Αποτελέσματα αναζήτησης - Alan Maclean

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  1. 1
    Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation

    Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation από Xinsheng Nan, Jianghui Hou, Alan Maclean, Jamal Nasir, María José Lafuente, Xinhua Shu, Skirmantas Kriaučionis, Adrian Bird

    Έκδοση 2007
    Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  2. 2
    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 από 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

    Έκδοση 2008
    Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  3. 3
    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 από 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

    Έκδοση 2009
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  4. 4
    Clustered Coding Variants in the Glutamate Receptor Complexes of Individuals with Schizophrenia and Bipolar Disorder

    Clustered Coding Variants in the Glutamate Receptor Complexes of Individuals with Schizophrenia and Bipolar Disorder από René Frank, Allan F. McRae, Andrew Pocklington, Louie N. van de Lagemaat, Pau Navarro, Mike D. R. Croning, Noboru H. Komiyama, Sophie J. Bradley, R. A. John Challiss, J. Douglas Armstrong, ROBERT FINN, M. P. Malloy, Alan Maclean, Sarah E. Harris, John M. Starr, Sanjeev S. Bhaskar, Eleanor Howard, Sarah Hunt, Alison J. Coffey, Venkatesh Ranganath, Panos Deloukas, Jane Rogers, Walter Muir, Ian J. Deary, Douglas Blackwood, Peter M. Visscher, Seth G. N. Grant

    Έκδοση 2011
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  5. 5
    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 από 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

    Έκδοση 2010
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Revisão
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  6. 6
    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 από 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

    Έκδοση 2008
    Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  7. 7
    Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

    Common polygenic variation contributes to risk of schizophrenia and bipolar disorder από 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

    Έκδοση 2009
    Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  8. 8
    Rare chromosomal deletions and duplications increase risk of schizophrenia

    Rare chromosomal deletions and duplications increase risk of schizophrenia από 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

    Έκδοση 2008
    Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  9. 9
    Repeated nebulisation of non-viral CFTR gene therapy in patients with cystic fibrosis: a randomised, double-blind, placebo-controlled, phase 2b trial

    Repeated nebulisation of non-viral CFTR gene therapy in patients with cystic fibrosis: a randomised, double-blind, placebo-controlled, phase 2b trial από Eric W.F.W. Alton, David K Armstrong, Deborah Ashby, Katie J Bayfield, Diana Bilton, Emily V Bloomfield, A. Christopher Boyd, June Brand, Ruaridh Buchan, Roberto Calcedo, Paula Carvelli, Mario Chan, Seng H. Cheng, David Collie, Steve Cunningham, Heather Davidson, Gwyneth Davies, Jane C. Davies, Lee A. Davies, Maria H Dewar, Ann Doherty, Jackie Donovan, Natalie S Dwyer, Hala I Elgmati, Rosanna F Featherstone, Jemyr Gavino, Sabrina Gea‐Sorlí, Duncan M. Geddes, James Sr Gibson, Deborah R. Gill, A P Greening, Uta Griesenbach, David M. Hansell, Katharine Harman, Tracy Higgins, Samantha L. Hodges, Stephen C. Hyde, Laura Hyndman, J. Alastair Innes, Joseph Jacob, Nancy E. Jones, Brian F Keogh, Maria P. Limberis, Paul Lloyd-Evans, Alan Maclean, Michelle C Manvell, Dominique McCormick, Michael McGovern, Gerry McLachlan, Cuixiang Meng, M Angeles Montero, Hazel Milligan, Laura Moyce, Gordon Murray, Andrew G. Nicholson, Tina Osadolor, Javier Parra-Leiton, David J. Porteous, Ian A. Pringle, Emma K Punch, Kamila M Pytel, Alexandra L. Quittner, Gina Rivellini, Clare Saunders, Ronald K. Scheule, Sarah Sheard, Nicholas J. Simmonds, Keith Smith, Stephen N. Smith, Najwa Soussi, Samia Soussi, Emma J Spearing, Barbara Stevenson, Stephanie Jones, Minna Turkkila, Rosa P Ureta, Michael D Waller, Marguerite Y Wasowicz, James M. Wilson, Paul Wolstenholme-Hogg

    Έκδοση 2015
    Λήψη πλήρους κειμένου
    Artigo
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:
  10. 10
    GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19

    GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19 από Erola Pairo‐Castineira, Konrad Rawlik, Andrew D. Bretherick, Ting Qi, Yang Wu, Isar Nassiri, Glenn A. McConkey, Marie Zechner, Lucija Klarić, Fiona Griffiths, Wilna Oosthuyzen, Athanasios Kousathanas, Anne Richmond, Jonathan Millar, Clark D Russell, Tomas Malinauskas, Ryan S. Thwaites, Kirstie Morrice, Seán Keating, David M. Maslove, Alistair Nichol, Malcolm G. Semple, Julian C. Knight, Manu Shankar‐Hari, Charlotte Summers, Charles Hinds, Peter Horby, Lowell Ling, Daniel F. McAuley, Hugh Montgomery, Peter Openshaw, Colin B. Begg, Timothy Walsh, Albert Tenesa, Carlos Flores, José A. Riancho, Augusto Rojas‐Martínez, Pablo Lapunzina, Sara Clohisey, Johnny Millar, Manu Shankar‐Hari, Emma Aitkin, Latha Aravindan, Ruth Armstrong, J. Kenneth Baillie, Heather Biggs, Ceilia Boz, Adam Brown, Primmy Chikowore, Richard Clark, Audrey Coutts, J. Terrence Coyle, Louise Cullum, Sukamal Das, Nicky Day, Lorna Donnelly, Esther Duncan, Paul Finernan, Max Head Fourman, Anita Furlong, James Furniss, Bernadette Gallagher, Tammy Gilchrist, Ailsa Golightly, Fiona Griffiths, Katarzyna Hafezi, Debbie Hamilton, Ross Hendry, Naomi Kearns, Dawn Law, R. M. Law, Sarah Law, Rebecca Lidstone-Scott, Christen Lauder, Louise MacGillivray, Alan Maclean, Hanning Mal, Sarah McCafferty, Ellie Mcmaster, Jen Meikle, Shona C. Moore, Sheena Murphy, Hellen Mybaya, Miranda Odam, Wilna Oosthuyzen, Chenqing Zheng, Jiantao Chen, Nick Parkinson, Trevor Paterson, Petra Tucker, Katherine Schon, Andrew Stenhouse, Mihaela Das, Maaike Swets, Helen Szoor-McElhinney, Filip Taneski, Lance Turtle, Tony Wackett, Mairi Ward, Jane Weaver

    Έκδοση 2023
    Λήψη πλήρους κειμένου Λήψη πλήρους κειμένου
    Revisão
    Προσθήκη στα αγαπημένα
    Αποθηκεύτηκε σε:

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