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    Miles Thompson

    TitleAssistant Project Scientist
    SchoolUniversity of California, San Diego
    DepartmentPediatrics
    Address9500 Gilman Drive #0830
    CA La Jolla 92093
    vCardDownload vCard

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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. Thompson M, Capra V, Clunes MT, Rovati GE, Stankova J, Maj MC, Duffy DL. Cysteinyl Leukotrienes Pathway Genes, Atopic Asthma and Drug Response: From Population Isolates to Large Genome-Wide Association Studies. Front Pharmacol. 2016; 7:299. PMID: 27990118.
        View in: PubMed
      2. Thompson M, Cole DE. Recessive PIGN Mutations in Fryns Syndrome: Evidence for Genetic Heterogeneity. Hum Mutat. 2016 Jul; 37(7):621. PMID: 27300081.
        View in: PubMed
      3. Knaus A, Awaya T, Helbig I, Afawi Z, Pendziwiat M, Abu-Rachma J, Thompson M, Cole DE, Skinner S, Annese F, Canham N, Schweiger MR, Robinson PN, Mundlos S, Kinoshita T, Munnich A, Murakami Y, Horn D, Krawitz PM. Rare Noncoding Mutations Extend the Mutational Spectrum in the PGAP3 Subtype of Hyperphosphatasia with Mental Retardation Syndrome. Hum Mutat. 2016 Aug; 37(8):737-44. PMID: 27120253.
        View in: PubMed
      4. Yaddaden L, Véronneau S, Thompson M, Rola-Pleszczynski M, Stankova J. Cellular signalling of cysteinyl leukotriene type 1 receptor variants CysLT1-G300S and CysLT1-I206S. Prostaglandins Leukot Essent Fatty Acids. 2016 Feb; 105:1-8. PMID: 26869085.
        View in: PubMed
      5. Thompson M, Kenna GA. Variation in the Serotonin Transporter Gene and Alcoholism: Risk and Response to Pharmacotherapy. Alcohol Alcohol. 2016 Mar; 51(2):164-71. PMID: 26311211; PMCID: PMC4755552 [Available on 03/01/17].
      6. Cole DE, Thompson M. Neurogenetic Aspects of Hyperphosphatasia in Mabry Syndrome. Subcell Biochem. 2015; 76:343-61. PMID: 26219719.
        View in: PubMed
      7. Thompson M, Xhaard H, Sakurai T, Rainero I, Kukkonen JP. OX1 and OX2 orexin/hypocretin receptor pharmacogenetics. Front Neurosci. 2014; 8:57. PMID: 24834023; PMCID: PMC4018553.
      8. Thompson M, Cole DE, Capra V, Siminovitch KA, Rovati GE, Burnham WM, Rana BK. Pharmacogenetics of the g protein-coupled receptors. Methods Mol Biol. 2014; 1175:189-242. PMID: 25150871.
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      9. Thompson M, Cole DE, Jose PA, Chidiac P. G protein-coupled receptor accessory proteins and signaling: pharmacogenomic insights. Methods Mol Biol. 2014; 1175:121-52. PMID: 25150869.
        View in: PubMed
      10. Thompson M, Hendy GN, Percy ME, Bichet DG, Cole DE. G protein-coupled receptor mutations and human genetic disease. Methods Mol Biol. 2014; 1175:153-87. PMID: 25150870.
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      11. Krawitz PM, Murakami Y, Hecht J, Krüger U, Holder SE, Mortier GR, Delle Chiaie B, De Baere E, Thompson M, Roscioli T, Kielbasa S, Kinoshita T, Mundlos S, Robinson PN, Horn D. Mutations in PIGO, a member of the GPI-anchor-synthesis pathway, cause hyperphosphatasia with mental retardation. Am J Hum Genet. 2012 Jul 13; 91(1):146-51. PMID: 22683086; PMCID: PMC3397269.
      12. Thompson M, Roscioli T, Marcelis C, Nezarati MM, Stolte-Dijkstra I, Sharom FJ, Lu P, Phillips JA, Sweeney E, Robinson PN, Krawitz P, Yntema HG, Andrade DM, Brunner HG, Cole DE. Phenotypic variability in hyperphosphatasia with seizures and neurologic deficit (Mabry syndrome). Am J Med Genet A. 2012 Mar; 158A(3):553-8. PMID: 22315194.
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      13. Thompson M, Noble-Topham S, Percy ME, Andrade DM, Ebers GC. Chromosome 1p36 in migraine with aura: association study of the 5HT(1D) locus. Neuroreport. 2012 Jan 04; 23(1):45-8. PMID: 22107845.
        View in: PubMed
      14. Krawitz PM, Schweiger MR, Rödelsperger C, Marcelis C, Kölsch U, Meisel C, Stephani F, Kinoshita T, Murakami Y, Bauer S, Isau M, Fischer A, Dahl A, Kerick M, Hecht J, Köhler S, Jäger M, Grünhagen J, de Condor BJ, Doelken S, Brunner HG, Meinecke P, Passarge E, Thompson M, Cole DE, Horn D, Roscioli T, Mundlos S, Robinson PN. Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome. Nat Genet. 2010 Oct; 42(10):827-9. PMID: 20802478.
