PubMed

Recessive Mutations of the Gene TRPM1 Abrogate ON Bipolar Cell Function and Cause Complete Congenital Stationary Night Blindness in Humans.

Li Z, Sergouniotis PI, Michaelides M, Mackay DS, Wright GA, Devery S, Moore AT, Holder GE, Robson AG, Webster AR.

Am J Hum Genet. 2009 Nov;85(5):711-9. Epub 2009 Oct 29.PMID: 19878917 [PubMed - in process]Related articles

Cataract surgery and primary intraocular lens implantation in children < or = 2 years old in the UK and Ireland: finding of national surveys.

Solebo AL, Russell-Eggitt I, Nischal KK, Moore AT, Cumberland P, Rahi JS; British Isles Congenital Cataract Interest Group.

Br J Ophthalmol. 2009 Nov;93(11):1495-8. Epub 2009 Jun 16.PMID: 19854739 [PubMed - in process]Related articles

Microcephaly with chorioretinal dysplasia: two case reports and a review of the literature.

Gupta A, Vasudevan P, Biswas S, Smith JC, Moore AT, Lloyd C, Dutton G.

Ophthalmic Genet. 2009 Dec;30(4):157-60.PMID: 19852571 [PubMed - in process]Related articles

Novel Mutations and Electrophysiologic Findings in RGS9- andR9AP-Associated Retinal Dysfunction (Bradyopsia).

Michaelides M, Li Z, Rana NA, Richardson EC, Hykin PG, Moore AT, Holder GE, Webster AR.

Ophthalmology. 2009 Oct 7. [Epub ahead of print]PMID: 19818506 [PubMed - as supplied by publisher]Related articles

Deficits in local and global motion perception arising from abnormal eye movements.

Neveu MM, Jeffery G, Moore AT, Dakin SC.

J Vis. 2009 Apr 6;9(4):9.1-15.PMID: 19757918 [PubMed - in process]Related articlesFree article

An unusual fundus phenotype of inner retinal sheen in X-linked retinoschisis.

Robson AG, Mengher LS, Tan MH, Moore AT.

Eye (Lond). 2009 Sep;23(9):1876-8. Epub 2008 Dec 5. No abstract available. PMID: 19741719 [PubMed - in process]Related articles

Winter Ecology of Buggy Creek Virus (Togaviridae, Alphavirus) in the Central Great Plains.

Brown CR, Strickler SA, Moore AT, Knutie SA, Padhi A, Brown MB, Young GR, O'Brien VA, Foster JE, Komar N.

Vector Borne Zoonotic Dis. 2009 Sep 2. [Epub ahead of print]PMID: 19725760 [PubMed - as supplied by publisher]Related articles

A Mutant Connexin50 with Enhanced Hemichannel Function Leads to Cell Death.

Minogue PJ, Tong JJ, Arora A, Russell-Eggitt I, Hunt DM, Moore AT, Ebihara L, Beyer E, Berthoud VM.

Invest Ophthalmol Vis Sci. 2009 Aug 13. [Epub ahead of print]PMID: 19684000 [PubMed - as supplied by publisher]Related articles

Childhood macular dystrophies.

Moore AT.

Curr Opin Ophthalmol. 2009 Sep;20(5):363-8. Review.PMID: 19587597 [PubMed - indexed for MEDLINE]Related articles

Motor-dependent microtubule disassembly driven by tubulin tyrosination.

Peris L, Wagenbach M, Lafanechère L, Brocard J, Moore AT, Kozielski F, Job D, Wordeman L, Andrieux A.

J Cell Biol. 2009 Jun 29;185(7):1159-66.PMID: 19564401 [PubMed - indexed for MEDLINE]Related articles

Initiation codon mutation in betaB1-crystallin (CRYBB1) associated with autosomal recessive nuclear pulverulent cataract.

Meyer E, Rahman F, Owens J, Pasha S, Morgan NV, Trembath RC, Stone EM, Moore AT, Maher ER.

