Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Jason, Corneveaux"'
Autor:
Alison A. Williams, Robin White, Ashley Siniard, Jason Corneveaux, Matt Huentelman, Carsten Duch
Publikováno v:
Neurobiology of Disease, Vol 91, Iss , Pp 284-291 (2016)
Using a Drosophila model of MECP2 gain-of-function, we identified memory associated KIBRA as a target of MECP2 in regulating dendritic growth. We found that expression of human MECP2 increased kibra expression in Drosophila, and targeted RNAi knockdo
Externí odkaz:
https://doaj.org/article/94da7e0ba07841ea826d51ffd67e82d4
Autor:
Perry G. Ridge, Kaitlyn B. Hoyt, Kevin Boehme, Shubhabrata Mukherjee, Paul K. Crane, Jonathan L. Haines, Richard Mayeux, Lindsay A. Farrer, Margaret A. Pericak-Vance, Gerard D. Schellenberg, John S.K. Kauwe, Perrie M. Adams, Marilyn S. Albert, Roger L. Albin, Liana G. Apostolova, Steven E. Arnold, Sanjay Asthana, Craig S. Atwood, Clinton T. Baldwin, Robert C. Barber, Michael M. Barmada, Lisa L. Barnes, Sandra Barral, Thomas G. Beach, James T. Becker, Gary W. Beecham, Duane Beekly, David A. Bennett, Eileen H. Bigio, Thomas D. Bird, Deborah Blacker, Bradley F. Boeve, James D. Bowen, Adam Boxer, James R. Burke, Jeffrey M. Burns, Joseph D. Buxbaum, Nigel J. Cairns, Laura B. Cantwell, Chuanhai Cao, Chris S. Carlson, Cynthia M. Carlsson, Regina M. Carney, Minerva M. Carrasquillo, Steven L. Carroll, Helena C. Chui, David G. Clark, Jason Corneveaux, David H. Cribbs, Elizabeth A. Crocco, Carlos Cruchaga, Philip L. De Jager, Charles DeCarli, F. Yesim Demirci, Malcolm Dick, Dennis W. Dickson, Rachelle S. Doody, Ranjan Duara, Nilufer Ertekin-Taner, Denis A. Evans, Kelley M. Faber, Thomas J. Fairchild, Kenneth B. Fallon, David W. Fardo, Martin R. Farlow, Steven Ferris, Tatiana M. Foroud, Matthew P. Frosch, Douglas R. Galasko, Marla Gearing, Daniel H. Geschwind, Bernardino Ghetti, John R. Gilbert, Alison M. Goate, Neill R. Graff-Radford, Robert C. Green, John H. Growdon, Hakon Hakonarson, Ronald L. Hamilton, Kara L. Hamilton-Nelson, John Hardy, Lindy E. Harrell, Lawrence S. Honig, Ryan M. Huebinger, Matthew J. Huentelman, Christine M. Hulette, Bradley T. Hyman, Gail P. Jarvik, Gregory A. Jicha, Lee-Way Jin, Gyungah Jun, M. Ilyas Kamboh, Anna Karydas, Mindy J. Katz, Jeffrey A. Kaye, Ronald Kim, Neil W. Kowall, Joel H. Kramer, Walter A. Kukull, Brian W. Kunkle, Frank M. LaFerla, James J. Lah, Eric B. Larson, James B. Leverenz, Allan I. Levey, Ge Li, Andrew P. Lieberman, Chiao-Feng Lin, Richard B. Lipton, Oscar L. Lopez, Kathryn L. Lunetta, Constantine G. Lyketsos, Wendy J. Mack, Daniel C. Marson, Eden R. Martin, Frank Martiniuk, Deborah C. Mash, Eliezer Masliah, Wayne C. McCormick, Susan M. McCurry, Andrew N. McDavid, Ann C. McKee, Marsel Mesulam, Bruce