Product
Help
Pricing
About
Jobs
Log in
Get started
Author
Add to collection
Kévin Jousselin
Observed names:
Jousselin, Kevin,
Kevin Jousselin
OpenAlex ID:
A5115780481
PFMG2025–integrating genomic medicine into the national healthcare system in France
2025
·
Caroline Abadie
, Aldja Abderrahmane
, et al.
·
The Lancet Regional Health - Europe
·
59
PDF
Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies
2026
·
Elsa Leitão
, Amandine Santini
, et al.
·
Nature Genetics
·
18
PDF
MYH6 in Congenital Heart Defects: A Genotype–Phenotype Characterization in a French Cohort
2025
·
Elise Daire
, Clément Sauvestre
, et al.
·
Pediatric Cardiology
·
1
Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies
2025
·
Leitão, Elsa
, Santini, Amandine
, et al.
·
RWTH Publications (RWTH Aachen)
Show more works
View as search
Works count:
4
Citation count:
78
H-index:
2
I10-index:
2
Year
Topic
Type
