Mike Michaelides - Publications

Affiliations: 
NIDA Intramural Research Program 

120 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2016 Strong SA, Gurbaxani A, Michaelides M. Treatment of Retinitis Pigmentosa-Associated Cystoid Macular Oedema Using Intravitreal Aflibercept (Eylea) despite Minimal Response to Ranibizumab (Lucentis): A Case Report. Case Reports in Ophthalmology. 7: 389-397. PMID 27721789 DOI: 10.1159/000448427  1
2016 Kotecha A, Webster AR, Wright G, Michaelides M, Rubin GS. Standing Balance Stability and the Effects of Light Touch in Adults With Profound Loss of Vision-An Exploratory Study. Investigative Ophthalmology & Visual Science. 57: 5053-5059. PMID 27661857 DOI: 10.1167/iovs.16-19606  1
2016 Georgiadis A, Duran Y, Ribeiro J, Abelleira-Hervas L, Robbie SJ, Sünkel-Laing B, Fourali S, Gonzalez-Cordero A, Cristante E, Michaelides M, Bainbridge JW, Smith AJ, Ali RR. Development of an optimized AAV2/5 gene therapy vector for Leber congenital amaurosis owing to defects in RPE65. Gene Therapy. PMID 27653967 DOI: 10.1038/gt.2016.66  1
2016 Arno G, Hull S, Carss K, Dev-Borman A, Chakarova C, Bujakowska K, van den Born I, Robson AG, Holder GE, Michaelides M, Cremers FP, Pierce E, Raymond FL, Moore AT, Webster AR. Reevaluation of the Retinal Dystrophy Due to Recessive Alleles of RGR With the Discovery of a Cis-Acting Mutation in CDHR1. Investigative Ophthalmology & Visual Science. 57: 4806-13. PMID 27623334 DOI: 10.1167/iovs.16-19687  1
2016 Raoof N, Bradley P, Theodorou M, Moore AT, Michaelides M. The New Pretender: A Large UK Case Series Of Retinal Injuries in Children Secondary to Hand-Held Lasers. American Journal of Ophthalmology. PMID 27590121 DOI: 10.1016/j.ajo.2016.08.027  1
2016 Fakin A, Robson AG, Fujinami K, Moore AT, Michaelides M, Pei-Wen Chiang J, E Holder G, Webster AR. Phenotype and Progression of Retinal Degeneration Associated With Nullizigosity of ABCA4. Investigative Ophthalmology & Visual Science. 57: 4668-78. PMID 27583828 DOI: 10.1167/iovs.16-19829  1
2016 Khan KN, Islam F, Moore AT, Michaelides M. Clinical and Genetic Features of Choroideremia in Childhood. Ophthalmology. PMID 27506488 DOI: 10.1016/j.ophtha.2016.06.051  1
2016 Tanna P, Strauss RW, Fujinami K, Michaelides M. Stargardt disease: clinical features, molecular genetics, animal models and therapeutic options. The British Journal of Ophthalmology. PMID 27491360 DOI: 10.1136/bjophthalmol-2016-308823  1
2016 Strauss RW, Muñoz B, Jha A, Ho A, Cideciyan AV, Kasilian ML, Wolfson Y, Sadda S, West S, Scholl HP, Michaelides M. Comparison of short-wavelength reduced-illuminance and conventional autofluorescence imaging in Stargardt Macular Dystrophy. American Journal of Ophthalmology. PMID 27296491 DOI: 10.1016/j.ajo.2016.06.003  1
2016 Arora R, Khan K, Kasilian M, Strauss RW, Holder GE, Robson AG, Thompson DA, Moore AT, Michaelides M. Unilateral BEST1-associated Retinopathy. American Journal of Ophthalmology. PMID 27287821 DOI: 10.1016/j.ajo.2016.05.024  1
2016 Oatts JT, Hull S, Michaelides M, Arno G, Webster AR, Moore AT. Novel heterozygous mutation in YAP1 in a family with isolated ocular colobomas. Ophthalmic Genetics. 1-3. PMID 27267789 DOI: 10.1080/13816810.2016.1188122  1
2016 Hull S, Arno G, Ku CA, Ge Z, Waseem N, Chandra A, Webster AR, Robson AG, Michaelides M, Weleber RG, Davagnanam I, Chen R, Holder GE, Pennesi ME, Moore AT. Molecular and Clinical Findings in Patients With Knobloch Syndrome. Jama Ophthalmology. PMID 27259167 DOI: 10.1001/jamaophthalmol.2016.1073  1
2016 Downs LM, Webster AR, Moore AT, Michaelides M, Ali RR, Hardcastle AJ, Mellersh CS. Investigation of SLA4A3 as a candidate gene for human retinal disease. Journal of Negative Results in Biomedicine. 15: 11. PMID 27211793 DOI: 10.1186/s12952-016-0054-z  1
2016 Khan KN, Mahroo OA, Khan R, Mohamed MD, McKibbin M, Bird A, Michaelides M, Tufail A, Moore AT. Differentiating drusen: Drusen and drusen-like appearances associated with ageing, age-related macular degeneration, inherited eye disease and other pathological processes. Progress in Retinal and Eye Research. PMID 27173377 DOI: 10.1016/j.preteyeres.2016.04.008  1
2016 Khan K, Chana R, N A, Wright G, Webster AR, Moore AT, Michaelides M. Advanced Diagnostic Genetic Testing In Inherited Retinal Disease:Experience from a Single Tertiary Referral Centre in the UK National Health Service. Clinical Genetics. PMID 27160483 DOI: 10.1111/cge.12798  1
