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Clinical and Epidemiologic Research July 2015

Time Outdoors and Myopia Progression Over 2 Years in Chinese Children: The Anyang Childhood Eye Study

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Shi-Ming Li; He Li; Si-Yuan Li; Luo-Ru Liu; Meng-Tian Kang; Yi-Peng Wang; Fengju Zhang; Si-Yan Zhan; Bamini Gopinath; Paul Mitchell; Ningli Wang; for the Anyang Childhood Eye Study Group
TAGS: child, chinese people, eye, myopia, cohort studies
Invest. Ophthalmol. Vis. Sci.. 2015; 56(8):4734-4740. doi: https://doi.org/10.1167/iovs.14-15474

ARVO Annual Meeting Abstract April 2014

APLP2 Regulates Refractive Error and Myopia Development in Mice and Humans

Andrei V Tkatchenko; Tatiana V Tkatchenko; Virginie JM Verhoeven; Pirro G Hysi; Pawan Kumar Singh; Ashok Kumar; Jeremy A Guggenheim; Cathy Williams; Consortium for Refractive Error and Myopia (CREAM), Avon Longitudinal Study of Parents and Children (ALSPAC)

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):4568. doi:

ARVO Annual Meeting Abstract April 2014

Next-Generation Exome Sequencing of Primary Congenital Glaucoma (PCG) Families

Roshanak Sharafieh; Peng Khaw; Brian W Fleck; Mustafa E Turacli; Francesc Lopez-Giraldez; Kaya Bilguvar; Richard P Lifton; Shrikant Mane; Anne H Child; Mansoor Sarfarazi

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):3808. doi:

ARVO Annual Meeting Abstract April 2014

Exome Sequencing of Familial and Sporadic Cases with Pseudoexfoliation Syndrome (XFS)

Mansoor Sarfarazi; Roshanak Sharafieh; Robert Ritch; Jeffrey M Liebmann; Ahti Tarkkanen; Francesc Lopez-Giraldez; Kaya Bilguvar; Richard P Lifton; Shrikant Mane; Anne H Child

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):3815. doi:

ARVO Annual Meeting Abstract June 2013

A study on visual status in children with autistic spectral disease at Shraddha Center in Hyderabad City

Shata Roopa reddy Pebbeti; Kiran Challa; Gowthami Vatti; Priyanka Jagana; Geeta Vemuganti; Autistic Children

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):5122. doi:

ARVO Annual Meeting Abstract June 2013

Ophthalmic abnormalities in children with Developmental Coordination Disorder: Data from the Avon Longitudinal Study of Parents and Children

Alex Creavin; Raghu Lingam; Kate Northstone; Cathy Williams; Avon Longitudinal Study of Parents and Children

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):5671. doi:

ARVO Annual Meeting Abstract June 2013

Peripheral Refraction in a Population of Schoolage Children in Central China: the Anyang Childhood Eye Study

Shi-Ming Li; Si-Yuan Li; Ningli Wang; Paul Mitchell; Anyang Childhood Eye Study (ACES) group

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):5703. doi:

Genetics July 2012

A Genotype-Phenotype Comparison of ADAMTSL4 and FBN1 in Isolated Ectopia Lentis

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Aman Chandra; Jose A. Aragon-Martin; Kathryn Hughes; Sabiha Gati; M. Ashwin Reddy; Charu Deshpande; Graham Cormack; Anne H. Child; David G. Charteris; Gavin Arno
TAGS: ectopia lentis, genotype, mutation, phenotype, cornea, cohort studies, eye
Invest. Ophthalmol. Vis. Sci.. 2012; 53(8):4889-4896. doi: https://doi.org/10.1167/iovs.12-9874

ARVO Annual Meeting Abstract April 2011

Genotype-phenotype Correlation In Fibrillin-1 And ADAMTSL4 Ectopia Lentis

Aman Chandra; Kathryn Hughes; Gavin Arno; Jan Poloniecki; David Charteris; Anne Child

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):2766. doi:

ARVO Annual Meeting Abstract April 2011

Association Study of American and British Normal-Tension Glaucoma Subjects with SRBD1 and ELOVL5 Gene Polymorphisms

Roshanak Sharafieh; Robert Ritch; Jeffrey M. Liebmann; Anne H. Child; Mansoor Sarfarazi

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):2415. doi:

ARVO Annual Meeting Abstract April 2011

Genetic Screening Of Ectopia Lentis Patients For Mutations In ADAMTSL4, ADAMTS17 and LTBP2

Anne H. Child; Jose A. Aragon-Martin; Kathryn B. Hughes; Roshanak Sharafieh; David Charteris; Gavin Arno

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):3932. doi:

ARVO Annual Meeting Abstract April 2010

Impact of LTBP2 Gene Variations on Primary Congenital Glaucoma

R. Sharafieh; A. Child; M. Sarfarazi

Invest. Ophthalmol. Vis. Sci.. 2010; 51(13):2183. doi:

ARVO Annual Meeting Abstract April 2010

Role of ADAMTSL4 Mutations in FBN1 Mutation Negative Ectopia Lentis Patients

A. H. Child; J. A. Aragon-Martin; D. Ahnood; D. Charteris; A. Saggar; G. Arno

Invest. Ophthalmol. Vis. Sci.. 2010; 51(13):4770. doi:

ARVO Annual Meeting Abstract April 2009

Analysis of Loxl1 Polymorphisms in Age-Related Sensorineural Hearing Loss

A. J. Kim; J. Aragon-Martin; R. Ritch; J. M. Liebmann; A. Child; M. Sarfarazi

Invest. Ophthalmol. Vis. Sci.. 2009; 50(13):887. doi:

ARVO Annual Meeting Abstract April 2009

Targeted Gene Association Studies of Primary Open Angle Glaucoma (POAG) at the GLC1B Locus

R. Sharafieh; A. Child; M. Sarfarazi

Invest. Ophthalmol. Vis. Sci.. 2009; 50(13):893. doi:

ARVO Annual Meeting Abstract April 2009

The Role of Fibrillin-1 Mutations in Families With Dominantly Inherited Ectopia Lentis

A. H. Child; D. Ahnood; P. Comeglio; L. Ocaka; D. Charteris; G. Arno

Invest. Ophthalmol. Vis. Sci.. 2009; 50(13):4115. doi:

ARVO Annual Meeting Abstract May 2008

Genetic Screening of LOXL1 in Exfoliation Glaucoma

J. A. Aragon-Martin; R. Ritch; J. Liebmann; C. O’Brien; K. Blaaow; F. Mercieca; K. Damji; T. Rezaie; A. Child; M. Sarfarazi

Invest. Ophthalmol. Vis. Sci.. 2008; 49(13):5868. doi:

ARVO Annual Meeting Abstract May 2007

Candidate Gene Screening of Primary Open Angle Glaucoma (POAG) at the GLC1C Locus

J. A. Aragon-Martin; A. Child; G. Brice; M. Sarfarazi

Invest. Ophthalmol. Vis. Sci.. 2007; 48(13):4036. doi:

ARVO Annual Meeting Abstract May 2007

Is WDR36 a Modifying Gene for Myocilin?

S. Monemi; A. Child; M. Sarfarazi

Invest. Ophthalmol. Vis. Sci.. 2007; 48(13):5592. doi:

ARVO Annual Meeting Abstract May 2007

Utilization of Genomic Convergence and Proteomic Streamlining Strategies for Selection and Mutation Screening of POAG Candidate Genes at the GLC1B Locus

R. Sharafieh; A. Child; M. Sarfarazi

Invest. Ophthalmol. Vis. Sci.. 2007; 48(13):5613. doi:

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Time Outdoors and Myopia Progression Over 2 Years in Chinese Children: The Anyang Childhood Eye Study

APLP2 Regulates Refractive Error and Myopia Development in Mice and Humans

Next-Generation Exome Sequencing of Primary Congenital Glaucoma (PCG) Families

Exome Sequencing of Familial and Sporadic Cases with Pseudoexfoliation Syndrome (XFS)

A study on visual status in children with autistic spectral disease at Shraddha Center in Hyderabad City

Ophthalmic abnormalities in children with Developmental Coordination Disorder: Data from the Avon Longitudinal Study of Parents and Children

Peripheral Refraction in a Population of Schoolage Children in Central China: the Anyang Childhood Eye Study

A Genotype-Phenotype Comparison of ADAMTSL4 and FBN1 in Isolated Ectopia Lentis

Genotype-phenotype Correlation In Fibrillin-1 And ADAMTSL4 Ectopia Lentis

Association Study of American and British Normal-Tension Glaucoma Subjects with SRBD1 and ELOVL5 Gene Polymorphisms

Genetic Screening Of Ectopia Lentis Patients For Mutations In ADAMTSL4, ADAMTS17 and LTBP2

Impact of LTBP2 Gene Variations on Primary Congenital Glaucoma

Role of ADAMTSL4 Mutations in FBN1 Mutation Negative Ectopia Lentis Patients

Analysis of Loxl1 Polymorphisms in Age-Related Sensorineural Hearing Loss

Targeted Gene Association Studies of Primary Open Angle Glaucoma (POAG) at the GLC1B Locus

The Role of Fibrillin-1 Mutations in Families With Dominantly Inherited Ectopia Lentis

Genetic Screening of LOXL1 in Exfoliation Glaucoma

Candidate Gene Screening of Primary Open Angle Glaucoma (POAG) at the GLC1C Locus

Is WDR36 a Modifying Gene for Myocilin?

Utilization of Genomic Convergence and Proteomic Streamlining Strategies for Selection and Mutation Screening of POAG Candidate Genes at the GLC1B Locus

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