Search Results - "Gayán, J."

Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder localizes pleiotropic loci by Gayán, J., Willcutt, E.G., Fisher, S.E., Francks, C., Cardon, L.R., Olson, R.K., Pennington, B.F., Smith, S.D., Monaco, A.P., DeFries, J.C.

“…Background:  There is a growing interest in the study of the genetic origins of comorbidity, a direct consequence of the recent findings of genetic loci that…”
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Genetic and Environmental Influences on Orthographic and Phonological Skills in Children With Reading Disabilities by Gayan, Javier, Olson, Richard K.

“…Data from identical and fraternal twins were analyzed to estimate the proportions of genetic and environmental influences on group deficits in accuracy and,…”
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Evidence for Linkage and Association with Reading Disability, on 6p21.3-22 by Kaplan, D.E., Gayán, J., Ahn, J., Won, T.-W., Pauls, D., Olson, R.K., DeFries, J.C., Wood, F., Pennington, B.F., Page, G.P., Smith, S.D., Gruen, J.R.

“…Reading disability (RD), or dyslexia, is a common heterogeneous syndrome with a large genetic component. Several studies have consistently found evidence for a…”
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Quantitative-Trait Locus for Specific Language and Reading Deficits on Chromosome 6p by Gayán, Javier, Smith, Shelley D., Cherny, Stacey S., Cardon, Lon R., Fulker, David W., Brower, Amy M., Olson, Richard K., Pennington, Bruce F., DeFries, John C.

“…Reading disability (RD), or dyslexia, is a complex cognitive disorder manifested by difficulties in learning to read, in otherwise normal individuals…”
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Reading disability: evidence for a genetic etiology by Gayán, J, Olson, R K

“…A review of evidence for genetic influences on reading disabilities (RD) is presented, with focus on twin study design and sib-pair linkage techniques…”
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ATP5H/KCTD2 locus is associated with Alzheimer's disease risk by Boada, M, Antúnez, C, Ramírez-Lorca, R, DeStefano, A L, González-Pérez, A, Gayán, J, López-Arrieta, J, Ikram, M A, Hernández, I, Marín, J, Galán, J J, Bis, J C, Mauleón, A, Rosende-Roca, M, Moreno-Rey, C, Gudnasson, V, Morón, F J, Velasco, J, Carrasco, J M, Alegret, M, Espinosa, A, Vinyes, G, Lafuente, A, Vargas, L, Fitzpatrick, A L, Launer, L J, Sáez, M E, Vázquez, E, Becker, J T, López, O L, Serrano-Ríos, M, Tárraga, L, van Duijn, C M, Real, L M, Seshadri, S, Ruiz, A

“…To identify loci associated with Alzheimer disease, we conducted a three-stage analysis using existing genome-wide association studies (GWAS) and genotyping in…”
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Replication of twelve association studies for Huntington’s disease residual age of onset in large Venezuelan kindreds by Andresen, J M, Gayán, J, Cherny, S S, Brocklebank, D, Alkorta-Aranburu, G, Addis, E A, Cardon, L R, Housman, D E, Wexler, N S

“…Background: The major determinant of age of onset in Huntington’s disease is the length of the causative triplet CAG repeat. Significant variance remains,…”
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Etiology of reading difficulties and rapid naming: the Colorado Twin Study of Reading Disability by Davis, C J, Gayán, J, Knopik, V S, Smith, S D, Cardon, L R, Pennington, B F, Olson, R K, DeFries, J C

“…Children with reading deficits perform more slowly than normally-achieving readers on speed of processing measures, such as rapid naming (RN). Although rapid…”
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Repeat instability in the 27-39 CAG range of the HD gene in the Venezuelan kindreds: Counseling implications by Brocklebank, D., Gayán, J., Andresen, J.M., Roberts, S.A., Young, A.B., Snodgrass, S.R., Penney, J.B., Ramos-Arroyo, M.A., Cha, J.J., Rosas, H.D., Hersch, S.M., Feigin, A., Cherny, S.S., Wexler, N.S., Housman, D.E., Cardon, L.R.

“…The instability of the CAG repeat size of the HD gene when transmitted intergenerationally has critical implications for genetic counseling practices. In…”
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Whole-genome conditional two-locus analysis identifies novel candidate genes for late-onset Parkinson’s disease by González-Pérez, A., Gayán, J., Marín, J., Galán, J. J., Sáez, M. E., Real, L. M., Antúnez, C., Ruiz, A.

“…Whole-genome epistasis analysis may add a new layer of knowledge to whole-genome association studies, permitting the identification of new candidate genes…”
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Reading Disability and Chromosome 6p21.3: Evaluation of MOG as a Candidate Gene by Smith, Shelley D., Kelley, Philip M., Askew, James W., Hoover, Denise M., Deffenbacher, Karen E., Gayán, Javier, Brower, Amy M., Olson, Richard K.

“…Linkage analysis has localized a gene influencing specific reading disability (dyslexia) to 6p213. The myelin oligodendrocyte glycoprotein (MOG) gene, which…”
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GAB2 gene does not modify the risk of Alzheimer’s disease in Spanish APOE 4 carriers by Ramírez-Lorca, Reposo, Boada, M., Saez, M. E., Hernandez, I., Mauleon, A., Rosende-Roca, M., Martinez-Lage, P., Gutierrez, M., Real, L. M., Lopez-Arrieta, J., Gayan, J., Antunez, C., Gonzalez-Perez, A., Tarraga, L., Ruiz, A.

