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For: Curia MC, Catalano T, Aceto GM. MUTYH: Not just polyposis. World J Clin Oncol 2020; 11(7): 428-449 [PMID: PMC7407923 DOI: 10.5306/wjco.v11.i7.428]
URL: https://www.wjgnet.com/1948-5204/full/v11/i7/428.htm
Number Citing Articles
1
Yunxiao Zhong, Xinya Zhang, Ruibing Feng, Yu Fan, Zhang Zhang, Qing‐Wen Zhang, Jian‐Bo Wan, Yitao Wang, Hua Yu, Guodong Li. OGG1: An emerging multifunctional therapeutic target for the treatment of diseases caused by oxidative DNA damageMedicinal Research Reviews 2024; 44(6): 2825 doi: 10.1002/med.22068
2
Patricia Esperon, Florencia Neffa, Walter Pavicic, Florencia Spirandelli, Karin Alvarez, María José Mullins, Benedito Mauro Rossi, Rodrigo Felipe Góngora e Silva, Carlos Vaccaro, Francisco Lopéz-Köstner, Jorge Rugeles, Adriana Della Valle, Mev Dominguez-Valentin. A comprehensive characterization of the spectrum of MUTYH germline pathogenic variants in Latin AmericaFamilial Cancer 2024; 23(4): 507 doi: 10.1007/s10689-024-00382-3
3
Khalid Mohamoud Abdullahi, Ahmed Faisal Ali, Mohamed Mohamoud Adan, Qiang Shu. Detection of Genetic Variations in Children with Tetralogy of Fallot Using Whole Exome Sequencing Technology Integrated Bioinformatics AnalysisGenetic Testing and Molecular Biomarkers 2024; 28(12): 474 doi: 10.1089/gtmb.2024.0350
4
Yushu Liu, Mohammadamin Edrisi, Zhi Yan, Huw A Ogilvie, Luay Nakhleh. NestedBD: Bayesian inference of phylogenetic trees from single-cell copy number profiles under a birth-death modelAlgorithms for Molecular Biology 2024; 19(1) doi: 10.1186/s13015-024-00264-4
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Yuri Mizuno, Nona Abolhassani, Guianfranco Mazzei, Kunihiko Sakumi, Takashi Saito, Takaomi C. Saido, Toshiharu Ninomiya, Toru Iwaki, Ryo Yamasaki, Jun-ichi Kira, Yusaku Nakabeppu, Zhao Zhong Chong. MUTYH Actively Contributes to Microglial Activation and Impaired Neurogenesis in the Pathogenesis of Alzheimer’s DiseaseOxidative Medicine and Cellular Longevity 2021; 2021(1) doi: 10.1155/2021/8635088
6
Joseph McGrath, Dillin J Rhatigan, Danielle Donahue, Mackenzie Fannin, Nuria Lawson. Infiltrating Ductal Breast Carcinoma in a Male Patient With Associated BARD1 MutationCureus 2024;  doi: 10.7759/cureus.66216
7
Pelin Ercoskun, Cigdem Yuce Kahraman, Guller Ozkan, Abdulgani Tatar. Genetic Characterization of Hereditary Cancer Syndromes Based on Targeted Next-Generation SequencingMolecular Syndromology 2022; 13(2): 123 doi: 10.1159/000518927
8
A.B. Semenova, M.M. Byakhova, M.V. Makarova, V.N. Galkin, M.V. Nemtsova, D.K. Chernevskiy, A.M. Danishevich, V.G. Shatalov, A.V. Babkina, N.G. Popova, S.M. Gadzhieva. The structure of pathogenic germline variants in colorectal cancer in Moscow patientsArkhiv patologii 2023; 85(6): 16 doi: 10.17116/patol20238506116
9
Matthew R. Trendowski, Christine M. Lusk, Angela S. Wenzlaff, Christine Neslund-Dudas, Kristen S. Purrington, Jennifer L. Beebe-Dimmer, Ann G. Schwartz. Association of Germline Pathogenic Variants in MUTYH and Other DNA Damage Response Genes With Lung Cancer Risk Among Non-Hispanic Whites and African Americans JCO Precision Oncology 2025; (9) doi: 10.1200/PO-24-00558
