Bibliography of Recent Articles by Our Faculty, Fellows, and Residents

Earlier Articles | Articles published before 2000

2012

1. Sanchez CI, Niemeijer M, Isgum I, Dumitrescu A, Suttorp-Schulten MS, Abramoff MD, et al. Contextual computer-aided detection: Improving bright lesion detection in retinal images and coronary calcification identification in CT scans. Med Image Anal. 2012;16(1):50-62.
2. Thurtell MJ, Tomsak RL, Daroff RB. Neuro-Ophthalmology. Oxford; New York: Oxford University Press; 2012.

2011

1. Abu-El-Haija M, Stasheff S, Atkins DL, Bishop WP. Rheumatic Fever in a Patient Receiving Infliximab Therapy for Crohn Disease. J Pediatr Gastroenterol Nutr. 2011;52(3):360-361.

2. Ahmed RM, Wilkinson M, Parker GD, Thurtell MJ, Macdonald J, McCluskey PJ, et al. Transverse Sinus Stenting for Idiopathic Intracranial Hypertension: A Review of 52 Patients and of Model Predictions. AJNR Am J Neuroradiol. 2011;32(8):1408-1414.

3. Aleman TS, Cideciyan AV, Aguirre GK, Huang WC, Mullins CL, Roman AJ, et al. Human CRB1-associated retinal degeneration: comparison with the rd8 Crb1-mutant mouse model. Invest Ophthalmol Vis Sci. 2011;52(9):6898-6910.

4. Allen RC, Murphy ML, Nerad JA. Benign Lid Tumors (volume 1. chapter 31). In: Krachmer JH, Mannis MJ, Holland EJ, editors. Cornea. St. Louis: Mosby; 2011. p. 367-386.

5. Allen RC, Saylor MA, Nerad JA. The current state of ptosis repair: a comparison of internal and external approaches. Curr Opin Ophthalmol. 2011;22(5):394-399.

6. Alsuhaibani AH, Carter KD, Nerad JA, Lee AG. Effect of Optic Nerve Sheath Fenestration on Papilledema of the Operated and the Contralateral Nonoperated Eyes in Idiopathic Intracranial Hypertension. Ophthalmology. 2011;118(2):412-414.

7. Alsuhaibani AH, Carter KD, Policeni B, Nerad JA. Effect of orbital bony decompression for Graves' orbitopathy on the volume of extraocular muscles. Br J Ophthalmol. 2011;95(9):1255-1258.

8. Alsuhaibani AH, Hitchon PW, Smoker WR, Lee AG, Nerad JA. Orbital Roof Encephalocele Mimicking a Destructive Neoplasm. Ophthal Plast Reconstr Surg. 2011;27(5):e121-123.

9. Alsuhaibani AH, Carter KD, Policeni B, Nerad JA. Orbital Volume and Eye Position Changes After Balanced Orbital Decompression. Ophthal Plast Reconstr Surg. 2011;27(3):158-163.

10. Alward WLM. Axenfeld-Rieger Syndrome and Peters' Anomaly (volume 1. chapter 58). In: Krachmer JH, Mannis MJ, Holland EJ, editors. Cornea. St. Louis: Mosby; 2011. p. 655-664.

11. Alward WL. A History of Gonioscopy. Optom Vis Sci. 2011;88(1):29-35.

12. Anderson AJ, Johnson CA, Werner JS. Measuring Visual Function in Age-Related Macular Degeneration with Frequency-Doubling (Matrix) Perimetry. Optom Vis Sci. 2011;88(7):806-815.

13. Antony B, Abramoff MD, Tang L, Ramdas WD, Vingerling JR, Jansonius NM, et al. Automated 3-D method for the correction of axial artifacts in spectral-domain optical coherence tomography images. Biomed Opt Express. 2011;2(8):2403-2416.

