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A novel computational approach for predicting complex phenotypes in Drosophila (starvation-sensitive and sterile) by deriving their gene expression signatures from public data.
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Bellou, Eftychia, Baker, Emily, Leonenko, Ganna, Bracher-Smith, Matthew, Daunt, Paula, Menzies, Georgina, Williams, Julie and Escott-Price, Valentina
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Meckelmann, Sven W., Hawksworth, Jade I., White, Daniel, Andrews, Robert, Rodrigues, Patricia, O'Connor, Anne, Alvarez-Jarreta, Jorge, Tyrrell, Victoria J., Hinz, Christine, Zhou, You, Williams, Julie, Aldrovandi, Maceler, Watkins, William J., Engler, Adam J., Lo Sardo, Valentina, Slatter, David A., Allen, Stuart M., Acharya, Jay, Mitchell, Jacquie, Cooper, Jackie, Aoki, Junken, Kano, Kuniyuki, Humphries, Steve E. and O'Donnell, Valerie B. 2020. Metabolic dysregulation of the lysophospholipid/autotaxin axis in the chromosome 9p21 gene SNP rs10757274. Circulation: Genomic and Precision Medicine 13 (3) , pp. 149-164. 10.1161/CIRCGEN.119.002806 |
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Sims, Rebecca, Hill, Matthew and Williams, Julie 2020. The multiplex model of the genetics of Alzheimer’s disease. Nature Neuroscience 23 , pp. 311-322. 10.1038/s41593-020-0599-5 |
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Leonenko, Ganna, Shoai, Maryam, Bellou, Eftychia, Sims, Rebecca, Williams, Julie, Hardy, John, Escott-Price, Valentina and the Alzheimer's Disease Neuroimaging Initiative,
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Genetic risk for Alzheimer's disease is distinct from genetic risk for amyloid deposition.
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Ma, Yiyi, Jun, Gyungah R., Chung, Jaeyoon, Zhang, Xiaoling, Kunkle, Brian W., Naj, Adam C., White, Charles C., Bennett, David A, De Jager, Philip L., Alzheimer’s Disease Genetics Consortium, , Mayeux, Richard, Haines, Jonathan L., Pericak-Vance, Margaret A., Schellenberg, Gerard D., Farrer, Lindsay A., Lunetta, Kathryn L. and Williams, Julie
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CpG‐related SNPs in the MS4A region have a dose‐dependent effect on risk of late–onset Alzheimer disease.
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Baker, Emily, Sims, Rebecca, Leonenko, Ganna, Frizzati, Aura, Harwood, Janet, Grozeva, Detelina, Morgan, Kevin, Passmore, Peter, Holmes, Clives, Powell, John, Brayne, Carol, Gill, Michael, Mead, Simon, Bossu, Paola, Spalletta, Gianfranco, Goate, Alison, Crunchaga, Carlos, Maier, Wolfgang, Heun, Reinhard, Jessen, Frank, Peters, Oliver, Dichgans, Martin, Frolich, Lutz, Ramirez, Alfredo, Jones, Lesley, Hardy, John, Ivanov, Dobril, Hill, Matthew, Holmans, Peter, Allen, Nicholas, Morgan, Paul, Seshadri, Sudha, Schellenberg, Gerard, Amouvel, Philippe, Williams, Julie and Escott-Price, Valentina
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Gene-based analysis in HRC imputed genome wide association data identifies three novel genes for Alzheimer’s disease.
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Lancaster, Thomas M., Hill, Matthew J., Sims, Rebecca and Williams, Julie
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Microglia - mediated immunity partly contributes to the genetic association between Alzheimer's disease and hippocampal volume.
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Hodgetts, Carl J., Shine, Jonathan P., Williams, Huw, Postans, Mark, Sims, Rebecca, WIlliams, Julie, Lawrence, Andrew D. and Graham, Kim S.
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Ahmad, Shahzad, Bannister, Christian, van der Lee, Sven J., Vojinovic, Dina, Adams, Hieab H.H., Ramirez, Alfredo, Escott-Price, Valentina, Sims, Rebecca, Baker, Emily, Williams, Julie, Holmans, Peter, Vernooij, Meike W., Ikram, M. Arfan, Amin, Najaf and van Duijn, Cornelia M. 2018. Disentangling the biological pathways involved in early features of Alzheimer's disease in the Rotterdam Study. Alzheimer's and Dementia 14 (7) , pp. 848-857. 10.1016/j.jalz.2018.01.005 |
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Baker, Emily, Schmidt, Karl Michael, Sims, Rebecca, O'Donovan, Michael C., Williams, Julie, Holmans, Peter and Escott-Price, Valentina 2018. POLARIS: polygenic LD-adjusted risk score approach for set-based analysis of GWAS data. Genetic Epidemiology 42 (4) , pp. 366-377. 10.1002/gepi.22117 |
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Escott-Price, Valentina, Shoai, Maryam, Pither, Richard, Williams, Julie and Hardy, John 2017. Polygenic score prediction captures nearly all common genetic risk for Alzheimer's disease. Neurobiology of Aging 49 , 214.e7-214.e11. 10.1016/j.neurobiolaging.2016.07.018 |
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2014.
Follow-up of loci from the International Genomics of Alzheimer's Disease Project identifies TRIP4 as a novel susceptibility gene.
Translational Psychiatry
4
, e358.
10.1038/tp.2014.2
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Baig, Shabnam, Palmer, Laura E., Owen, Michael John, Williams, Julie, Kehoe, Patrick G. and Love, Seth 2012. Clusterin mRNA and protein in Alzheimer's disease. Journal of Alzheimer's Disease 28 (2) , pp. 337-344. 10.3233/JAD-2011-110473 |
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Williams, Julie 2011. Interview: Julie Williams speaks to Personalized Medicine. Personalized Medicine 8 (4) , pp. 393-395. 10.2217/pme.11.41 |
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Hollingworth, Paul, Harold, Denise, Sims, Rebecca, Gerrish, Amy, Lambert, Jean-Charles, Carrasquillo, Minerva M., Abraham, Richard Alun, Hamshere, Marian Lindsay, Pahwa, Jaspreet Singh, Escott-Price, Valentina, Dowzell, Kimberley Frances, Denning, Nicola, Stretton, Alexandra, Thomas, Charlene, Richards, Alexander, Ivanov, Dobril, Widdowson, Caroline Susan, Chapman, Jade Alice, Lovestone, Simon, Powell, John, Proitsi, Petroula, Lupton, Michelle K., Brayne, Carol, Rubinsztein, David C., Gill, Michael, Lawlor, Brian, Lynch, Aoibhinn, Brown, Kristelle S., Passmore, Peter A., Craig, David, McGuinness, Bernadette, Todd, Stephen, Holmes, Clive, Mann, David, Smith, A David, Beaumont, Helen, Warden, Donald, Wilcock, Gordon, Love, Seth, Kehoe, Patrick G., Hooper, Nigel M., Vardy, Emma R. L. C., Hardy, John, Mead, Simon, Fox, Nick C, Rossor, Martin, Collinge, John, Maier, Wolfgang, Jessen, Frank, Rüther, Eckart, Schürmann, Britta, Heun, Reiner, Kölsch, Heike, van den Bussche, Hendrik, Heuser, Isabella, Kornhuber, Johannes, Wiltfang, Jens, Dichgans, Martin, Frölich, Lutz, Hampel, Harald, Gallacher, John Edward, Hüll, Michael, Rujescu, Dan, Giegling, Ina, Goate, Alison