Ionides A - Search Results

Year	Number of Results
1994	1
1996	3
1997	3
1998	2
1999	3
2000	2
2001	3
2003	3
2004	2
2005	1
2006	1
2007	3
2008	3
2009	2
2010	1
2011	2
2017	1
2018	2
2020	2
2021	4
2022	7
2023	4
2025	3

1

Gupta A, Ionides A. Gupta A, et al. Among authors: ionides a. Int Ophthalmol. 2023 Jan;43(1):1-2. doi: 10.1007/s10792-022-02419-x. Epub 2022 Jul 11. Int Ophthalmol. 2023. PMID: 35819740 No abstract available.

2

Multimorbidity due to novel pathogenic variants in the WFS1/RP1/NOD2 genes: autosomal dominant congenital lamellar cataract, retinitis pigmentosa and Crohn's disease in a British family.

Berry V, Ionides A, Georgiou M, Quinlan RA, Michaelides M. Berry V, et al. Among authors: ionides a. BMJ Open Ophthalmol. 2023 Jul;8(1):e001252. doi: 10.1136/bmjophth-2023-001252. BMJ Open Ophthalmol. 2023. PMID: 37493686 Free PMC article.

3

Application of real-time artificial intelligence to cataract surgery.

Shah N, Wawrzynski J, Hussain R, Singh B; Moorfields Cataract AI Study Group; Luengo I, Addis C, Barbarisi S, Mohammadi R, Culshaw L, Johnston E, Haikka P, Kerr K, Stoyanov D, Lindegger D, Saleh G. Shah N, et al. Br J Ophthalmol. 2025 Jul 15:bjo-2024-326111. doi: 10.1136/bjo-2024-326111. Online ahead of print. Br J Ophthalmol. 2025. PMID: 40664490

4

A locus for autosomal dominant posterior polar cataract on chromosome 1p.

Ionides AC, Berry V, Mackay DS, Moore AT, Bhattacharya SS, Shiels A. Ionides AC, et al. Hum Mol Genet. 1997 Jan;6(1):47-51. doi: 10.1093/hmg/6.1.47. Hum Mol Genet. 1997. PMID: 9002669

5

The genetic landscape of crystallins in congenital cataract.

Berry V, Ionides A, Pontikos N, Georgiou M, Yu J, Ocaka LA, Moore AT, Quinlan RA, Michaelides M. Berry V, et al. Among authors: ionides a. Orphanet J Rare Dis. 2020 Nov 26;15(1):333. doi: 10.1186/s13023-020-01613-3. Orphanet J Rare Dis. 2020. PMID: 33243271 Free PMC article.

6

Connexin 50 mutation in a family with congenital "zonular nuclear" pulverulent cataract of Pakistani origin.

Berry V, Mackay D, Khaliq S, Francis PJ, Hameed A, Anwar K, Mehdi SQ, Newbold RJ, Ionides A, Shiels A, Moore T, Bhattacharya SS. Berry V, et al. Among authors: ionides a. Hum Genet. 1999 Jul-Aug;105(1-2):168-70. doi: 10.1007/s004399900094. Hum Genet. 1999. PMID: 10480374

7

Whole-genome sequencing reveals a recurrent missense mutation in the Connexin 46 (GJA3) gene causing autosomal-dominant lamellar cataract.

Berry V, Ionides ACW, Pontikos N, Moghul I, Moore AT, Cheetham ME, Michaelides M. Berry V, et al. Among authors: ionides acw. Eye (Lond). 2018 May 1;32(10):1661-1668. doi: 10.1038/s41433-018-0154-8. Eye (Lond). 2018. PMID: 29934635 Free PMC article.

8

Variants in PAX6, PITX3 and HSF4 causing autosomal dominant congenital cataracts.

Berry V, Ionides A, Pontikos N, Moore AT, Quinlan RA, Michaelides M. Berry V, et al. Among authors: ionides a. Eye (Lond). 2022 Aug;36(8):1694-1701. doi: 10.1038/s41433-021-01711-x. Epub 2021 Aug 3. Eye (Lond). 2022. PMID: 34345029 Free PMC article.

9

A novel locus for autosomal dominant congenital cerulean cataract maps to chromosome 12q.

Berry V, Ionides AC, Moore AT, Bhattacharya SS. Berry V, et al. Among authors: ionides ac. Eur J Hum Genet. 2011 Dec;19(12):1289-91. doi: 10.1038/ejhg.2011.130. Epub 2011 Jul 6. Eur J Hum Genet. 2011. PMID: 21731060 Free PMC article.

10

Anterior polar cataract: clinical spectrum and genetic linkage in a single family.

Ionides A, Berry V, Mackay D, Shiels A, Bhattacharya S, Moore A. Ionides A, et al. Eye (Lond). 1998;12 ( Pt 2):224-6. doi: 10.1038/eye.1998.53. Eye (Lond). 1998. PMID: 9683943

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