Search Results - Ivan Nikolov

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  1. 1
    Pooled DNA genotyping on Affymetrix SNP genotyping arrays

    Pooled DNA genotyping on Affymetrix SNP genotyping arrays by George Kirov, Ivan Nikolov, Lyudmila Georgieva, Valentina Moskvina, Michael J. Owen, Michael O’Donovan

    Published 2006
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  2. 2
    Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk

    Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk by Valentina Moskvina, Nick Craddock, Peter Holmans, Ivan Nikolov, Jaspreet Singh Pahwa, E Green, Michael J. Owen, Michael O’Donovan

    Published 2008
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  3. 3
    Genetic and environmental influences on the relationship between peer alcohol use and own alcohol use in adolescents

    Genetic and environmental influences on the relationship between peer alcohol use and own alcohol use in adolescents by Tom Fowler, Katherine H. Shelton, Kate Lifford, Frances Rice, Andrew McBride, Ivan Nikolov, Michael C. Neale, Gordon T. Harold, Anita Thapar, Marianne B. M. van den Bree

    Published 2007
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  4. 4
    The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia

    The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia by E.K. Green, Detelina Grozeva, Ian Jones, Lisa Jones, George Kirov, Sian Caesar, Katherine Gordon‐Smith, Christine Fraser, Liz Forty, Elen Russell, M L Hamshere, Valentina Moskvina, Ivan Nikolov, Anne Farmer, Peter McGuffin, Peter Holmans, Michael J. Owen, Michael O’Donovan, Nick Craddock

    Published 2009
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  5. 5
    Convergent evidence that <i>oligodendrocyte lineage transcription factor 2</i> ( <i>OLIG2</i> ) and interacting genes influence susceptibility to schizophrenia

    Convergent evidence that <i>oligodendrocyte lineage transcription factor 2</i> ( <i>OLIG2</i> ) and interacting genes influence susceptibility to schizophrenia by Lyudmila Georgieva, Valentina Moskvina, Tim Peirce, Nadine Norton, Nicholas J. Bray, Lesley Jones, Peter Holmans, Stuart MacGregor, Stanley Zammit, Jennifer C. Wilkinson, Hywel Williams, Ivan Nikolov, Nigel Williams, Dobril Ivanov, Kenneth L. Davis, Vahram Haroutunian, Joseph D. Buxbaum, Nick Craddock, George Kirov, Michael J. Owen, Michael O’Donovan

    Published 2006
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  6. 6
    Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept

    Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept by Marian L. Hamshere, E K Green, Ian Jones, Lisa Jones, Valentina Moskvina, George Kirov, Detelina Grozeva, Ivan Nikolov, Damjan Vukcevic, Sian Caesar, Katherine Gordon‐Smith, Christine Fraser, Elen Russell, Gerome Breen, David St Clair, David Collier, Allan H. Young, I. Nicol Ferrier, Anne Farmer, Peter McGuffin, Peter Holmans, Michael J. Owen, Michael O’Donovan, N. Craddock

    Published 2009
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  7. 7
    Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype

    Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype by Nick Craddock, Lisa Jones, Ian Jones, George Kirov, E K Green, Detelina Grozeva, Valentina Moskvina, Ivan Nikolov, Marian L. Hamshere, Damjan Vukcevic, Sian Caesar, Katherine Gordon‐Smith, Christine Fraser, Ellie Russell, Nadine Norton, Gerome Breen, David St Clair, David Collier, Allan H. Young, I. Nicol Ferrier, Anne Farmer, Peter McGuffin, Peter Holmans, Peter Donnelly, Michael J. Owen, Michael O’Donovan

    Published 2008
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  8. 8
    De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia

    De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia by George Kirov, Andrew Pocklington, Peter Holmans, Dobril Ivanov, Masashi Ikeda, Douglas M. Ruderfer, Jennifer L. Moran, Kimberly Chambert, Драга Тончева, L. Georgieva, Detelina Grozeva, Marija Fjodorova, R Wollerton, Elliott Rees, Ivan Nikolov, Louie N. van de Lagemaat, Àlex Bayés, E Fernández, Pall I. Olason, Yvonne Böttcher, Noboru H. Komiyama, Mark O. Collins, Jyoti S. Choudhary, Kāri Stefánsson, Hreinn Stefánsson, Seth G. N. Grant, Shaun Purcell, Pamela Sklar, Michael O’Donovan, Michael J. Owen

    Published 2011
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  9. 9
    Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2

    Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2 by Michael O’Donovan, Nadine Norton, Hywel Williams, T Peirce, Valentina Moskvina, Ivan Nikolov, Marian L. Hamshere, Liam Carroll, L. Georgieva, Sarah Dwyer, Peter Holmans, Jonathan Marchini, Chris C. A. Spencer, Bryan Howie, H. T. T. Leung, Ina Giegling, Annette M. Hartmann, HJ Möller, Derek W. Morris, Yongyong Shi, Guofang Feng, Per Hoffmann, Peter Propping, Catalina Vasilescu, W. Maier, Marcella Rietschel, Stanley Zammit, J Schumacher, Emma M. Quinn, Thomas G. Schulze, Nakao Iwata, Masashi Ikeda, Ariel Darvasi, Sagiv Shifman, Lin He, Jubao Duan, Alan R. Sanders, Douglas F. Levinson, Rolf Adolfsson, Urban Ösby, Lars Terenius, Erik G. Jönsson, Sven Cichon, Markus M. Nöthen, Michael Gill, Aiden Corvin, Dan Rujescu, Pablo V. Gejman, George Kirov, Nick Craddock, Nigel Williams, Michael J. Owen

