Juan Carlos Zenteno Ruiz (Juan C Zenteno, Juan Carlos Zenteno)

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 24

Top Topics

Diabetic Retinopathy

Top Venues

American journal of medical genetics. Part A

Ophthalmic genetics

Molecular genetics and genomics : MGG

Molecular genetics & genomic medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Juan Carlos Zenteno Ruiz, Oscar F Chacón-Camacho, Vianey Ordoñez-Labastida, Antonio Miranda-Duarte, Camila Del Castillo, Jessica Nava, Fatima Mendoza, Luis Montes-Almanza, Germán Mora-Roldán, Karlen Gazarian
Identification of Genetic Variants for Diabetic Retinopathy Risk Applying Exome Sequencing in Extreme Phenotypes. BioMed research international 2024 (2024)
Víctor R López-Rodríguez, Rocío Arce-González, Alan Martínez-Aguilar, Carlos E Rodríguez-López, Sergio Groman-Lupa, M Isabel Neria-González, Genaro Rodríguez-Uribe, Juan Carlos Zenteno Ruiz
Mutational Profile and Retinal Phenotypes of PCARE -Related Cone-Rod Dystrophies in a Mexican Cohort. Journal of ophthalmology 2024 (2024)
Juan Carlos Zenteno Ruiz, Oscar F Chacón-Camacho, Vianey Ordoñez-Labastida, Antonio Miranda-Duarte, Camila Del Castillo, Jessica Nava, Fatima Mendoza, Luis Montes-Almanza, Germán Mora-Roldán, Karlen Gazarian
Identification of Genetic Variants for Diabetic Retinopathy Risk Applying Exome Sequencing in Extreme Phenotypes. BioMed research international 2024 (2024)
Oscar F Chacon-Camacho, Nancy Xilotl-de Jesús, Ernesto Calderón-Martínez, Vianey Ordoñez-Labastida, M Isabel Neria-Gonzalez, Rocío Villafuerte-de la Cruz, Augusto Martinez-Rojas, Juan Carlos Zenteno Ruiz
Genotypic spectrum of ABCA4-associated retinal degenerations in 211 unrelated Mexican patients: identification of 22 novel disease-causing variants. Molecular genetics and genomics : MGG 299 (1) (2024)
Oscar Francisco Chacon-Camacho, Thania Ordaz-Robles, Marion Aline Cid-García, María Enriqueta Hofmann-Blancas, Jasbeth Ledesma-Gil, María Magdalena García-Huerta, Carolina Prado-Larrea, Vianney Cortés-González, Rodrigo Isaac Lozano-Garza, Daphne García-Vega, JiHye Kim, Rin Khang, Eugene Lee, Juan Carlos Zenteno Ruiz
TEK gene-related primary congenital glaucoma: Phenotypic features and mutational spectrum in a Mexican cohort of 10 unrelated families. American journal of medical genetics. Part A (2024)
Víctor R López-Rodríguez, Rocío Arce-González, Alan Martínez-Aguilar, Carlos E Rodríguez-López, Sergio Groman-Lupa, M Isabel Neria-González, Genaro Rodríguez-Uribe, Juan Carlos Zenteno Ruiz
Mutational Profile and Retinal Phenotypes of PCARE -Related Cone-Rod Dystrophies in a Mexican Cohort. Journal of ophthalmology 2024 (2024)
Oscar F Chacon-Camacho, Nancy Xilotl-de Jesús, Ernesto Calderón-Martínez, Vianey Ordoñez-Labastida, M Isabel Neria-Gonzalez, Rocío Villafuerte-de la Cruz, Augusto Martinez-Rojas, Juan Carlos Zenteno Ruiz
Genotypic spectrum of ABCA4-associated retinal degenerations in 211 unrelated Mexican patients: identification of 22 novel disease-causing variants. Molecular genetics and genomics : MGG 299 (1) (2024)
Oscar F Chacon-Camacho, Nancy Xilotl-de Jesús, Ernesto Calderón-Martínez, Vianey Ordoñez-Labastida, M Isabel Neria-Gonzalez, Rocío Villafuerte-de la Cruz, Augusto Martinez-Rojas, Juan Carlos Zenteno Ruiz
