Academic Content and Language Evaluation of This Article
CrossCheck and Google Search of This Article
Academic Rules and Norms of This Article
Citation of this article
Corresponding Author of This Article
Research Domain of This Article
Article-Type of This Article
Open-Access Policy of This Article
Times Cited Counts in Google of This Article
Number of Hits and Downloads for This Article
- Total Article Views (24259)
All Articles published online
|
Featured Article
|
Publishing Process of This Article
|
Aug 21, 2015 (publication date) through Dec 20, 2024
Times Cited of This Article
Journal Information of This Article
Publication Name
World Journal of Gastroenterology
ISSN
1007-9327
Publisher of This Article
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Carethers JM, Stoffel EM. Lynch syndrome and Lynch syndrome mimics: The growing complex landscape of hereditary colon cancer. World J Gastroenterol 2015; 21(31): 9253-9261 [PMID: 26309352 DOI: 10.3748/wjg.v21.i31.9253] |
|---|---|
| URL: | https://www.wjgnet.com/1007-9327/full/v21/i31/9253.htm |
| Number | Citing Articles |
| 1 |
Angelo Cagnacci, Isabel Ramirez, Johannes Bitzer, Anne Gompel. Contraception in cancer survivors – an expert review Part II. Skin, gastrointestinal, haematological and endocrine cancers. The European Journal of Contraception & Reproductive Health Care 2019; 24(4): 299 doi: 10.1080/13625187.2019.1604947
|
| 2 |
F. Bourlond, C. Velter, B. Cribier. Clinicopathological study of 47 cases of sebaceoma. Annales de Dermatologie et de Vénéréologie 2016; 143(12): 814 doi: 10.1016/j.annder.2016.06.013
|
| 3 |
Dima Hamideh, Anirban Das, Vanessa Bianchi, Jiil Chung, Logine Negm, Adrian Levine, Maya Basbous, Santiago Sanchez-Ramirez, Leonie Mikael, Nada Jabado, Lamya Atweh, Mireille Lteif, Rami Mahfouz, Nidale Tarek, Miguel Abboud, Samar Muwakkit, Cynthia Hawkins, Uri Tabori, Raya Saab. Using comprehensive genomic and functional analyses for resolving genotype–phenotype mismatches in children with suspected CMMRD in Lebanon: an IRRDC study. Human Genetics 2023; 142(4): 563 doi: 10.1007/s00439-023-02530-8
|
| 4 |
Zachary S. Bohannan, Antonina Mitrofanova. Calling Variants in the Clinic: Informed Variant Calling Decisions Based on Biological, Clinical, and Laboratory Variables. Computational and Structural Biotechnology Journal 2019; 17: 561 doi: 10.1016/j.csbj.2019.04.002
|
| 5 |
Mujeeb Zafar Banday, Aga Syed Sameer, Saniya Nissar. Genetic Polymorphism and cancer susceptibility. 2021; : 119 doi: 10.1007/978-981-33-6699-2_5
|
| 6 |
Mengqi Zhang, Haojun Yang, Zhuohui Chen, Yishu Fan, Xinhang Hu, Weiping Liu. Lynch syndrome-associated repeated stroke with MLH1 frame-shift mutation. Neurological Sciences 2021; 42(4): 1631 doi: 10.1007/s10072-020-04987-1
|
| 7 |
Yun Xu, Zonghao Huang, Cong Li, Congcong Zhu, Yuqin Zhang, Tian’an Guo, Fangqi Liu, Ye Xu. Comparison of Molecular, Clinicopathological, and Pedigree Differences Between Lynch-Like and Lynch Syndromes. Frontiers in Genetics 2020; 11 doi: 10.3389/fgene.2020.00991
|
| 8 |
Hassan Ashktorab, Sonia S. Kupfer, Hassan Brim, John M. Carethers. Racial Disparity in Gastrointestinal Cancer Risk. Gastroenterology 2017; 153(4): 910 doi: 10.1053/j.gastro.2017.08.018
|
| 9 |
B. Peñas, E. Tavío, C. Teruel Sánchez-Vegazo, M. Aicart-Ramos. Protocolo sobre el manejo del paciente con carcinoma colorrectal familiar y hereditario. Medicine - Programa de Formación Médica Continuada Acreditado 2016; 12(6): 325 doi: 10.1016/j.med.2016.03.007
|
| 10 |
Vladimir Roudko, Cansu Cimen Bozkus, Theofano Orfanelli, Christopher B. McClain, Caitlin Carr, Timothy O’Donnell, Lauren Chakraborty, Robert Samstein, Kuan-lin Huang, Stephanie V. Blank, Benjamin Greenbaum, Nina Bhardwaj. Shared Immunogenic Poly-Epitope Frameshift Mutations in Microsatellite Unstable Tumors. Cell 2020; 183(6): 1634 doi: 10.1016/j.cell.2020.11.004
|
| 11 |
Pascale Palassin, Marion Lapierre, Samuel Pyrdziak, Antoine Wagner, Régine Stehle, Carole Corsini, Jacqueline Duffour, Sandrine Bonnet, Abdelhay Boulahtouf, Carmen Rodriguez, Alexandre Ho-Pun-Cheung, Evelyne Lopez-Crapez, Florence Boissière-Michot, Frédéric Bibeau, Simon Thezenas, Nabila Elarouci, Janick Selves, Jean-Sébastien Hoffmann, Paul Roepman, Thibault Mazard, Olivier Buhard, Alex Duval, Stéphan Jalaguier, Vincent Cavaillès, Audrey Castet-Nicolas. A Truncated NRIP1 Mutant Amplifies Microsatellite Instability of Colorectal Cancer by Regulating MSH2/MSH6 Expression, and Is a Prognostic Marker of Stage III Tumors. Cancers 2021; 13(17): 4449 doi: 10.3390/cancers13174449
|
| 12 |
Valerie Lee, Adrian Murphy, Dung T. Le, Luis A. Diaz. Mismatch Repair Deficiency and Response to Immune Checkpoint Blockade. The Oncologist 2016; 21(10): 1200 doi: 10.1634/theoncologist.2016-0046
|
| 13 |
Hassan Ashktorab, Zaki Sherif, Taraneh Tarjoman, Saman Azam, Edward Lee, Babak Shokrani, Ifeanyichukwu Okereke, Akbar Soleimani, John M. Carethers, Adeyinka O. Laiyemo, Farshad Aduli, Mehdi Nouraie, Aida Habtezion, Hassan Brim. Elevated Risk for Sessile Serrated Polyps in African Americans with Endometrial Polyps. Digestive Diseases and Sciences 2020; 65(9): 2686 doi: 10.1007/s10620-019-05991-y
