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For: Diskin SJ, Hou C, Glessner JT, Attiyeh EF, Laudenslager M, Bosse K, Cole K, Mossé YP, Wood A, Lynch JE. Copy number variation at 1q21.1 associated with neuroblastoma. Nature. 2009;459:987-991. [PMID: 19536264 DOI: 10.1038/nature08035] [Cited by in Crossref: 260] [Cited by in F6Publishing: 245] [Article Influence: 20.0] [Reference Citation Analysis]
Number Citing Articles
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2 Maris JM. Recent advances in neuroblastoma. N Engl J Med. 2010;362:2202-2211. [PMID: 20558371 DOI: 10.1056/nejmra0804577] [Cited by in Crossref: 1075] [Cited by in F6Publishing: 683] [Article Influence: 89.6] [Reference Citation Analysis]
3 Kuiper RP, Ligtenberg MJ, Hoogerbrugge N, Geurts van Kessel A. Germline copy number variation and cancer risk. Curr Opin Genet Dev. 2010;20:282-289. [PMID: 20381334 DOI: 10.1016/j.gde.2010.03.005] [Cited by in Crossref: 80] [Cited by in F6Publishing: 71] [Article Influence: 6.7] [Reference Citation Analysis]
4 O'Bleness MS, Dickens CM, Dumas LJ, Kehrer-Sawatzki H, Wyckoff GJ, Sikela JM. Evolutionary history and genome organization of DUF1220 protein domains. G3 (Bethesda) 2012;2:977-86. [PMID: 22973535 DOI: 10.1534/g3.112.003061] [Cited by in Crossref: 47] [Cited by in F6Publishing: 45] [Article Influence: 4.7] [Reference Citation Analysis]
5 Koroknai V, Ecsedi S, Vízkeleti L, Kiss T, Szász I, Lukács A, Papp O, Ádány R, Balázs M. Genomic profiling of invasive melanoma cell lines by array comparative genomic hybridization. Melanoma Res 2016;26:100-7. [PMID: 26656572 DOI: 10.1097/CMR.0000000000000227] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 1.4] [Reference Citation Analysis]
6 Speleman F, Park JR, Henderson TO. Neuroblastoma: A Tough Nut to Crack. Am Soc Clin Oncol Educ Book 2016;35:e548-57. [PMID: 27249766 DOI: 10.1200/EDBK_159169] [Cited by in Crossref: 10] [Cited by in F6Publishing: 19] [Article Influence: 2.0] [Reference Citation Analysis]
7 Roy S, Motsinger Reif A. Evaluation of calling algorithms for array-CGH. Front Genet 2013;4:217. [PMID: 24298279 DOI: 10.3389/fgene.2013.00217] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 0.8] [Reference Citation Analysis]
8 Kim S, Medvedev P, Paton TA, Bafna V. Reprever: resolving low-copy duplicated sequences using template driven assembly. Nucleic Acids Res 2013;41:e128. [PMID: 23658221 DOI: 10.1093/nar/gkt339] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 0.7] [Reference Citation Analysis]
9 Carr IM, Diggle CP, Khan K, Inglehearn C, McKibbin M, Bonthron DT, Markham AF, Anwar R, Dobbie A, Pena SD, Ali M. Rapid visualisation of microarray copy number data for the detection of structural variations linked to a disease phenotype. PLoS One 2012;7:e43466. [PMID: 22912880 DOI: 10.1371/journal.pone.0043466] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
10 Imielinski M, Hakonarson H. Breaking new ground in inflammatory bowel disease genetics: genome-wide association studies and beyond. Pharmacogenomics 2010;11:663-5. [PMID: 20415557 DOI: 10.2217/pgs.10.56] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 0.3] [Reference Citation Analysis]
11 Black HA, Khan FF, Tyson J, Al Armour J. Inferring mechanisms of copy number change from haplotype structures at the human DEFA1A3 locus. BMC Genomics 2014;15:614. [PMID: 25048054 DOI: 10.1186/1471-2164-15-614] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 0.8] [Reference Citation Analysis]
