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For: Leach FS, Nicolaides NC, Papadopoulos N, Liu B, Jen J, Parsons R, Peltomäki P, Sistonen P, Aaltonen LA, Nyström-Lahti M. Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer. Cell 1993;75:1215-25. [PMID: 8261515 DOI: 10.1016/0092-8674(93)90330-s] [Cited by in Crossref: 1588] [Cited by in F6Publishing: 1668] [Article Influence: 52.9] [Reference Citation Analysis]
Number Citing Articles
1 Imyanitov E, Sokolenko A. Integrative Genomic Tests in Clinical Oncology. IJMS 2022;23:13129. [DOI: 10.3390/ijms232113129] [Reference Citation Analysis]
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4 Scott RJ. Modifier genes and Lynch syndrome: some considerations. Hered Cancer Clin Pract 2022;20. [DOI: 10.1186/s13053-022-00240-2] [Reference Citation Analysis]
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7 Singh D, Prasad CB. DNA Damage Response: A Therapeutic Landscape For Breast Cancer Treatment. Breast Cancer: Current Trends in Molecular Research 2022. [DOI: 10.2174/9781681089522112010006] [Reference Citation Analysis]
8 Yao Z, Wang Q, Dai Z. Recent Advances in Directed Yeast Genome Evolution. J Fungi (Basel) 2022;8:635. [PMID: 35736118 DOI: 10.3390/jof8060635] [Reference Citation Analysis]
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11 Golas MM, Gunawan B, Cakir M, Cameron S, Enders C, Liersch T, Füzesi L, Sander B. Evolutionary patterns of chromosomal instability and mismatch repair deficiency in proximal and distal colorectal cancer. Colorectal Dis 2022;24:157-76. [PMID: 34623739 DOI: 10.1111/codi.15946] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
12 Dal Buono A, Gaiani F, Poliani L, Correale C, Laghi L. Defects in MMR Genes as a Seminal Example of Personalized Medicine: From Diagnosis to Therapy. J Pers Med 2021;11:1333. [PMID: 34945805 DOI: 10.3390/jpm11121333] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
13 Obayashi Y, Fujikane R, Morita S, Uechi Y, Hiraki A, Hidaka M. Suppression of TopBP1 function increases the efficacy of chemotherapeutic treatments by enhancing the induction of apoptosis. Oral Science International 2021;18:209-216. [DOI: 10.1002/osi2.1102] [Reference Citation Analysis]
14 Elez M. Mismatch Repair: From Preserving Genome Stability to Enabling Mutation Studies in Real-Time Single Cells. Cells 2021;10:1535. [PMID: 34207040 DOI: 10.3390/cells10061535] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
15 Song HR, Kim HK, Kim SG, Lim HJ, Kim HY, Han MK. Changes in the phosphorylation of nucleotide metabolism‑associated proteins by leukemia inhibitory factor in mouse embryonic stem cells. Mol Med Rep 2021;23:431. [PMID: 33846773 DOI: 10.3892/mmr.2021.12070] [Reference Citation Analysis]
16 Fountzilas E, Kurzrock R, Vo HH, Tsimberidou AM. Wedding of Molecular Alterations and Immune Checkpoint Blockade: Genomics as a Matchmaker. J Natl Cancer Inst 2021;113:1634-47. [PMID: 33823006 DOI: 10.1093/jnci/djab067] [Cited by in Crossref: 18] [Cited by in F6Publishing: 18] [Article Influence: 9.0] [Reference Citation Analysis]
