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Biblio

Found 148 results
Author Keyword Title [ Type(Asc)] Year
Journal Article
N. S. Raghavan, Brickman, A. M., Andrews, H., Manly, J. J., Schupf, N., Lantigua, R., Wolock, C. J., Kamalakaran, S., Petrovski, S., Tosto, G., Vardarajan, B. N., Goldstein, D. B., and Mayeux, R., Whole-exome sequencing in 20,197 persons for rare variants in Alzheimer's disease., Ann Clin Transl Neurol, vol. 5, no. 7, pp. 832-842, 2018.
B. N. Vardarajan, Barral, S., Jaworski, J., Beecham, G. W., Blue, E., Tosto, G., Reyes-Dumeyer, D., Medrano, M., Lantigua, R., Naj, A., Thornton, T., DeStefano, A., Martin, E., San Wang, L. -, Brown, L., Bush, W., van Duijn, C., Goate, A., Farrer, L., Haines, J. L., Boerwinkle, E., Schellenberg, G., Wijsman, E., Pericak-Vance, M. A., Mayeux, R., and San Wang, L. -, Whole genome sequencing of Caribbean Hispanic families with late-onset Alzheimer's disease., Ann Clin Transl Neurol, vol. 5, no. 4, pp. 406-417, 2018.
J. C. Bis, Jian, X., Kunkle, B. W., Chen, Y., Hamilton-Nelson, K. L., Bush, W. S., Salerno, W. J., Lancour, D., Ma, Y., Renton, A. E., Marcora, E., Farrell, J. J., Zhao, Y., Qu, L., Ahmad, S., Amin, N., Amouyel, P., Beecham, G. W., Below, J. E., Campion, D., Charbonnier, C., Chung, J., Crane, P. K., Cruchaga, C., L Cupples, A., Dartigues, J. - F., Debette, S., Deleuze, J. - F., Fulton, L., Gabriel, S. B., Genin, E., Gibbs, R. A., Goate, A., Grenier-Boley, B., Gupta, N., Haines, J. L., Havulinna, A. S., Helisalmi, S., Hiltunen, M., Howrigan, D. P., M Ikram, A., Kaprio, J., Konrad, J., Kuzma, A., Lander, E. S., Lathrop, M., Lehtimäki, T., Lin, H., Mattila, K., Mayeux, R., Muzny, D. M., Nasser, W., Neale, B., Nho, K., Nicolas, G., Patel, D., Pericak-Vance, M. A., Perola, M., Psaty, B. M., Quenez, O., Rajabli, F., Redon, R., Reitz, C., Remes, A. M., Salomaa, V., Sarnowski, C., Schmidt, H., Schmidt, M., Schmidt, R., Soininen, H., Thornton, T. A., Tosto, G., Tzourio, C., van der Lee, S. J., van Duijn, C. M., Vardarajan, B., Wang, W., Wijsman, E., Wilson, R. K., Witten, D., Worley, K. C., Zhang, X., Bellenguez, C., Lambert, J. - C., Kurki, M. I., Palotie, A., Daly, M., Boerwinkle, E., Lunetta, K. L., DeStefano, A. L., Dupuis, J., Martin, E. R., Schellenberg, G. D., Seshadri, S., Naj, A. C., Fornage, M., and Farrer, L. A., Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation., Mol Psychiatry, 2018.
D. Curtis, Bakaya, K., Sharma, L., and Bandyopadhyay, S., Weighted burden analysis of exome-sequenced late-onset Alzheimer's cases and controls provides further evidence for a role for PSEN1 and suggests involvement of the PI3K/Akt/GSK-3β and WNT signalling pathways., Ann Hum Genet, vol. 84, no. 3, pp. 291-302, 2020.
G. C. Román, Tatemichi, T. K., Erkinjuntti, T., Cummings, J. L., Masdeu, J. C., Garcia, J. H., Amaducci, L., Orgogozo, J. M., Brun, A., and Hofman, A., Vascular dementia: diagnostic criteria for research studies. Report of the NINDS-AIREN International Workshop., Neurology, vol. 43, no. 2, pp. 250-60, 1993.