|
| 14 |
Khalid El Bairi, Csongor Lengyel, Antonio Marra, Said Afqir. Illuminating Colorectal Cancer Genomics by Next-Generation Sequencing. 2020; : 29 doi: 10.1007/978-3-030-53821-7_2
|
| 15 |
Pandu P. Nugroho, Siti Alyaa S. Ghozali, Daniel D. Buchanan, Mia I. Pisano, Jeanette C. Reece. Risk of cancer in individuals with Lynch-like syndrome and their families: a systematic review. Journal of Cancer Research and Clinical Oncology 2023; 149(1): 25 doi: 10.1007/s00432-022-04397-0
|
| 16 |
Erell Guillerm, Magali Svrcek, Armelle Bardier-Dupas, Noémie Basset, Florence Coulet, Chrystelle Colas. Molecular tumor testing in patients with Lynch-like syndrome reveals a de novo mosaic variant of a mismatch repair gene transmitted to offspring. European Journal of Human Genetics 2020; 28(11): 1624 doi: 10.1038/s41431-020-0689-6
|
| 17 |
Ryan Ladd, Matthew Davis, Jonathan A. Dyer. Genodermatoses with malignant potential. Clinics in Dermatology 2020; 38(4): 432 doi: 10.1016/j.clindermatol.2020.03.007
|
| 18 |
Jennifer Y Ju, Megan E Dibbern, Mani S Mahadevan, Jinbo Fan, Paul R Kunk, Edward B Stelow. Mismatch Repair Protein Deficiency/Microsatellite Instability Is Rare in Cholangiocarcinomas and Associated With Distinctive Morphologies. American Journal of Clinical Pathology 2020; 153(5): 598 doi: 10.1093/ajcp/aqz199
|
| 19 |
Catuxa Celeiro Muñoz, María Sánchez Ares, José Ramón Antúnez López. Foundations of Colorectal Cancer. 2022; : 551 doi: 10.1016/B978-0-323-90055-3.00008-9
|
| 20 |
Suvradeep Mitra, Rajaguru Paramaguru, Prasenjit Das, Sanjeev Vasudev Katti. Surgical Pathology of the Gastrointestinal System. 2022; : 593 doi: 10.1007/978-981-16-6395-6_16
|
| 21 |
Divya S. Vundamati, Xiuxu Chen, Vivekanand Singh. Colonic Adenocarcinoma at Advanced Stage in Adolescence: Report of 2 Cases. Case Reports in Pathology 2020; 2020: 1 doi: 10.1155/2020/1848367
|
| 22 |
L. Adán-Merino, M. Aldeguer-Martínez, E. Alonso-Gamarra, F. Valentín-Gómez, C. Zaera-De la Fuente, S. Martín-Chávarri. Diagnóstico y comportamiento clínico de pacientes con sospecha de síndrome de Lynch sin mutación conocida. Revista de Gastroenterología de México 2018; 83(4): 470 doi: 10.1016/j.rgmx.2018.06.007
|
| 23 |
Frederick A. Jakobiec, Paula Cortes Barrantes, Daniel R. Lefebvre, Tatyana Milman. Intraductal sebaceous papilloma of a meibomian gland: a new entity possibly associated with the MSH6 subtype of the Muir-Torre syndrome. Survey of Ophthalmology 2020; 65(2): 227 doi: 10.1016/j.survophthal.2019.09.002
|
| 24 |
Racial disparities in cancer care, an eyeopener for developing better global cancer management strategies. Cancer Reports 2023; 6(S1) doi: 10.1002/cnr2.1807
|
| 25 |
Szymon Hryhorowicz, Marta Kaczmarek-Ryś, Emilia Lis-Tanaś, Jakub Porowski, Marcin Szuman, Natalia Grot, Alicja Kryszczyńska, Jacek Paszkowski, Tomasz Banasiewicz, Andrzej Pławski. Strong Hereditary Predispositions to Colorectal Cancer. Genes 2022; 13(12): 2326 doi: 10.3390/genes13122326
|
| 26 |
Kouki Kuwabara, Okihide Suzuki, Noriyasu Chika, Kensuke Kumamoto, Toshiharu Minabe, Tomoo Fukuda, Eiichi Arai, Jun-ichi Tamaru, Kiwamu Akagi, Hidetaka Eguchi, Yasushi Okazaki, Hideyuki Ishida. Prevalence and molecular characteristics of DNA mismatch repair protein-deficient sebaceous neoplasms and keratoacanthomas in a Japanese hospital-based population. Japanese Journal of Clinical Oncology 2018; 48(6): 514 doi: 10.1093/jjco/hyy055
|
| 27 |
Amitabh Srivastava. Adenomatous and serrated polyposis syndromes. Diagnostic Histopathology 2020; 26(1): 1 doi: 10.1016/j.mpdhp.2019.10.009
|
| 28 |
Christoffer B. Lambring, Chloe Smith, Sohail Siraj, Krishna Patel, Riyaz Basha. Theranostics Approaches to Gastric and Colon Cancer. Diagnostics and Therapeutic Advances in GI Malignancies 2020; : 209 doi: 10.1007/978-981-15-2017-4_12
|
| 29 |
Mara Carsote, Ionut Florin Turturea, Maria Roxana Turturea, Ana Valea, Claudiu Nistor, Ancuta-Augustina Gheorghisan-Galateanu. Pathogenic Insights into DNA Mismatch Repair (MMR) Genes–Proteins and Microsatellite Instability: Focus on Adrenocortical Carcinoma and Beyond. Diagnostics 2023; 13(11): 1867 doi: 10.3390/diagnostics13111867
|
| 30 |
Rong Bu, Abdul K. Siraj, Sandeep Kumar Parvathareddy, Kaleem Iqbal, Saud Azam, Zeeshan Qadri, Maha Al-Rasheed, Wael Haqawi, Mark Diaz, Khadija Alobaisi, Padmanaban Annaiyappanaidu, Nabil Siraj, Hamed AlHusaini, Osama Alomar, Ismail A. Al-Badawi, Fouad Al-Dayel, Khawla S. Al-Kuraya. Lynch Syndrome Identification in Saudi Cohort of Endometrial Cancer Patients Screened by Universal Approach. International Journal of Molecular Sciences 2022; 23(20): 12299 doi: 10.3390/ijms232012299
|
| 31 |
Kohji Tanakaya. Current clinical topics of Lynch syndrome. International Journal of Clinical Oncology 2019; 24(9): 1013 doi: 10.1007/s10147-018-1282-7