10
Katarína Fabišíková, Olívia Hamidová, Regína Lohajová Behulová, Katarína Závodná, Petra Priščáková, Vanda Repiská. Case Report: The Role of Molecular Analysis of the MUTYH Gene in Asymptomatic IndividualsFrontiers in Genetics 2020; 11 doi: 10.3389/fgene.2020.590486
11
Luca Savino, Maria Carmela Di Marcantonio, Carmelo Moscatello, Roberto Cotellese, Lucia Centurione, Raffaella Muraro, Gitana Maria Aceto, Gabriella Mincione. Effects of H2O2 Treatment Combined With PI3K Inhibitor and MEK Inhibitor in AGS Cells: Oxidative Stress Outcomes in a Model of Gastric CancerFrontiers in Oncology 2022; 12 doi: 10.3389/fonc.2022.860760
12
Yong Yang, Jieqing Yu, Yuanping Xiong, Jiansheng Xiao, Daofeng Dai, Feng Zhang. Prognostic Analysis of Differentially Expressed DNA Damage Repair Genes in Bladder CancerPathology and Oncology Research 2022; 28 doi: 10.3389/pore.2022.1610267
13
Melissa Duarte, Clara Milikowski. Gastrointestinal polyposis with associated cutaneous manifestationsPathology 2022; 54(2): 157 doi: 10.1016/j.pathol.2021.08.009
14
Sofia Tzoumpa, Nicolas Sevenet, Claudia‐Luisa Bejar‐Ardiles, Béatrice Villette, Coralie Zumelzu, Robert Benamouzig, Frédéric Caux, Eve Maubec. Multiple basal cell carcinomas revealing a biallelic MUTYH gene mutation in a 39‐year‐old male patientJournal of the European Academy of Dermatology and Venereology 2023; 37(3) doi: 10.1111/jdv.18592
15
Silvia Negro, Quoc Riccardo Bao, Marco Scarpa, Federico Scognamiglio, Salvatore Pucciarelli, Andrea Remo, Marco Agostini, Edoardo D'Angelo, Isabella Mammi, Francesca Schiavi, Silvia Rossi, Fabiana Zingone, Francesco Ferrara, Alberto Fantin, Chiara Cristofori, Ennio Guido, Erik Rosa Rizzotto, Rossana Intini, Francesca Bergamo, Matteo Fassan, Leonardo Salviati, Emanuele D.L. Urso. Multiple colorectal adenomas syndrome: The role of MUTYH mutation and the polyps’ number in clinical management and colorectal cancer riskDigestive and Liver Disease 2024; 56(6): 1087 doi: 10.1016/j.dld.2023.11.034
16
Irene Gagliardi, Federica Campolo, Patricia Borges de Souza, Lucrezia Rossi, Manuela Albertelli, Federica Grillo, Luigi Caputi, Massimiliano Mazza, Antongiulio Faggiano, Maria Chiara Zatelli. Comparative Targeted Genome Profiling between Solid and Liquid Biopsies in Gastroenteropancreatic Neuroendocrine Neoplasms: A Proof-of-Concept Pilot StudyNeuroendocrinology 2024; : 1 doi: 10.1159/000541346
17
Arthur S. Aelvoet, Francesco Buttitta, Luigi Ricciardiello, Evelien Dekker. Management of familial adenomatous polyposis and MUTYH-associated polyposis; new insightsBest Practice & Research Clinical Gastroenterology 2022; : 101793 doi: 10.1016/j.bpg.2022.101793
18
Luigi Magrin, Daniele Fanale, Chiara Brando, Lidia Rita Corsini, Ugo Randazzo, Marianna Di Piazza, Vittorio Gurrera, Erika Pedone, Tancredi Didier Bazan Russo, Salvatore Vieni, Gianni Pantuso, Antonio Russo, Viviana Bazan. MUTYH-associated tumor syndrome: The other face of MAPOncogene 2022; 41(18): 2531 doi: 10.1038/s41388-022-02304-y
