Wenric S - Search Results

1

Evaluation of BRCA1-related molecular features and microRNAs as prognostic factors for triple negative breast cancers.

Boukerroucha M, Josse C, ElGuendi S, Boujemla B, Frères P, Marée R, Wenric S, Segers K, Collignon J, Jerusalem G, Bours V. Boukerroucha M, et al. Among authors: wenric s. BMC Cancer. 2015 Oct 21;15:755. doi: 10.1186/s12885-015-1740-9. BMC Cancer. 2015. PMID: 26490435 Free PMC article.

2

Variations of circulating cardiac biomarkers during and after anthracycline-containing chemotherapy in breast cancer patients.

Frères P, Bouznad N, Servais L, Josse C, Wenric S, Poncin A, Thiry J, Moonen M, Oury C, Lancellotti P, Bours V, Jerusalem G. Frères P, et al. Among authors: wenric s. BMC Cancer. 2018 Jan 29;18(1):102. doi: 10.1186/s12885-018-4015-4. BMC Cancer. 2018. PMID: 29378531 Free PMC article.

3

Circulating microRNA-based screening tool for breast cancer.

Frères P, Wenric S, Boukerroucha M, Fasquelle C, Thiry J, Bovy N, Struman I, Geurts P, Collignon J, Schroeder H, Kridelka F, Lifrange E, Jossa V, Bours V, Josse C, Jerusalem G. Frères P, et al. Among authors: wenric s. Oncotarget. 2016 Feb 2;7(5):5416-28. doi: 10.18632/oncotarget.6786. Oncotarget. 2016. PMID: 26734993 Free PMC article.

4

Genomic studies of multiple myeloma reveal an association between X chromosome alterations and genomic profile complexity.

Sticca T, Caberg JH, Wenric S, Poulet C, Herens C, Jamar M, Josse C, El Guendi S, Max S, Beguin Y, Gothot A, Caers J, Bours V. Sticca T, et al. Among authors: wenric s. Genes Chromosomes Cancer. 2017 Jan;56(1):18-27. doi: 10.1002/gcc.22397. Epub 2016 Aug 18. Genes Chromosomes Cancer. 2017. PMID: 27454822 Free article.

5

Transcriptome-wide analysis of natural antisense transcripts shows their potential role in breast cancer.

Wenric S, ElGuendi S, Caberg JH, Bezzaou W, Fasquelle C, Charloteaux B, Karim L, Hennuy B, Frères P, Collignon J, Boukerroucha M, Schroeder H, Olivier F, Jossa V, Jerusalem G, Josse C, Bours V. Wenric S, et al. Sci Rep. 2017 Dec 12;7(1):17452. doi: 10.1038/s41598-017-17811-2. Sci Rep. 2017. PMID: 29234122 Free PMC article.

6

Exome copy number variation detection: Use of a pool of unrelated healthy tissue as reference sample.

Wenric S, Sticca T, Caberg JH, Josse C, Fasquelle C, Herens C, Jamar M, Max S, Gothot A, Caers J, Bours V. Wenric S, et al. Genet Epidemiol. 2017 Jan;41(1):35-40. doi: 10.1002/gepi.22019. Epub 2016 Nov 10. Genet Epidemiol. 2017. PMID: 27862228 Free article.

7

VPS51 biallelic variants cause microcephaly with brain malformations: A confirmatory report.

Uwineza A, Caberg JH, Hitayezu J, Wenric S, Mutesa L, Vial Y, Drunat S, Passemard S, Verloes A, El Ghouzzi V, Bours V. Uwineza A, et al. Among authors: wenric s. Eur J Med Genet. 2019 Aug;62(8):103704. doi: 10.1016/j.ejmg.2019.103704. Epub 2019 Jun 14. Eur J Med Genet. 2019. PMID: 31207318 Free article.

8

Using Supervised Learning Methods for Gene Selection in RNA-Seq Case-Control Studies.

Wenric S, Shemirani R. Wenric S, et al. Front Genet. 2018 Aug 3;9:297. doi: 10.3389/fgene.2018.00297. eCollection 2018. Front Genet. 2018. PMID: 30123241 Free PMC article.

9

EPS: automated feature selection in case-control studies using extreme pseudo-sampling.

Shemirani R, Wenric S, Kenny E, Ambite JL. Shemirani R, et al. Among authors: wenric s. Bioinformatics. 2021 Oct 11;37(19):3372-3373. doi: 10.1093/bioinformatics/btab214. Bioinformatics. 2021. PMID: 33774671

10

Toward a fine-scale population health monitoring system.

Belbin GM, Cullina S, Wenric S, Soper ER, Glicksberg BS, Torre D, Moscati A, Wojcik GL, Shemirani R, Beckmann ND, Cohain A, Sorokin EP, Park DS, Ambite JL, Ellis S, Auton A; CBIPM Genomics Team; Regeneron Genetics Center; Bottinger EP, Cho JH, Loos RJF, Abul-Husn NS, Zaitlen NA, Gignoux CR, Kenny EE. Belbin GM, et al. Among authors: wenric s. Cell. 2021 Apr 15;184(8):2068-2083.e11. doi: 10.1016/j.cell.2021.03.034. Cell. 2021. PMID: 33861964 Free article.

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