Karen Liddle

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 4

Top Topics

Intellectual Disability

Dna Methylation

Autism Spectrum Disorder

Top Venues

European journal of human genetics : EJHG

Journal of paediatrics and child health

This page only lists publications with an associated author ORCID identifier.

Publications

Rebecca Kriukelis, Michael T Gabbett, Rachael Beswick, Aideen M McInerney-Leo, Carlie Driscoll, Karen Liddle
The congenital hearing phenotype in GJB2 in Queensland, Australia: V37I and mild hearing loss predominates. European journal of human genetics : EJHG (2024)
Rebecca Kriukelis, Michael T Gabbett, Rachael Beswick, Aideen M McInerney-Leo, Carlie Driscoll, Karen Liddle
The congenital hearing phenotype in GJB2 in Queensland, Australia: V37I and mild hearing loss predominates. European journal of human genetics : EJHG (2024)
Rebecca Kriukelis, Michael T Gabbett, Rachael Beswick, Aideen M McInerney-Leo, Carlie Driscoll, Karen Liddle
The congenital hearing phenotype in GJB2 in Queensland, Australia: V37I and mild hearing loss predominates. European journal of human genetics : EJHG (2024)
Karen Liddle, Rachael Beswick, E Jane Fitzgibbons, Carlie Driscoll
Aetiology of permanent childhood hearing loss at a population level. Journal of paediatrics and child health (2021)