Zaragoza, Michael Vincent

Title(s)Associate Professor, Pediatrics
Phone(949) 824-8813
vCardDownload vCard

    Collapse Research 
    Collapse Research Activities and Funding
    Cardiac Functional and Structural Implications of Lamin A/C Mutations
    NIH/NHLBI R01HL129008Sep 4, 2015 - Apr 30, 2020
    Role: Co-Principal Investigator
    Mitochondrial Dysfunction &Noncompaction Cardiomyopathy
    NIH/NHLBI K08HL081222Sep 29, 2006 - Sep 30, 2011
    Role: Principal Investigator

    Collapse ORNG Applications 
    Collapse Clinical Trials

    Collapse Bibliographic 
    Collapse Publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help.
    List All   |   Timeline
    1. Tran RD, Siemens M, Nguyen CHH, Ochs AR, Zaragoza MV, Grosberg A. The Effect of Cyclic Strain on Human Fibroblasts with Lamin A/C Mutations and Its Relation to Heart Disease. J Biomech Eng. 2019 Jun 24. PMID: 31233093.
      View in: PubMed
    2. Core JQ, Mehrabi M, Robinson ZR, Ochs AR, McCarthy LA, Zaragoza MV, Grosberg A. Age of heart disease presentation and dysmorphic nuclei in patients with LMNA mutations. PLoS One. 2017; 12(11):e0188256. PMID: 29149195.
      View in: PubMed
    3. Zaragoza MV, Nguyen CHH, Widyastuti HP, McCarthy LA, Grosberg A. Dupuytren's and Ledderhose Diseases in a Family with LMNA-Related Cardiomyopathy and a Novel Variant in the ASTE1 Gene. Cells. 2017 Nov 01; 6(4). PMID: 29104234.
      View in: PubMed
    4. Zaragoza MV, Hakim SA, Hoang V, Elliott AM. Heart-hand syndrome IV: a second family with LMNA-related cardiomyopathy and brachydactyly. Clin Genet. 2017 03; 91(3):499-500. PMID: 27723096.
      View in: PubMed
    5. Zaragoza MV, Fung L, Jensen E, Oh F, Cung K, McCarthy LA, Tran CK, Hoang V, Hakim SA, Grosberg A. Exome Sequencing Identifies a Novel LMNA Splice-Site Mutation and Multigenic Heterozygosity of Potential Modifiers in a Family with Sick Sinus Syndrome, Dilated Cardiomyopathy, and Sudden Cardiac Death. PLoS One. 2016; 11(5):e0155421. PMID: 27182706.
      View in: PubMed
    6. Marshall LS, Simon J, Wood T, Peng M, Owen R, Feldman GS, Zaragoza MV. Deletion Xq27.3q28 in female patient with global developmental delays and skewed X-inactivation. BMC Med Genet. 2013 May 01; 14:49. PMID: 23634718.
      View in: PubMed
    7. Strauss KA, DuBiner L, Simon M, Zaragoza M, Sengupta PP, Li P, Narula N, Dreike S, Platt J, Procaccio V, Ortiz-González XR, Puffenberger EG, Kelley RI, Morton DH, Narula J, Wallace DC. Severity of cardiomyopathy associated with adenine nucleotide translocator-1 deficiency correlates with mtDNA haplogroup. Proc Natl Acad Sci U S A. 2013 Feb 26; 110(9):3453-8. PMID: 23401503.
      View in: PubMed
    8. Ronvelia D, Greenwood J, Platt J, Hakim S, Zaragoza MV. Intrafamilial variability for novel TAZ gene mutation: Barth syndrome with dilated cardiomyopathy and heart failure in an infant and left ventricular noncompaction in his great-uncle. Mol Genet Metab. 2012 Nov; 107(3):428-32. PMID: 23031367; PMCID: PMC3483384.
    9. Narula N, Zaragoza MV, Sengupta PP, Li P, Haider N, Verjans J, Waymire K, Vannan M, Wallace DC. Adenine nucleotide translocase 1 deficiency results in dilated cardiomyopathy with defects in myocardial mechanics, histopathological alterations, and activation of apoptosis. JACC Cardiovasc Imaging. 2011 Jan; 4(1):1-10. PMID: 21232697.
      View in: PubMed
    10. Zaragoza MV, Brandon MC, Diegoli M, Arbustini E, Wallace DC. Mitochondrial cardiomyopathies: how to identify candidate pathogenic mutations by mitochondrial DNA sequencing, MITOMASTER and phylogeny. Eur J Hum Genet. 2011 Feb; 19(2):200-7. PMID: 20978534; PMCID: PMC3025796.
    11. Zaragoza MV, Fass J, Diegoli M, Lin D, Arbustini E. Mitochondrial DNA variant discovery and evaluation in human Cardiomyopathies through next-generation sequencing. PLoS One. 2010 Aug 20; 5(8):e12295. PMID: 20808834.
      View in: PubMed
    12. Lindvall LE, Kormeili T, Chen E, Ramirez MC, Grum-Tokars V, Glucksman MJ, Martignetti JA, Zaragoza MV, Dyson SW. Infantile systemic hyalinosis: Case report and review of the literature. J Am Acad Dermatol. 2008 Feb; 58(2):303-7. PMID: 18222328.
      View in: PubMed
    13. Zaragoza MV, Arbustini E, Narula J. Noncompaction of the left ventricle: primary cardiomyopathy with an elusive genetic etiology. Curr Opin Pediatr. 2007 Dec; 19(6):619-27. PMID: 18025927.
      View in: PubMed
    14. Pop R, Zaragoza MV, Gaudette M, Dohrmann U, Scherer G. A homozygous nonsense mutation in SOX9 in the dominant disorder campomelic dysplasia: a case of mitotic gene conversion. Hum Genet. 2005 Jun; 117(1):43-53. PMID: 15806394.
      View in: PubMed
    15. Zaragoza MV, Lewis LE, Sun G, Wang E, Li L, Said-Salman I, Feucht L, Huang T. Identification of the TBX5 transactivating domain and the nuclear localization signal. Gene. 2004 Apr 14; 330:9-18. PMID: 15087119.
      View in: PubMed
    16. Zaragoza MV, Surti U, Redline RW, Millie E, Chakravarti A, Hassold TJ. Parental origin and phenotype of triploidy in spontaneous abortions: predominance of diandry and association with the partial hydatidiform mole. Am J Hum Genet. 2000 Jun; 66(6):1807-20. PMID: 10801385.
      View in: PubMed
    17. Zaragoza MV, Millie E, Redline RW, Hassold TJ. Studies of non-disjunction in trisomies 2, 7, 15, and 22: does the parental origin of trisomy influence placental morphology? J Med Genet. 1998 Nov; 35(11):924-31. PMID: 9832040.
      View in: PubMed
    18. Zaragoza MV, Jacobs PA, James RS, Rogan P, Sherman S, Hassold T. Nondisjunction of human acrocentric chromosomes: studies of 432 trisomic fetuses and liveborns. Hum Genet. 1994 Oct; 94(4):411-7. PMID: 7927339.
      View in: PubMed
    Michael's Networks
    Derived automatically from this person's publications.
    People in Profiles who have published with this person.
    Similar People
    People who share similar concepts with this person.
    Same Department