Michael Vincent Zaragoza

Title(s)Associate Professor, Pediatrics
SchoolSchool of Medicine
Address1001 Health Sciences Road
Irvine CA 92697-3950
Phone(949) 824-8813
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    Cardiac Functional and Structural Implications of Lamin A/C Mutations
    NIH R01HL129008Sep 4, 2015 - Apr 30, 2021
    Role: Co-Principal Investigator
    Mitochondrial Dysfunction &Noncompaction Cardiomyopathy
    NIH K08HL081222Sep 29, 2006 - Sep 30, 2011
    Role: Principal Investigator

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    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. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. A Study of Gene Expression, Structure, and Contractility of iPSC-Derived Cardiac Myocytes from a Family with Heart Disease due to LMNA Mutation. Ann Biomed Eng. 2021 Dec; 49(12):3524-3539. Mehrabi M, Morris TA, Cang Z, Nguyen CHH, Sha Y, Asad MN, Khachikyan N, Greene TL, Becker DM, Nie Q, Zaragoza MV, Grosberg A. PMID: 34585335; PMCID: PMC8671287.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    2. DNA methylation analysis reveals epimutation hotspots in patients with dilated cardiomyopathy-associated laminopathies. Clin Epigenetics. 2021 07 10; 13(1):139. Morival JLP, Widyastuti HP, Nguyen CHH, Zaragoza MV, Downing TL. PMID: 34246298; PMCID: PMC8272901.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    3. Gene expression profiling of fibroblasts in a family with LMNA-related cardiomyopathy reveals molecular pathways implicated in disease pathogenesis. BMC Med Genet. 2020 07 22; 21(1):152. Widyastuti HP, Norden-Krichmar TM, Grosberg A, Zaragoza MV. PMID: 32698886; PMCID: PMC7374820.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    4. The Effect of Cyclic Strain on Human Fibroblasts With Lamin A/C Mutations and Its Relation to Heart Disease. J Biomech Eng. 2020 06 01; 142(6). Tran RDH, Siemens M, Nguyen CHH, Ochs AR, Zaragoza MV, Grosberg A. PMID: 31233093; PMCID: PMC7104779.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    5. Databases to Efficiently Manage Medium Sized, Low Velocity, Multidimensional Data in Tissue Engineering. J Vis Exp. 2019 11 22; (153). Ochs AR, Mehrabi M, Becker D, Asad MN, Zhao J, Zaragoza MV, Grosberg A. PMID: 31814616; PMCID: PMC7156791.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    6. Age of heart disease presentation and dysmorphic nuclei in patients with LMNA mutations. PLoS One. 2017; 12(11):e0188256. Core JQ, Mehrabi M, Robinson ZR, Ochs AR, McCarthy LA, Zaragoza MV, Grosberg A. PMID: 29149195; PMCID: PMC5693421.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    7. 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). Zaragoza MV, Nguyen CHH, Widyastuti HP, McCarthy LA, Grosberg A. PMID: 29104234; PMCID: PMC5753070.
      View in: PubMed   Mentions: 3     Fields:    
    8. Heart-hand syndrome IV: a second family with LMNA-related cardiomyopathy and brachydactyly. Clin Genet. 2017 03; 91(3):499-500. Zaragoza MV, Hakim SA, Hoang V, Elliott AM. PMID: 27723096; PMCID: PMC5347894.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    9. 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. Zaragoza MV, Fung L, Jensen E, Oh F, Cung K, McCarthy LA, Tran CK, Hoang V, Hakim SA, Grosberg A. PMID: 27182706; PMCID: PMC4868298.
      View in: PubMed   Mentions: 21     Fields:    Translation:HumansCells
    10. Deletion Xq27.3q28 in female patient with global developmental delays and skewed X-inactivation. BMC Med Genet. 2013 May 01; 14:49. Marshall LS, Simon J, Wood T, Peng M, Owen R, Feldman GS, Zaragoza MV. PMID: 23634718; PMCID: PMC3643848.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansCells
    11. 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. 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. PMID: 23401503; PMCID: PMC3587196.
      View in: PubMed   Mentions: 55     Fields:    Translation:Humans
    12. 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. Ronvelia D, Greenwood J, Platt J, Hakim S, Zaragoza MV. PMID: 23031367; PMCID: PMC3483384.
      View in: PubMed   Mentions: 25     Fields:    Translation:Humans
    13. 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. Narula N, Zaragoza MV, Sengupta PP, Li P, Haider N, Verjans J, Waymire K, Vannan M, Wallace DC. PMID: 21232697; PMCID: PMC4023693.
      View in: PubMed   Mentions: 35     Fields:    Translation:AnimalsCells
    14. 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. Zaragoza MV, Brandon MC, Diegoli M, Arbustini E, Wallace DC. PMID: 20978534; PMCID: PMC3025796.
      View in: PubMed   Mentions: 29     Fields:    Translation:HumansCells
    15. Mitochondrial DNA variant discovery and evaluation in human Cardiomyopathies through next-generation sequencing. PLoS One. 2010 Aug 20; 5(8):e12295. Zaragoza MV, Fass J, Diegoli M, Lin D, Arbustini E. PMID: 20808834; PMCID: PMC2924892.
      View in: PubMed   Mentions: 31     Fields:    Translation:HumansCells
    16. Infantile systemic hyalinosis: Case report and review of the literature. J Am Acad Dermatol. 2008 Feb; 58(2):303-7. Lindvall LE, Kormeili T, Chen E, Ramirez MC, Grum-Tokars V, Glucksman MJ, Martignetti JA, Zaragoza MV, Dyson SW. PMID: 18222328.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    17. Noncompaction of the left ventricle: primary cardiomyopathy with an elusive genetic etiology. Curr Opin Pediatr. 2007 Dec; 19(6):619-27. Zaragoza MV, Arbustini E, Narula J. PMID: 18025927.
      View in: PubMed   Mentions: 31     Fields:    Translation:Humans
    18. 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. Pop R, Zaragoza MV, Gaudette M, Dohrmann U, Scherer G. PMID: 15806394.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
    19. Identification of the TBX5 transactivating domain and the nuclear localization signal. Gene. 2004 Apr 14; 330:9-18. Zaragoza MV, Lewis LE, Sun G, Wang E, Li L, Said-Salman I, Feucht L, Huang T. PMID: 15087119.
      View in: PubMed   Mentions: 26     Fields:    Translation:HumansAnimalsCells
    20. 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. Zaragoza MV, Surti U, Redline RW, Millie E, Chakravarti A, Hassold TJ. PMID: 10801385; PMCID: PMC1378061.
      View in: PubMed   Mentions: 59     Fields:    Translation:HumansCells
    21. 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. Zaragoza MV, Millie E, Redline RW, Hassold TJ. PMID: 9832040; PMCID: PMC1051486.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    22. Cytogenetic analysis of spontaneous abortions: comparison of techniques and assessment of the incidence of confined placental mosaicism. Am J Med Genet. 1997 Oct 31; 72(3):297-301. Griffin DK, Millie EA, Redline RW, Hassold TJ, Zaragoza MV. PMID: 9332658.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    23. Nondisjunction of human acrocentric chromosomes: studies of 432 trisomic fetuses and liveborns. Hum Genet. 1994 Oct; 94(4):411-7. Zaragoza MV, Jacobs PA, James RS, Rogan P, Sherman S, Hassold T. PMID: 7927339.
      View in: PubMed   Mentions: 25     Fields:    Translation:HumansCells
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