Search Results - "Arcos-Burgos, Mauricio"

A Neanderthal haplotype introgressed into the human genome confers protection against membranous nephropathy

Voinescu, Cătălin D., Mozere, Monika, Genovese, Giulio, Downie, Mallory L., Gupta, Sanjana, Gale, Daniel P., Bockenhauer, Detlef, Kleta, Robert, Arcos-Burgos, Mauricio, Stanescu, Horia C.

Mutations in sphingolipid metabolism genes are associated with ADHD.

Henriquez-Henriquez, Marcela, Acosta, Maria T, Martinez, Ariel F, Vélez, Jorge I, Lopera, Francisco, Pineda, David, Palacio, Juan D, Quiroga, Teresa, Worgall, Tilla S, Deckelbaum, Richard J, Mastronardi, Claudio, Molina, Brooke SG, MTA Cooperative Group, Arcos-Burgos, Mauricio, Muenke, Maximilian

application/pdf

Psychopathological Risk in Siblings of Subjects with Attention-Deficit/Hyperactivity Disorder: A cross-Sectional Study

Gómez-Álzate, Alejandra María, Hidalgo-López, Catalina, García-Valencia, Jenny, Martínez-Zamora, Marta, Aguirre-Acevedo, Daniel Camilo, Cuartas-Arias, Mauricio, Arcos-Burgos, Mauricio, Valencia-Evhecerry, Johanna, Lopez-Jaramillo, Carlos, Palacio-Ortiz, Juan David

Ancestry component as a major predictor of lithium response in the treatment of bipolar disorder

Díaz-Zuluaga, Ana M., Vélez, Jorge I., Cuartas, Mauricio, Valencia, Johanna, Castaño, Mauricio, Palacio, Juan David, Arcos-Burgos, Mauricio, López-Jaramillo, Carlos

This result is not displayed to guests.
Login for full access.

The role of psychosocial adversity in the aetiology and course of attention deficit hyperactivity disorder

Gómez-Cano, Sujey, Zapata-Ospina, Juan Pablo, Arcos-Burgos, Mauricio, Palacio-Ortiz, Juan David

CTBP1 and CTBP2 mutations underpinning neurological disorders: a systematic review

Acosta-Baena, Natalia^{Aff1, Aff2, IDs1004802200700w_cor1}, Tejada-Moreno, Johanna Alexandra, Arcos-Burgos, Mauricio, Villegas-Lanau, Carlos Andrés^{Aff1, Aff2}

Deficits of Alzheimer's Disease Neuropsychological Architecture Correlate with Specific Exosomal mRNA Expression: Evidence of a Continuum?

Barceló, Ernesto, Mosquera-Heredia, María I., Vidal, Oscar M., Bolívar, Daniel A., Allegri, Ricardo, Morales, Luis C., Silvera-Redondo, Carlos, Arcos-Burgos, Mauricio, Garavito-Galofre, Pilar, Vélez, Jorge I.

ADGRL3 (LPHN3) variants predict substance use disorder.

Arcos-Burgos, Mauricio, Vélez, Jorge I, Martinez, Ariel F, Ribasés, Marta, Ramos-Quiroga, Josep A, Sánchez-Mora, Cristina, Richarte, Vanesa, Roncero, Carlos, Cormand, Bru, Fernández-Castillo, Noelia, Casas, Miguel, Lopera, Francisco, Pineda, David A, Palacio, Juan D, Acosta-López, Johan E, Cervantes-Henriquez, Martha L, Sánchez-Rojas, Manuel G, Puentes-Rozo, Pedro J, Molina, Brooke SG, MTA Cooperative Group, Boden, Margaret T, Wallis, Deeann, Lidbury, Brett, Newman, Saul, Easteal, Simon, Swanson, James, Patel, Hardip, Volkow, Nora, Acosta, Maria T, Castellanos, Francisco X, de Leon, Jose, Mastronardi, Claudio A, Muenke, Maximilian

application/pdf

This result is not displayed to guests.
Login for full access.

