Stephane Wenric
Stephane Wenric
Computational Oncology Scientist, Tempus Labs
Verified email at - Homepage
Cited by
Cited by
Circulating microRNA-based screening tool for breast cancer
P Frères, S Wenric, M Boukerroucha, C Fasquelle, J Thiry, N Bovy, ...
Oncotarget 7 (5), 5416, 2015
Variations of circulating cardiac biomarkers during and after anthracycline-containing chemotherapy in breast cancer patients
P Frères, N Bouznad, L Servais, C Josse, S Wenric, A Poncin, J Thiry, ...
BMC cancer 18 (1), 1-9, 2018
Using Supervised Learning Methods for Gene Selection in RNA-Seq Case-Control Studies
S Wenric, R Shemirani
Frontiers in Genetics 9, 297, 2018
Transcriptome-wide analysis of natural antisense transcripts shows their potential role in breast cancer
S Wenric, S ElGuendi, JH Caberg, W Bezzaou, C Fasquelle, ...
Scientific Reports 7 (1), 17452, 2017
Evaluation of BRCA1-related molecular features and microRNAs as prognostic factors for triple negative breast cancers
M Boukerroucha, C Josse, S ElGuendi, B Boujemla, P Frères, R Marée, ...
BMC cancer 15 (1), 1-10, 2015
Exome sequencing reveals a high prevalence of BRCA1 and BRCA2 founder variants in a diverse population-based biobank
NS Abul-Husn, ER Soper, JA Odgis, S Cullina, D Bobo, A Moscati, ...
Genome medicine 12 (1), 1-12, 2020
De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population
MD Kessler, DP Loesch, JA Perry, NL Heard-Costa, D Taliun, BE Cade, ...
Proceedings of the National Academy of Sciences 117 (5), 2560-2569, 2020
VPS51 biallelic variants cause microcephaly with brain malformations: A confirmatory report
A Uwineza, JH Caberg, J Hitayezu, S Wenric, L Mutesa, Y Vial, S Drunat, ...
European journal of medical genetics 62 (8), 103704, 2019
Towards a fine-scale population health monitoring system
GM Belbin, S Wenric, S Cullina, BS Glicksberg, A Moscati, GL Wojcik, ...
bioRxiv, 780668, 2019
Derivation and validation of genome-wide polygenic score for urinary tract stone diagnosis
I Paranjpe, N Tsao, R Judy, M Paranjpe, K Chaudhary, D Klarin, I Forrest, ...
Kidney International 98 (5), 1323-1330, 2020
Genomic studies of multiple myeloma reveal an association between X chromosome alterations and genomic profile complexity
T Sticca, JH Caberg, S Wenric, C Poulet, C Herens, M Jamar, C Josse, ...
Genes, Chromosomes and Cancer 56 (1), 18-27, 2016
Rapid response to the alpha-1 adrenergic agent phenylephrine in the perioperative period is impacted by genomics and ancestry
S Wenric, JM Jeff, T Joseph, MC Yee, GM Belbin, AO Obeng, SB Ellis, ...
The Pharmacogenomics Journal, 1-16, 2020
Towards cancer mega-cohorts: A novel homogenization algorithm applied to diverse breast cancer RNA-Seq datasets.
T Ahmed, M Carty, S Wenric, R Pelossof
Journal of Clinical Oncology 38 (15_suppl), e13507-e13507, 2020
Normalization and correction for batch effects via RUV for RNA-seq data: practical implications for Breast Cancer
A Debit, S Wenric, C Josse, V Bours, K Van Steen
Study of the role played by natural antisens transcripts (NAT) in breast cancer through the regulation of the expression of their paired protein coding genes
S El Guendi, S Wenric, B Charloteaux, L Karim, B Hennuy, W Bezzaou, ...
Annals of Oncology 28 (suppl_1), 2017
Transcriptome wide analysis of natural antisense transcripts shows potential role in breast cancer
S Wenric, S El Guendi, JH Caberg, W Bezzaou, C Fasquelle, ...
European Society of Human Genetics 2017, 2017
Exome copy number variation detection: Use of a pool of unrelated healthy tissue as reference sample
S Wenric, T Sticca, JH Caberg, C Josse, C Fasquelle, C Herens, M Jamar, ...
Genetic epidemiology 41 (1), 35-40, 2016
Genetic study of triple negative breast cancers
M Boukerroucha, C Josse, S ElGuendi, P Freres, R Marée, S Wenric, ...
Annals of Oncology 26 (suppl 3), iii12-iii13, 2015
A miRNA expression based diagnostic tool for breast cancer using Random Forests
S Wenric, P Freres, C Josse, V Bours, G Jerusalem
Benelux Bioinformatics Conference 2013, 2013
Exome sequencing of tumors: relevance in copy-number alteration (CNA) analysis and fixed tissue samples.
S Wenric, C Josse, C Fasquelle, C Poulet, T Sticca, M Boukerroucha, ...
Belgian Society of Human Genetics 2013, 2013
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