2016 Burton E, Wattam-Bell J, S Rubin G, Aboshiha J, Michaelides M, Atkinson J, Braddick O, Nardini M. Dissociations in Coherence Sensitivity Reveal Atypical Development of Cortical Visual Processing in Congenital Achromatopsia. Investigative Ophthalmology & Visual Science. 57: 2251-9. PMID 27124317 DOI: 10.1167/iovs.15-18414  1
2016 Subash M, Comyn O, Samy A, Qatarneh D, Antonakis S, Mehat M, Tee J, Mansour T, Xing W, Bunce C, Viswanathan A, Rubin G, Weleber R, Peto T, Wickham L, ... Michaelides M, et al. The Effect of Multispot Laser Panretinal Photocoagulation on Retinal Sensitivity and Driving Eligibility in Patients With Diabetic Retinopathy. Jama Ophthalmology. PMID 27077924 DOI: 10.1001/jamaophthalmol.2016.0629  1
2016 Egervari G, Jutras-Aswad D, Landry J, Miller ML, Anderson SA, Michaelides M, Jacobs MM, Peter C, Yiannoulos G, Liu X, Hurd YL. A Functional 3'UTR Polymorphism (rs2235749) of Prodynorphin Alters microRNA-365 Binding in Ventral Striatonigral Neurons to Influence Novelty Seeking and Positive Reward Traits. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. PMID 27074815 DOI: 10.1038/npp.2016.53  1
2016 Silva L, Black R, Michaelides M, Hurd YL, Dow-Edwards D. Sex and age specific effects of delta-9-tetrahydrocannabinol during the periadolescent period in the rat: The unique susceptibility of the prepubescent animal. Neurotoxicology and Teratology. PMID 26898326 DOI: 10.1016/j.ntt.2016.02.005  1
2016 Majander A, Bitner-Glindzicz M, Chan CM, Duncan HJ, Chinnery PF, Subash M, Keane PA, Webster AR, Moore AT, Michaelides M, Yu-Wai-Man P. Lamination of the Outer Plexiform Layer in Optic Atrophy Caused by Dominant WFS1 Mutations. Ophthalmology. PMID 26875006 DOI: 10.1016/j.ophtha.2016.01.007  1
2016 Tee JJ, Smith AJ, Hardcastle AJ, Michaelides M. RPGR-associated retinopathy: clinical features, molecular genetics, animal models and therapeutic options. The British Journal of Ophthalmology. PMID 26843488 DOI: 10.1136/bjophthalmol-2015-307698  1
2016 Abozaid MA, Langlo CS, Dubis AM, Michaelides M, Tarima S, Carroll J. Reliability and Repeatability of Cone Density Measurements in Patients with Congenital Achromatopsia. Advances in Experimental Medicine and Biology. 854: 277-83. PMID 26427422 DOI: 10.1007/978-3-319-17121-0_37  1
2016 Gardner JC, Michaelides M, Hardcastle AJ. Cone opsins, colour blindness and cone dystrophy: Genotype-phenotype correlations South African Medical Journal. 106: S75-S78. DOI: 10.7196/SAMJ.2016.v106i6.11001  1
2016 Kousal B, Dudakova L, Gaillyova R, Hejtmankova M, Diblik P, Michaelides M, Liskova P. Phenotypic features of CRB1-associated early-onset severe retinal dystrophy and the different molecular approaches to identifying the disease-causing variants Graefe's Archive For Clinical and Experimental Ophthalmology. 254: 1833-1839. DOI: 10.1007/s00417-016-3358-2  1
2016 Michaelides M, Moore A. Sorsby fundus dystrophy Macular Dystrophies. 59-62. DOI: 10.1007/978-3-319-26621-3_7  1
2016 Michaelides M, Moore A. North Carolina macular dystrophy and North Carolina macular dystrophy-like disorders Macular Dystrophies. 53-58. DOI: 10.1007/978-3-319-26621-3_6  1
2015 Scholl HP, Moore AT, Koenekoop RK, Wen Y, Fishman GA, van den Born LI, Bittner A, Bowles K, Fletcher EC, Collison FT, Dagnelie G, Degli Eposti S, Michaelides M, Saperstein DA, Schuchard RA, et al. Safety and Proof-of-Concept Study of Oral QLT091001 in Retinitis Pigmentosa Due to Inherited Deficiencies of Retinal Pigment Epithelial 65 Protein (RPE65) or Lecithin:Retinol Acyltransferase (LRAT). Plos One. 10: e0143846. PMID 26656277 DOI: 10.1371/journal.pone.0143846  1
2015 Bellingham J, Davidson AE, Aboshiha J, Simonelli F, Bainbridge JW, Michaelides M, van der Spuy J. Investigation of Aberrant Splicing Induced by AIPL1 Variations as a Cause of Leber Congenital Amaurosis. Investigative Ophthalmology & Visual Science. 56: 7784-7793. PMID 26650897 DOI: 10.1167/iovs.15-18092  1
2015 Urban DJ, Zhu H, Marcinkiewcz CA, Michaelides M, Oshibuchi H, Rhea D, Aryal DK, Farrell MS, Lowery-Gionta E, Olsen RH, Wetsel WC, Kash TL, Hurd YL, Tecott LH, Roth BL. Elucidation of the Behavioral Program and Neuronal Network Encoded by Dorsal Raphe Serotonergic Neurons. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. PMID 26383016 DOI: 10.1038/npp.2015.293  1
2015 Strauss RW, Dubis AM, Cooper RF, Ba-Abbad R, Moore AT, Webster AR, Dubra A, Carroll J, Michaelides M. Retinal Architecture in ​RGS9- and ​R9AP-Associated Retinal Dysfunction (Bradyopsia). American Journal of Ophthalmology. PMID 26343007 DOI: 10.1016/j.ajo.2015.08.032  1
