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The Newcastle University research output collection, currently available on ePrints, will shortly be moving to a new open repository platform, Figshare. To prepare for the data migration we have paused adding new content to ePrints, and will resume once the new repository is launched. During this time you will continue to have access to ePrints (but no new content will appear). We will share updates here when available.

Browsing publications by Mohamed Al-Hamed

Newcastle AuthorsTitleYearFull text
Ruxandra Neatu
Mohamed Al-Hamed
Professor John Sayer
Network-based framework for studying etiology and phenotypic diversity in primary ciliopathies2026
Mohamed Al-Hamed
Professor John Sayer
Novel loss of function variants in FRAS1 AND FREM2 underlie renal agenesis in consanguineous families2021
Mohamed Al-Hamed
Professor John Sayer
Fetal anomalies associated with novel pathogenic variants in TMEM942020
Mohamed Al-Hamed
Dr Sarah Rice
Dr Noel Edwards
Professor John Sayer
Bialleleic PKD1 mutations underlie early-onset autosomal dominant polycystic kidney disease in Saudi Arabian families2019
Mohamed Al-Hamed
Professor John Sayer
Renal tubular dysgenesis: antenatal ultrasound scanning and molecular investigations in a Saudi Arabian family2016
Dr Noel Edwards
Dr Sarah Rice
Dr Ann Marie Hynes
Dr Shalabh Srivastava
Dr Iain Moore
et al.
A novel LMX1B mutation in a family with end-stage renal disease of ‘unknown cause’2015
Mohamed Al-Hamed
Dr Charles van Lennep
Dr Ann Marie Hynes
Paul Chrystal
Dr Lorraine Eley
et al.
Functional modelling of a novel mutation in BBS52014
Mohamed Al-Hamed
ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption2013
Dr Shalabh Srivastava
Dr Noel Edwards
Dr Ann Marie Hynes
Dr Katrina Wood
Mohamed Al-Hamed
et al.
Identification of compound heterozygous KCNJ1 mutations (Encoding ROMK) in a kindred with bartter’s syndrome and a functional analysis of their pathogenicity2013
Mohamed Al-Hamed
Dr Roslyn Simms
Professor John Sayer
Investigating Bardet Biedl syndrome: identification and modelling of a novel mutation in BBS52012
Mohamed Al-Hamed
Professor John Sayer
A novel mutation in NPHS2 causing nephrotic syndrome in a Saudi Arabian family2010
Mohamed Al-Hamed
Professor John Sayer
A Novel Mutation in NPHS2 Causing Steroid Resistant Nephrotic Syndrome in a Saudi Arabian Family2009