|
| 32 |
Luigi Ricciardiello, Dennis J. Ahnen, Patrick M. Lynch. Chemoprevention of hereditary colon cancers: time for new strategies. Nature Reviews Gastroenterology & Hepatology 2016; 13(6): 352 doi: 10.1038/nrgastro.2016.56
|
| 33 |
Yue Xue, Serdar Balci, Cisel Aydin Mericoz, Orhun C. Taskin, Hongmei Jiang, Burcin Pehlivanoglu, Takashi Muraki, Bahar Memis, Burcu Saka, Grace E. Kim, Sudeshna Bandopadhyay, Jessica Knight, Bassel F. El‐Rayes, Juan Sarmiento, Michelle D. Reid, Mert Erkan, Olca Basturk, Volkan Adsay. Frequency and clinicopathologic associations of DNA mismatch repair protein deficiency in ampullary carcinoma: Routine testing is indicated. Cancer 2020; 126(21): 4788 doi: 10.1002/cncr.33135
|
| 34 |
Stephanie S. Tseng-Rogenski, Koji Munakata, Daniel Y. Choi, Paul K. Martin, Supal Mehta, Minoru Koi, Wei Zheng, Yang Zhang, John M. Carethers. The Human DNA Mismatch Repair Protein MSH3 Contains Nuclear Localization and Export Signals That Enable Nuclear-Cytosolic Shuttling in Response to Inflammation. Molecular and Cellular Biology 2020; 40(13) doi: 10.1128/MCB.00029-20
|
| 35 |
Jessica M. Long, Jacquelyn M. Powers, Bryson W. Katona. Evaluation of Classic, Attenuated, and Oligopolyposis of the Colon. Gastrointestinal Endoscopy Clinics of North America 2022; 32(1): 95 doi: 10.1016/j.giec.2021.08.003
|
| 36 |
Jessica S. Thomas, Chanjuan Shi. Diagnostic Molecular Pathology. 2024; : 339 doi: 10.1016/B978-0-12-822824-1.00018-3
|
| 37 |
Raffaella Liccardo, Marina De Rosa, Giovanni Battista Rossi, Nicola Carlomagno, Paola Izzo, Francesca Duraturo. Incomplete Segregation of MSH6 Frameshift Variants with Phenotype of Lynch Syndrome. International Journal of Molecular Sciences 2017; 18(5): 999 doi: 10.3390/ijms18050999
|
| 38 |
Reginaldo Cruz Alves Rosa, Jessica Oliveira Santis, Lorena Alves Teixeira, Greice Andreotti Molfetta, Jennifer Thalita Targino dos Santos, Vanessa dos Santos Ribeiro, Fernando Chahud, Alfredo Ribeiro-Silva, Mariângela Ottoboni Brunaldi, Wilson Araújo Silva Jr, Victor Evangelista de Faria Ferraz. Lynch syndrome identification in a Brazilian cohort of endometrial cancer screened by a universal approach. Gynecologic Oncology 2020; 159(1): 229 doi: 10.1016/j.ygyno.2020.07.013
|
| 39 |
Huseyin Esin, Mehmet Fatih Ekici, Bulent Calik. Colon Polyps and Colorectal Cancer. 2021; : 153 doi: 10.1007/978-3-030-57273-0_8
|
| 40 |
Sherief Shawki, Matthew F. Kalady. Recent advances in understanding Lynch syndrome. F1000Research 2016; 5: 2889 doi: 10.12688/f1000research.9654.1
|
| 41 |
Anna Pellat, Jeanne Netter, Géraldine Perkins, Romain Cohen, Florence Coulet, Yann Parc, Magali Svrcek, Alex Duval, Thierry André. Syndrome de Lynch : quoi de neuf ?. Bulletin du Cancer 2019; 106(7-8): 647 doi: 10.1016/j.bulcan.2018.10.009
|
| 42 |
Kensuke Kumamoto, Hideyuki Ishida. Recent Advances in the Treatment of Colorectal Cancer. 2019; : 127 doi: 10.1007/978-981-13-3050-6_11
|
| 43 |
Larissa V. Furtado, Wade S. Samowitz. Colorectal cancer molecular profiling: from IHC to NGS in search of optimal algorithm. Virchows Archiv 2017; 471(2): 235 doi: 10.1007/s00428-017-2153-8
|
| 44 |
Wen-Xuan Fan, Fei Su, Yan Zhang, Xiao-Ling Zhang, Yun-Yi Du, Yang-Jun Gao, Wei-Ling Li, Wen-Qing Hu, Jun Zhao. Oncological characteristics, treatments and prognostic outcomes in MMR-deficient colorectal cancer. Biomarker Research 2024; 12(1) doi: 10.1186/s40364-024-00640-7
|
| 45 |
Kristina Lagerstedt-Robinson, Anna Rohlin, Christos Aravidis, Beatrice Melin, Margareta Nordling, Marie Stenmark-Askmalm, Annika Lindblom, Mef Nilbert. Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population. Oncology Reports 2016; 36(5): 2823 doi: 10.3892/or.2016.5060
|
| 46 |
Shumin Jia, Xiaodan Wu, Yiheng Zhang, Meifen Zhang. Chinese Lynch syndrome‐associated colorectal cancer patients' self‐concept and adherence to surveillance. European Journal of Cancer Care 2021; 30(2) doi: 10.1111/ecc.13379
|
| 47 |
Arianna Dal Buono, Federica Gaiani, Laura Poliani, Carmen Correale, Luigi Laghi. Defects in MMR Genes as a Seminal Example of Personalized Medicine: From Diagnosis to Therapy. Journal of Personalized Medicine 2021; 11(12): 1333 doi: 10.3390/jpm11121333
|
| 48 |
Beth K. Dray, Muthuswamy Raveendran, R. Alan Harris, Fernando Benavides, Stanton B. Gray, Carlos J. Perez, Mark J. McArthur, Lawrence E. Williams, Wallace B. Baze, Harsha Doddapaneni, Donna M. Muzny, Christian R. Abee, Jeffrey Rogers. Mismatch repair gene mutations lead to lynch syndrome colorectal cancer in rhesus macaques. Genes & Cancer 2018; 9(3-4): 142 doi: 10.18632/genesandcancer.170
|
| 49 |
Koji Munakata, Minoru Koi, Takahito Kitajima, Stephanie Tseng-Rogenski, Mamoru Uemura, Hiroshi Matsuno, Kenji Kawai, Yuki Sekido, Tsunekazu Mizushima, Yuji Toiyama, Takuya Yamada, Masayuki Mano, Eiji Mita, Masato Kusunoki, Masaki Mori, John M. Carethers. Inflammation-Associated Microsatellite Alterations Caused by MSH3 Dysfunction Are Prevalent in Ulcerative Colitis and Increase With Neoplastic Advancement. Clinical and Translational Gastroenterology 2019; 10(12): e00105 doi: 10.14309/ctg.0000000000000105