2015 Pappano WN, Guo J, He Y, Ferguson D, Jagadeeswaran S, Osterling DJ, Gao W, Spence JK, Pliushchev M, Sweis RF, Buchanan FG, Michaelides MR, Shoemaker AR, Tse C, Chiang GG. The Histone Methyltransferase Inhibitor A-366 Uncovers a Role for G9a/GLP in the Epigenetics of Leukemia. Plos One. 10: e0131716. PMID 26147105 DOI: 10.1371/journal.pone.0131716  1
2015 Smith J, Ward D, Michaelides M, Moore AT, Simpson S. New and emerging technologies for the treatment of inherited retinal diseases: a horizon scanning review. Eye (London, England). PMID 26113499 DOI: 10.1038/eye.2015.115  1
2015 Thanos PK, Michaelides M, Subrize M, Miller ML, Bellezza R, Cooney RN, Leggio L, Wang GJ, Rogers AM, Volkow ND, Hajnal A. Roux-en-Y Gastric Bypass Alters Brain Activity in Regions that Underlie Reward and Taste Perception. Plos One. 10: e0125570. PMID 26039080 DOI: 10.1371/journal.pone.0125570  1
2015 Lee H, Purohit R, Sheth V, McLean RJ, Kohl S, Leroy BP, Sundaram V, Michaelides M, Proudlock FA, Gottlob I. Retinal Development in Infants and Young Children with Achromatopsia. Ophthalmology. 122: 2145-7. PMID 25972256 DOI: 10.1016/j.ophtha.2015.03.033  1
2015 Bainbridge JW, Mehat MS, Sundaram V, Robbie SJ, Barker SE, Ripamonti C, Georgiadis A, Mowat FM, Beattie SG, Gardner PJ, Feathers KL, Luong VA, Yzer S, Balaggan K, Viswanathan A, ... ... Michaelides M, et al. Long-term effect of gene therapy on Leber's congenital amaurosis. The New England Journal of Medicine. 372: 1887-97. PMID 25938638 DOI: 10.1056/NEJMoa1414221  1
2015 Halford S, Liew G, Mackay DS, Sergouniotis PI, Holt R, Broadgate S, Volpi EV, Ocaka L, Robson AG, Holder GE, Moore AT, Michaelides M, Webster AR. Author reply: To PMID 24480711. Ophthalmology. 122: e22. PMID 25797088 DOI: 10.1016/j.ophtha.2014.08.041  1
2015 Aboshiha J, Dubis AM, Carroll J, Hardcastle AJ, Michaelides M. The cone dysfunction syndromes. The British Journal of Ophthalmology. PMID 25770143 DOI: 10.1136/bjophthalmol-2014-306505  1
2015 Langlo C, Dubis A, Michaelides M, Carroll J. CNGB3-Achromatopsia Clinical Trial With CNTF: Diminished Rod Pathway Responses With No Evidence of Improvement in Cone Function. Investigative Ophthalmology & Visual Science. 56: 1505. PMID 25737149 DOI: 10.1167/iovs.14-15897  1
2015 Liew G, Moore AT, Webster AR, Michaelides M. Efficacy and prognostic factors of response to carbonic anhydrase inhibitors in management of cystoid macular edema in retinitis pigmentosa. Investigative Ophthalmology & Visual Science. 56: 1531-6. PMID 25670491 DOI: 10.1167/iovs.14-15995  1
2015 Aboshiha J, Dubis AM, van der Spuy J, Nishiguchi KM, Cheeseman EW, Ayuso C, Ehrenberg M, Simonelli F, Bainbridge JW, Michaelides M. Preserved outer retina in AIPL1 Leber's congenital amaurosis: implications for gene therapy. Ophthalmology. 122: 862-4. PMID 25596619 DOI: 10.1016/j.ophtha.2014.11.019  1
2015 Michaelides M, Hurd YL. DREAMM: a biobehavioral imaging methodology for dynamic in vivo whole-brain mapping of cell type-specific functional networks. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 40: 239-40. PMID 25482170 DOI: 10.1038/npp.2014.233  1
2015 Fujinami K, Zernant J, Chana RK, Wright GA, Tsunoda K, Ozawa Y, Tsubota K, Robson AG, Holder GE, Allikmets R, Michaelides M, Moore AT. Clinical and molecular characteristics of childhood-onset Stargardt disease. Ophthalmology. 122: 326-34. PMID 25312043 DOI: 10.1016/j.ophtha.2014.08.012  1
2015 Miller ML, Chadwick B, Morris CV, Michaelides M, Hurd YL. Cannabinoid-opioid interactions Cannabinoid Modulation of Emotion, Memory, and Motivation. 393-407. DOI: 10.1007/978-1-4939-2294-9_15  1
2014 Kousal B, Skalicka P, Valesova L, Fletcher T, Hart-Holden N, O’grady A, Chakarova CF, Michaelides M, Hardcastle AJ, Liskova P. Severe retinal degeneration in women with a c.2543del mutation in ORF15 of the RPGR gene Molecular Vision. 20: 1307-1317. PMID 25352739  1
2014 Dubis AM, Cooper RF, Aboshiha J, Langlo CS, Sundaram V, Liu B, Collison F, Fishman GA, Moore AT, Webster AR, Dubra A, Carroll J, Michaelides M. Genotype-dependent variability in residual cone structure in achromatopsia: toward developing metrics for assessing cone health. Investigative Ophthalmology & Visual Science. 55: 7303-11. PMID 25277229 DOI: 10.1167/iovs.14-14225  1
2014 Aboshiha J, Luong V, Cowing J, Dubis AM, Bainbridge JW, Ali RR, Webster AR, Moore AT, Fitzke FW, Michaelides M. Dark-adaptation functions in molecularly confirmed achromatopsia and the implications for assessment in retinal therapy trials. Investigative Ophthalmology & Visual Science. 55: 6340-9. PMID 25168900 DOI: 10.1167/iovs.14-14910  1
