Gene expression levels as endophenotypes in genome-wide association studies of Alzheimer disease von ZOU, F, CARRASQUILLO, M. M, BURGESS, J. D, YOUNKIN, L. H, YOUNKIN, Samuel G, YOUNKIN, C. S, BISCEGLIO, G. D, CROOK, J. E, DICKSON, D. W, PETERSEN, Rc, GRAFF-RADFORD, N, YOUNKIN, Steven G, PANKRATZ, V. S, ERTEKIN-TANER, N, BELBIN, O, MORGAN, K, ALLEN, M, WILCOX, S. L, MA, L, WALKER, L. P, KOURI, N

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DJ-1 mutations are a rare cause of recessively inherited early onset parkinsonism mediated by loss of protein function von Lockhart, P J, Lincoln, S, Hulihan, M, Kachergus, J, Wilkes, K, Bisceglio, G, Mash, D C, Farrer, M J

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Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members von Finch, NiCole, Baker, Matt, Crook, Richard, Swanson, Katie, Kuntz, Karen, Surtees, Rebecca, Bisceglio, Gina, Rovelet-Lecrux, Anne, Boeve, Bradley, Petersen, Ronald C., Dickson, Dennis W., Younkin, Steven G., Deramecourt, Vincent, Crook, Julia, Graff-Radford, Neill R., Rademakers, Rosa

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Association and heterogeneity at the GAPDH locus in Alzheimer's disease von Allen, Mariet, Cox, Claire, Belbin, Olivia, Ma, Li, Bisceglio, Gina D, Wilcox, Samantha L, Howell, Chanley C, Hunter, Talisha A, Culley, Oliver, Walker, Louise P, Carrasquillo, Minerva M, Dickson, Dennis W, Petersen, Ronald C, Graff-Radford, Neill R, Younkin, Steven G, Ertekin-Taner, Nilüfer

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Parkin-proven disease: Common founders but divergent phenotypes von LINCOLN, S, WILEY, J, MARDER, K, KLEIN, C, BISCEGLIO, G, HUSSEY, J, WEST, A, HULIHAN, M, HARDY, J, FARRER, M, LYNCH, T, LANGSTON, J. W, CHEN, R, LANG, A, ROGAEVA, E, SA, D. S, MUNHOZ, R. P, HARRIS, J

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Parkinsonism, FXTAS, and FMR1 premutations von Toft, Mathias, Aasly, Jan, Bisceglio, Gina, Adler, Charles H., Uitti, Ryan J., Krygowska-Wajs, Anna, Lynch, Timothy, Wszolek, Zbigniew K., Farrer, Matthew J.

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The Tau H1 Haplotype is associated with Parkinson's disease in the Norwegian population von Farrer, Matt, Skipper, Lisa, Berg, Marianne, Bisceglio, Gina, Hanson, Melissa, Hardy, John, Adam, Amanda, Gwinn-Hardy, Katrina, Aasly, Jan

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Novel Late-Onset Alzheimer's Disease Loci Variants Associate with Brain Gene Expression (S54.001) von Allen, M., Zou, F., Chai, H. S., Younkin, C., Crook, J., Pankratz, V., Carrasquillo, M., Rowley, C., Nair, A., Middha, S., Maharjan, S., Nguyen, T., Ma, L., Malphrus, K., Palusak, R., Lincoln, S., Bisceglio, G., Georgescu, C., Kolbert, C., Jen, J., Petersen, R., Graff-Radford, N., Dickson, D., Younkin, S., Taner, N.

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Novel Progressive Supranuclear Palsy (PSP) Risk Loci Variants Associate with Brain Gene Expression Levels (S54.002) von Taner, N., Zou, F., Chai, H. S., Younkin, C., Crook, J., Pankratz, V., Allen, M., Carrasquillo, M., Rowley, C., Nair, A., Middha, S., Maharjan, S., Nguyen, T., Ma, L., Malphrus, K., Palusak, R., Lincoln, S., Bisceglio, G., Georgescu, C., Kouri, N., Kolbert, C., Jen, J., Petersen, R., Graff-Radford, N., Dickson, D., Younkin, S.

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Brain Expression Genome-Wide Association Study (eGWAS) Identifies Human Disease-Associated Variants (P05.069) von Taner, N., Zou, F., Chai, H. S., Younkin, C., Crook, J., Pankratz, V., Allen, M., Carrasquillo, M., Rowley, C., Nair, A., Middha, S., Maharjan, S., Nguyen, T., Ma, L., Malphrus, K., Palusak, R., Lincoln, S., Bisceglio, G., Georgescu, C., Kouri, N., Kolbert, C., Jen, J., Petersen, R., Graff-Radford, N., Dickson, D., Younkin, S.

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α-Synuclein missense and multiplication mutations in autosomal dominant Parkinson’s disease von Hope, Andrew D, Myhre, Ronny, Kachergus, Jennifer, Lincoln, Sarah, Bisceglio, Gina, Hulihan, Mary, Farrer, Matthew J

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Parkinson's disease in Ireland: Clinical presentation and genetic heterogeneity in patients with parkin mutations von Wiley, Joseph, Lynch, Timothy, Lincoln, Sarah, Skipper, Lisa, Hulihan, Mary, Gosal, David, Bisceglio, Gina, Kachergus, Jennifer, Hardy, John, Farrer, Matthew J.