Mol Vis. 2009 May 18;15:1014-9.PMID: 19461930 [PubMed - indexed for MEDLINE]Related articlesFree article

Blue cone monochromacy: causative mutations and associated phenotypes.

Gardner JC, Michaelides M, Holder GE, Kanuga N, Webb TR, Mollon JD, Moore AT, Hardcastle AJ.

Mol Vis. 2009;15:876-84. Epub 2009 May 1.PMID: 19421413 [PubMed - indexed for MEDLINE]Related articlesFree article

X-linked cataract and Nance-Horan syndrome are allelic disorders.

Coccia M, Brooks SP, Webb TR, Christodoulou K, Wozniak IO, Murday V, Balicki M, Yee HA, Wangensteen T, Riise R, Saggar AK, Park SM, Kanuga N, Francis PJ, Maher ER, Moore AT, Russell-Eggitt IM, Hardcastle AJ.

Hum Mol Genet. 2009 Jul 15;18(14):2643-55. Epub 2009 May 4.PMID: 19414485 [PubMed - indexed for MEDLINE]Related articlesFree article

Overwintering of infectious Buggy Creek virus (Togaviridae: Alphavirus) in Oeciacus vicarius (Hemiptera: Cimicidae) in North Dakota.

Brown CR, Moore AT, Knutie SA, Komar N.

J Med Entomol. 2009 Mar;46(2):391-4.PMID: 19351093 [PubMed - indexed for MEDLINE]Related articles

Isolation of Buggy Creek virus (Togaviridae: Alphavirus) from field-collected eggs of Oeciacus vicarius (Hemiptera: Cimicidae).

Brown CR, Moore AT, Young GR, Padhi A, Komar N.

J Med Entomol. 2009 Mar;46(2):375-9.PMID: 19351091 [PubMed - indexed for MEDLINE]Related articles

Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataract.

Zhang T, Hua R, Xiao W, Burdon KP, Bhattacharya SS, Craig JE, Shang D, Zhao X, Mackey DA, Moore AT, Luo Y, Zhang J, Zhang X.

Hum Mutat. 2009 May;30(5):E603-11.PMID: 19306328 [PubMed - indexed for MEDLINE]Related articles

Detailed ophthalmologic evaluation of 43 individuals with PAX6 mutations.

Hingorani M, Williamson KA, Moore AT, van Heyningen V.

Invest Ophthalmol Vis Sci. 2009 Jun;50(6):2581-90. Epub 2009 Feb 14.PMID: 19218613 [PubMed - indexed for MEDLINE]Related articles

Mutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfecta.

Parry DA, Mighell AJ, El-Sayed W, Shore RC, Jalili IK, Dollfus H, Bloch-Zupan A, Carlos R, Carr IM, Downey LM, Blain KM, Mansfield DC, Shahrabi M, Heidari M, Aref P, Abbasi M, Michaelides M, Moore AT, Kirkham J, Inglehearn CF.

Am J Hum Genet. 2009 Feb;84(2):266-73. Epub 2009 Feb 5.PMID: 19200525 [PubMed - indexed for MEDLINE]Related articlesFree article

Evaluation of the X-linked high-grade myopia locus (MYP1) with cone dysfunction and color vision deficiencies.

Metlapally R, Michaelides M, Bulusu A, Li YJ, Schwartz M, Rosenberg T, Hunt DM, Moore AT, Züchner S, Rickman CB, Young TL.

Invest Ophthalmol Vis Sci. 2009 Apr;50(4):1552-8. Epub 2008 Dec 20.PMID: 19098318 [PubMed - indexed for MEDLINE]Related articles

Phylogeographical structure and evolutionary history of two Buggy Creek virus lineages in the western Great Plains of North America.

Padhi A, Moore AT, Brown MB, Foster JE, Pfeffer M, Gaines KP, O'Brien VA, Strickler SA, Johnson AE, Brown CR.

J Gen Virol. 2008 Sep;89(Pt 9):2122-31.PMID: 18753221 [PubMed - indexed for MEDLINE]Related articlesFree article

Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice.

