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ARVO Annual Meeting Abstract June 2020

Scleral cross-linking using Rose Bengal-Green Light

Lupe Ivette Villegas Lopez; David Bronte; James Germann; Susana Marcos

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):3415. doi:

Glaucoma September 2018

Mitochondrial DNA Variation and Disease Susceptibility in Primary Open-Angle Glaucoma

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Larry N. Singh; Jonathan G. Crowston; M. Isabel G. Lopez Sanchez; Nicole J. Van Bergen; Lisa S. Kearns; Alex W. Hewitt; Seyhan Yazar; David A. Mackey; Douglas C. Wallace; Ian A. Trounce
TAGS: disease susceptibility, dna, mitochondrial, glaucoma, open-angle glaucoma
Invest. Ophthalmol. Vis. Sci.. 2018; 59(11):4598-4602. doi: https://doi.org/10.1167/iovs.18-25085

Includes: Supplemental Content

ARVO Annual Meeting Abstract July 2018

A Natural History Study of Visual Function in Patients with Usher Syndrome Type 1C.

Meredith Harrell Hartman; Katelyn N. Robillard; Vincent Sun; Irma Lopez; Mariam Ibrahim; Kelsey Walsdorf; Maria Reinoso; Robert K Koenekoop; Jennifer J Lentz

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):48. doi:

ARVO Annual Meeting Abstract June 2017

CLINICAL PRACTICE IN THE MANAGEMENT OF DIABETIC MACULAR EDEMA. RESULTS FROM A RETINOLOGISTS NATIONAL SURVEY

Isabel Pinilla Lozano; M Isabel Lopez; Rodrigo Abreu; Roberto Gallego-Pinazo; Maximino J Abraldes

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):941. doi:

Genetics February 2017

The Genetic Causes of Nonsyndromic Congenital Retinal Detachment: A Genetic and Phenotypic Study of Pakistani Families

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Vafa Keser; Ayesha Khan; Sorath Siddiqui; Irma Lopez; Huanan Ren; Raheel Qamar; Javad Nadaf; Jacek Majewski; Rui Chen; Robert K. Koenekoop
TAGS: family, genes, genetics, mutation, phenotype, retinal detachment, tissue dissection, homozygote, familial exudative vitreoretinopathies
Invest. Ophthalmol. Vis. Sci.. 2017; 58(2):1028-1036. doi: https://doi.org/10.1167/iovs.16-20281

Genetics February 2017

Analysis of the PRPF31 Gene in Spanish Autosomal Dominant Retinitis Pigmentosa Patients: A Novel Genomic Rearrangement

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Inmaculada Martin-Merida; Rocio Sanchez-Alcudia; Patricia Fernandez-San Jose; Fiona Blanco-Kelly; Raquel Perez-Carro; Luciana Rodriguez-Jacy da Silva; Berta Almoguera; Blanca Garcia-Sandoval; Maria Isabel Lopez-Molina; Almudena Avila-Fernandez; Miguel Carballo; Marta Corton; Carmen Ayuso
TAGS: family, gene rearrangement, genes, mutation, retinitis pigmentosa, spanish, cohort studies
Invest. Ophthalmol. Vis. Sci.. 2017; 58(2):1045-1053. doi: https://doi.org/10.1167/iovs.16-20515

Includes: Supplemental Content

ARVO Annual Meeting Abstract September 2016

Calcified crystalline material in peripheral lymphocytes in choroideremia- a novel discovery

Alice Yang Zhang; Vincent Sun; Hojatollah Vali; Jamie Koenekoop; Kelly Sears; Norma Fajardo; Irma Lopez; Nancy Braverman; Robert K Koenekoop

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):6600. doi:

ARVO Annual Meeting Abstract September 2016

A novel heterozygous mutation in PRPH2/RDS gene causing a spectrum of phenotypic manifestations in a family with autosomal dominant retinitis pigmentosa (adRP)

Fares Antaki; Razek Georges Coussa; Christina Chakarova; Susan Wakil; Vincent Sun; Pierre Lachapelle; Allison Dorfman; Irma Lopez; Kunka Kamenarova; Shomi S Bhattacharya; Robert K Koenekoop