17 Young SJ, West SC. Coordinated roles of SLX4 and MutSβ in DNA repair and the maintenance of genome stability. Crit Rev Biochem Mol Biol 2021;56:157-77. [PMID: 33596761 DOI: 10.1080/10409238.2021.1881433] [Cited by in Crossref: 7] [Cited by in F6Publishing: 3] [Article Influence: 3.5] [Reference Citation Analysis]
18 Monckton DG. The Contribution of Somatic Expansion of the CAG Repeat to Symptomatic Development in Huntington's Disease: A Historical Perspective. J Huntingtons Dis 2021;10:7-33. [PMID: 33579863 DOI: 10.3233/JHD-200429] [Cited by in Crossref: 21] [Cited by in F6Publishing: 23] [Article Influence: 10.5] [Reference Citation Analysis]
19 Gallon R, Gawthorpe P, Phelps RL, Hayes C, Borthwick GM, Santibanez-Koref M, Jackson MS, Burn J. How Should We Test for Lynch Syndrome? A Review of Current Guidelines and Future Strategies. Cancers (Basel) 2021;13:406. [PMID: 33499123 DOI: 10.3390/cancers13030406] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 6.5] [Reference Citation Analysis]
20 Te Paske IBAW, Ligtenberg MJL, Hoogerbrugge N, de Voer RM. Candidate Gene Discovery in Hereditary Colorectal Cancer and Polyposis Syndromes-Considerations for Future Studies. Int J Mol Sci 2020;21:E8757. [PMID: 33228212 DOI: 10.3390/ijms21228757] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
21 Chapel DB, Ritterhouse LL. Microsatellite Instability Testing and Therapy Implications. Advances in Molecular Pathology 2020;3:169-188. [DOI: 10.1016/j.yamp.2020.07.019] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
22 Lizardo DY, Kuang C, Hao S, Yu J, Huang Y, Zhang L. Immunotherapy efficacy on mismatch repair-deficient colorectal cancer: From bench to bedside. Biochim Biophys Acta Rev Cancer 2020;1874:188447. [PMID: 33035640 DOI: 10.1016/j.bbcan.2020.188447] [Cited by in Crossref: 34] [Cited by in F6Publishing: 44] [Article Influence: 11.3] [Reference Citation Analysis]
23 Khider H, Koual M, Nguyen-xuan H, Le Frère-belda M, Perkins G, Blons H, Crespel C, Nos C, Laurent-puig P, Bats A. Cáncer de endometrio en el síndrome de Lynch. EMC - Ginecología-Obstetricia 2020;56:1-10. [DOI: 10.1016/s1283-081x(20)44316-4] [Reference Citation Analysis]
24 Jansen AML, Goel A. Mosaicism in Patients With Colorectal Cancer or Polyposis Syndromes: A Systematic Review. Clin Gastroenterol Hepatol 2020;18:1949-60. [PMID: 32147591 DOI: 10.1016/j.cgh.2020.02.049] [Cited by in Crossref: 10] [Cited by in F6Publishing: 9] [Article Influence: 3.3] [Reference Citation Analysis]
25 Ryu SW, Stewart R, Pectol DC, Ender NA, Wimalarathne O, Lee JH, Zanini CP, Harvey A, Huibregtse JM, Mueller P, Paull TT. Proteome-wide identification of HSP70/HSC70 chaperone clients in human cells. PLoS Biol 2020;18:e3000606. [PMID: 32687490 DOI: 10.1371/journal.pbio.3000606] [Cited by in Crossref: 19] [Cited by in F6Publishing: 22] [Article Influence: 6.3] [Reference Citation Analysis]
26 Jia X, Burugula BB, Chen V, Lemons RM, Jayakody S, Maksutova M, Kitzman JO. Massively parallel functional testing of MSH2 missense variants conferring Lynch Syndrome risk.. [DOI: 10.1101/2020.06.03.133017] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