19
Exome sequencing identifies novel genes and variants in patients with Hirschsprung diseaseJournal of Pediatric Surgery 2023; 58(4): 723 doi: 10.1016/j.jpedsurg.2022.11.011
20
Samhita De, Sourav Paul, Anirban Manna, Chirantan Majumder, Koustav Pal, Nicolette Casarcia, Arijit Mondal, Sabyasachi Banerjee, Vinod Kumar Nelson, Suvranil Ghosh, Joyita Hazra, Ashish Bhattacharjee, Subhash Chandra Mandal, Mahadeb Pal, Anupam Bishayee. Phenolic Phytochemicals for Prevention and Treatment of Colorectal Cancer: A Critical Evaluation of In Vivo StudiesCancers 2023; 15(3): 993 doi: 10.3390/cancers15030993
21
Ghada Al-Kafaji, Ghufran Jassim, Amani AlHajeri, Amna Mohamed Tayeb Alawadhi, Mariam Fida, Ibrahim Sahin, Faisal Alali, Elias Fadel, Amy McCart Reed. Investigation of germline variants in Bahraini women with breast cancer using next-generation sequencing based-multigene panelPLOS ONE 2023; 18(9): e0291015 doi: 10.1371/journal.pone.0291015
22
Hyunjung Gu, Yao Yu, Saumya Dushyant Sisoudiya, Pamela Mishra, He Li, Jeremy M. Schraw, Michael E. Scheurer, Donna M. Muzny, Danielle Mitchell, Olga Taylor, Shalini N. Jhangiani, Shannon Dugan-Perez, Yifan Wu, Harsha Doddapaneni, Sravya Venkata Bhamidipati, Marie-Claude Gingras, Jennifer E. Posey, Richard A. Gibbs, Chad D. Huff, Sharon E. Plon, Philip J. Lupo, Aniko Sabo. An evaluation of genetic predisposition to congenital anomalies and pediatric cancer supports KAT6B as a novel neuroblastoma susceptibility geneGenetics in Medicine Open 2025; 3: 101901 doi: 10.1016/j.gimo.2024.101901
23
Polyanna Oliveira, Paula Correa, Angelina Acosta, Juliana Freitas, Taísa Machado-Lopes, Thais Bomfim-Palma, Ândrea Ribeiro-dos-Santos, Sidney Santos, Roberto Nascimento, Ivana Nascimento, Kiyoko Abe-Sandes. Screening for Mutations in Hereditary Cancer Susceptibility Genes in a Region with High Endogamy in BrazilGlobal Medical Genetics 2023; 10(04): 376 doi: 10.1055/s-0043-1777449
24
Zangbéwendé Guy Ouedraogo, Florian Ceruti, Mathis Lepage, Mathilde Gay-Bellile, Nancy Uhrhammer, Flora Ponelle-Chachuat, Yannick Bidet, Maud Privat, Mathias Cavaillé. Detection Rate and Spectrum of Pathogenic Variations in a Cohort of 83 Patients with Suspected Hereditary Risk of Kidney CancerGenes 2023; 14(11): 1991 doi: 10.3390/genes14111991
25
Fouad Bouso, Akhaled Zaher. Genetic Complexity in Recurrent Basal Cell Carcinoma: A MUTYH Variant Case ReportCureus 2024;  doi: 10.7759/cureus.55677
26
Marcella Nunziato, Federica Di Maggio, Matilde Pensabene, Maria Valeria Esposito, Flavio Starnone, Carmine De Angelis, Alessandra Calabrese, Massimiliano D’Aiuto, Gerardo Botti, Sabino De Placido, Valeria D’Argenio, Francesco Salvatore. Multi-gene panel testing increases germline predisposing mutations’ detection in a cohort of breast/ovarian cancer patients from Southern ItalyFrontiers in Medicine 2022; 9 doi: 10.3389/fmed.2022.894358
