Grigg JR - Search Results

1

Human iPSC-Derived Retinal Organoids and Retinal Pigment Epithelium for Novel Intronic RPGR Variant Assessment for Therapy Suitability.

Chahine Karam F, Loi TH, Ma A, Nash BM, Grigg JR, Parekh D, Riley LG, Farnsworth E, Bennetts B, Gonzalez-Cordero A, Jamieson RV. Chahine Karam F, et al. Among authors: grigg jr. J Pers Med. 2022 Mar 21;12(3):502. doi: 10.3390/jpm12030502. J Pers Med. 2022. PMID: 35330501 Free PMC article.

2

Deletion at 14q22-23 indicates a contiguous gene syndrome comprising anophthalmia, pituitary hypoplasia, and ear anomalies.

Nolen LD, Amor D, Haywood A, St Heaps L, Willcock C, Mihelec M, Tam P, Billson F, Grigg J, Peters G, Jamieson RV. Nolen LD, et al. Am J Med Genet A. 2006 Aug 15;140(16):1711-8. doi: 10.1002/ajmg.a.31335. Am J Med Genet A. 2006. PMID: 16835935

3

Secondary glaucoma after paediatric cataract surgery.

Swamy BN, Billson F, Martin F, Donaldson C, Hing S, Jamieson R, Grigg J, Smith JE. Swamy BN, et al. Br J Ophthalmol. 2007 Dec;91(12):1627-30. doi: 10.1136/bjo.2007.117887. Epub 2007 May 2. Br J Ophthalmol. 2007. PMID: 17475699 Free PMC article.

4

Chromosomal rearrangements and novel genes in disorders of eye development, cataract and glaucoma.

Mihelec M, St Heaps L, Flaherty M, Billson F, Rudduck C, Tam PP, Grigg JR, Peters GB, Jamieson RV. Mihelec M, et al. Among authors: grigg jr. Twin Res Hum Genet. 2008 Aug;11(4):412-21. doi: 10.1375/twin.11.4.412. Twin Res Hum Genet. 2008. PMID: 18637741 Review.

5

Novel SOX2 partner-factor domain mutation in a four-generation family.

Mihelec M, Abraham P, Gibson K, Krowka R, Susman R, Storen R, Chen Y, Donald J, Tam PP, Grigg JR, Flaherty M, Gole GA, Jamieson RV. Mihelec M, et al. Among authors: grigg jr. Eur J Hum Genet. 2009 Nov;17(11):1417-22. doi: 10.1038/ejhg.2009.79. Epub 2009 May 27. Eur J Hum Genet. 2009. PMID: 19471311 Free PMC article.

6

Port-wine vascular malformations and glaucoma risk in Sturge-Weber syndrome.

Sharan S, Swamy B, Taranath DA, Jamieson R, Yu T, Wargon O, Grigg JR. Sharan S, et al. Among authors: grigg jr. J AAPOS. 2009 Aug;13(4):374-8. doi: 10.1016/j.jaapos.2009.04.007. J AAPOS. 2009. PMID: 19683189

7

Twist2: role in corneal stromal keratocyte proliferation and corneal thickness.

Weaving L, Mihelec M, Storen R, Sosic D, Grigg JR, Tam PP, Jamieson RV. Weaving L, et al. Among authors: grigg jr. Invest Ophthalmol Vis Sci. 2010 Nov;51(11):5561-70. doi: 10.1167/iovs.09-5123. Epub 2010 Jun 23. Invest Ophthalmol Vis Sci. 2010. PMID: 20574024

8

A puzzle over several decades: eye anomalies with FRAS1 and STRA6 mutations in the same family.

Ng WY, Pasutto F, Bardakjian TM, Wilson MJ, Watson G, Schneider A, Mackey DA, Grigg JR, Zenker M, Jamieson RV. Ng WY, et al. Among authors: grigg jr. Clin Genet. 2013 Feb;83(2):162-8. doi: 10.1111/j.1399-0004.2012.01851.x. Epub 2012 Feb 20. Clin Genet. 2013. PMID: 22283518

9

Microphthalmia, anophthalmia, and coloboma and associated ocular and systemic features: understanding the spectrum.

Skalicky SE, White AJ, Grigg JR, Martin F, Smith J, Jones M, Donaldson C, Smith JE, Flaherty M, Jamieson RV. Skalicky SE, et al. Among authors: grigg jr. JAMA Ophthalmol. 2013 Dec;131(12):1517-24. doi: 10.1001/jamaophthalmol.2013.5305. JAMA Ophthalmol. 2013. PMID: 24177921

10

The importance of electrophysiology in revealing a complete homozygous deletion of KCNV2.

Grigg JR, Holder GE, Billson FA, Korsakova M, Jamieson RV. Grigg JR, et al. J AAPOS. 2013 Dec;17(6):641-3. doi: 10.1016/j.jaapos.2013.08.006. Epub 2013 Nov 7. J AAPOS. 2013. PMID: 24210337

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