A. J. Myers, Marshall, H., Holmans, P., Compton, D., Crook, R. J. P., Mander, A. P., Nowotny, P., Smemo, S., Dunstan, M., Jehu, L., Wang, J. C., Hamshere, M., Morris, J. C., Norton, J., Chakraventy, S., Tunstall, N., Lovestone, S., Petersen, R., O'Donovan, M., Jones, L., Williams, J., Owen, M. J., Hardy, J., and Goate, A., Variation in the urokinase-plasminogen activator gene does not explain the chromosome 10 linkage signal for late onset AD., Am J Med Genet B Neuropsychiatr Genet, vol. 124B, no. 1, pp. 29-37, 2004.
C. Reitz, Jun, G., Naj, A., Rajbhandary, R., Vardarajan, B. Narayan, San Wang, L. -, Valladares, O., Lin, C. - F., Larson, E. B., Graff-Radford, N. R., Evans, D., De Jager, P. L., Crane, P. K., Buxbaum, J. D., Murrell, J. R., Raj, T., Ertekin-Taner, N., Logue, M., Baldwin, C. T., Green, R. C., Barnes, L. L., Cantwell, L. B., M Fallin, D., Go, R. C. P., Griffith, P., Obisesan, T. O., Manly, J. J., Lunetta, K. L., M Kamboh, I., Lopez, O. L., Bennett, D. A., Hendrie, H., Hall, K. S., Goate, A. M., Byrd, G. S., Kukull, W. A., Foroud, T. M., Haines, J. L., Farrer, L. A., Pericak-Vance, M. A., Schellenberg, G. D., and Mayeux, R., Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans., JAMA, vol. 309, no. 14, pp. 1483-92, 2013.
P. Ryvkin, Leung, Y. Yee, Ungar, L. H., Gregory, B. D., and San Wang, L. -, Using machine learning and high-throughput RNA sequencing to classify the precursors of small non-coding RNAs., Methods, vol. 67, no. 1, pp. 28-35, 2014.
S. Smemo, Nowotny, P., Hinrichs, A. L., Kauwe, J. S. K., Cherny, S., Erickson, K., Myers, A. J., Kaleem, M., Marlowe, L., Gibson, A. M., Hollingworth, P., O'Donovan, M. C., Morris, C. M., Holmans, P., Lovestone, S., Morris, J. C., Thal, L., Li, Y., Grupe, A., Hardy, J., Owen, M. J., Williams, J., and Goate, A., Ubiquilin 1 polymorphisms are not associated with late-onset Alzheimer's disease., Ann Neurol, vol. 59, no. 1, pp. 21-6, 2006.
M. A. Slifer, Martin, E. R., Haines, J. L., and Pericak-Vance, M. A., The ubiquilin 1 gene and Alzheimer's disease., N Engl J Med, vol. 352, no. 26, pp. 2752-3; author reply 2752-3, 2005.
J. Mez, Chung, J., Jun, G., Kriegel, J., Bourlas, A. P., Sherva, R., Logue, M. W., Barnes, L. L., Bennett, D. A., Buxbaum, J. D., Byrd, G. S., Crane, P. K., Ertekin-Taner, N., Evans, D., M Fallin, D., Foroud, T., Goate, A., Graff-Radford, N. R., Hall, K. S., M Kamboh, I., Kukull, W. A., Larson, E. B., Manly, J. J., Haines, J. L., Mayeux, R., Pericak-Vance, M. A., Schellenberg, G. D., Lunetta, K. L., and Farrer, L. A., Two novel loci, COBL and SLC10A2, for Alzheimer's disease in African Americans., Alzheimers Dement, vol. 13, no. 2, pp. 119-129, 2017.
J. L. Del-Aguila, Benitez, B. A., Li, Z., Dube, U., Mihindukulasuriya, K. A., Budde, J. P., Farias, F. H. G., Fernández, M. Victoria, Ibañez, L., Jiang, S., Perrin, R. J., Cairns, N. J., Morris, J. C., Harari, O., and Cruchaga, C., TREM2 brain transcript-specific studies in AD and TREM2 mutation carriers., Mol Neurodegener, vol. 14, no. 1, p. 18, 2019.