27
A. V. Endutkin, D. O. Zharkov. GO System, a DNA Repair Pathway to Cope with Oxidative DamageMolecular Biology 2021; 55(2): 193 doi: 10.1134/S0026893321020072
28
Carmelo Moscatello, Maria Carmela Di Marcantonio, Luca Savino, Emira D’Amico, Giordano Spacco, Pasquale Simeone, Paola Lanuti, Raffaella Muraro, Gabriella Mincione, Roberto Cotellese, Gitana Maria Aceto. Emerging Role of Oxidative Stress on EGFR and OGG1-BER Cross-Regulation: Implications in Thyroid PhysiopathologyCells 2022; 11(5): 822 doi: 10.3390/cells11050822
29
Yuyue Qiu, Xinru Hu, Xiaoping Zeng, Hongmei Wang. Triple kill: DDR inhibitors, radiotherapy and immunotherapy leave cancer cells with no escapeActa Biochimica et Biophysica Sinica 2022; 54(11): 1569 doi: 10.3724/abbs.2022153
30
Giovanna D’Elia, Gemma Caliendo, Luana Passariello, Luisa Albanese, Jasmine Makker, Anna Maria Molinari, Maria Teresa Vietri. Hereditary Cancer Syndrome in a Family with Double Mutation in BRIP1 and MUTYH GenesGenes 2023; 14(2): 428 doi: 10.3390/genes14020428
31
Eugénie Chevalier, Robert Benamouzig. Chemoprevention in hereditary digestive neoplasia: A comprehensive reviewTherapeutic Advances in Gastroenterology 2023; 16 doi: 10.1177/17562848231215585
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Gábor Bedics, Lili Kotmayer, Erik Zajta, Lajos László Hegyi, Edit Ágota Brückner, Hajnalka Rajnai, Lilla Reiniger, Csaba Bödör, Miklós Garami, Bálint Scheich. Germline MUTYH mutations and high‐grade gliomas: Novel evidence for a potential associationGenes, Chromosomes and Cancer 2022; 61(10): 622 doi: 10.1002/gcc.23054
33
Edward J. Saunders, Tokhir Dadaev, Mark N. Brook, Sarah Wakerell, Koveela Govindasami, Reshma Rageevakumar, Nafisa Hussain, Andrea Osborne, Diana Keating, Artitaya Lophatananon, Kenneth R. Muir, Burcu F. Darst, David V. Conti, Christopher A. Haiman, Antonis C. Antoniou, Rosalind A. Eeles, Zsofia Kote-Jarai. Identification of Genes with Rare Loss of Function Variants Associated with Aggressive Prostate Cancer and SurvivalEuropean Urology Oncology 2024; 7(2): 248 doi: 10.1016/j.euo.2024.02.003
34
Ibrahim Sahin, Hanife Saat. New Perspectives on the Recurrent Monoallelic Germline Mutations of DNA Repair and Checkpoint Genes and Clinical VariabilityGenetic Testing and Molecular Biomarkers 2022; 26(1): 17 doi: 10.1089/gtmb.2021.0108
35
Seref Bugra Tuncer, Betul Celik, Seda Kilic Erciyas, Ozge Sukruoglu Erdogan, Busra Kurt Gültaslar, Demet Akdeniz Odemis, Mukaddes Avsar, Fatma Sen, Pınar Mualla Saip, Hulya Yazici. Germline mutational variants of Turkish ovarian cancer patients suspected of Hereditary Breast and Ovarian Cancer (HBOC) by next-generation sequencingPathology - Research and Practice 2024; 254: 155075 doi: 10.1016/j.prp.2023.155075
36
Hari Krishnan Krishnamurthy, Imbaasree R, Michelle Pereira, Vasanth Jayaraman, Karthik Krishna, Tianhao Wang, Kang Bei, John J. Rajasekaran. Inside the Genome: Understanding Genetic Influences on Oxidative StressSSRN Electronic Journal 2024;  doi: 10.2139/ssrn.4741633