|
| 50 |
Naim Abu Freha, Yaara Leibovici Weissman, Alexander Fich, Inbal Barnes Kedar, Marisa Halpern, Ignacio Sztarkier, Doron M. Behar, Orly Arbib Sneh, Alex Vilkin, Hagit N. Baris, Rachel Gingold, Flavio Lejbkowicz, Yaron Niv, Yael Goldberg, Zohar Levi. Constitutional mismatch repair deficiency and Lynch syndrome among consecutive Arab Bedouins with colorectal cancer in Israel. Familial Cancer 2018; 17(1): 79 doi: 10.1007/s10689-017-0009-7
|
| 51 |
G. A. Khakimov, A. A. Tryakin, G. G. Khakimova. Use of nivolumab for colon cancer with Lynch syndrome. Journal of Modern Oncology 2020; 22(3): 114 doi: 10.26442/18151434.2020.3.200350
|
| 52 |
Arato Takedachi, Erina Matsuishi, Shouji Mizusaki, Tomoki Nagasawa, Ryosuke Fujikane, Masumi Hidaka, Shigenori Iwai, Isao Kuraoka. Novel plasmids for the fluorescence-based evaluation of DNA mismatch repair in human cells. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 2022; 824: 111779 doi: 10.1016/j.mrfmmm.2022.111779
|
| 53 |
Konstantin R. Brawanski, Susanne Sprung, Christian F. Freyschlag, Romana Hoeftberger, Thomas Ströbel, Johannes Haybaeck, Claudius Thomé, Claudia Manzl, Anna M. Birkl-Toeglhofer. Influence of MMR, MGMT Promotor Methylation and Protein Expression on Overall and Progression-Free Survival in Primary Glioblastoma Patients Treated with Temozolomide. International Journal of Molecular Sciences 2023; 24(7): 6184 doi: 10.3390/ijms24076184
|
| 54 |
Ioannis A. Voutsadakis. Polymerase epsilon mutations and concomitant β2-microglobulin mutations in cancer. Gene 2018; 647: 31 doi: 10.1016/j.gene.2018.01.030
|
| 55 |
Mahdieh Nejadtaghi, Hamideh Jafari, Effat Farrokhi, Keihan Ghatreh Samani. Familial Colorectal Cancer Type X (FCCTX) and the correlation with various genes—A systematic review. Current Problems in Cancer 2017; 41(6): 388 doi: 10.1016/j.currproblcancer.2017.10.002
|
| 56 |
Makoto Kagawa, Satoru Kawakami, Azusa Yamamoto, Okihide Suzuki, Hidetaka Eguchi, Yasushi Okazaki, Kiwamu Akagi, Jun-ichi Tamaru, Tomio Arai, Tatsuro Yamaguchi, Hideyuki Ishida. Prevalence and clinicopathological/molecular characteristics of mismatch repair protein-deficient tumours among surgically treated patients with prostate cancer in a Japanese hospital-based population. Japanese Journal of Clinical Oncology 2021; 51(4): 639 doi: 10.1093/jjco/hyaa207
|
| 57 |
Mahmoud Elnaggar, Ponnuthurai Pratheepan, Baskaran Paramagurunathan, Josie Colemeadow, Basim Hussein, Varvara Bashkirova, Kavya Pillai, Lucy Singh, Mehar Chawla. Experience of a District General Hospital With a Diverse Community in Operated Colorectal Cancers According to Ethnic Background. Cureus 2023; doi: 10.7759/cureus.36917
|
| 58 |
J. Blount, A. Prakash. The changing landscape of Lynch syndrome due to PMS2 mutations. Clinical Genetics 2018; 94(1): 61 doi: 10.1111/cge.13205
|
| 59 |
Demetra Georgiou, Vicki Kiesel, Angela F. Brady, Kevin Monahan. Response to “Histology of colorectal adenocarcinoma with double somatic mismatch-repair mutations is indistinguishable from those caused by Lynch syndrome”. Human Pathology 2019; 89: 115 doi: 10.1016/j.humpath.2019.04.015
|
| 60 |
Melissa W. Taggart, Wai Chin Foo, Sun Mi Lee. Oncological Surgical Pathology. 2020; : 691 doi: 10.1007/978-3-319-96681-6_12
|
| 61 |
Anne-Sophie Sandner, Ramona Weggel, Yasmin Mehraein, Stephanie Schneider, Wolfgang Hiddemann, Karsten Spiekermann, Amanda Ewart Toland. Frequency of hematologic and solid malignancies in the family history of 50 patients with acute myeloid leukemia – a single center analysis. PLOS ONE 2019; 14(4): e0215453 doi: 10.1371/journal.pone.0215453
|
| 62 |
Satoshi Suzuki, Moriya Iwaizumi, Stephanie Tseng-Rogenski, Yasushi Hamaya, Hiroaki Miyajima, Shigeru Kanaoka, Ken Sugimoto, John M. Carethers. Production of truncated MBD4 protein by frameshift mutation in DNA mismatch repair-deficient cells enhances 5-fluorouracil sensitivity that is independent ofhMLH1status. Cancer Biology & Therapy 2016; 17(7): 760 doi: 10.1080/15384047.2016.1178430
|
| 63 |
Bryson W. Katona, John P. Lynch. Physiology of the Gastrointestinal Tract. 2018; : 1615 doi: 10.1016/B978-0-12-809954-4.00066-9
|
| 64 |
Yoshimi Kiyozumi, Hiroyuki Matsubayashi, Satomi Higashigawa, Yasue Horiuchi, Nobuhiro Kado, Yasuyuki Hirashima, Akio Shiomi, Takuma Oishi, Sumiko Ohnami, Keiichi Ohshima, Kenichi Urakami, Takeshi Nagashima, Ken Yamaguchi. Role of Tumor Mutation Burden Analysis in Detecting Lynch Syndrome in Precision Medicine: Analysis of 2,501 Japanese Cancer Patients. Cancer Epidemiology, Biomarkers & Prevention 2021; 30(1): 166 doi: 10.1158/1055-9965.EPI-20-0694
|
| 65 |
Shahid Mahmood Baig, Ambrin Fatima, Muhammad Tariq, Tahir Naeem Khan, Zafar Ali, Mohammad Faheem, Humera Mahmood, Patrick Killela, Matthew Waitkus, Yiping He, Fangping Zhao, Sizhen Wang, Yuchen Jiao, Hai Yan. Hereditary brain tumor with a homozygous germline mutation in PMS2: pedigree analysis and prenatal screening in a family with constitutional mismatch repair deficiency (CMMRD) syndrome. Familial Cancer 2019; 18(2): 261 doi: 10.1007/s10689-018-0112-4
