Similar articles for PMID: 22368298

Year	Number of Results
2000	1
2002	1
2004	3
2005	4
2006	4
2007	15
2008	25
2009	17
2010	24
2011	24
2012	27
2013	24
2014	36
2015	17
2016	10
2017	16
2018	28
2019	38
2020	31
2021	43
2022	33
2023	15
2024	0

1

Correlation of tumour BRAF mutations and MLH1 methylation with germline mismatch repair (MMR) gene mutation status: a literature review assessing utility of tumour features for MMR variant classification.

Parsons MT, Buchanan DD, Thompson B, Young JP, Spurdle AB. Parsons MT, et al. J Med Genet. 2012 Mar;49(3):151-7. doi: 10.1136/jmedgenet-2011-100714. J Med Genet. 2012. PMID: 22368298 Review.

2

Endometrial tumour BRAF mutations and MLH1 promoter methylation as predictors of germline mismatch repair gene mutation status: a literature review.

Metcalf AM, Spurdle AB. Metcalf AM, et al. Fam Cancer. 2014 Mar;13(1):1-12. doi: 10.1007/s10689-013-9671-6. Fam Cancer. 2014. PMID: 23880961 Review.

3

Incorporation of somatic BRAF mutation testing into an algorithm for the investigation of hereditary non-polyposis colorectal cancer.

Loughrey MB, Waring PM, Tan A, Trivett M, Kovalenko S, Beshay V, Young MA, McArthur G, Boussioutas A, Dobrovic A. Loughrey MB, et al. Fam Cancer. 2007;6(3):301-10. doi: 10.1007/s10689-007-9124-1. Epub 2007 Apr 24. Fam Cancer. 2007. PMID: 17453358

4

Distinction of hereditary nonpolyposis colorectal cancer and sporadic microsatellite-unstable colorectal cancer through quantification of MLH1 methylation by real-time PCR.

Bettstetter M, Dechant S, Ruemmele P, Grabowski M, Keller G, Holinski-Feder E, Hartmann A, Hofstaedter F, Dietmaier W. Bettstetter M, et al. Clin Cancer Res. 2007 Jun 1;13(11):3221-8. doi: 10.1158/1078-0432.CCR-06-3064. Clin Cancer Res. 2007. PMID: 17545526

5

BRAF V600E-specific immunohistochemistry for the exclusion of Lynch syndrome in MSI-H colorectal cancer.

Capper D, Voigt A, Bozukova G, Ahadova A, Kickingereder P, von Deimling A, von Knebel Doeberitz M, Kloor M. Capper D, et al. Int J Cancer. 2013 Oct 1;133(7):1624-30. doi: 10.1002/ijc.28183. Epub 2013 Apr 25. Int J Cancer. 2013. PMID: 23553055 Free article.

6

Prevalence of somatic mutl homolog 1 promoter hypermethylation in Lynch syndrome colorectal cancer.

Moreira L, Muñoz J, Cuatrecasas M, Quintanilla I, Leoz ML, Carballal S, Ocaña T, López-Cerón M, Pellise M, Castellví-Bel S, Jover R, Andreu M, Carracedo A, Xicola RM, Llor X, Boland CR, Goel A, Castells A, Balaguer F; Gastrointestinal Oncology Group of the Spanish Gastroenterological Association. Moreira L, et al. Cancer. 2015 May 1;121(9):1395-404. doi: 10.1002/cncr.29190. Epub 2014 Dec 29. Cancer. 2015. PMID: 25557234 Free PMC article.

7

Efficient molecular screening of Lynch syndrome by specific 3' promoter methylation of the MLH1 or BRAF mutation in colorectal cancer with high-frequency microsatellite instability.

Nakagawa H, Nagasaka T, Cullings HM, Notohara K, Hoshijima N, Young J, Lynch HT, Tanaka N, Matsubara N. Nakagawa H, et al. Oncol Rep. 2009 Jun;21(6):1577-83. doi: 10.3892/or_00000390. Oncol Rep. 2009. PMID: 19424639

8

Immunohistochemical staining for p16 and BRAFV600E is useful to distinguish between sporadic and hereditary (Lynch syndrome-related) microsatellite instable colorectal carcinomas.

Boissière-Michot F, Frugier H, Ho-Pun-Cheung A, Lopez-Crapez E, Duffour J, Bibeau F. Boissière-Michot F, et al. Virchows Arch. 2016 Aug;469(2):135-44. doi: 10.1007/s00428-016-1958-1. Epub 2016 May 25. Virchows Arch. 2016. PMID: 27220764

9

BRAF mutation analysis is a valid tool to implement in Lynch syndrome diagnosis in patients classified according to the Bethesda guidelines.

Molinari F, Signoroni S, Lampis A, Bertan C, Perrone F, Sala P, Mondini P, Crippa S, Bertario L, Frattini M. Molinari F, et al. Tumori. 2014 May-Jun;100(3):315-20. doi: 10.1700/1578.17214. Tumori. 2014. PMID: 25076244

10

Coexisting somatic promoter hypermethylation and pathogenic MLH1 germline mutation in Lynch syndrome.

Rahner N, Friedrichs N, Steinke V, Aretz S, Friedl W, Buettner R, Mangold E, Propping P, Walldorf C. Rahner N, et al. J Pathol. 2008 Jan;214(1):10-6. doi: 10.1002/path.2263. J Pathol. 2008. PMID: 17973250

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