Walid El‐Sayed

Mutations in CNNM4 Cause Jalili Syndrome, Consisting of Autosomal-Recessive Cone-Rod Dystrophy and Amelogenesis Imperfecta

David Parry, Alan J. Mighell, Walid El‐Sayed et al. · The American Journal of Human Genetics · 2009 · 166 citations · Full text

Mutations in the Beta Propeller WDR72 Cause Autosomal-Recessive Hypomaturation Amelogenesis Imperfecta

Walid El‐Sayed, David Parry, Mushtaq Ahmed et al. · The American Journal of Human Genetics · 2009 · 158 citations · Full text

Genetics, Pathology, Molecular Genetics +17

Mutations in C4orf26, Encoding a Peptide with In Vitro Hydroxyapatite Crystal Nucleation and Growth Activity, Cause Amelogenesis Imperfecta

David Parry, Steven J. Brookes, Clare V. Logan et al. · The American Journal of Human Genetics · 2012 · 100 citations · Full text

Mutations in the pH-Sensing G-protein-Coupled Receptor GPR68 Cause Amelogenesis Imperfecta

David Parry, Claire E. L. Smith, Walid El‐Sayed et al. · The American Journal of Human Genetics · 2016 · 71 citations · Full text

Whole-exome sequencing, without prior linkage, identifies a mutation in LAMB3 as a cause of dominant hypoplastic amelogenesis imperfecta

James A. Poulter, Walid El‐Sayed, Jennifer Kirkham et al. · European Journal of Human Genetics · 2013 · 69 citations · Full text

Family Members, Genetics, Genetic Epidemiology +16