|
| 66 |
Vassilis G Gorgoulis, Dafni‐Eleftheria Pefani, Ioannis S Pateras, Ioannis P Trougakos. Integrating the DNA damage and protein stress responses during cancer development and treatment. The Journal of Pathology 2018; 246(1): 12 doi: 10.1002/path.5097
|
| 67 |
Shih‐Ching Chang, Yuan‐Tzu Lan, Pei‐Ching Lin, Shung‐Haur Yang, Chien‐Hsing Lin, Wen‐Yi Liang, Wei‐Shone Chen, Jeng‐Kai Jiang, Jen‐Kou Lin. Patterns of germline and somatic mutations in 16 genes associated with mismatch repair function or containing tandem repeat sequences. Cancer Medicine 2020; 9(2): 476 doi: 10.1002/cam4.2702
|
| 68 |
Leila Cattelan, Jad Abi-Rafeh, Fadi Brimo, Roy Kazan, Margaret Redpath, May Chergui. Metastatic Prostatic Adenocarcinoma in Patient With Muir–Torre Syndrome Misdiagnosed as Metastatic Sebaceous Carcinoma: Case Report and Systematic Literature Review. The American Journal of Dermatopathology 2020; 42(9): 700 doi: 10.1097/DAD.0000000000001633
|
| 69 |
I. S. Reynolds, E. O’Connell, D. A. McNamara, J. H. M. Prehn, S. J. Furney, J. P. Burke. Clinical Oncogenomics and Personalized Medicine in Colorectal Cancer for the Surgeon: What We Need to Know and What the Future Holds. SN Comprehensive Clinical Medicine 2022; 4(1) doi: 10.1007/s42399-022-01144-x
|
| 70 |
Leslie E. Oldfield, Tiantian Li, Alicia Tone, Melyssa Aronson, Melissa Edwards, Spring Holter, Rene Quevedo, Emily Van de Laar, Jordan Lerner-Ellis, Aaron Pollett, Blaise Clarke, Uri Tabori, Steven Gallinger, Sarah E. Ferguson, Trevor J. Pugh. An Integrative DNA Sequencing and Methylation Panel to Assess Mismatch Repair Deficiency. The Journal of Molecular Diagnostics 2021; 23(2): 242 doi: 10.1016/j.jmoldx.2020.11.006
|
| 71 |
Jan Teuber, Annekathrin Reinhardt, David Reuss, Stefan Hähnel, Andreas Unterberg, Christopher Beynon. Aggressive pituitary adenoma in the context of Lynch syndrome: a case report and literature review on this rare coincidence. British Journal of Neurosurgery 2024; 38(3): 775 doi: 10.1080/02688697.2021.1967881
|
| 72 |
Matthew Symer, James Connolly, Heather Yeo. Management of the malignant colorectal polyp. Current Problems in Surgery 2022; 59(5): 101124 doi: 10.1016/j.cpsurg.2022.101124
|
| 73 |
Shizuko Sei, Aysel Ahadova, Derin B. Keskin, Lena Bohaumilitzky, Johannes Gebert, Magnus von Knebel Doeberitz, Steven M. Lipkin, Matthias Kloor. Lynch syndrome cancer vaccines: A roadmap for the development of precision immunoprevention strategies. Frontiers in Oncology 2023; 13 doi: 10.3389/fonc.2023.1147590
|
| 74 |
John M. Carethers, Chyke A. Doubeni. Causes of Socioeconomic Disparities in Colorectal Cancer and Intervention Framework and Strategies. Gastroenterology 2020; 158(2): 354 doi: 10.1053/j.gastro.2019.10.029
|
| 75 |
Maide Ö. Raeker, Jovan Pierre-Charles, John M. Carethers. Tetranucleotide Microsatellite Mutational Behavior Assessed in Real Time: Implications for Future Microsatellite Panels. Cellular and Molecular Gastroenterology and Hepatology 2020; 9(4): 689 doi: 10.1016/j.jcmgh.2020.01.006
|
| 76 |
John M. Carethers. Novel Approaches to Colorectal Cancer. Advances in Cancer Research 2021; 151: 197 doi: 10.1016/bs.acr.2021.02.007
|
| 77 |
Qian Liu, Xuefeng Zhu, Michelle Lindström, Yonghong Shi, Ju Zheng, Xinxin Hao, Claes M. Gustafsson, Beidong Liu, Jingyuan Fu. Yeast mismatch repair components are required for stable inheritance of gene silencing. PLOS Genetics 2020; 16(5): e1008798 doi: 10.1371/journal.pgen.1008798
|
| 78 |
E. Ryan, K. Sheahan, B. Creavin, H.M. Mohan, D.C. Winter. The current value of determining the mismatch repair status of colorectal cancer: A rationale for routine testing. Critical Reviews in Oncology/Hematology 2017; 116: 38 doi: 10.1016/j.critrevonc.2017.05.006
|
| 79 |
Danielle M. Pastor, Jeffrey Schlom. Immunology of Lynch Syndrome. Current Oncology Reports 2021; 23(8) doi: 10.1007/s11912-021-01085-z
|
| 80 |
Behyamet Onka, Daoud ali Mohamed, Romeo Thierry Tessi Yehouenou, Boris Adeyemi, Wend-Yam Mohammed Traore, Mbina Mbougou Kevin arthur, Hounayda Jerguigue, Rachida Latib, Youssef Omor. A tumor association to be aware: endometrial cancer and colon cancer in relation to Lynch syndrome. BJR|case reports 2022; 8(2) doi: 10.1259/bjrcr.20210230
|
| 81 |
John M. Carethers. GRG Profiles: John M. Carethers. Digestive Diseases and Sciences 2016; 61(6): 1429 doi: 10.1007/s10620-016-4058-9
|
| 82 |
Vladimir Roudko, Cansu Cimen Bozkus, Benjamin Greenbaum, Aimee Lucas, Robert Samstein, Nina Bhardwaj. Lynch Syndrome and MSI-H Cancers: From Mechanisms to “Off-The-Shelf” Cancer Vaccines. Frontiers in Immunology 2021; 12 doi: 10.3389/fimmu.2021.757804
|
| 83 |
