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For: Marvin ML, Mazzoni SM, Herron CM, Edwards S, Gruber SB, Petty EM. AXIN2-associated autosomal dominant ectodermal dysplasia and neoplastic syndrome. Am J Med Genet A. 2011;155A:898-902. [PMID: 21416598 DOI: 10.1002/ajmg.a.33927] [Cited by in Crossref: 53] [Cited by in F6Publishing: 45] [Article Influence: 5.3] [Reference Citation Analysis]
Number Citing Articles
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2 Valle L, de Voer RM, Goldberg Y, Sjursen W, Försti A, Ruiz-Ponte C, Caldés T, Garré P, Olsen MF, Nordling M, Castellvi-Bel S, Hemminki K. Update on genetic predisposition to colorectal cancer and polyposis. Mol Aspects Med 2019;69:10-26. [PMID: 30862463 DOI: 10.1016/j.mam.2019.03.001] [Cited by in Crossref: 39] [Cited by in F6Publishing: 26] [Article Influence: 19.5] [Reference Citation Analysis]
3 Yin W, Bian Z. The Gene Network Underlying Hypodontia. J Dent Res 2015;94:878-85. [PMID: 25910507 DOI: 10.1177/0022034515583999] [Cited by in Crossref: 59] [Cited by in F6Publishing: 44] [Article Influence: 9.8] [Reference Citation Analysis]
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8 Dinckan N, Du R, Akdemir ZC, Bayram Y, Jhangiani SN, Doddapaneni H, Hu J, Muzny DM, Guven Y, Aktoren O, Kayserili H, Boerwinkle E, Gibbs RA, Posey JE, Lupski JR, Uyguner ZO, Letra A. A biallelic ANTXR1 variant expands the anthrax toxin receptor associated phenotype to tooth agenesis. Am J Med Genet A 2018;176:1015-22. [PMID: 29436111 DOI: 10.1002/ajmg.a.38625] [Cited by in Crossref: 8] [Cited by in F6Publishing: 4] [Article Influence: 2.7] [Reference Citation Analysis]
9 Lamba A, Parekh P, Dvorak CC, Karlitz J. Pedigree analysis supports a correlation between an AXIN2 variant and polyposis/colorectal cancer. WJMG 2018;8:1-4. [DOI: 10.5496/wjmg.v8.i1.1] [Reference Citation Analysis]
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11 Järvinen E, Shimomura-Kuroki J, Balic A, Jussila M, Thesleff I. Mesenchymal Wnt/β-catenin signaling limits tooth number. Development 2018;145:dev158048. [PMID: 29437780 DOI: 10.1242/dev.158048] [Cited by in Crossref: 22] [Cited by in F6Publishing: 17] [Article Influence: 7.3] [Reference Citation Analysis]
12 Yue H, Liang J, Yang K, Hua B, Bian Z. Functional analysis of a novel missense mutation in AXIN2 associated with non-syndromic tooth agenesis. Eur J Oral Sci 2016;124:228-33. [PMID: 27090353 DOI: 10.1111/eos.12273] [Cited by in Crossref: 13] [Cited by in F6Publishing: 9] [Article Influence: 2.6] [Reference Citation Analysis]
13 Valle L, Vilar E, Tavtigian SV, Stoffel EM. Genetic predisposition to colorectal cancer: syndromes, genes, classification of genetic variants and implications for precision medicine. J Pathol 2019;247:574-88. [PMID: 30584801 DOI: 10.1002/path.5229] [Cited by in Crossref: 49] [Cited by in F6Publishing: 29] [Article Influence: 24.5] [Reference Citation Analysis]
14 Alldredge A, Fuhrmann S. Loss of Axin2 Causes Ocular Defects During Mouse Eye Development. Invest Ophthalmol Vis Sci 2016;57:5253-62. [PMID: 27701636 DOI: 10.1167/iovs.15-18599] [Cited by in Crossref: 14] [Cited by in F6Publishing: 9] [Article Influence: 3.5] [Reference Citation Analysis]
15 Andersson K, Malmgren B, Åström E, Nordgren A, Taylan F, Dahllöf G. Mutations in COL1A1/A2 and CREB3L1 are associated with oligodontia in osteogenesis imperfecta. Orphanet J Rare Dis 2020;15:80. [PMID: 32234057 DOI: 10.1186/s13023-020-01361-4] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
16 Ritwik P, Chrisentery-singleton TE. Oral and dental considerations in pediatric cancers. Cancer Metastasis Rev 2020;39:43-53. [DOI: 10.1007/s10555-020-09842-5] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 5.0] [Reference Citation Analysis]
17 Schubert SA, Morreau H, de Miranda NFCC, van Wezel T. The missing heritability of familial colorectal cancer. Mutagenesis 2020;35:221-31. [PMID: 31605533 DOI: 10.1093/mutage/gez027] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 8.0] [Reference Citation Analysis]
