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Meeting Abstract (13)
Journal Articles (2)

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Investigative Ophthalmology & Visual Science (15)

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ARVO Annual Meeting Abstract (13)
Biochemistry and Molecular Biology (2)

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Biochemistry and Molecular Biology (2)
Genetics (2)
Eye Anatomy and Disorders (1)
Retina (1)

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leber's amaurosis (2)
mutation (2)
alleles (1)
cohort studies (1)
genes (1)
genotype determination (1)
phenotype (1)
screening (1)

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ARVO Annual Meeting Abstract September 2016

BMP-7 Activation of Microglia Drives Reactive Retinal Gliosis

Subramanian Dharmarajan; Nader Sheibani; Teri L Belecky-Adams

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):2223. doi:

ARVO Annual Meeting Abstract June 2013

BMP7 CAN ACT AS A TRIGGER OF REACTIVE GLIOSIS IN MULLER GLIA

Subramanian Dharmarajan; Nader Sheibani; Teri Belecky-Adams

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):5592. doi:

ARVO Annual Meeting Abstract March 2012

Bmp Pathway And Retinal Astrogliosis

Subramanian Dharmarajan; Teri Belecky- Adams; Nader Sheibani

Invest. Ophthalmol. Vis. Sci.. 2012; 53(14):2013. doi:

ARVO Annual Meeting Abstract May 2006

Adjustable Sutures In The Correction Of Dysthyroid Vertical Deviation

S. Dharmaraj; C. Mocan; R. Ahuja; C. Kloek; N. Azar

Invest. Ophthalmol. Vis. Sci.. 2006; 47(13):2480. doi:

ARVO Annual Meeting Abstract May 2006

Genetic Basis of Extreme Hyperopia

O.H. Sundin; I.A. Bhutto; T. Hasegawa; G.A. Lutty; C.F. Parsa; I.H. Maumenee; E.D. Silva; E.I. Traboulsi; S. Dharmaraj

Invest. Ophthalmol. Vis. Sci.. 2006; 47(13):3137. doi:

Biochemistry and Molecular Biology September 2005

Genotyping Microarray (Disease Chip) for Leber Congenital Amaurosis: Detection of Modifier Alleles

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Jana Zernant; Maigi Külm; Sharola Dharmaraj; Anneke I. den Hollander; Isabelle Perrault; Markus N. Preising; Birgit Lorenz; Josseline Kaplan; Frans P. M. Cremers; Irene Maumenee; Robert K. Koenekoop; Rando Allikmets
TAGS: alleles, genes, genotype determination, leber's amaurosis, screening, cohort studies, mutation
Invest. Ophthalmol. Vis. Sci.. 2005; 46(9):3052-3059. doi: https://doi.org/10.1167/iovs.05-0111

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ARVO Annual Meeting Abstract May 2005

Retinal Findings and Docosahexanoic Acid (DHA) Therapy in Peroxisomal Disorders

S. Dharmaraj; E. Silva; G. Raymond; J. Sunness; I. Maumenee

Invest. Ophthalmol. Vis. Sci.. 2005; 46(13):4083. doi:

ARVO Annual Meeting Abstract May 2004

MULTIALLELIC INHERITANCE AND/OR MODIFIER ALLELES IN LEBER CONGENITAL AMAUROSIS: ANALYSIS WITH THE LCA DISEASE CHIP

R.L. Allikmets; J. Zernant; I. Perrault; A. den Hollander; S. Dharmaraj; F.P. M. Cremers; J. Kaplan; R.K. Koenekoop; I. Maumenee

Invest. Ophthalmol. Vis. Sci.. 2004; 45(13):2444. doi:

ARVO Annual Meeting Abstract May 2004

Recessive RPGRIP1 mutations can cause rod and cone dysfunction in the heterozygous parents.

S. Dharmaraj; I. Lopez; G. Fishman; J. Racine; A. Dorfman; P. Lachapelle; I. Maumenee; F. Cremers; R. Allikmets; R. Koenekoop

Invest. Ophthalmol. Vis. Sci.. 2004; 45(13):4728. doi:

ARVO Annual Meeting Abstract May 2004

Monogenic inheritance of Leber congenital amaurosis: causation by a novel mutation in CRB1.

H. Abouzeid; Y. Li; S. Dharmaraj; O. Sundin; I. Maumenee

Invest. Ophthalmol. Vis. Sci.. 2004; 45(13):4730. doi:

ARVO Annual Meeting Abstract May 2003

Analysis of CRX Mutations in LCA Patients

S. Dharmaraj; Y. Li; H. Abouzeid; E. Silva; X. Yao; R.K. Koenekoop; S. Chen; O. Sundin; R. Allikmets; I.H. Maumenee

Invest. Ophthalmol. Vis. Sci.. 2003; 44(13):2302. doi:

ARVO Annual Meeting Abstract May 2003

Mutations in the Gene Encoding RPE65 in Patients With Leber Congenital Amaurosis (LCA)

S. Yao; S. Dharmaraj; T. Millender-Swain; M. ElCherbini; I.H. Maumenee

Invest. Ophthalmol. Vis. Sci.. 2003; 44(13):2303. doi:

ARVO Annual Meeting Abstract May 2003

Genotyping Microarray (Disease Chip) for Leber Congenital Amaurosis

R.L. Allikmets; J. Zernant; M. Külm; I. Perrault; A. den Hollander; S. Dharmaraj; R. Koenekoop; J. Kaplan; F. Cremers; I. Maumenee

Invest. Ophthalmol. Vis. Sci.. 2003; 44(13):2851. doi:

ARVO Annual Meeting Abstract December 2002

Analysis of Developmental Genes in LCA Patients with CRX Mutations and Genotype-Phenotype Correlation

S Dharmaraj; S Bumgarner; Y Li; E Silva; M Loyer; J Yang; RK Koenekoop; O Sundin; IH Maumenee

Invest. Ophthalmol. Vis. Sci.. 2002; 43(13):1186. doi:

Biochemistry and Molecular Biology July 2000

A CRX Null Mutation Is Associated with Both Leber Congenital Amaurosis and a Normal Ocular Phenotype

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Eduardo Silva; Jun-Ming Yang; Yingying Li; Sharola Dharmaraj; Olof H. Sundin; Irene H. Maumenee
TAGS: leber's amaurosis, mutation, phenotype
Invest. Ophthalmol. Vis. Sci.. 2000; 41(8):2076-2079. doi:

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Online ISSN: 1552-5783

Investigative Ophthalmology & Visual Science
Journal of Vision
Translational Vision Science & Technology

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