SWOT: Analysis of Strategic Approaches in Total Force Fitness and Whole Health Summit von Triscari, Craig A, Rutherford, Ronald B, DiMercurio, Carlo, Franzos, M Alaric

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Neuroimaging signatures of frontotemporal dementia genetics: C9ORF72, tau, progranulin and sporadics von WHITWELL, Jennifer L, WEIGAND, Stephen D, PARIS, Joseph E, DICKSON, Dennis W, PETERSEN, Ronald C, RADEMAKERS, Rosa, JACK, Clifford R, JOSEPHS, Keith A, BOEVE, Bradley F, SENJEM, Matthew L, GUNTER, Jeffrey L, DEJESUS-HERNANDEZ, Mariely, RUTHERFORD, Nicola J, BAKER, Matthew, KNOPMAN, David S, WSZOLEK, Zbigniew K

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Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS von DeJesus-Hernandez, Mariely, Mackenzie, Ian R., Boeve, Bradley F., Boxer, Adam L., Baker, Matt, Rutherford, Nicola J., Nicholson, Alexandra M., Finch, NiCole A., Flynn, Heather, Adamson, Jennifer, Kouri, Naomi, Wojtas, Aleksandra, Sengdy, Pheth, Hsiung, Ging-Yuek R., Karydas, Anna, Seeley, William W., Josephs, Keith A., Coppola, Giovanni, Geschwind, Daniel H., Wszolek, Zbigniew K., Feldman, Howard, Knopman, David S., Petersen, Ronald C., Miller, Bruce L., Dickson, Dennis W., Boylan, Kevin B., Graff-Radford, Neill R., Rademakers, Rosa

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Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids von Rademakers, Rosa, Baker, Matt, Nicholson, Alexandra M, Rutherford, Nicola J, Finch, NiCole, Soto-Ortolaza, Alexandra, Lash, Jennifer, Wider, Christian, Wojtas, Aleksandra, DeJesus-Hernandez, Mariely, Adamson, Jennifer, Kouri, Naomi, Sundal, Christina, Shuster, Elizabeth A, Aasly, Jan, MacKenzie, James, Roeber, Sigrun, Kretzschmar, Hans A, Boeve, Bradley F, Knopman, David S, Petersen, Ronald C, Cairns, Nigel J, Ghetti, Bernardino, Spina, Salvatore, Garbern, James, Tselis, Alexandros C, Uitti, Ryan, Das, Pritam, Van Gerpen, Jay A, Meschia, James F, Levy, Shawn, Broderick, Daniel F, Graff-Radford, Neill, Ross, Owen A, Miller, Bradley B, Swerdlow, Russell H, Dickson, Dennis W, Wszolek, Zbigniew K

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Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72 von BOEVE, Bradley F, BOYLAN, Kevin B, DICKSON, Dennis W, JOSEPHS, Keith A, RUSH, Beth K, MACHULDA, Mary M, FIELDS, Julie A, FERMAN, Tanis J, BAKER, Matthew, RUTHERFORD, Nicola J, ADAMSON, Jennifer, WSZOLEK, Zbigniew K, GRAFF-RADFORD, Neill R, ADELI, Anahita, SAVICA, Rodolfo, BOOT, Brendon, KUNTZ, Karen M, GAVRILOVA, Ralitza, REEVES, Andrew, WHITWELL, Jennifer, KANTARCI, Kejal, JACK, Clifford R, PARISI, Joseph E, DEJESUS-HERNANDEZ, Mariely, LUCAS, John A, PETERSEN, Ronald C, RADEMAKERS, Rosa, KNOPMAN, David S, PEDRAZA, Otto, VEMURI, Prashanthi, JONES, David, LOWE, Val, MURRAY, Melissa E

