Beatriz Buentello‐Volante

Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinements

Feng Wang, Hui Wang, Han-Fang Tuan et al. · Human Genetics · 2013 · 242 citations

Medicine, Genetics, Molecular Genetics +16

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

Juan Carlos Zenteno, Beatriz Buentello‐Volante, Raúl Ayala-Ramírez et al. · American Journal of Medical Genetics Part A · 2011 · 50 citations

Life Sciences, Genetics, Molecular Genetics +17

Human Amniotic Membrane Mesenchymal Stem Cells inhibit Neutrophil Extracellular Traps through TSG-6

Fátima Sofía Magaña‐Guerrero, Alfredo Domínguez-López, Pamela Martínez-Aboytes et al. · Scientific Reports · 2017 · 48 citations · Full text

Life Sciences, Cell Biology, Immunology +17

Compound heterozygosity for a novel and a recurrent MFRP gene mutation in a family with the nanophthalmos-retinitis pigmentosa complex.

Juan Carlos Zenteno, Beatriz Buentello‐Volante, Miguel A. Quiroz-Gonzalez et al. · PubMed · 2009 · 46 citations

Life Sciences, Genetics, Ophthalmology +14

Homozygous FOXE3 mutations cause non-syndromic, bilateral, total sclerocornea, aphakia, microphthalmia and optic disc coloboma.

Manir Ali, Beatriz Buentello‐Volante, Martin McKibbin et al. · PubMed · 2010 · 42 citations

Life Sciences, Genetics, Ophthalmology +14