- Genetics of ARMD
- Genetics of glaucoma
- Genetics of nystagmus
- Stem cells for retinal / macular disease
- Association for Research in Vision and Ophthalmology (ARVO)
- Macula Society
- British Eye Research Group
- Senior Investigator, National Institute Health Research
Key Publications
- Ennis S, Jomary C, Mullins R, Cree A, Chen X, Macleod A et al.
Association between the SERPING1 gene and age-related macular degeneration: a two-stage case-control study.
Lancet 2008 October 6.
- Goverdhan SV, Khakoo SI, Gaston H, Chen X, Lotery A.
Age related macular degeneration is associated with the HLA Cw*0701 genotype and the Natural Killer cell receptor AA haplotype.
Invest Ophthalmol Vis Sci 2008 May 30.
- Ennis S, Goverdhan S, Cree A, Hoh J, Collins A, Lotery A.
Fine-scale linkage disequilibrium mapping of age-related macular degeneration in the complement factor H gene region.
British Journal of Ophthalmology 2007 July 1;91(7):966-70.
- Lotery AJ, Baas D, Ridley C, Jones RP, Klaver CC, Stone E et al.
Reduced secretion of fibulin 5 in age-related macular degeneration and cutis laxa.
Hum Mutat 2006 June;27(6):568-74.
- Goverdhan SV, Howell MW, Mullins RF, Osmond C, Hodgkins PR, Self J et al.
Association of HLA class I and class II polymorphisms with age-related macular degeneration.
Invest Ophthalmol Vis Sci 2005 May;46(5):1726-34.
- Stone EM, Braun TA, Russell SR, Kuehn MH, Lotery AJ, Moore PA et al.
Missense variations in the fibulin 5 gene and age-related macular degeneration.
N Engl J Med 2004 July 22;351(4):346-53.
- Guymer RH, Heon E, Lotery AJ, Munier FL, Schorderet DF, Baird PN et al.
Variation of codons 1961 and 2177 of the Stargardt disease gene is not associated with age-related macular degeneration.
Arch Ophthalmol 2001 May;119(5):745-51.
- Lotery AJ, Jacobson SG, Fishman GA, Weleber RG, Fulton AB, Namperumalsamy P et al.
Mutations in the CRB1 gene cause Leber congenital amaurosis.
Arch Ophthalmol 2001 March;119(3):415-20.
- Stone EM, Lotery AJ, Munier FL, Heon E, Piguet B, Guymer RH et al.
A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy.
Nat Genet 1999;22(2):199-202.
- Stone EM, Webster AR, Vandenburgh K, Streb LM, Hockey RR, Lotery AJ et al.
Allelic variation in ABCR associated with Stargardt disease but not age-related macular degeneration.
Nat Genet 1998 December;20(4):328-9.
Andrew John Lotery |
Research Group
Laboratory of Cellular and Molecular Pathophysiology of the Retina
Analysis of molecular mechanisms involved in retinal progenitor cell differentiation
Research Groups
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