Rethinking Oral Health in Aging: Ecosocial Theory and Intersectionality von Slack-Smith, L., Ng, T., Macdonald, M.E., Durey, A.

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Obstetric conditions and the placental weight ratio von Macdonald, E.M, Natale, R, Regnault, T.R.H, Koval, J.J, Campbell, M.K

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Loss of Huntingtin-Mediated BDNF Gene Transcription in Huntington's Disease von Zuccato, Chiara, Ciammola, Andrea, Rigamonti, Dorotea, Leavitt, Blair R., Goffredo, Donato, Conti, Luciano, MacDonald, Marcy E., Friedlander, Robert M., Silani, Vincenzo, Hayden, Michael R., Timmusk, Tõnis, Sipione, Simonetta, Cattaneo, Elena

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Meclizine is neuroprotective in models of Huntington's disease von GOHIL, Vishal M, OFFNER, Nicolas, WALKER, James A, SHETH, Sunil A, FOSSALE, Elisa, GUSELLA, James F, MACDONALD, Marcy E, NERI, Christian, MOOTHA, Vamsi K

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Factors associated with HD CAG repeat instability in Huntington disease von Wheeler, V C, Persichetti, F, McNeil, S M, Mysore, J S, Mysore, S S, MacDonald, M E, Myers, R H, Gusella, J F, Wexler, N S

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Oral health-related stigma: Describing and defining a ubiquitous phenomenon von Doughty, J, Macdonald, M E, Muirhead, V, Freeman, R

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The quantity and quality of the social networks of young people with early psychosis compared with closely matched controls von Macdonald, E.M, Hayes, R.L, Baglioni, A.J

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CAG repeat number governs the development rate of pathology in Huntington's disease von Penney Jr, John B., Vonsattel, Jean-Paul, Macdonald, Marcy E., Gusella, James F., Myers, Richard H.

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Huntingtin is required for neurogenesis and is not impaired by the Huntington's disease CAG expansion von White, Jacqueline K, Auerbach, Wojtek, Duyao, Mabel P, Vonsattel, Jean-Paul, Gusella, James F, Joyner, Alexandra L, MacDonald, Marcy E

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Huntingtin Interacts with a Family of WW Domain Proteins von Faber, Peter W., Barnes, Glenn T., Srinidhi, Jayalakshmi, Chen, Jianmin, Gusella, James F., MacDonald, Marcy E.

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Length-Dependent Gametic CAG Repeat Instability in the Huntington's Disease Knock-in Mouse von Wheeler, Vanessa C., Auerbach, Wojtek, White, Jacqueline K., Srinidhi, Jayalakshmi, Auerbach, Anna, Ryan, Angela, Duyao, Mabel P., Vrbanac, Vladimir, Weaver, Meredith, Gusella, James F., Joyner, Alexandra L., MacDonald, Marcy E.

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Hypogonadotropic hypogonadism and cleft lip and palate caused by a balanced translocation producing haploinsufficiency for FGFR1 von Kim, HG, Herrick, S R, Lemyre, E, Kishikawa, S, Salisz, J A, Seminara, S, MacDonald, M E, Bruns, G A P, Morton, C C, Quade, B J, Gusella, J F

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Evidence for the GluR6 gene associated with younger onset age of Huntington's disease von MACDONALD, M. E, VONSATTEL, J. P, SHRINIDHI, J, COUROPMITREE, N. N, CUPPLES, L. A, BIRD, E. D, GUSELLA, J. F, MYERS, R. H

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Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington disease von Djoussé, L., Knowlton, B., Hayden, M., Almqvist, E.W., Brinkman, R., Ross, C., Margolis, R., Rosenblatt, A., Durr, A., Dode, C., Morrison, P.J., Novelletto, A., Frontali, M., Trent, R.J.A., McCusker, E., Gómez-Tortosa, E., Mayo, D., Jones, R., Zanko, A., Nance, M., Abramson, R., Suchowersky, O., Paulsen, J., Harrison, M., Yang, Q., Cupples, L.A., Gusella, J.F., MacDonald, M.E., Myers, R.H.

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Herbicide exposure modifies GSTP1 haplotype association to parkinson onset age : The GenePD study von WILK, J. B, TOBIN, J. E, SINGER, C, GROWDON, J. H, LATOURELLE, J. C, SAINT-HILAIRE, M. H, DESTEFANO, A. L, PRAKASH, R, WILLIAMSON, S, BERG, C. J, SUN, M, GOLDWURM, S, SUCHOWERSKY, O, PEZZOLI, G, RACETTE, B. A, PERLMUTTER, J. S, PARSIAN, A, BAKER, K. B, GIROUX, M. L, LITVAN, I, PRAMSTALLER, P. P, NICHOLSON, G, BURN, D. J, SHILL, H. A, CHINNERY, P. F, VIEREGGE, P, SLEVIN, J. T, CAMBI, F, MACDONALD, M. E, GUSELLA, J. F, MYERS, R. H, GOLBE, L. I, KLEIN, C, WOOTEN, G. F, LEW, M. F, MARK, M. H, GUTTMAN, M, WATTS, R. L

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Clinical and genetic heterogeneity in benign hereditary chorea von BREEDVELD, G. J, PERCY, A. K, MACDONALD, M. E, DE VRIES, B. B. A, YAPIJAKIS, C, DURE, L. S, IPPEL, E. F, SANDKUIJL, L. A, HEUTINK, P, ARTS, W. F. M

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Reduced Penetrance of the Huntington's Disease Mutation von McNeil, Sandra M., Novelletto, Andrea, Srinidhi, Jayalakshmi, Barnes, Glenn, Kornbluth, Ira, Altherr, Michael R., Wasmuth, John J., Gusella, James F., MacDonald, Marcy E., Myers, Richard H.

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De novo expansion of a (CAG) n repeat in sporadic Huntington's disease von Myers, R. H, MacDonald, M. E, Koroshetz, W. J, Duyao, M. P, Ambrose, C. M, Taylor, S. A. M, Barnes, G, Srinidhi, J, Lin, C. S, Whaley, W. L, Lazzarini, A. M, Schwarz, M, Wolff, G, Bird, E. D, Vonsattel, J.-P. G, Gusella, J. F

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Molecular genetics: Unmasking polyglutamine triggers in neurodegenerative disease von Gusella, James F, MacDonald, Marcy E

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Huntingtin's WW domain partners in Huntington's disease post-mortem brain fulfill genetic criteria for direct involvement in Huntington's disease pathogenesis von PASSANI, L. A, BEDFORD, M. T, FABER, P. W, MCGINNIS, K. M, SHARP, A. H, GUSELLA, J. F, VONSATTEL, J.-P, MACDONALD, M. E

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