Selective impacts of subsistence hunting on mammal communities in Manu National Park, Peru von McFarlane, Jennifer Jane, Chacón, Oscar Mujica, Arauco‐Aliaga, Roxana Patricia, Braunholtz, Laura, Sanderson, Roy, Pfeifer, Marion

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Analysis of energy consumption bounds in CMOS current-steering digital-to-analog converters von Morales Chacón, Oscar, Wikner, J. Jacob, Svensson, Christer, Siek, Liter, Alvandpour, Atila

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Identification of Genetic Variants for Diabetic Retinopathy Risk Applying Exome Sequencing in Extreme Phenotypes von Zenteno, Juan C., Chacón-Camacho, Oscar F., Ordoñez-Labastida, Vianey, Miranda-Duarte, Antonio, Del Castillo, Camila, Nava, Jessica, Mendoza, Fatima, Montes-Almanza, Luis, Mora-Roldán, Germán, Gazarian, Karlen

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Clinical, histopathological, and in silico pathogenicity analyses in a pedigree with familial amyloidosis of the Finnish type (Meretoja syndrome) caused by a novel gelsolin mutatio... von Cabral-Macias, Jesus, Garcia-Montaño, Leopoldo A, Pérezpeña-Díazconti, Mario, Aguilar, Marisa-Cruz, Garcia, Guillermo, Vencedor-Meraz, Carlos I, Graue-Hernandez, Enrique O, Chacón-Camacho, Oscar F, Zenteno, Juan C

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Efficacy Prediction of Four Pharmaceutical Formulations for Intramammary Administration Containing Aloe vera (L.) Burm. f. Combined With Ceftiofur or Cloxacillin in Lactating Cows... von Forno-Bell, Natalia, Munoz, Marcos A, Chacón, Oscar, Pachá, Paulina, Iragüen, Daniela, Cornejo, Javiera, San Martín, Betty

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On maximum-sum matchings of points von Bereg, Sergey, Chacón-Rivera, Oscar P., Flores-Peñaloza, David, Huemer, Clemens, Pérez-Lantero, Pablo, Seara, Carlos

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Extracranial midline defects in a patient with craniofrontonasal syndrome with a novel EFNB1 mutation von Acosta‐Fernández, Elizabeth, Zenteno, Juan C., Chacón‐Camacho, Oscar F., Peña‐Padilla, Christian, Bobadilla‐Morales, Lucina, Corona‐Rivera, Alfredo, Romo‐Huerta, Carmen O., Zepeda‐Romero, Luz C., López‐Marure, Eloy, Acosta‐León, Jorge, García‐Cruz, Diana, Maciel‐Cruz, Eric Jonathan, Corona‐Rivera, Jorge Román

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Extensive genic and allelic heterogeneity underlying inherited retinal dystrophies in Mexican patients molecularly analyzed by next‐generation sequencing von Zenteno, Juan C., García‐Montaño, Leopoldo A., Cruz‐Aguilar, Marisa, Ronquillo, Josué, Rodas‐Serrano, Agustín, Aguilar‐Castul, Luis, Matsui, Rodrigo, Vencedor‐Meraz, Carlos I., Arce‐González, Rocío, Graue‐Wiechers, Federico, Gutiérrez‐Paz, Mario, Urrea‐Victoria, Tatiana, Dios Cuadras, Ulises, Chacón‐Camacho, Oscar F.

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A New Ocular Phenotype Combining Juvenile Glaucoma and Doyne Honeycomb Retinal Dystrophy (Malattia Leventinese) due to a Novel EFEMP1 Pathogenic Variant von Chacon‐Camacho, Oscar F., Ordaz‐Robles, Thania, Cid‐García, Marion A., Yepes‐Rodríguez, Olivia, Arce‐González, Rocio, Martínez‐Aguilar, Alan, Zenteno, Juan Carlos

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La enseñanza de la innovación para el desarrollo sostenible von Chacón, Oscar Antonio

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PAX6 allelic heterogeneity in Mexican congenital aniridia patients: expanding the mutational spectrum with seven novel pathogenic variants von Pérez‐Solórzano, Sofía, Chacón‐Camacho, Oscar F, Astiazarán, Mirena C, Ledesma‐Gil, Gerardo, Zenteno, Juan Carlos

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Charge Engineering of the Nucleic Acid Binding Cleft of a Thermostable HIV-1 Reverse Transcriptase Reveals Key Interactions and a Novel Mechanism of RNase H Inactivation von Martínez del Río, Javier, López-Carrobles, Nerea, Mendieta-Moreno, Jesús I., Herrera-Chacón, Óscar, Sánchez-Ibáñez, Adrián, Mendieta, Jesús, Menéndez-Arias, Luis

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ABCA4 mutational spectrum in Mexican patients with Stargardt disease: Identification of 12 novel mutations and evidence of a founder effect for the common p.A1773V mutation von Chacón-Camacho, Oscar F., Granillo-Alvarez, Mariella, Ayala-Ramírez, Raul, Zenteno, Juan C.

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Ophthalmic findings in patients with autosomal recessive lamellar ichthyosis due to TGM1 mutations in an isolated population von Macriz-Romero, Nicole, Vera-Duarte, Guillermo Raul, Guerrero-Becerril, Jesus, Chacón-Camacho, Oscar Francisco, Astiazarán, Mirena C, Zenteno, Juan Carlos, Graue-Hernandez, Enrique O.

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Review and update on the molecular basis of Leber congenital amaurosis von Chacon-Camacho, Oscar Francisco, Zenteno, Juan Carlos

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Exome sequencing identifies a SREBF1 recurrent ARG557CYS mutation as the cause of hereditary mucoepithelial dysplasia in a family with high clinical variability von Chacon‐Camacho, Oscar F., Arce‐Gonzalez, Rocio, Ordaz‐Robles, Thania, Perezpeña‐Diazconti, Mario, Nava‐Castañeda, Angel, Zenteno, Juan Carlos

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Exome sequencing identifies a de novo frameshift mutation in the imprinted gene ZDBF2 in a sporadic patient with Nasopalpebral Lipoma-coloboma syndrome von Chacón-Camacho, Oscar F., Sobreira, Nara, You, Jing, Piña-Aguilar, Raul E., Villegas-Ruiz, Vanessa, Zenteno, Juan C.

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Clinical characterization and identification of five novel FOXL2 pathogenic variants in a cohort of 12 Mexican subjects with the syndrome of blepharophimosis-ptosis-epicanthus inve... von Chacón-Camacho, Oscar F., Salgado-Medina, Acatzin, Alcaraz-Lares, Nayeli, López-Moreno, Daniel, Barragán-Arévalo, Tania, Nava-Castañeda, Angel, Rodríguez-Uribe, Genaro, Lieberman, Esther, Rodríguez-Cabrera, Lourdes, González-Del Angel, Ariadna, Borbolla, Ana María, Fernández-Hernández, Liliana, Graue-Hernández, Enrique O., Zenteno, Juan Carlos

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Analysis of energy consumption bounds in CMOS current-steering digital-to-analog cosnverters von Morales Chacon, Oscar Andres, Wikner, Jacob, Svensson, Christer, Siek, Liter, Alvandpour, Atila

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Learning from history in the midst of the COVID-19: epidemics/pandemics of antiquity up to the fall of the Western Roman Empire von Chacón-Camacho, Óscar F., Arce-González, Rocío, Zenteno, Juan C., Granillo, María T.

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