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Rare coding variants in PLCG2, ABI3 and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease.
Nature Genetics
49
, pp. 1373-1384.
10.1038/ng.3916
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Tansey, Katherine E., Guipponi, Michel, Perroud, Nader, Bondolfi, Guido, Domenici, Enrico, Evans, David, Hall, Stephanie K., Hauser, Joanna, Henigsberg, Neven, Hu, Xiaolan, Jerman, Borut, Maier, Wolfgang, Mors, Ole, O'Donovan, Michael Conlon, Peters, Tim J., Placentino, Anna, Rietschel, Marcella, Souery, Daniel, Aitchison, Katherine J., Craig, Ian, Farmer, Anne, Wendland, Jens R., Malafosse, Alain, Holmans, Peter Alan, Lewis, Glyn, Lewis, Cathryn M., Stensbøl, Tine Bryan, Kapur, Shitij, McGuffin, Peter and Uher, Rudolf 2012. Genetic predictors of response to serotonergic and noradrenergic antidepressants in major depressive disorder: a genome-wide analysis of individual-level data and a meta-analysis. Plos Medicine 9 (10) , e1001326. 10.1371/journal.pmed.1001326 |
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Levinson, Douglas F., Shi, Jianxin, Wang, Kai, Oh, Sang, Riley, Brien, Pulver, Ann E., Wildenauer, Dieter B., Laurent, Claudine, Mowry, Bryan J., Gejman, Pablo V., Owen, Michael John, Kendler, Kenneth S., Nestadt, Gerald, Schwab, Sibylle G., Mallet, Jacques, Nertney, Deborah, Sanders, Alan R., Williams, Nigel Melville, Wormley, Brandon, Lasseter, Virginia K., Albus, Margot, Godard-Bauché, Stephanie, Alexander, Madeline, Duan, Jubao, O'Donovan, Michael Conlon, Walsh, Dermot, O'Neill, Anthony, Papadimitriou, George N., Dikeos, Dimitris, Maier, Wolfgang, Lerer, Bernard, Campion, Dominique, Cohen, David, Jay, Maurice, Fanous, Ayman, Eichhammer, Peter, Silverman, Jeremy M., Norton, Nadine, Zhang, Nancy, Hakonarson, Hakon, Gao, Cynthia, Citri, Ami, Hansen, Mark, Ripke, Stephan, Dudbridge, Frank and Holmans, Peter Alan 2012. Genome-wide association study of multiplex schizophrenia pedigrees. American Journal of Psychiatry 169 (9) , pp. 963-973. 10.1176/appi.ajp.2012.11091423 |
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Hamilton, Gillian, Harris, Sarah E., Davies, Gail, Liewald, David C., Tenesa, Albert, Payton, Antony, Horan, Michael A., Ollier, William E.R., Pendleton, Neil, Starr, John M., Porteous, David, Deary, Ian J., Denning, Nicola, Escott-Price, Valentina, Gerrish, Amy, Hamshere, Marian Lindsay, Holmans, Peter Alan, O'Donovan, Michael Conlon, Owen, Michael John, Sims, Rebecca, Thomas, Charlene and Williams, Julie 2012. The role of ECE1 variants in cognitive ability in old age and Alzheimer's disease risk. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 159B (6) , pp. 696-709. 10.1002/ajmg.b.32073 |
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Shi, Hui, Belbin, Olivia, Medway, Christopher, Brown, Kristelle, Kalsheker, Noor, Carrasquillo, Minerva, Proitsi, Petroula, Powell, John, Lovestone, Simon, Goate, Alison, Younkin, Steven, Passmore, Peter, Morgan, Kevin, Chapman, Jade, Denning, Nicola, Escott-Price, Valentina, Gerrish, Amy, Hamshere, Marian Lindsay, Harold, Denise, Hollingworth, Paul, Holmans, Peter Alan, O'Donovan, Michael Conlon, Owen, Michael John, Pahwa, Jaspreet, Sims, Rebecca, Thomas, Charlene and Williams, Julie 2012. Genetic variants influencing human aging from late-onset Alzheimer's disease (LOAD) genome-wide association studies (GWAS). Neurobiology of Aging 33 (8) , 1849.e5. 10.1016/j.neurobiolaging.2012.02.014 |
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Hamilton, Gillian, Killick, Richard, Lambert, Jean-Charles, Amouyel, Philippe, Carrasquillo, Minerva M., Pankratz, V. Shane, Graff-Radford, Neill R., Dickson, Dennis W., Petersen, Ronald C., Younkin, Steven G., Powell, John F., Wade-Martins, Richard, Chapman, Jade, Denning, Nicola, Escott-Price, Valentina, Gerrish, Amy, Hamshere, Marian Lindsay, Harold, Denise, Hollingworth, Paul, Holmans, Peter Alan, O'Donovan, Michael Conlon, Owen, Michael John, Pahwa, Jaspreet, Russo, Giancarlo, Sims, Rebecca, Thomas, Charlene and Williams, Julie 2012. Functional and genetic analysis of haplotypic sequence variation at the nicastrin genomic locus. Neurobiology of Aging 33 (8) , 1848.e1. 10.1016/j.neurobiolaging.2012.02.005 |
