Microprobe X-ray Absorption Spectroscopic Determination of the Oxidation State of Intracellular Chromium following Exposure of V79 Chinese Hamster Lung Cells to Genotoxic Chromium... von Dillon, Carolyn T, Lay, Peter A, Cholewa, Marian, Legge, George J. F, Bonin, Antonio M, Collins, Terrence J, Kostka, Kimberley L, Shea-McCarthy, Grace

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Permeability, Cytotoxicity, and Genotoxicity of Cr(III) Complexes and Some Cr(V) Analogues in V79 Chinese Hamster Lung Cells von Dillon, Carolyn T, Lay, Peter A, Bonin, Antonio M, Cholewa, Marian, Legge, George J. F

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Secondary electron emission from boron-doped diamond under ion impact: Applications in single-ion detection von Kamiya, Tomihiro, Cholewa, Marian, Saint, Andrew, Prawer, Steven, Legge, George J. F., Butler, James E., Vestyck, Daniel J.

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Permeability, Cytotoxicity, and Genotoxicity of Chromium(V) and Chromium(VI) Complexes in V79 Chinese Hamster Lung Cells von Dillon, Carolyn T., Lay, Peter A., Bonin, Antonio M., Cholewa, Marian, Legge, George J. F., Collins, Terrence J., Kostka, Kimberly L.

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Elemental microanalysis of fibroblasts by a scanning proton microprobe and application to Menkes' disease von Allan, G.L, Camakaris, J, Legge, G.J.F

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Clinical indicators of treatment-resistant psychosis von Legge, Sophie E., Dennison, Charlotte A., Pardiñas, Antonio F., Rees, Elliott, Lynham, Amy J., Hopkins, Lucinda, Bates, Lesley, Kirov, George, Owen, Michael J., O'Donovan, Michael C., Walters, James T.R.

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Association of Genetic Liability to Psychotic Experiences With Neuropsychotic Disorders and Traits von Legge, Sophie E, Jones, Hannah J, Kendall, Kimberley M, Pardiñas, Antonio F, Menzies, Georgina, Bracher-Smith, Matthew, Escott-Price, Valentina, Rees, Elliott, Davis, Katrina A. S, Hotopf, Matthew, Savage, Jeanne E, Posthuma, Danielle, Holmans, Peter, Kirov, George, Owen, Michael J, O’Donovan, Michael C, Zammit, Stanley, Walters, James T. R

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Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection von Pardiñas, Antonio F., Holmans, Peter, Pocklington, Andrew J., Escott-Price, Valentina, Ripke, Stephan, Carrera, Noa, Legge, Sophie E., Bishop, Sophie, Cameron, Darren, Hamshere, Marian L., Han, Jun, Hubbard, Leon, Lynham, Amy, Mantripragada, Kiran, Rees, Elliott, MacCabe, James H., McCarroll, Steven A., Baune, Bernhard T., Breen, Gerome, Byrne, Enda M., Dannlowski, Udo, Eley, Thalia C., Hayward, Caroline, Martin, Nicholas G., McIntosh, Andrew M., Plomin, Robert, Porteous, David J., Wray, Naomi R., Caballero, Armando, Geschwind, Daniel H., Huckins, Laura M., Ruderfer, Douglas M., Santiago, Enrique, Sklar, Pamela, Stahl, Eli A., Won, Hyejung, Agerbo, Esben, Als, Thomas D., Andreassen, Ole A., Bækvad-Hansen, Marie, Mortensen, Preben Bo, Pedersen, Carsten Bøcker, Børglum, Anders D., Bybjerg-Grauholm, Jonas, Djurovic, Srdjan, Durmishi, Naser, Pedersen, Marianne Giørtz, Golimbet, Vera, Grove, Jakob, Hougaard, David M., Mattheisen, Manuel, Molden, Espen, Mors, Ole, Nordentoft, Merete, Pejovic-Milovancevic, Milica, Sigurdsson, Engilbert, Silagadze, Teimuraz, Hansen, Christine Søholm, Stefansson, Kari, Stefansson, Hreinn, Steinberg, Stacy, Tosato, Sarah, Werge, Thomas, Collier, David A., Rujescu, Dan, Kirov, George, Owen, Michael J., O’Donovan, Michael C., Walters, James T. R.