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      15. Thompson M, Nezarati MM, Gillessen-Kaesbach G, Meinecke P, Mendoza-Londono R, Mendoza R, Mornet E, Brun-Heath I, Squarcioni CP, Legeai-Mallet L, Munnich A, Cole DE. Hyperphosphatasia with seizures, neurologic deficit, and characteristic facial features: Five new patients with Mabry syndrome. Am J Med Genet A. 2010 Jul; 152A(7):1661-9. PMID: 20578257.
        View in: PubMed
      16. Thompson M, Cole DE, Ray JG. Vitamin B-12 and neural tube defects: the Canadian experience. Am J Clin Nutr. 2009 Feb; 89(2):697S-701S. PMID: 19116334.
        View in: PubMed
      17. Thompson M, Cole DE, Jose PA. Pharmacogenomics of G protein-coupled receptor signaling: insights from health and disease. Methods Mol Biol. 2008; 448:77-107. PMID: 18370232.
        View in: PubMed
      18. Thompson M, Percy ME, McIntyre Burnham W, Cole DE. G protein-coupled receptors disrupted in human genetic disease. Methods Mol Biol. 2008; 448:109-37. PMID: 18370233.
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      19. Thompson M, Siminovitch KA, Cole DE. G protein-coupled receptor pharmacogenetics. Methods Mol Biol. 2008; 448:139-85. PMID: 18370234.
        View in: PubMed
      20. Ray JG, Thompson M, Vermeulen MJ, Meier C, Wyatt PR, Wong PY, Summers AM, Farrell SA, Cole DE. Metabolic syndrome features and risk of neural tube defects. BMC Pregnancy Childbirth. 2007 Sep 19; 7:21. PMID: 17880716; PMCID: PMC2039731.
      21. Capra V, Thompson M, Sala A, Cole DE, Folco G, Rovati GE. Cysteinyl-leukotrienes and their receptors in asthma and other inflammatory diseases: critical update and emerging trends. Med Res Rev. 2007 Jul; 27(4):469-527. PMID: 16894531.
        View in: PubMed
      22. Thompson M, Capra V, Takasaki J, Maresca G, Rovati GE, Slutsky AS, Lilly C, Zamel N, McIntyre Burnham W, Cole DE, Siminovitch KA. A functional G300S variant of the cysteinyl leukotriene 1 receptor is associated with atopy in a Tristan da Cunha isolate. Pharmacogenet Genomics. 2007 Jul; 17(7):539-49. PMID: 17558309.
        View in: PubMed
      23. Ray JG, Wyatt PR, Thompson M, Vermeulen MJ, Meier C, Wong PY, Farrell SA, Cole DE. Vitamin B12 and the risk of neural tube defects in a folic-acid-fortified population. Epidemiology. 2007 May; 18(3):362-6. PMID: 17474166.
        View in: PubMed
      24. Thompson M, Killoran A, Percy ME, Nezarati M, Cole DE, Hwang PA. Hyperphosphatasia with neurologic deficit: a pyridoxine-responsive seizure disorder? Pediatr Neurol. 2006 Apr; 34(4):303-7. PMID: 16638507.
        View in: PubMed
      25. Thompson M, Takasaki J, Capra V, Rovati GE, Siminovitch KA, Burnham WM, Hudson TJ, Bossé Y, Cole DE. G-protein-coupled receptors and asthma endophenotypes: the cysteinyl leukotriene system in perspective. Mol Diagn Ther. 2006; 10(6):353-66. PMID: 17154652.
        View in: PubMed
      26. Thompson M, Burnham WM, Cole DE. The G protein-coupled receptors: pharmacogenetics and disease. Crit Rev Clin Lab Sci. 2005; 42(4):311-92. PMID: 16281738.
        View in: PubMed
      27. Thompson M, Bowen RA, Wong BY, Antal J, Liu Z, Yu H, Siminovitch K, Kreiger N, Rohan TE, Cole DE. Whole genome amplification of buccal cell DNA: genotyping concordance before and after multiple displacement amplification. Clin Chem Lab Med. 2005; 43(2):157-62. PMID: 15843209.
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      28. Thompson M, Comings DE, Abu-Ghazalah R, Jereseh Y, Lin L, Wade J, Sakurai T, Tokita S, Yoshida T, Tanaka H, Yanagisawa M, Burnham WM, Moldofsky H. Variants of the orexin2/hcrt2 receptor gene identified in patients with excessive daytime sleepiness and patients with Tourette's syndrome comorbidity. Am J Med Genet B Neuropsychiatr Genet. 2004 Aug 15; 129B(1):69-75. PMID: 15274044.
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      29. Thompson M, Storm van's Gravesande K, Galczenski H, Burnham WM, Siminovitch KA, Zamel N, Slutsky A, Drazen JM, George SR, Evans JF, O'Dowd BF. A cysteinyl leukotriene 2 receptor variant is associated with atopy in the population of Tristan da Cunha. Pharmacogenetics. 2003 Oct; 13(10):641-9. PMID: 14515063.
        View in: PubMed
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