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Allingham RR 24
Showing records 1 to 24 | Display all abstracts from Allingham RR60513 A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome
Aung T
Nature Genetics 2015; 47: 387-392
60445 The genetics of POAG in black South Africans: a candidate gene association study
Williams SE
Scientific reports 2015; 5: 8378
60754 Mathematical Modeling of Outflow Facility Increase With Trabecular Meshwork Bypass and Schlemm Canal Dilation
Yuan F
Journal of Glaucoma 2016; 25: 355-364
60170 Association of common SIX6 polymorphisms with peripapillary retinal nerve fiber layer thickness: the Singapore Chinese Eye Study
Cheng CY
Investigative Ophthalmology and Visual Science 2015; 56: 478-483
60513 A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome
Ozaki M
Nature Genetics 2015; 47: 387-392
60754 Mathematical Modeling of Outflow Facility Increase With Trabecular Meshwork Bypass and Schlemm Canal Dilation
Schieber AT
Journal of Glaucoma 2016; 25: 355-364
60445 The genetics of POAG in black South Africans: a candidate gene association study
Carmichael TR
Scientific reports 2015; 5: 8378
60170 Association of common SIX6 polymorphisms with peripapillary retinal nerve fiber layer thickness: the Singapore Chinese Eye Study
Allingham RR; Aung T
Investigative Ophthalmology and Visual Science 2015; 56: 478-483
60754 Mathematical Modeling of Outflow Facility Increase With Trabecular Meshwork Bypass and Schlemm Canal Dilation
Camras LJ
Journal of Glaucoma 2016; 25: 355-364
60445 The genetics of POAG in black South Africans: a candidate gene association study
Allingham RR
Scientific reports 2015; 5: 8378
60513 A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome
Mizoguchi T
Nature Genetics 2015; 47: 387-392
60445 The genetics of POAG in black South Africans: a candidate gene association study
Hauser M
Scientific reports 2015; 5: 8378
60754 Mathematical Modeling of Outflow Facility Increase With Trabecular Meshwork Bypass and Schlemm Canal Dilation
Harasymowycz PJ
Journal of Glaucoma 2016; 25: 355-364
60513 A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome
Allingham RR
Nature Genetics 2015; 47: 387-392
60170 Association of common SIX6 polymorphisms with peripapillary retinal nerve fiber layer thickness: the Singapore Chinese Eye Study
Tham YC; Hauser MA
Investigative Ophthalmology and Visual Science 2015; 56: 478-483
60445 The genetics of POAG in black South Africans: a candidate gene association study
Ramsay M
Scientific reports 2015; 5: 8378
60513 A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome
Li Z
Nature Genetics 2015; 47: 387-392
60754 Mathematical Modeling of Outflow Facility Increase With Trabecular Meshwork Bypass and Schlemm Canal Dilation
Herndon LW; Allingham RR
Journal of Glaucoma 2016; 25: 355-364
60170 Association of common SIX6 polymorphisms with peripapillary retinal nerve fiber layer thickness: the Singapore Chinese Eye Study
Vithana EN
Investigative Ophthalmology and Visual Science 2015; 56: 478-483
60513 A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome
Haripriya A; Nakano S
Nature Genetics 2015; 47: 387-392
60170 Association of common SIX6 polymorphisms with peripapillary retinal nerve fiber layer thickness: the Singapore Chinese Eye Study
Khor CC
Investigative Ophthalmology and Visual Science 2015; 56: 478-483
60513 A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome
Uebe S
Nature Genetics 2015; 47: 387-392
60170 Association of common SIX6 polymorphisms with peripapillary retinal nerve fiber layer thickness: the Singapore Chinese Eye Study
Wong TY
Investigative Ophthalmology and Visual Science 2015; 56: 478-483
60513 A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome
Harder JM; Chan AS; Lee MC; Burdon KP; Astakhov YS; Abu-Amero KK; Zenteno JC; Nilgün Y; Zarnowski T; Pakravan M; Safieh LA; Jia L; Wang YX; Williams S; Paoli D; Schlottm
Nature Genetics 2015; 47: 387-392