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De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia von Rees, Elliott, Han, Jun, Morgan, Joanne, Carrera, Noa, Escott-Price, Valentina, Pocklington, Andrew J., Duffield, Madeleine, Hall, Lynsey S., Legge, Sophie E., Pardiñas, Antonio F., Richards, Alexander L., Roth, Julian, Lezheiko, Tatyana, Kondratyev, Nikolay, Kaleda, Vasilii, Golimbet, Vera, Parellada, Mara, González-Peñas, Javier, Arango, Celso, Gawlik, Micha, Kirov, George, Walters, James T. R., Holmans, Peter, O’Donovan, Michael C., Owen, Michael J.

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Mapping genomic loci implicates genes and synaptic biology in schizophrenia von Trubetskoy, Vassily, Qi, Ting, Bryois, Julien, Chen, Chia-Yen, Magnusson, Sigurdur, Kim, Minsoo, Adams, Mark, Agartz, Ingrid, Agerbo, Esben, Athanasiu, Lavinia, Bacanu, Silviu A., Calkins, Monica E., Carr, Vaughan J., Consoli, Angèle, Costas, Javier, Davis, Kenneth L., Degenhardt, Franziska, Dickerson, Faith, Frustaci, Alessandra, Giegling, Ina, Goldstein, Jacqueline I., González Peñas, Javier, Hayward, Caroline, Howrigan, Daniel P., Ikeda, Masashi, Kam-Thong, Tony, Kamatani, Yoichiro, Khrunin, Andrey, Kim, Sung-Wan, Klovins, Janis, Kubo, Michiaki, Lazzeroni, Laura C., Lehrer, Douglas S., Li, Miaoxin, Liu, Chih-Min, Loughland, Carmel M., Mallet, Jacques, Mattheisen, Manuel, McCarley, Robert W., Meier, Sandra, Milani, Lili, Milanova, Vihra, Morley, Christopher P., Muntané, Gerard, Murphy, Kieran C., Olincy, Ann, Papadimitriou, George N., Parellada, Mara, Paunio, Tiina, Pellegrino, Renata, Radant, Allen D., Saker-Delye, Safaa, Sanjuan, Julio, Savitz, Adam, Seidman, Larry J., Sim, Kang, Stain, Helen J., Streit, Fabian, Strengman, Eric, Ta, Thi Minh Tam, Terao, Chikashi, Toncheva, Draga, Veijola, Juha, Waddington, John, Walter, Henrik, Webb, Bradley T., Wu, Jing Qin, Xu, Zhida, Ayub, Muhammad, Bertolino, Alessandro, Buccola, Nancy G., Byerley, William F., Hwu, Hai-Gwo, McCarroll, Steven A., Neil, Amanda L., Smoller, Jordan W., Vilella, Elisabet, Xu, Shuhua, Braff, David, Buxbaum, Joseph D., Cichon, Sven, Ehrenreich, Hannelore, Escott-Price, Valentina, Esko, Tõnu, Iwata, Nakao, Kirov, George, Lee, Jimmy, Li, Qingqin S., Malhotra, Anil K., Malhotra, Dheeraj, McQuillin, Andrew, Morgan, Vera A., Nöthen, Markus M., Saka, Meram C., Sanders, Alan R., Serretti, Alessandro, van Os, Jim, Yu, Xin, Neale, Benjamin M., Ripke, Stephan

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Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia von Rees, Elliott, Kendall, Kimberley, Pardiñas, Antonio F, Legge, Sophie E, Pocklington, Andrew, Escott-Price, Valentina, MacCabe, James H, Collier, David A, Holmans, Peter, O’Donovan, Michael C, Owen, Michael J, Walters, James T. R, Kirov, George

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Genetic and Phenotypic Features of Schizophrenia in the UK Biobank von Legge, Sophie E, Pardiñas, Antonio F, Woolway, Grace, Rees, Elliott, Cardno, Alastair G, Escott-Price, Valentina, Holmans, Peter, Kirov, George, Owen, Michael J, O'Donovan, Michael C, Walters, James T R

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Rare Copy Number Variants Are Associated With Poorer Cognition in Schizophrenia von Hubbard, Leon, Rees, Elliott, Morris, Derek W., Lynham, Amy J., Richards, Alex L., Pardiñas, Antonio F., Legge, Sophie E., Harold, Denise, Zammit, Stanley, Corvin, Aiden C., Gill, Michael G., Hall, Jeremy, Holmans, Peter, O’Donovan, Michael C., Owen, Michael J., Donohoe, Gary, Kirov, George, Pocklington, Andrew, Walters, James T.R.