Frederick A. Jakobiec, Paula Cortes Barrantes, Tatyana Milman, Nahyoung Grace Lee, Aaron Fay. Ocular Adnexal Adenomatoid Sebaceous Gland Hyperplasia: A Clinical and Immunopathologic Analysis in Relation to the Muir-Torre Syndrome. Ophthalmic Plastic & Reconstructive Surgery 2020; 36(1): e6 doi: 10.1097/IOP.0000000000001497
|
| 84 |
Olfat Khdair-Ahmad, Maysa Al Husaini, Sura Ghunaimat, Taleb Ismael, Nisreen Amayiri, Hadeel Halalsheh, Mahmoud Jaara, Iyad Sultan. Constitutional Mismatch Repair Deficiency in children with colorectal carcinoma: A jordanian center experience. Pediatric Hematology Oncology Journal 2021; 6(1): 18 doi: 10.1016/j.phoj.2020.10.004
|
| 85 |
Ladan Goshayeshi, Kamran Ghaffarzadegan, Alireza Khooei, Abbas Esmaeilzadeh, Mahla Rahmani Khorram, Hooman Mosannen Mozaffari, Behzad Kiani, Benyamin Hoseini. Prevalence and clinicopathological characteristics of mismatch repair-deficient colorectal carcinoma in early onset cases as compared with late-onset cases: a retrospective cross-sectional study in Northeastern Iran. BMJ Open 2018; 8(8): e023102 doi: 10.1136/bmjopen-2018-023102
|
| 86 |
L. Adán-Merino, M. Aldeguer-Martínez, E. Alonso-Gamarra, F. Valentín-Gómez, C. Zaera-De la Fuente, S. Martín-Chávarri. Diagnosis and clinical behavior in patients with Lynch-like syndrome. Revista de Gastroenterología de México (English Edition) 2018; 83(4): 470 doi: 10.1016/j.rgmxen.2018.06.012
|
| 87 |
Malene Djursby, Thomas van Overeem Hansen, Karin A. W. Wadt, Majbritt Busk Madsen, Lukas Adrian Berchtold, Charlotte Kvist Lautrup, Sara Markholt, Uffe Birk Jensen, Lotte Nylandsted Krogh, Malene Lundsgaard, Anne Marie Gerdes, Mef Nilbert, Christina Therkildsen. Clinical implications of genetic testing in familial intermediate and late-onset colorectal cancer. Human Genetics 2022; 141(12): 1925 doi: 10.1007/s00439-022-02470-9
|
| 88 |
Stephanie Histed Chung, Nina Woldenberg, Antoinette R. Roth, Rinat Masamed, Wendy Conlon, Joshua G. Cohen, Melissa M. Joines, Maitraya K. Patel. BRCAand Beyond: Comprehensive Image-rich Review of Hereditary Breast and Gynecologic Cancer Syndromes. RadioGraphics 2020; 40(2): 306 doi: 10.1148/rg.2020190084
|
| 89 |
Lobna S Shash, Shimaa A Elgohary, Riham A Ibrahim. FOXM1 and MMR genes immunohistochemical expression in colorectal cancer: promising prognostic insights and candidate therapeutic targets. Egyptian Journal of Pathology 2023; 43(1): 75 doi: 10.4103/egjp.egjp_6_23
|
| 90 |
Pasquale Paolisso, Giulia Saturi, Alberto Foà, Maristella Saponara, Margherita Nannini, Maria Abbondanza Pantaleo, Ornella Leone, Daniela Turchetti, Daniele Calistri, Carlo Savini, Davide Pacini, Carmine Pizzi, Nazzareno Galiè. Primary malignant pericardial tumour in Lynch syndrome. BMC Cancer 2020; 20(1) doi: 10.1186/s12885-020-6677-y
|
| 91 |
|
| 92 |
Daniel Czajkowski, Radosław Szmyd, Harriet E Gee. Impact ofDNAdamage response defects in cancer cells on response to immunotherapy and radiotherapy. Journal of Medical Imaging and Radiation Oncology 2022; 66(4): 546 doi: 10.1111/1754-9485.13413
|
| 93 |
Alban Zarzavadjian Le Bian, Christine Denet, Nicolas Tabchouri, Gianfranco Donatelli, Philippe Wind, Christophe Louvet, Mostefa Bennamoun, Christos Christidis, Thierry Perniceni, David Fuks, Brice Gayet. Specific features of colorectal cancer in patients with metabolic syndrome: a matched case-control analysis of 772 patients. Langenbeck's Archives of Surgery 2018; 403(4): 443 doi: 10.1007/s00423-018-1677-y
|
| 94 |
A. V. Semyanikhina, A. O. Rasulov, L. N. Lyubchenko. Clinical and genetic aspects of differential diagnostics of hereditary non-polyposis colorectal cancer. Advances in molecular oncology 2019; 6(2): 21 doi: 10.17650/2313-805X-2019-6-2-21-27
|
| 95 |
Quan M. Bui, David Lin, Wendy Ho. Approach to Lynch Syndrome for the Gastroenterologist. Digestive Diseases and Sciences 2017; 62(2): 299 doi: 10.1007/s10620-016-4346-4
|
| 96 |
Zhi-Gang Yao, Bei-Bei Lv, Hai-Yan Jing, Wen-Jing Su, Jia-Mei Li, Hui Fan, Miao-Qing Zhao, Ye-Jun Qin, Xi-Chao Sun. A practical screening strategy for Lynch syndrome and Lynch syndrome mimics in colorectal cancer. Journal of Cancer Research and Therapeutics 2021; 17(3): 790 doi: 10.4103/jcrt.jcrt_214_21
|
| 97 |
Fatma Hüsniye Dilek, Dilara İrem Arslan Kahraman. Prophylactic Surgery. 2021; : 279 doi: 10.1007/978-3-030-66853-2_26
|
| 98 |
Sotirios Doukas, Dimitra Vageli, Taxiarchis Nikolouzakis, Luca Falzone, Anca Docea, George Lazopoulos, Konstantinos Kalbakis, Aristidis Tsatsakis. Role of DNA mismatch repair genes in lung and head and neck cancer (Review). World Academy of Sciences Journal 2019; doi: 10.3892/wasj.2019.21
|
| 99 |
Jesse P. Wright, Kathleen W. Montgomery, Joshua Tierney, Jill Gilbert, Carmen C. Solórzano, Kamran Idrees. Ectopic, retroperitoneal adrenocortical carcinoma in the setting of Lynch syndrome. Familial Cancer 2018; 17(3): 381 doi: 10.1007/s10689-017-0042-6
|
| 100 |
Elena M. Stoffel, John M. Carethers. Current Approaches to Germline Cancer Genetic Testing. Annual Review of Medicine 2020; 71(1): 85 doi: 10.1146/annurev-med-052318-101009
|
| 101 |