2014 Gardner JC, Liew G, Quan YH, Ermetal B, Ueyama H, Davidson AE, Schwarz N, Kanuga N, Chana R, Maher ER, Webster AR, Holder GE, Robson AG, Cheetham ME, Liebelt J, ... ... Michaelides M, et al. Three different cone opsin gene array mutational mechanisms with genotype-phenotype correlation and functional investigation of cone opsin variants. Human Mutation. 35: 1354-62. PMID 25168334 DOI: 10.1002/humu.22679  1
2014 Aboshiha J, Dubis AM, Cowing J, Fahy RT, Sundaram V, Bainbridge JW, Ali RR, Dubra A, Nardini M, Webster AR, Moore AT, Rubin G, Carroll J, Michaelides M. A prospective longitudinal study of retinal structure and function in achromatopsia. Investigative Ophthalmology & Visual Science. 55: 5733-43. PMID 25103266 DOI: 10.1167/iovs.14-14937  1
2014 Sweis RF, Pliushchev M, Brown PJ, Guo J, Li F, Maag D, Petros AM, Soni NB, Tse C, Vedadi M, Michaelides MR, Chiang GG, Pappano WN. Discovery and development of potent and selective inhibitors of histone methyltransferase g9a. Acs Medicinal Chemistry Letters. 5: 205-9. PMID 24900801 DOI: 10.1021/ml400496h  1
2014 Sundaram V, Carroll J, Michaelides M. Author reply: To PMID 24148654. Ophthalmology. 121: e41. PMID 24793523 DOI: 10.1016/j.ophtha.2014.03.008  1
2014 Stockman A, Henning GB, Moore AT, Webster AR, Michaelides M, Ripamonti C. Visual consequences of molecular changes in the guanylate cyclase-activating protein. Investigative Ophthalmology & Visual Science. 55: 1930-40. PMID 24557353 DOI: 10.1167/iovs.13-13682  1
2014 Halford S, Liew G, MacKay DS, Sergouniotis PI, Holt R, Broadgate S, Volpi EV, Ocaka L, Robson AG, Holder GE, Moore AT, Michaelides M, Webster AR. Detailed phenotypic and genotypic characterization of bietti crystalline dystrophy Ophthalmology. 121: 1174-1184. PMID 24480711 DOI: 10.1016/j.ophtha.2013.11.042  1
2014 Errera MH, Michaelides M, Keane PA, Restori M, Paques M, Moore AT, Yeoh J, Chan D, Egan CA, Patel PJ, Tufail A. The extended clinical phenotype of dome-shaped macula Graefe's Archive For Clinical and Experimental Ophthalmology. 252: 499-508. PMID 24464468 DOI: 10.1007/s00417-013-2561-7  1
2014 Singh R, Fujinami K, Chen LL, Michaelides M, Moore AT. Longitudinal follow-up of siblings with a discordant Stargardt disease phenotype. Acta Ophthalmologica. 92: e331-2. PMID 24428930 DOI: 10.1111/aos.12280  1
2014 Ripamonti C, Aboshiha J, Henning GB, Sergouniotis PI, Michaelides M, Moore AT, Webster AR, Stockman A. Vision in observers with enhanced S-cone syndrome: an excess of s-cones but connected mainly to conventional s-cone pathways. Investigative Ophthalmology & Visual Science. 55: 963-76. PMID 24425859 DOI: 10.1167/iovs.13-12897  1
2014 Szutorisz H, DiNieri JA, Sweet E, Egervari G, Michaelides M, Carter JM, Ren Y, Miller ML, Blitzer RD, Hurd YL. Parental THC exposure leads to compulsive heroin-seeking and altered striatal synaptic plasticity in the subsequent generation. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 39: 1315-23. PMID 24385132 DOI: 10.1038/npp.2013.352  1
2014 Stockman A, Henning GB, Michaelides M, Moore AT, Webster AR, Cammack J, Ripamonti C. Cone dystrophy with "supernormal" rod ERG: psychophysical testing shows comparable rod and cone temporal sensitivity losses with no gain in rod function. Investigative Ophthalmology & Visual Science. 55: 832-40. PMID 24370833 DOI: 10.1167/iovs.13-12919  1
2014 Sundaram V, Wilde C, Aboshiha J, Cowing J, Han C, Langlo CS, Chana R, Davidson AE, Sergouniotis PI, Bainbridge JW, Ali RR, Dubra A, Rubin G, Webster AR, Moore AT, ... ... Michaelides M, et al. Retinal structure and function in achromatopsia: implications for gene therapy. Ophthalmology. 121: 234-45. PMID 24148654 DOI: 10.1016/j.ophtha.2013.08.017  1
2014 Fujinami K, Singh R, Carroll J, Zernant J, Allikmets R, Michaelides M, Moore AT. Fine central macular dots associated with childhood-onset Stargardt Disease. Acta Ophthalmologica. 92: e157-9. PMID 24020726 DOI: 10.1111/aos.12259  1
2014 Hurd YL, Michaelides M, Miller ML, Jutras-Aswad D. Trajectory of adolescent cannabis use on addiction vulnerability. Neuropharmacology. 76: 416-24. PMID 23954491 DOI: 10.1016/j.neuropharm.2013.07.028  1
2014 Michaelides M, Papas S, Pantziara M, Ioannidis K. High spatial resolution mri of cystic adventitial disease of the iliofemoral vein communicating with the hip joint Cardiovascular and Interventional Radiology. 37: 271-274. PMID 23670571 DOI: 10.1007/s00270-013-0645-8  1
