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Browsing publications by
Sumaya Alkanderi.
Newcastle Authors
Title
Year
Full text
Sumaya Alkanderi
Professor John Sayer
Biallelic
CYP24A1
variants presenting during pregnancy: Clinical and biochemical phenotypes
2020
Sumaya Alkanderi
Professor John Sayer
Novel
CYP24A1
Mutation in a Young Male Patient with Nephrolithiasis: Case Report
2019
Dr Elisa Molinari
Dr Simon Ramsbottom
Dr Shalabh Srivastava
Philip Booth
Sumaya Alkanderi
et al.
Targeted exon skipping rescues ciliary protein composition defects in Joubert syndrome patient fibroblasts
2019
Sumaya Alkanderi
Dr Elisa Molinari
Veronica Sammut
Dr Simon Ramsbottom
Dr Shalabh Srivastava
et al.
ARL3
Mutations Cause Joubert Syndrome by Disrupting Ciliary Protein Composition
2018
Dr Noel Edwards
Sumaya Alkanderi
Professor John Sayer
Acidosis and Deafness in Patients with Recessive Mutations in FOXI1
2018
Dr Elisa Molinari
Dr Holly Mabillard
Dr Shalabh Srivastava
Dr Katrina Wood
Sumaya Alkanderi
et al.
Human urine-derived renal epithelial cells provide insights into kidney-specific alternate splicing variants
2018
Dr Simon Ramsbottom
Dr Elisa Molinari
Dr Shalabh Srivastava
Sumaya Alkanderi
Laura Devlin
et al.
Targeted exon skipping of a
CEP290
mutation rescues Joubert syndrome phenotypes in vitro and in a murine model
2018
Dr Simon Ramsbottom
Dr Elisa Molinari
Dr Shalabh Srivastava
Sumaya Alkanderi
Laura Devlin
et al.
Targeted exon skipping of a CEP290 mutation rescues Joubert syndrome phenotypes in vitro and in a murine model
2018
Dr Shalabh Srivastava
Dr Simon Ramsbottom
Dr Elisa Molinari
Sumaya Alkanderi
Professor Andrew Filby
et al.
A human patient-derived cellular model of Joubert syndrome reveals ciliary defects which can be rescued with targeted therapies
2017
Sumaya Alkanderi
Dr Laura Yates
Dr Sally Johnson
Professor John Sayer
Lessons learned from a multidisciplinary renal genetics clinic
2017