27 Brondani VB, Montenegro L, Lacombe AMF, Magalhães BM, Nishi MY, Funari MFA, Narcizo AM, Cardoso LC, Siqueira SAC, Zerbini MCN, Denes FT, Latronico AC, Mendonca BB, Almeida MQ, Lerario AM, Soares IC, Fragoso MCBV. High Prevalence of Alterations in DNA Mismatch Repair Genes of Lynch Syndrome in Pediatric Patients with Adrenocortical Tumors Carrying a Germline Mutation on TP53. Cancers (Basel) 2020;12:E621. [PMID: 32156018 DOI: 10.3390/cancers12030621] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.7] [Reference Citation Analysis]
28 Eeles RA. The genetics of inherited cancers. Oxford Textbook of Medicine 2020. [DOI: 10.1093/med/9780198746690.003.0047] [Reference Citation Analysis]
29 Tamura K. Molecular Mechanism of Lynch Syndrome. Lynch Syndrome 2020. [DOI: 10.1007/978-981-15-6891-6_1] [Reference Citation Analysis]
30 Tseng D, Schultz L, Pardoll D, Mackall C. Cancer Immunology. Abeloff's Clinical Oncology 2020. [DOI: 10.1016/b978-0-323-47674-4.00006-2] [Reference Citation Analysis]
31 Palter VN. Lynch Syndrome. Encyclopedia of Gastroenterology 2020. [DOI: 10.1016/b978-0-12-801238-3.65755-0] [Reference Citation Analysis]
32 Franklin WA, Aisner DL, Davies KD, Crooks K, Post MD, Kleinschmidt-demasters BK, Ashwood E, Bunn PA, Varella-garcia M. Pathology, Biomarkers, and Molecular Diagnostics. Abeloff's Clinical Oncology 2020. [DOI: 10.1016/b978-0-323-47674-4.00015-3] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
33 Takeishi Y, Fujikane R, Rikitake M, Obayashi Y, Sekiguchi M, Hidaka M. SMARCAD1-mediated recruitment of the DNA mismatch repair protein MutLα to MutSα on damaged chromatin induces apoptosis in human cells. Journal of Biological Chemistry 2020;295:1056-65. [DOI: 10.1016/s0021-9258(17)49915-7] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 2.3] [Reference Citation Analysis]
34 Walsh MF, Cadoo K, Salo-mullen EE, Dubard-gault M, Stadler ZK, Offit K. Genetic Factors. Abeloff's Clinical Oncology 2020. [DOI: 10.1016/b978-0-323-47674-4.00013-x] [Cited by in Crossref: 2] [Article Influence: 0.7] [Reference Citation Analysis]
35 Takeishi Y, Fujikane R, Rikitake M, Obayashi Y, Sekiguchi M, Hidaka M. SMARCAD1-mediated recruitment of the DNA mismatch repair protein MutLα to MutSα on damaged chromatin induces apoptosis in human cells. J Biol Chem 2020;295:1056-65. [PMID: 31843968 DOI: 10.1074/jbc.RA119.008854] [Cited by in Crossref: 5] [Cited by in F6Publishing: 8] [Article Influence: 1.3] [Reference Citation Analysis]
36 Ryu SW, Stewart R, Pectol C, Ender N, Wimalarathne O, Lee J, Zanini CP, Harvey A, Huibregtse J, Mueller P, Paull TT. Comprehensive identification of HSP70/HSC70 Chaperone Clients in Human Cells.. [DOI: 10.1101/865030] [Reference Citation Analysis]
37 Ben Sghaier R, Jansen AML, Bdioui A, Van Wezel T, Ksiaa M, Elgolli L, Ben Fatma L, Ben Ahmed S, Azzouz MM, Hellara O, Elghali A, Darbel F, Skandrani K, Mokkni M, Gdissa A, Ltaief R, Saad A, Hmila F, Gribaa M, Morreau H. Targeted next generation sequencing screening of Lynch syndrome in Tunisian population. Fam Cancer 2019;18:343-8. [PMID: 31114938 DOI: 10.1007/s10689-019-00130-y] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.8] [Reference Citation Analysis]
38 Büttner R, Friedrichs N. [Hereditary colon cancer in Lynch syndrome/HNPCC syndrome in Germany]. Pathologe 2019;40:584-91. [PMID: 31372733 DOI: 10.1007/s00292-019-0643-y] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