2014 Liew G, Michaelides M, Bunce C. A comparison of the causes of blindness certifications in England and Wales in working age adults (16-64 years), 1999-2000 with 2009-2010 Bmj Open. 4. DOI: 10.1136/bmjopen-2013-004015  1
2013 Ba-Abbad R, Sergouniotis PI, Plagnol V, Robson AG, Michaelides M, Holder GE, Webster AR. Clinical characteristics of early retinal disease due to CDHR1 mutation. Molecular Vision. 19: 2250-9. PMID 24265541  1
2013 Fujinami K, Lois N, Mukherjee R, McBain VA, Tsunoda K, Tsubota K, Stone EM, Fitzke FW, Bunce C, Moore AT, Webster AR, Michaelides M. A longitudinal study of Stargardt disease: quantitative assessment of fundus autofluorescence, progression, and genotype correlations. Investigative Ophthalmology & Visual Science. 54: 8181-90. PMID 24265018 DOI: 10.1167/iovs.13-12104  1
2013 Scheepers MA, Lecuona KA, Rogers G, Bunce C, Corcoran C, Michaelides M. The value of routine polymerase chain reaction analysis of intraocular fluid specimens in the diagnosis of infectious posterior Uveitis The Scientific World Journal. 2013. PMID 24250270 DOI: 10.1155/2013/545149  1
2013 Michaelides M, Anderson SA, Ananth M, Smirnov D, Thanos PK, Neumaier JF, Wang GJ, Volkow ND, Hurd YL. Whole-brain circuit dissection in free-moving animals reveals cell-specific mesocorticolimbic networks. The Journal of Clinical Investigation. 123: 5342-50. PMID 24231358 DOI: 10.1172/JCI72117  1
2013 Anderson SA, Michaelides M, Zarnegar P, Ren Y, Fagergren P, Thanos PK, Wang GJ, Bannon M, Neumaier JF, Keller E, Volkow ND, Hurd YL. Impaired periamygdaloid-cortex prodynorphin is characteristic of opiate addiction and depression. The Journal of Clinical Investigation. 123: 5334-41. PMID 24231353 DOI: 10.1172/JCI70395  1
2013 Lee H, Sheth V, Bibi M, Maconachie G, Patel A, McLean RJ, Michaelides M, Thomas MG, Proudlock FA, Gottlob I. Potential of handheld optical coherence tomography to determine cause of infantile nystagmus in children by using foveal morphology Ophthalmology. 120: 2714-2724. PMID 24161406 DOI: 10.1016/j.ophtha.2013.07.018  1
2013 Cideciyan AV, Hufnagel RB, Carroll J, Sumaroka A, Luo X, Schwartz SB, Dubra A, Land M, Michaelides M, Gardner JC, Hardcastle AJ, Moore AT, Sisk RA, Ahmed ZM, Kohl S, et al. Human cone visual pigment deletions spare sufficient photoreceptors to warrant gene therapy. Human Gene Therapy. 24: 993-1006. PMID 24067079 DOI: 10.1089/hum.2013.153  1
2013 Sivaprasad S, Crosby-Nwaobi R, Esposti S, Peto T, Rajendram R, Michaelides M, Hykin P. Structural and Functional Measures of Efficacy in Response to Bevacizumab Monotherapy in Diabetic Macular Oedema: Exploratory Analyses of the BOLT Study (Report 4) Plos One. 8. PMID 24013651 DOI: 10.1371/journal.pone.0072755  1
2013 Fujinami K, Zernant J, Chana RK, Wright GA, Tsunoda K, Ozawa Y, Tsubota K, Webster AR, Moore AT, Allikmets R, Michaelides M. ABCA4 gene screening by next-generation sequencing in a British cohort. Investigative Ophthalmology & Visual Science. 54: 6662-74. PMID 23982839 DOI: 10.1167/iovs.13-12570  1
2013 Fujinami K, Sergouniotis PI, Davidson AE, Wright G, Chana RK, Tsunoda K, Tsubota K, Egan CA, Robson AG, Moore AT, Holder GE, Michaelides M, Webster AR. Clinical and molecular analysis of Stargardt disease with preserved foveal structure and function. American Journal of Ophthalmology. 156: 487-501.e1. PMID 23953153 DOI: 10.1016/j.ajo.2013.05.003  1
2013 Sivaprasad S, Crosby-Nwaobi R, Heng LZ, Peto T, Michaelides M, Hykin P. Injection frequency and response to bevacizumab monotherapy for diabetic macular oedema (BOLT Report 5). The British Journal of Ophthalmology. 97: 1177-80. PMID 23823078 DOI: 10.1136/bjophthalmol-2013-303168  1
2013 Fujinami K, Sergouniotis PI, Davidson AE, Mackay DS, Tsunoda K, Tsubota K, Robson AG, Holder GE, Moore AT, Michaelides M, Webster AR. The clinical effect of homozygous ABCA4 alleles in 18 patients. Ophthalmology. 120: 2324-31. PMID 23769331 DOI: 10.1016/j.ophtha.2013.04.016  1
2013 Thanos PK, Robison L, Nestler EJ, Kim R, Michaelides M, Lobo MK, Volkow ND. Mapping brain metabolic connectivity in awake rats with μPET and optogenetic stimulation. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 6343-9. PMID 23575833 DOI: 10.1523/JNEUROSCI.4997-12.2013  1
2013 Michaelides M, Miller ML, Subrize M, Kim R, Robison L, Hurd YL, Wang GJ, Volkow ND, Thanos PK. Limbic activation to novel versus familiar food cues predicts food preference and alcohol intake. Brain Research. 1512: 37-44. PMID 23506787 DOI: 10.1016/j.brainres.2013.03.006  1
