Olivia J Henry
3PUBLICATIONS
24CO-AUTHORS
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Publications (3)
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|Mar 30, 2026
Biallelic variants in RNU2-2 cause a remarkably frequent developmental and epileptic encephalopathy.Adam Jackson, Alexander J M Blakes, Bader Alhaddad
|Apr 04, 2025
Clinical whole genome sequencing in pediatric epilepsy: Genetic and phenotypic spectrum of 733 individuals.Olivia J Henry, Sofia Ygberg, Michela Barbaro
|Mar 26, 2023
Individualised human phenotype ontology gene panels improve clinical whole exome and genome sequencing analytical efficacy in a cohort of developmental and epileptic encephalopathies.Olivia J Henry, Tommy Stödberg, Sofia Båtelson
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Frequent Collaborators
1 joint publications
Chiara Rasi
1 joint publications
Leif Karlsson
1 joint publications
Adam Jackson
1 joint publications
Alexander J M Blakes
1 joint publications
Angelica M Delgado-Vega
1 joint publications
Irene Duba
1 joint publications
Frances Elmslie
1 joint publications
Jamie Ellingford
1 joint publications
Andrew P Fennell
1 joint publications
Simon P Heller