Yang Z, Chen Y, Lillo C, Chien J, Yu Z, Michaelides M, Klein M, Howes KA, Li Y, Kaminoh Y, Chen H, Zhao C, Chen Y, Al-Sheikh YT, Karan G, Corbeil D, Escher P, Kamaya S, Li C, Johnson S, Frederick JM, Zhao Y, Wang C, Cameron DJ, Huttner WB, Schorderet DF, Munier FL, Moore AT, Birch DG, Baehr W, Hunt DM, Williams DS, Zhang K.

J Clin Invest. 2008 Aug;118(8):2908-16.PMID: 18654668 [PubMed - indexed for MEDLINE]Related articlesFree article

ADVIRC is caused by distinct mutations in BEST1 that alter pre-mRNA splicing.

Burgess R, MacLaren RE, Davidson AE, Urquhart JE, Holder GE, Robson AG, Moore AT, Keefe RO, Black GC, Manson FD.

J Med Genet. 2009 Sep;46(9):620-5. Epub 2008 Jul 8.PMID: 18611979 [PubMed - in process]Related articles

Focus on molecules: retinol dehydrogenase 12 (RDH12).

Moradi P, Mackay D, Hunt DM, Moore AT.

Exp Eye Res. 2008 Sep;87(3):160-1. Epub 2008 Jul 2. Review. No abstract available. PMID: 18599039 [PubMed - indexed for MEDLINE]Related articles

Charles Bonnet syndrome in age-related macular degeneration: the nature and frequency of images in subjects with end-stage disease.

Khan JC, Shahid H, Thurlby DA, Yates JR, Moore AT.

Ophthalmic Epidemiol. 2008 May-Jun;15(3):202-8.PMID: 18569816 [PubMed - indexed for MEDLINE]Related articles

Effect of gene therapy on visual function in Leber's congenital amaurosis.

Bainbridge JW, Smith AJ, Barker SS, Robbie S, Henderson R, Balaggan K, Viswanathan A, Holder GE, Stockman A, Tyler N, Petersen-Jones S, Bhattacharya SS, Thrasher AJ, Fitzke FW, Carter BJ, Rubin GS, Moore AT, Ali RR.

N Engl J Med. 2008 May 22;358(21):2231-9. Epub 2008 Apr 27.PMID: 18441371 [PubMed - indexed for MEDLINE]Related articlesFree article

Phenotypic variation in enhanced S-cone syndrome.

Audo I, Michaelides M, Robson AG, Hawlina M, Vaclavik V, Sandbach JM, Neveu MM, Hogg CR, Hunt DM, Moore AT, Bird AC, Webster AR, Holder GE.

Invest Ophthalmol Vis Sci. 2008 May;49(5):2082-93.PMID: 18436841 [PubMed - indexed for MEDLINE]Related articlesFree article

Experimental inoculation of house sparrows (Passer domesticus) with buggy creek virus.

Huyvaert KP, Moore AT, Panella NA, Edwards EA, Brown MB, Komar N, Brown CR.

J Wildl Dis. 2008 Apr;44(2):331-40.PMID: 18436665 [PubMed - indexed for MEDLINE]Related articlesFree article

Host and vector movement affects genetic diversity and spatial structure of Buggy Creek virus (Togaviridae).

Brown CR, Bomberger Brown M, Padhi A, Foster JE, Moore AT, Pfeffer M, Komar N.

Mol Ecol. 2008 May;17(9):2164-73. Epub 2008 Mar 25.PMID: 18373533 [PubMed - indexed for MEDLINE]Related articles

Choroidal neovascularisation in children.

Sivaprasad S, Moore AT.

Br J Ophthalmol. 2008 Apr;92(4):451-4. Review.PMID: 18369058 [PubMed - indexed for MEDLINE]Related articles

The negative ERG: clinical phenotypes and disease mechanisms of inner retinal dysfunction.

Audo I, Robson AG, Holder GE, Moore AT.

