Emeline Davoine
Dijon, 21000, France
Last Updated: 09/26/2026
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Found 10 publications
Genomic newborn screening as a paradigm shift in rare disease management, with emphasis on endocrine conditions.
Journal: Annales d'endocrinologie
Published: May 08, 2026
Genomic newborn screening as a paradigm shift in rare disease management, with emphasis on endocrine conditions.
Journal: Annales d'endocrinologie
Published: March 21, 2026
PERIGENOMED-CLINICS 1-the first study on feasibility, acceptability and psychosocial impact of PERIGENOMED: a pilot project aimed at providing initial concrete evidence on the relevance of panel-based genome sequencing for newborn screening (NBS) in France.
Journal: BMJ open
Published: October 23, 2025
Sinus node dysfunction, Brugada syndrome and long QT syndrome affecting the same patient : when genetics can't make head or tail of it
Journal: Revue medicale suisse
Published: June 05, 2020
A New Variant in the MYH11 Gene in a Familial Case of Thoracic Aortic Aneurysm.
Journal: The Annals of thoracic surgery
Published: June 27, 2019
The Global State of the Genetic Counseling Profession.
Journal: European journal of human genetics : EJHG
Published: February 05, 2018
How were used recommendations for endometrial carcinoma? Britain retrospective study
Journal: Journal de gynecologie, obstetrique et biologie de la reproduction
Published: July 24, 2015
Consequences of combining siRNA-mediated DNA methyltransferase 1 depletion with 5-aza-2'-deoxycytidine in human leukemic KG1 cells.
Journal: Oncotarget
Published: December 28, 2014
Showing 1-10 of 10
Last Updated: 09/26/2026