Resultados de búsqueda - Paola Forabosco

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  1. 1
    Insights From Cerebellar Transcriptomic Analysis Into the Pathogenesis of Ataxia

    Insights From Cerebellar Transcriptomic Analysis Into the Pathogenesis of Ataxia por Conceição Bettencourt, Mina Ryten, Paola Forabosco, Stéphanie Schorge, Joshua Hersheson, John Hardy, Henry Houlden

    Publicado 2014
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  2. 2
    Genetic evidence for a pathogenic role for the vitamin D3 metabolizing enzyme CYP24A1 in multiple sclerosis

    Genetic evidence for a pathogenic role for the vitamin D3 metabolizing enzyme CYP24A1 in multiple sclerosis por Adaikalavan Ramasamy, Daniah Trabzuni, Paola Forabosco, Colin Smith, Robert Walker, Allissa Dillman, Sigurlaug Sveinbjörnsdóttir, John Hardy, Michael E. Weale, Mina Ryten

    Publicado 2013
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  3. 3
    An additional k-means clustering step improves the biological features of WGCNA gene co-expression networks

    An additional k-means clustering step improves the biological features of WGCNA gene co-expression networks por Juan A. Botía, Jana Vandrovcová, Paola Forabosco, Sebastian Guelfi, Karishma D’Sa, John Hardy, Cathryn M. Lewis, Mina Ryten, Michael E. Weale

    Publicado 2017
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  4. 4
    Frontotemporal dementia: insights into the biological underpinnings of disease through gene co-expression network analysis

    Frontotemporal dementia: insights into the biological underpinnings of disease through gene co-expression network analysis por Raffaele Ferrari, Paola Forabosco, Jana Vandrovcová, Juan A. Botía, Sebastian Guelfi, Jason D. Warren, Parastoo Momeni, Michael E. Weale, Mina Ryten, John Hardy

    Publicado 2016
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  5. 5
    Insights into TREM2 biology by network analysis of human brain gene expression data

    Insights into TREM2 biology by network analysis of human brain gene expression data por Paola Forabosco, Adaikalavan Ramasamy, Daniah Trabzuni, Robert Walker, Colin Smith, José Brás, Adam P. Levine, John Hardy, Jennifer M. Pocock, Rita Guerreiro, Michael E. Weale, Mina Ryten

    Publicado 2013
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  6. 6
    Genetic Mapping to 10q23.3-q24.2, in a Large Italian Pedigree, of a New Syndrome Showing Bilateral Cataracts, Gastroesophageal Reflux, and Spastic Paraparesis with Amyotrophy

    Genetic Mapping to 10q23.3-q24.2, in a Large Italian Pedigree, of a New Syndrome Showing Bilateral Cataracts, Gastroesophageal Reflux, and Spastic Paraparesis with Amyotrophy por Marco Seri, Roberto Cusano, Paola Forabosco, R. Cinti, Francesco Caroli, Paolo Picco, Rita Bini, Vincenzo Brescia Morra, Giuseppe De Michele, Margherita Lerone, Margherita Silengo, Ivana Pela, C Borrone, Giovanni Romeo, Marcella Devoto

    Publicado 1999
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  7. 7
    Genetic analysis in Italian families with inflammatory bowel disease supports linkage to the IBD1 locus – A GISC study

    Genetic analysis in Italian families with inflammatory bowel disease supports linkage to the IBD1 locus – A GISC study por Vito Annese, Anna Latiano, P. Bovio, Paola Forabosco, Ada Piepoli, Giovanni Lombardi, Arnaldo Andreoli, Marco Astegiano, Paolo Gionchetti, Gabriele Riegler, G Sturniolo, Maurizio Clementi, Eric Rappaport, Paolo Fortina, Marcella Devoto, Paolo Gasparini, Angelo Andriulli

    Publicado 1999
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  8. 8
    Predicting the Risk of Rheumatoid Arthritis and Its Age of Onset through Modelling Genetic Risk Variants with Smoking

    Predicting the Risk of Rheumatoid Arthritis and Its Age of Onset through Modelling Genetic Risk Variants with Smoking por Ian C. Scott, Seth Seegobin, Sophia Steer, Rachael Tan, Paola Forabosco, Anne Hinks, Stephen Eyre, Ann W. Morgan, Anthony G. Wilson, Lynne J. Hocking, P Wordsworth, Anne Barton, Jane Worthington, Andrew P. Cope, Cathryn M. Lewis

    Publicado 2013
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  9. 9
    Genetic Heterogeneity in Italian Families with IgA Nephropathy: Suggestive Linkage for Two Novel IgA Nephropathy Loci

