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    Iris Gonzalez, MSW

    TitleAdjunct Associate Professor, Dept. of Adults and Healthy Aging
    SchoolSchool of Social Work
    DepartmentSocial Work
    AddressOCC 2300 Michelson Dr, Irvine
    Off Campus
    Los Angeles California 90089-0411
    Phone+1 949 437 0043
    vCardDownload vCard

      Collapse Bibliographic 
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      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.
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      1. Kirwin SM, Manolakos A, Barnett SS, Gonzalez I. Tafazzin splice variants and mutations in Barth syndrome. Mol Genet Metab. 2014 Jan; 111(1):26-32. PMID: 24342716.
        View in: PubMed
      2. Kirwin SM, Vinette KM, Gonzalez I, Abdulwahed HA, Al-Sannaa N, Funanage VL. A homozygous double mutation in SMN1: a complicated genetic diagnosis of SMA. Mol Genet Genomic Med. 2013 Jul; 1(2):113-7. PMID: 24498607.
        View in: PubMed
      3. Fan Y, Steller J, Gonzalez I, Kulik W, Fox M, Chang R, Westerfield BA, Batra AS, Wang RY, Gallant NM, Pena LS, Wang H, Huang T, Bhuta S, Penny DJ, McCabe ER, Kimonis VE. A Novel Exonic Splicing Mutation in the TAZ (G4.5) Gene in a Case with Atypical Barth Syndrome. JIMD Rep. 2013; 11:99-106. PMID: 23606313.
        View in: PubMed
      4. Clarke SL, Bowron A, Gonzalez I, Groves SJ, Newbury-Ecob R, Clayton N, Martin RP, Tsai-Goodman B, Garratt V, Ashworth M, Bowen VM, McCurdy KR, Damin MK, Spencer CT, Toth MJ, Kelley RI, Steward CG. Barth syndrome. Orphanet J Rare Dis. 2013; 8:23. PMID: 23398819.
        View in: PubMed
      5. Steward CG, Newbury-Ecob RA, Hastings R, Smithson SF, Tsai-Goodman B, Quarrell OW, Kulik W, Wanders R, Pennock M, Williams M, Cresswell JL, Gonzalez I, Brennan P. Barth syndrome: an X-linked cause of fetal cardiomyopathy and stillbirth. Prenat Diagn. 2010 Oct; 30(10):970-6. PMID: 20812380.
        View in: PubMed
      6. Kirwin SM, Vinette KM, Schwartz SB, Funanage VL, Gonzalez I. Multiple transmissions of Barth syndrome through an oocyte donor with a de novo TAZ mutation. Fertil Steril. 2007 Apr; 87(4):976.e5-7. PMID: 17241629.
        View in: PubMed
      7. Sol-Church K, Stabley DL, Nicholson L, Gonzalez I, Gripp KW. Paternal bias in parental origin of HRAS mutations in Costello syndrome. Hum Mutat. 2006 Aug; 27(8):736-41. PMID: 16835863.
        View in: PubMed
      8. Spencer CT, Bryant RM, Day J, Gonzalez I, Colan SD, Thompson WR, Berthy J, Redfearn SP, Byrne BJ. Cardiac and clinical phenotype in Barth syndrome. Pediatrics. 2006 Aug; 118(2):e337-46. PMID: 16847078.
        View in: PubMed
      9. Gripp KW, Lin AE, Stabley DL, Nicholson L, Scott CI, Doyle D, Aoki Y, Matsubara Y, Zackai EH, Lapunzina P, Gonzalez-Meneses A, Holbrook J, Agresta CA, Gonzalez I, Sol-Church K. HRAS mutation analysis in Costello syndrome: genotype and phenotype correlation. Am J Med Genet A. 2006 Jan 1; 140(1):1-7. PMID: 16329078.
        View in: PubMed
      10. Gonzalez I. Barth syndrome: TAZ gene mutations, mRNAs, and evolution. Am J Med Genet A. 2005 May 1; 134(4):409-14. PMID: 15793838.
        View in: PubMed
      11. Doyle DA, Gonzalez I, Thomas B, Scavina M. Autosomal dominant transmission of congenital hypothyroidism, neonatal respiratory distress, and ataxia caused by a mutation of NKX2-1. J Pediatr. 2004 Aug; 145(2):190-3. PMID: 15289765.
        View in: PubMed
      12. Frisch R, Singleton KR, Moses PA, Gonzalez I, Carango P, Marks HG, Funanage VL. Effect of triplet repeat expansion on chromatin structure and expression of DMPK and neighboring genes, SIX5 and DMWD, in myotonic dystrophy. Mol Genet Metab. 2001 Sep-Oct; 74(1-2):281-91. PMID: 11592825.
        View in: PubMed
      13. Gonzalez I, Sylvester JE. Human rDNA: evolutionary patterns within the genes and tandem arrays derived from multiple chromosomes. Genomics. 2001 May 1; 73(3):255-63. PMID: 11350117.
        View in: PubMed
      14. Gonzalez I, Sylvester JE. Beyond ribosomal DNA: on towards the telomere. Chromosoma. 1997 Jun; 105(7-8):431-7. PMID: 9211970.
        View in: PubMed