Damien Sanlaville

13PUBLICATIONS
156CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Speciation and extinctionInfant and child healthGene mappingNeurosciences not elsewhere classified
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Journal

Publications (13)

|Apr 25, 2026
Compound heterozygous SLC12A5 variants expand the molecular and functional spectrum of KCC2-developmental and epileptic encephalopathy.

|Jun 26, 2025
Transposable element expression is associated with sex chromosome number in humans.

Jordan Teoli, Miriam Merenciano, Marie Fablet

|May 23, 2025
View of healthcare professionals on ultra-rapid genome sequencing and its future implementation in clinical practice for critically ill children.

Claire Caillot, Etienne Javouhey, Stéphane Hays

|Mar 21, 2024
Clinical and molecular cytogenetic studies of five new patients with 20q11q12 deletion and review of the literature: Proposition of two critical regions.

Souad Bensaid, Malika Bendahmane, Sara Loddo

|Mar 18, 2024
Novel syndromic neurodevelopmental disorder caused by de novo deletion of CHASERR, a long noncoding RNA.

Vijay S Ganesh, Kevin Riquin, Nicolas Chatron

|Feb 06, 2024
Creatinine levels in French children with Down syndrome up to ten years old.

Joanna Pautonnier, Sylvie Goutte, Laurence Derain Dubourg

Pageof 3

Frequent Collaborators

7 joint publications

Nicolas Chatron

4 joint publications

Gaetan Lesca

3 joint publications

Jill A Rosenfeld

2 joint publications

Gemma L Carvill