Methylation analysis by targeted bisulfite sequencing in large for gestational age (LGA) newborns: the LARGAN cohort von Carrizosa-Molina, Tamara, Casillas-Díaz, Natalia, Pérez-Nadador, Iris, Vales-Villamarín, Claudia, López-Martínez, Miguel Ángel, Riveiro-Álvarez, Rosa, Wilhelm, Larry, Cervera-Juanes, Rita, Garcés, Carmen, Lomniczi, Alejandro, Soriano-Guillén, Leandro

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Contested Cities and Urban Activism von Ngai Ming Yip, Miguel Angel Martínez López, Xiaoyi Sun, Ngai Ming Yip, Miguel Angel Martínez López, Xiaoyi Sun

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Clinical Exome Sequencing Reveals MKRN3 Pathogenic Variants in Familial and Nonfamilial Idiopathic Central Precocious Puberty von Ortiz-Cabrera, Nelmar Valentina, Riveiro-Álvarez, Rosa, López-Martínez, Miguel Ángel, Pérez-Segura, Pilar, Aragón-Gómez, Isabel, Trujillo-Tiebas, María José, Soriano-Guillén, Leandro

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Autonomous Activist-Research. The case of the squatters' movement in Madrid von Martinez Lopez, Miguel Angel, Fernandez, Elisabeth Lorenzi

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New Mutations in the RAB28 Gene in 2 Spanish Families With Cone-Rod Dystrophy von Riveiro-Álvarez, Rosa, Xie, Yajing (Angela), López-Martínez, Miguel-Ángel, Gambin, Tomasz, Pérez-Carro, Raquel, Ávila-Fernández, Almudena, López-Molina, María-Isabel, Zernant, Jana, Jhangiani, Shalini, Muzny, Donna, Yuan, Bo, Boerwinkle, Eric, Gibbs, Richard, Lupski, James R, Ayuso, Carmen, Allikmets, Rando

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Orquestación, despliegue y escalabilidad de un servicio de ejecución de código altamente disponible basado en contenedores von López Martínez, Miguel Ángel

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Analysis of the ABCA4 genomic locus in Stargardt disease von Zernant, Jana, Xie, Yajing Angela, Ayuso, Carmen, Riveiro-Alvarez, Rosa, Lopez-Martinez, Miguel-Angel, Simonelli, Francesca, Testa, Francesco, Gorin, Michael B, Strom, Samuel P, Bertelsen, Mette, Rosenberg, Thomas, Boone, Philip M, Yuan, Bo, Ayyagari, Radha, Nagy, Peter L, Tsang, Stephen H, Gouras, Peter, Collison, Frederick T, Lupski, James R, Fishman, Gerald A, Allikmets, Rando

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Squatters and migrants in Madrid: Interactions, contexts and cycles von Martinez, Miguel A.

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Outcome of ABCA4 Disease-Associated Alleles in Autosomal Recessive Retinal Dystrophies von Riveiro-Alvarez, Rosa, PhD, Lopez-Martinez, Miguel-Angel, SLT, Zernant, Jana, MSc, Aguirre-Lamban, Jana, PhD, Cantalapiedra, Diego, BSc, Avila-Fernandez, Almudena, PhD, Gimenez, Ascension, SLT, Lopez-Molina, Maria-Isabel, MD, Garcia-Sandoval, Blanca, MD, PhD, Blanco-Kelly, Fiona, MD, PhD, Corton, Marta, PhD, Tatu, Sorina, BSc, Fernandez-San Jose, Patricia, BSc, Trujillo-Tiebas, Maria-Jose, PhD, Ramos, Carmen, PhD, Allikmets, Rando, PhD, Ayuso, Carmen, MD, PhD

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Contribution of mutation load to the intrafamilial genetic heterogeneity in a large cohort of Spanish retinal dystrophies families von Sánchez-Alcudia, Rocío, Cortón, Marta, Ávila-Fernández, Almudena, Zurita, Olga, Tatu, Sorina D, Pérez-Carro, Raquel, Fernandez-San Jose, Patricia, Lopez-Martinez, Miguel Ángel, del Castillo, Francisco J, Millan, Jose M, Blanco-Kelly, Fiona, García-Sandoval, Blanca, Lopez-Molina, Maria Isabel, Riveiro-Alvarez, Rosa, Ayuso, Carmen

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The microbiology of sepsis is more than the application of new technologies in diagnosis von Larrosa Escartín, M N, Martínez-López, M A, Nadal-Barón, P

