded by the Korean government (MSIT)			PubMed
6-2019-0166	faculty research grant of Yonsei University College of Medicine			PubMed

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Trials0

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None in this release.

Comments and corrections0

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References38

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	15,872,200	Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).	N Engl J Med	2005	https://conductscience.org/library/papers/15872200	PubMed
2	34,115,236	Incidence of germline variants in Lynch syndrome-related genes among Japanese endometrial cancer patients aged 40 years or younger.	Int J Clin Oncol	2021	https://conductscience.org/library/papers/34115236	PubMed
3	32,060,377	Clinicopathological significance of deficient DNA mismatch repair and MLH1 promoter methylation in endometrioid endometrial carcinoma.	Mod Pathol	2020	https://conductscience.org/library/papers/32060377	PubMed
4	34,398,969	Endometrial cancer in Lynch syndrome.	Int J Cancer	2022	https://conductscience.org/library/papers/34398969	PubMed
5	23,531,335	Lynch syndrome related endometrial cancer: clinical significance beyond the endometrium.	J Hematol Oncol	2013	https://conductscience.org/library/papers/23531335	PubMed
6	26,977,831	Diagnosis and Management of Endometrial Cancer.	Am Fam Physician	2016	https://conductscience.org/library/papers/26977831	PubMed
7	35,128,854	A prospective comparison of the diagnostic accuracies of ultrasound and magnetic resonance imaging in preoperative staging of endometrial cancer.	J Gynecol Oncol	2022	https://conductscience.org/library/papers/35128854	PubMed
8	31,337,882	Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database.	Genet Med	2020	https://conductscience.org/library/papers/31337882	PubMed
9	31,383,734	Immune Activation in Mismatch Repair-Deficient Carcinogenesis: More Than Just Mutational Rate.	Clin Cancer Res	2020	https://conductscience.org/library/papers/31383734	PubMed
10	29,710,228	Immune Profiling of Premalignant Lesions in Patients With Lynch Syndrome.	JAMA Oncol	2018	https://conductscience.org/library/papers/29710228	PubMed

1 to 10 of 38

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Cited by0

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Genes0

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Drugs0

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Data0

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Data dates

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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

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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

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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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