14. Barriga ES, Pattichis M, Ts'o D, Abramoff M, Kardon R, Kwon Y, et al. Independent component analysis using prior information for signal detection in a functional imaging system of the retina. Med Image Anal. 2011;15(1):35-44.

15. Baye LM, Patrinostro XB, Swaminathan S, Beck JS, Zhang Y, Stone EM, et al. The N-terminal region of centrosomal protein 290 (CEP290) restores vision in a zebrafish model of human blindness. Hum Mol Genet. 2011;20(8):1467-1477.

16. Bayouth JE, Casavant TL, Graham MM, Sonka M, Muruganandham M, Buatti JM. Image-based biomarkers in clinical practice. Semin Radiat Oncol. 2011;21(2):157-166.

17. Berquam-Vrieze KE, Nannanpaneni K, Brett BT, Holmfeldt L, Ma J, Zagorodna O, et al. Cell of origin strongly influences genetic selection in mouse models of T-ALL. Blood. 2011;118(17):4646-4656.

18. Birkholz ES, Goins KM, Sutphin JE, Kitzmann AS, Wagoner MD. Treatment of ocular surface squamous cell intraepithelial neoplasia with and without mitomycin C. Cornea. 2011;30(1):37-41.

19. Borck G, Rehman AU, Lee K, Pogoda HM, Kakar N, von Ameln S, et al. Loss-of-Function Mutations of ILDR1 Cause Autosomal-Recessive Hearing Impairment DFNB42. Am J Hum Genet. 2011;88(2):127-137.

20. Brett BT, Berquam-Vrieze KE, Nannapaneni K, Huang J, Scheetz TE, Dupuy AJ. Novel molecular and computational methods improve the accuracy of insertion site analysis in sleeping beauty-induced tumors. PLOS One. 2011;6(9):e24668.

21. Campbell CA, Della Santina CC, Meyer NC, Smith NB, Myrie OA, Stone EM, et al. Polymorphisms in KCN epsilon 1 or KCN epsilon 3 are Not Associated With Meniere Disease in the Caucasian Population (Corrected Reprint of vol 152A, pg 67, 2010). American Journal of Medical Genetics Part A. 2011;155A(3):666+.

22. Capo H, Repka MX, Edmond JC, Drack AV, Blumenfeld L, Siatkowski RM. Optic nerve abnormalities in children: A practical approach. Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus / American Association for Pediatric Ophthalmology and Strabismus. 2011;15(3):281-290.

23. Checa-Casalengua P, Jiang C, Bravo-Osuna I, Tucker BA, Molina-Martinez IT, Young MJ, et al. Retinal ganglion cells survival in a glaucoma model by GDNF/Vit E PLGA microspheres prepared according to a novel microencapsulation procedure. Journal of controlled release : official journal of the Controlled Release Society. 2011;156(1):92-100.

24. Chen Y, Kardon R, Longmuir R. Arteritic Anterior Ischaemic Optic Neuropathy and Chronic Cough as Presenting Features of Churg-Strauss Syndrome. Neuro-Ophthalmology. 2011;35(5-6):269-271.

25. Cideciyan AV, Rachel RA, Aleman TS, Swider M, Schwartz SB, Sumaroka A, et al. Cone photoreceptors are the main targets for gene therapy of NPHP5 (IQCB1) or NPHP6 (CEP290) blindness: generation of an all-cone Nphp6 hypomorph mouse that mimics the human retinal ciliopathy. Hum Mol Genet. 2011;20(7):1411-1423.

26. Clements JL, Bouchard CS, Lee WB, Dunn SP, Mannis MJ, Reidy JJ, et al. Retrospective Review of Graft Dislocation Rate Associated With Descemet Stripping Automated Endothelial Keratoplasty After Primary Failed Penetrating Keratoplasty. Cornea. 2011;30(4):414-418.

27. Costello FE, Klistorner A, Kardon R. Optical coherence tomography in the diagnosis and management of optic neuritis and multiple sclerosis. Ophthalmic Surg Lasers Imaging. 2011;42(4):S28-40.

