檢索結果 - Nicholas Craddock

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  1. 1
    The genetics of schizophrenia and bipolar disorder: dissecting psychosis

    The genetics of schizophrenia and bipolar disorder: dissecting psychosis 由 Nicholas Craddock

    出版 2005
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  2. 2
    Genome-wide association studies: a primer

    Genome-wide association studies: a primer 由 Aiden Corvin, Nicholas Craddock, P. F. Sullivan

    出版 2009
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  3. 3
    Offspring of parents with recurrent depression: Which features of parent depression index risk for offspring psychopathology?

    Offspring of parents with recurrent depression: Which features of parent depression index risk for offspring psychopathology? 由 Becky Mars, Stephan Collishaw, Daniel J. Smıth, Ajay K Thapar, Robert Potter, Ruth Sellers, Gordon T. Harold, Nicholas Craddock, Frances Rice, Anita Thapar

    出版 2011
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  4. 4
    Association of DISC1 and TSNAX genes and affective disorders in the depression case–control (DeCC) and bipolar affective case–control (BACCS) studies

    Association of DISC1 and TSNAX genes and affective disorders in the depression case–control (DeCC) and bipolar affective case–control (BACCS) studies 由 Alexandra Schosser, Darya Gaysina, Sarah Cohen‐Woods, Philip C. Chow, Livia Martucci, Nicholas Craddock, Anne Farmer, Ania Korszun, Cerisse Gunasinghe, Joanna Gray, Lisa Jones, Federica Tozzi, J Perry, Pierandrea Muglia, Michael J. Owen, Ian Craig, Peter McGuffin

    出版 2009
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  5. 5
    Association Between Schizophrenia-Related Polygenic Liability and the Occurrence and Level of Mood-Incongruent Psychotic Symptoms in Bipolar Disorder

    Association Between Schizophrenia-Related Polygenic Liability and the Occurrence and Level of Mood-Incongruent Psychotic Symptoms in Bipolar Disorder 由 Judith Allardyce, Ganna Leonenko, Marian L. Hamshere, Antonio F. Pardiñas, Liz Forty, Sarah Knott, Katherine Gordon‐Smith, David J. Porteous, Caroline Haywood, Arianna Di Florio, Lisa Jones, Andrew M. McIntosh, Michael J. Owen, Peter Holmans, James Walters, Nicholas Craddock, Ian Jones, Michael O’Donovan, Valentina Escott‐Price

    出版 2017
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  6. 6
    Polygenic dissection of the bipolar phenotype

    Polygenic dissection of the bipolar phenotype 由 Marian L. Hamshere, Michael O’Donovan, Ian Jones, Lisa Jones, George Kirov, E K Green, Valentina Moskvina, Detelina Grozeva, Nicholas Bass, Andrew McQuillin, H. Gurling, David St Clair, Allan H. Young, I. Nicol Ferrier, Anne Farmer, Peter McGuffin, Pamela Sklar, Shaun Purcell, Peter Holmans, Michael J. Owen, Nicholas Craddock

    出版 2011
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  7. 7
    Depressive disorder moderates the effect of the FTO gene on body mass index

    Depressive disorder moderates the effect of the FTO gene on body mass index 由 Margarita Rivera, Sarah Cohen‐Woods, Karen Kapur, Gerome Breen, Ming‐Yen Ng, Amy W. Butler, Nicholas Craddock, Michael Gill, Ania Korszun, W. Maier, Ole Mors, M J Owen, Martin Preisig, S Bergmann, Federica Tozzi, John P. Rice, M. Rietschel, James Rucker, Alexandra Schosser, Katherine J. Aitchison, Rudolf Uher, Ian Craig, Cathryn M. Lewis, Anne Farmer, Peter McGuffin

    出版 2011
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  8. 8
    Genome-wide association study of cognitive functions and educational attainment in UK Biobank (N=112 151)

    Genome-wide association study of cognitive functions and educational attainment in UK Biobank (N=112 151) 由 Gail Davies, Riccardo E. Marioni, David C. Liewald, W. David Hill, Saskia P. Hagenaars, Sarah E. Harris, Stuart J. Ritchie, Michelle Luciano, Chloe Fawns‐Ritchie, Donald M. Lyall, Breda Cullen, Simon R. Cox, Caroline Hayward, David J. Porteous, Jonathan J. Evans, Andrew M. McIntosh, John Gallacher, Nicholas Craddock, Jill P. Pell, Daniel J. Smıth, Catharine R. Galé, Ian J. Deary

