Resultats de la cerca - Matt W. Wright

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  1. 1
    A short guide to long non-coding RNA gene nomenclature

    A short guide to long non-coding RNA gene nomenclature per Matt W. Wright

    Publicat 2014
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  2. 2
    Naming 'junk': Human non-protein coding RNA (ncRNA) gene nomenclature

    Naming 'junk': Human non-protein coding RNA (ncRNA) gene nomenclature per Matt W. Wright, Elspeth A. Bruford

    Publicat 2011
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  3. 3
    New Nomenclature for Mammalian BSP Genes1

    New Nomenclature for Mammalian BSP Genes1 per P. Manjunath, Jasmine Lefebvre, Prashanth Sirigeri Jois, Jinjiang Fan, Matt W. Wright

    Publicat 2008
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  4. 4
    A review of the new HGNC gene family resource

    A review of the new HGNC gene family resource per Kristian Gray, Ruth L. Seal, Susan Tweedie, Matt W. Wright, Elspeth A. Bruford

    Publicat 2016
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  5. 5
    Genenames.org: the HGNC resources in 2015

    Genenames.org: the HGNC resources in 2015 per Kristian Gray, Bethan Yates, Ruth L. Seal, Matt W. Wright, Elspeth A. Bruford

    Publicat 2014
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  6. 6
    The HGNC Database in 2008: a resource for the human genome

    The HGNC Database in 2008: a resource for the human genome per Elspeth A. Bruford, Michael Lush, Matt W. Wright, Tam P. Sneddon, S. Povey, Ewan Birney

    Publicat 2007
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  7. 7
    genenames.org: the HGNC resources in 2011

    genenames.org: the HGNC resources in 2011 per Ruth L. Seal, Susan M. Gordon, Michael Lush, Matt W. Wright, Elspeth A. Bruford

    Publicat 2010
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  8. 8
    Genenames.org: the HGNC resources in 2013

    Genenames.org: the HGNC resources in 2013 per Kristian Gray, Louise C. Daugherty, Susan M. Gordon, Ruth L. Seal, Matt W. Wright, Elspeth A. Bruford

    Publicat 2012
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  9. 9
    A revised nomenclature for mammalian acyl-CoA thioesterases/hydrolases

    A revised nomenclature for mammalian acyl-CoA thioesterases/hydrolases per Mary C. Hunt, Junji Yamada, Lois J. Maltais, Matt W. Wright, Ernesto J. Podestá, Stefan E.H. Alexson

    Publicat 2005
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  10. 10
    Evaluating the impact of in silico predictors on clinical variant classification

    Evaluating the impact of in silico predictors on clinical variant classification per Emma H. Wilcox, Mahdi Sarmady, Bryan Wulf, Matt W. Wright, Heidi L. Rehm, Leslie G. Biesecker, Ahmad Abou Tayoun

    Publicat 2021
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  11. 11
    Update of the human and mouse SERPINgene superfamily

    Update of the human and mouse SERPINgene superfamily per Claire Heit, Brian C. Jackson, Monica McAndrews, Matt W. Wright, David C. Thompson, Gary A. Silverman, Daniel W. Nebert, Vasilis Vasiliou

    Publicat 2013
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  12. 12
    New consensus nomenclature for mammalian keratins

    New consensus nomenclature for mammalian keratins per Jürgen Schweizer, Paul E. Bowden, Pierre A. Coulombe, Lutz Langbein, E. Birgitte Lane, Thomas M. Magin, Lois J. Maltais, M. Bishr Omary, David Parry, Michael A. Rogers, Matt W. Wright

    Publicat 2006
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  13. 13
    An Updated Nomenclature for Keratin-Associated Proteins (KAPs)

    An Updated Nomenclature for Keratin-Associated Proteins (KAPs) per Hua Gong, Huitong Zhou, Grant W McKenzie, Zhidong Yu, Stefan Clerens, Jolon M. Dyer, Jeffrey E. Plowman, Matt W. Wright, Reena Arora, C. Simon Bawden, Yulin Chen, Jinquan Li, Jon G. H. Hickford

    Publicat 2012
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  14. 14
    Recommendations for application of the functional evidence PS3/BS3 criterion using the ACMG/AMP sequence variant interpretation framework

    Recommendations for application of the functional evidence PS3/BS3 criterion using the ACMG/AMP sequence variant interpretation framework per Sarah E. Brnich, Ahmad Abou Tayoun, Fergus J. Couch, Garry R. Cutting, Marc S. Greenblatt, Christopher D. Heinen, Dona Kanavy, Xi Luo, Shannon McNulty, Lea M. Starita, Sean V. Tavtigian, Matt W. Wright, Steven M. Harrison, Leslie G. Biesecker, Jonathan S. Berg