28. Cyr AB, Nimmakayalu M, Longmuir SQ, Patil SR, Keppler-Noreuil KM, Shchelochkov OA. A novel 4p16.3 microduplication distal to WHSC1 and WHSC2 characterized by oligonucleotide array with new phenotypic features. American journal of medical genetics Part A. 2011;155A(9):2224-2228.

29. Davis L, Meyer K, Schindler E, Beck J, Rudd D, Grundstad AJ, et al. Copy Number Variations (CNVs) and Primary Open Angle Glaucoma (POAG). Invest Ophthalmol Vis Sci. 2011;52(10):7122-7133.

30. Donaghy C, Thurtell MJ, Pioro EP, Gibson JM, Leigh RJ. Eye movements in amyotrophic lateral sclerosis and its mimics: a review with illustrative cases. Journal of neurology, neurosurgery, and psychiatry. 2011;82(1):110-116.

31. Drack AV, Dumitrescu AV, Bhattarai S, Gratie D, Stone EM, Mullins R, et al. TUDCA slows retinal degeneration in two different mouse models of retinitis pigmentosa, and prevents obesity in Bardet Biedl Syndrome type 1 mice. Invest Ophthalmol Vis Sci. 2011;IN PRESS.

32. Dumitrescu AV, Milunsky JM, Longmuir SQ, Drack AV. A family with branchio-oculo-facial syndrome with primarily ocular involvement associated with mutation of the TFAP2A gene. Ophthalmic Genet. 2011;IN PRESS.

33. Dumitrescu AV, Moga DC, Longmuir SQ, Olson RJ, Drack AV. Prevalence and Characteristics of Abnormal Head Posture in Children with Down Syndrome A 20-Year Retrospective, Descriptive Review. Ophthalmology. 2011;118(9):1859-1864.

34. Dvorak L, Russell SR. Retinal drawing: a lost art of medicine. Perm J. 2011;15(3):74-75.

35. Echegaray S, Zamora G, Yu H, Luo W, Soliz P, Kardon R. Automated analysis of optic nerve images for detection and staging of papilledema. Invest Ophthalmol Vis Sci. 2011;52(10):7470-7478.

36. Fingert JH, Robin AL, Stone JL, Roos B, Davis LK, Scheetz TA, et al. Copy number variations on chromosome 12q14 in patients with normal tension glaucoma. Hum Mol Genet. 2011;20(12):2482-2494.

37. Fingert JH. Primary open-angle glaucoma genes. Eye. 2011;25(5):587-595.

38. Floyd MS, Kwon YH, Shah S, Benson C, Longmuir SQ. Unilateral congenital glaucoma in a child with optic nerve aplasia. Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus / American Association for Pediatric Ophthalmology and Strabismus. 2011;15(2):200-202.

39. Gandhi NG, Rogers GM, Kardon RH, Allen RC. Periodic Unilateral Eyelid Retraction in a Pediatric Patient. J Neuroophthalmol. 2011;31(4):350-352.

40. Gardiner SK, Demirel S, Johnson CA, Swanson WH. Assessment of linear-scale indices for perimetry in terms of progression in early glaucoma. Vision Res. 2011;51(6):1801-1810.

41. Gardiner SK, Johnson CA, Demirel S. Cup Size Predicts Subsequent Functional Change in Early Glaucoma. Optom Vis Sci. 2011;88(12):1470-1476.

42. Gardiner SK, Demirel S, Johnson CA. Perimetric Indices as Predictors of Future Glaucomatous Functional Change. Optom Vis Sci. 2011;88(1):56-62.

43. Genead MA, Fishman GA, Rha J, Dubis AM, Bonci DM, Dubra A, et al. Photoreceptor structure and function in patients with congenital achromatopsia. Invest Ophthalmol Vis Sci. 2011;52(10):7298-7308.