    出版 2016
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  9. 9
    A genome-wide association study of attempted suicide

    A genome-wide association study of attempted suicide 由 Virginia L. Willour, Fayaz Seifuddin, Pamela B. Mahon, Dubravka Jancic, Mehdi Pirooznia, J. Douglas Steele, Barbara Schweizer, Fernando S. Goes, Francis M. Mondimore, Dean F. MacKinnon, Roy H. Perlis, P. H. Lee, Jie Huang, John R. Kelsoe, Paul D. Shilling, Marcella Rietschel, Markus M. Nöthen, Sven Cichon, Hugh Gurling, Shaun Purcell, Jordan W. Smoller, Nicholas Craddock, J. Raymond DePaulo, Thomas G. Schulze, Francis J. McMahon, Peter P. Zandi, James B. Potash

    出版 2011
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  10. 10
    Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder

    Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder 由 Hywel Williams, N Norton, Sarah Dwyer, Valentina Moskvina, I Nikolov, Liam Carroll, L. Georgieva, Nigel Williams, Derek W. Morris, E M Quinn, I Giegling, Masashi Ikeda, Joel Wood, Todd Lencz, C Hultman, Paul Lichtenstein, D Thiselton, Brion S. Maher, A K Malhotra, B Riley, K S Kendler, Michael Gill, Patrick Sullivan, Pamela Sklar, Shaun Purcell, V L Nimgaonkar, George Kirov, Peter Holmans, Aiden Corvin, Dan Rujescu, Nicholas Craddock, M J Owen, Michael O’Donovan

    出版 2010
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  11. 11
    Evidence that duplications of 22q11.2 protect against schizophrenia

    Evidence that duplications of 22q11.2 protect against schizophrenia 由 Elliott Rees, George Kirov, A R Sanders, James Walters, Kimberly D. Chambert, Jianxin Shi, Jin Szatkiewicz, C O'Dushlaine, Alexander Richards, E K Green, I Jones, G Davies, Sophie E. Legge, Jennifer L. Moran, Carlos N. Pato, Michele T. Pato, Giulio Genovese, Douglas F. Levinson, Jubao Duan, Winton Moy, H.H.H. Göring, Derek W. Morris, Paul Cormican, Kenneth S. Kendler, F. Anthony O’Neill, Brien P. Riley, Michael Gill, Aiden Corvin, Nicholas Craddock, Pamela Sklar, Christina M. Hultman, Patrick F. Sullivan, Pablo V. Gejman, Steven A. McCarroll, Michael O’Donovan, Mike Owen

    出版 2013
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  12. 12
    Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia

    Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia 由 Duncan S. Palmer, Daniel P. Howrigan, Sinéad B. Chapman, Rolf Adolfsson, Nicholas Bass, Douglas Blackwood, Marco P. Boks, Chia‐Yen Chen, Claire Churchhouse, Aiden Corvin, Nicholas Craddock, David Curtis, Arianna Di Florio, Faith Dickerson, Nelson B. Freimer, Fernando S. Goes, Xiaoming Jia, Ian Jones, Lisa Jones, Lina Jönsson, René S. Kahn, Mikael Landén, Adam E. Locke, Andrew M. McIntosh, Andrew McQuillin, Derek W. Morris, Michael O’Donovan, Roel A. Ophoff, Michael J. Owen, Nancy L. Pedersen, Daniëlle Posthuma, Andreas Reif, Neil Risch, Catherine Schaefer, Laura J. Scott, Tarjinder Singh, Jordan W. Smoller, Matthew Solomonson, David St Clair, Eli A. Stahl, Annabel Vreeker, James Walters, Weiqing Wang, Nicholas A. Watts, Robert H. Yolken, Peter P. Zandi, Benjamin M. Neale

    出版 2022
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  13. 13
    Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes

    Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes 由 Kaixin Zhou, Céline Bellenguez, Chris C A Spencer, Amanda J. Bennett, Ruth L. Coleman, Roger Tavendale, Simon A. Hawley, Louise A. Donnelly, Chris Schofield, Christopher J. Groves, Lindsay Burch, Fiona Carr, Amy Strange, Colin Freeman, Jenefer M Blackwell, Elvira Bramon, Matthew A. Brown, Juan Pablo Casas, Aiden Corvin, Nicholas Craddock, Panos Deloukas, Serge Dronov, Audrey Duncanson, Sarah Edkins, Emma Gray, Sarah Hunt, Janusz Jankowski, Cordelia Langford, Hugh S Markus, Christopher G. Mathew, Robert Plomin, Anna Rautanen, Stephen J Sawcer, Nilesh J. Samani, Richard C. Trembath, Ananth C Viswanathan, Nicholas Wood, Lorna W. Harries, Andrew T. Hattersley, Alex S. F. Doney, Helen M. Colhoun, Andrew D. Morris, Calum Sutherland, D. Grahame Hardie, Leena Peltonen, Mark I. McCarthy, Rury R. Holman, Colin N. A. Palmer, Peter Donnelly, Ewan R. Pearson

