Shlien A - Search Results

1

Signatures of copy number alterations in human cancer.

Steele CD, Abbasi A, Islam SMA, Bowes AL, Khandekar A, Haase K, Hames-Fathi S, Ajayi D, Verfaillie A, Dhami P, McLatchie A, Lechner M, Light N, Shlien A, Malkin D, Feber A, Proszek P, Lesluyes T, Mertens F, Flanagan AM, Tarabichi M, Van Loo P, Alexandrov LB, Pillay N. Steele CD, et al. Among authors: shlien a. Nature. 2022 Jun;606(7916):984-991. doi: 10.1038/s41586-022-04738-6. Epub 2022 Jun 15. Nature. 2022. PMID: 35705804 Free PMC article.

2

The BRD4-NUT Fusion Alone Drives Malignant Transformation of NUT Carcinoma.

Durall RT, Huang J, Wojenski L, Huang Y, Gokhale PC, Leeper BA, Nash JO, Ballester PL, Davidson S, Shlien A, Sotirakis E, Bertaux F, Dubus V, Luo J, Wu CJ, Keskin DB, Eagen KP, Shapiro GI, French CA. Durall RT, et al. Among authors: shlien a. Cancer Res. 2023 Dec 1;83(23):3846-3860. doi: 10.1158/0008-5472.CAN-23-2545. Cancer Res. 2023. PMID: 37819236 Free PMC article.

3

Excessive genomic DNA copy number variation in the Li-Fraumeni cancer predisposition syndrome.

Shlien A, Tabori U, Marshall CR, Pienkowska M, Feuk L, Novokmet A, Nanda S, Druker H, Scherer SW, Malkin D. Shlien A, et al. Proc Natl Acad Sci U S A. 2008 Aug 12;105(32):11264-9. doi: 10.1073/pnas.0802970105. Epub 2008 Aug 6. Proc Natl Acad Sci U S A. 2008. PMID: 18685109 Free PMC article.

4

Copy number variations and cancer.

Shlien A, Malkin D. Shlien A, et al. Genome Med. 2009 Jun 16;1(6):62. doi: 10.1186/gm62. Genome Med. 2009. PMID: 19566914 Free PMC article.

5

IGF2 is highly expressed in pediatric undifferentiated sarcomas and reveals two distinct cytoplasmic trafficking patterns.

Somers GR, Ho M, Pienkowska M, Shlien A, Malkin D, Ackerley C, Zielenska M. Somers GR, et al. Among authors: shlien a. Pediatr Dev Pathol. 2010 May-Jun;13(3):169-77. doi: 10.2350/09-02-0613-OA.1. Pediatr Dev Pathol. 2010. PMID: 19586133

6

Copy number variations and cancer susceptibility.

Shlien A, Malkin D. Shlien A, et al. Curr Opin Oncol. 2010 Jan;22(1):55-63. doi: 10.1097/CCO.0b013e328333dca4. Curr Opin Oncol. 2010. Retraction in: Curr Opin Oncol. 2016 Sep;28(5):453. doi: 10.1097/01.cco.0000491182.00738.ba PMID: 19952747 Retracted. Review.

7

Recurrent focal copy-number changes and loss of heterozygosity implicate two noncoding RNAs and one tumor suppressor gene at chromosome 3q13.31 in osteosarcoma.

Pasic I, Shlien A, Durbin AD, Stavropoulos DJ, Baskin B, Ray PN, Novokmet A, Malkin D. Pasic I, et al. Among authors: shlien a. Cancer Res. 2010 Jan 1;70(1):160-71. doi: 10.1158/0008-5472.CAN-09-1902. Cancer Res. 2010. PMID: 20048075

8

TP53 alterations determine clinical subgroups and survival of patients with choroid plexus tumors.

Tabori U, Shlien A, Baskin B, Levitt S, Ray P, Alon N, Hawkins C, Bouffet E, Pienkowska M, Lafay-Cousin L, Gozali A, Zhukova N, Shane L, Gonzalez I, Finlay J, Malkin D. Tabori U, et al. Among authors: shlien a. J Clin Oncol. 2010 Apr 20;28(12):1995-2001. doi: 10.1200/JCO.2009.26.8169. Epub 2010 Mar 22. J Clin Oncol. 2010. PMID: 20308654

9

A common molecular mechanism underlies two phenotypically distinct 17p13.1 microdeletion syndromes.

Shlien A, Baskin B, Achatz MI, Stavropoulos DJ, Nichols KE, Hudgins L, Morel CF, Adam MP, Zhukova N, Rotin L, Novokmet A, Druker H, Shago M, Ray PN, Hainaut P, Malkin D. Shlien A, et al. Am J Hum Genet. 2010 Nov 12;87(5):631-42. doi: 10.1016/j.ajhg.2010.10.007. Am J Hum Genet. 2010. PMID: 21056402 Free PMC article.

10

Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: a prospective observational study.

Villani A, Tabori U, Schiffman J, Shlien A, Beyene J, Druker H, Novokmet A, Finlay J, Malkin D. Villani A, et al. Among authors: shlien a. Lancet Oncol. 2011 Jun;12(6):559-67. doi: 10.1016/S1470-2045(11)70119-X. Epub 2011 May 19. Lancet Oncol. 2011. PMID: 21601526

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