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):127. doi:

ARVO Annual Meeting Abstract September 2016

Albinism in Spain: Current genetic picture

Maria Isabel Lopez Molina; Blanco-Kelly Fiona; Martinez Garcia Monica; Ayuso Carmen; Corton Marta; Trujillo-Tiebas Maria Jose

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):6580. doi:

ARVO Annual Meeting Abstract September 2016

Rapid evaluation of risk factors linked to age-related macular degeneration (AMD): STARS questionnaire

M Isabel Lopez; Alfredo Garcia-Layana; Francisco Gomez Ulla; Jose María Ruiz-Moreno; Marta Suarez Figueroa; Jose-Carlos Pastor

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):3696. doi:

ARVO Annual Meeting Abstract September 2016

Variations in the size of retinal cysts as a tomographic factor predictor for retreatment with Ozurdex in patients with refractory diabetic macular edema

Félix Alexander Manco Lavado; María Rosalba Ramoa Osorio; M Isabel Lopez; Lucía Manzanas Leal; Ignacio Alonso de la Fuente; Mercedes Hernando Verdugo

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):3262. doi:

ARVO Annual Meeting Abstract September 2016

Circulating biomarkers of inflammation, oxidative stress and vascular risk for diabetic retinopathy. Effects of a nutraceutical supplementation in two year follow-up

Maria D Pinazo-Duran; VICENTE C ZANON-MORENO; Silvia M Sanz-Gonzalez; Jose J Garcia-Medina; CARMEN GALBIS-ESTRADA; Elena Bendala-Tufanisco; Rosa Dolz-Marco; M Isabel Lopez; Roberto Gallego-Pinazo

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):5429. doi:

ARVO Annual Meeting Abstract September 2016

Risk factors, clinical characteristics and management of patients with myopic choroidal neovascularization in clinical practice: Mypathway study

Laia Gomez; M Isabel Lopez; Jose María Ruiz-Moreno; Montserrat Roura

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):2479. doi:

Genetics December 2015

Genotype and Phenotype Studies in Autosomal Dominant Retinitis Pigmentosa (adRP) of the French Canadian Founder Population

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Razek Georges Coussa; Christina Chakarova; Radwan Ajlan; Mohammed Taha; Conrad Kavalec; Julius Gomolin; Ayesha Khan; Irma Lopez; Huanan Ren; Naushin Waseem; Kunka Kamenarova; Shomi S. Bhattacharya; Robert K. Koenekoop
TAGS: french, genotype, mutation, phenotype, retinitis pigmentosa, genes, cohort studies
Invest. Ophthalmol. Vis. Sci.. 2015; 56(13):8297-8305. doi: https://doi.org/10.1167/iovs.15-17104

Includes: Supplemental Content

Retina December 2015

Choroideremia Is a Systemic Disease With Lymphocyte Crystals and Plasma Lipid and RBC Membrane Abnormalities

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Alice Yang Zhang; Naveen Mysore; Hojatollah Vali; Jamie Koenekoop; Sang Ni Cao; Shen Li; Huanan Ren; Vafa Keser; Irma Lopez-Solache; Sorath Noorani Siddiqui; Ayesha Khan; Jeannie Mui; Kelly Sears; Jim Dixon; Jeremy Schwartzentruber; Jacek Majewski; Nancy Braverman; Robert K. Koenekoop
TAGS: choroideremia, fatty acids, lipids, lymphocytes, plasma, systemic disease, tissue membrane
Invest. Ophthalmol. Vis. Sci.. 2015; 56(13):8158-8165. doi: https://doi.org/10.1167/iovs.14-15751

ARVO Annual Meeting Abstract June 2015

A possible new gene for cone-rod dystrophy

Si-Liang Peng; Huanan Ren; Norma Fajardo; Irma Lopez; Robert K Koenekoop

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):1780. doi:

ARVO Annual Meeting Abstract June 2015

Systematic Evaluation of Noncoding Mutations in Inherited R etinal D egeneration (RD) Patients with Missing Heritability

Violet Gelowani; Eric Zaneveld; Feng Wang; Jason Scott Salvo; Irma Lopez; Huanan Ren; Ruifang Sui; Robert K Koenekoop; Rui Chen