39 Li L, Zhang X, Tian T, Pang L. Mathematical modelling the pathway of genomic instability in lung cancer. Sci Rep 2019;9:14136. [PMID: 31575883 DOI: 10.1038/s41598-019-50500-w] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.8] [Reference Citation Analysis]
40 Georgiadis A, Durham JN, Keefer LA, Bartlett BR, Zielonka M, Murphy D, White JR, Lu S, Verner EL, Ruan F, Riley D, Anders RA, Gedvilaite E, Angiuoli S, Jones S, Velculescu VE, Le DT, Diaz LA, Sausen M. Noninvasive Detection of Microsatellite Instability and High Tumor Mutation Burden in Cancer Patients Treated with PD-1 Blockade. Clin Cancer Res. 2019;25:7024-7034. [PMID: 31506389 DOI: 10.1158/1078-0432.ccr-19-1372] [Cited by in Crossref: 65] [Cited by in F6Publishing: 70] [Article Influence: 16.3] [Reference Citation Analysis]
41 Doukas S, Vageli D, Nikolouzakis T, Falzone L, Docea A, Lazopoulos G, Kalbakis K, Tsatsakis A. Role of DNA mismatch repair genes in lung and head and neck cancer (Review). Wrld Acd Sci 2019. [DOI: 10.3892/wasj.2019.21] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.3] [Reference Citation Analysis]
42 Nirwal S, Kulkarni DS, Sharma A, Rao DN, Nair DT. Mechanism of formation of a toroid around DNA by the mismatch sensor protein. Nucleic Acids Res 2018;46:256-66. [PMID: 29182773 DOI: 10.1093/nar/gkx1149] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 2.0] [Reference Citation Analysis]
43 Tamura K, Kaneda M, Futagawa M, Takeshita M, Kim S, Nakama M, Kawashita N, Tatsumi-Miyajima J. Genetic and genomic basis of the mismatch repair system involved in Lynch syndrome. Int J Clin Oncol 2019;24:999-1011. [PMID: 31273487 DOI: 10.1007/s10147-019-01494-y] [Cited by in Crossref: 31] [Cited by in F6Publishing: 30] [Article Influence: 7.8] [Reference Citation Analysis]
44 Sedhom R, Antonarakis ES. Clinical implications of mismatch repair deficiency in prostate cancer. Future Oncol 2019;15:2395-411. [PMID: 31237441 DOI: 10.2217/fon-2019-0068] [Cited by in Crossref: 12] [Cited by in F6Publishing: 12] [Article Influence: 3.0] [Reference Citation Analysis]
45 Van Esch H, Colnaghi R, Freson K, Starokadomskyy P, Zankl A, Backx L, Abramowicz I, Outwin E, Rohena L, Faulkner C, Leong GM, Newbury-Ecob RA, Challis RC, Õunap K, Jaeken J, Seuntjens E, Devriendt K, Burstein E, Low KJ, O'Driscoll M. Defective DNA Polymerase α-Primase Leads to X-Linked Intellectual Disability Associated with Severe Growth Retardation, Microcephaly, and Hypogonadism. Am J Hum Genet 2019;104:957-67. [PMID: 31006512 DOI: 10.1016/j.ajhg.2019.03.006] [Cited by in Crossref: 20] [Cited by in F6Publishing: 22] [Article Influence: 5.0] [Reference Citation Analysis]
46 Nakayama Y, Iijima T, Wakaume R, Takahashi K, Matsumoto H, Nakano D, Miyaki M, Yamaguchi T. Microsatellite instability is inversely associated with type 2 diabetes mellitus in colorectal cancer. PLoS One 2019;14:e0215513. [PMID: 31002690 DOI: 10.1371/journal.pone.0215513] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 1.3] [Reference Citation Analysis]
47 Felix GES, Zheng Y, Olopade OI. Mutations in context: implications of BRCA testing in diverse populations. Fam Cancer 2018;17:471-83. [PMID: 28918466 DOI: 10.1007/s10689-017-0038-2] [Cited by in Crossref: 15] [Cited by in F6Publishing: 15] [Article Influence: 3.8] [Reference Citation Analysis]
