NHCDRA: a non-uniform hierarchical clustering with dynamic route adjustment for mobile sink based heterogeneous wireless sensor networks von Jain, Shushant Kumar, Venkatadari, M., Shrivastava, Neeraj, Jain, Shubhra, Verma, Rahul Kumar

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Interactome Mapping Provides a Network of Neurodegenerative Disease Proteins and Uncovers Widespread Protein Aggregation in Affected Brains von Haenig, Christian, Atias, Nir, Taylor, Alexander K., Mazza, Arnon, Schaefer, Martin H., Russ, Jenny, Riechers, Sean-Patrick, Jain, Shushant, Coughlin, Maura, Fontaine, Jean-Fred, Freibaum, Brian D., Brusendorf, Lydia, Zenkner, Martina, Porras, Pablo, Stroedicke, Martin, Schnoegl, Sigrid, Arnsburg, Kristin, Boeddrich, Annett, Pigazzini, Lucia, Heutink, Peter, Taylor, J. Paul, Kirstein, Janine, Andrade-Navarro, Miguel A., Sharan, Roded, Wanker, Erich E.

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The Parkinson Disease-associated Leucine-rich Repeat Kinase 2 (LRRK2) Is a Dimer That Undergoes Intramolecular Autophosphorylation von Greggio, Elisa, Zambrano, Ibardo, Kaganovich, Alice, Beilina, Alexandra, Taymans, Jean-Marc, Daniëls, Veronique, Lewis, Patrick, Jain, Shushant, Ding, Jinhui, Syed, Ali, Thomas, Kelly J., Baekelandt, Veerle, Cookson, Mark R.

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Kinase activity is required for the toxic effects of mutant LRRK2/dardarin von Greggio, Elisa, Jain, Shushant, Kingsbury, Ann, Bandopadhyay, Rina, Lewis, Patrick, Kaganovich, Alice, van der Brug, Marcel P., Beilina, Alexandra, Blackinton, Jeff, Thomas, Kelly Jean, Ahmad, Rili, Miller, David W., Kesavapany, Sashi, Singleton, Andrew, Lees, Andrew, Harvey, Robert J., Harvey, Kirsten, Cookson, Mark R.

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The R1441C mutation of LRRK2 disrupts GTP hydrolysis von Lewis, Patrick A., Greggio, Elisa, Beilina, Alexandra, Jain, Shushant, Baker, Acacia, Cookson, Mark R.

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A common LRRK2 mutation in idiopathic Parkinson's disease von Gilks, William P, Abou-Sleiman, Patrick M, Gandhi, Sonia, Jain, Shushant, Singleton, Andrew, Lees, Andrew J, Shaw, Karen, Bhatia, Kailash P, Bonifati, Vincenzo, Quinn, Niall P, Lynch, John, Healy, Daniel G, Holton, Janice L, Revesz, Tamas, Wood, Nicholas W

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Drug repurposing screen for the rare disease ataxia-telangiectasia von Jayanth, Namrata, Mahé, Gurvan, Campbell, Matthew, Lipkin, Mike, Jain, Shushant, van de Bospoort, Rhea, Thornton, Jennifer, Margus, Brad, Fischer, David F.

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Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data von Khan, Naheed L., Jain, Shushant, Lynch, John M., Pavese, Nicola, Abou-Sleiman, Patrick, Holton, Janice L., Healy, Daniel G., Gilks, William P., Sweeney, Mary G., Ganguly, Milan, Gibbons, Vaneesha, Gandhi, Sonia, Vaughan, Jenny, Eunson, Louise H., Katzenschlager, Regina, Gayton, Juliet, Lennox, Graham, Revesz, Tamas, Nicholl, David, Bhatia, Kailash P., Quinn, Niall, Brooks, David, Lees, Andrew J., Davis, Mary B., Piccini, Paola, Singleton, Andrew B., Wood, Nicholas W.

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Virtual Grid-Based Routing for Query-Driven Wireless Sensor Networks von Jain, Shushant Kumar, Bhatia, Rinkoo, Shrivastava, Neeraj, Salunke, Sharad, Hashmi, Mohammad Farukh, Bokde, Neeraj Dhanraj

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From Single Genes to Gene Networks: High-Throughput-High-Content Screening for Neurological Disease von Jain, Shushant, Heutink, Peter

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The Complete Automation of Cell Culture: Improvements for High-Throughput and High-Content Screening von Jain, Shushant, Sondervan, David, Rizzu, Patrizia, Bochdanovits, Zoltan, Caminada, Daniel, Heutink, Peter