G. R. Jun, Chung, J., Mez, J., Barber, R., Beecham, G. W., Bennett, D. A., Buxbaum, J. D., Byrd, G. S., Carrasquillo, M. M., Crane, P. K., Cruchaga, C., De Jager, P., Ertekin-Taner, N., Evans, D., M Fallin, D., Foroud, T. M., Friedland, R. P., Goate, A. M., Graff-Radford, N. R., Hendrie, H., Hall, K. S., Hamilton-Nelson, K. L., Inzelberg, R., M Kamboh, I., Kauwe, J. S. K., Kukull, W. A., Kunkle, B. W., Kuwano, R., Larson, E. B., Logue, M. W., Manly, J. J., Martin, E. R., Montine, T. J., Mukherjee, S., Naj, A., Reiman, E. M., Reitz, C., Sherva, R., St George-Hyslop, P. H., Thornton, T., Younkin, S. G., Vardarajan, B. N., San Wang, L. -, Wendlund, J. R., Winslow, A. R., Haines, J., Mayeux, R., Pericak-Vance, M. A., Schellenberg, G., Lunetta, K. L., and Farrer, L. A., Transethnic genome-wide scan identifies novel Alzheimer's disease loci., Alzheimers Dement, vol. 13, no. 7, pp. 727-738, 2017.
A. Amlie-Wolf, Ryvkin, P., Tong, R., Dragomir, I., Suh, E. R., Xu, Y., Van Deerlin, V. M., Gregory, B. D., Kwong, L. K., Trojanowski, J. Q., Lee, V. M. - Y., San Wang, L. -, and Lee, E. B., Transcriptomic Changes Due to Cytoplasmic TDP-43 Expression Reveal Dysregulation of Histone Transcripts and Nuclear Chromatin., PLoS One, vol. 10, no. 10, p. e0141836, 2015.
A. J. Myers, J Gibbs, R., Webster, J. A., Rohrer, K., Zhao, A., Marlowe, L., Kaleem, M., Leung, D., Bryden, L., Nath, P., Zismann, V. L., Joshipura, K., Huentelman, M. J., Hu-Lince, D., Coon, K. D., Craig, D. W., Pearson, J. V., Holmans, P., Heward, C. B., Reiman, E. M., Stephan, D., and Hardy, J., A survey of genetic human cortical gene expression., Nat Genet, vol. 39, no. 12, pp. 1494-9, 2007.
C. A. Reynolds, Hong, M. - G., Eriksson, U. K., Blennow, K., Bennet, A. M., Johansson, B., Malmberg, B., Berg, S., Wiklund, F., Gatz, M., Pedersen, N. L., and Prince, J. A., A survey of ABCA1 sequence variation confirms association with dementia., Hum Mutat, vol. 30, no. 9, pp. 1348-54, 2009.
Y. Hu, Li, M., Lu, Q., Weng, H., Wang, J., Zekavat, S. M., Yu, Z., Li, B., Gu, J., Muchnik, S., Shi, Y., Kunkle, B. W., Mukherjee, S., Natarajan, P., Naj, A., Kuzma, A., Zhao, Y., Crane, P. K., Lu, H., and Zhao, H., A statistical framework for cross-tissue transcriptome-wide association analysis., Nat Genet, vol. 51, no. 3, pp. 568-576, 2019.
M. Victoria Fernández, Black, K., Carrell, D., Saef, B., Budde, J., Deming, Y., Howells, B., Del-Aguila, J. L., Ma, S., Bi, C., Norton, J., Chasse, R., Morris, J., Goate, A., and Cruchaga, C., SORL1 variants across Alzheimer's disease European American cohorts., Eur J Hum Genet, vol. 24, no. 12, pp. 1828-1830, 2016.
J. L. Del-Aguila, Li, Z., Dube, U., Mihindukulasuriya, K. A., Budde, J. P., Fernández, M. Victoria, Ibañez, L., Bradley, J., Wang, F., Bergmann, K., Davenport, R., Morris, J. C., Holtzman, D. M., Perrin, R. J., Benitez, B. A., Dougherty, J., Cruchaga, C., and Harari, O., A single-nuclei RNA sequencing study of Mendelian and sporadic AD in the human brain., Alzheimers Res Ther, vol. 11, no. 1, p. 71, 2019.
