A new methodology for analyzing vehicle network topologies for critical hacking von Ghadi, Maen, Sali, Ádám, Szalay, Zsolt, Török, Árpád

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Evidence of synergism among three genetic variants in a patient with LMNA-related lipodystrophy and amyotrophic lateral sclerosis leading to a remarkable nuclear phenotype von Volkening, Kathryn, Farhan, Sali M. K., Kao, Jessica, Leystra-Lantz, Cheryl, Ang, Lee Cyn, McIntyre, Adam, Wang, Jian, Hegele, Robert A., Strong, Michael J.

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A Novel LIPE Nonsense Mutation Found Using Exome Sequencing in Siblings With Late-Onset Familial Partial Lipodystrophy von Farhan, Sali M.K., BSc, Robinson, John F, McIntyre, Adam D., BSc, Marrosu, Maria G., MD, Ticca, Anna F., MD, Loddo, Sara, BSc, Carboni, Nicola, MD, PhD, Brancati, Francesco, MD, PhD, Hegele, Robert A., MD, FRCPC

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Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease von Dilliott, Allison A, Farhan, Sali M K, Ghani, Mahdi, Sato, Christine, Liang, Eric, Zhang, Ming, McIntyre, Adam D, Cao, Henian, Racacho, Lemuel, Robinson, John F, Strong, Michael J, Masellis, Mario, Bulman, Dennis E, Rogaeva, Ekaterina, Lang, Anthony, Tartaglia, Carmela, Finger, Elizabeth, Zinman, Lorne, Turnbull, John, Freedman, Morris, Swartz, Rick, Black, Sandra E, Hegele, Robert A

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Coherent control of single spins in silicon carbide at room temperature von Widmann, Matthias, Lee, Sang-Yun, Rendler, Torsten, Son, Nguyen Tien, Fedder, Helmut, Paik, Seoyoung, Yang, Li-Ping, Zhao, Nan, Yang, Sen, Booker, Ian, Denisenko, Andrej, Jamali, Mohammad, Momenzadeh, S. Ali, Gerhardt, Ilja, Ohshima, Takeshi, Gali, Adam, Janzén, Erik, Wrachtrup, Jörg

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Genetic Variation in the Ontario Neurodegenerative Disease Research Initiative von Dilliott, Allison A., Evans, Emily C., Farhan, Sali M.K., Ghani, Mahdi, Sato, Christine, Zhang, Ming, McIntyre, Adam D., Cao, Henian, Racacho, Lemuel, Robinson, John F., Strong, Michael J., Masellis, Mario, Bulman, Dennis E., Rogaeva, Ekaterina, Black, Sandra E., Finger, Elizabeth, Frank, Andrew, Freedman, Morris, Hassan, Ayman, Lang, Anthony, Shoesmith, Christen L., Swartz, Richard H., Tang-Wai, David, Tartaglia, Maria Carmela, Turnbull, John, Zinman, Lorne, Hegele, Robert A.

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Contribution of rare variant associations to neurodegenerative disease presentation von Dilliott, Allison A., Abdelhady, Abdalla, Sunderland, Kelly M., Farhan, Sali M. K., Abrahao, Agessandro, Binns, Malcolm A., Black, Sandra E., Borrie, Michael, Casaubon, Leanne K., Dowlatshahi, Dar, Finger, Elizabeth, Fischer, Corinne E., Frank, Andrew, Freedman, Morris, Grimes, David, Hassan, Ayman, Jog, Mandar, Kumar, Sanjeev, Kwan, Donna, Lang, Anthony E., Mandzia, Jennifer, Masellis, Mario, McIntyre, Adam D., Pasternak, Stephen H., Pollock, Bruce G., Rajji, Tarek K., Rogaeva, Ekaterina, Sahlas, Demetrios J., Saposnik, Gustavo, Sato, Christine, Seitz, Dallas, Shoesmith, Christen, Steeves, Thomas D. L., Swartz, Richard H., Tan, Brian, Tang-Wai, David F., Tartaglia, Maria C., Turnbull, John, Zinman, Lorne, Hegele, Robert A.

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Left-sided appendicitis managed laparoscopically: a case report von AlKeileh, Tamara B, Elsayed, Sali, Adam, Raheemah Mahomed, Nour, Mozamil, Bhagchandi, Tarun

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In Vivo Imaging of Tumor-Propagating Cells, Regional Tumor Heterogeneity, and Dynamic Cell Movements in Embryonal Rhabdomyosarcoma von Ignatius, Myron S., Chen, Eleanor, Elpek, Natalie M., Fuller, Adam Z., Tenente, Inês M., Clagg, Ryan, Liu, Sali, Blackburn, Jessica S., Linardic, Corinne M., Rosenberg, Andrew E., Nielsen, Petur G., Mempel, Thorsten R., Langenau, David M.