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A Comprehensive Analysis of Choroideremia: From Genetic Characterization to Clinical Practice von Sanchez-Alcudia, Rocio, Garcia-Hoyos, Maria, Lopez-Martinez, Miguel Angel, Sanchez-Bolivar, Noelia, Zurita, Olga, Gimenez, Ascension, Villaverde, Cristina, Rodrigues-Jacy da Silva, Luciana, Corton, Marta, Perez-Carro, Raquel, Torriano, Simona, Kalatzis, Vasiliki, Rivolta, Carlo, Avila-Fernandez, Almudena, Lorda, Isabel, Trujillo-Tiebas, Maria J, Garcia-Sandoval, Blanca, Lopez-Molina, Maria Isabel, Blanco-Kelly, Fiona, Riveiro-Alvarez, Rosa, Ayuso, Carmen

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Investigación activista autónoma. El caso del movimiento de okupaciones de Madrid von Miguel Ángel Martínez López, Elísabeth Lorenzi Fernández

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Panel-based NGS Reveals Novel Pathogenic Mutations in Autosomal Recessive Retinitis Pigmentosa von Perez-Carro, Raquel, Corton, Marta, Sánchez-Navarro, Iker, Zurita, Olga, Sanchez-Bolivar, Noelia, Sánchez-Alcudia, Rocío, Lelieveld, Stefan H., Aller, Elena, Lopez-Martinez, Miguel Angel, López-Molina, Mª Isabel, Fernandez-San Jose, Patricia, Blanco-Kelly, Fiona, Riveiro-Alvarez, Rosa, Gilissen, Christian, Millan, Jose M, Avila-Fernandez, Almudena, Ayuso, Carmen

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Outcome of ABCA4 disease-associated alleles in autosomal recessive retinal dystrophies: retrospective analysis in 420 Spanish families von Riveiro-Alvarez, Rosa, Lopez-Martinez, Miguel-Angel, Zernant, Jana, Aguirre-Lamban, Jana, Cantalapiedra, Diego, Avila-Fernandez, Almudena, Gimenez, Ascension, Lopez-Molina, Maria-Isabel, Garcia-Sandoval, Blanca, Blanco-Kelly, Fiona, Corton, Marta, Tatu, Sorina, Fernandez-San Jose, Patricia, Trujillo-Tiebas, Maria-Jose, Ramos, Carmen, Allikmets, Rando, Ayuso, Carmen

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Dominant Retinitis Pigmentosa, p.Gly56Arg Mutation in NR2E3: Phenotype in a Large Cohort of 24 Cases von Blanco-Kelly, Fiona, García Hoyos, María, Lopez Martinez, Miguel Angel, Lopez-Molina, Maria Isabel, Riveiro-Alvarez, Rosa, Fernandez-San Jose, Patricia, Avila-Fernandez, Almudena, Corton, Marta, Millan, Jose M, García Sandoval, Blanca, Ayuso, Carmen

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Targeted Next-Generation Sequencing Improves the Diagnosis of Autosomal Dominant Retinitis Pigmentosa in Spanish Patients von Fernandez-San Jose, Patricia, Corton, Marta, Blanco-Kelly, Fiona, Avila-Fernandez, Almudena, Lopez-Martinez, Miguel Angel, Sanchez-Navarro, Iker, Sanchez-Alcudia, Rocio, Perez-Carro, Raquel, Zurita, Olga, Sanchez-Bolivar, Noelia, Lopez-Molina, Maria Isabel, Garcia-Sandoval, Blanca, Riveiro-Alvarez, Rosa, Ayuso, Carmen

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Whole-exome sequencing reveals ZNF408 as a new gene associated with autosomal recessive retinitis pigmentosa with vitreal alterations von Avila-Fernandez, Almudena, Perez-Carro, Raquel, Corton, Marta, Lopez-Molina, Maria Isabel, Campello, Laura, Garanto, Alejandro, Fernandez-Sanchez, Laura, Duijkers, Lonneke, Lopez-Martinez, Miguel Angel, Riveiro-Alvarez, Rosa, Da Silva, Luciana Rodrigues Jacy, Sanchez-Alcudia, Rocío, Martin-Garrido, Esther, Reyes, Noelia, Garcia-Garcia, Francisco, Dopazo, Joaquin, Garcia-Sandoval, Blanca, Collin, Rob W J, Cuenca, Nicolas, Ayuso, Carmen

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Mutation Screening of 299 Spanish Families with Retinal Dystrophies by Leber Congenital Amaurosis Genotyping Microarray von Vallespin, Elena, Cantalapiedra, Diego, Riveiro-Alvarez, Rosa, Wilke, Robert, Aguirre-Lamban, Jana, Avila-Fernandez, Almudena, Lopez-Martinez, Miguel Angel, Gimenez, Ascension, Jose Trujillo-Tiebas, Maria, Ramos, Carmen, Ayuso, Carmen

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New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report von Blanco-Kelly, Fiona, Rodrigues-Jacy da Silva, Luciana, Sanchez-Navarro, Iker, Riveiro-Alvarez, Rosa, Lopez-Martinez, Miguel Angel, Corton, Marta, Ayuso, Carmen

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