2013 Fujinami K, Lois N, Davidson AE, Mackay DS, Hogg CR, Stone EM, Tsunoda K, Tsubota K, Bunce C, Robson AG, Moore AT, Webster AR, Holder GE, Michaelides M. A longitudinal study of stargardt disease: clinical and electrophysiologic assessment, progression, and genotype correlations. American Journal of Ophthalmology. 155: 1075-1088.e13. PMID 23499370 DOI: 10.1016/j.ajo.2013.01.018  1
2013 McClements M, Davies WI, Michaelides M, Carroll J, Rha J, Mollon JD, Neitz M, MacLaren RE, Moore AT, Hunt DM. X-linked cone dystrophy and colour vision deficiency arising from a missense mutation in a hybrid L/M cone opsin gene. Vision Research. 80: 41-50. PMID 23337435 DOI: 10.1016/j.visres.2012.12.012  1
2013 McClements M, Davies WI, Michaelides M, Young T, Neitz M, MacLaren RE, Moore AT, Hunt DM. Variations in opsin coding sequences cause x-linked cone dysfunction syndrome with myopia and dichromacy. Investigative Ophthalmology & Visual Science. 54: 1361-9. PMID 23322568 DOI: 10.1167/iovs.12-11156  1
2013 Soumplis V, Sergouniotis PI, Robson AG, Michaelides M, Moore AT, Holder GE, Webster AR. Phenotypic findings in C1QTNF5 retinopathy (late-onset retinal degeneration). Acta Ophthalmologica. 91: e191-5. PMID 23289492 DOI: 10.1111/aos.12010  1
2013 Davidson AE, Sergouniotis PI, Mackay DS, Wright GA, Waseem NH, Michaelides M, Holder GE, Robson AG, Moore AT, Plagnol V, Webster AR. RP1L1 variants are associated with a spectrum of inherited retinal diseases including retinitis pigmentosa and occult macular dystrophy. Human Mutation. 34: 506-14. PMID 23281133 DOI: 10.1002/humu.22264  1
2013 Thanos PK, Robison LS, Robinson JK, Michaelides M, Wang GJ, Volkow ND. Obese rats with deficient leptin signaling exhibit heightened sensitivity to olfactory food cues. Synapse (New York, N.Y.). 67: 171-8. PMID 23172699 DOI: 10.1002/syn.21627  1
2013 Sweis RF, Michaelides MR. Recent advances in small-molecule modulation of epigenetic targets: Discovery and development of histone methyltransferase and bromodomain inhibitors Annual Reports in Medicinal Chemistry. 48: 185-203. DOI: 10.1016/B978-0-12-417150-3.00013-2  1
2012 Michaelides M, Thanos PK, Volkow ND, Wang GJ. Translational neuroimaging in drug addiction and obesity. Ilar Journal / National Research Council, Institute of Laboratory Animal Resources. 53: 59-68. PMID 23520600  1
2012 Carroll J, Dubra A, Gardner JC, Mizrahi-Meissonnier L, Cooper RF, Dubis AM, Nordgren R, Genead M, Connor TB, Stepien KE, Sharon D, Hunt DM, Banin E, Hardcastle AJ, Moore AT, ... ... Michaelides M, et al. The effect of cone opsin mutations on retinal structure and the integrity of the photoreceptor mosaic. Investigative Ophthalmology & Visual Science. 53: 8006-15. PMID 23139274 DOI: 10.1167/iovs.12-11087  1
2012 Godara P, Cooper RF, Sergouniotis PI, Diederichs MA, Streb MR, Genead MA, McAnany JJ, Webster AR, Moore AT, Dubis AM, Neitz M, Dubra A, Stone EM, Fishman GA, Han DP, ... Michaelides M, et al. Assessing retinal structure in complete congenital stationary night blindness and Oguchi disease. American Journal of Ophthalmology. 154: 987-1001.e1. PMID 22959359 DOI: 10.1016/j.ajo.2012.06.003  1
2012 Glaser KB, Li J, Marcotte PA, Magoc TJ, Guo J, Reuter DR, Tapang P, Wei RQ, Pease LJ, Bui MH, Chen Z, Frey RR, Johnson EF, Osterling DJ, Olson AM, ... ... Michaelides MR, et al. Preclinical characterization of ABT-348, a kinase inhibitor targeting the aurora, vascular endothelial growth factor receptor/platelet-derived growth factor receptor, and Src kinase families. The Journal of Pharmacology and Experimental Therapeutics. 343: 617-27. PMID 22935731 DOI: 10.1124/jpet.112.197087  1
2012 Ji Z, Dai Y, Abad-Zapatero C, Albert DH, Bouska JJ, Glaser KB, Marcotte PA, Soni NB, Magoc TJ, Stewart KD, Wei RQ, Davidsen SK, Michaelides MR. Exploration of diverse hinge-binding scaffolds for selective Aurora kinase inhibitors Bioorganic and Medicinal Chemistry Letters. 22: 4528-4531. PMID 22727637 DOI: 10.1016/j.bmcl.2012.05.125  1
2012 Michaelides M, Thanos PK, Volkow ND, Wang GJ. Dopamine-related frontostriatal abnormalities in obesity and binge-eating disorder: emerging evidence for developmental psychopathology. International Review of Psychiatry (Abingdon, England). 24: 211-8. PMID 22724642 DOI: 10.3109/09540261.2012.679918  1
2012 Curtin ML, Heyman HR, Frey RR, Marcotte PA, Glaser KB, Jankowski JR, Magoc TJ, Albert DH, Olson AM, Reuter DR, Bouska JJ, Montgomery DA, Palma JP, Donawho CK, Stewart KD, ... ... Michaelides MR, et al. Pyrazole diaminopyrimidines as dual inhibitors of KDR and Aurora B kinases. Bioorganic & Medicinal Chemistry Letters. 22: 4750-5. PMID 22695126 DOI: 10.1016/j.bmcl.2012.05.067  1