Ataxia with Ocular Apraxia Type 1 (AOA1) (APTX, W279* Mutation): Neurological, Neuropsychological, and Molecular Outlining of a Heterogenous Phenotype in Four Colombian Siblings

Aguillon, David, Vasquez, Daniel, Madrigal, Lucia, Moreno, Sonia, Hernández, Dora, Isaza-Ruget, Mario, Lopez, Juan Javier, Landires, Iván, Nuñez-Samudio, Virginia, Restrepo, Carlos M., Vidal, Oscar M., Vélez, Jorge I., Arcos-Holzinger, Mauricio, Lopera, Francisco, Arcos-Burgos, Mauricio^{Aff7, IDs12035022028217_cor15}

Rare Functional Variants Associated with Antidepressant Remission in Mexican-Americans: Short title: Antidepressant remission and pharmacogenetics in Mexican-Americans

Wong, Ma-Li, Arcos-Burgos, Mauricio, Liu, Sha, Licinio, Alice W., Yu, Chenglong, Chin, Eunice W.M., Yao, Wei-Dong, Lu, Xin-Yun, Bornstein, Stefan R., Licinio, Julio

ADGRL3 genomic variation implicated in neurogenesis and ADHD links functional effects to the incretin polypeptide GIP

Vidal, Oscar M.^{Aff1, IDs4159802220343z_cor1}, Vélez, Jorge I.^{Aff3, IDs4159802220343z_cor2}, Arcos-Burgos, Mauricio

Young adult outcomes in the follow‐up of the multimodal treatment study of attention‐deficit/hyperactivity disorder: symptom persistence, source discrepancy, and height suppression

Swanson, James M, Arnold, L Eugene, Molina, Brooke SG, Sibley, Margaret H, Hechtman, Lily T, Hinshaw, Stephen P, Abikoff, Howard B, Stehli, Annamarie, Owens, Elizabeth B, Mitchell, John T, Nichols, Quyen, Howard, Andrea, Greenhill, Laurence L, Hoza, Betsy, Newcorn, Jeffrey H, Jensen, Peter S, Vitiello, Benedetto, Wigal, Timothy, Epstein, Jeffery N, Tamm, Leanne, Lakes, Kimberly D, Waxmonsky, James, Lerner, Marc, Etcovitch, Joy, Murray, Desiree W, Muenke, Maximilian, Acosta, Maria T, Arcos‐Burgos, Mauricio, Pelham, William E, Kraemer, Helena C, Group, the MTA Cooperative

application/pdf

This result is not displayed to guests.
Login for full access.

ADGRL3 (LPHN3) variants are associated with a refined phenotype of ADHD in the MTA study

Acosta, Maria T, Swanson, James, Stehli, Annamarie, Molina, Brooke SG, Team, the MTA, Martinez, Ariel F, Arcos‐Burgos, Mauricio, Muenke, Maximilian

application/pdf

Correction: Uveitis and Multiple Sclerosis: Potential Common Causal Mutations

de-la-Torre, Alejandra^{Aff1, IDs12035023032653_cor1}, Silva-Aldana, Claudia T., Muñoz-Ortiz, Juliana^{Aff1, Aff3}, Piñeros-Hernández, Laura B., Otero-Marquez, Oscar, Domínguez, Alejandra, Faciolince, León A.^{Aff1, Aff3}, Arcos-Holzinger, Mauricio, Mastronardi, Claudio, Contreras-Bravo, Nora Constanza, Restrepo, Carlos Martín, Arcos-Burgos, Mauricio

Origin of the PSEN1 E280A mutation causing early‐onset Alzheimer's disease

Lalli, Matthew A, Cox, Hannah C, Arcila, Mary L, Cadavid, Liliana, Moreno, Sonia, Garcia, Gloria, Madrigal, Lucia, Reiman, Eric M, Arcos‐Burgos, Mauricio, Bedoya, Gabriel, Brunkow, Mary E, Glusman, Gustavo, Roach, Jared C, Hood, Leroy, Kosik, Kenneth S, Lopera, Francisco

Role of the IL-1 Pathway in Dopaminergic Neurodegeneration and Decreased Voluntary Movement

Stojakovic, Andrea, Paz-Filho, Gilberto, Arcos-Burgos, Mauricio, Licinio, Julio, Wong, Ma-Li, Mastronardi, Claudio A.

electronic

Familial Alzheimer’s Disease and Recessive Modifiers

Vélez, Jorge I., Lopera, Francisco, Silva, Claudia T., Villegas, Andrés, Espinosa, Lady G., Vidal, Oscar M., Mastronardi, Claudio A., Arcos-Burgos, Mauricio^Aff4