Resultats de la cerca - Kevin A. McGhee

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  1. 1
    Variance in neurocognitive performance is associated with dysbindin-1 in schizophrenia: A preliminary study

    Variance in neurocognitive performance is associated with dysbindin-1 in schizophrenia: A preliminary study per Gary Donohoe, Derek W. Morris, Sarah Clarke, Kevin A. McGhee, Siobhan Schwaiger, Jeanne‐Marie Nangle, Hugh Garavan, Ian H. Robertson, Michael Gill, Aiden Corvin

    Publicat 2006
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  2. 2
    Common Variants of Large Effect in F12, KNG1, and HRG Are Associated with Activated Partial Thromboplastin Time

    Common Variants of Large Effect in F12, KNG1, and HRG Are Associated with Activated Partial Thromboplastin Time per Lorna M. Houlihan, Gail Davies, Albert Tenesa, Sarah E. Harris, Michelle Luciano, Alan J. Gow, Kevin A. McGhee, David C. Liewald, David J. Porteous, John M. Starr, Gordon Lowe, Peter M. Visscher, Ian J. Deary

    Publicat 2010
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  3. 3
    A common variant in the 3′UTR of the <i>GRIK4</i> glutamate receptor gene affects transcript abundance and protects against bipolar disorder

    A common variant in the 3′UTR of the <i>GRIK4</i> glutamate receptor gene affects transcript abundance and protects against bipolar disorder per Ben Pickard, Helen Miranda Knight, Russell S. Hamilton, Dinesh C. Soares, Robert Walker, J. K. F. Boyd, J. Machell, Alan Maclean, Kevin A. McGhee, Alison Condie, David J. Porteous, David St Clair, Ilan Davis, Douglas Blackwood, Walter Muir

    Publicat 2008
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  4. 4
    Whole genome association scan for genetic polymorphisms influencing information processing speed

    Whole genome association scan for genetic polymorphisms influencing information processing speed per Michelle Luciano, Narelle K. Hansell, Jari Lahti, Gail Davies, Sarah E. Medland, Katri Räikkönen, Albert Tenesa, Elisabeth Widén, Kevin A. McGhee, Aarno Palotie, David C. Liewald, David J. Porteous, John M. Starr, Grant W. Montgomery, Nicholas G. Martin, Johan G. Eriksson, Margaret J. Wright, Ian J. Deary

    Publicat 2010
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  5. 5
    A Cytogenetic Abnormality and Rare Coding Variants Identify ABCA13 as a Candidate Gene in Schizophrenia, Bipolar Disorder, and Depression

    A Cytogenetic Abnormality and Rare Coding Variants Identify ABCA13 as a Candidate Gene in Schizophrenia, Bipolar Disorder, and Depression per Helen Miranda Knight, Ben Pickard, Alan Maclean, M. P. Malloy, Dinesh C. Soares, Allan F. McRae, Alison Condie, Angela White, William E. Hawkins, Kevin A. McGhee, M. Van Beck, Donald J. MacIntyre, John M. Starr, Ian J. Deary, Peter M. Visscher, David J. Porteous, Ronald E. Cannon, David St Clair, Walter Muir, Douglas Blackwood

    Publicat 2009
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  6. 6
    Genome-wide association studies establish that human intelligence is highly heritable and polygenic

    Genome-wide association studies establish that human intelligence is highly heritable and polygenic per Gail Davies, Albert Tenesa, Antony Payton, Jian Yang, Sarah E. Harris, David C. Liewald, Xiayi Ke, Stéphanie Le Hellard, A. Christoforou, Michelle Luciano, Kevin A. McGhee, Lorna M. Lopez, Alan J. Gow, Janie Corley, Paul Redmond, Helen Fox, Paul Haggarty, Lawrence J. Whalley, Geraldine McNeill, Michael E. Goddard, Thomas Espeseth, Astri J. Lundervold, Ivar Reinvang, Andrew Pickles, Vidar M. Steen, William Ollier, David J. Porteous, M.A. Horan, John M. Starr, Neil Pendleton, Peter M. Visscher, Ian J. Deary

    Publicat 2011
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  7. 7
    Whole-genome association study of bipolar disorder