Belal A. Al-Husein, Bara’ Dawah, Saleem Bani-Hani, Samir M. Al Bashir, Khaled M. Al-Sawalmeh, Nehad M. Ayoub. Immunomodulatory effect of statins on Regulatory T Lymphocytes in human colorectal cancer is determined by the stage of disease. Oncotarget 2018; 9(87): 35752 doi: 10.18632/oncotarget.26293
|
| 102 |
Elizabeth V. Clarke, Kristin R. Muessig, Jamilyn Zepp, Jessica E. Hunter, Sapna Syngal, Louise S. Acheson, Georgia L. Wiesner, Susan K. Peterson, Kellene M. Bergen, Elizabeth Shuster, James V. Davis, Jennifer L. Schneider, Tia L. Kauffman, Marian J. Gilmore, Jacob A. Reiss, Alan F. Rope, Jennifer E. Cook, Katrina A. B. Goddard. Implementation of a Systematic Tumor Screening Program for Lynch Syndrome in an Integrated Health Care Setting. Familial Cancer 2019; 18(3): 317 doi: 10.1007/s10689-019-00123-x
|
| 103 |
Prerana Nagabhushana, Snigdha Kumari, Minakshi Rohilla, Radhika Srinivasan, Aashima Arora, Pulkit Rastogi. Discordant immunohistochemistry in an unusual MLH1 gene variant in a case of Lynch syndrome. Gynecologic Oncology Reports 2021; 37: 100854 doi: 10.1016/j.gore.2021.100854
|
| 104 |
Camille Evrard, Stéphane Messina, David Sefrioui, Éric Frouin, Marie-Luce Auriault, Romain Chautard, Aziz Zaanan, Marion Jaffrelot, Christelle De La Fouchardière, Thomas Aparicio, Romain Coriat, Julie Godet, Christine Silvain, Violaine Randrian, Jean-Christophe Sabourin, Rosine Guimbaud, Elodie Miquelestorena-Standley, Thierry Lecomte, Valérie Moulin, Lucie Karayan-Tapon, Gaëlle Tachon, David Tougeron. Heterogeneity of Mismatch Repair Status and Microsatellite Instability between Primary Tumour and Metastasis and Its Implications for Immunotherapy in Colorectal Cancers. International Journal of Molecular Sciences 2022; 23(8): 4427 doi: 10.3390/ijms23084427
|
| 105 |
Minoru Koi, John M Carethers. The colorectal cancer immune microenvironment and approach to immunotherapies. Future Oncology 2017; 13(18): 1633 doi: 10.2217/fon-2017-0145
|
| 106 |
Kenichi Chikatani, Noriyasu Chika, Okihide Suzuki, Takehiko Sakimoto, Keiichiro Ishibashi, Hidetaka Eguchi, Yasushi Okazaki, Hideyuki Ishida. Clinically applicable cases of anti-programmed cell death protein 1 immunotherapy for colorectal cancer patients. Surgery Today 2020; 50(12): 1694 doi: 10.1007/s00595-020-01998-5
|
| 107 |
Adrian C Bateman. DNA mismatch repair proteins: scientific update and practical guide. Journal of Clinical Pathology 2021; 74(4): 264 doi: 10.1136/jclinpath-2020-207281
|
| 108 |
Frederick A. Jakobiec, Paula Cortes Barrantes, Tatyana Milman, Michael Yoon. Sebaceoma of a Meibomian Gland of the Upper Eyelid. Ocular Oncology and Pathology 2020; 6(4): 297 doi: 10.1159/000504627
|
| 109 |
John M. Carethers. Microsatellite Instability Pathway and EMAST in Colorectal Cancer. Current Colorectal Cancer Reports 2017; 13(1): 73 doi: 10.1007/s11888-017-0352-y
|
| 110 |
Maria Beatriz de Matos, Laura Elisabete Barbosa, João Paulo Teixeira. Narrative review comparing the epidemiology, characteristics, and survival in sporadic colorectal carcinoma/Lynch syndrome. Journal of Coloproctology 2020; 40(01): 073 doi: 10.1016/j.jcol.2019.07.006
|
| 111 |
Tamara Alejandra Piñero, Omar Soukarieh, Marion Rolain, Karin Alvarez, Francisco López-Köstner, Giovana Tardin Torrezan, Dirce Maria Carraro, Ivana Lucia De Oliveira Nascimento, Thaís Ferreira Bomfim, Taísa Manuela Bonfim Machado-Lopes, Juliana Côrtes Freitas, Maria Betânia Toralles, Kiyoko Abe Sandes, Benedito Mauro Rossi, Samuel Aguiar Junior, Joanna Meira, Mev Dominguez-Valentin, Pål Møller, Carlos Alberto Vaccaro, Alexandra Martins, Walter Hernán Pavicic. MLH1 intronic variants mapping to + 5 position of splice donor sites lead to deleterious effects on RNA splicing. Familial Cancer 2020; 19(4): 323 doi: 10.1007/s10689-020-00182-5
|
| 112 |
Zarah Batulan, Nadia Maarouf, Vipul Shrivastava, Edward O’Brien. Prophylactic salpingo-oophorectomy & surgical menopause for inherited risks of cancer: the need to identify biomarkers to assess the theoretical risk of premature coronary artery disease. Women's Midlife Health 2018; 4(1) doi: 10.1186/s40695-018-0037-y
|
| 113 |
Alia Ghoneum, Amal Tazzite, Khalid El Bairi, Neveen Said. Ovarian Cancer Biomarkers. 2021; : 203 doi: 10.1007/978-981-16-1873-4_7
|
| 114 |
Luana Greco, Federica Rubbino, Arianna Dal Buono, Luigi Laghi. Microsatellite Instability and Immune Response: From Microenvironment Features to Therapeutic Actionability—Lessons from Colorectal Cancer. Genes 2023; 14(6): 1169 doi: 10.3390/genes14061169
|
| 115 |
Henry T. Lynch, Stephen Lanspa, Trudy Shaw, Murray Joseph Casey, Marc Rendell, Mark Stacey, Theresa Townley, Carrie Snyder, Megan Hitchins, Joan Bailey-Wilson. Phenotypic and genotypic heterogeneity of Lynch syndrome: a complex diagnostic challenge. Familial Cancer 2018; 17(3): 403 doi: 10.1007/s10689-017-0053-3
|
| 116 |
Wei Chen, Benjamin J. Swanson, Wendy L. Frankel. Molecular genetics of microsatellite-unstable colorectal cancer for pathologists. Diagnostic Pathology 2017; 12(1) doi: 10.1186/s13000-017-0613-8
