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Author #30958
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Craig JE
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Craig JE
79708
Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Lahola-Chomiak AA
Human Molecular Genetics
2019; 28: 1298-1311
79962
Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Siggs OM
JAMA ophthalmology
2019; 137: 348-355
79816
Prevalence and type of artefact with spectral domain optical coherence tomography macular ganglion cell imaging in glaucoma surveillance
Awadalla MS
PLoS ONE
2018; 13: e0206684
79962
Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Souzeau E
JAMA ophthalmology
2019; 137: 348-355
79816
Prevalence and type of artefact with spectral domain optical coherence tomography macular ganglion cell imaging in glaucoma surveillance
Fitzgerald J
PLoS ONE
2018; 13: e0206684
79708
Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Footz T; Nguyen-Phuoc K
Human Molecular Genetics
2019; 28: 1298-1311
79962
Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Pasutto F
JAMA ophthalmology
2019; 137: 348-355
79816
Prevalence and type of artefact with spectral domain optical coherence tomography macular ganglion cell imaging in glaucoma surveillance
Andrew NH; Zhou T
PLoS ONE
2018; 13: e0206684
79708
Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Neil GJ
Human Molecular Genetics
2019; 28: 1298-1311
79962
Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Dubowsky A; Smith JEH
JAMA ophthalmology
2019; 137: 348-355
79708
Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Fan B
Human Molecular Genetics
2019; 28: 1298-1311
79816
Prevalence and type of artefact with spectral domain optical coherence tomography macular ganglion cell imaging in glaucoma surveillance
Marshall H; Qassim A
PLoS ONE
2018; 13: e0206684
79708
Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Allen KF
Human Molecular Genetics
2019; 28: 1298-1311
79962
Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Taranath D
JAMA ophthalmology
2019; 137: 348-355
79816
Prevalence and type of artefact with spectral domain optical coherence tomography macular ganglion cell imaging in glaucoma surveillance
Hassall M
PLoS ONE
2018; 13: e0206684
79708
Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Greenfield DS
Human Molecular Genetics
2019; 28: 1298-1311
79962
Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Pater J
JAMA ophthalmology
2019; 137: 348-355
79708
Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Parrish RK
Human Molecular Genetics
2019; 28: 1298-1311
79962
Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Rait JL
JAMA ophthalmology
2019; 137: 348-355
79816
Prevalence and type of artefact with spectral domain optical coherence tomography macular ganglion cell imaging in glaucoma surveillance
Casson RJ; Graham SL
PLoS ONE
2018; 13: e0206684
79962
Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Narita A
JAMA ophthalmology
2019; 137: 348-355
79708
Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Linkroum K
Human Molecular Genetics
2019; 28: 1298-1311
79962
Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma
Mauri L
JAMA ophthalmology
2019; 137: 348-355
79816
Prevalence and type of artefact with spectral domain optical coherence tomography macular ganglion cell imaging in glaucoma surveillance
Healey PR
PLoS ONE
2018; 13: e0206684
79708
Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucoma
Pasquale LR
Human Molecular Genetics
2019; 28: 1298-1311
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