2012 Webb TR, Parfitt DA, Gardner JC, Martinez A, Bevilacqua D, Davidson AE, Zito I, Thiselton DL, Ressa JH, Apergi M, Schwarz N, Kanuga N, Michaelides M, Cheetham ME, Gorin MB, et al. Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23). Human Molecular Genetics. 21: 3647-54. PMID 22619378 DOI: 10.1093/hmg/dds194  1
2012 Michaelides M, Jeffery G, Moore AT. Developmental macular disorders: Phenotypes and underlying molecular genetic basis British Journal of Ophthalmology. 96: 917-924. PMID 22517799 DOI: 10.1136/bjophthalmol-2011-300994  1
2012 Rajendram R, Fraser-Bell S, Kaines A, Michaelides M, Hamilton RD, Esposti SD, Peto T, Egan C, Bunce C, Leslie RD, Hykin PG. A 2-year prospective randomized controlled trial of intravitreal bevacizumab or laser therapy (BOLT) in the management of diabetic macular edema: 24-month data: report 3. Archives of Ophthalmology (Chicago, Ill. : 1960). 130: 972-9. PMID 22491395 DOI: 10.1001/archophthalmol.2012.393  1
2012 Curtin ML, Frey RR, Heyman HR, Soni NB, Marcotte PA, Pease LJ, Glaser KB, Magoc TJ, Tapang P, Albert DH, Osterling DJ, Olson AM, Bouska JJ, Guan Z, Preusser LC, ... ... Michaelides MR, et al. Thienopyridine ureas as dual inhibitors of the VEGF and Aurora kinase families. Bioorganic & Medicinal Chemistry Letters. 22: 3208-12. PMID 22465635 DOI: 10.1016/j.bmcl.2012.03.035  1
2012 Tan MH, Mackay DS, Cowing J, Tran HV, Smith AJ, Wright GA, Dev-Borman A, Henderson RH, Moradi P, Russell-Eggitt I, MacLaren RE, Robson AG, Cheetham ME, Thompson DA, Webster AR, ... Michaelides M, et al. Leber congenital amaurosis associated with AIPL1: challenges in ascribing disease causation, clinical findings, and implications for gene therapy. Plos One. 7: e32330. PMID 22412862 DOI: 10.1371/journal.pone.0032330  1
2012 Webb TR, Matarin M, Gardner JC, Kelberman D, Hassan H, Ang W, Michaelides M, Ruddle JB, Pennell CE, Yazar S, Khor CC, Aung T, Yogarajah M, Robson AG, Holder GE, et al. X-linked megalocornea caused by mutations in CHRDL1 identifies an essential role for ventroptin in anterior segment development. American Journal of Human Genetics. 90: 247-59. PMID 22284829 DOI: 10.1016/j.ajhg.2011.12.019  1
2012 Gardner JC, Webb TR, Kanuga N, Robson AG, Holder GE, Stockman A, Ripamonti C, Ebenezer ND, Ogun O, Devery S, Wright GA, Maher ER, Cheetham ME, Moore AT, Michaelides M, et al. A novel missense mutation in both OPN1LW and OPN1MW cone opsin genes causes X-linked cone dystrophy (XLCOD5). Advances in Experimental Medicine and Biology. 723: 595-601. PMID 22183383 DOI: 10.1007/978-1-4614-0631-0_76  1
2012 Subash M, Rotsos T, Wright GA, Devery S, Holder GE, Robson AG, Pal B, Tufail A, Webster AR, Moore AT, Michaelides M. Unilateral vitelliform maculopathy: a comprehensive phenotype study with molecular screening of BEST1 and PRPH2. The British Journal of Ophthalmology. 96: 719-22. PMID 22174098 DOI: 10.1136/bjophthalmol-2011-300964  1
2012 Michaelides M, Thanos PK, Kim R, Cho J, Ananth M, Wang GJ, Volkow ND. PET imaging predicts future body weight and cocaine preference. Neuroimage. 59: 1508-13. PMID 21889993 DOI: 10.1016/j.neuroimage.2011.08.028  1
2012 Sergouniotis PI, Holder GE, Robson AG, Michaelides M, Webster AR, Moore AT. High-resolution optical coherence tomography imaging in KCNV2 retinopathy British Journal of Ophthalmology. 96: 213-217. PMID 21558291 DOI: 10.1136/bjo.2011.203638  1
2012 Vasiliadis K, Papavasiliou C, Fachiridis D, Pervana S, Michaelides M, Kiranou M, Makridis C. Retroperitoneal extra-adrenal ganglioneuroma involving the infrahepatic inferior vena cava, celiac axis and superior mesenteric artery: A case report International Journal of Surgery Case Reports. 3: 541-543. DOI: 10.1016/j.ijscr.2012.07.008  1
2011 McClellan WJ, Dai Y, Abad-Zapatero C, Albert DH, Bouska JJ, Glaser KB, Magoc TJ, Marcotte PA, Osterling DJ, Stewart KD, Davidsen SK, Michaelides MR. Discovery of potent and selective thienopyrimidine inhibitors of Aurora kinases. Bioorganic & Medicinal Chemistry Letters. 21: 5620-4. PMID 21778056 DOI: 10.1016/j.bmcl.2011.06.041  1
2011 Ali N, Child CS, Michaelides M, Olver JM. Recurrence of a rare skin tumour: Superficial angiomyxoma in the eyelid Canadian Journal of Ophthalmology. 46: 205-206. PMID 21708097 DOI: 10.3129/i11-005  1
