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ARVO Annual Meeting Abstract June 2020

Single cell RNA sequencing of retinal immune cells identifies activation of resident retinal microglia associated with subretinal pseudodrusen-like deposits

Asha Kumari; Raul Ayala; Juan Carlos Zenteno; Sasik Roman; Radha Ayyagari; Shyamanga Borooah

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):2748. doi:

ARVO Annual Meeting Abstract July 2019

Clinical and histopathological findings in a family with Meretoja’s syndrome carrying a novel gelsolin mutation

JOSE MARIO PEREZPEÑA-DIAZCONTI; Jesus Cabral-Macias; Enrique O Graue-Hernandez; Juan Carlos Zenteno; oscar Chacon

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):5427. doi:

ARVO Annual Meeting Abstract July 2019

Panel-based next generation sequencing reveals extensive locus and allelic heterogeneity underlying inherited retinal degenerations in Mexican population

Juan Carlos Zenteno; Leopoldo Garcia-Montaño; Marisa Cruz-Aguilar; Rodrigo Matsui-Serrano; Josue Ronquillo; Federico Graue-Wiechers; Luis Castul; Tatiana Urrea; Uises De Dios-Cuadras; Oscar Chacon-Camacho

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):2962. doi:

ARVO Annual Meeting Abstract July 2018

Clinico-epidemiologic features of oculocutaneous albinism in Mexico City

Carlos Muller Morales; Juan Carlos Zenteno; Ana María Beauregard

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):1065. doi:

ARVO Annual Meeting Abstract July 2018

Identification Of Five Somatic Mutations In KRAS And FGFR1 Genes In Mexican Patients With Oculocutaneous Syndromes

Sofía Pérez Solórzano; Óscar Francisco Chacón-Camacho; Bertha Irene Fuerte-Flores; Daniel López-Moreno; Enriqueta Hofmann; Juan Carlos Zenteno-Ruíz

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):5398. doi:

ARVO Annual Meeting Abstract July 2018

Identification of the rs121908120 polymorphism of the WNT10A gene as a risk factor for developing Keratoconus in a Mexican population sample

David Lozano-Giral; Beatriz Buentello; Juan Carlos Zenteno

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):5399. doi:

ARVO Annual Meeting Abstract July 2018

Sclerocornea-microphthalmia-aphakia complex: Description of two additional cases associated with novel FOXE3 mutations and review of the literature.

Natalia Paulina Quiroz-Casian; Oscar Chacon-Camacho; Tania Barragan-Arevalo; Jessica Nava-Valdez; Alejandro Navas; Enrique O Graue-Hernandez; Juan Carlos Zenteno

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):2925. doi:

ARVO Annual Meeting Abstract June 2017

A novel CYP1B1 mutation with the Von Hippel’s description of an internal corneal ulcer phenotype

Tania Albavera; Valeria Oliva; Alejandro Navas; Oscar Chacon; Juan Carlos Zenteno; Enrique O Graue-Hernandez; Mirena Astiazarán; Antonio Bermudez

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):968. doi:

ARVO Annual Meeting Abstract June 2017

CFH and HTRA1 genes associated with AMD in Mexican population

Antonieta Martínez-Velasco; Andric Christopher Perez-Ortiz; Juan Carlos Zenteno; ALEXA BERENICE LUNA-ANGULO; Antonio Rafael Villa-Romero; Lourdes Martínez-Villaseñor; Alvaro Rendon; Francisco Javier Estrada

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):2268. doi:

ARVO Annual Meeting Abstract June 2017

Clinical characterization of an uncommon ABCA4 mutation in Mexican Population

Rodrigo Matsui; Salvador Lopez-Rubio; Oscar Chacon; Juan Carlos Zenteno Ruiz

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):3222. doi:

ARVO Annual Meeting Abstract September 2016

Association between complement factor H polymorphism and response to antiangiogenic therapy in age-related macular degeneration

Lorena Ramirez; Federico Graue; Juan Carlos Zenteno; Antonio Bolaños; Beatriz Buentello

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):2641. doi:

ARVO Annual Meeting Abstract September 2016

Vortex pattern of corneal deposits in granular corneal dystrophy associated with the p.(ArgR555WTrp) mutation in TGFBI

Jaffer Kattan; Juan Carlos Serna-Ojeda; Eung Kweon Kim; Arturo J Ramirez-Miranda; Juan Carlos Zenteno; Anthony J Aldave

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):4828. doi:

ARVO Annual Meeting Abstract June 2015

Novel TACSTD2 gene Nonsense Mutation in a Family with Gelatinous Drop-Like Corneal Dystrophy (GDLD)

Jesus Cabral; Juan Carlos Zenteno; Beatriz Buentello-Volante; Enrique O Graue; Victor Boullosa-graña; Alejandro Navas; Patrick Gore; Arturo J Ramirez-Miranda