M., Kauwe, John S. K., Cruchaga, Carlos, Nowotny, Petra, Morris, John C., Mayo, Kevin, Sleegers, Kristel, Bettens, Karolien, Engelborghs, Sebastiaan, De Deyn, Peter P, Van Broeckhoven, Christine, Livingston, Gill, Bass, Nicholas J., Gurling, Hugh, McQuillin, Andrew, Gwilliam, Rhian, Deloukas, Panagiotis, Al-Chalabi, Ammar, Shaw, Christopher E., Tsolaki, Magda, Singleton, Andrew B., Guerreiro, Rita, Mühleisen, Thomas W., Nöthen, Markus M., Moebus, Susanne, Jöckel, Karl-Heinz, Klopp, Norman, Wichmann, H-Erich, Pankratz, V. Shane, Sando, Sigrid B., Aasly, Jan O., Barcikowska, Maria, Wszolek, Zbigniew K., Dickson, Dennis W., Graff-Radford, Neill R., Petersen, Ronald C., van Duijn, Cornelia M., Breteler, Monique M. B., Ikram, M. Arfan, DeStefano, Anita L., Fitzpatrick, Annette L., Lopez, Oscar, Launer, Lenore J., Seshadri, Sudha, Berr, Claudine, Campion, Dominique, Epelbaum, Jacques, Dartigues, Jean-François, Tzourio, Christophe, Alpérovitch, Annick, Lathrop, Mark, Feulner, Thomas M., Friedrich, Patricia, Riehle, Caterina, Krawczak, Michael, Schreiber, Stefan, Mayhaus, Manuel, Nicolhaus, S., Wagenpfeil, Stefan, Steinberg, Stacy, Stefansson, Hreinn, Stefansson, Kari, Snædal, Jon, Björnsson, Sigurbjörn, Jonsson, Palmi V., Chouraki, Vincent, Genier-Boley, Benjamin, Hiltunen, Mikko, Soininen, Hilkka, Combarros, Onofre, Zelenika, Diana, Delepine, Marc, Bullido, Maria J., Pasquier, Florence, Mateo, Ignacio, Frank-Garcia, Ana, Porcellini, Elisa, Hanon, Olivier, Coto, Eliecer, Alvarez, Victoria, Bosco, Paolo, Siciliano, Gabriele, Mancuso, Michelangelo, Panza, Francesco, Solfrizzi, Vincenzo, Nacmias, Benedetta, Sorbi, Sandro, Bossù, Paola, Piccardi, Paola, Arosio, Beatrice, Annoni, Giorgio, Seripa, Davide, Pilotto, Alberto, Scarpini, Elio, Galimberti, Daniela, Brice, Alexis, Hannequin, Didier, Licastro, Federico, Jones, Lesley, Holmans, Peter Alan, Jonsson, Thorlakur, Riemenschneider, Matthias, Morgan, Kevin, Younkin, Steven G., Owen, Michael John, O'Donovan, Michael Conlon, Amouyel, Philippe and Williams, Julie 2011. Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease. Nature Genetics 43 (5) , pp. 429-435. 10.1038/ng.803 |
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Schuermann, Britta, Wiese, Birgitt, Bickel, Horst, Weyerer, Siegfried, Riedel-Heller, Steffi G., Pentzek, Michael, Bachmann, Cadja, Williams, Julie, van den Bussche, Hendrik, Maier, Wolfgang and Jessen, Frank 2011. Association of the Alzheimer's disease clusterin risk allele with plasma clusterin concentration. Journal of Alzheimers Disease 25 (3) , pp. 421-424. |
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Belbin, Olivia, Brown, Kristelle, Shi, Hui, Medway, Christopher, Abraham, Richard, Passmore, Peter, Mann, David, Smith, A. David, Holmes, Clive, McGuinness, Bernadette, Craig, David, Warden, Donald, Heun, Reinhard, Koelsch, Heike, Love, Seth, Kalsheker, Noor, Williams, Julie, Owen, Michael John, Carrasquillo, Minerva, Younkin, Steven, Morgan, Kevin and Kehoe, Patrick G. 2011. A multi-center study of ACE and the risk of late-onset Alzheimer's disease. Journal of Alzheimer's Disease 24 (3) , pp. 587-597. 10.3233/JAD-2011-101914 |
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Reitz, Christine, Cheung, Rong, Rogaeva, Ekaterina, Lee, Joseph H., Tokuhiro, Shinya, Zou, Fanggeng, Bettens, Karolien, Sleegers, Kristel, Tan, Eng King, Kimura, Ryo, Shibata, Nobuto, Arai, Heii, Kamboh, Ilyas, Prince, Jonathan A., Maier, Wolfgang, Riemenschneider, Matthias, Owen, Michael John, Harold, Denise, Hollingworth, Paul, Cellini, Elena, Sorbi, Sandro, Nacmias, Benedetta, Takeda, Masatoshi, Pericak-Vance, Margaret A., Haines, Jonathan L., Younkin, Steven, Williams, Julie, van Broeckhoven, Christine, Farrer, Lindsay, St George-Hyslop, Peter and Mayeux, Richard 2011. Meta-analysis of the association between variants in SORL1 and Alzheimer Disease. Archives of Neurology 68 (1) , pp. 99-106. 10.1001/archneurol.2010.346 |
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Sims, Rebecca, Dwyer, Sarah Lynne, Harold, Denise, Gerrish, Amy, Hollingworth, Paul, Chapman, Jade Alice, Denning, Nicola, Abraham, Richard Alun, Ivanov, Dobril, Pahwa, Jaspreet Singh, Escott-Price, Valentina, Dowzell, Kimberley Frances, Thomas, Charlene, Stretton, Alexandra, Lovestone, Simon, Powell, John, Proitsi, Petroula, Lupton, Michelle K., Brayne, Carol, Rubinsztein, David C., Gill, Michael, Lawlor, Brian, Lynch, Aoibhinn, Morgan, Kevin, Brown, Kristelle S., Passmore, Peter A., Craig, David, McGuiness, Bernadette, Todd, Stephen, Johnston, Janet A., Holmes, Clive, Mann, David, Smith, A. David, Love, Seth, Kehoe, Patrick G., Hardy, John, Mead, Simon, Fox, Nick, Rossor, Martin, Collinge, John, Livingston, Gill, Bass, Nicholas J., Gurling, Hugh, McQuillin, Andrew, Jones, Lesley, Holmans, Peter Alan, O'Donovan, Michael Conlon, Owen, Michael John and Williams, Julie 2011. No evidence that extended tracts of homozygosity are associated with Alzheimer's disease. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 (7) , pp. 764-771. 10.1002/ajmg.b.31216 |
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Jones, Lesley, Holmans, Peter Alan, Hamshere, Marian Lindsay, Harold, Denise, Moskvina, Valentina, Ivanov, Dobril, Pocklington, Andrew, Abraham, Richard Alun, Hollingworth, Paul, Sims, Rebecca, Gerrish, Amy, Pahwa, Jaspreet Singh, Jones, Nicola, Stretton, Alexandra, Morgan, Angharad Rhys, Lovestone, Simon, Powell, John, Proitsi, Petroula, Lupton, Michelle K., Brayne, Carol, Rubinsztein, David C., Gill, Michael, Lawlor, Brian, Lynch, Aoibhinn, Morgan, Kevin, Brown, Kristelle S., Passmore, Peter A., Craig, David, McGuinness, Bernadette, Todd, Stephen, Holmes, Clive, Mann, David, Smith, A. David, Love, Seth, Kehoe, Patrick G., Mead, Simon, Fox, Nick, Rossor, Martin, Collinge, John, Maier, Wolfgang, Jessen, Frank, Schürmann, Britta, Heun, Reinhard, Kölsch, Heike, van den Bussche, Hendrik, Heuser, Isabella, Peters, Oliver, Kornhuber, Johannes, Wiltfang, Jens, Dichgans, Martin, Frölich, Lutz, Hampel, Harald, Hüll, Michael, Rujescu, Dan, Goate, Alison M., Kauwe, John S. K., Cruchaga, Carlos, Nowotny, Petra, Mayo, Kevin, Morris, John C., Livingston, Gill, Bass, Nicholas J., Gurling, Hugh, McQuillin, Andrew, Gwilliam, Rhian, Deloukas, Panos, Al-Chalabi, Ammar, Shaw, Christopher E., Singleton, Andrew B., Guerreiro, Rita, Mühleisen, Thomas W., Nöthen, Markus M., Moebus, Susanne, Jöckel, Karl-Heinz, Klopp, Norman, Wichmann, H.-Erich, Rüther, Eckhard, Carrasquillo, Minerva M., Pankratz, V. Shane, Younkin, Steven G., Hardy, John, O'Donovan, Michael Conlon, Williams, Julie and Owen, Michael John
2010.
Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease.
PLoS ONE
5
(11)
, e13950.