L. Miller, Carol A. Miller, Joshua W. Miller, Thomas J. Montine, John C. Morris, Jill R. Murrell, Amanda J. Myers, Adam C. Naj, Sid O'Bryant, John M. Olichney, Vernon S. Pankratz, Joseph E. Parisi, Amanda Partch, Henry L. Paulson, William Perry, Elaine Peskind, Ronald C. Petersen, Aimee Pierce, Wayne W. Poon, Huntington Potter, Joseph F. Quinn, Ashok Raj, Murray Raskind, Eric M. Reiman, Barry Reisberg, Joan S. Reisch, Christiane Reitz, John M. Ringman, Erik D. Roberson, Ekaterina Rogaeva, Howard J. Rosen, Roger N. Rosenberg, Donald R. Royall, Mark A. Sager, Mary Sano, Andrew J. Saykin, Julie A. Schneider, Lon S. Schneider, William W. Seeley, Amanda G. Smith, Joshua A. Sonnen, Salvatore Spina, Peter St George-Hyslop, Robert A. Stern, Russell H. Swerdlow, Rudolph E. Tanzi, Tricia A. Thornton-Wells, John Q. Trojanowski, Juan C. Troncoso, Debby W. Tsuang, Otto Valladares, Vivianna M. Van Deerlin, Linda J. Van Eldik, Badri N. Vardarajan, Harry V. Vinters, Jean Paul Vonsattel, Li-San Wang, Sandra Weintraub, Kathleen A. Welsh-Bohmer, Jens R. Wendland, Kirk C. Wilhelmsen, Jennifer Williamson, Thomas S. Wingo, Ashley R. Winslow, Sarah Wishnek, Randall L. Woltjer, Clinton B. Wright, Chuang-Kuo Wu, Steven G. Younkin, Chang-En Yu, Lei Yu
Publikováno v:
Neurobiology of Aging. 41:200.e13-200.e20
Alzheimer's disease (AD) is a complex genetic disorder with no effective treatments. More than 20 common markers have been identified, which are associated with AD. Recently, several rare variants have been identified in Amyloid Precursor Protein (AP
Autor:
Mariet, Allen, Fanggeng, Zou, High Seng, Chai, Curtis S, Younkin, Julia, Crook, V Shane, Pankratz, Minerva M, Carrasquillo, Christopher N, Rowley, Asha A, Nair, Sumit, Middha, Sooraj, Maharjan, Thuy, Nguyen, Li, Ma, Kimberly G, Malphrus, Ryan, Palusak, Sarah, Lincoln, Gina, Bisceglio, Constantin, Georgescu, Debra, Schultz, Fariborz, Rakhshan, Christopher P, Kolbert, Jin, Jen, Jonathan L, Haines, Richard, Mayeux, Margaret A, Pericak-Vance, Lindsay A, Farrer, Gerard D, Schellenberg, Ronald C, Petersen, Neill R, Graff-Radford, Dennis W, Dickson, Steven G, Younkin, Nilüfer, Ertekin-Taner, Liana G, Apostolova, Steven E, Arnold, Clinton T, Baldwin, Robert, Barber, Michael M, Barmada, Thomas, Beach, Gary W, Beecham, Duane, Beekly, David A, Bennett, Eileen H, Bigio, Thomas D, Bird, Deborah, Blacker, Bradley F, Boeve, James D, Bowen, Adam, Boxer, James R, Burke, Jacqueline, Buros, Joseph D, Buxbaum, Nigel J, Cairns, Laura B, Cantwell, Chuanhai, Cao, Chris S, Carlson, Regina M, Carney, Steven L, Carroll, Helena C, Chui, David G, Clark, Jason, Corneveaux, Carl W, Cotman, Paul K, Crane, Carlos, Cruchaga, Jeffrey L, Cummings, Philip L, De Jager, Charles, DeCarli, Steven T, DeKosky, F