Spontaneous chirality through mixing achiral components: a twist-bend nematic phase driven by hydrogen-bonding between unlike components von Walker, R, Pociecha, D, Abberley, J P, Martinez-Felipe, A, Paterson, D A, Forsyth, E, Lawrence, G B, Henderson, P A, Storey, J M D, Gorecka, E, Imrie, C T

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Metabolomic associations of impaired awareness of hypoglycaemia in type 1 diabetes von Varkevisser, R. D. M., Cecil, A., Prehn, C., Mul, D., Aanstoot, H. J., Paterson, A. D., Wolffenbuttel, B. H. R., van der Klauw, M. M.

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A study of the wetting of metal surfaces in order to understand the processes controlling atmospheric corrosion von COLE, I. S, GANTHER, W. D, SINCLAIR, J. D, LAU, D, PATERSON, D. A

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Monozygotic twins exhibit numerous epigenetic differences: clues to twin discordance? von Petronis, Arturas, Gottesman, Irving I, Kan, Peixiang, Kennedy, James L, Basile, Vincenzo S, Paterson, Andrew D, Popendikyte, Violeta

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Combined genome-wide linkage and targeted association analysis of head circumference in autism spectrum disorder families von Woodbury-Smith, M, Bilder, D A, Morgan, J, Jerominski, L, Darlington, T, Dyer, T, Paterson, A D, Coon, H

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Genetic linkage and association analysis in type 1 von Willebrand disease: results from the Canadian Type 1 VWD Study von JAMES, P. D., PATERSON, A. D., NOTLEY, C., CAMERON, C., HEGADORN, C., TINLIN, S., BROWN, C., O'BRIEN, L., LEGGO, J., LILLICRAP, D.

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Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes von Lionel, Anath C., Tammimies, Kristiina, Vaags, Andrea K., Rosenfeld, Jill A., Ahn, Joo Wook, Merico, Daniele, Noor, Abdul, Runke, Cassandra K., Pillalamarri, Vamsee K., Carter, Melissa T., Gazzellone, Matthew J., Thiruvahindrapuram, Bhooma, Fagerberg, Christina, Laulund, Lone W., Pellecchia, Giovanna, Lamoureux, Sylvia, Deshpande, Charu, Clayton-Smith, Jill, White, Ann C., Leather, Susan, Trounce, John, Melanie Bedford, H., Hatchwell, Eli, Eis, Peggy S., Yuen, Ryan K.C., Walker, Susan, Uddin, Mohammed, Geraghty, Michael T., Nikkel, Sarah M., Tomiak, Eva M., Fernandez, Bridget A., Soreni, Noam, Crosbie, Jennifer, Arnold, Paul D., Schachar, Russell J., Roberts, Wendy, Paterson, Andrew D., So, Joyce, Szatmari, Peter, Chrysler, Christina, Woodbury-Smith, Marc, Brian Lowry, R., Zwaigenbaum, Lonnie, Mandyam, Divya, Wei, John, MacDonald, Jeffrey R., Howe, Jennifer L., Nalpathamkalam, Thomas, Wang, Zhuozhi, Tolson, Daniel, Cobb, David S., Wilks, Timothy M., Sorensen, Mark J., Bader, Patricia I., An, Yu, Wu, Bai-Lin, Musumeci, Sebastiano Antonino, Romano, Corrado, Postorivo, Diana, Nardone, Anna M., Monica, Matteo Della, Scarano, Gioacchino, Zoccante, Leonardo, Novara, Francesca, Zuffardi, Orsetta, Ciccone, Roberto, Antona, Vincenzo, Carella, Massimo, Zelante, Leopoldo, Cavalli, Pietro, Poggiani, Carlo, Cavallari, Ugo, Argiropoulos, Bob, Chernos, Judy, Brasch-Andersen, Charlotte, Speevak, Marsha, Fichera, Marco, Ogilvie, Caroline Mackie, Shen, Yiping, Hodge, Jennelle C., Talkowski, Michael E., Stavropoulos, Dimitri J., Marshall, Christian R., Scherer, Stephen W.

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Genetic mapping of a new Lafora progressive myoclonus epilepsy locus (EPM2B) on 6p22 von Chan, E M, Bulman, D E, Paterson, A D, Turnbull, J, Andermann, E, Andermann, F, Rouleau, G A, Delgado-Escueta, A V, Scherer, S W, Minassian, B A

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Genome-wide association study of emotional empathy in children von Woodbury-Smith, M. R., Paterson, A. D., Szatmari, P., Scherer, S. W.

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An inversion inv(4)(p12–p15.3) in autistic siblings implicates the 4p GABA receptor gene cluster von Vincent, J B, Horike, SI, Choufani, S, Paterson, A D, Roberts, W, Szatmari, P, Weksberg, R, Fernandez, B, Scherer, S W

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Tailored surface roughnesses for enhanced deposition of fine liquid droplets from a flowing gas von Paterson, D.A., Threlfall, G., Griffin, G., Burke, N., Huang, S.H., Zhu, Y.

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Effect of Environmental Factors and Gender on the Heritability of Bone Mineral Density and Bone Size von Ng, M. Y. M., Sham, P. C., Paterson, A. D., Chan, V., Kung, A. W. C.

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Dopamine D4 Receptor Gene: Novelty or Nonsense? von Paterson, Andrew D, Sunohara, Glen A, Kennedy, James L

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The phenotypic manifestations of rare genic CNVs in autism spectrum disorder von Merikangas, A K, Segurado, R, Heron, E A, Anney, R J L, Paterson, A D, Cook, E H, Pinto, D, Scherer, S W, Szatmari, P, Gill, M, Corvin, A P, Gallagher, L

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Magnetically tunable selective reflection of light by heliconical cholesterics von Salili, S M, Xiang, J, Wang, H, Li, Q, Paterson, D A, Storey, J M D, Imrie, C T, Lavrentovich, O D, Sprunt, S N, Gleeson, J T, Jákli, A

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The associations of apolipoprotein E and angiotensin-converting enzyme polymorphisms and cognitive function in Type 1 diabetes based on an 18-year follow-up of the DCCT cohort von Jacobson, A. M., Paterson, A. D., Ryan, C. M., Cleary, P. A., Waberski, B. H., Weinger, K., Musen, G., Dahms, W., Bayless, M., Silvers, N., Harth, J., Boright, A. P.

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Association of the MscI Polymorphism of the Dopamine D3 Receptor Gene with Tardive Dyskinesia in Schizophrenia von Basile, Vincenzo S., Masellis, Mario, Badri, Farideh, Paterson, Andrew D., Meltzer, Herbert Y., Lieberman, Jeffrey A., Potkin, Steven G., Macciardi, Fabio, Kennedy, James L.

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The role of Self‐Defined Race/Ethnicity in Population Structure Control von Liu, X‐Q., Paterson, A. D., John, E. M., Knight, J. A.

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Psychiatric epigenetics : a new focus for the new century von PETRONIS, A, GOTTESMAN, I. I, CROW, T. J, DELISI, L. E, MACCIARDI, F, MCINNIS, M. G, MCMAHON, F. J, PATERSON, A. D, SKUSE, D, SUTHERLAND, G. R

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Schizophrenia: An Epigenetic Puzzle? von Petronis, Arturas, Paterson, Andrew D, Kennedy, James L

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