PubMed (RefSeq) for id: 2462509432

Year	Number of Results
1987	1
1988	1
1993	1
1995	1
1996	2
1998	1
1999	2
2000	2
2001	2
2002	6
2003	5
2004	14
2005	11
2006	19
2007	23
2008	25
2009	28
2010	35
2011	23
2012	21
2013	19
2014	16
2015	17
2016	11
2017	15
2018	6
2019	14
2020	10
2021	10
2022	12
2023	5
2024	3

1

Pan-Cancer Interrogation of MUTYH Variants Reveals Biallelic Inactivation and Defective Base Excision Repair Across a Spectrum of Solid Tumors.

Paller CJ, Tukachinsky H, Maertens A, Decker B, Sampson JR, Cheadle JP, Antonarakis ES. Paller CJ, et al. JCO Precis Oncol. 2024 Feb;8:e2300251. doi: 10.1200/PO.23.00251. JCO Precis Oncol. 2024. PMID: 38394468 Free PMC article.

2

Breast cancers in monoallelic MUTYH germline mutation carriers have clinicopathological features overlapping with those in BRCA1 germline mutation carriers.

Keske A, Weisman P, Ospina-Romero M, Raut P, Smith-Simmer K, Zakas AL, Flynn C, Xu J. Keske A, et al. Breast Cancer Res Treat. 2024 Feb;204(1):151-158. doi: 10.1007/s10549-023-07173-x. Epub 2023 Dec 7. Breast Cancer Res Treat. 2024. PMID: 38062336

3

A one-stop approach to diagnosing hereditary colorectal cancer in the Chinese population.

Li C, Song W, Xu Y, Guo T, Zhou X, Liu F, Xu Y. Li C, et al. J Gastroenterol Hepatol. 2023 Nov;38(11):1980-1987. doi: 10.1111/jgh.16319. Epub 2023 Sep 25. J Gastroenterol Hepatol. 2023. PMID: 37749864

4

Increased KRAS G12C Prevalence, High Tumor Mutational Burden, and Specific Mutational Signatures Are Associated With MUTYH Mutations: A Pan-Cancer Analysis.

Disel U, Sivakumar S, Pham T, Fleischmann Z, Anu RI, Sokol ES, Kurzrock R. Disel U, et al. Oncologist. 2024 Feb 2;29(2):e213-e223. doi: 10.1093/oncolo/oyad230. Oncologist. 2024. PMID: 37589222 Free PMC article.

5

Evolutionary Origin of MUTYH Germline Pathogenic Variations in Modern Humans.

Xiao F, Li J, Lagniton PNP, Kou SH, Lei H, Tam B, Wang SM. Xiao F, et al. Biomolecules. 2023 Feb 24;13(3):429. doi: 10.3390/biom13030429. Biomolecules. 2023. PMID: 36979362 Free PMC article.

6

Structural snapshots of base excision by the cancer-associated variant MutY N146S reveal a retaining mechanism.

Demir M, Russelburg LP, Lin WJ, Trasviña-Arenas CH, Huang B, Yuen PK, Horvath MP, David SS. Demir M, et al. Nucleic Acids Res. 2023 Feb 22;51(3):1034-1049. doi: 10.1093/nar/gkac1246. Nucleic Acids Res. 2023. PMID: 36631987 Free PMC article.

7

MUTYH and KLF6 gene expression fluctuations in tumor tissue and tumor margins tissues of colorectal cancer.

Naebi H, Bandegi A, Talebinasab F, Samidoust P, Norollahi SE, Vahidi S, Samadani AA. Naebi H, et al. J Egypt Natl Canc Inst. 2022 Dec 5;34(1):57. doi: 10.1186/s43046-022-00158-9. J Egypt Natl Canc Inst. 2022. PMID: 36464752

8

Concurrent Pathogenic Variants of BRCA1, MUTYH and CHEK2 in a Hereditary Cancer Family.

Agaoglu NB, Ng OH, Unal B, Dogan OA, Amanvermez U, Yildiz J, Doganay L, Ghazani AA, Rana HQ. Agaoglu NB, et al. Cancer Genet. 2022 Nov;268-269:128-136. doi: 10.1016/j.cancergen.2022.10.144. Epub 2022 Nov 1. Cancer Genet. 2022. PMID: 36368126

9

Summary of the experiences, knowledge, medical management, and family communication of monoallelic MUTYH carriers.

McKenna DB, Sanchez P, Powers J, Brower J, Wang L, Mueller R, Symecko H, Hamilton JG, Wildman T, Domchek SM, Couch FJ, Garber JE, Offit K, Robson ME, Katona BW. McKenna DB, et al. J Genet Couns. 2023 Apr;32(2):342-350. doi: 10.1002/jgc4.1641. Epub 2022 Oct 17. J Genet Couns. 2023. PMID: 36245263 Free PMC article.

10

Inherited MUTYH mutations cause elevated somatic mutation rates and distinctive mutational signatures in normal human cells.

Robinson PS, Thomas LE, Abascal F, Jung H, Harvey LMR, West HD, Olafsson S, Lee BCH, Coorens THH, Lee-Six H, Butlin L, Lander N, Truscott R, Sanders MA, Lensing SV, Buczacki SJA, Ten Hoopen R, Coleman N, Brunton-Sim R, Rushbrook S, Saeb-Parsy K, Lalloo F, Campbell PJ, Martincorena I, Sampson JR, Stratton MR. Robinson PS, et al. Nat Commun. 2022 Jul 8;13(1):3949. doi: 10.1038/s41467-022-31341-0. Nat Commun. 2022. PMID: 35803914 Free PMC article.

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