Iris Gonzalez, MSW

TitleSenior Lecturer of Social Work, Dept. of Adult Mental Health and Wellness
InstitutionUniversity of Southern California
DepartmentSocial Work
AddressOCC 2300 Michelson Dr, Irvine
University Park Campus
Los Angeles CA 90089-0411
Phone+1 949 437 0043
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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; PMCID: PMC3865576.
    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; PMCID: PMC3755548.
    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 Feb 12; 8:23. PMID: 23398819; PMCID: PMC3583704.
    5. 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
    6. 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
    7. 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
    8. 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 01; 140(1):1-7. PMID: 16329078.
      View in: PubMed
    9. Gonzalez I. Barth syndrome: TAZ gene mutations, mRNAs, and evolution. Am J Med Genet A. 2005 May 01; 134(4):409-14. PMID: 15793838.
      View in: PubMed
    10. 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
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