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Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis von Rutherford, Nicola J, Zhang, Yong-Jie, Baker, Matt, Gass, Jennifer M, Finch, Nicole A, Xu, Ya-Fei, Stewart, Heather, Kelley, Brendan J, Kuntz, Karen, Crook, Richard J P, Sreedharan, Jemeen, Vance, Caroline, Sorenson, Eric, Lippa, Carol, Bigio, Eileen H, Geschwind, Daniel H, Knopman, David S, Mitsumoto, Hiroshi, Petersen, Ronald C, Cashman, Neil R, Hutton, Mike, Shaw, Christopher E, Boylan, Kevin B, Boeve, Bradley, Graff-Radford, Neill R, Wszolek, Zbigniew K, Caselli, Richard J, Dickson, Dennis W, Mackenzie, Ian R, Petrucelli, Leonard, Rademakers, Rosa

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Conservation of herpetofauna in northern landscapes: Threats and challenges from a Canadian perspective von Lesbarrères, David, Ashpole, Sara L., Bishop, Christine A., Blouin-Demers, Gabriel, Brooks, Ronald J., Echaubard, Pierre, Govindarajulu, Purnima, Green, David M., Hecnar, Stephen J., Herman, Tom, Houlahan, Jeff, Litzgus, Jacqueline D., Mazerolle, Marc J., Paszkowski, Cynthia A., Rutherford, Pamela, Schock, Danna M., Storey, Kenneth B., Lougheed, Stephen C.

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Length of normal alleles of C9ORF72 GGGGCC repeat do not influence disease phenotype von Rutherford, Nicola J, Heckman, Michael G, DeJesus-Hernandez, Mariely, Baker, Matt C, Soto-Ortolaza, Alexandra I, Rayaprolu, Sruti, Stewart, Heather, Finger, Elizabeth, Volkening, Kathryn, Seeley, William W, Hatanpaa, Kimmo J, Lomen-Hoerth, Catherine, Kertesz, Andrew, Bigio, Eileen H, Lippa, Carol, Knopman, David S, Kretzschmar, Hans A, Neumann, Manuela, Caselli, Richard J, White, Charles L, Mackenzie, Ian R, Petersen, Ronald C, Strong, Michael J, Miller, Bruce L, Boeve, Bradley F, Uitti, Ryan J, Boylan, Kevin B, Wszolek, Zbigniew K, Graff-Radford, Neill R, Dickson, Dennis W, Ross, Owen A, Rademakers, Rosa

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Ataxin-2 repeat-length variation and neurodegeneration von Ross, Owen A., Rutherford, Nicola J., Baker, Matt, Soto-Ortolaza, Alexandra I., Carrasquillo, Minerva M., DeJesus-Hernandez, Mariely, Adamson, Jennifer, Li, Ma, Volkening, Kathryn, Finger, Elizabeth, Seeley, William W., Hatanpaa, Kimmo J., Lomen-Hoerth, Catherine, Kertesz, Andrew, Bigio, Eileen H., Lippa, Carol, Woodruff, Bryan K., Knopman, David S., White, Charles L., Van Gerpen, Jay A., Meschia, James F., Mackenzie, Ian R., Boylan, Kevin, Boeve, Bradley F., Miller, Bruce L., Strong, Michael J., Uitti, Ryan J., Younkin, Steven G., Graff-Radford, Neill R., Petersen, Ronald C., Wszolek, Zbigniew K., Dickson, Dennis W., Rademakers, Rosa