44. Gibson J, Griffiths H, Collins A, Yates JR, Folk JC, East JS, et al. Genetic variants within chromosome 4q28.3 are not reproducibly associated with Age-related Macular Degeneration (AMD). Acta Ophthalmol. 2011;89(7):E603-E604.

45. Goins KM. Donor Preparation for Endothelial Keratoplasty (volume 2. chapter 134). In: Krachmer JH, Mannis MJ, Holland EJ, editors. Cornea. St. Louis: Mosby; 2011. p. 1535-1541.

46. Golnik KC, Haripriya A, Beaver H, Gauba V, Lee AG, Mayorga E, et al. Cataract surgery skill assessment (reply). Ophthalmology. 2011;118(10):2094.

47. Golnik KC, Beaver H, Gauba V, Lee AG, Mayorga E, Palis G, et al. Cataract surgical skill assessment. Ophthalmology. 2011;118(2):427-427.

48. Gopalakrishna KN, Doddapuneni K, Boyd KK, Masuho I, Martemyanov KA, Artemyev NO. Interaction of transducin with uncoordinated 119 protein (UNC119): implications for the model of transducin trafficking in rod photoreceptors. The Journal of biological chemistry. 2011;286(33):28954-18962.

49. Grau T, Artemyev NO, Rosenberg T, Dollfus H, Haugen OH, Sener EC, et al. Decreased catalytic activity and altered activation properties of PDE6C mutants associated with autosomal recessive achromatopsia. Hum Mol Genet. 2011;20(4):719-730.

50. Gulati A, Yalamanchili S, Golnik KC, Lee AG. Cat Scratch Neuroretinitis: The Role of Acute and Convalescent Titers for Diagnosis. J Neuroophthalmol. 2011;IN PRESS.

51. Guo DF, Beyer AM, Yang BL, Nishimura DY, Sheffield VC, Rahmouni K. Inactivation of Bardet-Biedl syndrome genes causes kidney defects. American Journal of Physiology-Renal Physiology. 2011;300(2):F574-F580.

52. Haines SR, Thurtell MJ. Treatment of Ocular Myasthenia Gravis. Current treatment options in neurology. 2011;IN PRESS.

53. Han DF, Bayouth J, Bhatia S, Sonka M, Wu XD. Characterization and identification of spatial artifacts during 4D-CT imaging. Med Phys. 2011;38(4):2074-2087.

54. Han D, Bayouth J, Song Q, Bhatia S, Sonka M, Wu X. Feature guided motion artifact reduction with structure-awareness in 4D CT images. Proc IEEE Comput Soc Conf Comput Vis Pattern Recognit. 2011;2011:1057-1064.

55. Han D, Bayouth J, Song Q, Taurani A, Sonka M, Buatti J, et al. Globally optimal tumor segmentation in PET-CT images: A graph-based co-segmentation method. Inf Process Med Imaging. 2011;22:245-256.

56. Han D, Bayouth J, Bhatia S, Sonka M, Wu X. Motion Artifact Reduction in 4D Helical CT: Graph-Based Structure Alignment. Lecture Notes in Computer Science. 2011;6533(Medical Computer Vision. Recognition Techniques and Applications in Medical Imaging):63-73.

57. Haraszti T, Trantow CM, Hedberg-Buenz A, Grunze M, Anderson MG. Spectral analysis by XANES reveals that GPNMB influences the chemical composition of intact melanosomes. Pigment Cell & Melanoma Research. 2011;24(1):187-196.

58. Harper MM, Grozdanic SD, Blits B, Kuehn MH, Zamzow D, Buss JE, et al. Transplantation of BDNF secreting mesenchymal stem cells provides neuroprotection in chronic hypertensive rat eyes. Invest Ophthalmol Vis Sci. 2011;52(7):4506-4515.

