Mohamed Al-Hamed Professor John Sayer
| Novel loss of function variants in FRAS1 AND FREM2 underlie renal agenesis in consanguineous families | 2021 |
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Mohamed Al-Hamed Professor John Sayer
| Fetal anomalies associated with novel pathogenic variants in TMEM94 | 2020 |
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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 families | 2019 |
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Mohamed Al-Hamed Professor John Sayer
| Renal tubular dysgenesis: antenatal ultrasound scanning and molecular investigations in a Saudi Arabian family | 2016 |
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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 |
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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 BBS5 | 2014 |
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Mohamed Al-Hamed
| ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption | 2013 |
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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 pathogenicity | 2013 |
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Mohamed Al-Hamed Dr Roslyn Simms Professor John Sayer
| Investigating Bardet Biedl syndrome: identification and modelling of a novel mutation in BBS5 | 2012 |
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Mohamed Al-Hamed Professor John Sayer
| A novel mutation in NPHS2 causing nephrotic syndrome in a Saudi Arabian family | 2010 |
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Mohamed Al-Hamed Professor John Sayer
| A Novel Mutation in NPHS2 Causing Steroid Resistant Nephrotic Syndrome in a Saudi Arabian Family | 2009 |
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