Resultados da pesquisa - Elaine Kenny

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  1. 1
    The SNP ratio test: pathway analysis of genome-wide association datasets

    The SNP ratio test: pathway analysis of genome-wide association datasets Por Colm Ó'Dúshláine, Elaine Kenny, Elizabeth A. Heron, Ricardo Segurado, Michael Gill, Derek W. Morris, Aiden Corvin

    Publicado em 2009
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  2. 2
    Development of Strategies for SNP Detection in RNA-Seq Data: Application to Lymphoblastoid Cell Lines and Evaluation Using 1000 Genomes Data

    Development of Strategies for SNP Detection in RNA-Seq Data: Application to Lymphoblastoid Cell Lines and Evaluation Using 1000 Genomes Data Por Emma M. Quinn, Paul Cormican, Elaine Kenny, Matthew Hill, Richard Anney, Michael Gill, Aiden Corvin, Derek W. Morris

    Publicado em 2013
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  3. 3
    Identification of mechanosensitive genes during skeletal development: alteration of genes associated with cytoskeletal rearrangement and cell signalling pathways

    Identification of mechanosensitive genes during skeletal development: alteration of genes associated with cytoskeletal rearrangement and cell signalling pathways Por Rebecca A. Rolfe, Niamh C. Nowlan, Elaine Kenny, Paul Cormican, Derek W. Morris, Patrick J. Prendergast, Daniel J. Kelly, Paula Murphy

    Publicado em 2014
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  4. 4
    Delineating the genetic heterogeneity of ALS using targeted high-throughput sequencing

    Delineating the genetic heterogeneity of ALS using targeted high-throughput sequencing Por Kevin P. Kenna, Russell L. McLaughlin, Susan Byrne, Marwa Elamin, Mark Heverin, Elaine Kenny, Paul Cormican, Derek W. Morris, Colette Donaghy, Daniel G. Bradley, Orla Hardiman

    Publicado em 2013
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  5. 5
    Translation of 5′ leaders is pervasive in genes resistant to eIF2 repression

    Translation of 5′ leaders is pervasive in genes resistant to eIF2 repression Por Dmitry E. Andreev, Patrick B. F. O’Connor, Ciara Fahey, Elaine Kenny, Ilya M. Terenin, Sergey E. Dmitriev, Paul Cormican, Derek W. Morris, Ivan N. Shatsky, Pavel V. Baranov

    Publicado em 2015
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  6. 6
    Detection of novel germline mutations for breast cancer in non‐<i><scp>BRCA</scp>1</i>/<i>2</i> families

    Detection of novel germline mutations for breast cancer in non‐<i><scp>BRCA</scp>1</i>/<i>2</i> families Por Fatima Aloraifi, Trudi McDevitt, Rui Martiniano, Jonah McGreevy, Russell L. McLaughlin, Catherine Egan, Nuala Cody, Marie Meany, Elaine Kenny, Andrew Green, Daniel G. Bradley, James Geraghty, Adrian P. Bracken

    Publicado em 2015
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  7. 7
    Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders

    Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders Por Elaine Kenny, Paul Cormican, Sarah Furlong, Elizabeth A. Heron, G. N. C. Kenny, Ciara Fahey, Eric Kelleher, Sean Ennis, Daniela Tropea, Richard Anney, Aiden Corvin, Gary Donohoe, Louise Gallagher, Michael Gill, Derek W. Morris

    Publicado em 2013
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  8. 8
    First implication of<i>STRA6</i>mutations in isolated anophthalmia, microphthalmia, and coloboma: A new dimension to the<i>STRA6</i>phenotype

    First implication of<i>STRA6</i>mutations in isolated anophthalmia, microphthalmia, and coloboma: A new dimension to the<i>STRA6</i>phenotype Por Jillian P. Casey, Riki Kawaguchi, Maria E. Morrissey, Hui Sun, Paul McGettigan, Jens Erik Nielsen, Judith Conroy, Regina Regan, Elaine Kenny, Paul Cormican, Derek W. Morris, Peter Tormey, Muireann Ní Chróinín, Breandán N. Kennedy, Sally Ann Lynch, Andrew Green, Sean Ennis

    Publicado em 2011
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  9. 9
    Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study

    Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study Por Richard Anney, Jessica Lasky‐Su, Colm Ó'Dúshláine, Elaine Kenny, Benjamin M. Neale, Aisling Mulligan, Barbara Franke, Kaixin Zhou, Wai Chen, Hanna Christiansen, Alejandro Arias Vásquez, Tobias Banaschewski, Jan K. Buitelaar, Richard P. Ebstein, Ana Miranda, Fernando Mulas, Robert D. Oades, Herbert Roeyers, Aribert Rothenberger, Joseph A. Sergeant, Edmund Sonuga‐Barke, Hans‐Christoph Steinhausen, Philip Asherson, Stephen V. Faraone, Michael Gill

    Publicado em 2008
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  10. 10
    Targeted Sequencing of 10,198 Samples Confirms Abnormalities in Neuronal Activity and Implicates Voltage-Gated Sodium Channels in Schizophrenia Pathogenesis

    Targeted Sequencing of 10,198 Samples Confirms Abnormalities in Neuronal Activity and Implicates Voltage-Gated Sodium Channels in Schizophrenia Pathogenesis Por Elliott Rees, Noa Carrera, Joanne Morgan, Kirsty Hambridge, Valentina Escott‐Price, Andrew Pocklington, Alexander Richards, Antonio F. Pardiñas, Colm McDonald, Gary Donohoe, Derek W. Morris, Elaine Kenny, Eric Kelleher, Michael Gill, Aiden Corvin, George Kirov, James Walters, Peter Holmans, Michael J. Owen, Michael O’Donovan, Behrooz Z. Alizadeh, Thérèse van Amelsvoort, Agna A. Bartels‐Velthuis, Nico J. van Beveren, Richard Bruggeman, Wiepke Cahn, Lieuwe de Haan, Philippe Delespaul, Carin J. Meijer, Inez Myin‐Germeys, René S. Kahn, Frederike Schirmbeck, Claudia J.P. Simons, Neeltje E.M. van Haren, Jim van Os, Ruud van Winkel, Jurjen J. Luykx

    Publicado em 2018
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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 Por 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

    Publicado em 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 Por 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

    Publicado em 2008
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  13. 13
    New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis

    New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis Por Sang Lee, Enda M. Byrne, Christina M. Hultman, Anna K. Kähler, Anna A. E. Vinkhuyzen, Stephan Ripke, Ole A. Andreassen, Thomas Frisell, Alexander Gusev, Xinli Hu, Robert Karlsson, Vasilis X Mantzioris, John J. McGrath, Divya Mehta, Eli A. Stahl, Qiongyi Zhao, Kenneth S. Kendler, Patrick F. Sullivan, Alkes L. Price, Michael O’Donovan, Yukinori Okada, Bryan Mowry, Soumya Raychaudhuri, Naomi R. Wray, William Byerley, Wiepke Cahn, Rita M. Cantor, Sven Cichon, Paul Cormican, David Curtis, Srdjan Djurovic, Valentina Escott‐Price, Pablo V. Gejman, Lyudmila Georgieva, Ina Giegling, Thomas Hansen, Andrés Ingason, Yunjung Kim, Bettina Konte, Sang Hyuck Lee, Andrew M. McIntosh, Andrew McQuillin, Derek W. Morris, Markus M. Nöthen, Colm Ó'Dúshláine, Ann Olincy, Line Olsen, Carlos N. Pato, Michele T. Pato, Ben Pickard, Daniëlle Posthuma, Henrik Berg Rasmussen, Marcella Rietschel, Dan Rujescu, Thomas G. Schulze, Jeremy M. Silverman, Srinivasa Thirumalai, Thomas Werge, Ingrid Agartz, Farooq Amin, Maria Helena Pinto de Azevedo, Nicholas Bass, Donald W. Black, Douglas Blackwood, Richard Bruggeman, Nancy G. Buccola, Khalid Choudhury, Robert Cloninger, Aiden Corvin, Nicholas John Craddock, Mark J. Daly, Susmita Datta, Gary Donohoe, Jubao Duan, Frank Dudbridge, Ayman H. Fanous, Robert Freedman, Nelson B. Freimer, Marion Friedl, Michael Gill, Hugh Gurling, Lieuwe de Haan, Marian L. Hamshere, Annette M. Hartmann, Peter Holmans, René S. Kahn, Matthew C. Keller, Elaine Kenny, George Kirov, Lydia Krabbendam, Robert Krasucki, Jacob Lawrence, Todd Lencz, Douglas F. Levinson, Jeffrey A. Lieberman, D. Y. Lin, Don Linszen, Patrik K. E. Magnusson, Wolfgang Maier, Anil K. Malhotra

    Publicado em 2015
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