Genotypic spectrum of ABCA4-associated retinal degenerations in 211 unrelated Mexican patients: identification of 22 novel disease-causing variants. Molecular genetics and genomics : MGG 299 (1) (2024)
Oscar Francisco Chacon-Camacho, Thania Ordaz-Robles, Marion A Cid-García, Olivia Yepes-Rodríguez, Rocio Arce-González, Alan Martínez-Aguilar, Juan Carlos Zenteno Ruiz
A New Ocular Phenotype Combining Juvenile Glaucoma and Doyne Honeycomb Retinal Dystrophy (Malattia Leventinese) due to a Novel EFEMP1 Pathogenic Variant. American journal of medical genetics. Part A (2024)
Nicole Macriz-Romero, Guillermo Raul Vera-Duarte, Jesus Guerrero-Becerril, Oscar Francisco Chacón-Camacho, Mirena C Astiazarán, Juan Carlos Zenteno Ruiz, Enrique Octavio Graue-Hernández
Ophthalmic findings in patients with autosomal recessive lamellar ichthyosis due to TGM1 mutations in an isolated population. International ophthalmology (2023)
Leire Irusteta, Arturo Ramírez-Miranda, Alejandro Navas-Pérez, Luis Montes-Almanza, José Arteaga, Froylán García-Martínez, Enrique Graue-Hernández, Juan Carlos Zenteno Ruiz
Detailed phenotypic description of stromal corneal dystrophy in a large pedigree carrying the uncommon TGFBI p.Ala546Asp pathogenic variant. Ophthalmic genetics 43 (5) (2022)
Rocío Arce-González, Oscar Francisco Chacon-Camacho, Vianey Ordoñez-Labastida, Enrique O Graue-Hernandez, Alejandro Navas-Pérez, Juan Carlos Zenteno Ruiz
A novel homozygous ZNF469 variant causing brittle cornea syndrome is associated with corneal ectasias in heterozygous carriers. International ophthalmology (2022)
Juan Carlos Zenteno Ruiz, Rocio Arce-Gonzalez, Rodrigo Matsui, Antonio Lopez-Bolaños, Luis Montes, Alan Martinez-Aguilar, Oscar F Chacon-Camacho
Clinical-genetic findings in a group of subjects with macular dystrophies due to mutations in rare inherited retinopathy genes. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie (2022)
German A Mora-Roldan, Carlos Galaviz-Hernandez, Jose Hiebert-Froese, Arturo Hernandez, Luis Montes, Maria L Duran-Pasten, Karlen Gazarian, Juan Carlos Zenteno Ruiz
A new missense variant in RAB3GAP2 in a family with muscular dystrophy-short stature and defective autophagy: An expansion of the micro/Martsolf spectrum or a new phenotype? American journal of medical genetics. Part A 188 (7) (2022)
Rocio Arce-Gonzalez, Oscar F Chacon-Camacho, Alejandro Navas-Perez, María C Gonzalez-Gonzalez, Alan Martinez-Aguilar, Juan Carlos Zenteno Ruiz
Novel CHRDL1 mutation causing X-linked megalocornea in a family with mild anterior segment manifestations in carrier females. Ophthalmic genetics (2021)
Grecia Yael Ortiz-Ramirez, Cristina Villanueva-Mendoza, Juan Carlos Zenteno Ruiz, Mariana Reyes, Vianney Cortés-González
Autofluorescence in female carriers with choroideremia: A familial case with a novel mutation in the CHM gene. Ophthalmic genetics 41 (6) (2020)
Oscar Francisco Chacon-Camacho, Rocio Arce-Gonzalez, Thania Ordaz-Robles, Mario Perezpeña-Diazconti, Angel Nava-Castañeda, Juan Carlos Zenteno Ruiz
