Andrew Paul Fennell
6PUBLICATIONS
48CO-AUTHORS
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Publications (6)
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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
|Jul 02, 2025
Lifesaving Diagnosis through Prenatal Genomic Sequencing.Andrew P Fennell, Tony Roscioli, Michael Buckley
|Feb 02, 2023
Elusive variants in autosomal recessive disease: how can we improve timely diagnosis?Ari E Horton, Sebastian Lunke, Simon Sadedin
|Nov 11, 2022
The diverse pleiotropic effects of spliceosomal protein PUF60: A case series of Verheij syndrome.Andrew Paul Fennell, Anne Elizabeth Baxter, Samuel Frank Berkovic
|Jul 12, 2019
The changing face of clinical genetics service delivery in the era of genomics: a framework for monitoring service delivery and data from a comprehensive metropolitan general genetics service.Andrew Paul Fennell, Matthew Frank Hunter, Gregory Philip Corboy
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Frequent Collaborators
2 joint publications
Sebastian Lunke
2 joint publications
Zornitza Stark
2 joint publications
Matthew Frank Hunter
1 joint publications
Ari E Horton
1 joint publications
Adam Jackson
1 joint publications
Alexander J M Blakes
1 joint publications
Olivia J Henry
1 joint publications
Angelica M Delgado-Vega
1 joint publications
Irene Duba
1 joint publications
Frances Elmslie