| 1 |
DeSisto J, Lucas JT Jr, Xu K, Donson A, Lin T, Sanford B, Wu G, Tran QT, Hedges D, Hsu CY, Armstrong GT, Arnold M, Bhatia S, Flannery P, Lemma R, Hardie L, Schüller U, Venkataraman S, Hoffman LM, Dorris K, Mulcahy Levy JM, Hankinson TC, Handler M, Liu AK, Foreman N, Vibhakar R, Jones K, Allen S, Zhang J, Baker SJ, Merchant TE, Orr BA, Green AL. Comprehensive molecular characterization of pediatric radiation-induced high-grade glioma. Nat Commun 2021;12:5531. [PMID: 34545084 DOI: 10.1038/s41467-021-25709-x] [Cited by in Crossref: 7] [Cited by in F6Publishing: 9] [Article Influence: 3.5] [Reference Citation Analysis]
|
| 2 |
Nissar B, Shah IA, ul Afshan F, Ganai BA. A decade in unravelling the etiology of gastric carcinogenesis in Kashmir, India – A high risk region. Gene Reports 2020;21:100832. [DOI: 10.1016/j.genrep.2020.100832] [Reference Citation Analysis]
|
| 3 |
Desisto J, Lucas JT, Xu K, Donson A, Lin T, Sanford B, Wu G, Tran QT, Hedges D, Hsu C, Armstrong GT, Arnold M, Bhatia S, Flannery P, Lemma R, Hardie L, Schüller U, Hoffman LM, Dorris K, Levy JM, Hankinson TC, Handler M, Liu A, Foreman N, Vibhakar R, Jones K, Allen S, Zhang J, Baker SJ, Merchant TE, Orr BA, Green AL. Comprehensive molecular characterization of pediatric treatment-induced high-grade glioma: A distinct entity despite disparate etiologies with defining molecular characteristics and potential therapeutic targets.. [DOI: 10.1101/809772] [Reference Citation Analysis]
|
| 4 |
Dominguez-Valentin M, Wernhoff P, Cajal AR, Kalfayan PG, Piñero TA, Gonzalez ML, Ferro A, Sammartino I, Causada Calo NS, Vaccaro CA. MLH1 Ile219Val Polymorphism in Argentinean Families with Suspected Lynch Syndrome. Front Oncol 2016;6:189. [PMID: 27606285 DOI: 10.3389/fonc.2016.00189] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.6] [Reference Citation Analysis]
|
| 5 |
Leite M, Corso G, Sousa S, Carvalho J, Roviello F, Oliveira C, Figueiredo C, Seruca R. Non-CDH1-Associated Familial Gastric Cancer and Epigenetics Factors. Spotlight on Familial and Hereditary Gastric Cancer 2013. [DOI: 10.1007/978-94-007-6570-2_10] [Reference Citation Analysis]
|
| 6 |
Hudler P. Genetic aspects of gastric cancer instability. ScientificWorldJournal. 2012;2012:761909. [PMID: 22606061 DOI: 10.1100/2012/761909] [Cited by in Crossref: 67] [Cited by in F6Publishing: 74] [Article Influence: 6.1] [Reference Citation Analysis]
|
| 7 |
Medeiros F, Lindor NM, Couch FJ, Highsmith WE Jr. The germline MLH1 K618A variant and susceptibility to Lynch syndrome-associated tumors. J Mol Diagn 2012;14:264-73. [PMID: 22426235 DOI: 10.1016/j.jmoldx.2012.01.006] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 0.6] [Reference Citation Analysis]
|
| 8 |
Sui H, Wang KB, Bai YX. DNA methylation and gastric cancer. Shijie Huaren Xiaohua Zazhi 2011; 19(32): 3347-3352 [DOI: 10.11569/wcjd.v19.i32.3347] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
|
| 9 |
Webb EA, Smith TD, Cotton RG. Difficulties in finding DNA mutations and associated phenotypic data in web resources using simple, uncomplicated search terms, and a suggested solution. Hum Genomics 2011;5:141-55. [PMID: 21504866 DOI: 10.1186/1479-7364-5-3-141] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
|
| 10 |
Vogelsang M, Komel R. Non-truncating hMLH1 variants identified in Slovenian gastric cancer patients are not associated with Lynch Syndrome: a functional analysis report. Familial Cancer 2011;10:255-63. [DOI: 10.1007/s10689-010-9409-7] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
|
| 11 |
Vogelsang M, Comino A, Zupanec N, Hudler P, Komel R. Assessing pathogenicity of MLH1 variants by co-expression of human MLH1 and PMS2 genes in yeast. BMC Cancer 2009;9:382. [PMID: 19863800 DOI: 10.1186/1471-2407-9-382] [Cited by in Crossref: 9] [Cited by in F6Publishing: 11] [Article Influence: 0.6] [Reference Citation Analysis]
|
| 12 |
Nejda N, Iglesias D, Moreno Azcoita M, Medina Arana V, González-Aguilera JJ, Fernández-Peralta AM. A MLH1 polymorphism that increases cancer risk is associated with better outcome in sporadic colorectal cancer. Cancer Genet Cytogenet 2009;193:71-7. [PMID: 19665066 DOI: 10.1016/j.cancergencyto.2009.04.011] [Cited by in Crossref: 18] [Cited by in F6Publishing: 20] [Article Influence: 1.3] [Reference Citation Analysis]
|
| 13 |
Vietri MT, Riegler G, De Paola M, Simeone S, Boggia M, Improta A, Parisi M, Molinari AM, Cioffi M. I219V polymorphism in hMLH1 gene in patients affected with ulcerative colitis. Genet Test Mol Biomarkers 2009;13:193-7. [PMID: 19371218 DOI: 10.1089/gtmb.2008.0088] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 0.4] [Reference Citation Analysis]
|
| 14 |
Zhao Y, Miyashita K, Ando T, Kakeji Y, Yamanaka T, Taguchi K, Ushijima T, Oda S, Maehara Y. Exclusive KRAS mutation in microsatellite-unstable human colorectal carcinomas with sequence alterations in the DNA mismatch repair gene, MLH1. Gene 2008;423:188-93. [PMID: 18692554 DOI: 10.1016/j.gene.2008.07.014] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 0.6] [Reference Citation Analysis]
|
| 15 |
Fredriksson H, Ikonen T, Autio V, Matikainen MP, Helin HJ, Tammela TL, Koivisto PA, Schleutker J. Identification of germline MLH1 alterations in familial prostate cancer. Eur J Cancer 2006;42:2802-6. [PMID: 16963262 DOI: 10.1016/j.ejca.2006.04.024] [Cited by in Crossref: 24] [Cited by in F6Publishing: 25] [Article Influence: 1.4] [Reference Citation Analysis]
|