12 Zhang YP, Deng FY, Yang TL, Zhang F, Chen XD, Shen H, Zhu XZ, Tian Q, Deng HW. Genome-wide association study identified CNP12587 region underlying height variation in Chinese females. PLoS One 2012;7:e44292. [PMID: 22957059 DOI: 10.1371/journal.pone.0044292] [Cited by in Crossref: 1] [Article Influence: 0.1] [Reference Citation Analysis]
13 Stahl PD, Wainszelbaum MJ. Human-specific genes may offer a unique window into human cell signaling. Sci Signal 2009;2:pe59. [PMID: 19797272 DOI: 10.1126/scisignal.289pe59] [Cited by in Crossref: 22] [Cited by in F6Publishing: 25] [Article Influence: 1.7] [Reference Citation Analysis]
14 Walsh KM, Choi M, Oberg K, Kulke MH, Yao JC, Wu C, Jurkiewicz M, Hsu LI, Hooshmand SM, Hassan M, Janson ET, Cunningham JL, Vosburgh E, Sackler RS, Lifton RP, Dewan AT, Hoh J. A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum. Endocr Relat Cancer 2011;18:171-80. [PMID: 21139019 DOI: 10.1677/ERC-10-0248] [Cited by in Crossref: 15] [Cited by in F6Publishing: 7] [Article Influence: 1.4] [Reference Citation Analysis]
15 Lin P, Hartz SM, Wang JC, Krueger RF, Foroud TM, Edenberg HJ, Nurnberger JI Jr, Brooks AI, Tischfield JA, Almasy L, Webb BT, Hesselbrock VM, Porjesz B, Goate AM, Bierut LJ, Rice JP; COGA Collaborators., COGEND Collaborators., GENEVA Investigators. Copy number variation accuracy in genome-wide association studies. Hum Hered 2011;71:141-7. [PMID: 21778733 DOI: 10.1159/000324683] [Cited by in Crossref: 11] [Cited by in F6Publishing: 9] [Article Influence: 1.0] [Reference Citation Analysis]
16 Leyva-Vega M, Gerfen J, Thiel BD, Jurkiewicz D, Rand EB, Pawlowska J, Kaminska D, Russo P, Gai X, Krantz ID, Kamath BM, Hakonarson H, Haber BA, Spinner NB. Genomic alterations in biliary atresia suggest region of potential disease susceptibility in 2q37.3. Am J Med Genet A 2010;152A:886-95. [PMID: 20358598 DOI: 10.1002/ajmg.a.33332] [Cited by in Crossref: 44] [Cited by in F6Publishing: 37] [Article Influence: 3.7] [Reference Citation Analysis]
17 Giwa A, Fatai A, Gamieldien J, Christoffels A, Bendou H. Identification of novel prognostic markers of survival time in high-risk neuroblastoma using gene expression profiles. Oncotarget 2020;11:4293-305. [PMID: 33245713 DOI: 10.18632/oncotarget.27808] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
18 Paar V, Gluncic M, Rosandic M, Basar I, Vlahovic I. Intragene Higher Order Repeats in Neuroblastoma BreakPoint Family Genes Distinguish Humans from Chimpanzees. Molecular Biology and Evolution 2011;28:1877-92. [DOI: 10.1093/molbev/msr009] [Cited by in Crossref: 12] [Cited by in F6Publishing: 12] [Article Influence: 1.1] [Reference Citation Analysis]
19 Wolf M, Korja M, Karhu R, Edgren H, Kilpinen S, Ojala K, Mousses S, Kallioniemi A, Haapasalo H. Array-based gene expression, CGH and tissue data defines a 12q24 gain in neuroblastic tumors with prognostic implication. BMC Cancer 2010;10:181. [PMID: 20444257 DOI: 10.1186/1471-2407-10-181] [Cited by in Crossref: 17] [Cited by in F6Publishing: 17] [Article Influence: 1.4] [Reference Citation Analysis]
20 Ott J, Kamatani Y, Lathrop M. Family-based designs for genome-wide association studies.Nat Rev Genet. 2011;12:465-474. [PMID: 21629274 DOI: 10.1038/nrg2989] [Cited by in Crossref: 194] [Cited by in F6Publishing: 150] [Article Influence: 17.6] [Reference Citation Analysis]
