Self, Jay - University of Southampton

个人简介

Mr Self is a joint Academic/Clinical Ophthalmologist who works as a Consultant Ophthalmologist at Southampton General Hospital and runs a group at the University of Southampton as an Associate Professor. He completed his higher specialist training in Paediatric Ophthalmology in Southampton and Manchester and his research training through an MRC Clinical Research Training Fellowship/PhD in Ophthalmic Molecular Genetics. He has an interest in translation of basic science findings into clinical practice in Paediatric Ophthalmology and has published widely in addition to writing book chapters and documents for the Royal College of Ophthalmologists. He is a medical advisor for 3 charities, is a board member for a third and sits on the University Hospital Southampton charity committee. He has a particular research interest in nystagmus and genetic eye diseases and has a focus on improving the lives of children and families with eye disease. He also works with both local and national community groups and schools in order to promote public awareness of eye diseases affecting children. Mr Self is a joint Academic/Clinical Ophthalmologist who works as a Consultant Paediatric Ophthalmologist at Southampton General Hospital and as a Senior Lecturer at the University of Southampton. He completed his higher specialist training in Paediatric Ophthalmology in Southampton and Manchester and his research training through an MRC Clinical Research Training Fellowship/PhD in Ophthalmic Molecular Genetics. He has an interest in translation of basic science findings into clinical practice in Paediatric Ophthalmology and has published widely in addition to writing book chapters and documents for the Royal College of Ophthalmologists. He is a medical advisor for two charities and as a board member for a third. He has a particular research focus in the group of disorders collectively termed congenital Nystagmus and utilizes genetic techniques, eye tracking technology and modeling to achieve his aim of improving the lives of children and families with this disorder. He also works with both local and national community groups and schools in order to promote public awareness and engagement in science.

研究领域

Mr Self is a Consultant Ophthalmologist and a Senior Lecturer. As a clinical academic he is particularly interested in translation of research findings into meaningful benefit for his patients. He has a particular clinical interest in paediatric genetic eye disease including nystagmus and congenital cataract. His research interests are accordingly tailored towards nystagmus and translational genetics and he continues to prioritize his research according to the needs as identified by patients through his work with three vision support charities and his dedication to a public engagement in science program. He benefits from significant collaboration both within the university and the Universities of Plymouth, Bristol, Cardiff, Manchester and worldwide.

近期论文

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Mutation of EPT1 (SELENOI) underlies a new disorder of Kennedy pathway phospholipid biosynthesis - Ahmed, Mustafa Y., Al-Khayat, Aisha, Al-Murshedi, Fathiya, Al-Futaisi, Amna, Choiza, Barry A., Fernandez-Murray, Pedro, Self, Jay E., Salter, Claire G., Harlalka, Gaurav V., Rawlins, Lettie E., Al-Zuhaibi, Sana, Al-Azri, Faisal, Al-Rashdi, Fatma, Cazenave Gassiot, Amaury, Wenk, Marcus R., Al-Salmi, Fatema, Patton, Michael A., Silver, David L., Baple, Emma L., McMaster, Christopher R. and Crosby, Andrew H. Published:2017Publication:BrainPage Range:1-8doi:10.1093/brain/aww318 The emerging ophthalmological phenotype of XXYY syndrome - Ashraf, Tazeen, Shalaby, Ahmed, Mercer, Catherine, Bolton, Kate and Self, James Published:2016Publication:Journal of Clinical & Experimental OphthalmologyPage Range:1-9 Is an iris claw IOL a good option for correcting surgically induced aphakia in children? A review of the literature and illustrative case study - Self, James, Barbara, Ramez, Tan, Nicole and Rufai, Sohaib Published:2016Publication:EyeVolume:30, (9)Page Range:1155-1159doi:10.1038/eye.2016.140PMID:27391934 Expanding the ocular phenotype of 14q terminal deletions: a novel presentation of microphthalmia and coloboma in ring 14 syndrome with associated 14q32.31 deletion and review of the literature - Salter, Claire G., Baralle, Diana, Collinson, Morag N. and Self, James E. Published:2016Publication:American Journal of Medical Genetics Part AVolume:170, (4)Page Range:1017-1022doi:10.1002/ajmg.a.37436PMID:26773965