“…Objectives The genetic basis of Alzheimer’s disease (AD) is being analyzed in multiple whole genome association studies (WGAS). The GAB2 gene has been proposed…”
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644 GENOME-WIDE ASSOCIATION AND HIGH THROUGHPUT GENOTYPE IMPUTATION STUDIES CONFIRM A SUSCEPTIBILITY LOCUS TO HCV INFECTION ON 6P22.1–P21.31 by Del Campo, J.A, Maraver, M, Pardo, B, Grande, L, Diago, M, Carmona, I, Andrade, R, Rivero, M.C, Velasco, J, Saez, M.E, Galán, J.J, Ramírez-Lorca, R, Morón, F.J, Carrasco, J.M, Salinas, A, Molero, E, Royo, J.L, Moreno, C, González Pérez, A, Gayan, J, Real, L.M, Ruiz, A, Romero-Gómez, M

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4CPS-060 Prevalence of vancomycin-related neutropaenia, thrombocytopaenia and acute kidney injury by Landa Alberdi, J, Lombera Saez, L, Aldalur Uranga, I, Zurutuza Lopez, A, García Echeverría, D, Gonzalez Fernandez, T, Gayan Lera, MJ, Pascual Gonzalez, P, Bachiller Cacho, MP, Carmona Oyaga, MP

“…BackgroundVancomycin is a glucopeptide antibiotic widely used to treat Gram positive related infections. It is well known for its nefrotoxic and ototoxic…”
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1ISG-005 A cost-effective strategy: switching from one to two tablets, in a once-daily regimen in HIV patients by Carmona Oyaga, MP, Bachiller Cacho, MP, Landa Alberdi, J, Lombera Saez, L, Mendarte Barrenechea, L, Lopez Arzoz, G, Mauelon Echeverria, MD, Zurutuza Lopez, A, Iribarren Loyarte, JA, Gayan Lera, MJ

“…BackgroundFollowing a request by the Central Management Organisation of our Health System (HS), a decision was made to change from a patented drug of three…”
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Genetic and environmental influences on individual differences in printed word recognition by Gayán, Javier, Olson, Richard K

“…The genetic and environmental etiologies of individual differences in printed word recognition and related skills were explored in 440 identical and fraternal…”
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1st Conference Clinical Trials on Alzheimer’s Disease September 17-18-19, 2008 School of Medecine Montpellier, France by Portet, F., Lehmann, S., Shapiro, F., Vanderstichele, H., Vanmechelen, E., De Deyn, P. P., Shaw, L., Trojanowski, J., Nestor, S. M., Borrie, M., De Meyer, G., Minthon, L., Wiltfang, J., Grundke-Iqbal, I., Gertz, H. J., Berwig, M., Leicht, H., Zhu, C. W., Townsend, R., Scarmeas, N., Albert, M., Stern, Y., Bravo, G., Dubois, M. F., Deudon, A., Gervais, X., Leone, E., Lavallart, B., Green, R. C., Van Kan, G. Abellan, Carrie, I., Gardette, J., Dangour, A. D., Elbourne, D., Richards, M., Uauy, R., Zavitz, K. H., Wurtman, R. J., Möller, H. J., Owenius, R., Nelissen, N., Koole, M., Van Laere, K., Ortiz, P., López, O., Pla, R., Grifols, J. R., Paez, A., Núñez, L., Ferrer, I., Siemers, E. R., Willey, M. B., Sáez, M. E., Mauleón, A., Gutiérrez, M., González-Pérez, A., Bchiri, J. El, Fraisse, M. L., Husson, J. M., Melis, R. J. F., Krabbe, P. F., Yik, P. Y., Mok, W., Doody, R., Fox, N. C., Orgogozo, J. M., Molloy, D. W., Diloreto, P., Clarke, J., Robert, P. H., Cantet, C., Erder, M. H., Setyawan, J., Fridman, M., Ramirez, B., Anglés, N., Boada, M., Roca, I., Cuberas, G., Tramoni, E., Elkhoury, C., Mattner, F., Gatignol, P., David, C., Guitton, C., German, P., Hajas, G., Wesnes, K., Wetten, S., Andrieu, S., Ousset, P. J., Verwey, N. A., Clark, C., Cole, G. M., Lannfelt, L., Pirttila, T., Verbeek, M. M., Younkin, S., Viswanathan, A., Weil, J.

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Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia by Richardson, Alex J, Fisher, Simon E, Pennington, Bruce F, Stein, John F, Cardon, Lon R, Marlow, Angela J, Gayán, Javier, Francks, Clyde, Ishikawa-Brush, Yumiko, MacPhie, I. Laurence, Talcott, Joel B, Newbury, Dianne F, DeFries, John C, Monaco, Anthony P, Smith, Shelley D, Olson, Richard K

“…Developmental dyslexia is defined as a specific and significant impairment in reading ability that cannot be explained by deficits in intelligence, learning…”
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DD-003 Implementation of an automated dispensing cabinet linked to an electronic prescribing programme in a home care service by Lizardi, A, Ripa, C, Ercilla, M, Gayán, MJ, Odriozola, B, López, G, Lombera, L, Zurutuza, A, Urretavizcaya, M, García, D

“…BackgroundBefore October 2015, the dispensing procedure in the Home Care Service (HCS) was manual where medication for each patient was sent from the pharmacy…”
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Diagnóstico diferencial de la dorsalgia crónica: a propósito de 2 casos by Esteban-Zubero, E, Aranguren-García, F.J, Gayan-Ordás, J, Ruiz-Ruiz, F.J

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