21 Zhang T, Cai J, Chang J, Yu D, Wu C, Yan T, Zhai K, Bi X, Zhao H, Xu J. Evidence of associations of APOBEC3B gene deletion with susceptibility to persistent HBV infection and hepatocellular carcinoma. Hum Mol Genet. 2013;22:1262-1269. [PMID: 23213177 DOI: 10.1093/hmg/dds513] [Cited by in Crossref: 39] [Cited by in F6Publishing: 44] [Article Influence: 3.9] [Reference Citation Analysis]
22 Shi J, Li P. An integrative segmentation method for detecting germline copy number variations in SNP arrays. Genet Epidemiol 2012;36:373-83. [PMID: 22539397 DOI: 10.1002/gepi.21631] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]
23 Diskin SJ, Capasso M, Schnepp RW, Cole KA, Attiyeh EF, Hou C, Diamond M, Carpenter EL, Winter C, Lee H, Jagannathan J, Latorre V, Iolascon A, Hakonarson H, Devoto M, Maris JM. Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastoma. Nat Genet 2012;44:1126-30. [PMID: 22941191 DOI: 10.1038/ng.2387] [Cited by in Crossref: 170] [Cited by in F6Publishing: 175] [Article Influence: 17.0] [Reference Citation Analysis]
24 Kim H, Sung S, Cho S, Kim TH, Seo K, Kim H. VCS: Tool for Visualizing Copy Number Variation and Single Nucleotide Polymorphism. Asian-Australas J Anim Sci 2014;27:1691-4. [PMID: 25358361 DOI: 10.5713/ajas.2014.14143] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
25 Venkataramany AS, Schieffer KM, Lee K, Cottrell CE, Wang PY, Mardis ER, Cripe TP, Chandler DS. Alternative RNA Splicing Defects in Pediatric Cancers: New Insights in Tumorigenesis and Potential Therapeutic Vulnerabilities. Ann Oncol 2022:S0923-7534(22)00390-8. [PMID: 35339647 DOI: 10.1016/j.annonc.2022.03.011] [Reference Citation Analysis]
26 Liu GE, Bickhart DM. Copy number variation in the cattle genome. Funct Integr Genomics 2012;12:609-24. [DOI: 10.1007/s10142-012-0289-9] [Cited by in Crossref: 32] [Cited by in F6Publishing: 31] [Article Influence: 3.2] [Reference Citation Analysis]
27 Owens C, Irwin M. Neuroblastoma: the impact of biology and cooperation leading to personalized treatments. Crit Rev Clin Lab Sci 2012;49:85-115. [PMID: 22646747 DOI: 10.3109/10408363.2012.683483] [Cited by in Crossref: 29] [Cited by in F6Publishing: 25] [Article Influence: 2.9] [Reference Citation Analysis]
28 Gamazon ER, Pinto N, Konkashbaev A, Im HK, Diskin SJ, London WB, Maris JM, Dolan ME, Cox NJ, Cohn SL. Trans-population analysis of genetic mechanisms of ethnic disparities in neuroblastoma survival. J Natl Cancer Inst 2013;105:302-9. [PMID: 23243203 DOI: 10.1093/jnci/djs503] [Cited by in Crossref: 24] [Cited by in F6Publishing: 22] [Article Influence: 2.4] [Reference Citation Analysis]
29 Huang L, Yu D, Wu C, Zhai K, Jiang G, Cao G, Wang C, Liu Y, Sun M, Li Z, Tan W, Lin D. Copy number variation at 6q13 functions as a long-range regulator and is associated with pancreatic cancer risk. Carcinogenesis 2012;33:94-100. [PMID: 22016467 DOI: 10.1093/carcin/bgr228] [Cited by in Crossref: 27] [Cited by in F6Publishing: 22] [Article Influence: 2.5] [Reference Citation Analysis]
30 Whittle SB, Smith V, Doherty E, Zhao S, McCarty S, Zage PE. Overview and recent advances in the treatment of neuroblastoma. Expert Rev Anticancer Ther. 2017;17:369-386. [PMID: 28142287 DOI: 10.1080/14737140.2017.1285230] [Cited by in Crossref: 115] [Cited by in F6Publishing: 111] [Article Influence: 23.0] [Reference Citation Analysis]