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):2523. doi:

ARVO Annual Meeting Abstract June 2015

Genetic association of polymorphisms in the p53 and LTA genes with proliferative vitreoretinopathy after retinal detachment surgery in Mexican population

Natalia Paulina Quiroz Casian; José Luis Rodríguez; Salvador Lopez-Rubio; Antonio Miranda Duarte; Juan C Zenteno; Genetics

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):404. doi:

ARVO Annual Meeting Abstract June 2015

Exome sequencing in Nasopalpebral-Lipoma-Coloboma Syndrome identifies a pathogenic mutation in an imprinted locus

Oscar Francisco Chacon-Camacho; RAUL EDUARDO PIÑA-AGUILAR; Angel Nava-Castaneda; Juan Carlos Zenteno; GENETICS

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):5987. doi:

ARVO Annual Meeting Abstract June 2015

Identification of RB1 gene germline mutations in Mexican patients with sporadic unilateral retinoblastoma

Dalia Consuelo Guadarrama Vallejo; Juan C Zenteno; Arturo Flores Cuevas

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):81. doi:

ARVO Annual Meeting Abstract April 2014

TGFBI, CHST6 and Gelsolin gene analysis in mexican patients with stromal corneal dystrophies

Johanna Gonzalez; Arturo J Ramirez-Miranda; Sergio Hernandez-da Mota; Juan Carlos Zenteno

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):1000. doi:

ARVO Annual Meeting Abstract June 2013

Tietz syndrome (albinism and congenital deafness): Description of a familiar case carrying a novel MITF gene mutation and associated with nanophthalmos

Luz Cortés; Martin Guzman-Sanchez; Dalia Guadarrama; Juan Zenteno; Cristina Villanueva-Mendoza

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):1337. doi:

ARVO Annual Meeting Abstract June 2013

Exome sequencing identifies RDH12 gene compound heterozygous mutations in a Mexican inbred family with severe autosomal recessive retinitis pigmentosa

Juan Zenteno; Oscar Chacon-Camacho; Beatriz Buentello; Serguei Jitskii

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):3345. doi:

ARVO Annual Meeting Abstract June 2013

Association of the T allele of rs41435250 of LOXL1 with elevated risk of exfoliation syndrome and exfoliation glaucoma in a Mexican population

Dalia Guadarrama; Juan Zenteno; Antonio Miranda; Celia Elizondo

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):1598. doi:

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Single cell RNA sequencing of retinal immune cells identifies activation of resident retinal microglia associated with subretinal pseudodrusen-like deposits

Clinical and histopathological findings in a family with Meretoja’s syndrome carrying a novel gelsolin mutation

Panel-based next generation sequencing reveals extensive locus and allelic heterogeneity underlying inherited retinal degenerations in Mexican population

Clinico-epidemiologic features of oculocutaneous albinism in Mexico City

Identification Of Five Somatic Mutations In KRAS And FGFR1 Genes In Mexican Patients With Oculocutaneous Syndromes

Identification of the rs121908120 polymorphism of the WNT10A gene as a risk factor for developing Keratoconus in a Mexican population sample

Sclerocornea-microphthalmia-aphakia complex: Description of two additional cases associated with novel FOXE3 mutations and review of the literature.

A novel CYP1B1 mutation with the Von Hippel’s description of an internal corneal ulcer phenotype

CFH and HTRA1 genes associated with AMD in Mexican population

Clinical characterization of an uncommon ABCA4 mutation in Mexican Population

Association between complement factor H polymorphism and response to antiangiogenic therapy in age-related macular degeneration

Vortex pattern of corneal deposits in granular corneal dystrophy associated with the p.(ArgR555WTrp) mutation in TGFBI

Novel TACSTD2 gene Nonsense Mutation in a Family with Gelatinous Drop-Like Corneal Dystrophy (GDLD)

Genetic association of polymorphisms in the p53 and LTA genes with proliferative vitreoretinopathy after retinal detachment surgery in Mexican population

Exome sequencing in Nasopalpebral-Lipoma-Coloboma Syndrome identifies a pathogenic mutation in an imprinted locus

Identification of RB1 gene germline mutations in Mexican patients with sporadic unilateral retinoblastoma

TGFBI, CHST6 and Gelsolin gene analysis in mexican patients with stromal corneal dystrophies

Tietz syndrome (albinism and congenital deafness): Description of a familiar case carrying a novel MITF gene mutation and associated with nanophthalmos

Exome sequencing identifies RDH12 gene compound heterozygous mutations in a Mexican inbred family with severe autosomal recessive retinitis pigmentosa

Association of the T allele of rs41435250 of LOXL1 with elevated risk of exfoliation syndrome and exfoliation glaucoma in a Mexican population

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