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    Hayes, Ian

    TitleUC GSRA
    SchoolLawrence Berkeley National Lab
    DepartmentMaterials Sciences
    Address1 Cyclotron Road
    Berkeley CA 94720
    vCardDownload vCard

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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.
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      1. Di Gioia SA, Connors S, Matsunami N, Cannavino J, Rose MF, Gilette NM, Artoni P, de Macena Sobreira NL, Chan WM, Webb BD, Robson CD, Cheng L, Van Ryzin C, Ramirez-Martinez A, Mohassel P, Leppert M, Scholand MB, Grunseich C, Ferreira CR, Hartman T, Hayes I, Morgan T, Markie DM, Fagiolini M, Swift A, Chines PS, Speck-Martins CE, Collins FS, Jabs EW, Bönnemann CG, Olson EN, Carey JC, Robertson SP, Manoli I, Engle EC. A defect in myoblast fusion underlies Carey-Fineman-Ziter syndrome. Nat Commun. 2017 Jul 06; 8:16077. PMID: 28681861.
        View in: PubMed
      2. Low K, Ashraf T, Canham N, Clayton-Smith J, Deshpande C, Donaldson A, Fisher R, Flinter F, Foulds N, Fryer A, Gibson K, Hayes I, Hills A, Holder S, Irving M, Joss S, Kivuva E, Lachlan K, Magee A, McConnell V, McEntagart M, Metcalfe K, Montgomery T, Newbury-Ecob R, Stewart F, Turnpenny P, Vogt J, Fitzpatrick D, Williams M, Smithson S. Clinical and genetic aspects of KBG syndrome. Am J Med Genet A. 2016 Nov; 170(11):2835-2846. PMID: 27667800.
        View in: PubMed
      3. Coman DJ, Hayes I, Collins V, Sahhar M, Wraith JE, Delatycki MB. Enzyme replacement therapy and extended newborn screening for mucopolysaccharidoses: opinions of treating physicians. JIMD Rep. 2011; 1:9-15. PMID: 23430821; PMCID: PMC3509829.
      4. Goudie DR, D'Alessandro M, Merriman B, Lee H, Szeverényi I, Avery S, O'Connor BD, Nelson SF, Coats SE, Stewart A, Christie L, Pichert G, Friedel J, Hayes I, Burrows N, Whittaker S, Gerdes AM, Broesby-Olsen S, Ferguson-Smith MA, Verma C, Lunny DP, Reversade B, Lane EB. Multiple self-healing squamous epithelioma is caused by a disease-specific spectrum of mutations in TGFBR1. Nat Genet. 2011 Feb 27; 43(4):365-9. PMID: 21358634.
        View in: PubMed
      5. George A, Marquis-Nicholson R, Zhang LT, Love JM, Ashton F, Aftimos S, Hayes I, Williams LC, Love DR. Chromosome microarray analysis in a clinical environment: new perspective and new challenge. Br J Biomed Sci. 2011; 68(2):100-8. PMID: 21706924.
        View in: PubMed
      6. Marquis-Nicholson R, Aftimos S, Hayes I, George A, Love DR. Array comparative genomic hybridisation: a new tool in the diagnostic genetic armoury. N Z Med J. 2010 Jul 16; 123(1318):50-61. PMID: 20651866.
        View in: PubMed
      7. Hoischen A, van Bon BW, Gilissen C, Arts P, van Lier B, Steehouwer M, de Vries P, de Reuver R, Wieskamp N, Mortier G, Devriendt K, Amorim MZ, Revencu N, Kidd A, Barbosa M, Turner A, Smith J, Oley C, Henderson A, Hayes I, Thompson EM, Brunner HG, de Vries BB, Veltman JA. De novo mutations of SETBP1 cause Schinzel-Giedion syndrome. Nat Genet. 2010 Jun; 42(6):483-5. PMID: 20436468.
        View in: PubMed
      8. Hayes I, Perry D, Aftimos S. Fryns-Aftimos syndrome with milder clinical manifestations. Clin Dysmorphol. 2009 Apr; 18(2):95-7. PMID: 19449464.
        View in: PubMed
      9. Al-Mudaffer M, Oley C, Price S, Hayes I, Stewart A, Hall CM, Reardon W. Clinical and radiological findings in Schinzel-Giedion syndrome. Eur J Pediatr. 2008 Dec; 167(12):1399-407. PMID: 18461363.
        View in: PubMed
      10. Coman DJ, Hayes I, Collins V, Sahhar M, Wraith JE, Delatycki MB. Enzyme replacement therapy for mucopolysaccharidoses: opinions of patients and families. J Pediatr. 2008 May; 152(5):723-7. PMID: 18410781.
        View in: PubMed
      11. Hayes I, Collins V, Sahhar M, Wraith JE, Delatycki MB. Newborn screening for mucopolysaccharidoses: opinions of patients and their families. Clin Genet. 2007 May; 71(5):446-50. PMID: 17489850.
        View in: PubMed
      12. Kannu P, Hayes I, Mandelstam S, Donnan L, Savarirayan R. Medial temporal lobe dysgenesis in hypochondroplasia. Am J Med Genet A. 2005 Nov 01; 138(4):389-91. PMID: 16222682.
        View in: PubMed
      13. Hayes I, Varigos G, Upjohn EJ, Orchard DC, Penny DJ, Savarirayan R. Unilateral acheiria and fatal primary pulmonary hypertension in a girl with incontinentia pigmenti. Am J Med Genet A. 2005 Jun 15; 135(3):302-3. PMID: 15884011.
        View in: PubMed

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