The uses and misuses of uneven and combined development: an anatomy of a concept von Allinson, Jamie C, Anievas, Alexander

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The uneven and combined development of the Meiji Restoration: A passive revolutionary road to capitalist modernity von Allinson, Jamie C., Anievas, Alexander

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Benchmarking Organic Micropollutants in Wastewater, Recycled Water and Drinking Water with In Vitro Bioassays von Escher, Beate I, Allinson, Mayumi, Altenburger, Rolf, Bain, Peter A, Balaguer, Patrick, Busch, Wibke, Crago, Jordan, Denslow, Nancy D, Dopp, Elke, Hilscherova, Klara, Humpage, Andrew R, Kumar, Anu, Grimaldi, Marina, Jayasinghe, B. Sumith, Jarosova, Barbora, Jia, Ai, Makarov, Sergei, Maruya, Keith A, Medvedev, Alex, Mehinto, Alvine C, Mendez, Jamie E, Poulsen, Anita, Prochazka, Erik, Richard, Jessica, Schifferli, Andrea, Schlenk, Daniel, Scholz, Stefan, Shiraishi, Fujio, Snyder, Shane, Su, Guanyong, Tang, Janet Y. M, Burg, Bart van der, Linden, Sander C. van der, Werner, Inge, Westerheide, Sandy D, Wong, Chris K. C, Yang, Min, Yeung, Bonnie H. Y, Zhang, Xiaowei, Leusch, Frederic D. L

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A rare case of paediatric astroblastoma with concomitant MN1‐GTSE1 and EWSR1‐PATZ1 gene fusions altering management von Chadda, Karan R., Holland, Katherine, Scoffings, Daniel, Dean, Andrew, Pickles, Jessica C., Behjati, Sam, Jacques, Thomas S., Trotman, Jamie, Tarpey, Patrick, Allinson, Kieren, Murray, Matthew J.

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Characterisation of regional variations in a stitched CMOS active pixel sensor von Zin, Hafiz M., Konstantinidis, Anastasios C., Harris, Emma J., Osmond, John P.F., Olivo, Alesandro, Bohndiek, Sarah E., Clark, Andy T., Turchetta, Renato, Guerrini, Nicola, Crooks, Jamie, Allinson, Nigel M., Speller, Robert, Evans, Philip M.

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The NHS England 100,000 Genomes Project: feasibility and utility of centralised genome sequencing for children with cancer von Trotman, Jamie, Armstrong, Ruth, Firth, Helen, Trayers, Claire, Watkins, James, Allinson, Kieren, Jacques, Thomas S, Nicholson, James C, Burke, GA Amos, Genomics England Research Consortium, Behjati, Sam, Murray, Matthew J, Hook, Catherine E, Tarpey, Patrick

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The NHS England 100,000 Genomes Project: feasibility and utility of centralised genome sequencing for children with cancer von Trotman, Jamie, Armstrong, Ruth, Firth, Helen, Trayers, Claire, Watkins, James, Allinson, Kieren, Jacques, Thomas S, Nicholson, James C, Burke, GA Amos, Genomics England Research Consortium, Behjati, Sam, Murray, Matthew J, Hook, Catherine E, Tarpey, Patrick

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The NHS England 100,000 Genomes Project: feasibility and utility of centralised genome sequencing for children with cancer von Trotman, Jamie, Armstrong, Ruth, Firth, Helen, Trayers, Claire, Watkins, James, Allinson, Kieren, Jacques, Thomas S, Nicholson, James C, Burke, GA Amos, Genomics England Research Consortium, Behjati, Sam, Murray, Matthew, Hook, Catherine E, Tarpey, Patrick

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Demographic, clinical, biomarker, and neuropathological correlates of posterior cortical atrophy: an international cohort study and individual participant data meta-analysis von Chapleau, Marianne, La Joie, Renaud, Yong, Keir, Agosta, Federica, Allen, Isabel Elaine A, Best, John, Boon, Baayla DC, Crutch, Sebastian, Filippi, Massimo, Fumagalli, Giorgio Giulio, Galimberti, Daniela, Graff-Radford, Jonathan, Grinberg, Lea T, Irwin, David J, Josephs, Keith A, Mendez, Mario F, Mendez, Patricio Chrem, Migliaccio, Raffaella, Miller, Zachary A, Montembeault, Maxime, Murray, Melissa E, Nemes, Sára, Pelak, Victoria, Perani, Daniela, Phillips, Jeffrey, Pijnenburg, Yolande, Rogalski, Emily, Schott, Jonathan M, Seeley, William, Sullivan, A Campbell, Spina, Salvatore, Tanner, Jeremy, Walker, Jamie, Whitwell, Jennifer L, Wolk, David A, Ossenkoppele, Rik, Rabinovici, Gil D, Abdi, Z, Ahmed, S, Alcolea, D, Allinson, KSJ, Arighi, A, Balasa, M, Barkhof, F, Brandt, KD, Brosch, J, Burrell, J, Butler, CR, Calandri, I, Caminiti, SP, Canu, E, Carrillo, MC, Caso, F, Chu, M, Cordato, N, Costa, AS, Cui, Y, Dickerson, B, Dickson, DW, Duara, R, Dubois, B, Eldaief, M, Farlow, M, Feneglio, C, Fliessbach, K, Formaglio, M, Fortea, J, Fox, N, Foxe, D, Tilikete, CF, Frosch, MP, Galasko, D, Garat, O, Giardinieri, G, Graff-Radford, NR, Groot, C, Hake, AM, Hansson, O, Headley, A, Hernandez, M, Hochberg, D, Hodges, JR, Hof, PR, Holton, J, Hromas, G, Illán Gala, I, Jaunmuktane, Z, Jing, D, Kagerer, SM, Kasuga, K, Kong, Y, Kövari, E, Lacombe-Thibault, M, Lleó Plarrumaní, A, Lucente, DE, Machulda, MM, Magnani, G, Magnin, E, Malpetti, M, PCA International Work Group

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A rare case of paediatric astroblastoma with concomitant MN1-GTSE1 and EWSR1-PATZ1 gene fusions altering management von Chadda, Karan R, Holland, Katherine, Scoffings, Daniel, Dean, Andrew, Pickles, Jessica C, Behjati, Sam, Jacques, Thomas S, Trotman, Jamie, Tarpey, Patrick, Allinson, Kieren, Murray, Matthew J, Genomics England Research Consortium

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A rare case of paediatric astroblastoma with concomitant MN1 ‐ GTSE1 and EWSR1 ‐ PATZ1 gene fusions altering management von Chadda, Karan R, Holland, Katherine, Scoffings, Daniel, Dean, Andrew, Pickles, Jessica C, Behjati, Sam, Jacques, Thomas S, Trotman, Jamie, Tarpey, Patrick, Allinson, Kieren, Murray, Matthew J, Genomics England Research Consortium

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A rare case of paediatric astroblastoma with concomitant MN1-GTSE1 and EWSR1-PATZ1 gene fusions altering management von Chadda, Karan R, Holland, Katherine, Scoffings, Daniel, Dean, Andrew, Pickles, Jessica C, Behjati, Sam, Jacques, Thomas S, Trotman, Jamie, Tarpey, Patrick, Allinson, Kieren, Murray, Matthew J

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