Mosse Y - Search Results

1

Percutaneous biopsy for the diagnosis, risk stratification, and molecular profiling of neuroblastoma: A single-center retrospective study.

Schoeman S, Bagatell R, Cahill AM, Maris J, Mattei P, Mosse Y, Pogoriler J, Srinivasan A, Acord M. Schoeman S, et al. Among authors: mosse y. Pediatr Blood Cancer. 2024 Apr;71(4):e30887. doi: 10.1002/pbc.30887. Epub 2024 Jan 30. Pediatr Blood Cancer. 2024. PMID: 38291721

2

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. Among authors: mosse y. Cancer Res. 2002 Nov 15;62(22):6651-8. Cancer Res. 2002. PMID: 12438263

3

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: mosse y. Cancer Res. 2003 Apr 1;63(7):1631-5. Cancer Res. 2003. PMID: 12670915

4

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. Lancet Oncol. 2003 Dec;4(12):769-71. doi: 10.1016/s1470-2045(03)01283-x. Lancet Oncol. 2003. PMID: 14662434 No abstract available.

5

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: mosse y. Mod Pathol. 2003 Dec;16(12):1248-56. doi: 10.1097/01.MP.0000097364.64566.81. Mod Pathol. 2003. PMID: 14681326

6

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. Genes Chromosomes Cancer. 2005 Aug;43(4):390-403. doi: 10.1002/gcc.20198. Genes Chromosomes Cancer. 2005. PMID: 15892104

7

Measurement and relevance of neuroblastoma DNA copy number changes in the post-genome era.

Mosse YP, Greshock J, Weber BL, Maris JM. Mosse YP, et al. Cancer Lett. 2005 Oct 18;228(1-2):83-90. doi: 10.1016/j.canlet.2005.02.052. Cancer Lett. 2005. PMID: 15967571 Review.

8

Chromosome 1p and 11q deletions and outcome in neuroblastoma.

Attiyeh EF, London WB, Mossé YP, Wang Q, Winter C, Khazi D, McGrady PW, Seeger RC, Look AT, Shimada H, Brodeur GM, Cohn SL, Matthay KK, Maris JM; Children's Oncology Group. Attiyeh EF, et al. N Engl J Med. 2005 Nov 24;353(21):2243-53. doi: 10.1056/NEJMoa052399. N Engl J Med. 2005. PMID: 16306521 Free article.

9

Integrative genomics identifies distinct molecular classes of neuroblastoma and shows that multiple genes are targeted by regional alterations in DNA copy number.

Wang Q, Diskin S, Rappaport E, Attiyeh E, Mosse Y, Shue D, Seiser E, Jagannathan J, Shusterman S, Bansal M, Khazi D, Winter C, Okawa E, Grant G, Cnaan A, Zhao H, Cheung NK, Gerald W, London W, Matthay KK, Brodeur GM, Maris JM. Wang Q, et al. Among authors: mosse y. Cancer Res. 2006 Jun 15;66(12):6050-62. doi: 10.1158/0008-5472.CAN-05-4618. Cancer Res. 2006. PMID: 16778177

10

STAC: A method for testing the significance of DNA copy number aberrations across multiple array-CGH experiments.

Diskin SJ, Eck T, Greshock J, Mosse YP, Naylor T, Stoeckert CJ Jr, Weber BL, Maris JM, Grant GR. Diskin SJ, et al. Genome Res. 2006 Sep;16(9):1149-58. doi: 10.1101/gr.5076506. Epub 2006 Aug 9. Genome Res. 2006. PMID: 16899652 Free PMC article.

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