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SFRS7-mediated splicing of tau exon 10 is directly regulated by STOX1A in glial cells von van Abel, Daan, Hölzel, Dennis R, Jain, Shushant, Lun, Fiona M F, Zheng, Yama W L, Chen, Eric Z, Sun, Hao, Chiu, Rossa W K, Lo, Y M Dennis, van Dijk, Marie, Oudejans, Cees B M

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Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing von Jansen, Iris E, Ye, Hui, Heetveld, Sasja, Lechler, Marie C, Michels, Helen, Seinstra, Renée I, Lubbe, Steven J, Drouet, Valérie, Lesage, Suzanne, Majounie, Elisa, Gibbs, J Raphael, Nalls, Mike A, Ryten, Mina, Botia, Juan A, Vandrovcova, Jana, Simon-Sanchez, Javier, Castillo-Lizardo, Melissa, Rizzu, Patrizia, Blauwendraat, Cornelis, Chouhan, Amit K, Li, Yarong, Yogi, Puja, Amin, Najaf, van Duijn, Cornelia M, Morris, Huw R, Brice, Alexis, Singleton, Andrew B, David, Della C, Nollen, Ellen A, Jain, Shushant, Shulman, Joshua M, Heutink, Peter

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The carbon source in the culture media modulates the cardiotoxic effects of doxorubicin on human stem cell-derived cardiomyocytes von Obejero-Paz, Carlos A., Snow, Tiffany, Lachize, Servane, Hawryluk, Peter, Jain, Shushant, Bruening-Wright, Andrew

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Abstract 986: High content analysis of 2D and 3D oncology models for target and phenotypic drug discovery von Lachize, Servane, Bospoort, Rhea van de, Silva, Marta da Silva da, Steentraten, Niki van der, Gowers, Ian, Clark, Roger, DeGroot, Jeroen, Waddell, Ian, Schiewe, Hajo, Jain, Shushant

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Cloning of the Gene Containing Mutations that Cause PARK8-Linked Parkinson's Disease von Paisán-Ruı́z, Coro, Jain, Shushant, Evans, E.Whitney, Gilks, William P., Simón, Javier, van der Brug, Marcel, de Munain, Adolfo López, Aparicio, Silvia, Gil, Angel Martı́nez, Khan, Naheed, Johnson, Janel, Martinez, Javier Ruiz, Nicholl, David, Carrera, Itxaso Marti, Peňa, Amets Saénz, de Silva, Rohan, Lees, Andrew, Martı́-Massó, José Félix, Pérez-Tur, Jordi, Wood, Nick W., Singleton, Andrew B.

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Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease von Nichols, William C, Pankratz, Nathan, Hernandez, Dena, Paisán-Ruíz, Coro, Jain, Shushant, Halter, Cheryl A, Michaels, Veronika E, Reed, Terry, Rudolph, Alice, Shults, Clifford W, Singleton, Andrew, Foroud, Tatiana

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Discovery and systematic functional validation of Parkinson’s disease genes from exome sequencing (S1.003) von Shulman, Joshua, Jansen, Iris, Ye, Hui, Heetveld, Sasja, Gibbs, J Raphael, Chouhan, Amit, Singleton, Andrew, Jain, Shushant, Heutink, Peter

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Clinical and Neuropathological Features of Spastic Ataxia in a Spanish Family with Novel Compound Heterozygous Mutations in STUB1 von Bettencourt, Conceição, de Yébenes, Justo García, López-Sendón, José Luis, Shomroni, Orr, Zhang, Xingqian, Qian, Shu-Bing, Bakker, Ingrid M. C., Heetveld, Sasja, Ros, Raquel, Quintáns, Beatriz, Sobrido, María-Jesús, Bevova, Marianna R., Jain, Shushant, Bugiani, Marianna, Heutink, Peter, Rizzu, Patrizia

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Analysis of IFT74as a candidate gene for chromosome 9p-linked ALS-FTD von Momeni, Parastoo, Schymick, Jennifer, Jain, Shushant, Cookson, Mark R, Cairns, Nigel J, Greggio, Elisa, Greenway, Matthew J, Berger, Stephen, Pickering-Brown, Stuart, Chiò, Adriano, Fung, Hon Chung, Holtzman, David M, Huey, Edward D, Wassermann, Eric M, Adamson, Jennifer, Hutton, Michael L, Rogaeva, Ekaterina, St George-Hyslop, Peter, Rothstein, Jeffrey D, Hardiman, Orla, Grafman, Jordan, Singleton, Andrew, Hardy, John, Traynor, Bryan J

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