    Whole-genome association study of bipolar disorder per Pamela Sklar, Jordan W. Smoller, Jinbo Fan, Manuel A. R. Ferreira, Roy H. Perlis, Kim Chambert, Vishwajit L. Nimgaonkar, Matthew B. McQueen, Stephen V. Faraone, Andrew Kirby, Paul I. W. de Bakker, Matthew N. Ogdie, Michael E. Thase, Gary S. Sachs, Katherine EO Todd-Brown, Stacey B. Gabriel, Carrie Sougnez, Camille Gates, Brendan Blumenstiel, Matthew DeFelice, Kristin Ardlie, Jennifer Franklin, W.J. Muir, Kevin A. McGhee, Donald J. MacIntyre, Alan McLean, MP D VanBeck, Andrew McQuillin, Nicholas Bass, Mark W. Robinson, Jacob Lawrence, Adebayo Anjorin, David Curtis, Edward M. Scolnick, Mark J. Daly, Douglas Blackwood, Hugh Gurling, Shaun Purcell

    Publicat 2008
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  8. 8
    Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned

    Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned per Naomi R. Wray, Michele L. Pergadia, Douglas Blackwood, Brenda W.J.H. Penninx, Scott D. Gordon, Dale R. Nyholt, Stephan Ripke, Donald J. MacIntyre, Kevin A. McGhee, Alan Maclean, Johannes H. Smit, Jouke‐Jan Hottenga, Gonneke Willemsen, Christel M. Middeldorp, Eco J. C. de Geus, Cathryn M. Lewis, Peter McGuffin, Ian B. Hickie, Edwin J.C.G. van den Oord, J. Z. Liu, Stuart MacGregor, Brian P. McEvoy, Enda M. Byrne, Sarah E. Medland, Dixie J. Statham, Anjali K. Henders, Andrew C. Heath, Grant W. Montgomery, Nicholas G. Martin, Dorret I. Boomsma, Pamela A. F. Madden, P F Sullivan

    Publicat 2010
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  9. 9
    Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo

    Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo per Patrick F. Sullivan, Eco J. C. de Geus, Gonneke Willemsen, M R James, Johannes H. Smit, T. Zandbelt, Volker Arolt, B. Baune, Douglas Blackwood, Sven Cichon, William L. Coventry, Katharina Domschke, Anne Farmer, M. Fava, Scott D. Gordon, Qianchuan He, Andrew C. Heath, Peter Heutink, Herta Flor, Witte J.G. Hoogendijk, Jouke‐Jan Hottenga, Yi Hu, M. Kohli, D. Y. Lin, Susanne Lucae, Donald J. MacIntyre, Wolfgang Maier, Kevin A. McGhee, Peter McGuffin, Grant W. Montgomery, Walter Muir, Willem A. Nolen, Markus M. Nöthen, Roy H. Perlis, Katrina Pirlo, Daniëlle Posthuma, Marcella Rietschel, Patrizia Rizzu, Alexandra Schosser, August B. Smit, Jordan W. Smoller, J.‐W. Tzeng, Richard van Dyck, Matthijs Verhage, Frans G. Zitman, Nicholas G. Martin, Naomi R. Wray, Dorret I. Boomsma, Brenda W.J.H. Penninx

    Publicat 2008
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  10. 10
    Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

    Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder per Manuel A. R. Ferreira, Michael O’Donovan, Yan Meng, Ian Jones, Douglas M. Ruderfer, Lisa Jones, Jinbo Fan, George Kirov, Roy H. Perlis, Elaine Green, Jordan W. Smoller, Detelina Grozeva, Jennifer Stone, Ivan Nikolov, Kimberly Chambert, Marian L. Hamshere, Vishwajit L. Nimgaonkar, Valentina Moskvina, Michael E. Thase, Sian Caesar, Gary S. Sachs, Jennifer Franklin, Katherine Gordon‐Smith, Kristin G. Ardlie, Stacey Gabriel, Christine Fraser, Brendan Blumenstiel, Matthew DeFelice, Gerome Breen, Michael Gill, Derek W. Morris, Amanda Elkin, Walter Muir, Kevin A. McGhee, Richard Williamson, Donald J. MacIntyre, Alan Maclean, David St Clair, Michelle Robinson, M. Van Beck, Ana Carla Pereira, Radhika Kandaswamy, Andrew McQuillin, David Collier, Nicholas Bass, Allan H. Young, Jacob Lawrence, I. Nicol Ferrier, Adebayo Anjorin, Anne Farmer, David Curtis, Edward M. Scolnick, Peter McGuffin, Mark J. Daly, Aiden Corvin, Peter Holmans, Douglas Blackwood, Hugh Gurling, Michael J. Owen, Shaun Purcell, Pamela Sklar, Nick Craddock