48 Moon JJ, Lu A, Moon C. Role of genomic instability in human carcinogenesis. Exp Biol Med (Maywood) 2019;244:227-40. [PMID: 30760030 DOI: 10.1177/1535370219826031] [Cited by in Crossref: 20] [Cited by in F6Publishing: 22] [Article Influence: 5.0] [Reference Citation Analysis]
49 Yurgelun MB, Kastrinos F. Tumor Testing for Microsatellite Instability to Identify Lynch Syndrome: New Insights Into an Old Diagnostic Strategy. J Clin Oncol 2019;37:263-5. [PMID: 30550362 DOI: 10.1200/JCO.18.01664] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
50 Antonarakis SE, Cooper DN. Human Genomic Variants and Inherited Disease. Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics 2019. [DOI: 10.1016/b978-0-12-812537-3.00006-8] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
51 Hatfield E, Green JS, Woods MO, Warden G, Parfrey PS. Impact of colonoscopic screening in Familial Colorectal Cancer Type X. Mol Genet Genomic Med 2018;6:1021-30. [PMID: 30300963 DOI: 10.1002/mgg3.478] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 1.0] [Reference Citation Analysis]
52 Turnbull C, Sud A, Houlston RS. Cancer genetics, precision prevention and a call to action. Nat Genet 2018;50:1212-8. [PMID: 30158684 DOI: 10.1038/s41588-018-0202-0] [Cited by in Crossref: 62] [Cited by in F6Publishing: 65] [Article Influence: 12.4] [Reference Citation Analysis]
53 Huang D, Matin SF, Lawrentschuk N, Roupret M. Systematic Review: An Update on the Spectrum of Urological Malignancies in Lynch Syndrome. Bladder Cancer 2018;4:261-8. [PMID: 30112437 DOI: 10.3233/BLC-180180] [Cited by in Crossref: 17] [Cited by in F6Publishing: 18] [Article Influence: 3.4] [Reference Citation Analysis]
54 Jonchere V, Marisa L, Greene M, Virouleau A, Buhard O, Bertrand R, Svrcek M, Cervera P, Goloudina A, Guillerm E, Coulet F, Landman S, Ratovomanana T, Job S, Ayadi M, Elarouci N, Armenoult L, Merabtene F, Dumont S, Parc Y, Lefèvre JH, André T, Fléjou JF, Guilloux A, Collura A, de Reyniès A, Duval A. Identification of Positively and Negatively Selected Driver Gene Mutations Associated With Colorectal Cancer With Microsatellite Instability. Cell Mol Gastroenterol Hepatol 2018;6:277-300. [PMID: 30116770 DOI: 10.1016/j.jcmgh.2018.06.002] [Cited by in Crossref: 14] [Cited by in F6Publishing: 13] [Article Influence: 2.8] [Reference Citation Analysis]
55 Evans DR, Venkitachalam S, Revoredo L, Dohey AT, Clarke E, Pennell JJ, Powell AE, Quinn E, Ravi L, Gerken TA, Green JS, Woods MO, Guda K. Evidence for GALNT12 as a moderate penetrance gene for colorectal cancer. Hum Mutat 2018;39:1092-101. [PMID: 29749045 DOI: 10.1002/humu.23549] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 2.2] [Reference Citation Analysis]
56 Kim D, Fishel R, Lee JB. Coordinating Multi-Protein Mismatch Repair by Managing Diffusion Mechanics on the DNA. J Mol Biol 2018;430:4469-80. [PMID: 29792877 DOI: 10.1016/j.jmb.2018.05.032] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 1.6] [Reference Citation Analysis]