Surv Ophthalmol. 2008 Jan-Feb;53(1):16-40. Review.PMID: 18191655 [PubMed - indexed for MEDLINE]Related articles

An assessment of the apex microarray technology in genotyping patients with Leber congenital amaurosis and early-onset severe retinal dystrophy.

Henderson RH, Waseem N, Searle R, van der Spuy J, Russell-Eggitt I, Bhattacharya SS, Thompson DA, Holder GE, Cheetham ME, Webster AR, Moore AT.

Invest Ophthalmol Vis Sci. 2007 Dec;48(12):5684-9.PMID: 18055820 [PubMed - indexed for MEDLINE]Related articlesFree article

A novel connexin50 mutation associated with congenital nuclear pulverulent cataracts.

Arora A, Minogue PJ, Liu X, Addison PK, Russel-Eggitt I, Webster AR, Hunt DM, Ebihara L, Beyer EC, Berthoud VM, Moore AT.

J Med Genet. 2008 Mar;45(3):155-60. Epub 2007 Nov 15.PMID: 18006672 [PubMed - indexed for MEDLINE]Related articlesFree article

Functional characteristics of patients with retinal dystrophy that manifest abnormal parafoveal annuli of high density fundus autofluorescence; a review and update.

Robson AG, Michaelides M, Saihan Z, Bird AC, Webster AR, Moore AT, Fitzke FW, Holder GE.

Doc Ophthalmol. 2008 Mar;116(2):79-89. Epub 2007 Nov 6. Review.PMID: 17985165 [PubMed - indexed for MEDLINE]Related articlesFree article

Functional correlates of fundus autofluorescence abnormalities in patients with RPGR or RIMS1 mutations causing cone or cone rod dystrophy.

Robson AG, Michaelides M, Luong VA, Holder GE, Bird AC, Webster AR, Moore AT, Fitzke FW.

Br J Ophthalmol. 2008 Jan;92(1):95-102. Epub 2007 Oct 25.PMID: 17962389 [PubMed - indexed for MEDLINE]Related articles

In vitro and in vivo analysis of microtubule-destabilizing kinesins.

Stumpff J, Cooper J, Domnitz S, Moore AT, Rankin KE, Wagenbach M, Wordeman L.

Methods Mol Biol. 2007;392:37-49.PMID: 17951709 [PubMed - indexed for MEDLINE]Related articles

Molecular genetics of infantile-onset retinal dystrophies.

Moradi P, Moore AT.

Eye (Lond). 2007 Oct;21(10):1344-51. Review.PMID: 17914438 [PubMed - indexed for MEDLINE]Related articles

The first case of vesico-vaginal fistula in a patient with primary lymphoma of the bladder - a case report.

Evans DA, Moore AT.

J Med Case Reports. 2007 Sep 27;1:105.PMID: 17900354 [PubMed - in process]Related articlesFree article

Bird movement predicts Buggy Creek virus infection in insect vectors.

Brown CR, Brown MB, Moore AT, Komar N.

Vector Borne Zoonotic Dis. 2007 Fall;7(3):304-14.PMID: 17760513 [PubMed - indexed for MEDLINE]Related articles

Complement C3 variant and the risk of age-related macular degeneration.

Yates JR, Sepp T, Matharu BK, Khan JC, Thurlby DA, Shahid H, Clayton DG, Hayward C, Morgan J, Wright AF, Armbrecht AM, Dhillon B, Deary IJ, Redmond E, Bird AC, Moore AT; Genetic Factors in AMD Study Group.

N Engl J Med. 2007 Aug 9;357(6):553-61. Epub 2007 Jul 18.PMID: 17634448 [PubMed - indexed for MEDLINE]Related articlesFree article

Autofluorescence imaging in a case of benign familial fleck retina.

Audo I, Tsang SH, Fu AD, Barnes JA, Holder GE, Moore AT.