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Risk of variceal hemorrhage and pretransplant mortality in children with biliary atresia von Bass, Lee M., Ye, Wen, Leung, Daniel H., Murray, Karen F., Molleston, Jean P., Romero, Rene, Rosenthal, Philip, Loomes, Kathleen M., Wang, Kasper S., Squires, Robert H., Miethke, Alexander, Ng, Vicky L., Kyle Jensen, M., Sokol, Ronald J., Magee, John C., Alonso, Estella, Bass, Lee, Kelly, Susan, Melin‐Aldana, Hector, Bove, Kevin, Heubi, James, Miethke, Alexander, Tiao, Greg, Chapman, Erin, Sokol, Ronald, Feldman, Amy, Mack, Cara, Narkewicz, Michael, Sundaram, Shikha, Van Hove, Johan, Garcia, Benigno, Kauma, Mikaela, Kocher, Kendra, Steinbeiss, Matthew, Lovell, Mark, Loomes, Kathleen, Rand, Elizabeth, Russo, Pierre, Spinner, Nancy, Erlichman, Jessi, Pakstis, Dina, King, Sakya, Squires, Robert, Sindhi, Rakesh, Venkat, Veena, McKiernan, Patrick, Haberstroh, Lori, Curry, Joanna, Langlois, Camille, Kim, Grace, Teckman, Jeffery, Kociela, Vikki, Nagy, Rosemary, Patel, Shraddha, Cerkoski, Jacqueline, Bozic, Molly, Subbarao, Girish, Klipsch, Ann, Cummings, Oscar, Hsu, Evelyn, Cooper, Kara, Young, Melissa, Finn, Laura, Kamath, Binita, Ng, Vicky, Quammie, Claudia, Putra, Juan, Sharma, Deepika, Guthery, Stephen, Rutherford, Ann, Lowichik, Amy, Book, Linda, Meyers, Rebecka, Hall, Tyler, Wang, Kasper, Thomas, Danny, Goodhue, Catherine, Wang, Larry, Soufi, Nisreen, Thomas, Daniel, Karpen, Saul, Romero, Rene, Tory, Rita, Abramowsky, Carlos, McFall, Jeanette, Shneider, Benjamin, Harpavat, Sanjiv, Leung, Daniel, Tessier, Mary, Schady, Deborah, Olvera, Diego, Banks, Christina, Thompson, Richard, Doo, Edward, Hoofnagle, Jay, Sherker, Averell, Hall, Sherry, Merion, Robert, Spino, Cathie, Ye, Wen

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Genome sequence of the human malaria parasite Plasmodium falciparum von Gardner, Malcolm J, Hall, Neil, Fung, Eula, White, Owen, Berriman, Matthew, Hyman, Richard W, Carlton, Jane M, Pain, Arnab, Nelson, Karen E, Bowman, Sharen, Paulsen, Ian T, James, Keith, Eisen, Jonathan A, Rutherford, Kim, Salzberg, Steven L, Craig, Alister, Kyes, Sue, Chan, Man-Suen, Nene, Vishvanath, Shallom, Shamira J, Suh, Bernard, Peterson, Jeremy, Angiuoli, Sam, Pertea, Mihaela, Allen, Jonathan, Selengut, Jeremy, Haft, Daniel, Mather, Michael W, Vaidya, Akhil B, Martin, David M. A, Fairlamb, Alan H, Fraunholz, Martin J, Roos, David S, Ralph, Stuart A, McFadden, Geoffrey I, Cummings, Leda M, Subramanian, G. Mani, Mungall, Chris, Venter, J. Craig, Carucci, Daniel J, Hoffman, Stephen L, Newbold, Chris, Davis, Ronald W, Fraser, Claire M, Barrell, Bart