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Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects von Merico, Daniele, Antaki, Danny, Shetty, Aniket, Gujral, Madhusudan, Brandler, William M, Malhotra, Dheeraj, Alexander, Madeline, Belliveau, Richard A, Bergen, Sarah E, Bertalan, Marcelo, Bevilacqua, Elizabeth, Cantor, Rita M, Carrera, Noa, Cormican, Paul, Crespo-Facorro, Benedicto, Curtis, David, Davidson, Michael, Degenhardt, Franziska, Del Favero, Jurgen, DeLisi, Lynn E, Dudbridge, Frank, Eichhammer, Peter, Eriksson, Johan, Essioux, Laurent, Farrell, Martilias S, Freedman, Robert, Freimer, Nelson B, Georgieva, Lyudmila, Gershon, Elliot S, Giegling, Ina, Godard, Stephanie, Goldstein, Jacqueline I, Hamshere, Marian L, Hartmann, Annette M, Hofman, Andrea, Kähler, Anna K, Kalaydjieva, Luba, Kelly, Brian J, Lee, S Hong, Legge, Sophie E, Lerer, Bernard, Levy, Deborah L, Maher, Brion S, Mattingsdal, Morten, McDonald, Colm, Metspalu, Andres, Milanova, Vihra, Morris, Derek W, Murray, Robin M, Nestadt, Gerald, Nicodemus, Kristin K, Nordin, Annelie, Oh, Sang-Yun, Olsen, Line, Van Os, Jim, Pantelis, Christos, Pers, Tune H, Powell, John, Price, Alkes, Pulver, Ann E, Purcell, Shaun M, Rasmussen, Henrik B, Richards, Alexander L, Roussos, Panos, Schall, Ulrich, Schwab, Sibylle G, Smoller, Jordan W, Spencer, Chris C A, Stahl, Eli A, Stroup, T Scott, Suvisaari, Jaana, Svrakic, Dragan M, Szatkiewicz, Jin P, Veijola, Juha, Waddington, John, Webb, Bradley T, Williams, Nigel M, Williams, Stephanie, Wolen, Aaron R, Adolfsson, Rolf, Blackwood, Douglas H R, Bramon, Elvira, Buxbaum, Joseph D, Collier, David A, Daly, Mark J, Darvasi, Ariel, Domenici, Enrico, Gill, Michael, Iwata, Nakao, Jablensky, Assen V, Jönsson, Erik G, Kirov, George, Knight, Jo, Levinson, Douglas F, Ophoff, Roel A, Owen, Michael J, Rietschel, Marcella, Rujescu, Dan, O'Donovan, Michael C, Neale, Benjamin M

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Using genetic variants to evaluate the causal effect of cholesterol lowering on head and neck cancer risk: A Mendelian randomization study von Gormley, Mark, Yarmolinsky, James, Dudding, Tom, Burrows, Kimberley, Martin, Richard M., Thomas, Steven, Tyrrell, Jessica, Brennan, Paul, Pring, Miranda, Boccia, Stefania, Olshan, Andrew F., Diergaarde, Brenda, Hung, Rayjean J., Liu, Geoffrey, Legge, Danny, Tajara, Eloiza H., Severino, Patricia, Lacko, Martin, Ness, Andrew R., Smith, George Davey, Vincent, Emma E., Richmond, Rebecca C.

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Impact of schizophrenia genetic liability on the association between schizophrenia and physical illness: data-linkage study von Kendall, Kimberley M., John, Ann, Lee, Sze Chim, Rees, Elliott, Pardiñas, Antonio F., Banos, Marcos Del Pozo, Owen, Michael J., O'Donovan, Michael C., Kirov, George, Lloyd, Keith, Jones, Ian, Legge, Sophie E., Walters, James T. R.

