Maris JM - Search Results

1

Phenotype restricted genome-wide association study using a gene-centric approach identifies three low-risk neuroblastoma susceptibility Loci.

Nguyen le B, Diskin SJ, Capasso M, Wang K, Diamond MA, Glessner J, Kim C, Attiyeh EF, Mosse YP, Cole K, Iolascon A, Devoto M, Hakonarson H, Li HK, Maris JM. Nguyen le B, et al. Among authors: maris jm. PLoS Genet. 2011 Mar;7(3):e1002026. doi: 10.1371/journal.pgen.1002026. Epub 2011 Mar 17. PLoS Genet. 2011. PMID: 21436895 Free PMC article.

2

Novel regions of chromosomal loss in familial neuroblastoma by comparative genomic hybridization.

Altura RA, Maris JM, Li H, Boyett JM, Brodeur GM, Look AT. Altura RA, et al. Among authors: maris jm. Genes Chromosomes Cancer. 1997 Jul;19(3):176-84. doi: 10.1002/(sici)1098-2264(199707)19:3<176::aid-gcc7>3.0.co;2-v. Genes Chromosomes Cancer. 1997. PMID: 9218999

3

Molecular biology of neuroblastoma.

Maris JM, Matthay KK. Maris JM, et al. J Clin Oncol. 1999 Jul;17(7):2264-79. doi: 10.1200/JCO.1999.17.7.2264. J Clin Oncol. 1999. PMID: 10561284 Review.

4

Evidence for a hereditary neuroblastoma predisposition locus at chromosome 16p12-13.

Maris JM, Weiss MJ, Mosse Y, Hii G, Guo C, White PS, Hogarty MD, Mirensky T, Brodeur GM, Rebbeck TR, Urbanek M, Shusterman S. Maris JM, et al. Cancer Res. 2002 Nov 15;62(22):6651-8. Cancer Res. 2002. PMID: 12438263

5

ID2 expression is not associated with MYCN amplification or expression in human neuroblastomas.

Wang Q, Hii G, Shusterman S, Mosse Y, Winter CL, Guo C, Zhao H, Rappaport E, Hogarty MD, Maris JM. Wang Q, et al. Among authors: maris jm. Cancer Res. 2003 Apr 1;63(7):1631-5. Cancer Res. 2003. PMID: 12670915

6

Identification and high-resolution mapping of a constitutional 11q deletion in an infant with multifocal neuroblastoma.

Mosse Y, Greshock J, King A, Khazi D, Weber BL, Maris JM. Mosse Y, et al. Among authors: maris jm. Lancet Oncol. 2003 Dec;4(12):769-71. doi: 10.1016/s1470-2045(03)01283-x. Lancet Oncol. 2003. PMID: 14662434 No abstract available.

7

Detection of single-copy chromosome 17q gain in human neuroblastomas using real-time quantitative polymerase chain reaction.

Morowitz M, Shusterman S, Mosse Y, Hii G, Winter CL, Khazi D, Wang Q, King R, Maris JM. Morowitz M, et al. Among authors: maris jm. Mod Pathol. 2003 Dec;16(12):1248-56. doi: 10.1097/01.MP.0000097364.64566.81. Mod Pathol. 2003. PMID: 14681326

8

Germline PHOX2B mutation in hereditary neuroblastoma.

Mosse YP, Laudenslager M, Khazi D, Carlisle AJ, Winter CL, Rappaport E, Maris JM. Mosse YP, et al. Among authors: maris jm. Am J Hum Genet. 2004 Oct;75(4):727-30. doi: 10.1086/424530. Am J Hum Genet. 2004. PMID: 15338462 Free PMC article. No abstract available.

9

The biologic basis for neuroblastoma heterogeneity and risk stratification.

Maris JM. Maris JM. Curr Opin Pediatr. 2005 Feb;17(1):7-13. doi: 10.1097/01.mop.0000150631.60571.89. Curr Opin Pediatr. 2005. PMID: 15659956 Review.

10

High-resolution detection and mapping of genomic DNA alterations in neuroblastoma.

Mosse YP, Greshock J, Margolin A, Naylor T, Cole K, Khazi D, Hii G, Winter C, Shahzad S, Asziz MU, Biegel JA, Weber BL, Maris JM. Mosse YP, et al. Among authors: maris jm. Genes Chromosomes Cancer. 2005 Aug;43(4):390-403. doi: 10.1002/gcc.20198. Genes Chromosomes Cancer. 2005. PMID: 15892104

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