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Longitudinal Outcomes in Young Patients with Alpha-1-Antitrypsin Deficiency with Native Liver Reveal that Neonatal Cholestasis is a Poor Predictor of Future Portal Hypertension von Teckman, Jeffrey, Rosenthal, Philip, Hawthorne, Kieran, Spino, Cathie, Bass, Lee M., Kerkar, Nanda, Magee, John C., Karpen, Saul, Heubi, James E., Molleston, Jean P., Kamath, Binita M., Guthery, Stephen L., Sherker, Averell H., Alonso, Estella, Bass, Lee, Kelly, Susan, Melin-Aldana, Hector, Bove, Kevin, Heubi, James, Miethke, Alexander, Tiao, Greg, Denlinger, Julie, Chapman, Erin, Feldman, Amy, Narkewicz, Michael, Suchy, Frederick, Sundaram, Shikha, Van Hove, Johan, Garcia, Benigno, Kauma, Mikaela, Kocher, Kendra, Steinbeiss, Matthew, Lovell, Mark, Rand, Elizabeth, Russo, Pierre, Erlichman, Jessi, Pakstis, Dina, King, Sakya, Squires, Robert, Sindhi, Rakesh, Venkat, Veena, McKiernan, Patrick, Haberstroh, Lori, Squires, James, Curry, Joanna, Langlois, Camille, Kim, Grace, Teckman, Jeffery, Kociela, Vikki, Nagy, Rosemary, Patel, Shraddha, Cerkoski, Jacqueline, Molleston, Jean P., Bozic, Molly, Subbarao, Girish, Klipsch, Ann, Sawyers, Cindy, Cummings, Oscar, Horslen, Simon, Murray, Karen, Hsu, Evelyn, Cooper, Kara, Young, Melissa, Finn, Laura, Ng, Vicky, Quammie, Claudia, Putra, Juan, Sharma, Deepika, Guthery, Stephen, Rutherford, Ann, Lowichik, Amy, Book, Linda, Meyers, Rebecka, Hall, Tyler, Wang, Kasper, Thomas, Danny, Goodhue, Catherine, Kohli, Rohit, Soufi, Nisreen, Thomas, Daniel, Karpen, Saul, Gupta, Nitika, Tory, Rita, Berauer, John-Paul, Abramowsky, Carlos, McFall, Jeanette, Shneider, Benjamin, Harpavat, Sanjiv, Hertel, Paula, Leung, Daniel, Schady, Deborah, Banks, Christina, Doo, Edward, Hoofnagle, Jay, Sherker, Averell, Hall, Sherry, Magee, John, Merion, Robert, Spino, Cathie, Ye, Wen

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C9ORF72 repeat expansions in cases with previously identified pathogenic mutations von van Blitterswijk, Marka, Baker, Matthew C, DeJesus-Hernandez, Mariely, Ghidoni, Roberta, Benussi, Luisa, Finger, Elizabeth, Hsiung, Ging-Yuek R, Kelley, Brendan J, Murray, Melissa E, Rutherford, Nicola J, Brown, Patricia E, Ravenscroft, Thomas, Mullen, Bianca, Ash, Peter E.A, Bieniek, Kevin F, Hatanpaa, Kimmo J, Karydas, Anna, Wood, Elisabeth McCarty, Coppola, Giovanni, Bigio, Eileen H, Lippa, Carol, Strong, Michael J, Beach, Thomas G, Knopman, David S, Huey, Edward D, Mesulam, Marsel, Bird, Thomas, White, Charles L, Kertesz, Andrew, Geschwind, Dan H, Van Deerlin, Vivianna M, Petersen, Ronald C, Binetti, Giuliano, Miller, Bruce L, Petrucelli, Leonard, Wszolek, Zbigniew K, Boylan, Kevin B, Graff-Radford, Neill R, Mackenzie, Ian R, Boeve, Bradley F, Dickson, Dennis W, Rademakers, Rosa

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Numerical investigation of auroral cyclotron maser processes von Speirs, D. C., Ronald, K., McConville, S. L., Gillespie, K. M., Phelps, A. D. R., Cross, A. W., Bingham, R., Robertson, C. W., Whyte, C. G., He, W., Vorgul, I., Cairns, R. A., Kellett, B. J.

