Browsing by Author Baird, Paul

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Issue DateTitleAuthor(s)Citation
2008Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic peopleMitchell, Ronald (Paul); Wang, Jie Jin; Baird, Paul; Burdon, Kathryn P; Craig, Jamie E.; Dimasi, David P; Hewitt, Alex W.; Mackey, David A.; Sharma, Shiwani; Western Clinical School: Westmead Millennium Institute; Western Clinical School: Westmead Millennium InstituteAncestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic people, Human Molecular Genetics, vol.17,(5),2008,pp 710-716
2009Fine mapping linkage analysis identifies a novel susceptibility locus for myopia on chromosome 2q37 adjacent to but not overlapping MYP12Mitchell, Paul; Baird, Paul; Chen, Christine Yi-Chin; Dirani, M; Pertile, Kelly Kathleen; Richardson, Andrea Jane; Schache, Maria; Western Clinical School: Westmead Millennium InstituteFine mapping linkage analysis identifies a novel susceptibility locus for myopia on chromosome 2q37 adjacent to but not overlapping MYP12, Molecular Vision, vol.15, N/A, 2009,pp 722-730
2013A rare functional haplotype of the P2RX4 and P2RX7 genes leads to loss of innate phagocytosis and confers increased risk of age-related macular degenerationFuller, Stephen; Skarratt, Kristen; Wiley, James; Baird, Paul; Fletcher, Erica; Gu, Ben; Guymer, Robyn; Richardson, Andrea; Vessey, Kirstan; Nepean Clinical School: Medicine; Nepean Clinical School: Medicine; Nepean Clinical School: MedicineA rare functional haplotype of the P2RX4 and P2RX7 genes leads to loss of innate phagocytosis and confers increased risk of age-related macular degeneration, The FASEB Journal, vol.27, 4, 2013,pp 1479-1487