    Genetic Heterogeneity in Italian Families with IgA Nephropathy: Suggestive Linkage for Two Novel IgA Nephropathy Loci por Luigi Bisceglia, Giuseppina Cerullo, Paola Forabosco, Diletta Domenica Torres, Francesco Scolari, Michele Di Perna, Marina Foramitti, Antonio Amoroso, Sara Bertok, Jürgen Floege, Peter R. Mertens, Klaus Zerres, Efstathios Alexopoulos, Dimitrios Kirmizis, Ermelinda Mazzucco, Leopoldo Zelante, Francesco Paolo Schena

    Publicado 2006
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  10. 10
    Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopy

    Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopy por Emmanuelle Bouzigon, Paola Forabosco, Gerard H. Koppelman, William Cookson, Marie‐Hélène Dizier, David L. Duffy, David M. Evans, Manuel A. R. Ferreira, Juha Kere, Tarja Laitinen, Giovanni Malerba, Deborah A. Meyers, Miriam F. Moffatt, Nicholas G. Martin, Mandy Ng, Pier Franco Pignatti, M Wjst, F. Kauffmann, Florence Démenais, Cathryn M. Lewis

    Publicado 2010
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  11. 11
    Dystonia genes functionally converge in specific neurons and share neurobiology with psychiatric disorders

    Dystonia genes functionally converge in specific neurons and share neurobiology with psychiatric disorders por Niccolò E. Mencacci, Regina H. Reynolds, Sonia García-Ruiz, Jana Vandrovcová, Paola Forabosco, Álvaro Sánchez‐Ferrer, Viola Volpato, Juan A. Botía, Karishma D’Sa, Paola Forabosco, Sebastian Guelfi, John Hardy, Jana Vandrovcová, C. L. MacKenzie, Adaikalavan Ramasamy, Mina Ryten, Colin Smith, Daniah Trabzuni, Michael E. Weale, Alastair Noyce, Rauan Kaiyrzhanov, Ben Middlehurst, Demis A. Kia, Manuela Tan, Henry Houlden, Huw R. Morris, Hélène Plun‐Favreau, Peter Holmans, John Hardy, Daniah Trabzuni, José Brás, John P. Quinn, Kin Y. Mok, Kerri J. Kinghorn, Kimberley J. Billingsley, Nicholas Wood, Patrick A. Lewis, Rita Guerreiro, Ruth C. Lovering, Lea R’Bibo, Claudia Manzoni, Mie Rizig, Mina Ryten, Sebastian Guelfi, Valentina Escott‐Price, Viorica Chelban, Thomas Foltynie, Nigel Williams, Chingiz Shashakin, Nazira Zharkinbekova, Elena Zholdybayeva, Akbota Aitkulova, Kirsten Harvey, Michael E. Weale, Kailash P. Bhatia, Caleb Webber, John Hardy, Juan A. Botía, Mina Ryten

    Publicado 2020
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  12. 12
    A Missense Mutation in KCTD17 Causes Autosomal Dominant Myoclonus-Dystonia

    A Missense Mutation in KCTD17 Causes Autosomal Dominant Myoclonus-Dystonia por Niccolò E. Mencacci, Ignacio Rubio‐Agusti, Anselm A. Zdebik, Friedrich Asmus, Marthe H. R. Ludtmann, Mina Ryten, Vincent Plagnol, Ann‐Kathrin Hauser, Sara Bandrés‐Ciga, Conceição Bettencourt, Paola Forabosco, Deborah Hughes, Marc P. M. Soutar, Kathryn J. Peall, Huw R. Morris, Daniah Trabzuni, Mehmet Tekman, Horia Stanescu, Robert Kleta, Miryam Carecchio, Giovanna Zorzi, Nardo Nardocci, Barbara Garavaglia, Ebba Lohmann, Anne Weißbach, Christine Klein, John Hardy, Alan Pittman, Thomas Foltynie, Andrey Y. Abramov, Thomas Gasser, Kailash P. Bhatia, Nicholas Wood

    Publicado 2015
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  13. 13
    Meta‐analysis of genome‐wide linkage scans of attention deficit hyperactivity disorder

    Meta‐analysis of genome‐wide linkage scans of attention deficit hyperactivity disorder por Kaixin Zhou, Astrid Dempfle, Mauricio Arcos‐Burgos, Steven C. Bakker, Tobias Banaschewski, Joseph Biederman, Jan Buitelaar, F. Xavier Castellanos, Alysa E. Doyle, Richard P. Ebstein, Jenny Ekholm, Paola Forabosco, Barbara Franke, Christine M. Freitag, Susann Friedel, Michael Gill, Johannes Hebebrand, Anke Hinney, Christian Jacob, Klaus‐Peter Lesch, Sandra K. Loo, Francisco Lopera, James T. McCracken, James J. McGough, Jobst Meyer, Eric Mick, Ana Miranda, Maximilian Muenke, Fernando Mulas, Stanley F. Nelson, Trang Nguyen, Robert D. Oades, Matthew N. Ogdie, Juan David Palacio, David Pineda, Andreas Reif, Tobias Renner, Herbert Roeyers, Marcel Romanos, Aribert Rothenberger, H. Schäfer, Joseph A. Sergeant, Richard J. Sinke, Susan L. Smalley, Edmund Sonuga‐Barke, Hans‐Christoph Steinhausen, Emma van der Meulen, Susanne Walitza, Andreas Warnke, Cathryn M. Lewis, Stephen V. Faraone, Philip Asherson

