Work

Understanding the molecular basis and pathogenesis of hereditary optic neuropathies: towards improved diagnosis and management

Year: 2022

Type: review

Source: The Lancet Neurology

DOI: 10.1016/s1474-4422(22)00174-0

Authors: Nancy J Newman, Patrick Yu-Wai-Man, Valérie Biousse, Valerio Carelli

Institutions: Emory University, University of Cambridge, Moorfields Eye Hospital, Addenbrooke's Hospital, University College London, MRC Mitochondrial Biology Unit, Istituto delle Scienze Neurologiche di Bologna, University of Bologna

Language: English

Topic: Hereditary Neurological Disorders

Subfield: Cellular and Molecular Neuroscience

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: bronze

Funders: Research to Prevent Blindness, Fight for Sight, National Institute for Health and Care Research, Sight Research UK, Fondazione Telethon, Ministero della Salute, Ministero dell’Istruzione, dell’Università e della Ricerca, Isaac Newton Trust, Moorfields Eye Hospital NHS Foundation Trust, Moorfields Eye Charity, National Institutes of Health, Manchester Biomedical Research Centre, Medical Research Council, UCL Institute of Ophthalmology, University College London, NIHR Cambridge Biomedical Research Centre, National Eye Institute

Awards: G1221422246, G139696651, G2318304826, Evaluating Patient Outcomes and Therapies for Inherited Optic Neuropathies, G3714030281, G4341238149, Keeping mitochondrial DNA in shape in health and disease: cracking the elusive relationship between the fusion protein OPA1, mitochondrial membrane lipid composition and maintenance of membrane-anchored mtDNA nucleoids, G6831032312, G7715181091, G7989623481

OpenAlex ID: W4296901011

FWCI: 2.639

Cites: 102

Cited by: 96

Related to: 10