31 Xu G, Wang J, Wu Z, Qian L, Dai L, Wan X, Tan M, Zhao Y, Wu Y. SAHA regulates histone acetylation, Butyrylation, and protein expression in neuroblastoma. J Proteome Res 2014;13:4211-9. [PMID: 25160476 DOI: 10.1021/pr500497e] [Cited by in Crossref: 21] [Cited by in F6Publishing: 18] [Article Influence: 2.6] [Reference Citation Analysis]
32 Liu GE, Hou Y, Zhu B, Cardone MF, Jiang L, Cellamare A, Mitra A, Alexander LJ, Coutinho LL, Dell'Aquila ME, Gasbarre LC, Lacalandra G, Li RW, Matukumalli LK, Nonneman D, Regitano LC, Smith TP, Song J, Sonstegard TS, Van Tassell CP, Ventura M, Eichler EE, McDaneld TG, Keele JW. Analysis of copy number variations among diverse cattle breeds. Genome Res 2010;20:693-703. [PMID: 20212021 DOI: 10.1101/gr.105403.110] [Cited by in Crossref: 201] [Cited by in F6Publishing: 183] [Article Influence: 16.8] [Reference Citation Analysis]
33 Zhu L, Su X. Case Report: Neuroblastoma Breakpoint Family Genes Associate With 1q21 Copy Number Variation Disorders. Front Genet 2021;12:728816. [PMID: 34646304 DOI: 10.3389/fgene.2021.728816] [Reference Citation Analysis]
34 Atkinson EJ, Eckel-Passow JE, Wang A, Greenberg AJ, Scott CG, Pankratz VS, Purrington KN, Sellers TA, Rider DN, Heit JA, de Andrade M, Cunningham JM, Couch FJ, Vachon CM. The association of copy number variation and percent mammographic density. BMC Res Notes 2015;8:297. [PMID: 26152678 DOI: 10.1186/s13104-015-1212-y] [Cited by in Crossref: 1] [Article Influence: 0.1] [Reference Citation Analysis]
35 Choy K, Setlur S, Lee C, Lau T. The impact of human copy number variation on a new era of genetic testing: Copy number variation in genetic testing. BJOG: An International Journal of Obstetrics & Gynaecology 2010;117:391-8. [DOI: 10.1111/j.1471-0528.2009.02470.x] [Cited by in Crossref: 37] [Cited by in F6Publishing: 34] [Article Influence: 3.1] [Reference Citation Analysis]
36 Talukder AK, Agarwal M, Buetow KH, Denèfle PP. Tracking Cancer Genetic Evolution using OncoTrack. Sci Rep 2016;6:29647. [PMID: 27412732 DOI: 10.1038/srep29647] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
37 Bae JS, Jung MH, Lee BC, Cheong HS, Park BL, Kim LH, Kim J, Pasaje CFA, Lee JS, Jung KH, Chai YG, Shin HD, Choi I. The Genetic Effect of Copy Number Variations on the Risk of Alcoholism in a Korean Population: ANALYSIS OF CNV IN ALCOHOLISM. Alcoholism: Clinical and Experimental Research 2012;36:35-42. [DOI: 10.1111/j.1530-0277.2011.01578.x] [Cited by in Crossref: 9] [Cited by in F6Publishing: 6] [Article Influence: 0.8] [Reference Citation Analysis]
38 Ewing A, Semple C. Breaking point: the genesis and impact of structural variation in tumours. F1000Res 2018;7:F1000 Faculty Rev-1814. [PMID: 30519450 DOI: 10.12688/f1000research.16079.1] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 1.5] [Reference Citation Analysis]
39 Hungate EA, Applebaum MA, Skol AD, Vaksman Z, Diamond M, McDaniel L, Volchenboum SL, Stranger BE, Maris JM, Diskin SJ, Onel K, Cohn SL. Evaluation of Genetic Predisposition for MYCN-Amplified Neuroblastoma. J Natl Cancer Inst 2017;109. [PMID: 29117357 DOI: 10.1093/jnci/djx093] [Cited by in Crossref: 15] [Cited by in F6Publishing: 14] [Article Influence: 3.0] [Reference Citation Analysis]
40 Krepischi AC, Achatz MI, Santos EM, Costa SS, Lisboa BC, Brentani H, Santos TM, Gonçalves A, Nóbrega AF, Pearson PL, Vianna-Morgante AM, Carraro DM, Brentani RR, Rosenberg C. Germline DNA copy number variation in familial and early-onset breast cancer. Breast Cancer Res 2012;14:R24. [PMID: 22314128 DOI: 10.1186/bcr3109] [Cited by in Crossref: 63] [Cited by in F6Publishing: 59] [Article Influence: 6.3] [Reference Citation Analysis]
