Rezultati - Colin Veal

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  1. 1
    The Major Psoriasis Susceptibility Locus PSORS1 Is not a Risk Factor for Late-Onset Psoriasis

    The Major Psoriasis Susceptibility Locus PSORS1 Is not a Risk Factor for Late-Onset Psoriasis od Michael H. Allen, Hahreen Ameen, Colin Veal, Julie Evans, V.S. Ramrakha‐Jones, Alexander Marsland, A. David Burden, C.E.M. Griffiths, Richard C. Trembath, Juliet N. Barker

    Izdano 2005
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  2. 2
    Family-Based Analysis Using a Dense Single-Nucleotide Polymorphism–Based Map Defines Genetic Variation at PSORS1, the Major Psoriasis-Susceptibility Locus

    Family-Based Analysis Using a Dense Single-Nucleotide Polymorphism–Based Map Defines Genetic Variation at PSORS1, the Major Psoriasis-Susceptibility Locus od Colin Veal, Francesca Capon, Michael H. Allen, Emma Heath, Julie Evans, A. Rocyn Jones, Shanta Patel, David Burden, David M. Tillman, Juliet N. Barker, Richard C. Trembath

    Izdano 2002
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  3. 3
    Identification of a novel psoriasis susceptibility locus at 1p and evidence of epistasis between PSORS1 and candidate loci

    Identification of a novel psoriasis susceptibility locus at 1p and evidence of epistasis between PSORS1 and candidate loci od Colin Veal, R. Lee Clough, Ruth Barber, Sara S. Mason, D Tillman, Berne Ferry, ANTHONY JONES, M. Ameen, Nalini Balendran, Stephen H. Powis, A. David Burden, Juliet N. Barker, Richard C. Trembath

    Izdano 2001
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  4. 4
    Beacon v2 and Beacon networks: A “lingua franca” for federated data discovery in biomedical genomics, and beyond

    Beacon v2 and Beacon networks: A “lingua franca” for federated data discovery in biomedical genomics, and beyond od Jordi Rambla, Michael Baudis, Roberto Ariosa, Tim Beck, Lauren A. Fromont, Arcadi Navarro, Rahel Paloots, Manuel Rueda, Gary Saunders, Babita Singh, Dylan Spalding, Juha Törnroos, Claudia Vasallo, Colin Veal, Anthony J. Brookes

    Izdano 2022
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  5. 5
    Characterization of the Major Susceptibility Region for Psoriasis at Chromosome 6p21.3

    Characterization of the Major Susceptibility Region for Psoriasis at Chromosome 6p21.3 od Nalini Balendran, R. Lee Clough, J. Rafael Argüello, Ruth Barber, Colin Veal, Andrew B. Jones, Jane L. Rosbotham, Anne-Margaret Little, J. Alejandro Madrigal, Juliet N. Barker, Stephen H. Powis, Richard C. Trembath

    Izdano 1999
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  6. 6
    Inherited Chromosomally Integrated Human Herpesvirus 6 Genomes Are Ancient, Intact, and Potentially Able To Reactivate from Telomeres

    Inherited Chromosomally Integrated Human Herpesvirus 6 Genomes Are Ancient, Intact, and Potentially Able To Reactivate from Telomeres od Enjie Zhang, Adam J. Bell, Gavin S. Wilkie, Nicolás M. Suárez, Chiara Batini, Colin Veal, Isaac Armendáriz‐Castillo, Rita Neumann, Victoria E. Cotton, Yan Huang, David J. Porteous, Ruth F. Jarrett, Andrew J. Davison, Nicola J. Royle

    Izdano 2017
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  7. 7
    Responsible sharing of biomedical data and biospecimens via the “Automatable Discovery and Access Matrix” (ADA-M)

    Responsible sharing of biomedical data and biospecimens via the “Automatable Discovery and Access Matrix” (ADA-M) od J. Patrick Woolley, Emily Kirby, Josh Leslie, Francis Jeanson, Moran N. Cabili, Gregory T. Rushton, James G. Hazard, Vagelis Ladas, Colin Veal, Spencer Gibson, Anne-Marie Tassé, Stephanie O. M. Dyke, Clara Gaff, Adrian Thorogood, Bartha Maria Knoppers, John Wilbanks, Anthony J. Brookes

    Izdano 2018
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  8. 8
    The International Psoriasis Genetics Study: Assessing Linkage to 14 Candidate Susceptibility Loci in a Cohort of 942 Affected Sib Pairs

    The International Psoriasis Genetics Study: Assessing Linkage to 14 Candidate Susceptibility Loci in a Cohort of 942 Affected Sib Pairs od M H Allen, Jwn Barker, A. Bowcock, AD Burden, Francesca Capon, Nicholas V.C. Chia, Enno Christophers, MJ Daly, JT Elder, Cynthia Helms, Tilo Henseler, Stefan Jenisch, Alan Menter, Ragini M. Mistry, RP Nair, P. E. Stuart, D Tillman, Richard C. Trembath, Colin Veal, JJ Voorhees