2011 Thanos PK, Subrize M, Lui W, Puca Z, Ananth M, Michaelides M, Wang GJ, Volkow ND. D-cycloserine facilitates extinction of cocaine self-administration in C57 mice. Synapse (New York, N.Y.). 65: 1099-105. PMID 21584863 DOI: 10.1002/syn.20944  1
2011 Buch PK, Mihelec M, Cottrill P, Wilkie SE, Pearson RA, Duran Y, West EL, Michaelides M, Ali RR, Hunt DM. Dominant cone-rod dystrophy: a mouse model generated by gene targeting of the GCAP1/Guca1a gene. Plos One. 6: e18089. PMID 21464903 DOI: 10.1371/journal.pone.0018089  1
2011 Michaelides M, Rha J, Dees EW, Baraas RC, Wagner-Schuman ML, Mollon JD, Dubis AM, Andersen MK, Rosenberg T, Larsen M, Moore AT, Carroll J. Integrity of the cone photoreceptor mosaic in oligocone trichromacy. Investigative Ophthalmology & Visual Science. 52: 4757-64. PMID 21436275 DOI: 10.1167/iovs.10-6659  1
2011 Michaelides M, Stover NB, Francis PJ, Weleber RG. Retinal toxicity associated with hydroxychloroquine and chloroquine: Risk factors, screening, and progression despite cessation of therapy Archives of Ophthalmology. 129: 30-39. PMID 21220626 DOI: 10.1001/archophthalmol.2010.321  1
2011 Thanos PK, Cho J, Kim R, Michaelides M, Primeaux S, Bray G, Wang GJ, Volkow ND. Bromocriptine increased operant responding for high fat food but decreased chow intake in both obesity-prone and resistant rats Behavioural Brain Research. 217: 165-170. PMID 21034777 DOI: 10.1016/j.bbr.2010.10.027  1
2011 Sohn EH, Michaelides M, Bird AC, Roberts CJ, Moore AT, Smyth D, Brady AF, Hungerford JL. Novel mutation in PANK2 associated with retinal telangiectasis. The British Journal of Ophthalmology. 95: 149-50. PMID 20974629 DOI: 10.1136/bjo.2010.183616  1
2011 Thanos PK, Gopez V, Delis F, Michaelides M, Grandy DK, Wang GJ, Kunos G, Volkow ND. Upregulation of cannabinoid type 1 receptors in dopamine D2 receptor knockout mice is reversed by chronic forced ethanol consumption. Alcoholism, Clinical and Experimental Research. 35: 19-27. PMID 20958329 DOI: 10.1111/j.1530-0277.2010.01318.x  1
2011 Arrigoni FI, Matarin M, Thompson PJ, Michaelides M, McClements ME, Redmond E, Clarke L, Ellins E, Mohamed S, Pavord I, Klein N, Hunt DM, Moore AT, Halcox J, Sisodiya SM. Extended extraocular phenotype of PROM1 mutation in kindreds with known autosomal dominant macular dystrophy. European Journal of Human Genetics : Ejhg. 19: 131-7. PMID 20859302 DOI: 10.1038/ejhg.2010.147  1
2011 Weleber RG, Michaelides M, Trzupek KM, Stover NB, Stone EM. The phenotype of Severe Early Childhood Onset Retinal Dystrophy (SECORD) from mutation of RPE65 and differentiation from Leber congenital amaurosis. Investigative Ophthalmology & Visual Science. 52: 292-302. PMID 20811047 DOI: 10.1167/iovs.10-6106  1
2011 Michaelides M, Dimarelos V, Stratilati S, Tsitouridis I. Intramural dissection of the renal collecting system during percutaneous nephrostomy: Computed tomography findings of a rare complication Cardiovascular and Interventional Radiology. 34. PMID 20532773 DOI: 10.1007/s00270-010-9910-2  1
2011 Michaelides M, Pervana S, Sotiridadis C, Tsitouridis I. Cystic adventitial disease of the popliteal artery Diagnostic and Interventional Radiology. 17: 166-168. PMID 20039232 DOI: 10.4261/1305-3825.DIR.2790-09.2  1
2011 Michaelides M, Thanos PK, Volkow ND, Wang GJ. Functional neuroimaging in obesity Psychiatric Annals. 41: 496-500. DOI: 10.3928/00485713-20110921-09  1
2011 Michaelides M, Nikolaidou A, Konstantinou D, Balis GC, Tsitouridis I. Posterior mediastinal Castelman's disease presented as hypervascular lipomatous tumor Hippokratia. 15: 361-362.  1
2011 Michaelides M, Dimarelos V, Kostantinou D, Bintoudi A, Tzikos F, Kyriakou V, Rodokalakis G, Tsitouridis I. A new variant of Todani type I choledochal cyst. Imaging evaluation Hippokratia. 15: 174-177.  1
2010 Thanos PK, Kim R, Cho J, Michaelides M, Anderson BJ, Primeaux SD, Bray GA, Wang GJ, Robinson JK, Volkow ND. Obesity-resistant S5B rats showed greater cocaine conditioned place preference than the obesity-prone OM rats. Physiology & Behavior. 101: 713-8. PMID 20801137 DOI: 10.1016/j.physbeh.2010.08.011  1
2010 Michaelides M, Foster PJ. Retinal vein occlusion and angle closure: A retrospective case series Journal of Glaucoma. 19: 643-649. PMID 20179618 DOI: 10.1097/IJG.0b013e3181d12dea  1
2004 Li J, Staver MJ, Curtin ML, Holms JH, Frey RR, Edalji R, Smith R, Michaelides MR, Davidsen SK, Glaser KB. Expression and functional characterization of recombinant human HDAC1 and HDAC3. Life Sciences. 74: 2693-705. PMID 15043985 DOI: 10.1016/j.lfs.2003.09.070  1
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