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Expanded van der GCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS von DeJesus-Hernandez, Mariely, Mackenzie, Ian R, Boeve, Bradley F, Boxer, Adam L, Baker, Matt, Rutherford, Nicola J, Nicholson, Alexandra M, Finch, NiCole A, Flynn, Heather, Adamson, Jennifer, Kouri, Naomi, Wojtas, Aleksandra, Sengdy, Pheth, Hsiung, Ging-Yuek R, Karydas, Anna, Seeley, William W, Josephs, Keith A, Coppola, Giovanni, Geschwind, Daniel H, Wszolek, Zbigniew K, Feldman, Howard, Knopman, David S, Petersen, Ronald C, Miller, Bruce L, Dickson, Dennis W, Boylan, Kevin B, Graff-Radford, Neill R, Rademakers, Rosa

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Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region ofC9ORF72Causes Chromosome 9p-Linked FTD and ALS von DeJesus-Hernandez, Mariely, Mackenzie, Ian R, Boeve, Bradley F, Boxer, Adam L, Baker, Matt, Rutherford, Nicola J, Nicholson, Alexandra M, Finch, NiCole A, Flynn, Heather, Adamson, Jennifer, Kouri, Naomi, Wojtas, Aleksandra, Sengdy, Pheth, Hsiung, Ging-Yuek R, Karydas, Anna, Seeley, William W, Josephs, Keith A, Coppola, Giovan ni, Geschwind, Daniel H, Wszolek, Zbigniew K, Feldman, Howard, Knopman, David S, Petersen, Ronald C, Miller, Bruce L, Dickson, Dennis W, Boylan, Kevin B, Graff-Radford, Neill R, Rademakers, Rosa

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The use of the L-plastin promoter for adenoviral-mediated, tumor-specific gene expression in ovarian and bladder cancer cell lines von Peng, X Y, Won, J H, Rutherford, T, Fujii, T, Zelterman, D, Pizzorno, G, Sapi, E, Leavitt, J, Kacinski, B, Crystal, R, Schwartz, P, Deisseroth, A

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Mutations in the colony stimulating factor 1 receptor (CSF1R) cause hereditary diffuse leukoencephalopathy with spheroids von Rademakers, Rosa, Baker, Matt, Nicholson, Alexandra M., Rutherford, Nicola J., Finch, NiCole, Soto-Ortolaza, Alexandra, Lash, Jennifer, Wider, Christian, Wojtas, Aleksandra, DeJesus-Hernandez, Mariely, Adamson, Jennifer, Kouri, Naomi, Sundal, Christina, Shuster, Elizabeth A., Aasly, Jan, MacKenzie, James, Roeber, Sigrun, Kretzschmar, Hans A., Boeve, Bradley F., Knopman, David S., Petersen, Ronald C., Cairns, Nigel J., Ghetti, Bernardino, Spina, Salvatore, Garbern, James, Tselis, Alexandros C., Uitti, Ryan, Das, Pritam, Van Gerpen, Jay A., Meschia, James F., Levy, Shawn, Broderick, Daniel F., Graff-Radford, Neill, Ross, Owen A., Miller, Bradley B., Swerdlow, Russell H., Dickson, Dennis W., Wszolek, Zbigniew K.

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Length of normal alleles of C9ORF72 GGGGCC repeat do not influence disease phenotype von Rutherford, Nicola J, Heckman, Michael G, Dejesus-Hernandez, Mariely, Baker, Matt C, Soto-Ortolaza, Alexandra I, Rayaprolu, Sruti, Stewart, Heather, Finger, Elizabeth, Volkening, Kathryn, Seeley, William W, Hatanpaa, Kimmo J, Lomen-Hoerth, Catherine, Kertesz, Andrew, Bigio, Eileen H, Lippa, Carol, Knopman, David S, Kretzschmar, Hans A, Neumann, Manuela, Caselli, Richard J, White, Charles L, Mackenzie, Ian R, Petersen, Ronald C, Strong, Michael J, Miller, Bruce L, Boeve, Bradley F, Uitti, Ryan J, Boylan, Kevin B, Wszolek, Zbigniew K, Graff-Radford, Neill R, Dickson, Dennis W, Ross, Owen A, Rademakers, Rosa

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Immune thrombocytopenic purpura during pregnancy: laparoscopic treatment von Anglin, B V, Rutherford, C, Ramus, R, Lieser, M, Jones, D B

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