Exome sequencing identifies a SREBF1 recurrent ARG557CYS mutation as the cause of hereditary mucoepithelial dysplasia in a family with high clinical variability. American journal of medical genetics. Part A 182 (11) (2020)
Antonieta Martínez-Velasco, Andric C Perez-Ortiz, Bani Antonio-Aguirre, Lourdes Martínez-Villaseñor, Esmeralda Lira-Romero, Claudia Palacio Pastrana, Juan Carlos Zenteno Ruiz, Israel Ramirez, Claudia Zepeda-Palacio, Cristina Mendoza-Velásquez, Azyadeh Camacho-Ordóñez, Daniela Michelle Ortiz Bibriesca, Francisco J Estrada-Mena
Assessment of CFH and HTRA1 polymorphisms in age-related macular degeneration using classic and machine-learning approaches. Ophthalmic genetics 41 (6) (2020)
Elizabeth Acosta-Fernández, Juan Carlos Zenteno Ruiz, Oscar F Chacón-Camacho, Christian Peña-Padilla, Lucina Bobadilla-Morales, Alfredo Corona-Rivera, Carmen O Romo-Huerta, Luz C Zepeda-Romero, Eloy López-Marure, Jorge Acosta-León, Diana García-Cruz, Eric Jonathan Maciel-Cruz, Jorge Román Corona Rivera
Extracranial midline defects in a patient with craniofrontonasal syndrome with a novel EFNB1 mutation. American journal of medical genetics. Part A 182 (5) (2020)
Valeria Kheir, Vianney Cortés-González, Juan Carlos Zenteno Ruiz, Daniel F Schorderet
Mutation update: TGFBI pathogenic and likely pathogenic variants in corneal dystrophies. Human mutation 40 (6) (2019)
Juan Carlos Zenteno Ruiz, Leopoldo A García-Montaño, Marisa Cruz-Aguilar, Josué Ronquillo, Agustín Rodas-Serrano, Luis Aguilar-Castul, Rodrigo Matsui, Carlos I Vencedor-Meraz, Rocío Arce-González, Federico Graue-Wiechers, Mario Gutiérrez-Paz, Tatiana Urrea-Victoria, Ulises de Dios Cuadras, Oscar F Chacón-Camacho
Extensive genic and allelic heterogeneity underlying inherited retinal dystrophies in Mexican patients molecularly analyzed by next-generation sequencing. Molecular genetics & genomic medicine 8 (1) (2019)
Oscar F Chacon-Camacho, Daniel Lopez-Moreno, Martha A Morales-Sanchez, Enriqueta Hofmann, Michelle Pacheco-Quito, Ilse Wieland, Vianney Cortes-Gonzalez, Cristina Villanueva-Mendoza, Martin Zenker, Juan Carlos Zenteno Ruiz
Expansion of the phenotypic spectrum and description of molecular findings in a cohort of patients with oculocutaneous mosaic RASopathies. Molecular genetics & genomic medicine 7 (5) (2019)
Patrick R Blackburn, Oscar F Chacon-Camacho, Xilma R Ortiz-González, Mariana Reyes, Graciela A Lopez-Uriarte, Shabnam Zarei, Elizabeth Joyce Bhoj, Sofia Perez-Solorzano, Rachael A Vaubel, Marine I Murphree, Jessica Nava, Vianney Cortes-Gonzalez, Joseph E Parisi, Cristina Villanueva-Mendoza, Iris G Tirado-Torres, Dong Li, Eric W Klee, Pavel N Pichurin, Juan Carlos Zenteno Ruiz
Extension of the mutational and clinical spectrum of SOX2 related disorders: Description of six new cases and a novel association with suprasellar teratoma. American journal of medical genetics. Part A 176 (12) (2018)
Mirena C Astiazarán, Leopoldo A García-Montaño, Francisco Sánchez-Moreno, Humberto Matiz-Moreno, Juan Carlos Zenteno Ruiz
Next generation sequencing-based molecular diagnosis in familial congenital cataract expands the mutational spectrum in known congenital cataract genes. American journal of medical genetics. Part A 176 (12) (2018)