59. Hayreh SS. Acute retinal arterial occlusive disorders. Prog Retin Eye Res. 2011;30(5):359-394.

60. Hayreh SS, Podhajsky PA, Zimmerman MB. Central and Hemicentral Retinal Vein Occlusion Role of Anti-Platelet Aggregation Agents and Anticoagulants. Ophthalmology. 2011;118(8):1603-1611.

61. Hayreh SS, Zimmerman MB. Hemicentral Retinal Vein Occlusion: Natural History of Visual Outcome. Retina. 2011;32(1):68-76.

62. Hayreh SS. Ischemic Optic Neuropathies. Berlin; Heidelberg: Springer-Verlag; 2011.

63. Hayreh SS. Management of ischemic optic neuropathies. Indian J Ophthalmol. 2011;59(2):123-136.

64. Hayreh SS, Podhajsky PA, Zimmerman MB. Natural history of visual outcome in central retinal vein occlusion. Ophthalmology. 2011;118(1):119-133 e112.

65. Hayreh SS. Treatment of non-arteritic anterior ischaemic optic neuropathy. Br J Ophthalmol. 2011;95(11):1617-1618.

66. Hayreh SS. Vascular disorders in neuro-ophthalmology. Curr Opin Neurol. 2011;24(1):6-11.

67. Hegg R, Lee AG, Tagg NT, Zimmerman MB. Statin or Nonsteroidal Anti-Inflammatory Drug Use Is Associated With Lower Erythrocyte Sedimentation Rate in Patients With Giant Cell Arteritis. J Neuroophthalmol. 2011;31(2):135-138.

68. Hildebrand MS, Morin M, Meyer NC, Mayo F, Modamio-Hoybjor S, Mencia A, et al. DFNA8/12 caused by TECTA mutations is the most identified subtype of non-syndromic autosomal dominant hearing loss. Hum Mutat. 2011;32(6):825-834.

69. Hong ES, Longmuir SQ, Goins KM. Ocular myeloid sarcoma in a 10-year-old child. J AAPOS. 2011;15(5):504-505.

70. Houston SK, 3rd, Markoe AM, Boldt HC, Murray TG. Juxtapapillary uveal melanomas: patient outcomes after treatment with proton irradiation for peripapillary and parapapillary melanomas. Arch Ophthalmol. 2011;129(9):1218-1220.

71. Iannaccone A, Kerr NC, Kinnick TR, Calzada JI, Stone EM. Autosomal recessive best vitelliform macular dystrophy: report of a family and management of early-onset neovascular complications. Arch Ophthalmol. 2011;129(2):211-217.

72. Jacobson SG, Cideciyan AV, Ratnakaram R, Heon E, Schwartz SB, Roman AJ, et al. Gene Therapy for Leber Congenital Amaurosis Caused by RPE65 Mutations: Safety and Efficacy in 15 Children and Adults Followed Up to 3 Years. Arch Ophthalmol. 2011;IN PRESS.

73. Jacobson SG, Cideciyan AV, Aleman TS, Sumaroka A, Roman AJ, Swider M, et al. Human Retinal Disease from AIPL1 Gene Mutations: Foveal Cone Loss with Minimal Macular Photoreceptors and Rod Function Remaining. Invest Ophthalmol Vis Sci. 2011;52(1):70-79.

74. Jacobson SG, Cideciyan AV, Gibbs D, Sumaroka A, Roman AJ, Aleman TS, et al. Retinal Disease Course in Usher Syndrome 1B due to MYO7A Mutations. Invest Ophthalmol Vis Sci. 2011;52(11):7924-7936.

75. Johnson CA, Anderson D, Fingeret M, Garway-Heath DT, Harwerth R. Glaucoma: recent discoveries and patient care. Optom Vis Sci. 2011;88(1):2-3.

76. Johnson CA, Wall M, Thompson HS. A History of Perimetry and Visual Field Testing. Optom Vis Sci. 2011;88(1):E8-E15.

77. Johnson RK, Premraj S, Patel SS, Wahle A, Stolpen A, Sonka M, et al. Quantitative assessment of the entire thoracic aorta from magnetic resonance images. Cardiol Young. 2011;21(2):170-177.