41 Bosse KR, Diskin SJ, Cole KA, Wood AC, Schnepp RW, Norris G, Nguyen le B, Jagannathan J, Laquaglia M, Winter C, Diamond M, Hou C, Attiyeh EF, Mosse YP, Pineros V, Dizin E, Zhang Y, Asgharzadeh S, Seeger RC, Capasso M, Pawel BR, Devoto M, Hakonarson H, Rappaport EF, Irminger-Finger I, Maris JM. Common variation at BARD1 results in the expression of an oncogenic isoform that influences neuroblastoma susceptibility and oncogenicity. Cancer Res 2012;72:2068-78. [PMID: 22350409 DOI: 10.1158/0008-5472.CAN-11-3703] [Cited by in Crossref: 71] [Cited by in F6Publishing: 53] [Article Influence: 7.1] [Reference Citation Analysis]
42 Mocellin S, Verdi D, Pooley KA, Nitti D. Genetic variation and gastric cancer risk: a field synopsis and meta-analysis. Gut. 2015;64:1209-1219. [PMID: 25731870 DOI: 10.1136/gutjnl-2015-309168] [Cited by in Crossref: 106] [Cited by in F6Publishing: 113] [Article Influence: 15.1] [Reference Citation Analysis]
43 Tyson J, Majerus TM, Walker S, Armour JA. Screening for common copy-number variants in cancer genes. Cancer Genet Cytogenet 2010;203:316-23. [PMID: 21156252 DOI: 10.1016/j.cancergencyto.2010.08.008] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 0.1] [Reference Citation Analysis]
44 Davis LE, Jeng S, Svalina MN, Huang E, Pittsenbarger J, Cantor EL, Berlow N, Seguin B, Mansoor A, McWeeney SK, Keller C. Integration of genomic, transcriptomic and functional profiles of aggressive osteosarcomas across multiple species. Oncotarget 2017;8:76241-56. [PMID: 29100308 DOI: 10.18632/oncotarget.19532] [Cited by in Crossref: 9] [Cited by in F6Publishing: 7] [Article Influence: 1.8] [Reference Citation Analysis]
45 Shlien A, Malkin D. Copy number variations and cancer susceptibility. Curr Opin Oncol 2010;22:55-63. [PMID: 19952747 DOI: 10.1097/CCO.0b013e328333dca4] [Cited by in Crossref: 59] [Cited by in F6Publishing: 30] [Article Influence: 4.9] [Reference Citation Analysis]
46 Wang Y, Huang B, Edelmann L, Kolodner RD, Edelmann W. Genes essential for cell viability that are linked to tumor suppressor genes play a role in cancer susceptibility. Cell Cycle 2010;9:3144-5. [PMID: 20703099 DOI: 10.4161/cc.9.16.12951] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.2] [Reference Citation Analysis]
47 Schwienbacher C, De Grandi A, Fuchsberger C, Facheris MF, Svaldi M, Wjst M, Pramstaller PP, Hicks AA. Copy number variation and association over T-cell receptor genes--influence of DNA source. Immunogenetics 2010;62:561-7. [PMID: 20582410 DOI: 10.1007/s00251-010-0459-7] [Cited by in Crossref: 9] [Cited by in F6Publishing: 8] [Article Influence: 0.8] [Reference Citation Analysis]
48 Latorre V, Diskin SJ, Diamond MA, Zhang H, Hakonarson H, Maris JM, Devoto M. Replication of neuroblastoma SNP association at the BARD1 locus in African-Americans. Cancer Epidemiol Biomarkers Prev 2012;21:658-63. [PMID: 22328350 DOI: 10.1158/1055-9965.EPI-11-0830] [Cited by in Crossref: 38] [Cited by in F6Publishing: 38] [Article Influence: 3.8] [Reference Citation Analysis]
49 Barbieri CE, Demichelis F, Rubin MA. Molecular genetics of prostate cancer: emerging appreciation of genetic complexity: Genomic complexity of prostate cancer. Histopathology 2012;60:187-98. [DOI: 10.1111/j.1365-2559.2011.04041.x] [Cited by in Crossref: 48] [Cited by in F6Publishing: 38] [Article Influence: 4.4] [Reference Citation Analysis]
