Audrey Guilmatre - Publications

Safety and immunogenicity of BNT162b2 vaccine in children with acute leukaemia: results and perspectives of an open-label, two-centre, phase 1/2 trial with dose finding study.

Journal: Vaccine

Published: December 18, 2024

Suspicion of constitutional abnormality at diagnosis of childhood leukemia: Update of the leukemia committee of the French Society of Childhood Cancers

Journal: Bulletin du cancer

Published: August 18, 2023

Prognostic impact of RUNX1 mutations and deletions in pediatric acute myeloid leukemia: results from the French ELAM02 study group.

Journal: Leukemia

Published: September 23, 2022

What are the genetic practices of SFCE oncopediatricians? A study of the CONECT-AML ethical group

Journal: Bulletin du cancer

Published: June 13, 2022

Ex vivo drug sensitivity profiling-guided treatment of a relapsed pediatric mixed-phenotype acute leukemia with venetoclax and azacitidine.

Journal: Pediatric blood & cancer

Published: December 21, 2021

Solid organ transplantation after hematopoietic stem cell transplantation in childhood: A multicentric retrospective survey.

Journal: American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons

Published: September 13, 2018

Polymorphic tandem repeats within gene promoters act as modifiers of gene expression and DNA methylation in humans.

Journal: Nucleic acids research

Published: November 16, 2015

Abundant contribution of short tandem repeats to gene expression variation in humans.

Journal: Nature genetics

Published: August 17, 2015

Digital genotyping of macrosatellites and multicopy genes reveals novel biological functions associated with copy number variation of large tandem repeats.

Journal: PLoS genetics

Published: July 16, 2013

The emerging role of SHANK genes in neuropsychiatric disorders.

Journal: Developmental neurobiology

Published: March 28, 2013

Rapid multiplexed genotyping of simple tandem repeats using capture and high-throughput sequencing.

Journal: Human mutation

Published: February 09, 2013