| Issue Date | Title | Author(s) |
| 2017-03-14 | 2017 update on the relationship between diabetes and colorectal cancer: epidemiology, potential molecular mechanisms and therapeutic implications. | González, Nieves; Prieto, Isabel; Del Puerto-Nevado, Laura; Portal-Nuñez, Sergio; Ardura, Juan Antonio; Corton, Marta; Fernández-Fernández, Beatriz; Aguilera, Oscar; Gomez-Guerrero, Carmen; Mas, Sebastián; Moreno, Juan Antonio; Ruiz-Ortega, Marta; Sanz, Ana Belen; Sanchez-Niño, Maria Dolores; Rojo, Federico; Vivanco, Fernando; Esbrit, Pedro; Ayuso, Carmen; Alvarez-Llamas, Gloria; Egido, Jesús; García-Foncillas, Jesús; Ortiz, Alberto |
| 2016-01-08 | Attention deficit hyperactivity disorder: genetic association study in a cohort of Spanish children. | Gomez-Sanchez, Clara I; Riveiro-Alvarez, Rosa; Soto-Insuga, Victor; Rodrigo, Maria; Tirado-Requero, Pilar; Mahillo-Fernandez, Ignacio; Abad-Santos, Francisco; Carballo, Juan J; Dal-Ré, Rafael; Ayuso, Carmen |
| 2016 | Functional Characterization of Three Concomitant MtDNA LHON Mutations Shows No Synergistic Effect on Mitochondrial Activity. | Cruz-Bermúdez, Alberto; Vicente-Blanco, Ramiro J; Hernández-Sierra, Rosana; Montero, Mayte; Alvarez, Javier; González Manrique, Mar; Blázquez, Alberto; Martín, Miguel Angel; Ayuso, Carmen; Garesse, Rafael; Fernández-Moreno, Miguel A |
| 2015 | Hypo- and hypermorphic FOXC1 mutations in dominant glaucoma: transactivation and phenotypic variability. | Medina-Trillo, Cristina; Sánchez-Sánchez, Francisco; Aroca-Aguilar, José-Daniel; Ferre-Fernández, Jesús-José; Morales, Laura; Méndez-Hernández, Carmen-Dora; Blanco-Kelly, Fiona; Ayuso, Carmen; García-Feijoo, Julián; Escribano, Julio |
| 2017 | Improving molecular diagnosis of aniridia and WAGR syndrome using customized targeted array-based CGH. | Blanco-Kelly, Fiona; Palomares, María; Vallespín, Elena; Villaverde, Cristina; Martín-Arenas, Rubén; Vélez-Monsalve, Camilo; Lorda-Sánchez, Isabel; Nevado, Julián; Trujillo-Tiebas, María José; Lapunzina, Pablo; Ayuso, Carmen; Corton, Marta |
| 2018 | Parental Mosaicism in PAX6 Causes Intra-Familial Variability: Implications for Genetic Counseling of Congenital Aniridia and Microphthalmia. | Tarilonte, María; Morín, Matías; Ramos, Patricia; Galdós, Marta; Blanco-Kelly, Fiona; Villaverde, Cristina; Rey-Zamora, Dolores; Rebolleda, Gema; Muñoz-Negrete, Francisco J; Tahsin-Swafiri, Saoud; Gener, Blanca; Moreno-Pelayo, Miguel-Angel; Ayuso, Carmen; Villamar, Manuela; Corton, Marta |
| 2017 | Pharmacogenetics of methylphenidate in childhood attention-deficit/hyperactivity disorder: long-term effects. | |
| 2017 | Whole-Exome Sequencing of Congenital Glaucoma Patients Reveals Hypermorphic Variants in GPATCH3, a New Gene Involved in Ocular and Craniofacial Development. | Ferre-Fernández, Jesús-José; Aroca-Aguilar, José-Daniel; Medina-Trillo, Cristina; Bonet-Fernández, Juan-Manuel; Méndez-Hernández, Carmen-Dora; Morales-Fernández, Laura; Corton, Marta; Cabañero-Valera, María-José; Gut, Marta; Tonda, Raul; Ayuso, Carmen; Coca-Prados, Miguel; García-Feijoo, Julián; Escribano, Julio |