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Escott-Price, Valentina, Schmidt, Karl Michael, Vedernikov, Alexey, Owen, Michael John, Craddock, Nicholas John, Holmans, Peter Alan and O'Donovan, Michael Conlon 2012. Permutation-based approaches do not adequately allow for linkage disequilibrium in gene-wide multi-locus association analysis. European Journal of Human Genetics 20 (8) , pp. 890-896. 10.1038/ejhg.2012.8 |
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Le Foll, Bernard, Chen, Jingchun, Brunzell, Darlene H., Jackson, Kia, van der Vaart, Andrew, Ma, Jennie Z., Payne, Thomas J., Sherva, Richard, Farrer, Lindsay A., Gejman, Pablo, Levinson, Douglas F., Holmans, Peter Alan, Aggen, Steven H., Damaj, Imad, Kuo, Po-Hsiu, Webb, Bradley T., Anton, Raymond, Kranzler, Henry R., Gelernter, Joel, Li, Ming D., Kendler, Kenneth S. and Chen, Xiangning 2012. Correction: ACSL6 is associated with the number of cigarettes smoked and its expression is altered by chronic nicotine exposure. PLoS ONE 7 (8) 10.1371/annotation/071abcbd-6f0c-4c4b-9507-dae42450457e |
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Jia, Peilin, Wang, Lily, Fanous, Ayman H., Pato, Carlos N., Edwards, Todd L., Zhao, Zhongming, Craddock, Nicholas John, Holmans, Peter Alan, Kirov, George, O'Donovan, Michael Conlon and Williams, Nigel Melville 2012. Network-assisted investigation of combined causal signals from genome-wide association studies in schizophrenia. PLoS Computational Biology 8 (7) , e1002587. 10.1371/journal.pcbi.1002587 |
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Goes, F. S., McCusker, M. G., Bienvenu, O. J., MacKinnon, D. F., Mondimore, F. M., Schweizer, B., DePaulo, J. R., Potash, J. B. and Holmans, Peter Alan 2012. Co-morbid anxiety disorders in bipolar disorder and major depression: familial aggregation and clinical characteristics of co-morbid panic disorder, social phobia, specific phobia and obsessive-compulsive disorder. Psychological Medicine 42 (07) , pp. 1449-1459. 10.1017/S0033291711002637 |
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Derks, Eske M., Vorstman, Jacob A. S., Ripke, Stephan, Kahn, Rene S., Ophoff, Roel A., Craddock, Nicholas John, Escott-Price, Valentina, Hamshere, Marian Lindsay, Holmans, Peter Alan, Kirov, George, O'Donovan, Michael Conlon, Owen, Michael John and Zammit, Stanley 2012. Investigation of the genetic association between quantitative measures of psychosis and schizophrenia: A polygenic risk score analysis. PLoS ONE 7 (6) , e37852. 10.1371/journal.pone.0037852 |
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Sabunciyan, Sarven, Aryee, Martin J., Irizarry, Rafael A., Rongione, Michael, Webster, Maree J., Kaufman, Walter E., Murakami, Peter, Lessard, Andree, Yolken, Robert H., Feinberg, Andrew P., Potash, James B., Consortium, GenRED and Holmans, Peter Alan 2012. Genome-Wide DNA methylation scan in major depressive disorder. PLoS ONE 7 (4) , e34451. 10.1371/journal.pone.0034451 |
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Hudson, G., Sims, Rebecca, Harold, Denise, Chapman, Jade Alice, Hollingworth, Paul, Gerrish, Amy, Russo, Giancarlo, Hamshere, Marian Lindsay, Escott-Price, Valentina, Denning, Nicola, Thomas, Charlene, Stretton, Alexandra, Holmans, Peter Alan, O'Donovan, Michael Conlon, Owen, Michael John, Williams, Julie and Chinnery, P. F. 2012. No consistent evidence for association between mtDNA variants and Alzheimer disease. Neurology 78 (14) , pp. 1038-1042. 10.1212/WNL.0b013e31824e8f1d |
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Keller, Matthew C., Simonson, Matthew A., Ripke, Stephan, Neale, Ben M., Gejman, Pablo V., Howrigan, Daniel P., Lee, Sang Hong, Lencz, Todd, Levinson, Douglas F., Sullivan, Patrick F., Kirov, George, O'Donovan, Michael Conlon, Holmans, Peter Alan, Georgieva, Lyudmila, Nikolov, Ivan, Williams, Hywel John, Owen, Michael John, Craddock, Nicholas John, Hamshere, Marian Lindsay, Escott-Price, Valentina, Dwyer, Sarah Lynne and Zammit, Stanley 2012. Runs of homozygosity implicate autozygosity as a schizophrenia risk factor. Plos Genetics 8 (4) , e1002656. 10.1371/journal.pgen.1002656 |