10.1371/journal.pone.0013950
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Pagnamenta, Alistair T., Bacchelli, Elena, de Jonge, Maretha V., Mirza, Ghazala, Scerri, Thomas S., Minopoli, Fiorella, Chiocchetti, Andreas, Ludwig, Kerstin U., Hoffmann, Per, Paracchini, Silvia, Lowy, Ernesto, Harold, Denise, Chapman, Jade Alice, Klauck, Sabine M., Poustka, Fritz, Houben, Renske H., Staal, Wouter G., Ophoff, Roel A., O'Donovan, Michael Conlon, Williams, Julie, Nöthen, Markus M., Schulte-Körne, Gerd, Deloukas, Panos, Ragoussis, Jiannis, Bailey, Anthony J., Maestrini, Elena and Monaco, Anthony P. 2010. Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia. Biological psychiatry 68 (4) , pp. 320-328. 10.1016/j.biopsych.2010.02.002 |
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Seshadri, Sudha, Fitzpatrick, Annette L., Ikram, M. Arfan, DeStefano, Anita L., Gudnason, Vilmunder, Boada, Merce, Bis, Joshua C., Smith, Albert V., Carrasquillo, Minerva M., Lambert, Jean Charles, Harold, Denise, Schrijvers, Elizabeth M. C., Ramirez-Lorca, Reposo, Debette, Stephanie, Longstreth, W. T., Janssens, A. Cecile J. W., Pankratz, V. Shane, Dartigues, Jean Francois, Hollingworth, Paul, Aspelund, Thor, Hernandez, Isabel, Beiser, Alexa, Kuller, Lewis H., Koudstaal, Peter J., Dickson, Dennis W., Tzourio, Christope, Abraham, Richard Alun, Antunez, Carmen, Du, Yangchun, Rotter, Jerome I., Aulchenko, Yurii S., Harris, Tamara B., Petersen, Ronald C., Berr, Claudine, Owen, Michael John, Lopez-Arrieta, Jesus, Vardarajan, Bardi N., Becker, James T., Rivadeneira, Fernando, Nalls, Michael A., Graff-Radford, Neill R., Campion, Dominique, Auerbach, Sanford, Rice, Kenneth, Hofman, Albert, Jonsson, Palmi V., Schmidt, Helena, Lathrop, Mark, Mosley, Thomas H., Au, Rhoda, Psaty, Bruce M., Uitterlinden, Andre G., Farrer, Lindsay A., Lumley, Thomas, Ruiz, Agustin, Williams, Julie, Amouyel, Philippe, Younkin, Steve G., Wolf, Philip A., Launer, Lenore J., Lopez, Oscar L., van Duijn, Cornelia M. and Breteler, Monique M. B. 2010. Genome-wide analysis of genetic loci associated with Alzheimer Disease. JAMA - The Journal of the American Medical Association 303 (18) , pp. 1832-1840. 10.1001/jama.2010.574 |
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Williams, Julie 2010. Pinpointing key mechanisms in Alzheimer's disease development [Commentary]. Alzheimer's Research & Therapy 2 (2) , p. 4. 10.1186/alzrt27 |
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Hardy, John and Williams, Julie 2010. Identification of Alzheimer risk factors through whole-genome analysis. Archives of Neurology 67 (6) , pp. 663-664. |
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Hollingworth, Paul, Harold, Denise, Jones, Lesley, Owen, Michael John and Williams, Julie 2010. Alzheimer's disease genetics: current knowledge and future challenges. International Journal of Geriatric Psychiatry 26 (8) , pp. 793-802. 10.1002/gps.2628 |
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Lupton, Michelle K, Stahl, Daniel, Archer, Nicola, Foy, Catherine, Poppe, Michaela, Lovestone, Simon, Hollingworth, Paul, Williams, Julie, Owen, Michael John, Dowzell, Kimberley Frances, Abraham, Richard Alun, Sims, Rebecca, Brayne, Carol, Rubinsztein, David, Gill, Michael, Lawlor, Brian, Lynch, Aoibhinn and Powell, John F 2010. Education, occupation and retirement age effects on the age of onset of Alzheimer's disease. International Journal of Geriatric Psychiatry 25 (1) , pp. 30-36. 10.1002/gps.2294 |
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Jones, Lesley, Harold, Denise and Williams, Julie 2010. Genetic evidence for the involvement of lipid metabolism in Alzheimer's disease. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids 1801 (8) , pp. 754-761. 10.1016/j.bbalip.2010.04.005 |
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Cruchaga, Carlos, Kauwe, John S. K., Mayo, Kevin, Spiegel, Noah, Bertelsen, Sarah, Nowotny, Petra, Shah, Aarti R., Abraham, Richard, Hollingworth, Paul, Harold, Denise, Owen, Michael John, Williams, Julie, Lovestone, Simon, Peskind, Elaine R., Li, Ge, Leverenz, James B., Galasko, Douglas, Morris, John C., Fagan, Anne M., Holtzman, David M. and Goate, Alison M. 2010. SNPS associated with cerebrospinal fluid phospho-tau levels influence rate of decline in Alzheimer's disease. PLoS Genetics 6 (9) , e1001101. 10.1371/journal.pgen.1001101 |
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Baig, Shabnam, Joseph, Sally A., Tayler, Hannah, Abraham, Richard Alun, Owen, Michael John, Williams, Julie, Kehoe, Patrick G. and Love, Seth 2010. Distribution and expression of picalm in alzheimer disease. Journal of Neuropathology and Experimental Neurology 69 (10) , pp. 1071-1077. 10.1097/NEN.0b013e3181f52e01 |
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Harold, Denise, Abraham, Richard Alun, Hollingworth, Paul, Sims, Rebecca, Gerrish, Amy, Hamshere, Marian Lindsay, Pahwa, Jaspreet Singh, Escott-Price, Valentina, Dowzell, Kimberley Frances, Williams, Amy, Denning, Nicola, Thomas, Charlene, Stretton, Alexandra, Morgan, Angharad Rhys, Lovestone, Simon, Powell, John, Proitsi, Petroula, Lupton, Michelle K., Brayne, Carol, Rubinsztein, David C., Gill, Michael, Lawlor, Brian, Lynch, Aoibhinn, Morgan, Kevin, Brown, Kristelle S., Passmore, Peter A., Craig, David, McGuinness, Bernadette, Todd, Stephen, Holmes, Clive, Mann, David, Smith, A. David, Love, Seth, Kehoe, Patrick G., Hardy, John, Mead, Simon, Fox, Nick, Rossor, Martin, Collinge, John, Maier, Wolfgang, Jessen, Frank, Schürmann, Britta, van den Bussche, Hendrik, Heuser, Isabella, Kornhuber, Johannes, Wiltfang, Jens, Dichgans, Martin, Frölich, Lutz, Hampel, Harald, Hüll, Michael, Rujescu, Dan, Goate, Alison M., Kauwe, John S. K., Cruchaga, Carlos, Nowotny, Petra, Morris, John C., Mayo, Kevin, Sleegers, Kristel, Bettens, Karolien, Engelborghs, Sebastiaan, De Deyn, Peter P., Van Broeckhoven, Christine, Livingston, Gill, Bass, Nicholas J., Gurling, Hugh, McQuillin, Andrew, Gwilliam, Rhian, Deloukas, Panagiotis, Al-Chalabi, Ammar, Shaw, Christopher E., Tsolaki, Magda, Singleton, Andrew B., Guerreiro, Rita, Mühleisen, Thomas W., Nöthen, Markus M., Moebus, Susanne, Jöckel, Karl-Heinz, Klopp, Norman, Wichmann, H.-Erich, Carrasquillo, Minerva M., Pankratz, V. Shane, Younkin, Steven G., Holmans, Peter Alan, O'Donovan, Michael Conlon, Owen, Michael John and Williams, Julie 2009. Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease [Letter]. Nature Genetics 41 (10) , pp. 1088-1093. 10.1038/ng.440 |
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Harold, Denise, Abraham, Richard Alun, Hollingworth, Paul, Sims, Rebecca, Gerrish, Amy, Hamshere, Marian Lindsay, Pahwa, Jaspreet Singh, Escott-Price, Valentina, Dowzell, Kimberley Frances, Williams, Amy, Denning, Nicola, Thomas, Charlene, Stretton, Alexandra, Morgan, Angharad Rhys, Lovestone, Simom, Powell, John, Proitsi, Petroula, Lupton, Michelle K., Brayne, Carol, Rubinsztein, David C., Gill, Michael, Lawlor, Brian, Lynch, Aoibhinn, Morgan, Kevin, Brown, Kristelle S., Passmore, Peter A., Craig, David, McGuinness, Bernadette, Todd, Stephen, Holmes, Clive, Mann, David, Smith, A. David, Love, Seth, Kehoe, Patrick G., Hardy, John, Mead, Simon, Fox, Nick, Rossor, Martin, Collinge, John, Maier, Wolfgang, Jessen, Frank, Schürmann, Britta, van den Bussche, Hendrik, Heuser, Isabella, Kornhuber, Johannes, Wiltfang, Jens, Dichgans, Martin, Frölich, , Hampel, Harald, Hüll, Michael, Rujescu, Dan, Goate, Alison M., Kauwe, John S. K., Cruchaga, Carlos, Nowotny, Petra, Morris, John C., Mayo, Kevin, Sleegers, Kristel, Bettens, Karolien, Engelborghs, Sebastiaan, De Deyn, Peter P., Van Broeckhoven, Christine, Livingston, Gill, Bass, Nicholas J., Gurling, Hugh, McQuillin, Andrew, Gwilliam, Rhian, Deloukas, Panagiotis, Al-Chalabi, Ammar, Shaw, Christopher E., Tsolaki, Magda, Singleton, Andrew B., Guerreiro, Rita, Mühleisen, Thomas W., Nöthen, Markus M., Moebus, Susanne, Jöckel, Karl-Heinz, Klopp, Norman, Wichmann, H-Erich, Carrasquillo, Minerva M., Pankratz, V. Shane, Younkin, Steven G., Holmans, Peter Alan, O'Donovan, Michael Conlon, Owen, Michael John and Williams, Julie 2009. Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease [Corrigendum]. Nature Genetics 41 (10) , p. 1156. 10.1038/ng1009-1156d |
