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Research

Dr Matt Hodges

Part-time Laboratory Safety Officer, Physiological Services Facility Manager

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  1. 2008
  2. Published

    Systemic aminoglycoside treatment in rodent models of retinitis pigmentosa

    Guerin, K., Gregory-Evans, C. Y., Hodges, M., Moosajee, M., Mackay, D. S., Gregory-Evans, K. & Flannery, J. G., 09/2008, In: Experimental Eye Research. 87, 3, p. 197-207 11 p.

    Research output: Contribution to Journal/Magazine › Journal article › peer-review

  3. Published

    A clearer view of stem cells in retinal disease

    Hodges, M., Gregory-Evans, C. Y. & Gregory-Evans, K., 2008, Stem cell repair and regeneration. Leviécar, N., Habib, N. A., Gordon, M. Y. & Dimarakis, I. (eds.). London: Imperial College Press, Vol. 3. p. 227-245 19 p.

    Research output: Contribution in Book/Report/Proceedings - With ISBN/ISSN › Chapter

  4. 2007
  5. Published

    SNP genome scanning localizes oto-dental syndrome to chromosome 11q13 and microdeletions at this locus implicate FGF3 in dental and inner-ear disease and FADD in ocular coloboma.

    Gregory-Evans, C. Y., Moosajee, M., Hodges, M., Mackay, D. S., Game, L., Vargesson, N., Bloch-Zupan, A., Rüschendorf, F., Santos-Pintos, L., Wackens, G. & Gregory-Evans, K., 2007, In: Human Molecular Genetics. 16, 20, p. 2482-2493 12 p.

    Research output: Contribution to Journal/Magazine › Journal article › peer-review

  6. 2006
  7. Published

    Evaluation of deletions in 7q11.2 and 8p12-p21 as prognostic indicators of tumour development following molar pregnancy

    Burke, B., Sebire, N. J., Moss, J., Hodges, M., Seckl, M. J., Newlands, E. S. & Fisher, R. A., 11/2006, In: Gynecologic Oncology. 103, 2, p. 642-648 7 p.

    Research output: Contribution to Journal/Magazine › Journal article › peer-review

  8. Published

    Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans

    Aitman, T. J., Dong, R., Vyse, T. J., Norsworthy, P. J., Johnson, M. D., Smith, J., Mangion, J., Roberton-Lowe, C., Marshall, A. J., Petretto, E., Hodges, M., Bhangal, G., Patel, S. G., Sheehan-Rooney, K., Duda, M., Cook, P. R., Evans, D. J., Domin, J., Flint, J. & Boyle, J. J. & 2 others, Pusey, C. D. & Cook, H. T., 16/02/2006, In: Nature. 439, p. 851-855 5 p.

    Research output: Contribution to Journal/Magazine › Journal article › peer-review

  9. 2004
  10. Published

    Familial recurrent hydatidiform mole: a review

    Fisher, R. A., Hodges, M. & Newlands, E. S., 08/2004, In: Journal of Reproductive Medicine. 49, 8, p. 595-601 7 p.

    Research output: Contribution to Journal/Magazine › Journal article › peer-review

  11. 2003
  12. Published

    Genomic imprinting in gestational trophoblastic disease: a review

    Fisher, R. A. & Hodges, M., 04/2003, In: Placenta. 24, Suppl. A, p. s111-s118 8 p.

    Research output: Contribution to Journal/Magazine › Journal article › peer-review

  13. Published

    Genetic refinement and physical mapping of a biparental complete hydatidiform mole locus on chromosome 19q13.4.

    Hodges, M., Rees, H. C., Seckl, M. J., Newlands, E. S. & Fisher, R. A., 2003, In: Journal of Medical Genetics. 40, 8, 6 p., e95.

    Research output: Contribution to Journal/Magazine › Journal article › peer-review

  14. 2002
  15. Published

    Characterization of the genomic and transcriptional structure of the CRX gene: substantial differences between human and mouse.

    Hodges, M., Vieira, H., Gregory-Evans, K. & Gregory-Evans, C. Y., 11/2002, In: Genomics. 80, 5, p. 531-542 12 p.

    Research output: Contribution to Journal/Magazine › Journal article › peer-review

  16. Published

    The maternally transcribed gene p57KIP2 (CDNK1C) is abnormally expressed in both androgenetic and biparental complete hydatidiform moles

    Fisher, R. A., Hodges, M., Rees, H. C., Seibre, N. J., Seckl, M. J., Newlands, E. S., Genest, D. R. & Castrillon, D. H., 2002, In: Human Molecular Genetics. 11, 26, p. 3267-3272 6 p.

    Research output: Contribution to Journal/Magazine › Journal article › peer-review

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