Bilateral Teleoperation Over Networks Based on Stochastic Switching Approach von Walker, K.C., Ya-Jun Pan, Gu, J.

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Volunteer potential of genetically modified oilseed rape with altered fatty acid content von Walker, R.L., Booth, E.J., Whytock, G.P., Walker, K.C.

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Mineral concentrations in serum/plasma and liver tissue of captive and free-ranging rhinoceros species von Dierenfeld, E.S, Atkinson, S, Craig, A.M, Walker, K.C, Streich, W.J, Clauss, M

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Crop protection--what will shape the future picture? von Atkinson, D, Litterick, A.M, Walker, K.C, Walker, R, Watson, C.A

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Assessment of serum concentrations and sedative effects of fentanyl after transdermal adminstration at three dosages in healthy llamas von Grubb, T.L, Gold, J.R, Schlipf, J.W, Craig, A.M, Walker, K.C, Riebold, T.W

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effect of site and foliar sulfur on oilseed rape: comparison of sulfur responsive and nonresponsive seasons von Booth, E.J, Walker, K.C

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Energy analysis of rape methyl ester (RME) production from winter oilseed rape von Batchelor, Sheila E., Booth, Elaine J., Walker, Kerr C.

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Absolute calebration of scatir with comparison to measurements of fly height on the DFHT II von Walker, K.C., Sides, P.J.

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time-course study of the effect of sulphur on glucosinolates in oilseed rape (Brassica napus) from the vegetative stage to maturity von Booth, E.J, Walker, K.C, Griffiths, D.W

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Economics of bioethanol production from wheat in the UK von Batchelor, S.E., Cook, P., Booth, E.J., Walker, K.C.

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Wet deposition monitoring—Effect of sampling period von De Pena, R.G., Walker, K.C., Lebowitz, L., Micka, J.G.

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So Many Variables: Joint Modeling in Community Ecology von Warton, David I., Blanchet, F. Guillaume, O’Hara, Robert B., Ovaskainen, Otso, Taskinen, Sara, Walker, Steven C., Hui, Francis K.C.

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Whole-genome sequencing of quartet families with autism spectrum disorder von Yuen, Ryan K C, Thiruvahindrapuram, Bhooma, Merico, Daniele, Walker, Susan, Tammimies, Kristiina, Hoang, Ny, Chrysler, Christina, Nalpathamkalam, Thomas, Pellecchia, Giovanna, Liu, Yi, Gazzellone, Matthew J, D'Abate, Lia, Deneault, Eric, Howe, Jennifer L, Liu, Richard S C, Thompson, Ann, Zarrei, Mehdi, Uddin, Mohammed, Marshall, Christian R, Ring, Robert H, Zwaigenbaum, Lonnie, Ray, Peter N, Weksberg, Rosanna, Carter, Melissa T, Fernandez, Bridget A, Roberts, Wendy, Szatmari, Peter, Scherer, Stephen W

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Detection of Clinically Relevant Genetic Variants in Autism Spectrum Disorder by Whole-Genome Sequencing von Jiang, Yong-hui, Yuen, Ryan K.C., Jin, Xin, Wang, Mingbang, Chen, Nong, Wu, Xueli, Ju, Jia, Mei, Junpu, Shi, Yujian, He, Mingze, Wang, Guangbiao, Liang, Jieqin, Wang, Zhe, Cao, Dandan, Carter, Melissa T., Chrysler, Christina, Drmic, Irene E., Howe, Jennifer L., Lau, Lynette, Marshall, Christian R., Merico, Daniele, Nalpathamkalam, Thomas, Thiruvahindrapuram, Bhooma, Thompson, Ann, Uddin, Mohammed, Walker, Susan, Luo, Jun, Anagnostou, Evdokia, Zwaigenbaum, Lonnie, Ring, Robert H., Wang, Jian, Lajonchere, Clara, Wang, Jun, Shih, Andy, Szatmari, Peter, Yang, Huanming, Dawson, Geraldine, Li, Yingrui, Scherer, Stephen W.

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Complete Disruption of Autism-Susceptibility Genes by Gene Editing Predominantly Reduces Functional Connectivity of Isogenic Human Neurons von Deneault, Eric, White, Sean H., Rodrigues, Deivid C., Ross, P. Joel, Faheem, Muhammad, Zaslavsky, Kirill, Wang, Zhuozhi, Alexandrova, Roumiana, Pellecchia, Giovanna, Wei, Wei, Piekna, Alina, Kaur, Gaganjot, Howe, Jennifer L., Kwan, Vickie, Thiruvahindrapuram, Bhooma, Walker, Susan, Lionel, Anath C., Pasceri, Peter, Merico, Daniele, Yuen, Ryan K.C., Singh, Karun K., Ellis, James, Scherer, Stephen W.