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Multiplication of the alpha-synuclein gene is not a common disease mechanism in Lewy body disease von Lockhart, Paul J, Kachergus, Jennifer, Lincoln, Sarah, Hulihan, Mary, Bisceglio, Gina, Thomas, Natalie, Dickson, Dennis, Farrer, Matthew J

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Polygenic risk and hazard scores for Alzheimer's disease prediction von Leonenko, G, Shoai, M, Frizzati, A, Bossu, P, Fox, NC, Williams, J, Tsolaki, M, Avramidou, D, Germanou, A, Love, S, McGuinness, B, Passmore, P, Warren, JD, Kawalia, A, Hughes, JT, Lupton, MK, Powell, J, Bonuccelli, U, Uphill, J, Fisher, E, Soininen, H, Bisceglio, G, Ma, L, Carrasquillo, MM, Daniilidou, M, Galimberti, D, Scarpini, E, Peters, O, Ramirez, A, Pichler, S, Riemenschneider, M, Heun, R, Kolsch, H, Heuser, I, Rujescu, D, Giegling, I, Hull, M, Lovestone, S, Cruchaga, C, Feulner, T, Holmes, C, Mann, D, Pickering-Brown, S, Livingston, G, Bass, NJ, Vronskaya, M, Morgan, T, Cushion, TD, Jones, L, Marshall, R, Grozeva, D, O'Donovan, MC, Owen, MJ, Russo, G, Maier, W, Jessen, F, Wichmann, H-E, Vellas, B, Vardy, E, Moebus, S, Dichgans, M, Klopp, N, Turton, J, Brown, K, Medway, C, Hoffmann, P, Daniele, A, Gallacher, J, van den Bussche, H, Brayne, C, Riedel-Heller, S, Powell, JF, Al-Chalabi, A, Pastor, P, Diez-Fairen, M, Lynch, A, Lawlor, B, Coto, E, Alvarez, V, Mead, S, Ryan, N, Nacmias, B, Rodriguez-Rodriguez, E, Sanchez-Juan, P, Shofany, J, Banaj, N, Sacchinelli, E, Smith, AD, Warden, D, Cupidi, C, Bruni, AC, Gallo, M, Harold, D, Cecchetti, R, Mecocci, P, Warner, N, Wilcock, G, Deloukas, P, Corcoran, C, Tschanz, J

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Identification of the Human Ubiquitin Specific Protease 31 (USP31) Gene: Structure, Sequence and Expression Analysis von Lockhart, Paul J., Hulihan, Mary, Lincoln, Sarah, Hussey, Jennifer, Skipper, Lisa, Bisceglio, Gina, Wilkes, Kristen, Farrer, Matthew J.

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Human whole genome genotype and transcriptome data for Alzheimer’s and other neurodegenerative diseases von Allen, Mariet, Carrasquillo, Minerva M., Funk, Cory, Heavner, Benjamin D., Zou, Fanggeng, Younkin, Curtis S., Burgess, Jeremy D., Chai, High-Seng, Crook, Julia, Eddy, James A., Li, Hongdong, Logsdon, Ben, Peters, Mette A., Dang, Kristen K., Wang, Xue, Serie, Daniel, Wang, Chen, Nguyen, Thuy, Lincoln, Sarah, Malphrus, Kimberly, Bisceglio, Gina, Li, Ma, Golde, Todd E., Mangravite, Lara M., Asmann, Yan, Price, Nathan D., Petersen, Ronald C., Graff-Radford, Neill R., Dickson, Dennis W., Younkin, Steven G., Ertekin-Taner, Nilüfer

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Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease von Younkin, Steven G, Carrasquillo, Minerva M, Zou, Fanggeng, Pankratz, V Shane, Wilcox, Samantha L, Ma, Li, Walker, Louise P, Younkin, Samuel G, Younkin, Curtis S, Younkin, Linda H, Bisceglio, Gina D, Ertekin-Taner, Nilufer, Crook, Julia E, Dickson, Dennis W, Petersen, Ronald C, Graff-Radford, Neill R

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Replication of EPHA1 and CD33 associations with late-onset Alzheimer's disease: a multi-centre case-control study von Carrasquillo, Minerva M, Belbin, Olivia, Hunter, Talisha A, Ma, Li, Bisceglio, Gina D, Zou, Fanggeng, Crook, Julia E, Pankratz, V Shane, Sando, Sigrid B, Aasly, Jan O, Barcikowska, Maria, Wszolek, Zbigniew K, Dickson, Dennis W, Graff-Radford, Neill R, Petersen, Ronald C, Passmore, Peter, Morgan, Kevin, Younkin, Steven G

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Genome-wide Screen Identifies rs646776 near Sortilin as a Regulator of Progranulin Levels in Human Plasma von Carrasquillo, Minerva M., Nicholson, Alexandra M., Finch, NiCole, Gibbs, J. Raphael, Baker, Matt, Rutherford, Nicola J., Hunter, Talisha A., DeJesus-Hernandez, Mariely, Bisceglio, Gina D., Mackenzie, Ian R., Singleton, Andrew, Cookson, Mark R., Crook, Julia E., Dillman, Allissa, Hernandez, Dena, Petersen, Ronald C., Graff-Radford, Neill R., Younkin, Steven G., Rademakers, Rosa

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ABCA7 Deficiency Accelerates Amyloid-β Generation and Alzheimer's Neuronal Pathology von Sakae, Nobutaka, Liu, Chia-Chen, Shinohara, Mitsuru, Frisch-Daiello, Jessica, Ma, Li, Yamazaki, Yu, Tachibana, Masaya, Younkin, Linda, Kurti, Aishe, Carrasquillo, Minerva M, Zou, Fanggeng, Sevlever, Daniel, Bisceglio, Gina, Gan, Ming, Fol, Romain, Knight, Patrick, Wang, Miao, Han, Xianlin, Fryer, John D, Fitzgerald, Michael L, Ohyagi, Yasumasa, Younkin, Steven G, Bu, Guojun, Kanekiyo, Takahisa

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