18 Wong S, Liu H, Bai B, Chang H, Zhao H, Wang Y, Han D, Feng H. Novel missense mutations in the AXIN2 gene associated with non-syndromic oligodontia. Arch Oral Biol 2014;59:349-53. [PMID: 24581859 DOI: 10.1016/j.archoralbio.2013.12.009] [Cited by in Crossref: 16] [Cited by in F6Publishing: 13] [Article Influence: 2.0] [Reference Citation Analysis]
19 Ritwik P, Patterson KK. Diagnosis of Tooth Agenesis in Childhood and Risk for Neoplasms in Adulthood. Ochsner J 2018;18:345-50. [PMID: 30559619 DOI: 10.31486/toj.18.0060] [Cited by in Crossref: 9] [Cited by in F6Publishing: 5] [Article Influence: 3.0] [Reference Citation Analysis]
20 Aval SF, Lotfi H, Sheervalilou R, Zarghami N. Tuning of major signaling networks (TGF-β, Wnt, Notch and Hedgehog) by miRNAs in human stem cells commitment to different lineages: Possible clinical application. Biomed Pharmacother 2017;91:849-60. [PMID: 28501774 DOI: 10.1016/j.biopha.2017.05.020] [Cited by in Crossref: 16] [Cited by in F6Publishing: 15] [Article Influence: 4.0] [Reference Citation Analysis]
21 Macklin-Mantia SK, Hines SL, Chaichana KL, Donaldson AM, Ko SL, Zhai Q, Samadder NJ, Riegert-Johnson DL. Case report expanding the germline AXIN2- related phenotype to include olfactory neuroblastoma and gastric adenoma. BMC Med Genet 2020;21:161. [PMID: 32807118 DOI: 10.1186/s12881-020-01103-0] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
22 Liu H, Ding T, Zhan Y, Feng H. A Novel AXIN2 Missense Mutation Is Associated with Non-Syndromic Oligodontia. PLoS One 2015;10:e0138221. [PMID: 26406231 DOI: 10.1371/journal.pone.0138221] [Cited by in Crossref: 12] [Cited by in F6Publishing: 10] [Article Influence: 2.0] [Reference Citation Analysis]
23 Mazzoni SM, Petty EM, Stoffel EM, Fearon ER. An AXIN2 Mutant Allele Associated With Predisposition to Colorectal Neoplasia Has Context-Dependent Effects on AXIN2 Protein Function. Neoplasia 2015;17:463-72. [PMID: 26025668 DOI: 10.1016/j.neo.2015.04.006] [Cited by in Crossref: 11] [Cited by in F6Publishing: 9] [Article Influence: 2.2] [Reference Citation Analysis]
24 Valle L. Recent Discoveries in the Genetics of Familial Colorectal Cancer and Polyposis. Clinical Gastroenterology and Hepatology 2017;15:809-19. [DOI: 10.1016/j.cgh.2016.09.148] [Cited by in Crossref: 43] [Cited by in F6Publishing: 27] [Article Influence: 10.8] [Reference Citation Analysis]
25 Itin PH. Etiology and pathogenesis of ectodermal dysplasias. Am J Med Genet A 2014;164A:2472-7. [PMID: 24715647 DOI: 10.1002/ajmg.a.36550] [Cited by in Crossref: 30] [Cited by in F6Publishing: 14] [Article Influence: 4.3] [Reference Citation Analysis]
26 Zhang T, Zhao X, Hou F, Sun Y, Wu J, Ma T, Zhang X. A novel PAX9 mutation found in a Chinese patient with hypodontia via whole exome sequencing. Oral Dis 2018;25:234-41. [DOI: 10.1111/odi.12982] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
27 Lorans M, Dow E, Macrae FA, Winship IM, Buchanan DD. Update on Hereditary Colorectal Cancer: Improving the Clinical Utility of Multigene Panel Testing. Clin Colorectal Cancer 2018;17:e293-305. [PMID: 29454559 DOI: 10.1016/j.clcc.2018.01.001] [Cited by in Crossref: 34] [Cited by in F6Publishing: 17] [Article Influence: 11.3] [Reference Citation Analysis]
28 Tabibzadeh A, Tameshkel FS, Moradi Y, Soltani S, Moradi-Lakeh M, Ashrafi GH, Motamed N, Zamani F, Motevalian SA, Panahi M, Esghaei M, Ajdarkosh H, Mousavi-Jarrahi A, Niya MHK. Signal transduction pathway mutations in gastrointestinal (GI) cancers: a systematic review and meta-analysis. Sci Rep 2020;10:18713. [PMID: 33127962 DOI: 10.1038/s41598-020-73770-1] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
29 Qin H, Xu HZ, Xuan K. Clinical and genetic evaluation of a Chinese family with isolated oligodontia. Arch Oral Biol 2013;58:1180-6. [PMID: 23731659 DOI: 10.1016/j.archoralbio.2013.04.007] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
30 Ruf S, Klimas D, Hönemann M, Jabir S. Genetic background of nonsyndromic oligodontia: a systematic review and meta-analysis. J Orofac Orthop 2013;74:295-308. [PMID: 23828301 DOI: 10.1007/s00056-013-0138-z] [Cited by in Crossref: 34] [Cited by in F6Publishing: 25] [Article Influence: 4.3] [Reference Citation Analysis]