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Abraham, Richard Alun, Sims, Rebecca, Carroll, Liam Stuart, Hollingworth, Paul, O'Donovan, Michael Conlon, Williams, Julie and Owen, Michael John 2009. An association study of common variation at theMAPTlocus with late-onset Alzheimer's disease. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 150B (8) , pp. 1152-1155. 10.1002/ajmg.b.30951 |
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Kauwe, J. S. K., Bertelsen, S., Mayo, K., Cruchaga, C., Abraham, Richard Alun, Hollingworth, Paul, Harold, Denise, Owen, Michael John, Williams, Julie, Lovestone, S., Morris, J. C. and Goate, A. M. 2009. Suggestive synergy between genetic variants in TF and HFE as risk factors for Alzheimer's disease. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (4) , pp. 955-959. 10.1002/ajmg.b.31053 |
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Filippini, Nicola, Rao, Anil, Wetten, Sally, Gibson, Rachel A., Borrie, Michael, Guzman, Danilo, Kertesz, Andrew, Loy-English, Inge, Williams, Julie, Nichols, Thomas, Whitcher, Brandon and Matthews, Paul M. 2009. Anatomically-distinctgeneticassociations of APOE ɛ4 alleleload with regionalcorticalatrophy in Alzheimer's disease. NeuroImage 44 (3) , pp. 724-728. 10.1016/j.neuroimage.2008.10.003 |
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Blom, Elin S., Giedraitis, Vilmantas, Arepalli, Sampath, Hamshere, Marian Lindsay, Adighibe, Omanma, Goate, Alison, Williams, Julie, Lannfelt, Lars, Hardy, John, Vrièze, Fabienne and Glaser, Anna 2009. Further analysis of previously implicated linkage regions for Alzheimer's disease in affected relative pairs. BMC Medical Genetics 10 , pp. 1-6. 10.1186/1471-2350-10-122 |
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Abraham, Richard, Escott-Price, Valentina, Sims, Rebecca, Hollingworth, Paul, Morgan, Angharad, Georgieva, Lyudmila, Dowzell, Kimberley, Cichon, Sven, Hillmer, Axel M, O'Donovan, Michael Conlon, Williams, Julie, Owen, Michael John and Kirov, George 2008. A genome-wide association study for late-onset Alzheimer's disease using DNA pooling. BMC Medical Genomics 1 (1) , 44. 10.1186/1755-8794-1-44 |
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Li, Hao, Wetten, Sally, Li, Li, St. Jean, Pamela L., Upmanyu, Ruchi, Surh, Linda, Hosford, David, Barnes, Michael R., Briley, James David, Borrie, Michael, Coletta, Natalie, Delisle, Richard, Dhalla, Daniella, Ehm, Margaret G., Feldman, Howard H., Fornazzari, Luis, Gauthier, Serge, Goodgame, Neil, Guzman, Danilo, Hammond, Sandra, Hollingworth, Paul, Hsiung, Ging - Yuek, Johnson, Joan, Kelly, Devon D., Keren, Ron, Kertesz, Andrew, King, Karen S., Lovestone, Simon, Loy-English, Inge, Matthews, Paul M., Owen, Michael John, Plumpton, Mary, Pryse-Phillips, William, Prinjha, Rab K., Richardson, Jill C., Saunders, Ann, Slater, Andrew J., St. George-Hyslop, Peter H., Stinnett, Sandra W., Swartz, Jina E., Taylor, Rachel L., Wherrett, John, Williams, Julie, Yarnall, David P., Gibson, Rachel A., Irizarry, Michael C., Middleton, Lefkos T. and Roses, Allen D. 2008. Candidate single-nucleotide polymorphisms from a genomewide association study of alzheimer disease. Archives of Neurology 65 (1) , pp. 45-53. 10.1001/archneurol.2007.3 |
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Kwok, John B. J., Loy, Clement T., Hamilton, Gillian, Lau, Edmond, Hallupp, Marianne, Williams, Julie, Owen, Michael John, Broe, G. Anthony, Tang, Nelson, Lam, Linda, Powell, John F., Lovestone, Simon and Schofield, Peter R. 2008. Glycogen synthase kinase-3β and tau genes interact in Alzheimer's disease. Annals of Neurology 64 (4) , pp. 446-454. 10.1002/ana.21476 |
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Li, Y., Grupe, A., Rowland, C., Holmans, Peter Alan, Segurado, Ricardo, Abraham, Richard Alun, Jones, Lesley, Catanese, J., Ross, D., Mayo, K., Martinez, M., Hollingworth, Paul, Goate, A., Cairns, N. J., Racette, B. A., Perlmutter, J. S., O'Donovan, Michael Conlon, Morris, J. C., Brayne, C., Rubinsztein, D. C., Lovestone, S., Thal, L. J., Owen, Michael John and Williams, Julie 2008. Evidence that common variation in NEDD9 is associated with susceptibility to late-onset Alzheimer's and Parkinson's disease. Human Molecular Genetics 17 (5) , pp. 759-767. 10.1093/hmg/ddm348 |
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Blom, Elin S., Holmans, Peter Alan, Arepalli, Sampath, Adighibe, Omanma, Hamshere, Marian Lindsay, Gatz, Margaret, Pedersen, Nancy L., Bergem, A. L. Mina, Owen, Michael John, Hollingworth, Paul, Goate, Alison, Williams, Julie, Lannfelt, Lars, Hardy, John, Wavrant-De Vrièze, Fabienne and Glaser, Anna 2008. Does APOE explain the linkage of Alzheimer's disease to chromosome 19q13? American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B (6) , pp. 778-783. 10.1002/ajmg.b.30681 |
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Foy, Catherine M. L., Nicholas, Helen, Hollingworth, Paul, Boothby, Harry, Williams, Julie, Brown, Richard G., Al-Sarraj, Safa and Lovestone, Simon 2007. Diagnosing Alzheimer's disease--non-clinicians and computerised algorithms together are as accurate as the best clinical practice. International Journal of Geriatric Psychiatry 22 (11) , pp. 1154-1163. 10.1002/gps.1810 |
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Hollingworth, Paul, Hamshere, Marian Lindsay, Holmans, Peter Alan, O'Donovan, Michael Conlon, Sims, Rebecca, Powell, J., Lovestone, S., Myers, A., DeVrieze, F.W., Hardy, J., Goate, A., Owen, Michael John and Williams, Julie 2007. Increased familial risk and genomewide significant linkage for Alzheimer's disease with psychosis. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 144B (7) , pp. 841-848. 10.1002/ajmg.b.30515 |
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Morgan, A.R., Turic, Darko, Jehu, Luke, Hamilton, G., Hollingworth, Paul, Escott-Price, Valentina, Jones, Lesley, Lovestone, S., Brayne, C., Rubinsztein, D.C., Lawlor, B., Gill, M., O'Donovan, Michael Conlon, Owen, Michael John and Williams, Julie 2007. Association studies of 23 positional/functional candidate genes on chromosome 10 in late-onset Alzheimer's disease. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 144B (6) , pp. 762-770. 10.1002/ajmg.b.30509 |
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Hamshere, Marian Lindsay, Holmans, Peter Alan, Avramopoulos, Dimitrios, Bassett, Susan S., Blacker, Deborah, Bertram, Lars, Wiener, Howard, Rochberg, Nan, Tanzi, Rudolph E., Myers, Amanda, Wavrant-De Vrièze, Fabienne, Go, Rodney, Fallin, Daniele, Lovestone, Simon, Hardy, John, Goate, Alison, O'Donovan, Michael Conlon, Williams, Julie and Owen, Michael John 2007. Genome-wide linkage analysis of 723 affected relative pairs with late-onset Alzheimer's disease. Human Molecular Genetics Advanc , pp. 1-34. 10.1093/hmg/ddm224 |
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Harold, Denise, Jehu, Luke, Turic, Darko, Hollingworth, Paul, Moore, P., Summerhayes, P., Escott-Price, Valentina, Foy, C., Archer, N., Hamilton, B.A., Lovestone, S., Powell, J., Brayne, C., Rubinsztein, D.C., Jones, Lesley, O'Donovan, Michael Conlon, Owen, Michael John and Williams, Julie 2007. Interaction between theADAM12 andSH3MD1 genes may confer susceptibility to late-onset Alzheimer's disease. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 144B (4) , pp. 448-452. 10.1002/ajmg.b.30456 |
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Hamilton, Gillian, Proitsi, Petra, Jehu, Luke, Morgan, Angharad, Williams, Julie, O'Donovan, Michael Conlon, Owen, Michael John, Powell, John F. and Lovestone, Simon 2007. Candidate gene association study of insulin signaling genes and Alzheimer's disease: Evidence for SOS2, PCK1, and PPARgamma as susceptibility loci. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 144B (4) , pp. 508-516. 10.1002/ajmg.b.30503 |