Arch Ophthalmol. 2007 May;125(5):714-5. No abstract available. PMID: 17502520 [PubMed - indexed for MEDLINE]Related articles

Auditory interhemispheric transfer deficits, hearing difficulties, and brain magnetic resonance imaging abnormalities in children with congenital aniridia due to PAX6 mutations.

Bamiou DE, Free SL, Sisodiya SM, Chong WK, Musiek F, Williamson KA, van Heyningen V, Moore AT, Gadian D, Luxon LM.

Arch Pediatr Adolesc Med. 2007 May;161(5):463-9.PMID: 17485622 [PubMed - indexed for MEDLINE]Related articlesFree article

Residual cone vision without alpha-transducin.

Stockman A, Smithson HE, Michaelides M, Moore AT, Webster AR, Sharpe LT.

J Vis. 2007 Mar 23;7(4):8.PMID: 17461692 [PubMed - indexed for MEDLINE]Related articlesFree article

Metal hip joint: a case report. 1942.

Moore AT, Bohlman HR.

Clin Orthop Relat Res. 2006 Dec;453:22-4. No abstract available. PMID: 17312585 [PubMed - indexed for MEDLINE]Related articles

Ecological correlates of buggy creek virus infection in Oeciacus vicarius, southwestern Nebraska, 2004.

Moore AT, Edwards EA, Brown MB, Komar N, Brown CR.

J Med Entomol. 2007 Jan;44(1):42-9.PMID: 17294919 [PubMed - indexed for MEDLINE]Related articles

Genetic enhancement of cognition in a kindred with cone-rod dystrophy due to RIMS1 mutation.

Sisodiya SM, Thompson PJ, Need A, Harris SE, Weale ME, Wilkie SE, Michaelides M, Free SL, Walley N, Gumbs C, Gerrelli D, Ruddle P, Whalley LJ, Starr JM, Hunt DM, Goldstein DB, Deary IJ, Moore AT.

J Med Genet. 2007 Jun;44(6):373-80. Epub 2007 Jan 19.PMID: 17237123 [PubMed - indexed for MEDLINE]Related articles

Increased crystalline lens thickness and phacomorphic glaucoma in patients with Fanconi anemia.

Elgohary MA, Lim KS, Siriwardena D, Moore AT, Wormald RP.

J Cataract Refract Surg. 2006 Oct;32(10):1771-4.PMID: 17010885 [PubMed - indexed for MEDLINE]Related articles

Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause "cone dystrophy with supernormal rod electroretinogram" in humans.

Wu H, Cowing JA, Michaelides M, Wilkie SE, Jeffery G, Jenkins SA, Mester V, Bird AC, Robson AG, Holder GE, Moore AT, Hunt DM, Webster AR.

Am J Hum Genet. 2006 Sep;79(3):574-9. Epub 2006 Jul 24.PMID: 16909397 [PubMed - indexed for MEDLINE]Related articlesFree article

Progressive cone and cone-rod dystrophies: phenotypes and underlying molecular genetic basis.

Michaelides M, Hardcastle AJ, Hunt DM, Moore AT.

Surv Ophthalmol. 2006 May-Jun;51(3):232-58. Review.PMID: 16644365 [PubMed - indexed for MEDLINE]Related articles

Congenital stationary night blindness associated with mutations in GRM6 encoding glutamate receptor MGluR6.

O'Connor E, Allen LE, Bradshaw K, Boylan J, Moore AT, Trump D.

Br J Ophthalmol. 2006 May;90(5):653-4. No abstract available. PMID: 16622103 [PubMed - indexed for MEDLINE]Related articlesFree article

Mutation in Rab3 GTPase-activating protein (RAB3GAP) noncatalytic subunit in a kindred with Martsolf syndrome.

Aligianis IA, Morgan NV, Mione M, Johnson CA, Rosser E, Hennekam RC, Adams G, Trembath RC, Pilz DT, Stoodley N, Moore AT, Wilson S, Maher ER.

Am J Hum Genet. 2006 Apr;78(4):702-7. Epub 2006 Feb 14.PMID: 16532399 [PubMed - indexed for MEDLINE]Related articlesFree article