| 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 | 42 | 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 | 33 | 2018 |
| Using Supervised Learning Methods for Gene Selection in RNA-Seq Case-Control Studies S Wenric, R Shemirani Frontiers in Genetics 9, 297, 2018 | 25 | 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 | 22 | 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 | 21 | 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 | 15 | 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 | 8 | 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 | 6 | 2019 |
| Towards a fine-scale population health monitoring system GM Belbin, S Wenric, S Cullina, BS Glicksberg, A Moscati, GL Wojcik, ... bioRxiv, 780668, 2019 | 6 | 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 | 2 | 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 | 1 | 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 | | 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 | | 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 EUROPEAN JOURNAL OF HUMAN GENETICS 26, 995-995, 2018 | | 2018 |
| 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 | | 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 | | 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 | | 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 | | 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 | | 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 | | 2013 |
Vincent BoursUniversité de LiègeVerified email at uliege.be