Yesim, Demirci, Ramon, Diaz-Arrastia, Malcolm, Dick, Beth A, Dombroski, Ranjan, Duara, William D, Ellis, Denis, Evans, Kelley M, Faber, Kenneth B, Fallon, Martin R, Farlow, Steven, Ferris, Tatiana M, Foroud, Matthew, Frosch, Douglas R, Galasko, Paul J, Gallins, Mary, Ganguli, Marla, Gearing, Daniel H, Geschwind, Bernardino, Ghetti, John R, Gilbert, Sid, Gilman, Bruno, Giordani, Jonathan D, Glass, Alison M, Goate, Robert C, Green, John H, Growdon, Hakon, Hakonarson, Ronald L, Hamilton, John, Hardy, Lindy E, Harrell, Elizabeth, Head, Lawrence S, Honig, Matthew J, Huentelman, Christine M, Hulette, Bradley T, Hyman, Gail P, Jarvik, Gregory A, Jicha, Lee-Way, Jin, Gyungah, Jun, M Ilyas, Kamboh, Jason, Karlawish, Anna, Karydas, John S K, Kauwe, Jeffrey A, Kaye, Nancy, Kennedy, Ronald, Kim, Edward H, Koo, Neil W, Kowall, Patricia, Kramer, Walter A, Kukull, James J, Lah, Eric B, Larson, Allan I, Levey, Andrew P, Lieberman, Oscar L, Lopez, Kathryn L, Lunetta, Wendy J, Mack, Daniel C, Marson, Eden R, Martin, Frank, Martiniuk, Deborah C, Mash, Eliezer, Masliah, Wayne C, McCormick, Susan M, McCurry, Andrew N, McDavid, Ann C, McKee, Marsel, Mesulam, Bruce L, Miller, Carol A, Miller, Joshua W, Miller, Thomas J, Montine, John C, Morris, Amanda J, Myers, Adam C, Naj, Petra, Nowotny, Joseph E, Parisi, Daniel P, Perl, Elaine, Peskind, Wayne W, Poon, Huntington, Potter, Joseph F, Quinn, Ashok, Raj, Ruchita A, Rajbhandary, Murray, Raskind, Eric M, Reiman, Barry, Reisberg, Christiane, Reitz, John M, Ringman, Erik D, Roberson, Ekaterina, Rogaeva, Roger N, Rosenberg, Mary, Sano, Andrew J, Saykin, Julie A, Schneider, Lon S, Schneider, William, Seeley, Michael L, Shelanski, Michael A, Slifer, Charles D, Smith, Joshua A, Sonnen, Salvatore, Spina, Peter, St George-Hyslop, Robert A, Stern, Rudolph E, Tanzi, John Q, Trojanowski, Juan C, Troncoso, Debby W, Tsuang, Vivianna M, Van Deerlin, Badri Narayan, Vardarajan, Harry V, Vinters, Jean Paul, Vonsattel, Li-San, Wang, Sandra, Weintraub, Kathleen A, Welsh-Bohmer, Jennifer, Williamson, Randall L, Woltjer
Publikováno v:
Neurology. 79(3)
Objective: Recent genome-wide association studies (GWAS) of late-onset Alzheimer disease (LOAD) identified 9 novel risk loci. Discovery of functional variants within genes at these loci is required to confirm their role in Alzheimer disease (AD). Sin
Autor:
Ramsey, Keri1 (AUTHOR), Belnap, Newell1 (AUTHOR), Bonfitto, Anna1 (AUTHOR), Jepsen, Wayne1 (AUTHOR), Naymik, Marcus1 (AUTHOR), Sanchez‐Castillo, Meredith1 (AUTHOR), Craig, David W.2 (AUTHOR), Szelinger, Szabolcs1 (AUTHOR), Huentelman, Matthew J.1 (AUTHOR), Narayanan, Vinodh1 (AUTHOR) vnarayanan2@tgen.org, Rangasamy, Sampath1 (AUTHOR)
Publikováno v:
Molecular Genetics & Genomic Medicine. Feb2022, Vol. 10 Issue 2, p1-4. 4p.
