Oliver VF - Search Results

1

Genotypic and phenotypic characterisation of RP2- and RPGR-associated X-linked inherited retinal dystrophy, including female manifestations.

Kuruvilla SE, Song E, Raoof N, van Bysterveldt K, Oliver VF, Hong SC, Al-Taie R, Wilson G, Vincent AL. Kuruvilla SE, et al. Among authors: oliver vf. Clin Exp Ophthalmol. 2023 May-Jun;51(4):300-312. doi: 10.1111/ceo.14220. Epub 2023 Mar 15. Clin Exp Ophthalmol. 2023. PMID: 36882936

2

Next-generation sequencing targeted disease panel in rod-cone retinal dystrophies in Māori and Polynesian reveals novel changes and a common founder mutation.

Vincent AL, Abeysekera N, van Bysterveldt KA, Oliver VF, Ellingford JM, Barton S, Black GC. Vincent AL, et al. Among authors: oliver vf. Clin Exp Ophthalmol. 2017 Dec;45(9):901-910. doi: 10.1111/ceo.12983. Epub 2017 Jun 13. Clin Exp Ophthalmol. 2017. PMID: 28488341

3

ADAMTSL4 assessment in ectopia lentis reveals a recurrent founder mutation in Polynesians.

van Bysterveldt KA, Al Taie R, Ikink W, Oliver VF, Vincent AL. van Bysterveldt KA, et al. Among authors: oliver vf. Ophthalmic Genet. 2017 Dec;38(6):537-543. doi: 10.1080/13816810.2017.1309552. Epub 2017 Apr 10. Ophthalmic Genet. 2017. PMID: 28394649

4

The Genetics and Pathophysiology of IC3D Category 1 Corneal Dystrophies: A Review.

Oliver VF, Vincent AL. Oliver VF, et al. Asia Pac J Ophthalmol (Phila). 2016 Jul-Aug;5(4):272-81. doi: 10.1097/APO.0000000000000205. Asia Pac J Ophthalmol (Phila). 2016. PMID: 27213768 Free article. Review.

5

A COL17A1 Splice-Altering Mutation Is Prevalent in Inherited Recurrent Corneal Erosions.

Oliver VF, van Bysterveldt KA, Cadzow M, Steger B, Romano V, Markie D, Hewitt AW, Mackey DA, Willoughby CE, Sherwin T, Crosier PS, McGhee CN, Vincent AL. Oliver VF, et al. Ophthalmology. 2016 Apr;123(4):709-22. doi: 10.1016/j.ophtha.2015.12.008. Epub 2016 Jan 16. Ophthalmology. 2016. PMID: 26786512 Free article.

6

Prediction of promoters and enhancers using multiple DNA methylation-associated features.

Hwang W, Oliver VF, Merbs SL, Zhu H, Qian J. Hwang W, et al. Among authors: oliver vf. BMC Genomics. 2015;16 Suppl 7(Suppl 7):S11. doi: 10.1186/1471-2164-16-S7-S11. Epub 2015 Jun 11. BMC Genomics. 2015. PMID: 26099324 Free PMC article.

7

Differential DNA methylation identified in the blood and retina of AMD patients.

Oliver VF, Jaffe AE, Song J, Wang G, Zhang P, Branham KE, Swaroop A, Eberhart CG, Zack DJ, Qian J, Merbs SL. Oliver VF, et al. Epigenetics. 2015;10(8):698-707. doi: 10.1080/15592294.2015.1060388. Epigenetics. 2015. PMID: 26067391 Free PMC article.

8

Characterization of tissue-specific differential DNA methylation suggests distinct modes of positive and negative gene expression regulation.

Wan J, Oliver VF, Wang G, Zhu H, Zack DJ, Merbs SL, Qian J. Wan J, et al. Among authors: oliver vf. BMC Genomics. 2015 Feb 5;16(1):49. doi: 10.1186/s12864-015-1271-4. BMC Genomics. 2015. PMID: 25652663 Free PMC article.

9

Hypomethylation of the IL17RC promoter in peripheral blood leukocytes is not a hallmark of age-related macular degeneration.

Oliver VF, Franchina M, Jaffe AE, Branham KE, Othman M, Heckenlively JR, Swaroop A, Campochiaro B, Vote BJ, Craig JE, Saffery R, Mackey DA, Qian J, Zack DJ, Hewitt AW, Merbs SL. Oliver VF, et al. Cell Rep. 2013 Dec 26;5(6):1527-35. doi: 10.1016/j.celrep.2013.11.042. Cell Rep. 2013. PMID: 24373284 Free PMC article.

10

Integrative analysis of tissue-specific methylation and alternative splicing identifies conserved transcription factor binding motifs.

Wan J, Oliver VF, Zhu H, Zack DJ, Qian J, Merbs SL. Wan J, et al. Among authors: oliver vf. Nucleic Acids Res. 2013 Oct;41(18):8503-14. doi: 10.1093/nar/gkt652. Epub 2013 Jul 24. Nucleic Acids Res. 2013. PMID: 23887936 Free PMC article.

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