78. Johnson CA, Wall M. The visual field. In: Levin LA, Nilsson SFE, Ver Hoeve J, Wu SM, editors. Adler's physiology of the eye. 11th ed. Edinburgh: Saunders, Elsevier; 2011. p. 655-676.

79. Jonas JB, Hayreh SS, Yong T. Thickness of the lamina cribrosa and peripapillary sclera in Rhesus monkeys with nonglaucomatous or glaucomatous optic neuropathy. Acta Ophthalmol (Copenh). 2011;89(5):e423-e427.

80. Joshi VS, Garvin MK, Reinhardt JM, Abramoff MD. Automated method for the identification and analysis of vascular tree structures in retinal vessel network. Progress in Biomedical Optics and Imaging - Proceedings of SPIE:Medical Imaging 2011: Computer-Aided Diagnosis. 2011;7963.

81. Joshi V, Garvin M, Reinhardt J, Abramoff M. Identification and reconnection of interrupted vessels in retinal vessel segmentation. International Symposium on Biomedical Imaging, March 30- April 1, 2011. 2011;2011 IEEE International Symposium in Biomedical Imaging: From Nano to Macro(Image Segmentation Methods):1416-1420. Paper FR-PS1413a.1417 http://www.biomedicalimaging.org/Papers/viewpapers.asp?papernum=1658

82. Kaplowitz K, Lee AG. Horner syndrome following a selective cervical nerve root block. J Neuroophthalmol. 2011;31(1):54-55.

83. Kardon R, Anderson SC, Damarjian TG, Grace EM, Stone E, Kawasaki A. Chromatic Pupillometry in Patients with Retinitis Pigmentosa. Ophthalmology. 2011;118(2):376-381.

84. Kardon RH, Scott CJ, Lee AG, Frisen L, Wall M. Optical coherence tomography for optic disc edema--reply. Arch Ophthalmol. 2011;129(9):1246-1247.

85. Kardon R. Regulation of light through the pupil. In: Levin LA, Nilsson SFE, Ver Hoeve J, Wu SM, editors. Adler's physiology of the eye. 11th ed. Edinburgh: Saunders, Elsevier; 2011. p. 502-525.

86. Kardon RH. Role of the macular optical coherence tomography scan in neuro-ophthalmology. J Neuroophthalmol. 2011;31(4):353-361.

87. Kay CN, Abramoff MD, Mullins RF, Kinnick TR, Lee K, Eyestone ME, et al. Three-dimensional Distribution of the Vitelliform Lesion, Photoreceptors, and Retinal Pigment Epithelium in the Macula of Patients With Best Vitelliform Macular Dystrophy. Arch Ophthalmol. 2011;IN PRESS.

88. Kay CN, Sohn EH, Abràmoff MD. Using biomarkers for retinal disease risk assessment and management. Retinal Physician. 2011;8(6):23-27.

89. Kay CN, Tarantola RM, Gehrs KM, Folk JC, Mahajan VB, Boldt HC, et al. Uveitis following intravitreal bevacizumab: a non-infectious cluster. Ophthalmic Surg Lasers Imaging. 2011;42(4):292-296.

90. Kerov V, Artemyev NO. Diffusion and light-dependent compartmentalization of transducin. Molecular and Cellular Neuroscience. 2011;46(1):340-346.

91. Kimberling WJ, Borsa N, Smith RJ. Hearing loss disorders associated with renal disease. Adv Otorhinolaryngol. 2011;70:75-83.

92. Kinnick TR, Mullins RF, Dev S, Leys M, Mackey DA, Kay CN, et al. Autosomal Recessive Vitelliform Macular Dystrophy in a Large Cohort of Vitelliform Macular Dystrophy Patients. Retina. 2011;31(3):581-595.

