Silvestri G - Search Results

1

Further assessment of the complement component 2 and factor B region associated with age-related macular degeneration.

McKay GJ, Silvestri G, Patterson CC, Hogg RE, Chakravarthy U, Hughes AE. McKay GJ, et al. Among authors: silvestri g. Invest Ophthalmol Vis Sci. 2009 Feb;50(2):533-9. doi: 10.1167/iovs.08-2275. Epub 2008 Sep 20. Invest Ophthalmol Vis Sci. 2009. PMID: 18806297

2

Is genetic predisposition an important risk factor in age-related macular degeneration?

Silvestri G, Johnston PB, Hughes AE. Silvestri G, et al. Eye (Lond). 1994;8 ( Pt 5):564-8. doi: 10.1038/eye.1994.138. Eye (Lond). 1994. PMID: 7835454

3

Localisation of a gene for central areolar choroidal dystrophy to chromosome 17p.

Lotery AJ, Ennis KT, Silvestri G, Nicholl S, McGibbon D, Collins AD, Hughes AE. Lotery AJ, et al. Among authors: silvestri g. Hum Mol Genet. 1996 May;5(5):705-8. doi: 10.1093/hmg/5.5.705. Hum Mol Genet. 1996. PMID: 8733141

4

Age-related macular degeneration: genetics and implications for detection and treatment.

Silvestri G. Silvestri G. Mol Med Today. 1997 Feb;3(2):84-91. doi: 10.1016/S1357-4310(96)10057-5. Mol Med Today. 1997. PMID: 9060006 Review.

5

Fine localisation of the gene for central areolar choroidal dystrophy on chromosome 17p.

Hughes AE, Lotery AJ, Silvestri G. Hughes AE, et al. Among authors: silvestri g. J Med Genet. 1998 Sep;35(9):770-2. doi: 10.1136/jmg.35.9.770. J Med Genet. 1998. PMID: 9733038 Free PMC article.

6

A physical and expression map of the D17S1810-D17S1353 region spanning the central areolar choroidal dystrophy locus.

Lichanska AM, McGibbon D, Silvestri G, Hughes AE. Lichanska AM, et al. Among authors: silvestri g. Cytogenet Cell Genet. 2001;93(1-2):43-7. doi: 10.1159/000056946. Cytogenet Cell Genet. 2001. PMID: 11474177

7

Familial keratoconus with cataract: linkage to the long arm of chromosome 15 and exclusion of candidate genes.

Hughes AE, Dash DP, Jackson AJ, Frazer DG, Silvestri G. Hughes AE, et al. Among authors: silvestri g. Invest Ophthalmol Vis Sci. 2003 Dec;44(12):5063-6. doi: 10.1167/iovs.03-0399. Invest Ophthalmol Vis Sci. 2003. PMID: 14638698

8

A novel diagnostic test detects a low frequency of the hemicentin Gln5345Arg variant among Northern Irish age related macular degeneration patients.

McKay GJ, Clarke S, Hughes A, McConnell V, Schultz DW, Klein ML, Silvestri G, Simpson DA. McKay GJ, et al. Among authors: silvestri g. Mol Vis. 2004 Sep 24;10:682-7. Mol Vis. 2004. PMID: 15467524 Free article.

9

Pigmented paravenous chorioretinal atrophy is associated with a mutation within the crumbs homolog 1 (CRB1) gene.

McKay GJ, Clarke S, Davis JA, Simpson DA, Silvestri G. McKay GJ, et al. Among authors: silvestri g. Invest Ophthalmol Vis Sci. 2005 Jan;46(1):322-8. doi: 10.1167/iovs.04-0734. Invest Ophthalmol Vis Sci. 2005. PMID: 15623792

10

A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degeneration.

Hageman GS, Anderson DH, Johnson LV, Hancox LS, Taiber AJ, Hardisty LI, Hageman JL, Stockman HA, Borchardt JD, Gehrs KM, Smith RJ, Silvestri G, Russell SR, Klaver CC, Barbazetto I, Chang S, Yannuzzi LA, Barile GR, Merriam JC, Smith RT, Olsh AK, Bergeron J, Zernant J, Merriam JE, Gold B, Dean M, Allikmets R. Hageman GS, et al. Among authors: silvestri g. Proc Natl Acad Sci U S A. 2005 May 17;102(20):7227-32. doi: 10.1073/pnas.0501536102. Epub 2005 May 3. Proc Natl Acad Sci U S A. 2005. PMID: 15870199 Free PMC article.

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