    Publicat 2019
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  15. 15
    Recommendations for application of the functional evidence PS3/BS3 criterion using the ACMG/AMP sequence variant interpretation framework

    Recommendations for application of the functional evidence PS3/BS3 criterion using the ACMG/AMP sequence variant interpretation framework per Sarah E. Brnich, Ahmad Abou Tayoun, Fergus J. Couch, Garry R. Cutting, Marc S. Greenblatt, Christopher D. Heinen, Dona Kanavy, Xi Luo, Shannon McNulty, Lea M. Starita, Sean V. Tavtigian, Matt W. Wright, Steven M. Harrison, Leslie G. Biesecker, Jonathan S. Berg

    Publicat 2019
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  16. 16
    The clinical imperative for inclusivity: Race, ethnicity, and ancestry (REA) in genomics

    The clinical imperative for inclusivity: Race, ethnicity, and ancestry (REA) in genomics per Alice B. Popejoy, Deborah Ritter, Kristy Crooks, Erin Currey, Stephanie M. Fullerton, Lucia A. Hindorff, Barbara A. Koenig, Erin M. Ramos, Elena P. Sorokin, Hannah Wand, Matt W. Wright, James Zou, Christopher R. Gignoux, Vence L. Bonham, Sharon E. Plon, Carlos D. Bustamante

    Publicat 2018
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  17. 17
    Clinical Genetics Lacks Standard Definitions and Protocols for the Collection and Use of Diversity Measures

    Clinical Genetics Lacks Standard Definitions and Protocols for the Collection and Use of Diversity Measures per Alice B. Popejoy, Kristy Crooks, Stephanie M. Fullerton, Lucia A. Hindorff, Gillian W. Hooker, Barbara A. Koenig, Natalie Pino, Erin M. Ramos, Deborah Ritter, Hannah Wand, Matt W. Wright, Michael Yudell, James Zou, Sharon E. Plon, Carlos D. Bustamante, Kelly E. Ormond

    Publicat 2020
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  18. 18
    Recommended nomenclature for five mammalian carboxylesterase gene families: human, mouse, and rat genes and proteins

    Recommended nomenclature for five mammalian carboxylesterase gene families: human, mouse, and rat genes and proteins per Roger S. Holmes, Matt W. Wright, Stanley J. F. Laulederkind, Laura A. Cox, Masakiyo Hosokawa, Teruko Imai, Shun Ishibashi, Richard Lehner, Masao Miyazaki, E.J. Perkins, Philip M. Potter, Matthew R. Redinbo, Jacques Robert, Tetsuo Satoh, Tetsuro Yamashita, Bingfan Yan, Tsuyoshi Yokoi, Rudolf Zechner, Lois J. Maltais

    Publicat 2010
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  19. 19
    ClinGen Allele Registry links information about genetic variants

    ClinGen Allele Registry links information about genetic variants per Piotr Pawliczek, Ronak Y. Patel, Lillian Ashmore, Andrew R. Jackson, Chris Bizon, Tristan Nelson, Bradford C. Powell, Robert R. Freimuth, Natasha T. Strande, Neethu Shah, Sameer Paithankar, Matt W. Wright, Selina S. Dwight, Jimmy Zhen, Melissa Landrum, Peter B. McGarvey, Lawrence Babb, Sharon E. Plon, Aleksandar Milosavljevic

    Publicat 2018
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  20. 20
    Unique aspects of sequence variant interpretation for inborn errors of metabolism (IEM): The ClinGen IEM Working Group and the Phenylalanine Hydroxylase Gene

    Unique aspects of sequence variant interpretation for inborn errors of metabolism (IEM): The ClinGen IEM Working Group and the Phenylalanine Hydroxylase Gene per Diane B. Zastrow, Heather Baudet, Wei Shen, Amanda Thomas‐Wilson, Yue Si, Meredith Weaver, Angela M. Lager, Jixia Liu, Rachel Mangels, Selina S. Dwight, Matt W. Wright, Steven F. Dobrowolski, Karen Eilbeck, Gregory M. Enns, Annette Feigenbaum, Uta Lichter‐Konecki, Elaine Lyon, Marzia Pasquali, Michael S. Watson, Nenad Blau, Robert D. Steiner, William J. Craigen, Rong Mao

    Publicat 2018
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