57 Vaccaro CA, Piñero T, Herrando AI, Cajal R, Ferro A, Kalfayan P, Santino JP, Falconi MD, Verzura A, Guerrero G, Riggi MC, Pavicic W, González ML. Síndrome de Lynch: impacto de la caracterización de familias en base a estudios genéticos. RevOnco 2018;23. [DOI: 10.56969/oc.v23i1.63] [Reference Citation Analysis]
58 Jiao X, Liu W, Mahdessian H, Bryant P, Ringdahl J, Timofeeva M, Farrington SM, Dunlop M, Lindblom A. Recurrent, low-frequency coding variants contributing to colorectal cancer in the Swedish population. PLoS One 2018;13:e0193547. [PMID: 29547645 DOI: 10.1371/journal.pone.0193547] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 1.2] [Reference Citation Analysis]
59 Brammer DW, Gillespie PJ, Tian M, Young D, Raveendran M, Williams LE, Gagea M, Benavides FJ, Perez CJ, Broaddus RR, Bernacky BJ, Barnhart KF, Alauddin MM, Bhutani MS, Gibbs RA, Sidman RL, Pasqualini R, Arap W, Rogers J, Abee CR, Gelovani JG. MLH1-rheMac hereditary nonpolyposis colorectal cancer syndrome in rhesus macaques. Proc Natl Acad Sci U S A 2018;115:2806-11. [PMID: 29490919 DOI: 10.1073/pnas.1722106115] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.0] [Reference Citation Analysis]
60 Zeinalian M, Hashemzadeh-Chaleshtori M, Salehi R, Emami MH. Clinical Aspects of Microsatellite Instability Testing in Colorectal Cancer. Adv Biomed Res 2018;7:28. [PMID: 29531926 DOI: 10.4103/abr.abr_185_16] [Cited by in Crossref: 29] [Cited by in F6Publishing: 30] [Article Influence: 5.8] [Reference Citation Analysis]
61 Koi M, Tseng-Rogenski SS, Carethers JM. Inflammation-associated microsatellite alterations: Mechanisms and significance in the prognosis of patients with colorectal cancer. World J Gastrointest Oncol 2018; 10(1): 1-14 [PMID: 29375743 DOI: 10.4251/wjgo.v10.i1.1] [Cited by in CrossRef: 28] [Cited by in F6Publishing: 33] [Article Influence: 5.6] [Reference Citation Analysis]
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64 Stoffel EM, Yurgelun MB, Boland CR. Lynch Syndrome. Hereditary Colorectal Cancer 2018. [DOI: 10.1007/978-3-319-74259-5_1] [Reference Citation Analysis]
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66 Coleman WB. The Human Genome. Molecular Pathology 2018. [DOI: 10.1016/b978-0-12-802761-5.00006-7] [Reference Citation Analysis]
67 Campos S, Amaro P, Cunha I, Fraga J, Cipriano MA, Tomé L. Uncertainties in the Management of a Lynch Syndrome Patient: A Case Report. GE Port J Gastroenterol 2017;24:241-6. [PMID: 29255760 DOI: 10.1159/000461590] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
68 Liu W, Jiao X, Thutkawkorapin J, Mahdessian H, Lindblom A. Cancer risk susceptibility loci in a Swedish population. Oncotarget 2017;8:110300-10. [PMID: 29299148 DOI: 10.18632/oncotarget.22687] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 1.0] [Reference Citation Analysis]
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70 Cabreira V, Pinto C, Pinheiro M, Lopes P, Peixoto A, Santos C, Veiga I, Rocha P, Pinto P, Henrique R, Teixeira MR. Performance of Lynch syndrome predictive models in quantifying the likelihood of germline mutations in patients with abnormal MLH1 immunoexpression. Fam Cancer 2017;16:73-81. [PMID: 27581132 DOI: 10.1007/s10689-016-9926-0] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
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