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Comment
. 2015 Jun 16;107(8):djv174.
doi: 10.1093/jnci/djv174. Print 2015 Aug.

Response

Matthew Bainbridge  1 , Melissa L Bondy  2
Affiliations
Comment

Response

Matthew Bainbridge et al. J Natl Cancer Inst. .
No abstract available

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Comment on

  • Germline mutations in shelterin complex genes are associated with familial glioma.
    Bainbridge MN, Armstrong GN, Gramatges MM, Bertuch AA, Jhangiani SN, Doddapaneni H, Lewis L, Tombrello J, Tsavachidis S, Liu Y, Jalali A, Plon SE, Lau CC, Parsons DW, Claus EB, Barnholtz-Sloan J, Il'yasova D, Schildkraut J, Ali-Osman F, Sadetzki S, Johansen C, Houlston RS, Jenkins RB, Lachance D, Olson SH, Bernstein JL, Merrell RT, Wrensch MR, Walsh KM, Davis FG, Lai R, Shete S, Aldape K, Amos CI, Thompson PA, Muzny DM, Gibbs RA, Melin BS, Bondy ML; Gliogene Consortium. Bainbridge MN, et al. J Natl Cancer Inst. 2014 Dec 7;107(1):384. doi: 10.1093/jnci/dju384. Print 2015 Jan. J Natl Cancer Inst. 2014. PMID: 25482530 Free PMC article.
  • RE: Germline Mutations in Shelterin Complex Genes Are Associated With Familial Glioma.
    Cooke JG. Cooke JG. J Natl Cancer Inst. 2015 Jun 16;107(8):djv173. doi: 10.1093/jnci/djv173. Print 2015 Aug. J Natl Cancer Inst. 2015. PMID: 26079288 Free PMC article. No abstract available.

References

    1. Ostrom QT, Gittleman H, Liao P, et al. CBTRUS Statistical Report: Primary Brain and Central Nervous System Tumors Diagnosed in the United States in 2007–2011. Neuro Oncol. 2014;16(Suppl 4):iv1-iv63. - PMC - PubMed
    1. Bainbridge MN, Armstrong GN, Gramatges MM, et al. Germline mutations in shelterin complex genes are associated with familial glioma. J Natl Cancer Inst. 2014;107 (1):384. - PMC - PubMed
    1. Walsh KM, Codd V, Smirnov et al. Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk. Nat Genet. 2014;46 (7):731–735. - PMC - PubMed
    1. Robles-Espinoza CD, Harland M, Ramsay AJ, et al. POT1 loss-of-function variants predispose to familial melanoma. Nat Genet. 2014;46 (5):478–481. - PMC - PubMed
    1. Shi J, Yang XR, Ballew B, et al. Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma. Nat Genet. 2014;46 (5):482–486. - PMC - PubMed

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