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Matthew Taylor

InstitutionUniversity of Colorado Denver - Anschutz Medical Campus

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    Our research interests are in the genetic basis of hereditary cardiomyopathies, with a current focus on arrhythmogenic forms of dilated cardiomyopathy. We have ongoing projects in our molecular genetics lab in RC2 and also have some clinical-phenotyping database mining projects. I will be serving as a cardiology mentor for the 2018-2019 academic year.

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    K23HL067915     (TAYLOR, MATTHEW R)Sep 13, 2002 - Feb 29, 2008
    Familial Dilated Cardiomyopathy:Genetic Characterization
    Role: Principal Investigator

    R01HL109209     (TAYLOR, MATTHEW R)Apr 1, 2012 - Feb 28, 2017
    Whole genome DNA sequencing to identify novel genes in dilated cardiomyopathy
    Role: Principal Investigator

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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    1. Taylor M, Graw S, Sinagra G, Barnes C, Slavov D, Brun F, Pinamonti B, Salcedo EE, Sauer W, Pyxaras S, Anderson B, Simon B, Bogomolovas J, Labeit S, Granzier H, Mestroni L. Genetic variation in titin in arrhythmogenic right ventricular cardiomyopathy-overlap syndromes. Circulation. 2011 Aug 23; 124(8):876-85. PMID: 21810661.
      View in: PubMed
    2. Taylor MR, Jirikowic J, Wells C, Springer M, McGavran L, Lunt B, Swisshelm K. High prevalence of array comparative genomic hybridization abnormalities in adults with unexplained intellectual disability. Genet Med. 2010 Jan; 12(1):32-8. PMID: 20009761.
      View in: PubMed
    3. Taylor MR, Slavov D, Humphrey K, Zhao L, Cockroft J, Zhu X, Lavori P, Bristow MR, Mestroni L, Lazzeroni LC. Pharmacogenetic effect of an endothelin-1 haplotype on response to bucindolol therapy in chronic heart failure. Pharmacogenet Genomics. 2009 Jan; 19(1):35-43. PMID: 18953265.
      View in: PubMed
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