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Physician Global Assessment International Standardisation COnsensus in Systemic Lupus Erythematosus: the PISCOS study von Piga, Matteo, Chessa, Elisabetta, Morand, Eric F, Ugarte-Gil, Manuel F, Tektonidou, Maria, van Vollenhoven, Ronald, Petri, Michelle, Arnaud, Laurent, Appenzeller, Simone, Aranow, Cynthia, Askanase, Anca, Avcin, Tadej, Bae, Sang-Cheol, Bertsias, George, Bonfa, Eloisa, Cairoli, Ernesto, Cardiel, Mario H, Cervera, Ricard, Chasset, François, Chizzolini, Carlo, Clarke, Ann E, Conti, Fabrizio, Costedoat-Chalumeau, Nathalie, Czirják, László, Doria, Andrea, Dörner, Thomas, Espinosa, Gerard, Fischer-Betz, Rebecca, Garcìa, Mercedes, Gladman, Dafna D, González, Luis A, Gunnarsson, Iva, Hamijoyo, Laniyati, Hanly, John G, Hasni, Sarfaraz A, Houssiau, Frédéric A, Inanç, Murat, Inês, Luís S, Isenberg, David, Jacobsen, Soren, Jan Wu, Yeong-Jian, Kaneko, Yuko, Katsumata, Yasuhiro, Lau, Chak S, Legge, Alexandra C, Lerang, Karoline, Limper, Maarten, Louthrenoo, Worawit, Luo, Shue-Fen, Marinho, António, Massardo, Loreto, Mathian, Alexis, Mosca, Marta, Nikpour, Mandana, Pego-Reigosa, José M, Peschken, Christine A, Pons-Estel, Bernardo A, Pons-Estel, Guillermo J, Rahman, Anisur, Rednic, Simona, Ribi, Camillo, Ruiz-Irastorza, Guillermo, Sato, Emilia I, Saxena, Amit, Schneider, Matthias, Sebastiani, Gian Domenico, Strand, Vibeke, Svenungsson, Elisabet, Tanaka, Yoshiya, Tazi Mezalek, Zoubida, Tee, Michael L, Tincani, Angela, Touma, Zahi, Troldborg, Anne, Vasconcelos, Carlos, Vinet, Évelyne, Vital, Edward M, Voskuyl, Alexandre E, Voss, Anne, Wallace, Daniel, Ward, Michael, Zamora, Leonid D

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Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia von Legge, Sophie E, Hamshere, Marian L, Ripke, Stephan, Pardinas, Antonio F, Goldstein, Jacqueline I, Rees, Elliott, Richards, Alexander L, Leonenko, Ganna, Jorskog, L Fredrik, Chambert, Kimberly D, Collier, David A, Genovese, Giulio, Giegling, Ina, Holmans, Peter, Jonasdottir, Adalbjorg, Kirov, George, McCarroll, Steven A, MacCabe, James H, Mantripragada, Kiran, Moran, Jennifer L, Neale, Benjamin M, Stefansson, Hreinn, Rujescu, Dan, Daly, Mark J, Sullivan, Patrick F, Owen, Michael J, O’Donovan, Michael C, Walters, James T R

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CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1 von Rees, Elliott, Walters, James T.R, Chambert, Kimberly D, O'Dushlaine, Colm, Szatkiewicz, Jin, Richards, Alexander L, Georgieva, Lyudmila, Mahoney-Davies, Gerwyn, Legge, Sophie E, Moran, Jennifer L, Genovese, Giulio, Levinson, Douglas, Morris, Derek W, Cormican, Paul, Kendler, Kenneth S, O'Neill, Francis A, Riley, Brien, Gill, Michael, Corvin, Aiden, Sklar, Pamela, Hultman, Christina, Pato, Carlos, Pato, Michele, Sullivan, Patrick F, Gejman, Pablo V, McCarroll, Steven A, O'Donovan, Michael C, Owen, Michael J, Kirov, George

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Analysis of the distribution of Cu, Fe and Zn and other elements in brindled mouse kidney using a scanning proton microprobe von Kirby, Brendan J, M. Danks, David, Legge, George J.F, Mercer, Julian F.B

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