PubMed (GeneRIF) for id: 5395

Year	Number of Results
2002	4
2003	2
2004	4
2005	5
2006	9
2007	10
2008	17
2009	19
2010	13
2011	11
2012	6
2013	12
2014	11
2015	12
2016	11
2017	10
2018	8
2019	4
2020	9
2021	6
2022	6
2023	3
2024	2

1

Genotype-phenotype correlations in carriers of the PMS2 founder variant c.1831dup.

Gass M, Seebauer B, Thommen A, Fischler A, Heinimann K. Gass M, et al. Mol Genet Genomic Med. 2024 Jan;12(1):e2360. doi: 10.1002/mgg3.2360. Mol Genet Genomic Med. 2024. PMID: 38284451 Free PMC article.

2

PMS2 or PMS2CL? Characterization of variants detected in the 3' of the PMS2 gene.

Bouras A, Lefol C, Ruano E, Grand-Masson C, Wang Q. Bouras A, et al. Genes Chromosomes Cancer. 2024 Jan;63(1):e23193. doi: 10.1002/gcc.23193. Epub 2023 Aug 3. Genes Chromosomes Cancer. 2024. PMID: 37534630

3

Diabetes mellitus impacts on expression of DNA mismatch repair protein PMS2 and tumor microenvironment in pancreatic ductal adenocarcinoma.

Pan X, Mizukami H, Hara Y, Yamada T, Yamazaki K, Kudoh K, Takeuchi Y, Sasaki T, Kushibiki H, Igawa A, Hakamada K. Pan X, et al. J Diabetes Investig. 2023 Jan;14(1):132-144. doi: 10.1111/jdi.13929. Epub 2022 Dec 1. J Diabetes Investig. 2023. PMID: 36453157 Free PMC article.

4

Exome sequencing in a Swedish family with PMS2 mutation with varying penetrance of colorectal cancer: investigating the presence of genetic risk modifiers in colorectal cancer risk.

Bryant P, Walton Bernstedt S, Thutkawkorapin J, Backman AS, Lindblom A, Lagerstedt-Robinson K. Bryant P, et al. Eur J Cancer Prev. 2023 Mar 1;32(2):113-118. doi: 10.1097/CEJ.0000000000000769. Epub 2022 Dec 6. Eur J Cancer Prev. 2023. PMID: 36134613

5

Germline variants screening of MLH1, MSH2, MSH6 and PMS2 genes in 64 Algerian Lynch syndrome families: The first nationwide study.

Boumehdi AL, Cherbal F, Khider F, Oukkal M, Mahfouf H, Zebboudj F, Maaoui M. Boumehdi AL, et al. Ann Hum Genet. 2022 Nov;86(6):328-352. doi: 10.1111/ahg.12482. Epub 2022 Sep 8. Ann Hum Genet. 2022. PMID: 36073783

6

Predictive functional assay-based classification of PMS2 variants in Lynch syndrome.

Rayner E, Tiersma Y, Fortuno C, van Hees-Stuivenberg S, Drost M, Thompson B, Spurdle AB, de Wind N. Rayner E, et al. Hum Mutat. 2022 Sep;43(9):1249-1258. doi: 10.1002/humu.24387. Epub 2022 Apr 28. Hum Mutat. 2022. PMID: 35451539 Free PMC article.

7

Early age of onset and broad cancer spectrum persist in MSH6- and PMS2-associated Lynch syndrome.

Liu YL, Cadoo KA, Maio A, Patel Z, Kemel Y, Salo-Mullen E, Catchings A, Ranganathan M, Kane S, Soslow R, Ceyhan-Birsoy O, Mandelker D, Carlo MI, Walsh MF, Shia J, Markowitz AJ, Offit K, Stadler ZK, Latham A. Liu YL, et al. Genet Med. 2022 Jun;24(6):1187-1195. doi: 10.1016/j.gim.2022.02.016. Epub 2022 Mar 26. Genet Med. 2022. PMID: 35346574 Free PMC article.

8

Analysis of the MLH1, MLH2, MLH6, PMS2 genes and their correlations with clinical data in rectal mucinous adenocarcinoma.

Graur F, Puia A, Mois E, Pop P, Berar M, Elisei R, Zaharie F, Nechita V, Rusu I, Buiga R, Puia C, Al Hajjar N. Graur F, et al. Ann Ital Chir. 2022;93:188-194. Ann Ital Chir. 2022. PMID: 34807001

9

A novel mouse model of PMS2 founder mutation that causes mismatch repair defect due to aberrant splicing.

Biswas K, Couillard M, Cavallone L, Burkett S, Stauffer S, Martin BK, Southon E, Reid S, Plona TM, Baugher RN, Mellott SD, Pike KM, Albaugh ME, Maedler-Kron C, Hamel N, Tessarollo L, Marcus V, Foulkes WD, Sharan SK. Biswas K, et al. Cell Death Dis. 2021 Sep 6;12(9):838. doi: 10.1038/s41419-021-04130-8. Cell Death Dis. 2021. PMID: 34489406 Free PMC article.

10

The coding microsatellite mutation profile of PMS2-deficient colorectal cancer.

Bajwa-Ten Broeke SW, Ballhausen A, Ahadova A, Suerink M, Bohaumilitzky L, Seidler F, Morreau H, van Wezel T, Krzykalla J, Benner A, de Miranda NF, von Knebel Doeberitz M, Nielsen M, Kloor M. Bajwa-Ten Broeke SW, et al. Exp Mol Pathol. 2021 Oct;122:104668. doi: 10.1016/j.yexmp.2021.104668. Epub 2021 Jul 22. Exp Mol Pathol. 2021. PMID: 34302852 Free article.

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