    Publicado 2008
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  14. 14
    Meta-analysis of 32 genome-wide linkage studies of schizophrenia

    Meta-analysis of 32 genome-wide linkage studies of schizophrenia por Mandy Ng, Douglas F. Levinson, Stephen V. Faraone, Brian K. Suarez, Lynn E. DeLisi, Tadao Arinami, Brien P. Riley, Tiina Paunio, Ann E. Pulver, Irmansyah, Peter Holmans, Michael Escamilla, Dieter B. Wildenauer, Nigel Williams, Claudine Laurent, Bryan Mowry, Linda M. Brzustowicz, Michel Maziade, Pamela Sklar, D. Garver, Gonçalo R. Abecasis, Bernard Lerer, M. Daniele Fallin, Hugh Gurling, Pablo V. Gejman, Eva Lindholm, Hans W. Moises, William Byerley, Ellen M. Wijsman, Paola Forabosco, Ming T. Tsuang, Hai‐Gwo Hwu, Yozo Okazaki, Kenneth S. Kendler, Brandon Wormley, Ayman H. Fanous, Dermot Walsh, F. Anthony O’Neill, L. Peltonen, Gerald Nestadt, Virginia K. Lasseter, Kung‐Yee Liang, G. Papadimitriou, Dimitris Dikeos, Sibylle G. Schwab, Michael J. Owen, Michael O’Donovan, Nadine Norton, Elizabeth Hare, Henriette Raventós, Humberto Nicolini, Margot Albus, W. Maier, Vishwajit L. Nimgaonkar, Lars Terenius, Jacques Mallet, Melanie Jay, Stephanie Godard, Deborah A. Nertney, Madeline Alexander, R R Crowe, Jeremy M. Silverman, Anne S. Bassett, M-A Roy, Chantal Mérette, Carlos N. Pato, Michele T. Pato, Johannes L. Roos, Yoav Kohn, Daniela Amann‐Zalcenstein, G. Kalsi, Andrew McQuillin, David Curtis, Jon Brynjolfson, Thordur Sigmundsson, Hannes Pétursson, Alan R. Sanders, Jubao Duan, Elena Jazin, Marina Myles‐Worsley, Maria Karayiorgou, Cathryn M. Lewis

    Publicado 2008
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  15. 15
    Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease

    Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer’s disease por Carlos Cruchaga, Celeste M. Karch, Sheng Chih Jin, Bruno A. Benítez, Yefei Cai, Rita Guerreiro, Oscar Harari, Joanne Norton, John Budde, Sarah Bertelsen, Amanda T. Jeng, Breanna Cooper, Tara Skorupa, David Carrell, Denise Levitch, Simon Hsu, Jiyoon Choi, Mina Ryten, John Hardy, Mina Ryten, Daniah Trabzuni, Michael E. Weale, Adaikalavan Ramasamy, Colin Smith, Celeste Sassi, José Brás, J. Raphael Gibbs, Dena G. Hernandez, Michelle K. Lupton, John Powell, Paola Forabosco, Perry G. Ridge, Christopher Corcoran, JoAnn T. Tschanz, Maria C. Norton, Ronald G. Munger, Cameron Schmutz, Maegan Leary, F. Yesim Demirci, Mikhil Bamne, Xingbin Wang, Oscar L. López, Mary Ganguli, Christopher Medway, James Turton, Jenny Lord, Anne Braae, Imelda Barber, Kristelle Brown, Peter Passmore, David Craig, Janet Johnston, Bernadette McGuinness, Stephen Todd, Reinhard Heun, Heike Kölsch, Patrick G. Kehoe, Nigel M. Hooper, Emma Vardy, David Mann, Stuart Pickering‐Brown, Kristelle Brown, Noor Kalsheker, James Lowe, Kevin Morgan, A. David Smith, Gordon Wilcock, Donald Warden, Clive Holmes, Pau Pástor, Oswaldo Lorenzo‐Betancor, Zoran Brkanac, Erick R. Scott, Eric J. Topol, Kevin Morgan, Ekaterina Rogaeva, Andrew B. Singleton, John Hardy, M. Ilyas Kamboh, Peter St George‐Hyslop, Nigel J. Cairns, John C. Morris, John Kauwe, Alison Goate

    Publicado 2013
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