    出版 2010
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  14. 14
    Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder

    Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder 由 Jie Song, Sarah E. Bergen, Arianna Di Florio, Robert Karlsson, Alexander W. Charney, Douglas M. Ruderfer, Eli A. Stahl, Kimberly D. Chambert, Jennifer L. Moran, Katherine Gordon‐Smith, Liz Forty, E K Green, Ian Jones, Lisa Jones, Edward M. Scolnick, Pamela Sklar, Jordan W. Smoller, Paul Lichtenstein, Christina M. Hultman, Nicholas Craddock, M Landén, Jordan W. Smoller, Roy H. Perlis, Phil Hyoun Lee, Víctor M. Castro, Alison G. Hoffnagle, Pamela Sklar, Eli A. Stahl, Shaun Purcell, Douglas M. Ruderfer, Alexander W. Charney, Panos Roussos, Carlos Pato Michele Pato, Helen Medeiros, Janet Sobel, Nick Craddock, Ian Jones, Liz Forty, Arianna Di Florio, Elaine Green, Lisa Jones, Katherine Gordon‐Smith, Mikael Landén, Christina M. Hultman, Anders Juréus, Sarah E. Bergen, Steven A. McCarroll, Jennifer L. Moran, Jordan W. Smoller, Kimberly Chambert, Richard A. Belliveau

    出版 2015
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  15. 15
    Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region

    Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region 由 Jeffrey C. Barrett, James Lee, Charlie W. Lees, Natalie J. Prescott, Carl A. Anderson, Anne Phillips, Emma Wesley, Kirstie Parnell, Hu Zhang, Hazel E. Drummond, Elaine R. Nimmo, Dunecan Massey, Kasia Blaszczyk, Timothy R. Elliott, Lynn Cotterill, Helen Dallal, Alan Lobo, Craig Mowat, Jeremy Sanderson, Derek P. Jewell, William G. Newman, Cathryn Edwards, Tariq Ahmad, John Mansfield, Jack Satsangi, Miles Parkes, Christopher G. Mathew, Peter Donnelly, Leena Peltonen, Jenefer M. Blackwell, Elvira Bramon, Matthew A. Brown, Juan P. Casas, Aiden Corvin, Nicholas Craddock, Panos Deloukas, Audrey Duncanson, Janusz Jankowski, Hugh S Markus, Mark I. McCarthy, Colin N. A. Palmer, Robert Plomin, Anna Rautanen, Stephen J Sawcer, Nilesh J. Samani, Richard C. Trembath, Ananth C Viswanathan, Nicholas Wood, Chris C. A. Spencer, Céline Bellenguez, Daniel B. Davison, Colin L. Freeman, Amy Strange, Cordelia Langford, Sarah Hunt, Sarah Edkins, Rhian Gwilliam, Hannah Blackburn, Suzannah J Bumpstead, Serge Dronov, Matthew Gillman, Emma Gray, Naomi Hammond, Alagurevathi Jayakumar, Owen T McCann, Jennifer Liddle, M. L. Perez, Simon Potter, Rathi Ravindrarajah, Michelle Ricketts, Matthew Waller, Paul A. Weston, Sara Widaa, Pamela Whittaker, Antony Attwood, Jonathan Stephens, Jennifer Sambrook, Willem H. Ouwehand, Wendy L. McArdle, Susan M. Ring, David P. Strachan

    出版 2009
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  16. 16
    Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility

    Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility 由 David M. Evans, Chris C. A. Spencer, Jennifer J. Pointon, Zhan Su, David Harvey, Grazyna Kochan, Udo Oppermann, Alexander Dilthey, Matti Pirinen, Millicent Stone, Louise Appleton, Loukas Moutsianas, Stephen Leslie, Tom Wordsworth, Tony Kenna, Tugce Karaderi, Gethin Thomas, Michael M. Ward, Michael H. Weisman, Claire Farrar, Linda A. Bradbury, Patrick Danoy, Robert D. Inman, Walter P. Maksymowych, Dafna Gladman, Proton Rahman, Ann W. Morgan, Helena Marzo-Ortega, Paul Bowness, Karl Gaffney, J. S. Hill Gaston, Malcolm Smith, Jácome Bruges‐Armas, Ana Rita Couto, Rosa Sorrentino, Fabiana Paladini, Manuel A. R. Ferreira, Huji Xu, Yu Liu, Lei Jiang, Carlos López‐Larrea, Roberto Díaz‐Peña, Antonio López‐Vázquez, Tetyana Zayats, Gavin Band, Céline Bellenguez, Hannah Blackburn, Jenefer M. Blackwell, Elvira Bramon, Suzannah J. Bumpstead, Juan Pablo Casas, Aiden Corvin, Nicholas Craddock, Panos Deloukas, Serge Dronov, Audrey Duncanson, Sarah Edkins, Colin Freeman, Matthew Gillman, Emma Gray, Rhian Gwilliam, Naomi Hammond, Sarah Hunt, Janusz Jankowski, Alagurevathi Jayakumar, Cordelia Langford, Jennifer Liddle, Hugh S. Markus, Christopher G. Mathew, Owen T McCann, Mark I. McCarthy, Colin N. A. Palmer, Leena Peltonen, Robert Plomin, Simon Potter, Anna Rautanen, Rathi Ravindrarajah, Michelle Ricketts, Nilesh J. Samani, Stephen Sawcer, Amy Strange, Richard C. Trembath, Ananth C. Viswanathan, Matthew Waller, Paul A. Weston, Pamela Whittaker, Sara Widaa, Nicholas Wood, Gil McVean, John D. Reveille, B P Wordsworth, Matthew A. Brown, Peter Donnelly

    出版 2011
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  17. 17
    Rare coding variants in ten genes confer substantial risk for schizophrenia

    Rare coding variants in ten genes confer substantial risk for schizophrenia 由 Tarjinder Singh, Timothy Poterba, David Curtis, Huda Akil, Mariam Al Eissa, Jack D. Barchas, Nicholas Bass, Tim B. Bigdeli, Gerome Breen, Evelyn J. Bromet, P.F. Buckley, William E. Bunney, Jonas Bybjerg‐Grauholm, William Byerley, Sinéad B. Chapman, Wei J. Chen, Claire Churchhouse, Nicholas Craddock, Caroline Cusick, Lynn E. DeLisi, Sheila Dodge, Michael Escamilla, Saana Eskelinen, Ayman H. Fanous, Stephen V. Faraone, Alessia Fiorentino, Laurent C. Francioli, Stacey Gabriel, Diane Gage, Sarah A. Gagliano Taliun, Andrea Ganna, Giulio Genovese, David C. Glahn, Jakob Grove, Mei‐Hua Hall, Eija Hämäläinen, Henrike Heyne, Matti Holi, David M. Hougaard, Daniel P. Howrigan, Hailiang Huang, Hai‐Gwo Hwu, René S. Kahn, Hyun Min Kang, Konrad J. Karczewski, George Kirov, James A. Knowles, Francis S. Lee, Douglas S. Lehrer, Francesco Lescai, Dolores Malaspina, Stephen R. Marder, Steven A. McCarroll, Andrew M. McIntosh, Helena Medeiros, Lili Milani, Christopher P. Morley, Derek W. Morris, Preben Bo Mortensen, R Myers, Merete Nordentoft, Niamh L. O’Brien, Ana Maria Olivares, Döst Öngür, Willem H. Ouwehand, Duncan S. Palmer, Tiina Paunio, Digby Quested, Mark Hyman Rapaport, Elliott Rees, Brandi Rollins, F. Kyle Satterstrom, Alan F. Schatzberg, Edward M. Scolnick, Laura J. Scott, Sally I. Sharp, Pamela Sklar, Jordan W. Smoller, Janet L. Sobell, Matthew Solomonson, Eli A. Stahl, Christine Stevens, Jaana Suvisaari, Grace Tiao, Stanley J. Watson, Nicholas A. Watts, Douglas Blackwood, Anders D. Børglum, Bruce M. Cohen, Aiden Corvin, Tõnu Esko, Nelson B. Freimer, Stephen J. Glatt, Christina M. Hultman, Andrew McQuillin, Aarno Palotie, Carlos N. Pato, Michele T. Pato, Ann E. Pulver, David St Clair

    出版 2022
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