Paper · 42129295

Follow-up, cancer risk and mortality in Peutz-Jeghers syndrome: Data from the PRED-IdF network.

Rémond M and 23 others. Eur J Hum Genet, 2026. Cited by 0 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

Cite this record

ConductScience Library. Follow-up, cancer risk and mortality in Peutz-Jeghers syndrome: Data from the PRED-IdF network. Papers, record 42129295. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/42129295

On this page

Paper

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

Title: Follow-up, cancer risk and mortality in Peutz-Jeghers syndrome: Data from the PRED-IdF network.; PubMed
Journal: Eur J Hum Genet; PubMed
Year: 2026; PubMed
Publication types: Journal Article; PubMed
PubMed: https://pubmed.ncbi.nlm.nih.gov/42129295/; PubMed
DOI: https://doi.org/10.1038/s41431-026-02116-8; PubMed
The journal: https://conductscience.org/library/journal-index/9302235; PubMed
Citations, by iCite: 0; iCite
Revised in PubMed: 2026-07-04; PubMed

Authors24

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

Order	Author	Forename	ORCID iD
1	Rémond M	Maxime	https://orcid.org/0000-0001-7147-6936
2	Drouet Y	Youenn	https://orcid.org/0000-0003-2963-558X
3	Dardenne A	Antoine
4	Perrod G	Guillaume
5	Netter J	Jeanne
6	Parc Y	Yann
7	Cellier C	Christophe
8	Coriat R	Romain
9	Farelly S	Solenne
10	Maksimovic F	Fanny

1 to 10 of 24Source PubMed

See all 24 authors

Topics0

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

None in this release.

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 corrections1

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

Kind	PMID	Title	In Papers
Erratum in	42,399,437	Correction: follow-up, cancer risk and mortality in Peutz-Jeghers syndrome: data from the PRED-IdF network.	https://conductscience.org/library/papers/42399437

Source PubMed

References24

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	9,425,897	Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase.	Nat Genet	1998	https://conductscience.org/library/papers/9425897	PubMed
2	9,428,765	A serine/threonine kinase gene defective in Peutz-Jeghers syndrome.	Nature	1998	https://conductscience.org/library/papers/9428765	PubMed
3	26,746,637	Update on our investigation of malignant tumors associated with Peutz-Jeghers syndrome in Japan.	Surg Today	2016	https://conductscience.org/library/papers/26746637	PubMed
4	11,113,065	Very high risk of cancer in familial Peutz-Jeghers syndrome.	Gastroenterology	2000	https://conductscience.org/library/papers/11113065	PubMed
5	23,240,097	Pancreatic cancer risk in Peutz-Jeghers syndrome patients: a large cohort study and implications for surveillance.	J Med Genet	2013	https://conductscience.org/library/papers/23240097	PubMed
6	23,415,580	Cancer risk associated with STK11/LKB1 germline mutations in Peutz-Jeghers syndrome patients: results of an Italian multicenter study.	Dig Liver Dis	2013	https://conductscience.org/library/papers/23415580	PubMed
7	33,513,864	The Management of Peutz-Jeghers Syndrome: European Hereditary Tumour Group (EHTG) Guideline.	J Clin Med	2021	https://conductscience.org/library/papers/33513864	PubMed
8	20,924,409	Estimating penetrance from multiple case families with predisposing mutations: extension of the 'genotype-restricted likelihood' (GRL) method.	Eur J Hum Genet	2011	https://conductscience.org/library/papers/20924409	PubMed
9	36,038,258	First estimates of diffuse gastric cancer risks for carriers of CTNNA1 germline pathogenic variants.	J Med Genet	2022	https://conductscience.org/library/papers/36038258	PubMed
10	38,182,527	International evidence-based Kyoto guidelines for the management of intraductal papillary mucinous neoplasm of the pancreas.	Pancreatology	2024	https://conductscience.org/library/papers/38182527	PubMed

1 to 10 of 24

See all 24 references

Cited by0

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 0 citations.

None in this release.

Genes0

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

None in this release.

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.

For software

Read this paper from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/papers/v1/42129295

GET https://conductscience.org/api/papers/v1/42129295/authors?page=2

API reference For AI assistants