Paper ยท 21193451
Metachronous colorectal cancer risk for mismatch repair gene mutation carriers: the advantage of more extensive colon surgery.
Parry S and 21 others. Gut, 2011. Cited by 206 papers, by iCite.
11 sourcespapers-2026-11-12-0.1.0
Cite this record
ConductScience Library. Metachronous colorectal cancer risk for mismatch repair gene mutation carriers: the advantage of more extensive colon surgery. Papers, record 21193451. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/21193451
On this page
Paper
PubMed's record of the paper, with iCite's citation figures. No abstract is shown.
- Title
- Metachronous colorectal cancer risk for mismatch repair gene mutation carriers: the advantage of more extensive colon surgery.
- PubMed
Topics26
NLM's MeSH indexing of the paper, its major topics first.
| MeSH term | Major |
|---|---|
| Colorectal Neoplasms, Hereditary Nonpolyposis | Major topic |
| DNA Mismatch Repair | Major topic |
| Adaptor Proteins, Signal Transducing | |
| Adenosine Triphosphatases | |
| Adult | |
| Age Distribution | |
| Aged | |
| Colectomy | |
| Colonoscopy | |
| DNA Mutational Analysis | |
| DNA Repair Enzymes | |
| DNA-Binding Proteins | |
| Epidemiologic Methods | |
| Female | |
| Heterozygote | |
| Humans | |
| Male | |
| Middle Aged | |
| Mismatch Repair Endonuclease PMS2 | |
| MutL Protein Homolog 1 | |
| MutS Homolog 2 Protein | |
| Neoplasm Staging | |
| Neoplasms, Second Primary | |
| Nuclear Proteins | |
| Sex Distribution | |
| Young Adult |
Source PubMed
Grants10
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 it | Agency | Country | NIH project | Stated by | Source |
|---|---|---|---|---|---|
| U01 CA074799 | NCI NIH HHS | United States | U01CA074799 | PubMed and NIH | NIH RePORTER |
| U01 CA074794 | NCI NIH HHS | United States | U01CA074794 | PubMed and NIH | NIH RePORTER |
| U01 CA097735 | NCI NIH HHS | United States | U01CA097735 | PubMed and NIH | NIH RePORTER |
| U01 CA074783 | NCI NIH HHS | United States | U01CA074783 | PubMed and NIH | NIH RePORTER |
| U01 CA074806 | NCI NIH HHS | United States | U01CA074806 | PubMed and NIH | NIH RePORTER |
| UO1 CA074799 | NCI NIH HHS | United States | U01CA074799 | PubMed and NIH | NIH RePORTER |
| U24 CA074794 | NCI NIH HHS | United States | U01CA074794 | PubMed and NIH | NIH RePORTER |
| P30 CA071789 | NCI NIH HHS | United States | P30CA071789 | PubMed and NIH | NIH RePORTER |
| U01 CA074800 | NCI NIH HHS | United States | U01CA074800 | PubMed and NIH | NIH RePORTER |
| U24CA074794 | NIH | NIH 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 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 |
|---|---|---|---|
| Comment in | 21,873,468 | Cumulative incidence of metachronous colorectal cancer risk for mismatch repair gene mutation carriers is overestimated. | https://conductscience.org/library/papers/21873468 |
Source PubMed
References20
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 | 20,206,180 | One to 2-year surveillance intervals reduce risk of colorectal cancer in families with Lynch syndrome. | Gastroenterology | 2010 | https://conductscience.org/library/papers/20206180 | PubMed |
| 2 | 20,028,993 | Risks of Lynch syndrome cancers for MSH6 mutation carriers. | J Natl Cancer Inst | 2010 | https://conductscience.org/library/papers/20028993 | PubMed |
| 3 | 12,473,880 | Surveillance for hereditary nonpolyposis colorectal cancer: a long-term study on 114 families. | Dis Colon Rectum | 2002 | https://conductscience.org/library/papers/12473880 | PubMed |
| 4 | 14,633,956 | Decision analysis in the surgical treatment of colorectal cancer due to a mismatch repair gene defect. | Gut | 2003 | https://conductscience.org/library/papers/14633956 | PubMed |
| 5 | 10,784,581 | Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer. | Gastroenterology | 2000 | https://conductscience.org/library/papers/10784581 | PubMed |
| 6 | 10,348,829 | New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC. | Gastroenterology | 1999 | https://conductscience.org/library/papers/10348829 | PubMed |
| 7 | 12,792,437 | Patterns of surgery in patients belonging to amsterdam-positive families. | Dis Colon Rectum | 2003 | https://conductscience.org/library/papers/12792437 | PubMed |
| 8 | 17,327,285 | Guidelines for the clinical management of Lynch syndrome (hereditary non-polyposis cancer). | J Med Genet | 2007 | https://conductscience.org/library/papers/17327285 | PubMed |
| 9 | 17,003,399 | Recommendations for the care of individuals with an inherited predisposition to Lynch syndrome: a systematic review. | JAMA | 2006 | https://conductscience.org/library/papers/17003399 | PubMed |
| 10 | 10,877,330 | A note on robust variance estimation for cluster-correlated data. | Biometrics | 2000 | https://conductscience.org/library/papers/10877330 | PubMed |
1 to 10 of 20
See all 20 referencesCited by108
The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 206 citations.
| PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|
| 42,882,890 | Second Primary Malignancies in Gastrointestinal Cancer Survivors: Epidemiology, Risk Factors, and Future Prediction Models. | Cancers (Basel) | 2026 | https://conductscience.org/library/papers/42882890 | PubMed |
| 41,287,493 | Cost-Utility Analysis of Universal Lynch Syndrome Screening among Colorectal Cancer Patients in a Low-Middle-Income Country. | Yonsei Med J | 2025 | https://conductscience.org/library/papers/41287493 | PubMed |
| 40,873,251 | Contemporary Surgical Management of Colorectal Cancer in Lynch Syndrome: Considering the Implications of Known Genotype. | ANZ J Surg | 2025 | https://conductscience.org/library/papers/40873251 | PubMed |
| 40,765,665 | Segmental versus Extended Resection for Colon Cancer in Lynch Syndrome. | Clin Colon Rectal Surg | 2025 | https://conductscience.org/library/papers/40765665 | PubMed |
| 40,292,001 | Hereditary Colorectal Cancer: From Diagnosis to Surgical Options. | Clin Colon Rectal Surg | 2025 | https://conductscience.org/library/papers/40292001 | PubMed |
| 40,231,433 | Metachronous colorectal cancer risks after extended or segmental resection in MLH1, MSH2, and MSH6 Lynch syndrome: multicentre study from the Prospective Lynch Syndrome Database. | Br J Surg | 2025 | https://conductscience.org/library/papers/40231433 | PubMed |
| 40,158,390 | Intratumoural pks+Escherichia coli is associated with risk of metachronous colorectal cancer and adenoma development in people with Lynch syndrome. | EBioMedicine | 2025 | https://conductscience.org/library/papers/40158390 | PubMed |
| 39,906,700 | DMMR status and synchronous lesions predicts metachronous lesions after curative resection for rectal cancer. | Front Surg | 2025 | https://conductscience.org/library/papers/39906700 | PubMed |
| 39,859,102 | Lynch Syndrome-Impact of the Type of Deficient Mismatch Repair Gene Mutation on Diagnosis, Clinical Presentation, Surveillance and Therapeutic Approaches. | Medicina (Kaunas) | 2025 | https://conductscience.org/library/papers/39859102 | PubMed |
| 39,502,732 | High risk of multiple gastric cancers in Japanese individuals with Lynch syndrome. | Ann Gastroenterol Surg | 2024 | https://conductscience.org/library/papers/39502732 | PubMed |
1 to 10 of 108
See all 108 cited byGenes4
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 |
|---|---|---|---|---|
| MLH1 | 4,292 | PubTator's text mining | https://conductscience.org/library/genes/4292 | NCBI Gene |
| MSH2 | 4,436 | PubTator's text mining | https://conductscience.org/library/genes/4436 | NCBI Gene |
| MSH6 | 2,956 | PubTator's text mining | https://conductscience.org/library/genes/2956 | NCBI Gene |
| PMS2 | 5,395 | PubTator's text mining | https://conductscience.org/library/genes/5395 | 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.
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/v1/21193451
GET https://conductscience.org/api/papers/v1/21193451/authors?page=2