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Chacon-Camacho, Oscar F. [Author]; Lopez-Moreno, Daniel [Author]; Morales-Sanchez, Martha A. [Author]; Hofmann, Enriqueta [Author]; Pacheco-Quito, Michelle [Author]; Wieland, Ilse [Author]; Cortes-Gonzalez, Vianney [Author]; Villanueva-Mendoza, Cristina [Author]; Zenker, Martin [Author]; Zenteno, Juan Carlos [Author]

Expansion of the phenotypic spectrum and description of molecular findings in a cohort of patients with oculocutaneous mosaic RASopathies

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2019

Published in: Molecular genetics & genomic medicine ; Bd. 7.2019, 5, Art.-Nr. e625, insges. 12 S.
Cortés-González, Vianney; Villanueva-Mendoza, Cristina

Epidemiología del glaucoma congénito en la Asociación para Evitar la Ceguera en México, revisión de 5 años

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Elsevier BV, 2015

Published in: Revista Mexicana de Oftalmología, 89 (2015) 3, Seite 150-153
Olivares-de Emparan, Juan Pablo; Villanueva-Mendoza, Cristina

Microscopia confocal en opacidades corneales asociadas a ictiosis ligada a X: reporte de caso

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Elsevier BV, 2014

Published in: Revista Mexicana de Oftalmología, 88 (2014) 2, Seite 85-88
Pelcastre, Erika L; Villanueva‐Mendoza, Cristina; Zenteno, Juan C

Novel and recurrent NDP gene mutations in familial cases of Norrie disease and X‐linked exudative vitreoretinopathy

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Wiley, 2010

Published in: Clinical & Experimental Ophthalmology, 38 (2010) 4, Seite 367-374
Hernández-Medrano, Cristina; Hidalgo-Bravo, Alberto; Villanueva-Mendoza, Cristina; Bautista-Tirado, Teresa; Apam-Garduño, David

Mosaic cat eye syndrome in a child with unilateral iris coloboma

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Informa UK Limited, 2021

Published in: Ophthalmic Genetics, 42 (2021) 1, Seite 84-87
Hortal, Alejandro M.; Villanueva, Ana; Arellano, Irene; Prieto, Cristina; Mendoza, Pilar; Bustelo, Xosé R.; Alarcón, Balbino

Mice Overexpressing Wild-Type RRAS2 Are a Novel Model for Preclinical Testing of Anti-Chronic Lymphocytic Leukemia Therapies

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MDPI AG, 2023

Published in: Cancers, 15 (2023) 24, Seite 5817
Ortiz-Ramirez, Grecia Yael; Villanueva-Mendoza, Cristina; Zenteno Ruiz, Juan Carlos; Reyes, Mariana; Cortés-González, Vianney

Autofluorescence in female carriers with choroideremia: A familial case with a novel mutation in the CHM gene

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Informa UK Limited, 2020

Published in: Ophthalmic Genetics, 41 (2020) 6, Seite 625-628
Villafuerte-de la Cruz, Rocío; Salinas-Longoria, Samantha; Cortés-González, Vianney; Villanueva-Mendoza, Cristina

Ruptura de globo ocular y síndrome de Ehlers-Danlos VI

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Jaypee Brothers Medical Publishing, 2018

Published in: Revista Mexicana de Oftalmología, 92 (2018) 4S, Seite 209-213
Cortés-González, Vianney; González-Chávez, Victoria; Robles-López, Karla L.; Villanueva-Mendoza, Cristina

Nervios corneales prominentes como manifestación inicial en el síndrome de neoplasia endocrina múltiple tipo 2B

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Elsevier BV, 2015

Published in: Revista Mexicana de Oftalmología, 89 (2015) 4, Seite 246-249
Zenteno, Juan Carlos; Buentello‐Volante, Beatriz; Ayala‐Ramirez, Raul; Villanueva‐Mendoza, Cristina

Homozygosity mapping identifies the Crumbs homologue 1 (Crb1) gene as responsible for a recessive syndrome of retinitis pigmentosa and nanophthalmos

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Wiley, 2011

Published in: American Journal of Medical Genetics Part A, 155 (2011) 5, Seite 1001-1006
Zenteno, Juan Carlos; Correa-Gomez, Vicente; Santacruz-Valdez, Concepción; Suarez-Sanchez, Raul; Villanueva-Mendoza, Cristina

Clinical and genetic features of TGFBI-linked corneal dystrophies in Mexican population: Description of novel mutations and novel genotype–phenotype correlations

