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Year | Number of Results |
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2012 | 1 |
2017 | 1 |
2019 | 1 |
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Page 1
The clinical utility of integrative genomics in childhood cancer extends beyond targetable mutations.
Nat Cancer. 2023 Feb;4(2):203-221. doi: 10.1038/s43018-022-00474-y. Epub 2022 Dec 30.
Nat Cancer. 2023.
PMID: 36585449
Free PMC article.
Miglustat as a therapeutic agent: prospects and caveats.
Venier RE, Igdoura SA.
Venier RE, et al.
J Med Genet. 2012 Sep;49(9):591-7. doi: 10.1136/jmedgenet-2012-101070. Epub 2012 Aug 14.
J Med Genet. 2012.
PMID: 22892202
Review.
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BRCA1-associated RING domain-1 (BARD1) loss and GBP1 expression enhance sensitivity to DNA damage in Ewing sarcoma.
Maurer LM, Daley JD, Mukherjee E, Venier RE, Julian CM, Bailey NG, Jacobs MF, Kumar-Sinha C, Raphael H, Periyapatna N, Weiss K, Janeway KA, Mody R, Lucas PC, McAllister-Lucas LM, Bailey KM.
Maurer LM, et al. Among authors: venier re.
Cancer Res Commun. 2022 Apr;2(4):220-232. doi: 10.1158/2767-9764.crc-21-0047. Epub 2022 Apr 20.
Cancer Res Commun. 2022.
PMID: 36187937
Free PMC article.
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Lineage-defined leiomyosarcoma subtypes emerge years before diagnosis and determine patient survival.
Anderson ND, Babichev Y, Fuligni F, Comitani F, Layeghifard M, Venier RE, Dentro SC, Maheshwari A, Guram S, Wunker C, Thompson JD, Yuki KE, Hou H, Zatzman M, Light N, Bernardini MQ, Wunder JS, Andrulis IL, Ferguson P, Razak ARA, Swallow CJ, Dowling JJ, Al-Awar RS, Marcellus R, Rouzbahman M, Gerstung M, Durocher D, Alexandrov LB, Dickson BC, Gladdy RA, Shlien A.
Anderson ND, et al. Among authors: venier re.
Nat Commun. 2021 Jul 23;12(1):4496. doi: 10.1038/s41467-021-24677-6.
Nat Commun. 2021.
PMID: 34301934
Free PMC article.
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Evaluation of barriers to referral for cancer predisposition syndromes in pediatric oncology patients in the United States.
Venier RE, Grubs RE, Kessler E, Cooper KL, Bailey KM, Meade J.
Venier RE, et al.
J Genet Couns. 2022 Aug;31(4):901-911. doi: 10.1002/jgc4.1559. Epub 2022 Feb 11.
J Genet Couns. 2022.
PMID: 35147246
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Neuronal pentraxin 1 depletion delays neurodegeneration and extends life in Sandhoff disease mice.
Hooper AWM, Alamilla JF, Venier RE, Gillespie DC, Igdoura SA.
Hooper AWM, et al. Among authors: venier re.
Hum Mol Genet. 2017 Feb 15;26(4):661-673. doi: 10.1093/hmg/ddw422.
Hum Mol Genet. 2017.
PMID: 28007910
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A germline BARD1 mutation in a patient with Ewing Sarcoma: Implications for familial testing and counseling.
Venier RE, Maurer LM, Kessler EM, Ranganathan S, McGough RL, Weiss KR, Malek MM, Meade J, Tersak JM, Bailey KM.
Venier RE, et al.
Pediatr Blood Cancer. 2019 Sep;66(9):e27824. doi: 10.1002/pbc.27824. Epub 2019 Jun 3.
Pediatr Blood Cancer. 2019.
PMID: 31157509
No abstract available.
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