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Altered TAOK2 activity causes autism-related neurodevelopmental and cognitive abnormalities through RhoA signaling von Richter, Melanie, Murtaza, Nadeem, Scharrenberg, Robin, White, Sean H., Johanns, Ole, Walker, Susan, Yuen, Ryan K. C., Schwanke, Birgit, Bedürftig, Bianca, Henis, Melad, Scharf, Sarah, Kraus, Vanessa, Dörk, Ronja, Hellmann, Jakob, Lindenmaier, Zsuzsa, Ellegood, Jacob, Hartung, Henrike, Kwan, Vickie, Sedlacik, Jan, Fiehler, Jens, Schweizer, Michaela, Lerch, Jason P., Hanganu-Opatz, Ileana L., Morellini, Fabio, Scherer, Stephen W., Singh, Karun K., Calderon de Anda, Froylan

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A Comprehensive Workflow for Read Depth-Based Identification of Copy-Number Variation from Whole-Genome Sequence Data von Trost, Brett, Walker, Susan, Wang, Zhuozhi, Thiruvahindrapuram, Bhooma, MacDonald, Jeffrey R., Sung, Wilson W.L., Pereira, Sergio L., Whitney, Joe, Chan, Ada J.S., Pellecchia, Giovanna, Reuter, Miriam S., Lok, Si, Yuen, Ryan K.C., Marshall, Christian R., Merico, Daniele, Scherer, Stephen W.

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The population genomic legacy of the second plague pandemic von Gopalakrishnan, Shyam, Ebenesersdóttir, S. Sunna, Lundstrøm, Inge K.C., Turner-Walker, Gordon, Moore, Kristjan H.S., Luisi, Pierre, Margaryan, Ashot, Martin, Michael D., Ellegaard, Martin Rene, Magnússon, Ólafur þ., Sigurðsson, Ásgeir, Snorradóttir, Steinunn, Magnúsdóttir, Droplaug N., Laffoon, Jason E., van Dorp, Lucy, Liu, Xiaodong, Moltke, Ida, Ávila-Arcos, María C., Schraiber, Joshua G., Rasmussen, Simon, Juan, David, Gelabert, Pere, de-Dios, Toni, Fotakis, Anna K., Iraeta-Orbegozo, Miren, Vågene, Åshild J., Denham, Sean Dexter, Christophersen, Axel, Stenøien, Hans K., Vieira, Filipe G., Liu, Shanlin, Günther, Torsten, Kivisild, Toomas, Moseng, Ole Georg, Skar, Birgitte, Cheung, Christina, Sandoval-Velasco, Marcela, Wales, Nathan, Schroeder, Hannes, Campos, Paula F., Guðmundsdóttir, Valdís B., Sicheritz-Ponten, Thomas, Petersen, Bent, Halgunset, Jostein, Gilbert, Edmund, Cavalleri, Gianpiero L., Hovig, Eivind, Kockum, Ingrid, Olsson, Tomas, Alfredsson, Lars, Hansen, Thomas F., Werge, Thomas, Willerslev, Eske, Balloux, Francois, Marques-Bonet, Tomas, Lalueza-Fox, Carles, Nielsen, Rasmus, Stefánsson, Kári, Helgason, Agnar, Gilbert, M. Thomas P.

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DIXDC1 Phosphorylation and Control of Dendritic Morphology Are Impaired by Rare Genetic Variants von Kwan, Vickie, Meka, Durga Praveen, White, Sean H., Hung, Claudia L., Holzapfel, Nicholas T., Walker, Susan, Murtaza, Nadeem, Unda, Brianna K., Schwanke, Birgit, Yuen, Ryan K.C., Habing, Kendra, Milsom, Chloe, Hope, Kristin J., Truant, Ray, Scherer, Stephen W., Calderon de Anda, Froylan, Singh, Karun K.

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Predictive impact of rare genomic copy number variations in siblings of individuals with autism spectrum disorders von D’Abate, L., Walker, S., Yuen, R. K. C., Tammimies, K., Buchanan, J. A., Davies, R. W., Thiruvahindrapuram, B., Wei, J., Brian, J., Bryson, S. E., Dobkins, K., Howe, J., Landa, R., Leef, J., Messinger, D., Ozonoff, S., Smith, I. M., Stone, W. L., Warren, Z. E., Young, G., Zwaigenbaum, L., Scherer, S. W.

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