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Archer, Nicola, Brown, Richard G., Reeves, Suzanne J., Boothby, Harry, Nicholas, Helen, Foy, Catherine, Williams, Julie and Lovestone, Simon 2007. Premorbid personality and behavioral and psychological symptoms in probable Alzheimer disease. American Journal of Geriatric Psychiatry 15 (3) , pp. 202-213. |
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Grupe, Andrew, Abraham, Richard Alun, Li, Yonghong, Rowland, Charles, Hollingworth, Paul, Morgan, Angharad Rhys, Jehu, Luke, Segurado, Ricardo, Stone, David, Schadt, Eric, Karnoub, Maha, Nowotny, Petra, Tacey, Kristina, Catanese, Joseph, Sninsky, John, Brayne, Carol, Rubinsztein, David, Gill, Michael, Lawlor, Brian, Lovestone, Simo, Holmans, Peter Alan, O'Donovan, Michael Conlon, Morris, John C., Thal, Leon, Goate, Alison, Owen, Michael John and Williams, Julie 2007. Evidence for novel susceptibility genes for late-onset Alzheimer's disease from a genome-wide association study of putative functional variants. Human Molecular Genetics 16 (8) , pp. 865-873. 10.1093/hmg/ddm031 |
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Hamilton, Gillian, Proitsi, Petra, Williams, Julie, O'Donovan, Michael Conlon, Owen, Michael John, Powell, John and Lovestone, Simon 2007. Complement factor H Y402H polymorphism is not associated with late-onset Alzheimer's disease. Neuromolecular Medicine 9 (4) , pp. 331-334. 10.1007/s12017-007-8013-y |
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Morgan, A.R., Hamilton, G., Turic, Dragana, Jehu, L., Harold, Denise, Abraham, Richard Alun, Hollingworth, Paul, Escott-Price, Valentina, Brayne, C., Rubinsztein, D.C., Lynch, A., Lawlor, B., Gill, M., O'Donovan, Michael Conlon, Powell, J., Lovestone, S., Williams, Julie and Owen, Michael John 2007. Association analysis of 528 intra-genic SNPs in a region of chromosome 10 linked to late onset Alzheimer's disease. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147B (6) , pp. 727-731. 10.1002/ajmg.b.30670 |
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Hollingworth, Paul, Hamshere, Marian Lindsay, Escott-Price, Valentina, Dowzell, Kimberley, Moore, Pamela J., Foy, Catherine, Archer, Nicola, Lynch, Aoibhinn, Lovestone, Simon, Brayne, Carol, Rubinsztein, David C., Lawlor, Brian, Gill, Mike, Owen, Michael John and Williams, Julie 2006. Four Components Describe Behavioral Symptoms in 1,120 Individuals with Late-Onset Alzheimer's Disease. Journal of the American Geriatrics Society 54 (9) , pp. 1348-1354. 10.1111/j.1532-5415.2006.00854.x |
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Li, Yonghong, O'Donovan, Michael Conlon, Williams, Julie, Brayne, Carol, Rowland, Charles, Owen, Michael John, Morris, John C and Maxwell, Taylor J 2006. DAPK1 variants are associated with Alzheimer's disease and allele-specific expression. Human Molecular Genetics 15 (17) , pp. 2560-2568. 10.1093/hmg/ddl178 |
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Williams, Julie and O'Donovan, Michael Conlon 2006. The genetics of developmental dyslexia. European Journal of Human Genetics 14 (6) , pp. 681-89. 10.1038/sj.ejhg.5201575 |
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Hamilton, Gillian, Samedi, Farzana, Knight, Jo, Archer, Nicola, Foy, Catherine, Walter, Sarah, Turic, Dragana, Jehu, Luke, Moore, Pamela, Hollingworth, Paul, O'Donovan, Michael Conlon, Williams, Julie, Owen, Michael John, Lovestone, Simon and Powell, John F. 2006. Polymorphisms in the phosphate and tensin homolog gene are not associated with late-onset Alzheimer's disease. Neuroscience Letters 401 (1-2) , pp. 77-80. 10.1016/j.neulet.2006.03.021 |
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Harold, Denise, Macgregor, S., Patterson, C. E., Hollingworth, P., Moore, P., Owen, Michael John, Williams, Julie, O'Donovan, Michael Conlon, Passmore, P., McIlroy, S. and Jones, Lesley 2006. A single nucleotide polymorphism in CHAT influences response to acetylcholinesterase inhibitors in Alzheimer's disease. Pharmacogenetics and genomics 16 (2) , pp. 75-77. |
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Grupe, Andrew, Li, Yonghong, Rowland, Charles, Nowotny, Petra, Hinrichs, Anthony L., Smemo, Scott, Kauwe, John S. K., Maxwell, Taylor J., Cherny, Sara, Doil, Lisa, Tacey, Kristina, Luchene, Ryan van, Myers, Amanda, Wavrant-De Vrièze, Fabienne, Kaleem, Mona, Hollingworth, Paul, Jehu, Luke, Foy, Catherine, Archer, Nicola, Hamilton, Gillian, Holmans, Peter Alan, Morris, Chris M., Catanese, Joseph, Sninsky, John, White, Thomas J., Powell, John, Hardy, John, O'Donovan, Michael Conlon, Lovestone, Simon, Jones, Lesley, Morris, John C., Thal, Leon, Owen, Michael John, Williams, Julie and Goate, Alison 2006. A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease. The American Journal of Human Genetics 78 (1) , pp. 78-88. |
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Li, Y., Rowland, C., Tacey, K., Catanese, J., Sninsky, J., Hardy, J., Powell, J., Lovestone, S., Morris, J. C., Thal, L., Goate, A., Owen, Michael John, Williams, Julie and Grupe, A. 2005. The BDNF Val66Met polymorphism is not associated with late onset Alzheimer's disease in three case-control samples. Molecular Psychiatry 10 (9) , pp. 809-810. 10.1038/sj.mp.4001702 |
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Holmans, Peter Alan, Hamshere, Marian Lindsay, Hollingworth, P., Rice, Frances, Tunstall, N., Jones, S., Moore, P., Wavrant DeVrieze, F., Myers, A., Crook, R., Compton, D., Marshall, H., Meyer, D., Shears, S., Booth, J., Ramic, D., Williams, Nigel Melville, Norton, N., Abraham, R., Kehoe, P., Williams, H., Rudrasingham, V., O'Donovan, Michael Conlon, Jones, Lesley, Hardy, J., Goate, A., Lovestone, S., Owen, Michael John and Williams, Julie 2005. Genome screen for loci influencing age at onset and rate of decline in late onset Alzheimer's disease. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 135B (1) , pp. 24-32. 10.1002/ajmg.b.30114 |
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Cope, Natalie Alexandra, Harold, Denise, Hill, Gary Trevor, Escott-Price, Valentina, Stevenson, Jim, Holmans, Peter Alan, Owen, Michael John, O’Donovan, Michael Conlon and Williams, Julie 2005. Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia. American Journal of Human Genetics 76 (4) , pp. 581-591. 10.1086/429131 |
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Li, Y., Hollingworth, P., Moore, P., Foy, C., Archer, N., Powell, J., Nowotny, P., Holmans, Peter Alan, O'Donovan, Michael Conlon, Tacey, K., Doil, L., van Luchene, R., Garcia, V., Rowland, V., Lau, K., Cantanese, J., Sninsky, J., Hardy, J., Thal, L., Morris, J. C., Goate, A., Lovestone, S., Owen, Michael John, Williams, Julie and Grupe, A. 2005. Genetic association of the APP binding protein 2 gene (APBB2) with late onset Alzheimer disease. Human Mutation 25 (3) , pp. 270-277. 10.1002/humu.20138 |
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Cope, N. A., Hill, G., van den Bree, Marianne Bernadette, Harold, D., Escott-Price, Valentina, Green, E. K., Owen, Michael John, Williams, Julie and O'Donovan, Michael Conlon 2005. No support for association between dyslexia susceptibility 1 candidate 1 and developmental dyslexia. Molecular Psychiatry 10 (3) , pp. 237-238. 10.1038/sj.mp.4001596 |
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Cook, L. J., Ho, L. W., Wang, L., Terrenoire, E., Brayne, C., Evans, J. G., Xuereb, J., Cairns, N. J., Turic, D., Hollingworth, P., Moore, P. J., Jehu, L., Archer, N., Walter, S., Foy, C., Edmonson, A., Powell, J., Lovestone, S., Williams, Julie and Rubinsztein, D. C. 2005. Candidate gene association studies of genes involved in neuronal cholinergic transmission in Alzheimer's disease suggests choline acetyltransferase as a candidate deserving further study. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 132B (1) , pp. 5-8. 10.1002/ajmg.b.30068 |
