Search Results - 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 by Matt W. Wright

    Published 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 by Matt W. Wright, Elspeth A. Bruford

    Published 2011
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  3. 3
    New Nomenclature for Mammalian BSP Genes1

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

    Published 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 by Kristian Gray, Ruth L. Seal, Susan Tweedie, Matt W. Wright, Elspeth A. Bruford

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

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

    Published 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 by Elspeth A. Bruford, Michael Lush, Matt W. Wright, Tam P. Sneddon, S. Povey, Ewan Birney

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

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

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

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

    Published 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 by Mary C. Hunt, Junji Yamada, Lois J. Maltais, Matt W. Wright, Ernesto J. Podestá, Stefan E.H. Alexson

    Published 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 by Emma H. Wilcox, Mahdi Sarmady, Bryan Wulf, Matt W. Wright, Heidi L. Rehm, Leslie G. Biesecker, Ahmad Abou Tayoun

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

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

    Published 2013
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  12. 12
    New consensus nomenclature for mammalian keratins

    New consensus nomenclature for mammalian keratins by 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

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

    An Updated Nomenclature for Keratin-Associated Proteins (KAPs) by 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

    Published 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 by 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

    Published 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 by 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

    Published 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 by 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

    Published 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 by 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

    Published 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 by 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

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

    ClinGen Allele Registry links information about genetic variants by 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

    Published 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 by 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

    Published 2018
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