Moore T - Search Results

1

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: moore t. Hum Genet. 1999 Jul-Aug;105(1-2):168-70. doi: 10.1007/s004399900094. Hum Genet. 1999. PMID: 10480374

2

The clinical and genetic heterogeneity of autosomal dominant cataract.

Ionides A, Berry V, Moore T, Bhattacharya S, Shiels A. Ionides A, et al. Among authors: moore t. Acta Ophthalmol Scand Suppl. 1996;(219):40-1. doi: 10.1111/j.1600-0420.1996.tb00383.x. Acta Ophthalmol Scand Suppl. 1996. PMID: 8741116 Review. No abstract available.

3

Evidence for a major retinitis pigmentosa locus on 19q13.4 (RP11) and association with a unique bimodal expressivity phenotype.

Al-Maghtheh M, Vithana E, Tarttelin E, Jay M, Evans K, Moore T, Bhattacharya S, Inglehearn CF. Al-Maghtheh M, et al. Among authors: moore t. Am J Hum Genet. 1996 Oct;59(4):864-71. Am J Hum Genet. 1996. PMID: 8808602 Free PMC article.

4

Dominant cataract formation in association with a vimentin assembly disrupting mutation.

Müller M, Bhattacharya SS, Moore T, Prescott Q, Wedig T, Herrmann H, Magin TM. Müller M, et al. Among authors: moore t. Hum Mol Genet. 2009 Mar 15;18(6):1052-7. doi: 10.1093/hmg/ddn440. Epub 2009 Jan 6. Hum Mol Genet. 2009. PMID: 19126778

5

Genetic analysis of the guanylate cyclase activator 1B (GUCA1B) gene in patients with autosomal dominant retinal dystrophies.

Payne AM, Downes SM, Bessant DA, Plant C, Moore T, Bird AC, Bhattacharya SS. Payne AM, et al. Among authors: moore t. J Med Genet. 1999 Sep;36(9):691-3. J Med Genet. 1999. PMID: 10507726 Free PMC article.

6

Segregation of a PRKCG mutation in two RP11 families.

Al-Maghtheh M, Vithana EN, Inglehearn CF, Moore T, Bird AC, Bhattacharya SS. Al-Maghtheh M, et al. Among authors: moore t. Am J Hum Genet. 1998 May;62(5):1248-52. doi: 10.1086/301819. Am J Hum Genet. 1998. PMID: 9545390 Free PMC article. No abstract available.

7

Biallelic mutations in the autophagy regulator DRAM2 cause retinal dystrophy with early macular involvement.

El-Asrag ME, Sergouniotis PI, McKibbin M, Plagnol V, Sheridan E, Waseem N, Abdelhamed Z, McKeefry D, Van Schil K, Poulter JA; UK Inherited Retinal Disease Consortium; Johnson CA, Carr IM, Leroy BP, De Baere E, Inglehearn CF, Webster AR, Toomes C, Ali M. El-Asrag ME, et al. Am J Hum Genet. 2015 Jun 4;96(6):948-54. doi: 10.1016/j.ajhg.2015.04.006. Epub 2015 May 14. Am J Hum Genet. 2015. PMID: 25983245 Free PMC article.

8

Missense mutations in the most ancient residues of the PAX6 paired domain underlie a spectrum of human congenital eye malformations.

Hanson I, Churchill A, Love J, Axton R, Moore T, Clarke M, Meire F, van Heyningen V. Hanson I, et al. Among authors: moore t. Hum Mol Genet. 1999 Feb;8(2):165-72. doi: 10.1093/hmg/8.2.165. Hum Mol Genet. 1999. PMID: 9931324

9

Restoring retinal function in a mouse model of hereditary blindness.

Moore T. Moore T. PLoS Med. 2005 Nov;2(11):e399. doi: 10.1371/journal.pmed.0020399. Epub 2005 Nov 29. PLoS Med. 2005. PMID: 16288566 Free PMC article.

10

Understanding psychotic-like experiences in children in the context of dimensions of psychological problems.

Jeong HJ, Lahey BB, Reimann GE, Durham EL, Archer C, Moore TM, Shah K, Kaczkurkin AN. Jeong HJ, et al. Among authors: moore tm. Front Child Adolesc Psychiatry. 2024 Aug 2;3:1410804. doi: 10.3389/frcha.2024.1410804. eCollection 2024. Front Child Adolesc Psychiatry. 2024. PMID: 39816605 Free PMC article.

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