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Li, Yonghong, Nowotny, Petra, Holmans, Peter Alan, Smemo, Scott, Kauwe, John S. K., Hinrichs, Anthony L., Tacey, Kristina, Doil, Lisa, Luchene, Ryan van, Garcia, Veronica, Rowland, Charles, Schrodi, Steve, Leong, Diane, Gogic, Goran, Chan, Joanne, Cravchik, Anibal, Ross, David, Lau, Kit, Kwok, Shirley, Chang, Sheng-Yung, Catanese, Joseph, Sninsky, John, White, Thomas J., Hardy, John, Powell, John, Lovestone, Simon, Morris, John C., Thal, Leon, Owen, Michael John, Williams, Julie, Goate, Alison and Grupe, Andrew 2004. Association of late-onset Alzheimer's disease with genetic variation in multiple members of the GAPD gene family. Proceedings of the National Academy of Sciences 101 (44) , pp. 15688-15693. 10.1073/pnas.0403535101 |
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Bray, Nicholas John, Jehu, Luke, Escott-Price, Valentina, Buckland, Paul Robert, Williams, Julie, Owen, Michael John and O'Donovan, Michael Conlon 2004. Allelic expression of APOE in brain [Conference Abstract]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 130B (1) , p. 61. |
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Bray, Nicholas John, Jehu, Luke, Escott-Price, Valentina, Buckland, Paul Robert, Owen, Michael John, Williams, Julie and O'Donovan, Michael Conlon 2004. P4-101 Allelic expression of APOE in brain [Conference Abstract]. Neurobiology of Aging 25 , S503-S503. 10.1016/S0197-4580(04)81659-2 |
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Cook, Lynnette J., Ho, Luk W., Taylor, Alison E., Brayne, Carol, Evans, John Grimley, Xuereb, John, Cairns, Nigel J., Pritchard, Antonia, Lemmon, Helen, Mann, David, St Clair, David, Turic, Dragana, Hollingworth, Paul, Moore, Pamela J., Jehu, Luke, Archer, Nicola, Walter, Sarah, Foy, Catherine, Edmondson, Amanda, Powell, John, Lovestone, Simon, Owen, Michael John, Williams, Julie, Lendon, Corinne and Rubinsztein, David C. 2004. Candidate gene association studies of the alpha 4 (CHRNA4) and beta 2 (CHRNB2) neuronal nicotinic acetylcholine receptor subunit genes in Alzheimer's disease. Neuroscience Letters 358 (2) , pp. 142-146. 10.1016/j.neulet.2004.01.016 |
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Myers, Amanda J., Marshall, Helen, Holmans, Peter Alan, Compton, Danielle, Crook, Richard J.P., Mander, Adrian P., Nowotny, Petra, Smemo, Scott, Dunstan, Melanie, Jehu, Luke, Wang, Jen C., Hamshere, Marian Lindsay, Morris, John C., Norton, Joanne, Chakraventy, Sumi, Tunstall, Nigel, Lovestone, Simon, Petersen, Ronald, O'Donovan, Michael Conlon, Jones, Lesley, Williams, Julie, Owen, Michael John, Hardy, John and Goate, Alison 2004. Variation in the urokinase-plasminogen activator gene does not explain the chromosome 10 linkage signal for late onset AD. American Journal of Medical Genetics 124B (1) , pp. 29-37. 10.1002/ajmg.b.20036 |
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Busby, Victoria, Goossens, Steven, Nowotny, Petra, Hamilton, Gillian, Smemo, Scott, Harold, Denise, Turic, Dragana, Jehu, Luke, Myers, Amanda, Womick, Meredith, Woo, Daniel, Compton, Danielle, Doil, Lisa M., Tacey, Kristina M., Lau, Kit F., Al-Saraj, Safa, Killick, Richard, Pickering-Brown, Stuart, Moore, Pamela, Hollingworth, Paul, Archer, Nicola, Foy, Catherine, Walter, Sarah, Lovestone, Simon, O'Donovan, Michael Conlon, Owen, Michael John, Jones, Lesley, Williams, Julie and Holmans, Peter Alan 2004. Alpha-T-Catenin Is Expressed in Human Brain and Interacts With the Wnt Signaling Pathway But Is Not Responsible for Linkage to Chromosome 10 in Alzheimer's Disease. Neuromolecular Medicine 5 (2) , pp. 133-146. 10.1385/NMM:5:2:133 |
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Bray, Nicholas John, Jehu, Luke, Moskvina, Vanentina, Buxbaum, Joseph D., Dracheva, Stella, Haroutunian, Vahram, Williams, Julie, Buckland, Paul Robert, Owen, Michael John and O'Donovan, Michael Conlon 2004. Allelic expression of APOE in human brain: effects of epsilon status and promoter haplotypes. Human Molecular Genetics 13 (22) , pp. 2885-2892. 10.1093/hmg/ddh299 |
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Harold, Denise, Peirce, Timothy, Escott-Price, Valentina, Lovestone, Simon, Powell, John, Foy, Catherine, Archer, Nicola, Walter, Sarah, Edmonson, Amanda, McIlroy, Stephen, Craig, David, Passmore, Peter A., Goate, Alison, Hardy, John, O'Donovan, Michael Conlon, Williams, Julie, Liddell, Malcolm, Owen, Michael John, Jones, Lesley, Myers, Amanda, Jones, Susan, Hollingworth, Paul and Moore, Pamela 2003. Sequence variation in the CHAT locus shows no association with late-onset Alzheimer's disease. Human Genetics 113 (3) , pp. 258-267. 10.1007/s00439-003-0960-2 |
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Rice, Frances, Abraham, Richard, Rudrasingham, Varuni, Owen, Michael John and Williams, Julie 2003. Memory for new information as a cognitive marker of liability to Alzheimer's disease in a high risk group: a research note. International Journal of Geriatric Psychiatry 18 (2) , pp. 155-160. 10.1002/gps.808 |
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Turic, D, Robinson, L, Duke, M, Morris, D W, Webb, V, Hamshere, Marian Lindsay, Milham, C, Hopkin, E, Pound, K, Fernando, S, Grierson, A, Easton, M, Williams, Nigel Melville, van den Bree, Marianne Bernadette, Chowdhury, R, Gruen, J, Stevenson, J, Krawczak, M, Owen, Michael John, O'Donovan, Michael Conlon and Williams, Julie 2003. Linkage disequilibrium mapping provides further evidence of a gene for reading disability on chromosome 6p21.3-22. Molecular Psychiatry 8 (2) , pp. 176-185. 10.1038/sj.mp.4001216 |
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Heron, J., Jones, Ian Richard, Williams, Julie, Owen, Michael John, Craddock, Nicholas John and Jones, L. 2003. Self-reported schizotypy and bipolar disorder: demonstration of a lack of specificity of the Kings Schizotypy Questionnaire. Schizophrenia Research 65 (2-3) , pp. 153-158. 10.1016/S0920-9964(03)00004-5 |
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Walter, S., Archer, N., Foy, C., Lovestone, Simon, Davis, G., Hollingsworth, P., Jones, S., Moore, P., Owen, Michael John and Williams, Julie 2002. The retained ability to display affection and emotion in Alzheimer's disease. Neurobiology of Aging 23 (1) , S44-S45. |
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Archer, N., Foy, C., Walter, S., Lovestone, Simon, Davis, G., Hollingworth, Paul, Jones, S., Moore, P, Owen, Michael John and Williams, Julie 2002. Delusions in dementia - An investigation into their persistence and predictive value. Neurobiology of Aging 23 (1) , S156-S156. |
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Myers, Amanda, Wavrant De-Vrieze, Fabienne, Holmans, Peter Alan, Hamshere, Marian Lindsay, Crook, Richard, Compton, Danielle, Marshall, Helen, Meyer, David, Shears, Shantia, Booth, Jeremy, Ramic, Dzanan, Knowles, Heather, Morris, John C., Williams, Nigel Melville, Norton, Nadine, Abraham, Richard, Kehoe, Pat, Williams, Hywel, Rudrasingham, Varuni, Rice, Frances, Giles, Peter, Tunstall, Nigel, Jones, Lesley, Lovestone, Simon, Williams, Julie, Owen, Michael John, Hardy, John and Goate, Alison 2002. Full genome screen for Alzheimer disease: Stage II analysis. American Journal Of Medical Genetics Part A 114 (2) , pp. 235-244. 10.1002/ajmg.10183 |
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Abraham, Richard, Myers, Amanda, Wavrant-DeVrieze, Fabienne, Hamshere, Marian Lindsay, Thomas, Hollie Victoria, Marshall, Helen, Compton, Danielle, Spurlock, Gillian, Turic, Dragana, Hoogendoorn, Bastiaan, Kwon, Jennifer M., Petersen, Ronald C., Tangalos, Eric, Norton, Joanne, Morris, John C., Bullock, Roger, Liolitsa, Danae, Lovestone, Simon, Hardy, John, Goate, Alison, O'Donovan, Michael Conlon, Williams, Julie, Owen, Michael John and Jones, Lesley 2001. Substantial linkage disequilibrium across the insulin-degrading enzyme locus but no association with late-onset Alzheimer's disease. Human Genetics 109 (6) , pp. 646-652. 10.1007/s00439-001-0614-1 |
