Hasil Pencarian - Paul Wordsworth

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  1. 1
    Perspectives on the Genetic Associations of Ankylosing Spondylitis

    Perspectives on the Genetic Associations of Ankylosing Spondylitis oleh B. Paul Wordsworth, B. Paul Wordsworth, Carla J. Cohen, Connor Davidson, Matteo Vecellio, Matteo Vecellio, Matteo Vecellio

    Diterbitkan 2021-03-01
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  2. 2
    Disruption of c-MYC Binding and Chromosomal Looping Involving Genetic Variants Associated With Ankylosing Spondylitis Upstream of the RUNX3 Promoter

    Disruption of c-MYC Binding and Chromosomal Looping Involving Genetic Variants Associated With Ankylosing Spondylitis Upstream of the RUNX3 Promoter oleh Carla J. Cohen, Carla J. Cohen, Connor Davidson, Connor Davidson, Connor Davidson, Carlo Selmi, Paul Bowness, Paul Bowness, Julian C. Knight, B. Paul Wordsworth, B. Paul Wordsworth, Matteo Vecellio, Matteo Vecellio, Matteo Vecellio

    Diterbitkan 2022-01-01
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  3. 3
    The IL-17/IL-23 Axis and Its Genetic Contribution to Psoriatic Arthritis

    The IL-17/IL-23 Axis and Its Genetic Contribution to Psoriatic Arthritis oleh Matteo Vecellio, Matteo Vecellio, Vivien Xanath Hake, Connor Davidson, Maria Cristina Carena, B. Paul Wordsworth, Carlo Selmi

    Diterbitkan 2021-01-01
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  4. 4
    Chromosome conformation capture approaches to investigate 3D genome architecture in Ankylosing Spondylitis

    Chromosome conformation capture approaches to investigate 3D genome architecture in Ankylosing Spondylitis oleh Connor Davidson, Connor Davidson, B. Paul Wordsworth, Carla J. Cohen, Carla J. Cohen, Julian C. Knight, Matteo Vecellio, Matteo Vecellio

    Diterbitkan 2023-01-01
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  5. 5
    Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients.

    Novel mutations in ACVR1 result in atypical features in two fibrodysplasia ossificans progressiva patients. oleh Kirsten A Petrie, Wen Hwa Lee, Alex N Bullock, Jenny J Pointon, Roger Smith, R Graham G Russell, Matthew A Brown, B Paul Wordsworth, James T Triffitt

    Diterbitkan 2009-01-01
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  6. 6
    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. oleh Ian C Scott, Seth D Seegobin, Sophia Steer, Rachael Tan, Paola Forabosco, Anne Hinks, Stephen Eyre, Ann W Morgan, Anthony G Wilson, Lynne J Hocking, Paul Wordsworth, Anne Barton, Jane Worthington, Andrew P Cope, Cathryn M Lewis

    Diterbitkan 2013-01-01
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  7. 7
    Correction: Predicting the Risk of Rheumatoid Arthritis and Its Age of Onset through Modelling Genetic Risk Variants with Smoking.

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

    Diterbitkan 2013-10-01
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  8. 8
    Correction: Association of Variants at 1q32 and with Ankylosing Spondylitis Suggests Genetic Overlap with Crohn's Disease.

    Correction: Association of Variants at 1q32 and with Ankylosing Spondylitis Suggests Genetic Overlap with Crohn's Disease. oleh Patrick Danoy, Karena Pryce, Johanna Hadler, Linda A. Bradbury, Claire Farrar, Jennifer Pointon, Michael Ward, Michael Weisman, John D. Reveille, B. Paul Wordsworth, Millicent A. Stone, Walter P. Maksymowych, Proton Rahman, Dafna Gladman, Robert D. Inman, Matthew A. Brown

    Diterbitkan 2011-02-01
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  9. 9
    Correction: Association of Variants at 1q32 and with Ankylosing Spondylitis Suggests Genetic Overlap with Crohn's Disease.