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):1239. doi:

ARVO Annual Meeting Abstract June 2015

Hypomorphic mutations in CLUAP1 cause Leber congenital amaurosis

Zachry Soens; Yuanyuan Li; Li Zhao; Yumei Li; Zhaoxia Sun; Ayesha Khan; Norma Fajardo; Irma Lopez; Robert K Koenekoop; Rui Chen; Genetics of Leber congenital amaurosis

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):4349. doi:

ARVO Annual Meeting Abstract June 2015

Identification of two novel mutations in CDHR1 in consanguineous Spanish families with autosomal recessive retinal dystrophy

Konstantinos Nikopoulos; Almudena Avila-Fernandez; Marta Corton; Maria Isabel Lopez-Molina; Raquel Perez-Carro; Olga Zurita; Blanca Garcia-Sandoval; Carlo Rivolta; Carmen Ayuso

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):1098. doi:

Genetics April 2015

Targeted Next-Generation Sequencing Improves the Diagnosis of Autosomal Dominant Retinitis Pigmentosa in Spanish Patients

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Patricia Fernandez-San Jose; Marta Corton; Fiona Blanco-Kelly; Almudena Avila-Fernandez; Miguel Angel Lopez-Martinez; Iker Sanchez-Navarro; Rocio Sanchez-Alcudia; Raquel Perez-Carro; Olga Zurita; Noelia Sanchez-Bolivar; Maria Isabel Lopez-Molina; Blanca Garcia-Sandoval; Rosa Riveiro-Alvarez; Carmen Ayuso
TAGS: family, massively-parallel genome sequencing, mutation, retinitis pigmentosa, spanish, genes
Invest. Ophthalmol. Vis. Sci.. 2015; 56(4):2173-2182. doi: https://doi.org/10.1167/iovs.14-16178

Includes: Supplemental Content

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Scleral cross-linking using Rose Bengal-Green Light

Mitochondrial DNA Variation and Disease Susceptibility in Primary Open-Angle Glaucoma

A Natural History Study of Visual Function in Patients with Usher Syndrome Type 1C.

CLINICAL PRACTICE IN THE MANAGEMENT OF DIABETIC MACULAR EDEMA. RESULTS FROM A RETINOLOGISTS NATIONAL SURVEY

The Genetic Causes of Nonsyndromic Congenital Retinal Detachment: A Genetic and Phenotypic Study of Pakistani Families

Analysis of the PRPF31 Gene in Spanish Autosomal Dominant Retinitis Pigmentosa Patients: A Novel Genomic Rearrangement

Calcified crystalline material in peripheral lymphocytes in choroideremia- a novel discovery

A novel heterozygous mutation in PRPH2/RDS gene causing a spectrum of phenotypic manifestations in a family with autosomal dominant retinitis pigmentosa (adRP)

Albinism in Spain: Current genetic picture

Rapid evaluation of risk factors linked to age-related macular degeneration (AMD): STARS questionnaire

Variations in the size of retinal cysts as a tomographic factor predictor for retreatment with Ozurdex in patients with refractory diabetic macular edema

Circulating biomarkers of inflammation, oxidative stress and vascular risk for diabetic retinopathy. Effects of a nutraceutical supplementation in two year follow-up

Risk factors, clinical characteristics and management of patients with myopic choroidal neovascularization in clinical practice: Mypathway study

Genotype and Phenotype Studies in Autosomal Dominant Retinitis Pigmentosa (adRP) of the French Canadian Founder Population

Choroideremia Is a Systemic Disease With Lymphocyte Crystals and Plasma Lipid and RBC Membrane Abnormalities

A possible new gene for cone-rod dystrophy

Systematic Evaluation of Noncoding Mutations in Inherited R etinal D egeneration (RD) Patients with Missing Heritability

Hypomorphic mutations in CLUAP1 cause Leber congenital amaurosis

Identification of two novel mutations in CDHR1 in consanguineous Spanish families with autosomal recessive retinal dystrophy

Targeted Next-Generation Sequencing Improves the Diagnosis of Autosomal Dominant Retinitis Pigmentosa in Spanish Patients

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