Autor:
Saulnier Sholler, Giselle L.1,2, Bond, Jeffrey P.3, Bergendahl, Genevieve1, Dutta, Akshita1, Dragon, Julie3, Neville, Kathleen4, Ferguson, William5, Roberts, William6, Eslin, Don7, Kraveka, Jacqueline8, Kaplan, Joel9, Mitchell, Deanna1, Parikh, Nehal10, Merchant, Melinda11, Ashikaga, Takamaru12, Hanna, Gina7, Lescault, Pamela Jean13, Siniard, Ashley14, Corneveaux, Jason14, Huentelman, Matthew14
Publikováno v:
Cancer Medicine. Jun2015, Vol. 4 Issue 6, p871-886. 16p.
Autor:
Miyashita, Akinori1, Koike, Asako2, Jun, Gyungah3, Wang, Li-San4, Takahashi, Satoshi5, Matsubara, Etsuro6, Kawarabayashi, Takeshi6, Shoji, Mikio6, Tomita, Naoki7, Arai, Hiroyuki7, Asada, Takashi8, Harigaya, Yasuo9, Ikeda, Masaki10, Amari, Masakuni10, Hanyu, Haruo11, Higuchi, Susumu12, Ikeuchi, Takeshi13, Nishizawa, Masatoyo13, Suga, Masaichi14, Kawase, Yasuhiro15
Publikováno v:
PLoS ONE. Apr2013, Vol. 8 Issue 4, p1-11. 11p.
Brain Expression Genome-Wide Association Study (eGWAS) Identifies Human Disease-Associated Variants.
Autor:
Zou, Fanggeng1, High Seng Chai2, Younkin, Curtis S.1, Allen, Mariet1, Crook, Julia3, Pankratz, V. Shane2, Carrasquillo, Minerva M.1, Rowley, Christopher N.1, Nair, Asha A.2, Middha, Sumit2, Maharjan, Sooraj2, Li Ma1, Malphrus, Kimberly G.1, Palusak, Ryan1, Lincoln, Sarah1, Bisceglio, Gina1, Georgescu, Constantin1, Kouri, Naomi1, Kolbert, Christopher P.4, Jen, Jin4
Publikováno v:
PLoS Genetics. Jun2012, Vol. 8 Issue 6, Special section p1-16. 16p. 1 Diagram, 5 Charts.
Autor:
Dunn, P., Prigatano, G. P., Szelinger, S., Roth, J., Siniard, A. L., Claasen, A. M., Richholt, R. F., De Both, M., Corneveaux, J. J., Moskowitz, A. M., Balak, C., Piras, I. S., Russell, M., Courtright, A. L., Belnap, N., Rangasamy, S., Ramsey, K., Opitz, J. M., Craig, D. W., Narayanan, V.
Publikováno v:
American Journal of Medical Genetics. Part A; Mar2017, Vol. 173 Issue 3, p611-617, 7p
Autor:
Huentelman, Matt1,2 (AUTHOR) mhuentelman@tgen.org, De Both, Matthew1,2 (AUTHOR), Jepsen, Wayne1,2 (AUTHOR), Piras, Ignazio S.1,2 (AUTHOR), Talboom, Joshua S.1,2 (AUTHOR), Willeman, Mari1,2 (AUTHOR), Reiman, Eric M.2,3,4,5 (AUTHOR), Hardy, John6 (AUTHOR), Myers, Amanda J.7 (AUTHOR)
Publikováno v:
Scientific Reports. 7/3/2019, Vol. 9 Issue 1, pN.PAG-N.PAG. 1p.
Autor:
Escott-Price, Valentina, Sims, Rebecca, Bannister, Christian, Harold, Denise, Vronskaya, Maria, Majounie, Elisa, Badarinarayan, Nandini, Morgan, Kevin, Passmore, Peter, Holmes, Clive, Powell, John, Brayne, Carol, Gill, Michael, Mead, Simon, Goate, Alison, Cruchaga, Carlos, Lambert, Jean-Charles, van Duijn, Cornelia, Maier, Wolfgang, Ramirez, Alfredo
Publikováno v:
Brain: A Journal of Neurology; 12/1/2015, Vol. 138 Issue 12, p3673-3684, 12p