Výsledky vyhledávání - Johanna Hadler

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  1. 1
    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 Autor Patrick Danoy, Karena Pryce, Johanna Hadler, Linda A. Bradbury, Claire Farrar, Jennifer J. Pointon, Michael M. Ward, Michael H. Weisman, John D. Reveille, B P Wordsworth, Millicent Stone, Walter P. Maksymowych, Proton Rahman, Dafna Gladman, Robert D. Inman, Matthew A. Brown

    Vydáno 2010
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  2. 2
    Specifications of the ACMG/AMP variant curation guidelines for myocilin: Recommendations from the clingen glaucoma expert panel

    Specifications of the ACMG/AMP variant curation guidelines for myocilin: Recommendations from the clingen glaucoma expert panel Autor Kathryn P. Burdon, Patricia Graham, Johanna Hadler, John D. Hulleman, Francesca Pasutto, Erin A. Boese, Jamie E. Craig, John H. Fingert, Alex W. Hewitt, Owen M. Siggs, Kristina N. Whisenhunt, Terri L. Young, David A. Mackey, Andrew Dubowsky, Emmanuelle Souzeau

    Vydáno 2022
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  3. 3
    Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci

    Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci Autor John D. Reveille, Anne-Marie Sims, Patrick Danoy, David M. Evans, Paul Leo, Jennifer J. Pointon, Rui Jin, Xiaodong Zhou, Linda A. Bradbury, Louise Appleton, John C. Davis, Laura Diekman, Tracey Doan, Alison Dowling, Ran Duan, Emma L. Duncan, Claire Farrar, Johanna Hadler, David Harvey, Tugce Karaderi, R Mogg, Emma Pomeroy, Karena Pryce, Jacqueline Taylor, Laurie Savage, Panos Deloukas, Vasudev Kumanduri, Leena Peltonen, Susan M. Ring, Pamela Whittaker, Evgeny A. Glazov, Gethin Thomas, Walter P. Maksymowych, Robert D. Inman, Michael M. Ward, Millicent Stone, Michael H. Weisman, B P Wordsworth, Matthew A. Brown

    Vydáno 2010
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  4. 4
    Evidence-based recommendations for gene-specific ACMG/AMP variant classification from the ClinGen ENIGMA BRCA1 and BRCA2 Variant Curation Expert Panel

    Evidence-based recommendations for gene-specific ACMG/AMP variant classification from the ClinGen ENIGMA BRCA1 and BRCA2 Variant Curation Expert Panel Autor Michael T. Parsons, Miguel de la Hoya, Marcy E. Richardson, Emma Tudini, Michael G. Anderson, Windy Berkofsky‐Fessler, Sandrine M. Caputo, Raymond C. Chan, Melissa Cline, Bing Feng, Cristina Fortuño, E. Gómez, Johanna Hadler, Susan Hiraki, Megan Holdren, Claude Houdayer, Kathleen S. Hruska, Paul A. James, Rachid Karam, Huei San Leong, Alexandra Martins, Arjen R. Mensenkamp, Álvaro N.A. Monteiro, Vaishnavi Nathan, Robert O’Connor, Inge Søkilde Pedersen, Tina Pesaran, Paolo Radice, Gunnar Schmidt, Melissa C. Southey, Sean V. Tavtigian, Bryony A. Thompson, Amanda E. Toland, Clare Turnbull, Maartje J. Vogel, Jamie Weyandt, George A. R. Wiggins, Lauren Zec, Fergus J. Couch, Logan C. Walker, Maaike P.G. Vreeswijk, David E. Goldgar, Amanda B. Spurdle

    Vydáno 2024
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