Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder localizes pleiotropic loci von 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.

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ATP5H/KCTD2 locus is associated with Alzheimer's disease risk von 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

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Evidence for Linkage and Association with Reading Disability, on 6p21.3-22 von 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.

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Quantitative-Trait Locus for Specific Language and Reading Deficits on Chromosome 6p von 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.

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Replication of twelve association studies for Huntington’s disease residual age of onset in large Venezuelan kindreds von 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

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Reading disability: evidence for a genetic etiology von Gayán, J, Olson, R K

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Repeat instability in the 27-39 CAG range of the HD gene in the Venezuelan kindreds: Counseling implications von 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.

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Etiology of reading difficulties and rapid naming: the Colorado Twin Study of Reading Disability von Davis, C J, Gayán, J, Knopik, V S, Smith, S D, Cardon, L R, Pennington, B F, Olson, R K, DeFries, J C

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Whole-genome conditional two-locus analysis identifies novel candidate genes for late-onset Parkinson’s disease von González-Pérez, A., Gayán, J., Marín, J., Galán, J. J., Sáez, M. E., Real, L. M., Antúnez, C., Ruiz, A.

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Genetic and environmental influences on individual differences in printed word recognition von Gayán, Javier, Olson, Richard K

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Reading Disability and Chromosome 6p21.3: Evaluation of MOG as a Candidate Gene von Smith, Shelley D., Kelley, Philip M., Askew, James W., Hoover, Denise M., Deffenbacher, Karen E., Gayán, Javier, Brower, Amy M., Olson, Richard K.

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GAB2 gene does not modify the risk of Alzheimer’s disease in Spanish APOE 4 carriers von 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.

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Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia von 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

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1ISG-005 A cost-effective strategy: switching from one to two tablets, in a once-daily regimen in HIV patients von 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

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4CPS-060 Prevalence of vancomycin-related neutropaenia, thrombocytopaenia and acute kidney injury von 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

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Quantitative trait locus for reading disability on chromosome 6p is pleiotropic for attention-deficit/hyperactivity disorder von Willcutt, Erik G., Pennington, Bruce F., Smith, Shelley D., Cardon, Lon R., Gayán, Javier, Knopik, Valerie S., Olson, Richard K., DeFries, John C.

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The trans-ancestral genomic architecture of glycemic traits von Chen, J, Spracklen, CN, Varshney, A, Luan, J, Willems, SM, Waage, J, Hottenga, J-J, Louie, T, Maerz, W, Ndungu, A, Nolte, IM, Raulerson, CK, Rohde, R, Wu, P, Bielak, LF, Brody, JA, Burtt, NP, Cade, BE, Chitrala, KN, Delgado, GE, Hartwig, FP, Hwang, MY, Jensen, RA, Kooner, IK, Loh, M, Long, J, Mangino, M, Noce, D, Preuss, M, Rasmussen-Torvik, LJ, Ryan, K, Strawbridge, RJ, Wang, C, Wen, W, Wilsgaard, T, Zhao, W, Dehghan, A, Farmaki, AE, Franberg, M, Fuchsberger, C, Gjesing, AP, Goel, A, Herder, C, Igase, M, Kalyani, RR, Katsuya, T, Khor, CC, Kuulasmaa, T, Kuusisto, J, Mingrone, G, Nadler, JL, Neville, MJ, Norris, JM, Polasek, O, Sandow, K, Sattar, N, Teslovich, TM, Tsai, MY, Abecasis, GR, Black, C, Boehm, BO, Canouil, M, Caulfield, MJ, Cheng, C-Y, Elmstahl, S, Ferrannini, E, Grimsgaard, S, Gudnason, V, Hamsten, A, Hayward, C, Huang, W, Ingelsson, E, Kaleebu, P, Kardia, SLR, Keinanen-Kiukaanniemi, SM, Kooner, JS, Kumari, M, Lind, L, Lindgren, C, Magnusson, PKE, Munroe, PB, Padmanabhan, S, Pedersen, O, Qi, L, Raffel, LJ, Scott, LJ, Sever, P, Snieder, H, Stumvoll, M, Tabara, Y, Tuomilehto, J, Vitart, V, Vrijkotte, TGM, Watanabe, RM, Wickremasinghe, AR, Yengo, L, Zheng, W, Zonderman, AB, Dupuis, J, Meigs, JB

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DD-003 Implementation of an automated dispensing cabinet linked to an electronic prescribing programme in a home care service von Lizardi, A, Ripa, C, Ercilla, M, Gayán, MJ, Odriozola, B, López, G, Lombera, L, Zurutuza, A, Urretavizcaya, M, García, D

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Hereditary transthyretin amyloidosis caused by Val142Ile variant in Spain: phenotypic characteristics, geographic distribution and population frequency von De Frutos Seminario, F, Peiro Aventin, B, Eiros, R, Limeres Freire, J, Sevilla, T, Carbayo, A, Llongueras, P, Garcia-Alvarez, A, Ripoll-Vera, T, Macias, R, Vilches, S, Ruiz-Bustillo, S, Arana Achaga, X, Gayan Ordas, J, Gonzalez-Costello, J

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Factors associated with the presence of thrombus in the left atrial appendage and usefulness of the D-Dimer to rule out its presence von Irigaray Sierra, P, Gayan Ordas, J, Pueo Crespo, E M, Fernandez-Rodriguez, D, Pastor Pueyo, P, Blanco Ponce, E, Matute-Blanco, L, Pueyo Balsells, N, Barriuso Barrado, I, Ramirez Martinez, T, Papiol Morales, E, Worner Diz, F

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