    Izdano 2003
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  9. 9
    Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

    Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus od Patrick Tarpey, Shery Thomas, Nagini Sarvananthan, Uma Mallya, Steven Lisgo, Chris J. Talbot, E.O. Roberts, Musarat Awan, Mylvaganam Surendran, Rebecca J. McLean, Robert Reinecke, Andrea Langmann, S. Lindner, Martina Koch, Sunila Jain, Geoffrey Woodruff, Richard Gale, Andrew Bastawrous, Chris Degg, Konstantinos Droutsas, Ioannis Asproudis, Alina A. Zubcov, Christina Pieh, Colin Veal, Rajiv D. Machado, O Backhouse, Laura Baumber, Cris S. Constantinescu, Michael C. Brodsky, David G. Hunter, Richard W. Hertle, Randy J. Read, Sarah Edkins, Sarah O’Meara, Adrian G. Parker, Claire Stevens, Jon W. Teague, Richard Wooster, P. Andrew Futreal, Richard C. Trembath, Michael R. Stratton, F. Lucy Raymond, Irène Gottlob

    Izdano 2006
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  10. 10
    Erratum: Corrigendum: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus

    Erratum: Corrigendum: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus od Patrick Tarpey, Shery Thomas, Nagini Sarvananthan, Uma Mallya, Steven Lisgo, Chris J. Talbot, E.O. Roberts, Musarat Awan, Mylvaganam Surendran, Rebecca J. McLean, Robert Reinecke, Andrea Langmann, S. Lindner, Martina Koch, Sunila Jain, Geoffrey Woodruff, Richard Gale, Chris Degg, Konstantinos Droutsas, Ioannis Asproudis, Alina A. Zubcov, Christina Pieh, Colin Veal, Rajiv D. Machado, O Backhouse, Laura Baumber, Cris S. Constantinescu, Michael C. Brodsky, David G. Hunter, Richard W. Hertle, Randy J. Read, Sarah Edkins, Sarah O’Meara, Adrian G. Parker, Claire Stevens, Jon W. Teague, Richard Wooster, P. Andrew Futreal, Richard C. Trembath, Michael R. Stratton, F. Lucy Raymond, Irène Gottlob

    Izdano 2011
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  11. 11
    Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

    Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases od Birte Zurek, Kornelia Ellwanger, Lisenka E.L.M. Vissers, Rebecca Schüle, Matthis Synofzik, Ana Töpf, Richarda M. de Voer, Steven Laurie, Leslie Matalonga, Christian Gilissen, Stephan Ossowski, Peter A.C. ‘t Hoen, Antonio Vitobello, Julia M. Schulze‐Hentrich, Olaf Rieß, Han G. Brunner, Anthony J. Brookes, Ana Rath, Gisèle Bonne, Gulcin Gumus, Alain Verloès, Nicoline Hoogerbrugge, Teresinha Evangelista, Tina Harmuth, Morris A. Swertz, Dylan Spalding, Alexander Hoischen, Sergi Beltrán, Holm Graeßner, Tobias B. Haack, Birte Zurek, Kornelia Ellwanger, German Demidov, Marc Sturm, Christoph Keßler, Melanie Wayand, Carlo Wilke, Andreas Traschütz, Lüdger Schöls, Holger Hengel, Peter Heutink, Han G. Brunner, Hans Scheffer, Wouter Steyaert, Karolis Sablauskas, Richarda M. de Voer, Erik-Jan Kamsteeg, Bart van de Warrenburg, Nienke van Os, Iris te Paske, Erik Janssen, Elke de Boer, Marloes Steehouwer, Burcu Yaldız, Tjitske Kleefstra, Colin Veal, Spencer Gibson, Marc Wadsley, Mehdi Mehtarizadeh, Umar Riaz, Greg Warren, Farid Yavari Dizjikan, Thomas Shorter, Volker Straub, Chiara Marini Bettolo, Sabine Specht, Jill Clayton‐Smith, Siddharth Banka, Elizabeth Alexander, Adam Jackson, Laurence Faivre, Christel Thauvin, Antonio Vitobello, Anne‐Sophie Denommé‐Pichon, Yannis Duffourd, Émilie Tisserant, Ange‐Line Bruel, Christine Peyron, Aurore Pélissier, Sergi Beltrán, Marta Gut, Steven Laurie, Davide Piscia, Leslie Matalonga, Anastasios Papakonstantinou, Gemma Bullich, Alberto Corvò, Carles García, Marcos Fernandez-Callejo, Carles Hernández-Ferrer, Daniel Picó, Ida Paramonov, Hanns Lochmüller, Gulcin Gumus, Virginie Bros‐Facer, Marc Hanauer, Annie Olry, David Lagorce, Svitlana Havrylenko, Katia Izem

    Izdano 2021
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