Early signals of parasitism expressed through behaviour but modulated by social context von Morris, Alex M.M., Innocent, Giles T., Cunningham, Emma J.A., Athanasiadou, Spiridoula, Hutchings, Michael R., Smith, Lesley A.

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Association studies indicate that protein disulfide isomerase is a risk factor in amyotrophic lateral sclerosis von Kwok, Chun Tak, Morris, Alex G., Frampton, Jenny, Smith, Bradley, Shaw, Christopher E., de Belleroche, Jackie

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Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase von Mitchell, John, Paul, Praveen, Chen, Han-Jou, Morris, Alex, Payling, Miles, Falchi, Mario, Habgood, James, Panoutsou, Stefania, Winkler, Sabine, Tisato, Veronica, Hajitou, Amin, Smith, Bradley, Vance, Caroline, Shaw, Christopher, Mazarakis, Nicholas D, de Belleroche, Jacqueline

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Characterization of the Properties of a Novel Mutation in VAPB in Familial Amyotrophic Lateral Sclerosis von Chen, Han-Jou, Anagnostou, Georgia, Chai, Andrea, Withers, James, Morris, Alex, Adhikaree, Jason, Pennetta, Giuseppa, de Belleroche, Jackie S.

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Further insights into the molecular complexity of the human sinus node – The role of ‘novel’ transcription factors and microRNAs von Aminu, Abimbola J., Petkova, Maria, Atkinson, Andrew J., Yanni, Joseph, Morris, Alex D., Simms, Robert T., Chen, Weixuan, Yin, Zeyuan, Kuniewicz, Marcin, Holda, Mateusz K., Kuzmin, Vladislav S., Perde, Filip, Molenaar, Peter, Dobrzynski, Halina

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Animal Behaviour Packs a Punch: From Parasitism to Production, Pollution and Prevention in Grazing Livestock von Smith, Lesley A, Fox, Naomi J, Marion, Glenn, Booth, Naomi J, Morris, Alex M M, Athanasiadou, Spiridoula, Hutchings, Michael R

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The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder von Smith, Bradley N, Newhouse, Stephen, Shatunov, Aleksey, Vance, Caroline, Topp, Simon, Johnson, Lauren, Miller, Jack, Lee, Younbok, Troakes, Claire, Scott, Kirsten M, Jones, Ashley, Gray, Ian, Wright, Jamie, Hortobágyi, Tibor, Al-Sarraj, Safa, Rogelj, Boris, Powell, John, Lupton, Michelle, Lovestone, Simon, Sapp, Peter C, Weber, Markus, Nestor, Peter J, Schelhaas, Helenius J, Asbroek, Anneloor Alm Ten, Silani, Vincenzo, Gellera, Cinzia, Taroni, Franco, Ticozzi, Nicola, Van den Berg, Leonard, Veldink, Jan, Van Damme, Phillip, Robberecht, Wim, Shaw, Pamela J, Kirby, Janine, Pall, Hardev, Morrison, Karen E, Morris, Alex, de Belleroche, Jacqueline, Vianney de Jong, J M B, Baas, Frank, Andersen, Peter M, Landers, John, Brown, Jr, Robert H, Weale, Michael E, Al-Chalabi, Ammar, Shaw, Christopher E

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Variants in the zinc transporter-3 encoding gene (SLC30A3) in schizophrenia and bipolar disorder: Effects on brain glutamate-A pilot study von Jelen, Luke A, Green, Mark S, King, Sinead, Morris, Alex G, Zhang, Xinyuan, Lythgoe, David J, Young, Allan H, De Belleroche, Jacqueline, Stone, James M

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High prevalence of posterior polymorphous corneal dystrophy in the Czech Republic; linkage disequilibrium mapping and dating an ancestral mutation von Liskova, Petra, Gwilliam, Rhian, Filipec, Martin, Jirsova, Katerina, Reinstein Merjava, Stanislava, Deloukas, Panos, Webb, Tom R, Bhattacharya, Shomi S, Ebenezer, Neil D, Morris, Alex G, Hardcastle, Alison J

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The dilemma of digital colonialism : unmasking facial recognition technology and data sovereignty in Aotearoa New Zealand von Morris, Alex

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VCP mutations are not a major cause of familial amyotrophic lateral sclerosis in the UK von Kwok, Chun Tak, Wang, Hsiang-Ya, Morris, Alex G, Smith, Bradley, Shaw, Christopher, de Belleroche, Jackie

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Reply to Millecamps et al.: Elucidating the role of D amino acid oxidase in familial amyotrophic lateral sclerosis von de Belleroche, Jacqueline, Morris, Alex

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Genomic organisation and alternative splicing of human RIM1, a gene implicated in autosomal dominant cone-rod dystrophy (CORD7) von Johnson, Samantha, Halford, Stephanie, Morris, Alex G, Patel, Reshma J, Wilkie, Susan E, Hardcastle, Alison J, Moore, Anthony T, Zhang, Kang, Hunt, David M

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Preparing students for university: A guide for senior English teachers von Alex Harty-Morris

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A major marker for normal tension glaucoma: association with polymorphisms in the OPA1 gene von AUNG, Tin, OCAKA, Louise, FRANCIS, Peter J, HITCHINGS, Roger A, LEHMANN, Ordan J, BHATTACHARYA, Shomi S, EBENEZER, Neil D, MORRIS, Alex G, KRAWCZAK, Michael, THISELTON, Dawn L, ALEXANDER, Christiane, VOTRUBA, Marcela, BRICE, Glen, CHILD, Anne H

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Based on 0.35 T magnetic resonance-guided radiotherapy, what are the nonisotropic PTV margins required for conventional prostate radiotherapy? von Drabble, Joseph, Das, Prantik, George, Ben, Camilleri, Philip, Morris, Alex

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Effect of intravenous magnesium on post-operative pain following Latarjet shoulder reconstruction von Soeding, Paul, Morris, Alex, Soeding, Adam, Hoy, Gregory

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Sequestosome-1 (SQSTM1) sequence variants in ALS cases in the UK: prevalence and coexistence of SQSTM1 mutations in ALS kindred with PDB von Kwok, Chun T, Morris, Alex, de Belleroche, Jacqueline S

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Investigating the association between OPA1 polymorphisms and glaucoma: comparison between normal tension and high tension primary open angle glaucoma von TIN AUNG, OCAKA, Louise, EBENEZER, Neil D, MORRIS, Alex G, BRICE, Glen, CHILD, Anne H, HITCHINGS, Roger A, LEHMANN, Ordan J, BHATTACHARYA, Shomi S

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Nelson Rockefeller, a biography von Morris, Joe Alex, 1904-1990

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