Publications by authors named "Stephane Wenric"

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Real-World Validation of the Purity Independent Subtyping of Tumors Classifier for Informing Therapy Selection in Pancreatic Ductal Adenocarcinoma.
Stephane Wenric, Chithra Sangli, John Guittar, Farahnaz Islam, Alia Zander

JCO Precis Oncol· September 2025

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Molecular profiling of a real-world breast cancer cohort with genetically inferred ancestries reveals actionable tumor biology differences between European ancestry and African ancestry patient populations.
Minoru Miyashita, Joshua S K Bell, Stephane Wenric, Ezgi Karaesmen, Brooke Rhead

Breast Cancer Res· May 2023

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Privacy preserving validation for multiomic prediction models.
Talal Ahmed, Mark A Carty, Stephane Wenric, Jonathan R Dry, Ameen A Salahudeen

Brief Bioinform· May 2022

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EPS: automated feature selection in case-control studies using extreme pseudo-sampling.
Ruhollah Shemirani, Stephane Wenric, Eimear Kenny, José Luis Ambite

Bioinformatics· October 2021

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Rapid response to the alpha-1 adrenergic agent phenylephrine in the perioperative period is impacted by genomics and ancestry.
Stephane Wenric, Janina M Jeff, Thomas Joseph, Muh-Ching Yee, Gillian M Belbin

Pharmacogenomics J· April 2021

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Toward a fine-scale population health monitoring system.
Gillian M Belbin, Sinead Cullina, Stephane Wenric, Emily R Soper, Benjamin S Glicksberg

Cell· April 2021

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VPS51 biallelic variants cause microcephaly with brain malformations: A confirmatory report.
Annette Uwineza, Jean-Hubert Caberg, Janvier Hitayezu, Stephane Wenric, Leon Mutesa

Eur J Med Genet· August 2019

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Using Supervised Learning Methods for Gene Selection in RNA-Seq Case-Control Studies.
Stephane Wenric, Ruhollah Shemirani

Front Genet· August 2018

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Variations of circulating cardiac biomarkers during and after anthracycline-containing chemotherapy in breast cancer patients.
Pierre Frères, Nassim Bouznad, Laurence Servais, Claire Josse, Stéphane Wenric

BMC Cancer· January 2018

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Transcriptome-wide analysis of natural antisense transcripts shows their potential role in breast cancer.
Stephane Wenric, Sonia ElGuendi, Jean-Hubert Caberg, Warda Bezzaou, Corinne Fasquelle

Sci Rep· December 2017

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Genomic studies of multiple myeloma reveal an association between X chromosome alterations and genomic profile complexity.
Tiberio Sticca, Jean-Hubert Caberg, Stephane Wenric, Christophe Poulet, Christian Herens

Genes Chromosomes Cancer· January 2017

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Exome copy number variation detection: Use of a pool of unrelated healthy tissue as reference sample.
Stephane Wenric, Tiberio Sticca, Jean-Hubert Caberg, Claire Josse, Corinne Fasquelle

Genet Epidemiol· January 2017

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Circulating microRNA-based screening tool for breast cancer.
Pierre Frères, Stéphane Wenric, Meriem Boukerroucha, Corinne Fasquelle, Jérôme Thiry

Oncotarget· February 2016

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Evaluation of BRCA1-related molecular features and microRNAs as prognostic factors for triple negative breast cancers.
Meriem Boukerroucha, Claire Josse, Sonia ElGuendi, Bouchra Boujemla, Pierre Frères, Stephane Wenric

BMC Cancer· October 2015

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