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Jones, L. A., Cardno, A. G., Sanders, R. D., Owen, Michael John and Williams, Julie 2001. Sustained and selective attention as measures of genetic liability to schizophrenia. Schizophrenia Research 48 (2-3) , pp. 263-267. |
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Myers, A., Holmans, Peter Alan, Marshall, H., Kwon, J., Meyer, D., Ramic, D., Shears, S., Booth, J., DeVrieze, F. W., Crook, R., Hamshere, Marian Lindsay, Abraham, R., Tunstall, N., Rice, Frances, Carty, S., Lillystone, S., Kehoe, P., Rudrasingham, V., Jones, Lesley, Lovestone, S., Perez-Tur, J., Williams, Julie, Owen, Michael John, Hardy, J. and Goate, A. M. 2000. Susceptibility locus for Alzheimer's disease on chromosome 10. Science 290 (5500) , pp. 2304-2305. 10.1126/science.290.5500.2304 |
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Deb, S., Williams, Julie and Owen, Michael John 2000. Apolipoprotein E, Alzheimer's disease and Down's syndrome - Reply. British Journal of Psychiatry 177 , pp. 469-470. |
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Jones, L. A., Cardno, A. G., Murphy, K. C., Sanders, R. D., Gray, M. Y., McCarthy, G., McGuffin, P., Owen, Michael John and Williams, Julie 2000. The kings schizotypy questionnaire as a quantitative measure of schizophrenia liability. Schizophrenia Research 45 (3) , pp. 213-221. 10.1016/S0920-9964(99)00183-8 |
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Kington, J. M., Jones, L. A., Watt, A. A., Hopkin, E. J. and Williams, Julie 2000. Impaired eye expression recognition in schizophrenia. Journal of Psychiatric Research 34 (4-5) , pp. 341-347. |
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Deb, S., Braganza, J., Norton, N., Williams, H., Kehoe, P. G., Williams, Julie and Owen, Michael John 2000. APOE epsilon 4 influences the manifestation of Alzheimer's disease in adults with Down's syndrome. British Journal of Psychiatry 176 , pp. 468-472. 10.1192/bjp.176.5.468 |
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Morris, D. W., Robinson, L., Turic, D., Duke, M., Webb, V., Milham, C., Hopkin, E., Pound, K., Fernando, S., Easton, M., Hamshere, Marian Lindsay, Williams, Nigel Melville, McGuffin, P., Stephenson, Jessica, Krawczak, M., Owen, Michael John, O'Donovan, Michael and Williams, Julie 2000. Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q. Human Molecular Genetics 9 (5) , pp. 843-848. 10.1093/hmg/9.5.843 |
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Tunstall, N., Owen, Michael John, Williams, Julie, Rice, Frances, Carty, S., Lillystone, S., Fraser, L., Kehoe, P., Neill, D., Rudrasingham, V., Sham, P. and Lovestone, S. 2000. Familial influence on variation in age of onset and behavioural phenotype in Alzheimer's disease. British Journal of Psychiatry 176 , pp. 156-159. 10.1192/bjp.176.2.156 |
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Deb, S., Braganza, J., Norton, N., Williams, H., Kehoe, P. G., Williams, Julie and Owen, Michael John 2000. Presence of the Apolipoprotein E e4 allele is associated with the manifestation of Alzheimer dementia in adults with Down syndrome. Journal of Intellectual Disability Research 44 , p. 259. |
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Jones, L. A., Sanders, R. D., Cardno, A. G., Owen, Michael John and Williams, Julie 1999. Sustained and selective attention as quantitative measures of schizophrenia liability. Molecular Psychiatry 4 , S117-S117. |
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Sanders, R. D., Norton, Nadine, Williams, Julie and Owen, Michael John 1999. Pre-pulse inhibition in the functional psychoses. Molecular Psychiatry 4 , S121-S121. |
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Wavrant-De Vrieze, F., Crook, R., Holmans, Peter Alan, Kehoe, P., Owen, Michael John, Williams, Julie, Roehl, K., Laliiri, D. K., Shears, S., Booth, J., Wu, W., Goate, A., Chartier-Harlin, M. C., Hardy, J. and Perez-Tur, J. 1999. Genetic variability at the amyloid-beta precursor protein locus may contribute to the risk of late-onset Alzheimer's disease. Neuroscience Letters 269 (2) , pp. 67-70. |
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Williams, Julie, Kehoe, P. G. and Owen, Michael John 1999. Case-control study of presenelin-1 intronic polymorphism. Journal of Neurology, Neurosurgery & Psychiatry 66 (6) , p. 702. 10.1136/jnnp.66.6.702 |
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Wavrant-DeVrieze, F., Rudrasingham, V., Lambert, J. C., Chakraverty, S., Kehoe, P., Crook, R., Amouyel, P., Wu, W., Holmans, Peter Alan, Rice, Frances, Perez-Tur, J., Frigard, B., Morric, J. C., Carty, S., Cottel, D., Tunstall, N., Lovestone, S., Petersen, R. C., Chartier-Harlin, M. C., Goate, A., Owen, Michael John, Williams, Julie and Hardy, J. 1999. No association between the alpha-2 macroglobulin I1000V polymorphism and Alzheimer's disease. Neuroscience Letters 262 (2) , pp. 137-139. 10.1016/S0304-3940(99)00035-X |
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Kehoe, P., Wavrant-De Vrieze, F., Crook, R., Wu, W. S., Holmans, Peter Alan, Fenton, I., Williams, Nigel Melville, Lovestone, S., Perez-Tur, J., Hutton, M., Chartier-Harlin, M. C., Shears, S., Roehl, K., Booth, J., Van Voorst, W., Ramic, D., Williams, Julie, Goate, A., Hardy, J. and Owen, Michael John 1999. A full genome scan for late onset Alzheimer's disease. Human Molecular Genetics 8 (2) , pp. 237-245. 10.1093/hmg/8.2.237 |
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Kehoe, P. G., Russ, C., McIlory, S., Williams, H., Powell, J., McGleenon, B., Liddell, M., Plomin, R., Dynan, K., Williams, Nigel Melville, Neal, J., Cairns, N. J., Wilcock, G., Passmore, P., Lovestone, S., Williams, Julie and Owen, Michael John 1999. Variation in DCP1, encoding ACE, is associated with susceptibility to Alzheimer disease. Nature Genetics 21 (1) , pp. 71-72. 10.1038/5009 |
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Wu, W. S., Holmans, Peter Alan, Wavrant-DeVrieze, F., Shears, S., Kehoe, P., Crook, R., Booth, J., Williams, Nigel Melville, Perez-Tur, J., Roehl, K., Fenton, I., Chartier-Harlin, M. C., Lovestone, S., Williams, Julie, Hutton, M., Hardy, J., Owen, Michael John and Goate, A. 1998. Genetic studies on chromosome 12 in late-onset Alzheimer disease. JAMA - The Journal of the American Medical Association 280 (7) , pp. 619-622. 10.1001/jama.280.7.619 |
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Bowen, Timothy, Guy, Carol, Craddock, Nicholas John, Cardno, A. G., Williams, Nigel Melville, Spurlock, G., Murphy, K. C., Jones, L. A., Gray, M., Sanders, Rebecca, McCarthy, G, Chandy, K. G., Fantino, E, Kalman, K, Gutman, G. A., Gargus, J. J., Williams, Julie, McGuffin, P., Owen, Michael John and O'Donovan, Michael Conlon 1998. Further support for an association between a polymorphic CAG repeat in the hKCa3 gene and schizophrenia. Molecular Psychiatry 3 (3) , pp. 266-269. 10.1038/sj.mp.4000400 |
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Williams, Julie, Spurlock, G., Holmans, Peter Alan, Mant, R., Murphy, K., Jones, L., Cardno, A., Asherson, P., Blackwood, D., Muir, W., Meszaros, K., Aschauer, H., Mallet, J., Laurent, C., Pekkarinen, P., Seppala, J., Stefanis, C. N., Papadimitriou, G. N., Macciardi, F., Verga, M., Pato, C., Azevedo, H., Crocq, M. A., Gurling, H. and Owen, Michael John 1998. A meta-analysis and transmission disequilibrium study of association between the dopamine D3 receptor gene and schizophrenia. Molecular Psychiatry 3 (2) , pp. 141-149. |