    Publicat 2008
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  11. 11
    Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

    Common polygenic variation contributes to risk of schizophrenia and bipolar disorder per Shaun Purcell, Naomi R. Wray, Jennifer Stone, Peter M. Visscher, Michael O’Donovan, Patrick F. Sullivan, Pamela Sklar, Douglas M. Ruderfer, Andrew McQuillin, Derek W. Morris, Colm O’Dushlaine, Aiden Corvin, Peter Holmans, Stuart MacGregor, Hugh Gurling, Douglas Blackwood, Nick Craddock, Michael Gill, Christina M. Hultman, George Kirov, Paul Lichtenstein, Walter Muir, Michael J. Owen, Carlos N. Pato, Edward M. Scolnick, David St Clair, Nigel Williams, Lyudmila Georgieva, Ivan Nikolov, Nadine Norton, Hywel Williams, Драга Тончева, Mariofanna Milanova, Emma Flordal Thelander, Patrick Sullivan, Elaine Kenny, Emma M. Quinn, Khalid Choudhury, Susmita Datta, Jonathan Pimm, Srinivasa Thirumalai, Vinay Puri, Robert Krasucki, Jacob Lawrence, Digby Quested, Nicholas Bass, Caroline Crombie, Gillian Fraser, Soh Leh Kuan, Nicholas Walker, Kevin A. McGhee, Ben Pickard, P. Malloy, Alan Maclean, M. Van Beck, Michele T. Pato, Helena Medeiros, Frank A. Middleton, Célia Barreto Carvalho, Christopher P. Morley, Ayman H. Fanous, David V. Conti, James A. Knowles, Carlos Paz Ferreira, A. Macedo, M.H. Azevedo, Andrew Kirby, Manuel A. R. Ferreira, Mark Daly, Kimberly Chambert, Finny G. Kuruvilla, Stacey B. Gabriel, Kristin Ardlie, Jennifer L. Moran

    Publicat 2009
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  12. 12
    Rare chromosomal deletions and duplications increase risk of schizophrenia

    Rare chromosomal deletions and duplications increase risk of schizophrenia per Jennifer Stone, Michael O’Donovan, Hugh Gurling, George Kirov, Douglas H. R. Blackwood, Aiden Corvin, Nick Craddock, Michael Gill, Christina M. Hultman, Paul Lichtenstein, Andrew McQuillin, Carlos N. Pato, Douglas M. Ruderfer, Michael J. Owen, David St Clair, Patrick F. Sullivan, Pamela Sklar, Shaun Purcell, Joshua M. Korn, Stuart MacGregor, Derek W. Morris, Colm Ó'Dúshláine, Mark Daly, Peter M. Visscher, Peter Holmans, Edward M. Scolnick, Nigel Williams, L. Georgieva, Ivan Nikolov, Nadine Norton, Hywel Williams, Драга Тончева, Vihra Milanova, Emma Flordal Thelander, Patrick Sullivan, Elaine Kenny, John L. Waddington, Khalid Choudhury, Susmita Datta, Jonathan Pimm, Srinivasa Thirumalai, Vinay Puri, Robert Krasucki, Jacob Lawrence, Digby Quested, Nicholas Bass, David Curtis, Caroline Crombie, Gillian Fraser, Soh Leh Kwan, Nicholas Walker, Walter J. Muir, Kevin A. McGhee, Ben Pickard, P. Malloy, Alan Maclean, M. Van Beck, Michele T. Pato, Helena Medeiros, Frank A. Middleton, Célia Barreto Carvalho, Christopher P. Morley, Ayman H. Fanous, David V. Conti, James A. Knowles, Carlos Paz Ferreira, A. Macedo, Maria Helena Pinto de Azevedo, Steve McCarroll, Mark Daly, Kimberly Chambert, Casey Gates, Stacey B. Gabriel, Scott Mahon, Kristen Ardlie

    Publicat 2008
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