H. Wang, Lo, M. - T., Rosenthal, S. Brin, Makowski, C., Andreassen, O. A., Salem, R. M., McEvoy, L. K., Fiecas, M., and Chen, C. - H., Similar Genetic Architecture of Alzheimer's Disease and Differential Effect Between Sexes., Front Aging Neurosci, vol. 13, p. 674318, 2021.
R. C. Green, L Cupples, A., Go, R., Benke, K. S., Edeki, T., Griffith, P. A., Williams, M., Hipps, Y., Graff-Radford, N., Bachman, D., and Farrer, L. A., Risk of dementia among white and African American relatives of patients with Alzheimer disease., JAMA, vol. 287, no. 3, pp. 329-36, 2002.
Y. - J. Li, Scott, W. K., Zhang, L., Lin, P. - I., Oliveira, S. A., Skelly, T., Doraiswamy, M. P., Welsh-Bohmer, K. A., Martin, E. R., Haines, J. L., Pericak-Vance, M. A., and Vance, J. M., Revealing the role of glutathione S-transferase omega in age-at-onset of Alzheimer and Parkinson diseases., Neurobiol Aging, vol. 27, no. 8, pp. 1087-93, 2006.
L. - San Wang, Naj, A. C., Graham, R. R., Crane, P. K., Kunkle, B. W., Cruchaga, C., Murcia, J. D. Gonzalez, Cannon-Albright, L., Baldwin, C. T., Zetterberg, H., Blennow, K., Kukull, W. A., Faber, K. M., Schupf, N., Norton, M. C., Tschanz, J. A. T., Munger, R. G., Corcoran, C. D., Rogaeva, E., Lin, C. - F., Dombroski, B. A., Cantwell, L. B., Partch, A., Valladares, O., Hakonarson, H., St George-Hyslop, P., Green, R. C., Goate, A. M., Foroud, T. M., Carney, R. M., Larson, E. B., Behrens, T. W., Kauwe, J. S. K., Haines, J. L., Farrer, L. A., Pericak-Vance, M. A., Mayeux, R., Schellenberg, G. D., Albert, M. S., Albin, R. L., Apostolova, L. G., Arnold, S. E., Barber, R., Barmada, M., Barnes, L. L., Beach, T. G., Becker, J. T., Beecham, G. W., Beekly, D., Bennett, D. A., Bigio, E. H., Bird, T. D., Blacker, D., Boeve, B. F., Bowen, J. D., Boxer, A., Burke, J. R., Buxbaum, J. D., Cairns, N. J., Cao, C., Carlson, C. S., Carroll, S. L., Chui, H. C., Clark, D. G., Cribbs, D. H., Crocco, E. A., DeCarli, C., DeKosky, S. T., F Demirci, Y., Dick, M., Dickson, D. W., Duara, R., Ertekin-Taner, N., Fallon, K. B., Farlow, M. R., Ferris, S., Frosch, M. P., Galasko, D. R., Ganguli, M., Gearing, M., Geschwind, D. H., Ghetti, B., Gilbert, J. R., Glass, J. D., Graff-Radford, N. R., Growdon, J. H., Hamilton, R. L., Hamilton-Nelson, K. L., Harrell, L. E., Head, E., Honig, L. S., Hulette, C. M., Hyman, B. T., Jarvik, G. P., Jicha, G. A., Jin, L. - W., Jun, G., Jun, G., M Kamboh, I., Karydas, A., Kaye, J. A., Kim, R., Koo, E. H., Kowall, N. W., Kramer, J. H., LaFerla, F. M., Lah, J. J., Leverenz, J. B., Levey, A. I., Li, G., Lieberman, A. P., Lopez, O. L., Lunetta, K. L., Lyketsos, C. G., Mack, W. J., Marson, D. C., Martin, E. R., Martiniuk, F., Mash, D. C., Masliah, E., McCormick, W. C., McCurry, S. M., McDavid, A. N., McKee, A. C., W