|
| 117 |
A.H. Mohammad, E. Rohr, A. Moise, R.M. Abdulsalam, W. Davalan, A. Rizzolo, A.S. Liberman, C. Goudie, L. Palma, W.D. Foulkes. This is not Lynch syndrome: lessons from misattributed diagnoses in constitutional mismatch repair deficiency. ESMO Gastrointestinal Oncology 2024; 6: 100111 doi: 10.1016/j.esmogo.2024.100111
|
| 118 |
Teresa Marple, Mi Young Son, Xiaodong Cheng, Jun Ho Ko, Patrick Sung, Paul Hasty. TREX2 deficiency suppresses spontaneous and genotoxin-associated mutagenesis. Cell Reports 2024; 43(1): 113637 doi: 10.1016/j.celrep.2023.113637
|
| 119 |
Jennifer K. Maratt, Elena Stoffel. Identification of Lynch Syndrome. Gastrointestinal Endoscopy Clinics of North America 2022; 32(1): 45 doi: 10.1016/j.giec.2021.09.002
|
| 120 |
Maya Eiger-Moscovich, Ralph C. Eagle Jr., Carol L. Shields, Hilary Racher, Sara E. Lally, Rona Z. Silkiss, Jerry A. Shields, Tatyana Milman. Muir-Torre Syndrome Associated Periocular Sebaceous Neoplasms: Screening Patterns in the Literature and in Clinical Practice. Ocular Oncology and Pathology 2020; 6(4): 226 doi: 10.1159/000504984
|
| 121 |
Daniele Fanale, Lidia Rita Corsini, Chiara Brando, Alessandra Dimino, Clarissa Filorizzo, Luigi Magrin, Roberta Sciacchitano, Alessia Fiorino, Tancredi Didier Bazan Russo, Valentina Calò, Juan Lucio Iovanna, Edoardo Francini, Antonio Russo, Viviana Bazan. Impact of Different Selection Approaches for Identifying Lynch Syndrome-Related Colorectal Cancer Patients: Unity Is Strength. Frontiers in Oncology 2022; 12 doi: 10.3389/fonc.2022.827822
|
| 122 |
Yusuke Tajima, Hidetaka Eguchi, Noriyasu Chika, Tomonori Nagai, Sariya Dechamethakun, Kensuke Kumamoto, Tetsuhiko Tachikawa, Kiwamu Akagi, Jun-ichi Tamaru, Hiroyuki Seki, Yasushi Okazaki, Hideyuki Ishida. Prevalence and molecular characteristics of defective mismatch repair epithelial ovarian cancer in a Japanese hospital-based population. Japanese Journal of Clinical Oncology 2018; 48(8): 728 doi: 10.1093/jjco/hyy081
|
| 123 |
Ashleigh C. Hamilton, Finian J. Bannon, Philip D. Dunne, Jacqueline James, Stephen McQuaid, Ronan T. Gray, Manuel Salto-Tellez, Chris R. Cardwell, Maurice B. Loughrey, Helen G. Coleman. Distinct Molecular Profiles of Sporadic Early-Onset Colorectal Cancer: A Population-Based Cohort and Systematic Review. Gastro Hep Advances 2023; 2(3): 347 doi: 10.1016/j.gastha.2022.11.005
|
| 124 |
G. G. Khakimova, A. A. Tryakin, G. A. Khakimov. The Use of Nivolumab in Colorectal Cancer with Lynch Syndrome. A Case Report. Malignant tumours 2020; 10(1): 41 doi: 10.18027/2224-5057-2020-10-41-48
|
| 125 |
M. Sierra Morales, I. Bartolomé Oterino, S. Redondo Evangelista, P. García Centeno, A. Santos Rodríguez. Síndrome de Lynch. Cáncer de colon familiar no sindrómico. Medicine - Programa de Formación Médica Continuada Acreditado 2024; 14(4): 175 doi: 10.1016/j.med.2024.02.020
|
| 126 |
Pauline Rochefort, Françoise Desseigne, Valérie Bonadona, Sophie Dussart, Clélia Coutzac, Matthieu Sarabi, Christelle de la Fouchardiere. Immune Checkpoint Inhibitor Sensitivity of DNA Repair Deficient Tumors. Immunotherapy 2021; 13(14): 1205 doi: 10.2217/imt-2021-0024
|
| 127 |
Aleksandra Stajkovska, Sanja Mehandziska, Rodney Rosalia, Margarita Stavrevska, Marija Janevska, Martina Markovska, Ivan Kungulovski, Zan Mitrev, Goran Kungulovski. A Pediatric Case of Glioblastoma Multiforme Associated With a Novel Germline p.His112CysfsTer9 Mutation in the MLH1 Gene Accompanied by a p.Arg283Cys Mutation in the TP53 Gene: A Case Report. Frontiers in Genetics 2019; 10 doi: 10.3389/fgene.2019.00952
|
| 128 |
Zornitsa Bogomilova Kamburova, Polina Damyanova Dimitrova, Diana Strateva Dimitrova, Katya Stefanova Kovacheva, Savelina Lubenova Popovska, Slavena Enkova Nikolova. Lynch-like syndrome with germline WRN mutation in Bulgarian patient with synchronous endometrial and ovarian cancer. Hereditary Cancer in Clinical Practice 2023; 21(1) doi: 10.1186/s13053-023-00257-1
|
| 129 |
Carlos A. Vaccaro, Tamara Piñero, Alberto I. Herrando, Romina Cajal, Alejandra Ferro, Pablo Kalfayan, Juan Pablo Santino, María Dalva Falconi, Alicia Verzura, Gisela Guerrero, María Cecilia Riggi, Walter Pavicic, María Laura González. Síndrome de Lynch: impacto de la caracterización de familias en base a estudios genéticos. Oncología Clínica 2018; 23(1) doi: 10.56969/oc.v23i1.63
|
| 130 |
Samuel G.W. Ow, Kar Tong Tan, Henry Yang, Hui-Ling Yap, Nur Sabrina Binte Sapari, Pei Yi Ong, Richie Soong, Soo-Chin Lee. Next Generation Sequencing Reveals Novel Mutations in Mismatch Repair Genes and Other Cancer Predisposition Genes in Asian Patients with Suspected Lynch Syndrome. Clinical Colorectal Cancer 2019; 18(4): e324 doi: 10.1016/j.clcc.2019.05.007
|
| 131 |
Mahalakshmi S. Biradar, Shankar Thapa, Sonali S. Shinde, Aniket P. Sarkate, Kalusing S. Padvi. Systems Biology Approaches: Prevention, Diagnosis, and Understanding Mechanisms of Complex Diseases. 2024; : 467 doi: 10.1007/978-981-99-9462-5_18
|