Genetic Predisposition to External Apical Root Resorption in Orthodontic Patients: Linkage of Chromosome-18 Marker von Al-Qawasmi, R.A., Hartsfield, J.K., Everett, E.T., Flury, L., Liu, L., Foroud, T.M., Macri, J.V., Roberts, W.E.

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APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study von Ramanan, V K, Risacher, S L, Nho, K, Kim, S, Swaminathan, S, Shen, L, Foroud, T M, Hakonarson, H, Huentelman, M J, Aisen, P S, Petersen, R C, Green, R C, Jack, C R, Koeppe, R A, Jagust, W J, Weiner, M W, Saykin, A J

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The Alzheimer's Disease Sequencing Project: Study design and sample selection von Beecham, Gary W, Bis, J C, Martin, E R, Choi, S-H, DeStefano, A L, van Duijn, C M, Fornage, M, Gabriel, S B, Koboldt, D C, Larson, D E, Naj, A C, Psaty, B M, Salerno, W, Bush, W S, Foroud, T M, Wijsman, E, Farrer, L A, Goate, A, Haines, J L, Pericak-Vance, Margaret A, Boerwinkle, E, Mayeux, R, Seshadri, S, Schellenberg, G

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FASTKD2 is associated with memory and hippocampal structure in older adults von Ramanan, V K, Nho, K, Shen, L, Risacher, S L, Kim, S, McDonald, B C, Farlow, M R, Foroud, T M, Gao, S, Soininen, H, Kłoszewska, I, Mecocci, P, Tsolaki, M, Vellas, B, Lovestone, S, Aisen, P S, Petersen, R C, Jack, C R, Shaw, L M, Trojanowski, J Q, Weiner, M W, Green, R C, Toga, A W, De Jager, P L, Yu, L, Bennett, D A, Saykin, A J

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Oculomotor control in asymptomatic and recently diagnosed individuals with the genetic marker for Huntington’s disease von Blekher, T.M., Yee, R.D., Kirkwood, S.C., Hake, A.M., Stout, J.C., Weaver, M.R., Foroud, T.M.

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Alcohol Dehydrogenase-22 Allele is Associated With Decreased Prevalence of Fetal Alcohol Syndrome in the Mixed-Ancestry Population of the Western Cape Province, South Africa von Viljoen, D.L., Carr, L.G., Foroud, T.M., Brooke, L., Ramsay, M., Li, T.K.

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Alcohol dehydrogenase-22 allele is associated with decreased prevalence of fetal alcohol syndrome in the mixed-ancestry population of the Western Cape Province, South Africa von VILJOEN, D. L, CARR, L. G, FOROUD, T. M, BROOKE, L, RAMSAY, M, LI, T. K

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Supplementary Material for: APOL1 G3 Variant Is Associated with Cardiovascular Mortality and Sudden Cardiac Death in Patients Receiving Maintenance Hemodialysis of European Ancestr... von T.-H., Schwantes-An, C., Robinson-Cohen, S., Liu, N., Zheng, M., Stedman, L., Wetherill, H.J., Edenberg, M., Vatta, T.M., Foroud, G.M., Chertow, S.M., Moe

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Supplementary Material for: Fibroblast Growth Factor 23 Genotype and Cardiovascular Disease in Patients Undergoing Hemodialysis von Schwantes-An, T.-H., Liu, S., Stedman, M., Decker, B.S., Wetherill, L., Edenberg, H.J., Vatta, M., Foroud, T.M., Chertow, G.M., Moe, S.M.

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Supplementary Material for: Copy Number Variation Accuracy in Genome-Wide Association Studies von Lin, P., Hartz, S.M., Wang, J.-C., Krueger, R.F., Foroud, T.M., Edenberg, H.J., Nurnberger, Jr J.I., Brooks, A.I., Tischfield, J.A., Almasy, L.

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