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Simón-Sánchez, Javier, Kilarski, Laura, Nalls, Michael A., Martinez, Maria, Schulte, Claudia, Holmans, Peter Alan, Gasser, Thomas, Hardy, John, Singleton, Andrew B., Wood, Nicholas W., Brice, Alexis, Heutink, Peter, Williams, Nigel Melville and Morris, Huw Rees 2012. Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's Disease. PLoS ONE 7 (3) , e28787. 10.1371/journal.pone.0028787 |
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Kirov, George, Pocklington, Andrew, Holmans, Peter Alan, Ivanov, Dobril, Ikeda, M., Ruderfer, D., Moran, J., Chambert, K., Toncheva, D., Georgieva, Lyudmila, Grozeva, Detelina, Fjodorova, Marija, Wollerton, Rebecca Louise, Rees, Elliott, Nikolov, Ivan, van de Lagemaat, L. N., Bayés, À., Fernandez, E., Olason, P. I., Böttcher, Y., Komiyama, N. H., Collins, M. O., Choudhary, J., Stefansson, K., Stefansson, H., Grant, S. G. N., Purcell, S., Sklar, P., O'Donovan, Michael Conlon and Owen, Michael John 2012. De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia. Molecular Psychiatry 17 (2) , pp. 142-153. 10.1038/mp.2011.154 |
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Jia, P., Wang, L., Fanous, A. H., Chen, X., Kendler, K. S., Zhao, Z., Craddock, Nicholas John, Georgieva, Lyudmila, Holmans, Peter Alan, Kirov, George, O'Donovan, Michael Conlon, Owen, Michael John, Ruderfer, D.M., Williams, H. and Williams, Nigel Melville 2012. A bias-reducing pathway enrichment analysis of genome-wide association data confirmed association of the MHC region with schizophrenia. Journal of Medical Genetics 49 (2) , pp. 96-103. 10.1136/jmedgenet-2011-100397 |
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Richards, Alexander, Jones, Lesley, Escott-Price, Valentina, Kirov, George, Gejman, P. V., Levinson, D. F., Sanders, A. R., Molecular Genetics of Schizophrenia Collaboration (MGS), International Schizophrenia Consortium (ISC), Purcell, S., Visscher, P. M., Craddock, Nicholas John, Owen, Michael John, Holmans, Peter Alan and O'Donovan, Michael Conlon 2012. Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain. Molecular Psychiatry 17 (2) , pp. 193-201. 10.1038/mp.2011.11 |
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Stergiakouli, Evangelia, Hamshere, Marian Lindsay, Holmans, Peter Alan, Langley, Kate, Zaharieva, Irina, Hawi, Ziarah, Kent, Lindsey, Gill, Michael, Williams, Nigel Melville, Owen, Michael John, O'Donovan, Michael Conlon and Thapar, Anita 2012. Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD. American Journal of Psychiatry 169 (2) , pp. 186-194. 10.1176/appi.ajp.2011.11040551 |
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Williams, Nigel Melville, Franke, Barbara, Mick, Eric, Anney, Richard, Freitag, Christine M., Gill, Michael, Thapar, Anita, O'Donovan, Michael Conlon, Owen, Michael John, Holmans, Peter Alan, Kent, Lindsey, Middleton, Frank, Zhang-James, Yanli, Liu, Lu, Meyer, Jobst, Nguyen, Thuy Trang, Romanos, Jasmin, Romanos, Marcel, Seitz, Christiane, Renner, Tobias J., Walitza, Susanne, Warnke, Andreas, Palmason, Haukur, Buitelaar, Jan, Rommelse, Nanda, Vasquez, Alejandro Arias, Hawi, Ziarih, Langley, Kate, Sergeant, Joseph, Steinhausen, Hans-Christoph, Roeyers, Herbert, Biederman, Joseph, Zaharieva, Irina, Hakonarson, Hakon, Elia, Josephine, Lionel, Anath C., Crosbie, Jennifer, Marshall, Christian R., Schachar, Russell, Scherer, Stephen W., Todorov, Alexandre, Smalley, Susan L., Loo, Sandra, Nelson, Stanley, Shtir, Corina, Asherson, Philip, Reif, Andreas, Lesch, Klaus-Peter and Faraone, Stephen V. 2012. Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3. American Journal of Psychiatry 169 (2) , pp. 195-204. 10.1176/appi.ajp.2011.11060822 |
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Gerrish, Amy, Russo, Giancarlo, Richards, Alexander, Escott-Price, Valentina, Ivanov, Dobril, Harold, Denise, Sims, Rebecca, Abraham, Richard Alun, Hollingworth, Paul, Chapman, Jade Alice, Hamshere, Marian Lindsay, Pahwa, Jaspreet Singh, 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, 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, Maier, Wolfgang, Jessen, Frank, Kölsch, Heike, Heun, Reinhard, 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, Livingston, Gill, Bass, Nicholas J., Gurling, Hugh, McQuillin, Andrew, Gwilliam, Rhian, Deloukas, Panagiotis, Davies, Gail, Harris, Sarah E., Starr, John M., Deary, Ian J., 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., Jones, Lesley, Holmans, Peter Alan, O'Don |