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Elsevier BV, 2009

Published in: Experimental Eye Research, 89 (2009) 2, Seite 172-177
Villanueva-Mendoza, Cristina; Martínez-Guzmán, Oswaldo; Rivera-Parra, David; Zenteno, Juan Carlos

Triple A or Allgrove Syndrome. A Case Report with Ophthalmic Abnormalities and a Novel Mutation in theAAASGene

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Informa UK Limited, 2009

Published in: Ophthalmic Genetics, 30 (2009) 1, Seite 45-49
Salcedo-Villanueva, Guillermo; Paciuc-Beja, Miguel; Villanueva-Mendoza, Cristina; Harasawa, Mariana; Smith, Jesse M.; Velez-Montoya, Raul; Olson, Jeffrey L.; Oliver, Scott C.; Mandava, Naresh; Quiroz-Mercado, Hugo

Progression of gyrate atrophy measured with ultra-wide-field imaging

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Springer Science and Business Media LLC, 2016

Published in: International Ophthalmology, 36 (2016) 1, Seite 111-120
Apam-Garduño, David; Cortés-González, Vianney; Quintana-Fernández, Luis; Martínez-Anaya, Daniel; Pérez-Vera, Patricia; Villanueva-Mendoza, Cristina

The relevance of the cytogenetic analysis in syndromic microphthalmia/anophthalmia

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Informa UK Limited, 2019

Published in: Ophthalmic Genetics, 40 (2019) 6, Seite 584-587
Serrano-Ahumada, Ana Silvia; Cortes-González, Vianney; González-Huerta, Luz María; Cuevas, Sergio; Aguilar-Lozano, Luis; Villanueva-Mendoza, Cristina

Severe Phenotype of Keratitis–Ichthyosis–Deafness Syndrome With Presumed Ocular Surface Squamous Neoplasia

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Ovid Technologies (Wolters Kluwer Health), 2018

Published in: Cornea, 37 (2018) 2, Seite 252-254
Villanueva-Mendoza, Cristina; Arellanes-García, Lourdes; Cubas-Lorenzo, Victoria; Jimenez-Martinez, Maria C.; Flores-Suárez, Luis Felipe; Zenteno, Juan Carlos

Familial case of Blau syndrome associated with aCARD15/NOD2mutation

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Informa UK Limited, 2010

Published in: Ophthalmic Genetics, 31 (2010) 3, Seite 155-158
Treviño-Herrera, Alan Baltazar; Bustamante-Vargas, Ana Patricia; Lisker-Cervantes, Andrés; Ríos Y Valles Valles, Dolores; Villanueva-Mendoza, Cristina; González-Duarte, Alejandra; Concha-Del-Río, Luz Elena

Vitreous involvement as initial presentation of hereditary transthyretin amyloidosis related to the rare TTR Ile107Met (p.Ile127Met) pathogenic variant

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Informa UK Limited, 2022

Published in: Ophthalmic Genetics, 43 (2022) 3, Seite 413-419
Villanueva-Mendoza, Cristina; Tuson, Miquel; Apam-Garduño, David; de Castro-Miró, Marta; Tonda, Raul; Trotta, Jean Remi; Marfany, Gemma; Valero, Rebeca; Cortés-González, Vianney; Gonzàlez-Duarte, Roser

The Genetic Landscape of Inherited Retinal Diseases in a Mexican Cohort: Genes, Mutations and Phenotypes

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MDPI AG, 2021

Published in: Genes, 12 (2021) 11, Seite 1824
Toulis, Vasileios; Cortés-González, Vianney; de Castro-Miró, Marta; Ferraz Sallum, Juliana; Català-Mora, Jaume; Villanueva-Mendoza, Cristina; Ciccioli, Marcela; Gonzàlez-Duarte, Roser; Valero, Rebeca; Marfany, Gemma

Increasing the Genetic Diagnosis Yield in Inherited Retinal Dystrophies: Assigning Pathogenicity to Novel Non-canonical Splice Site Variants

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MDPI AG, 2020

Published in: Genes, 11 (2020) 4, Seite 378
Lo Faro, Valeria; Siddiqui, Sorath N.; Khan, Muhammad I.; Villanueva‐Mendoza, Cristina; Cortés‐González, Vianney; Jansonius, Nomdo; Bergen, Arthur A. B.; Micheal, Shazia

Novel mutations in the PITX2 gene in Pakistani and Mexican families with Axenfeld‐Rieger syndrome

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Wiley, 2020

Published in: Molecular Genetics & Genomic Medicine, 8 (2020) 7

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