31 Beard C, Purvis R, Winship IM, Macrae FA, Buchanan DD. Phenotypic confirmation of oligodontia, colorectal polyposis and cancer in a family carrying an exon 7 nonsense variant in the AXIN2 gene. Familial Cancer 2019;18:311-5. [DOI: 10.1007/s10689-019-00120-0] [Cited by in Crossref: 8] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
32 Rivera B, Perea J, Sánchez E, Villapún M, Sánchez-Tomé E, Mercadillo F, Robledo M, Benítez J, Urioste M. A novel AXIN2 germline variant associated with attenuated FAP without signs of oligondontia or ectodermal dysplasia. Eur J Hum Genet 2014;22:423-6. [PMID: 23838596 DOI: 10.1038/ejhg.2013.146] [Cited by in Crossref: 23] [Cited by in F6Publishing: 19] [Article Influence: 2.9] [Reference Citation Analysis]
33 Ye X, Attaie AB. Genetic Basis of Nonsyndromic and Syndromic Tooth Agenesis. J Pediatr Genet 2016;5:198-208. [PMID: 27895972 DOI: 10.1055/s-0036-1592421] [Cited by in Crossref: 18] [Cited by in F6Publishing: 12] [Article Influence: 3.6] [Reference Citation Analysis]
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35 Mazzoni SM, Fearon ER. AXIN1 and AXIN2 variants in gastrointestinal cancers. Cancer Lett. 2014;355:1-8. [PMID: 25236910 DOI: 10.1016/j.canlet.2014.09.018] [Cited by in Crossref: 66] [Cited by in F6Publishing: 54] [Article Influence: 9.4] [Reference Citation Analysis]
36 Lam KK, Thean LF, Cheah PY. Advances in colorectal cancer genomics and transcriptomics drive early detection and prevention. Int J Biochem Cell Biol 2021;137:106032. [PMID: 34182137 DOI: 10.1016/j.biocel.2021.106032] [Reference Citation Analysis]
37 Novellasdemunt L, Antas P, Li VS. Targeting Wnt signaling in colorectal cancer. A Review in the Theme: Cell Signaling: Proteins, Pathways and Mechanisms. Am J Physiol Cell Physiol. 2015;309:C511-C521. [PMID: 26289750 DOI: 10.1152/ajpcell.00117.2015] [Cited by in Crossref: 182] [Cited by in F6Publishing: 146] [Article Influence: 30.3] [Reference Citation Analysis]
38 Fournier BP, Bruneau MH, Toupenay S, Kerner S, Berdal A, Cormier-Daire V, Hadj-Rabia S, Coudert AE, de La Dure-Molla M. Patterns of Dental Agenesis Highlight the Nature of the Causative Mutated Genes. J Dent Res 2018;97:1306-16. [PMID: 29879364 DOI: 10.1177/0022034518777460] [Cited by in Crossref: 20] [Cited by in F6Publishing: 14] [Article Influence: 6.7] [Reference Citation Analysis]
39 Dhooge M, Baert-Desurmont S, Corsini C, Caron O, Andrieu N, Berthet P, Bonadona V, Cohen-Haguenauer O, De Pauw A, Delnatte C, Dussart S, Lasset C, Leroux D, Maugard C, Moretta-Serra J, Popovici C, Buecher B, Colas C, Noguès C; GGC-Unicancer Group. National recommendations of the French Genetics and Cancer Group - Unicancer on the modalities of multi-genes panel analyses in hereditary predispositions to tumors of the digestive tract. Eur J Med Genet 2020;63:104080. [PMID: 33039684 DOI: 10.1016/j.ejmg.2020.104080] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
40 Bonczek O, Krejci P, Izakovicova-Holla L, Cernochova P, Kiss I, Vojtesek B. Tooth agenesis: What do we know and is there a connection to cancer? Clin Genet 2021;99:493-502. [PMID: 33249565 DOI: 10.1111/cge.13892] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
41 Yin W, Bian Z. Hypodontia, a prospective predictive marker for tumor? Oral Dis 2016;22:265-73. [DOI: 10.1111/odi.12400] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 1.6] [Reference Citation Analysis]
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43 Lorca V, Garre P. Current status of the genetic susceptibility in attenuated adenomatous polyposis. World J Gastrointest Oncol. 2019;11:1101-1114. [PMID: 31908716 DOI: 10.4251/wjgo.v11.i12.1101] [Cited by in CrossRef: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
44 Williams MA, Letra A. The Changing Landscape in the Genetic Etiology of Human Tooth Agenesis. Genes (Basel) 2018;9:E255. [PMID: 29772684 DOI: 10.3390/genes9050255] [Cited by in Crossref: 16] [Cited by in F6Publishing: 9] [Article Influence: 5.3] [Reference Citation Analysis]
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