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Limits of ligand selectivity from docking to models: in silico screening for A(1) adenosine receptor antagonists von Kolb, Peter, Phan, Khai, Gao, Zhan-Guo, Marko, Adam C, Sali, Andrej, Jacobson, Kenneth A

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Finding Suitable Clinical Endpoints for a Potential Treatment of a Rare Genetic Disease: the Case of ARID1B von Kruizinga, Matthijs D., Zuiker, Rob G.J.A., Sali, Elif, de Kam, Marieke L., Doll, Robert J., Groeneveld, Geert Jan, Santen, Gijs W.E., Cohen, Adam F.

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Outcome of a Workshop on Applications of Protein Models in Biomedical Research von Schwede, Torsten, Sali, Andrej, Honig, Barry, Levitt, Michael, Berman, Helen M., Jones, David, Brenner, Steven E., Burley, Stephen K., Das, Rhiju, Dokholyan, Nikolay V., Dunbrack, Roland L., Fidelis, Krzysztof, Fiser, Andras, Godzik, Adam, Huang, Yuanpeng Janet, Humblet, Christine, Jacobson, Matthew P., Joachimiak, Andrzej, Krystek, Stanley R., Kortemme, Tanja, Kryshtafovych, Andriy, Montelione, Gaetano T., Moult, John, Murray, Diana, Sanchez, Roberto, Sosnick, Tobin R., Standley, Daron M., Stouch, Terry, Vajda, Sandor, Vasquez, Max, Westbrook, John D., Wilson, Ian A.

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Limits of Ligand Selectivity from Docking to Models: In Silico Screening for A1 Adenosine Receptor Antagonists von Kolb, Peter, Phan, Khai, Gao, Zhan-Guo, Marko, Adam C., Sali, Andrej, Jacobson, Kenneth A.

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The ONDRISeq panel: custom-designed next-generation sequencing of genes related to neurodegeneration von Farhan, Sali M K, Dilliott, Allison A, Ghani, Mahdi, Sato, Christine, Liang, Eric, Zhang, Ming, McIntyre, Adam D, Cao, Henian, Racacho, Lemuel, Robinson, John F, Strong, Michael J, Masellis, Mario, St George-Hyslop, Peter, Bulman, Dennis E, Rogaeva, Ekaterina, Hegele, Robert A

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Limits of Ligand Selectivity from Docking to Models: In Silico Screening for A.sub.1 Adenosine Receptor Antagonists von Kolb, Peter, Phan, Khai, Gao, Zhan-Guo, Marko, Adam C, Sali, Andrej, Jacobson, Kenneth A

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Outcome of a Workshop on Archiving Structural Models of Biological Macromolecules von Berman, Helen M., Burley, Stephen K., Chiu, Wah, Sali, Andrej, Adzhubei, Alexei, Bourne, Philip E., Bryant, Stephen H., Dunbrack, Roland L., Fidelis, Krzysztof, Frank, Joachim, Godzik, Adam, Henrick, Kim, Joachimiak, Andrzej, Heymann, Bernard, Jones, David, Markley, John L., Moult, John, Montelione, Gaetano T., Orengo, Christine, Rossmann, Michael G., Rost, Burkhard, Saibil, Helen, Schwede, Torsten, Standley, Daron M., Westbrook, John D.

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Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease von Dilliott, Allison A., Farhan, Sali M.K., Ghani, Mahdi, Sato, Christine, Liang, Eric, Zhang, Ming, McIntyre, Adam D., Cao, Henian, Racacho, Lemuel, Robinson, John F., Strong, Michael J., Masellis, Mario, Bulman, Dennis E., Rogaeva, Ekaterina, Lang, Anthony, Tartaglia, Carmela, Finger, Elizabeth, Zinman, Lorne, Turnbull, John, Freedman, Morris, Swartz, Rick, Black, Sandra E., Hegele, Robert A.

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Genetic Variation in the Ontario Neurodegenerative Disease Research Initiative von Dilliott, Allison A., Evans, Emily C., Farhan, Sali M.K., Ghani, Mahdi, Sato, Christine, Zhang, Ming, McIntyre, Adam D., Cao, Henian, Racacho, Lemuel, Robinson, John F., Strong, Michael J., Masellis, Mario, Bulman, Dennis E., Rogaeva, Ekaterina, Black, Sandra E., Finger, Elizabeth, Frank, Andrew, Freedman, Morris, Hassan, Ayman, Lang, Anthony, Shoesmith, Christen L., Swartz, Richard H., Tang-Wai, David, Tartaglia, Maria Carmela, Turnbull, John, Zinman, Lorne, Hegele, Robert A.

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Identifying the Genetic Basis of Vascular Cognitive Impairment Using a Custom Designed Next-generation Sequencing-based Gene Panel von Dilliott, Allison A., Farhan, Sali M., McIntyre, Adam A., Robinson, John F., Kwan, Donna, Swartz, Rick, Hassan, Ayman, Dowlatshahi, Dar, Sahlas, Demetrios, Saposnik, Gustavo, Mandzia, Jennifer, Casaubon, Leanne, Strong, Michael J., Masellis, Mario, Bulman, Dennis E., Rogaeva, Ekaterina, Hegele, Robert A.

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