| A mutation of EPT1 (SELENOI) underlies a new disorder of Kennedy pathway phospholipid biosynthesis MY Ahmed, A Al-Khayat, F Al-Murshedi, A Al-Futaisi, BA Chioza, ... Brain 140 (3), 547-554, 2017 | 88 | 2017 |
| PRUNE is crucial for normal brain development and mutated in microcephaly with neurodevelopmental impairment M Zollo, M Ahmed, V Ferrucci, V Salpietro, F Asadzadeh, M Carotenuto, ... Brain 140 (4), 940-952, 2017 | 73 | 2017 |
| Loss of PCLO function underlies pontocerebellar hypoplasia type III MY Ahmed, BA Chioza, A Rajab, K Schmitz-Abe, A Al-Khayat, S Al-Turki, ... Neurology 84 (17), 1745-1750, 2015 | 62 | 2015 |
| Biallelic mutations of Prune-1 are causing PEHO-like syndrome with microcephaly and neurodevelopmental impairment V Ferrucci, V Salpietro, F Asadzadeh, J Jemielity, F Pennino, M Ahmed, ... EUROPEAN JOURNAL OF HUMAN GENETICS 26, 60-61, 2018 | | 2018 |
| Defining the genetic basis of three novel neurodevelopmental disorders identified in families from Oman MY Ahmed St George's, University of London, 2017 | | 2017 |
