Delattre O - Search Results

1

Multimodal analysis of cell-free DNA whole-genome sequencing for pediatric cancers with low mutational burden.

Peneder P, Stütz AM, Surdez D, Krumbholz M, Semper S, Chicard M, Sheffield NC, Pierron G, Lapouble E, Tötzl M, Ergüner B, Barreca D, Rendeiro AF, Agaimy A, Boztug H, Engstler G, Dworzak M, Bernkopf M, Taschner-Mandl S, Ambros IM, Myklebost O, Marec-Bérard P, Burchill SA, Brennan B, Strauss SJ, Whelan J, Schleiermacher G, Schaefer C, Dirksen U, Hutter C, Boye K, Ambros PF, Delattre O, Metzler M, Bock C, Tomazou EM. Peneder P, et al. Among authors: delattre o. Nat Commun. 2021 May 28;12(1):3230. doi: 10.1038/s41467-021-23445-w. Nat Commun. 2021. PMID: 34050156 Free PMC article.

2

Variability of EWS chimaeric transcripts in Ewing tumours: a comparison of clinical and molecular data.

Zoubek A, Pfleiderer C, Salzer-Kuntschik M, Amann G, Windhager R, Fink FM, Koscielniak E, Delattre O, Strehl S, Ambros PF, et al. Zoubek A, et al. Among authors: delattre o. Br J Cancer. 1994 Nov;70(5):908-13. doi: 10.1038/bjc.1994.419. Br J Cancer. 1994. PMID: 7524604 Free PMC article.

3

A multiplex PCR assay for routine evaluation of deletion of the short arm of chromosome 1 in neuroblastoma.

Schleiermacher G, Peter M, Michon J, Zucker JM, Thomas G, Magdelénat H, Delattre O. Schleiermacher G, et al. Among authors: delattre o. Eur J Cancer. 1995;31A(4):535-8. doi: 10.1016/0959-8049(95)00008-7. Eur J Cancer. 1995. PMID: 7576961

4

The Ewing family of tumors--a subgroup of small-round-cell tumors defined by specific chimeric transcripts.

Delattre O, Zucman J, Melot T, Garau XS, Zucker JM, Lenoir GM, Ambros PF, Sheer D, Turc-Carel C, Triche TJ, et al. Delattre O, et al. N Engl J Med. 1994 Aug 4;331(5):294-9. doi: 10.1056/NEJM199408043310503. N Engl J Med. 1994. PMID: 8022439 Free article.

5

Clinical relevance of loss heterozygosity of the short arm of chromosome 1 in neuroblastoma: a single-institution study.

Schleiermacher G, Delattre O, Peter M, Mosseri V, Delonlay P, Vielh P, Thomas G, Zucker JM, Magdelénat H, Michon J. Schleiermacher G, et al. Among authors: delattre o. Int J Cancer. 1996 Apr 22;69(2):73-8. doi: 10.1002/(SICI)1097-0215(19960422)69:2<73::AID-IJC1>3.0.CO;2-S. Int J Cancer. 1996. PMID: 8608986 Free article.

6

Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer.

Versteege I, Sévenet N, Lange J, Rousseau-Merck MF, Ambros P, Handgretinger R, Aurias A, Delattre O. Versteege I, et al. Among authors: delattre o. Nature. 1998 Jul 9;394(6689):203-6. doi: 10.1038/28212. Nature. 1998. PMID: 9671307

7

[Detection of micrometastases and circulating tumour cells using molecular biology technics in solid tumours].

Schleiermacher G, Delattre O. Schleiermacher G, et al. Among authors: delattre o. Bull Cancer. 2001 Jun;88(6):561-70. Bull Cancer. 2001. PMID: 11459702 Free article. French.

8

CGH analysis of secondary genetic changes in Ewing tumors: correlation with metastatic disease in a series of 43 cases.

Brisset S, Schleiermacher G, Peter M, Mairal A, Oberlin O, Delattre O, Aurias A. Brisset S, et al. Among authors: delattre o. Cancer Genet Cytogenet. 2001 Oct 1;130(1):57-61. doi: 10.1016/s0165-4608(01)00454-x. Cancer Genet Cytogenet. 2001. PMID: 11672775 Review.

9

Increased risk of systemic relapses associated with bone marrow micrometastasis and circulating tumor cells in localized ewing tumor.

Schleiermacher G, Peter M, Oberlin O, Philip T, Rubie H, Mechinaud F, Sommelet-Olive D, Landman-Parker J, Bours D, Michon J, Delattre O; Société Française d'Oncologie Pédiatrique. Schleiermacher G, et al. Among authors: delattre o. J Clin Oncol. 2003 Jan 1;21(1):85-91. doi: 10.1200/JCO.2003.03.006. J Clin Oncol. 2003. PMID: 12506175

10

Combined 24-color karyotyping and comparative genomic hybridization analysis indicates predominant rearrangements of early replicating chromosome regions in neuroblastoma.

Schleiermacher G, Janoueix-Lerosey I, Combaret V, Derré J, Couturier J, Aurias A, Delattre O. Schleiermacher G, et al. Among authors: delattre o. Cancer Genet Cytogenet. 2003 Feb;141(1):32-42. doi: 10.1016/s0165-4608(02)00644-1. Cancer Genet Cytogenet. 2003. PMID: 12581896

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