    Published 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 by 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

    Published 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 by 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

    Published 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 by 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

    Published 2008
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  13. 13
    Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

    Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants by Paul R. Burton, David Clayton, Lon R. Cardon, Nick Craddock, Panos Deloukas, Audrey Duncanson, Dominic Kwiatkowski, Mark I. McCarthy, Willem H. Ouwehand, Nilesh J. Samani, John A. Todd, Peter Donnelly, Jeffrey C. Barrett, Dan Davison, Doug Easton, David M. Evans, H.T. Leung, Jonathan Marchini, Andrew P. Morris, Chris C. A. Spencer, Martin D. Tobin, Antony Attwood, James P. Boorman, Barbara Cant, Ursula Everson, Judith M. Hussey, Jennifer D. Jolley, Alexandra S. Knight, Kerstin Koch, Elizabeth Meech, Sarah Nutland, C V Prowse, H. E. Stevens, Niall Taylor, Graham R. Walters, Neil Walker, Nicholas A. Watkins, Thilo Winzer, Richard W. Jones, Wendy L. McArdle, Susan M. Ring, David P. Strachan, Marcus Pembrey, Gerome Breen, David St Clair, Sian Caesar, Katharine Gordon-Smith, Lisa Jones, Christine Fraser, Elaine Green, Detelina Grozeva, Marian L. Hamshere, Peter Holmans, Ian Jones, George Kirov, Valentina Moskivina, Ivan Nikolov, Michael O’Donovan, Michael J. Owen, David Collier, Amanda Elkin, Anne Farmer, Richard Williamson, Peter McGuffin, Allan H. Young, I. Nicol Ferrier, Stephen G. Ball, Anthony J. Balmforth, Jennifer H. Barrett, D. Timothy Bishop, Mark M. Iles, Azhar Maqbool, Nadira Yuldasheva, Alistair S. Hall, Peter S. Braund, Richard J. Dixon, Massimo Mangino, Suzanne Stevens, John R. Thompson, Francesca Bredin, Mark Tremelling, Miles Parkes, Hazel E. Drummond, Charlie W. Lees, Elaine R. Nimmo, Jack Satsangi, Sheila Fisher, Alastair Forbes, Cathryn M. Lewis, Clive M. Onnie, Natalie J. Prescott, Jeremy Sanderson, Christopher G Matthew, Jamie Barbour, Mohamed Khalid Mohiuddin, Catherine E Todhunter, John Mansfield, Tariq Ahmad, Fraser Cummings, Derek P. Jewell

    Published 2007
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  14. 14
    Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

    Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls by Paul R. Burton, David Clayton, Lon R. Cardon, Nick Craddock, Panos Deloukas, Audrey Duncanson, Dominic Kwiatkowski, Mark I. McCarthy, Willem H. Ouwehand, Nilesh J. Samani, John A. Todd, Peter Donnelly, Jeffrey C. Barrett, Paul R. Burton, Doug Easton, Peter Donnelly, H.T. Leung, Jonathan L. Marchini, Andrew P. Morris, Jonathan L. Marchini, Martin D. Tobin, Antony Attwood, Martin D. Tobin, Lon R. Cardon, David Clayton, Antony Attwood, James P. Boorman, Barbara Cant, Ursula Everson, Judith M. Hussey, Jennifer D. Jolley, Alexandra S. Knight, Kerstin Koch, Elizabeth Meech, Nicholas J. Timpson, C V Prowse, Eleftheria Zeggini, Niall Taylor, Graham R. Walters, Melanie J. Newport, Nicholas A. Watkins, Thilo Winzer, John A. Todd, Willem H. Ouwehand, Richard W. Jones, Wendy L. McArdle, Susan M. Ring, David P. Strachan, Marcus Pembrey, Gerome Breen, David St Clair, Sian Caesar, Katherine Gordon‐Smith, Lisa Jones, Christine Fraser, Elaine Green, Detelina Grozeva, Marian L. Hamshere, Peter Holmans, Ian Jones, George Kirov, Valentina Moskvina, Ivan Nikolov, Michael O’Donovan, Michael J. Owen, Nick Craddock, David Collier, Amanda Elkin, Anne Farmer, Richard Williamson, Peter McGuffin, Allan H. Young, I. Nicol Ferrier, Stephen G. Ball, Anthony J. Balmforth, Jennifer H. Barrett, D. Timothy Bishop, Mark M. Iles, Azhar Maqbool, Nadira Yuldasheva, Alistair S. Hall, Peter S. Braund, Paul R. Burton, Richard J. Dixon, Massimo Mangino, Suzanne Stevens, Martin D. Tobin, J. Thompson, Nilesh J. Samani, Francesca Bredin, Mark Tremelling, Miles Parkes, Hazel E. Drummond, Charlie W. Lees, Elaine R. Nimmo, Jack Satsangi, Sheila Fisher, Alastair Forbes, Cathryn M. Lewis, Clive M. Onnie

    Published 2007
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