    Correction: Association of Variants at 1q32 and with Ankylosing Spondylitis Suggests Genetic Overlap with Crohn's Disease. oleh Patrick Danoy, Karena Pryce, Johanna Hadler, Linda A. Bradbury, Claire Farrar, Jennifer Pointon, Michael Ward, Michael Weisman, John D. Reveille, B. Paul Wordsworth, Millicent A. Stone, Walter P. Maksymowych, Proton Rahman, Dafna Gladman, Robert D. Inman, Matthew A. Brown

    Diterbitkan 2011-02-01
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  10. 10
    Association of variants at 1q32 and STAT3 with ankylosing spondylitis suggests genetic overlap with Crohn's disease.

    Association of variants at 1q32 and STAT3 with ankylosing spondylitis suggests genetic overlap with Crohn's disease. oleh Patrick Danoy, Karena Pryce, Johanna Hadler, Linda A Bradbury, Claire Farrar, Jennifer Pointon, Australo-Anglo-American Spondyloarthritis Consortium, Michael Ward, Michael Weisman, John D Reveille, B Paul Wordsworth, Millicent A Stone, Spondyloarthritis Research Consortium of Canada, Walter P Maksymowych, Proton Rahman, Dafna Gladman, Robert D Inman, Matthew A Brown

    Diterbitkan 2010-12-01
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  11. 11
    Informed conditioning on clinical covariates increases power in case-control association studies.

    Informed conditioning on clinical covariates increases power in case-control association studies. oleh Noah Zaitlen, Sara Lindström, Bogdan Pasaniuc, Marilyn Cornelis, Giulio Genovese, Samuela Pollack, Anne Barton, Heike Bickeböller, Donald W Bowden, Steve Eyre, Barry I Freedman, David J Friedman, John K Field, Leif Groop, Aage Haugen, Joachim Heinrich, Brian E Henderson, Pamela J Hicks, Lynne J Hocking, Laurence N Kolonel, Maria Teresa Landi, Carl D Langefeld, Loic Le Marchand, Michael Meister, Ann W Morgan, Olaide Y Raji, Angela Risch, Albert Rosenberger, David Scherf, Sophia Steer, Martin Walshaw, Kevin M Waters, Anthony G Wilson, Paul Wordsworth, Shanbeh Zienolddiny, Eric Tchetgen Tchetgen, Christopher Haiman, David J Hunter, Robert M Plenge, Jane Worthington, David C Christiani, Debra A Schaumberg, Daniel I Chasman, David Altshuler, Benjamin Voight, Peter Kraft, Nick Patterson, Alkes L Price

    Diterbitkan 2012-01-01
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  12. 12
    Novel pathogenic variants and quantitative phenotypic analyses of Robinow syndrome: WNT signaling perturbation and phenotypic variability

    Novel pathogenic variants and quantitative phenotypic analyses of Robinow syndrome: WNT signaling perturbation and phenotypic variability oleh Chaofan Zhang, Angad Jolly, Brian J. Shayota, Juliana F. Mazzeu, Haowei Du, Moez Dawood, Patricia Celestino Soper, Ariadne Ramalho de Lima, Bárbara Merfort Ferreira, Zeynep Coban-Akdemir, Janson White, Deborah Shears, Fraser Robert Thomson, Sarah Louise Douglas, Andrew Wainwright, Kathryn Bailey, Paul Wordsworth, Mike Oldridge, Tracy Lester, Alistair D. Calder, Katja Dumic, Siddharth Banka, Dian Donnai, Shalini N. Jhangiani, Lorraine Potocki, Wendy K. Chung, Sara Mora, Hope Northrup, Myla Ashfaq, Jill A. Rosenfeld, Kati Mason, Lynda C. Pollack, Allyn McConkie-Rosell, Wei Kelly, Marie McDonald, Natalie S. Hauser, Peter Leahy, Cynthia M. Powell, Raquel Boy, Rachel Sayuri Honjo, Fernando Kok, Lucia R. Martelli, Vicente Odone Filho, Genomics England Research Consortium, Donna M. Muzny, Richard A. Gibbs, Jennifer E. Posey, Pengfei Liu, James R. Lupski, V. Reid Sutton, Claudia M.B. Carvalho

    Diterbitkan 2022-01-01
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