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Spurlock, G., Williams, Julie, McGuffin, P., Aschauer, H. N., Lenzinger, E., Fuchs, K., Sieghart, W. C., Meszaros, K., Fathi, N., Laurent, C., Mallet, J., Macciardi, F., Pedrini, S., Gill, M., Hawi, Z., Gibson, S., Jazin, E. E., Yang, H. T., Adolfsson, R., Pato, C. N., Dourado, A. M. and Owen, Michael John 1998. European Multicentre Association Study of Schizophrenia: a study of the DRD2 Ser311Cys and DRD3 Ser9Gly polymorphisms. American Journal of Medical Genetics 81 (1) , pp. 24-28. 10.1002/(SICI)1096-8628(19980207)81:1<24::AID-AJMG5>3.0.CO;2-N |
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Williams, Julie, McGuffin, P., Nothen, . and Owen, Michael John 1997. A meta analysis of association between the 5-HT2a receptor, T102C polymorphism and schizophrenia. American Journal of Medical Genetics 74 (6) , p. 612. |
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Williams, Julie, McGuffin, Peter, Nothen, Markus and Owen, Michael John 1997. Meta-analysis of association between the 5-HT2a receptor T102C polymorphism and schizophrenia. The Lancet 349 (9060) , p. 1221. 10.1016/S0140-6736(05)62413-0 |
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Spurlock, Gillian, Williams, Julie, McGuffin, Peter, Mallet, Jacques, Nöthen, Markus, Gill, Michael, Aschauer, Harald, Adlfsson, Rolf, Macciardi, Fabio and Owen, Michael John 1997. Meta-analysis of association studies between schizophrenia and polymorphisms of the 5-hydroxytryptamine type 2A receptor gene. Schizophrenia Research 24 (1-2) , p. 91. 10.1016/S0920-9964(97)82247-5 |
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Williams, Nigel Melville, Jones, L. A., Murphy, K. C., Cardno, A. G., Asherson, P., Williams, Julie, McGuffin, P. and Owen, Michael John 1997. No evidence for an allelic association between schizophrenia and markers D22S278 and D22S283. American Journal of Medical Genetics 74 (1) , pp. 37-39. 10.1002/(SICI)1096-8628(19970221)74:1<37::AID-AJMG8>3.0.CO;2-S |
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Cardno, A. G., Jones, L. A., Murphy, K. C., Asherson, P., Scott, L. C., Williams, Julie, Owen, Michael John and McGuffin, P. 1996. Factor analysis of schizophrenic symptoms using the OPCRIT checklist. Schizophrenia Research 22 (3) , pp. 233-239. 10.1016/S0920-9964(96)00060-6 |
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O'Donovan, Michael Conlon, Guy, Carol, Craddock, Nicholas John, Bowen, Timothy, McKeon, P., Macedo, A., Maier, W., Wildenauer, D., Aschauer, H. N., Sorbi, S., Feldman, E., Mynett-Johnson, L., Claffey, E., Nacmias, B., Valente, J., Dourado, A., Grassi, E., Lenzinger, E., Heiden, A. M., Moorhead, S., Harrison, D., Williams, Julie, McGuffin, P. and Owen, Michael John 1996. Confirmation of association between expanded CAG/CTG repeats and both schizophrenia and bipolar disorder. Psychological Medicine -London- 26 (6) , pp. 1145-1153. 10.1017/s0033291700035868 |
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Kehoe, P., Williams, Julie, Holmans, Peter Alan, Liddell, M., Lovestone, S., Holmes, C., Powell, J., Neal, J., Wilcock, G. and Owen, Michael John 1996. Association between a PS-1 intronic polymorphism and late onset Alzheimer's disease. NeuroReport 7 (13) , pp. 2155-2158. 10.1097/00001756-199609020-00019 |
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Owen, Michael John, Kehoe, P. and Williams, Julie 1996. Presenilin-1 polymorphism and Alzheimer's disease. The Lancet 348 (9024) , p. 414. 10.1016/S0140-6736(05)65041-6 |
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Williams, Julie, Farmer, A. E., Ackenheil, M., Kaufmann, C. A. and McGuffin, P. 1996. A multicentre inter-rater reliability study using the OPCRIT computerized diagnostic system. Psychological Medicine 26 (4) , pp. 775-783. 10.1017/S003329170003779X |
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Williams, Julie, Spurlock, G., McGuffin, P., Mallet, J., Nothen, M. M., Gill, M., Aschauer, H., Nylander, P. O., Macciardi, F. and Owen, Michael John 1996. Association between schizophrenia and T102C polymorphism of the 5-hydroxytryptamine type 2a-receptor gene. European Multicentre Association Study of Schizophrenia (EMASS) Group. The Lancet 347 (9011) , pp. 1294-1296. 10.1016/S0140-6736(96)90939-3 |
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Asherson, P., Mant, R., Holmans, Peter Alan, Williams, Julie, Cardno, A., Murphy, K., Jones, L., Collier, D., McGuffin, P. and Owen, Michael John 1996. Linkage, association and mutational analysis of the dopamine D3 receptor gene in schizophrenia. Molecular Psychiatry 1 (2) , pp. 125-132. |
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Kehoe, P., Williams, Julie, Lovestone, S., Wilcock, G. and Owen, Michael John 1996. Presenilin-1 polymorphism and Alzheimer's disease. The UK Alzheimer's Disease Collaborative Group. The Lancet 347 (9009) , p. 1185. |
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Daniels, J. K., Williams, Nigel Melville, Williams, Julie, Jones, L. A., Cardno, A. G., Murphy, K. C., Spurlock, G., Riley, B., Scambler, P., Asherson, P., McGuffin, P. and Owen, Michael John 1996. No evidence for allelic association between schizophrenia and a polymorphism determining high or low catechol O-methyltransferase activity. American Journal of Psychiatry 153 (2) , pp. 268-270. 10.1176/ajp.153.2.268 |
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Daniels, J., Williams, Julie, Asherson, P, McGuffin, P. and Owen, Michael John 1995. No association between schizophrenia and polymorphisms within the genes for debrisoquine 4-hydroxylase (CYP2D6) and the dopamine transporter (DAT). American Journal of Medical Genetics 60 (1) , pp. 85-87. 10.1002/ajmg.1320600115 |
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Farmer, A. E., Williams, Julie and Jones, Ian Richard 1994. Phenotypic definitions of psychotic illness for molecular genetic research. American Journal of Medical Genetics 54 (4) , pp. 365-371. 10.1002/ajmg.1320540416 |
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Daniels, J., Williams, Julie, Mant, R., Asherson, P., McGuffin, P. and Owen, Michael John 1994. Repeat length variation in the dopamine D4 receptor gene shows no evidence of association with schizophrenia. American Journal of Medical Genetics 54 (3) , pp. 256-258. 10.1002/ajmg.1320540313 |
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Liddell, Malcolm Brandon, Williams, Julie, Bayer, Antony James, Kaiser, F. and Owen, Michael John 1994. Confirmation of association between the e4 allele of apolipoprotein E and Alzheimer's disease. Journal of Medical Genetics 31 (3) , pp. 197-200. 10.1136/jmg.31.3.197 |
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Williams, Julie, Farmer, Anne E., Wessely, Simon, Castle, David J. and McGuffin, Peter 1993. Heterogeneity in schizophrenia: An extended replication of the hebephrenic-like and paranoid-like subtypes. Psychiatry Research 49 (3) , pp. 199-210. 10.1016/0165-1781(93)90061-K |
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Farmer, Anne E. and Williams, Julie 1993. Defining the phenotype for molecular-genetic research into psychotic illness - problems and solutions. Behavior Genetics 23 (6) , p. 551. |
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Mant, R., Williams, Julie, Asherson, P., Parfitt, E., McGuffin, P. and Owen, Michael John 1993. Susceptibility to schizophrenia and the dopamine d3 receptor gene. American Journal of Human Genetics 53 (3) , p. 1654. |
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Crocq, M A, Mant, R, Asherson, P, Williams, Julie, Hode, Y, Mayerova, A, Collier, D, Lannfelt, L, Sokoloff, P and Schwartz, J C 1992. Association between schizophrenia and homozygosity at the dopamine D3 receptor gene. Journal of Medical Genetics 29 (12) , pp. 858-860. 10.1136/jmg.29.12.858 |
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Owen, Michael John, Mant, R., Parfitt, E., Williams, Julie, Asherson, P., O'Mahoney, G., Van Os, J., Llewellyn, D., Collier, D., Gill, M. and McGuffin, P. 1992. No association between RFLPs at the porphobilinogen deaminase gene and schizophrenia. Human Genetics 90 (1-2) , pp. 131-132. 10.1007/BF00210756 |
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