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    Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic people 

    Baird, Paul N; Wang, Jie Jin; Mackey, David A; Mitchell, Paul; Sharma, Shiwani; Burdon, Kathryn Penelope; Hewitt, Alex W; Dimasi, David Paul; Craig, Jamie E (2008)
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    The role of the Met98Lys optineurin variant in inherited optic nerve diseases 

    Craig, Jamie E; Hewitt, Alex W; Dimasi, David Paul; Howell, Neil; Toomes, Carmel; Cohn, Amy C; Mackey, David A (2006)
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    Identification of a novel oligomerization disrupting mutation in CRYAA associated with congenital cataract in a South Australian family 

    Laurie, Kate; Dave, Alpana; Straga, Tania; Souzeau, Emmanuelle; Chataway, Timothy Kennion; Sykes, Matthew James; Casey, Theresa; Teo, Theodosia; Pater, John Brian; Craig, Jamie E; Sharma, Shiwani; Burdon, Kathryn Penelope (Wiley-Blackwell, 2013-03)
    Congenital cataract is a heterogeneous disorder causing severe visual impairment in affected children. We screened four South Australian families with autosomal dominant congenital cataract for mutations in 10 crystallin ...
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    The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genes 

    McKay, James D; Patterson, B; Russell-Eggit, Isabelle M; Wirth, M Gabriela; Burdon, Kathryn Penelope; Cohn, Amy C; Kerdraon, Y; Mackey, David A; Craig, Jamie E; Hewitt, Alex W (2005)
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    Apparent autosomal dominant keratoconus in a large Australian pedigree accounted for by digenic inheritance of two novel loci 

    Giunta, Cecilia; Hewitt, Alex W; Craig, Jamie E; Latimer, Paul; Burdon, Kathryn Penelope; Coster, Douglas John; Charlesworth, Jac C; Mills, Richard Arthur; Laurie, Kate (2008)
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    A glaucoma case-control study of the WDR36 gene D658G sequence variant 

    Hewitt, Alex W; Mackey, David A; Craig, Jamie E; Dimasi, David Paul (2006)
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    Linkage to 10q22 for maximum intraocular pressure and 1p32 for maximum cup-to-disc ratio in an extended primary open-angle glaucoma pedigree 

    Charlesworth, Jac C; Dyer, Thomas D; Stankovich, Jim M; Blangero, John; Mackey, David A; Craig, Jamie E; Green, Catherine M; Baird, Paul N; Sale, Michele M; Foote, Simon J (2005)
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    Evaluation of optinueurin sequence variations in 1,048 patients with open-angle glaucoma 

    Yamamoto, Tetsuya; Craig, Jamie E; Affatigato, Louisa M; Alward, Wallace L M; Mackey, David A; Kwon, Young H; Johnson, A Tim; Hayreh, Sohan S; Kawase, Kazuhide; Khanna, Cheryl L; Sheffield, Val C; Roos, Benjamin R; Stone, Edwin M (2003)
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    Glaucoma phenotype in pedigrees with the myocilin Thr377Met mutation 

    Wong, T L; Wilkinson, C H; Craig, Jamie E; Mackey, David A; Coote, M A; De Graaf, A P; Fingert, John H; McCartney, Paul J; Healey, D L; Rait, J; Stone, Edwin M (2003)
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    Does the association between TMEM98 and nanophthalmos require further confirmation?-Reply 

    Awadalla, Mona S; Burdon, Kathryn Penelope; Craig, Jamie E (American Medical Association, 2015-03)
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    Craig, Jamie E (162)
    Burdon, Kathryn Penelope (103)Hewitt, Alex W (90)Mackey, David A (82)Souzeau, Emmanuelle (50)Sharma, Shiwani (34)Landers, John (26)Mills, Richard Arthur (24)Mitchell, Paul (24)Dimasi, David Paul (19)... View MoreSubject1113 Ophthalmology and Optometry (58)1103 Clinical Sciences (19)Glaucoma (14)Genetics (12)0604 Genetics (10)Opthalmology (10)1117 Public Health and Health Services (8)1109 Neurosciences (4)Cataract (4)Genome-wide association studies (4)... View MoreDate Issued2010 - 2020 (109)2003 - 2009 (53)

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