37
Igor Gavrić, Edin Hodžić, Lana Sarajlić, Mirhan Salibašić, Salem Bajramagić, Advan Dizdarević, Edin Kulović. Analysis of TP53, APC, KRAS, and MMR Genetic mutations in colorectal cancer: A review articleSanamed 2024; 19(3): 333 doi: 10.5937/sanamed0-52803
38
Kazunori Takada, Kinichi Hotta, Yoshihiro Kishida, Sayo Ito, Kenichiro Imai, Hiroyuki Ono. Comprehensive Analysis of Early-onset Colorectal Cancer: A ReviewJournal of the Anus, Rectum and Colon 2023; 7(4): 241 doi: 10.23922/jarc.2023-032
39
Chloe J. Cohan, Caroline Chinchilla Putzeys, Brianna Pruniski, Paul Tran. Colorectal cancer in a 13‐year‐old with constitutional mismatch repair deficiency and MUTYH heterozygosityJPGN Reports 2025;  doi: 10.1002/jpr3.70001
40
KristenM. Shannon,, LindaH. Rodgers‐Foucheand, DanielC. Chung. Cancer Consult2023; : 625 doi: 10.1002/9781119823766.ch47
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A. Calabrese, C. von Arx, A.A. Tafuti, M. Pensabene, M. De Laurentiis. Prevention, diagnosis and clinical management of hereditary breast cancer beyond BRCA1/2 genesCancer Treatment Reviews 2024; 129: 102785 doi: 10.1016/j.ctrv.2024.102785
42
Maria Cecilia Mathias-Machado, Renata D. Peixoto, Patricia Ashton-Prolla, Leonard Medeiros da Silva, Rodrigo Dienstmann. Complete Response to Immunotherapy in a Patient with MUTYH-Associated Polyposis and Gastric Cancer: A Case ReportCase Reports in Oncology 2023; : 510 doi: 10.1159/000530965
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Jaeyoung Moon, Ichiwa Kitty, Kusuma Renata, Sisi Qin, Fei Zhao, Wootae Kim. DNA Damage and Its Role in Cancer TherapeuticsInternational Journal of Molecular Sciences 2023; 24(5): 4741 doi: 10.3390/ijms24054741
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Kum Hei Ryu, Min-Chae Kang, Ye-Ryeong Jung, Mi-Ae Jang, Jong Eun Park, Namhee Kim, Dongju Won, Boyoung Park, Sun-Young Kong. Clinical Significance of MUTYH Germline VariantLaboratory Medicine Online 2023; 13(4): 301 doi: 10.47429/lmo.2023.13.4.301
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Lupe Sanchez-Mete, Lorenzo Mosciatti, Marco Casadio, Luigi Vittori, Aline Martayan, Vittoria Stigliano. <i>MUTYH-</i>associated polyposis: Is it time to change upper gastrointestinal surveillance? A single-center case series and a literature overviewWorld Journal of Gastrointestinal Oncology 2023; 15(11): 1891-1899 doi: 10.4251/wjgo.v15.i11.1891
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Yousif M. Shakroo, Charles A. Seabury, Kenneth A. Iczkowski, Kinloch Nelson, Junqi Qian, Dharam M. Ramnani. Germline pathogenic variants in prostate cancerPathology - Research and Practice 2024; 264: 155718 doi: 10.1016/j.prp.2024.155718
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King C, Edwards H, Thompson E, Abdelmasseh M, Cuaranta A, Pacioles A, Sanabria J. Constitutional mismatch repair deficiency: a case on a commonly misinterpreted mutation in colon cancerClinical Journal of Gastroenterology 2024; 17(5): 866 doi: 10.1007/s12328-024-02015-9