Mesulam, M., Miller, B. L., Miller, C. A., Miller, J. W., Montine, T. J., Morris, J. C., Murrell, J. R., Olichney, J. M., Parisi, J. E., Perry, W., Peskind, E., Petersen, R. C., Pierce, A., Poon, W. W., Potter, H., Quinn, J. F., Raj, A., Raskind, M., Reiman, E. M., Reisberg, B., Reitz, C., Ringman, J. M., Roberson, E. D., Rosen, H. J., Rosenberg, R. N., Sano, M., Saykin, A. J., Schneider, J. A., Schneider, L. S., Seeley, W. W., Smith, A. G., Sonnen, J. A., Spina, S., Stern, R. A., Tanzi, R. E., Thornton-Wells, T. A., Trojanowski, J. Q., Troncoso, J. C., Tsuang, D. W., Van Deerlin, V. M., Van Eldik, L. J., Vardarajan, B. N., Vinters, H. V., Vonsattel, J. Paul, Weintraub, S., Welsh-Bohmer, K. A., Williamson, J., Wishnek, S., Woltjer, R. L., Wright, C. B., Younkin, S. G., Yu, C. - E., and Yu, L., Rarity of the Alzheimer disease-protective APP A673T variant in the United States., JAMA Neurol, vol. 72, no. 2, pp. 209-16, 2015.
C. Cruchaga, Karch, C. M., Jin, S. Chih, Benitez, B. A., Cai, Y., Guerreiro, R., Harari, O., Norton, J., Budde, J., Bertelsen, S., Jeng, A. T., Cooper, B., Skorupa, T., Carrell, D., Levitch, D., Hsu, S., Choi, J., Ryten, M., Sassi, C., Brás, J., Gibbs, R. J., Hernandez, D. G., Lupton, M. K., Powell, J., Forabosco, P., Ridge, P. G., Corcoran, C. D., Tschanz, J. A. T., Norton, M. C., Munger, R. G., Schmutz, C., Leary, M., F Demirci, Y., Bamne, M. N., Wang, X., Lopez, O. L., Ganguli, M., Medway, C., Turton, J., Lord, J., Braae, A., Barber, I., Brown, K., Pastor, P., Lorenzo-Betancor, O., Brkanac, Z., Scott, E., Topol, E., Morgan, K., Rogaeva, E., Singleton, A., Hardy, J., M Kamboh, I., St George-Hyslop, P., Cairns, N., Morris, J. C., Kauwe, J. S. K., and Goate, A. M., Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer's disease., Nature, vol. 505, no. 7484, pp. 550-554, 2014.
R. Sims, van der Lee, S. J., Naj, A. C., Bellenguez, C., Badarinarayan, N., Jakobsdottir, J., Kunkle, B. W., Boland, A., Raybould, R., Bis, J. C., Martin, E. R., Grenier-Boley, B., Heilmann-Heimbach, S., Chouraki, V., Kuzma, A. B., Sleegers, K., Vronskaya, M., Ruiz, A., Graham, R. R., Olaso, R., Hoffmann, P., Grove, M. L., Vardarajan, B. N., Hiltunen, M., Nöthen, M. M., White, C. C., Hamilton-Nelson, K. L., Epelbaum, J., Maier, W., Choi, S. - H., Beecham, G. W., Dulary, C., Herms, S., Smith, A. V., Funk, C. C., Derbois, C., Forstner, A. J., Ahmad, S., Li, H., Bacq, D., Harold, D., Satizabal, C. L., Valladares, O., Squassina, A., Thomas, R., Brody, J. A., Qu, L., Sánchez-Juan, P., Morgan, T., Wolters, F. J., Zhao, Y., Garcia, F. Sanchez, Denning, N., Fornage, M., Malamon, J., Naranjo, M. Candida De, Majounie, E., Mosley, T. H., Dombroski, B., Wallon, D., Lupton, M. K., Dupuis, J., Whitehead, P., Fratiglioni, L., Medway, C., Jian, X., Mukherjee, S., Keller, L., Brown, K., Lin, H., Cantwell, L. B., Panza, F., McGuinness, B., Moreno-Grau, S., Burgess, J. D., Solfrizzi, V., Proitsi, P., Adams, H. H., Allen, M., Seripa, D., Pastor, P., L