50 Sharma A, Kumar A, Kumari N, Krishnani N, Rastogi N. Genome-wide copy number profiling in gallbladder carcinoma - A study from north India. Meta Gene 2017;14:42-8. [DOI: 10.1016/j.mgene.2017.07.009] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.4] [Reference Citation Analysis]
51 Kuusisto KM, Akinrinade O, Vihinen M, Kankuri-Tammilehto M, Laasanen SL, Schleutker J. copy number variation analysis in familial BRCA1/2-negative Finnish breast and ovarian cancer. PLoS One 2013;8:e71802. [PMID: 23967248 DOI: 10.1371/journal.pone.0071802] [Cited by in Crossref: 23] [Cited by in F6Publishing: 18] [Article Influence: 2.6] [Reference Citation Analysis]
52 Zhou Z, Wang W, Wang LS, Zhang NR. Integrative DNA copy number detection and genotyping from sequencing and array-based platforms. Bioinformatics 2018;34:2349-55. [PMID: 29992253 DOI: 10.1093/bioinformatics/bty104] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
53 Fang Z, Xiong Y, Li J, Liu L, Li M, Zhang C, Zhang W, Wan J. Copy-number increase of AURKA in gastric cancers in a Chinese population: a correlation with tumor progression. Med Oncol 2011;28:1017-22. [PMID: 20585902 DOI: 10.1007/s12032-010-9602-4] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 0.6] [Reference Citation Analysis]
54 Al-Sukhni W, Joe S, Lionel AC, Zwingerman N, Zogopoulos G, Marshall CR, Borgida A, Holter S, Gropper A, Moore S, Bondy M, Klein AP, Petersen GM, Rabe KG, Schwartz AG, Syngal S, Scherer SW, Gallinger S. Identification of germline genomic copy number variation in familial pancreatic cancer. Hum Genet 2012;131:1481-94. [PMID: 22665139 DOI: 10.1007/s00439-012-1183-1] [Cited by in Crossref: 17] [Cited by in F6Publishing: 17] [Article Influence: 1.7] [Reference Citation Analysis]
55 Need AC, Goldstein DB. Whole genome association studies in complex diseases: where do we stand? Dialogues Clin Neurosci 2010;12:37-46. [PMID: 20373665 [PMID: 20373665 DOI: 10.31887/dcns.2010.12.1/aneed] [Cited by in Crossref: 5] [Article Influence: 0.4] [Reference Citation Analysis]
56 Russell MR, Penikis A, Oldridge DA, Alvarez-Dominguez JR, McDaniel L, Diamond M, Padovan O, Raman P, Li Y, Wei JS, Zhang S, Gnanchandran J, Seeger R, Asgharzadeh S, Khan J, Diskin SJ, Maris JM, Cole KA. CASC15-S Is a Tumor Suppressor lncRNA at the 6p22 Neuroblastoma Susceptibility Locus. Cancer Res 2015;75:3155-66. [PMID: 26100672 DOI: 10.1158/0008-5472.CAN-14-3613] [Cited by in Crossref: 89] [Cited by in F6Publishing: 82] [Article Influence: 12.7] [Reference Citation Analysis]
57 Diskin SJ, Capasso M, Diamond M, Oldridge DA, Conkrite K, Bosse KR, Russell MR, Iolascon A, Hakonarson H, Devoto M, Maris JM. Rare variants in TP53 and susceptibility to neuroblastoma. J Natl Cancer Inst 2014;106:dju047. [PMID: 24634504 DOI: 10.1093/jnci/dju047] [Cited by in Crossref: 67] [Cited by in F6Publishing: 74] [Article Influence: 8.4] [Reference Citation Analysis]
58 Zhou F, Xing Y, Xu X, Yang Y, Zhang J, Ma Z, Wang J. NBPF is a potential DNA-binding transcription factor that is directly regulated by NF-κB. Int J Biochem Cell Biol 2013;45:2479-90. [PMID: 23939288 DOI: 10.1016/j.biocel.2013.07.022] [Cited by in Crossref: 19] [Cited by in F6Publishing: 18] [Article Influence: 2.1] [Reference Citation Analysis]
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