Christelle Borel

Lyon, France

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 36 publications

HPV circulating tumor DNA to monitor response to pembrolizumab and vorinostat combination in patients with advanced HPV-related squamous-cell carcinomas.

HPV circulating tumor DNA to monitor response to pembrolizumab and vorinostat combination in patients with advanced HPV-related squamous-cell carcinomas.

Journal: ESMO open

Published: June 06, 2025

Rare variant enrichment analysis supports GREB1L as a contributory driver gene in the etiology of Mayer-Rokitansky-Küster-Hauser syndrome.

Rare variant enrichment analysis supports GREB1L as a contributory driver gene in the etiology of Mayer-Rokitansky-Küster-Hauser syndrome.

Journal: HGG advances

Published: November 02, 2022

FOXI3 pathogenic variants cause one form of craniofacial microsomia.

FOXI3 pathogenic variants cause one form of craniofacial microsomia.

Journal: Nature communications

Published: April 09, 2022

Functional characteristics of a broad spectrum of TBX6 variants in Mayer-Rokitansky-Küster-Hauser syndrome.

Functional characteristics of a broad spectrum of TBX6 variants in Mayer-Rokitansky-Küster-Hauser syndrome.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: December 02, 2021

French national overview of the inclusion of environmental criteria in the public purchasing of health products (drugs and sterile medical devices)

French national overview of the inclusion of environmental criteria in the public purchasing of health products (drugs and sterile medical devices)

Journal: Annales pharmaceutiques francaises

Published: March 12, 2021

Dominant monoallelic variant in the PAK2 gene causes Knobloch syndrome type 2.

Dominant monoallelic variant in the PAK2 gene causes Knobloch syndrome type 2.

Journal: Human molecular genetics

Published: October 06, 2020

Perturbations of genes essential for Müllerian duct and Wölffian duct development in Mayer-Rokitansky-Küster-Hauser syndrome.

Perturbations of genes essential for Müllerian duct and Wölffian duct development in Mayer-Rokitansky-Küster-Hauser syndrome.

Journal: American journal of human genetics

Published: July 11, 2020

Single cell transcriptome in aneuploidies reveals mechanisms of gene dosage imbalance.

Single cell transcriptome in aneuploidies reveals mechanisms of gene dosage imbalance.

Journal: Nature communications

Published: February 28, 2019

Extensive cellular heterogeneity of X inactivation revealed by single-cell allele-specific expression in human fibroblasts.

Extensive cellular heterogeneity of X inactivation revealed by single-cell allele-specific expression in human fibroblasts.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: December 05, 2018

Multi-omic measurements of heterogeneity in HeLa cells across laboratories.

Multi-omic measurements of heterogeneity in HeLa cells across laboratories.

Journal: Nature biotechnology

Published: April 29, 2018

Chromatin three-dimensional interactions mediate genetic effects on gene expression.

Chromatin three-dimensional interactions mediate genetic effects on gene expression.

Journal: Science (New York, N.Y.)

Published: April 09, 2018

Deciphering Cell Lineage Specification during Male Sex Determination with Single-Cell RNA Sequencing.

Deciphering Cell Lineage Specification during Male Sex Determination with Single-Cell RNA Sequencing.

Journal: Cell reports

Published: September 19, 2017

Showing 1-12 of 36

Last Updated: 09/26/2026