Cupples, A., Price, N. D., Hannequin, D., Frank-Garcia, A., Levy, D., Chakrabarty, P., Caffarra, P., Giegling, I., Beiser, A. S., Giedraitis, V., Hampel, H., Garcia, M. E., Wang, X., Lannfelt, L., Mecocci, P., Eiriksdottir, G., Crane, P. K., Pasquier, F., Boccardi, V., Henández, I., Barber, R. C., Scherer, M., Tarraga, L., Adams, P. M., Leber, M., Chen, Y., Albert, M. S., Riedel-Heller, S., Emilsson, V., Beekly, D., Braae, A., Schmidt, R., Blacker, D., Masullo, C., Schmidt, H., Doody, R. S., Spalletta, G., Longstreth, W. T., Fairchild, T. J., Bossù, P., Lopez, O. L., Frosch, M. P., Sacchinelli, E., Ghetti, B., Yang, Q., Huebinger, R. M., Jessen, F., Li, S., M Kamboh, I., Morris, J., Sotolongo-Grau, O., Katz, M. J., Corcoran, C., Dunstan, M., Braddel, A., Thomas, C., Meggy, A., Marshall, R., Gerrish, A., Chapman, J., Aguilar, M., Taylor, S., Hill, M., Fairén, M. Díez, Hodges, A., Vellas, B., Soininen, H., Kloszewska, I., Daniilidou, M., Uphill, J., Patel, Y., Hughes, J. T., Lord, J., Turton, J., Hartmann, A. M., Cecchetti, R., Fenoglio, C., Serpente, M., Arcaro, M., Caltagirone, C., Orfei, M. Donata, Ciaramella, A., Pichler, S., Mayhaus, M., Gu, W., Lleó, A., Fortea, J., Blesa, R., Barber, I. S., Brookes, K., Cupidi, C., Maletta, R. Giovanni, Carrell, D., Sorbi, S., Moebus, S., Urbano, M., Pilotto, A., Kornhuber, J., Bosco, P., Todd, S., Craig, D., Johnston, J., Gill, M., Lawlor, B., Lynch, A., Fox, N. C., Hardy, J., Albin, R. L., Apostolova, L. G., Arnold, S. E., Asthana, S., Atwood, C. S., Baldwin, C. T., Barnes, L. L., Barral, S., Beach, T. G., Becker, J. T., Bigio, E. H., Bird, T. D., Boeve, B. F., Bowen, J. D., Boxer, A., Burke, J. R., Burns, J. M., Buxbaum, J. D., Cairns, N. J., Cao, C., Carlson, C. S., Carlsson, C. M., Carney, R. M., Carrasquillo, M. M., Carroll, S. L., Diaz, C. Ceballos, Chui, H. C., Clark, D. G., Cribbs, D. H., Crocco, E. A., DeCarli, C., Dick, M., Duara, R., Evans, D. A., Faber, K. M., Fallon, K. B., Fardo, D. W., Farlow, M. R., Ferris, S., Foroud, T. M., Galasko, D. R., Gearing, M., Geschwind, D. H., Gilbert, J. R., Graff-Radford, N. R., Green, R. C., Growdon, J. H., Hamilton, R. L., Harrell, L. E., Honig, L. S., Huentelman, M. J., Hulette, C. M., Hyman, B. T., Jarvik, G. P., Abner, E., Jin, L. - W., Jun, G., Karydas, A., Kaye, J. A., Kim, R., Kowall, N. W., Kramer, J. H., LaFerla, F. M., Lah, J. J., Leverenz, J. B., Levey, A. I., Li, G., Lieberman, A. P., Lunetta, K. L., Lyketsos, C. G., Marson, D. C., Martiniuk, F., Mash, D. C., Masliah, E., McCormick, W. C., McCurry, S. M., McDavid, A. N., McKee, A. C., Mesulam, M., Miller, B. L., Miller, C. A., Miller, J. W., Morris, J. C., Murrell, J. R., Myers, A. J., O'Bryant, S., Olichney, J. 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