93. Kitzmann AS, Fethke NB, Baratz KH, Zimmerman MB, Hackbarth DJ, Gehrs KM. A Survey Study of Musculoskeletal Disorders Among Eye Care Physicians Compared with Family Medicine Physicians. Ophthalmology. 2011;IN PRESS.

94. Ko AC, Brinton JP, Mahajan VB, Zimmerman B, Brinton GS, Stone EM, et al. Seroreactivity against aqueous-soluble and detergent-soluble retinal proteins in posterior uveitis. Arch Ophthalmol. 2011;129(4):415-420.

95. Kondratowicz AS, Lennemann NJ, Sinn PL, Davey RA, Hunt CL, Moller-Tank S, et al. T-cell immunoglobulin and mucin domain 1 (TIM-1) is a receptor for Zaire Ebolavirus and Lake Victoria Marburgvirus. Proc Natl Acad Sci U S A. 2011;108(20):8426-8431.

96. Kovárník T, Mintz GS, Sonka M. The late stent malapposition develops also after paclitaxel balloon predilatation before bare-metal stent implantation: case description. Eur Heart J. 2011;32(11):1432.

97. Kovárník T, Mintz GS, Skalicka H, Král A, Horák J, Skulec R, et al. Virtual Histology Evaluation of Atherosclerosis Regression During Atorvastatin and Ezetimibe Administration. Circ J. 2011;76(1):176-183.

98. Král A, Kovárník T, Králík L, Skalická H, Horák J, Mintz GS, et al. Genetic variants in haem oxygenase-1 and endothelial nitric oxide synthase influence the extent and evolution of coronary artery atherosclerosis. Folia Biol (Praha). 2011;57(5):182-190.

99. Kuehn MH, Wang K, Roos B, Stone EM, Kwon YH, Alward WL, et al. Chromosome 7q31 POAG locus: ocular expression of caveolins and lack of association with POAG in a US cohort. Mol Vis. 2011;17:430-435.

100. Kupersmith MJ, Mandel G, Anderson S, Meltzer DE, Kardon R. Baseline, one and three month changes in the peripapillary retinal nerve fiber layer in acute optic neuritis: Relation to baseline vision and MRI. J Neurol Sci. 2011;308(1-2):117-123.

101. Kupersmith MJ, Sibony P, Mandel G, Durbin M, Kardon RH. Optical coherence tomography of the swollen optic nerve head: deformation of the peripapillary RPE layer in papilledema. Invest Ophthalmol Vis Sci. 2011;59(2):6558-6564.

102. Lachke SA, Alkuraya FS, Kneeland SC, Ohn T, Aboukhalil A, Howell GR, et al. Mutations in the RNA granule component TDRD7 cause cataract and glaucoma. Science. 2011;331(6024):1571-1576.

103. Lavik E, Kuehn MH, Kwon YH. Novel drug delivery systems for glaucoma. Eye. 2011;25(5):578-586.

104. Lee K, Abràmoff MD, Sonka M, Garvin MK. Automated segmentation of intraretinal layers from spectral-domain macular OCT: Reproducibility of layer thickness measurements. Progress in Biomedical Optics and Imaging - Proceedings of SPIE: Medical Imaging 2011: Biomedical Applications in Molecular, Structural, and Functional Imaging. 2011;7965:796523.

105. Lee AG. Patient Safety Issues. In: Oetting TA, editor. Basic Principles of Ophthalmic Surgery. Second ed. San Francisco: American Academy of Ophthalmology; 2011. p. 117-130.

106. Lee AG. Resident selection. Ophthalmology. 2011;118(4):783.

107. Lee J, Carter KD. Suture Materials and Needles. In: Oetting TA, editor. Basic Principles of Ophthalmic Surgery. Second ed. San Francisco: American Academy of Ophthalmology; 2011. p. 83-92.

108. Li HK, Horton M, Bursell SE, Cavallerano J, Zimmer-Galler I, Tennant M, et al. Telehealth Practice Recommendations for Diabetic Retinopathy, Second Edition. Telemedicine journal and e-health : the official journal of the American Telemedicine Association. 2011;17(10):814-837.

109. Longmuir S, Dumitrescu A, Kwon Y, Boldt HC, Hong S. Juvenile xanthogranulomatosis with bilateral and multifocal ocular lesions of the iris, cornealscleral limbus, and choroid. J AAPOS. 2011;15(6):598-600.

110. Ma J, Kabiel M, Tucker BA, Ge J, Young MJ. Combining chondroitinase ABC and growth factors promotes the integration of murine retinal progenitor cells transplanted into Rho -/- mice. Mol Vis. 2011;17:1759-1770.

111. Macdonald JT, Kutzbach BR, Holleschau AM, Wyckoff S, Summers CG. Reading Skills in Children and Adults With Albinism: The Role of Visual Impairment. J Pediatr Ophthalmol Strabismus. 2011;IN PRESS.

112. Mader TH, Gibson CR, Pass AF, Kramer LA, Lee AG, Fogarty J, et al. Optic Disc Edema, Globe Flattening, Choroidal Folds, and Hyperopic Shifts Observed in Astronauts after Long-duration Space Flight. Ophthalmology. 2011;118(10):2058-2069.

113. Mahajan VB, Elkins KA, Russell SR, Boldt HC, Gehrs KM, Weingeist TA, et al. Bilateral intravitreal injection of antivascular endothelial growth factor therapy. Retina. 2011;31(1):31-35.

114. Mahajan VB, Skeie JM, Assefnia AH, Mahajan M, Tsang SH. Mouse Eye Enucleation for Remote High-throughput Phenotyping. J Vis Exp. 2011;Nov 19(57):(online at http://www.jove.com/video/3184/mouse-eye-enucleation-for-remote-high-throughput-phenotyping).

115. Mahajan VB, Tarantola RM, Graff JM, Boldt HC, Abramoff MD, Russell SR, et al. Sutureless triplanar sclerotomy for 23-gauge vitrectomy. Arch Ophthalmol. 2011;129(5):585-590.

116. Malm E, Ponjavic V, Moller C, Kimberling WJ, Andreasson S. Phenotypes in Defined Genotypes Including Siblings with Usher Syndrome. Ophthalmic Genet. 2011;32(2):65-74.

117. Mao M, Hedberg-Buenz A, Koehn D, John SW, Anderson MG. Anterior segment dysgenesis and early-onset glaucoma in nee mice with mutation of Sh3pxd2b. Invest Ophthalmol Vis Sci. 2011;52(5):2679-2688.

118. Mazor M, Alkrinawi S, Chalifa-Caspi V, Manor E, Sheffield VC, Aviram M, et al. Primary Ciliary Dyskinesia Caused by Homozygous Mutation in DNAL1, Encoding Dynein Light Chain 1. Am J Hum Genet. 2011;88(5):599-607.

119. McKendrick AM, Johnson CA. Temporal properties of vision. In: Levin LA, Nilsson SFE, Ver Hoeve J, Wu SM, editors. Adler's physiology of the eye. 11th ed. Edinburgh: Saunders, Elsevier; 2011. p. 698-712.

120. Meyer KJ, Davis LK, Schindler EI, Beck JS, Rudd DS, Grundstad AJ, et al. Genome-wide analysis of copy number variants in age-related macular degeneration. Hum Genet. 2011;129(1):91-100.

121. Meyer KJ, Axelsen MS, Sheffield VC, Patil SR, Wassink TH. Germline mosaic transmission of a novel duplication of PXDN and MYT1L to two male half-siblings with autism. Psychiatr Genet 2011 Dec 12. 2011;IN PRESS.

122. Milunsky JM, Maher TM, Zhao G, Wang Z, Mulliken JB, Chitayat D, et al. Genotype-phenotype analysis of the branchio-oculo-facial syndrome. Am J Med Genet A. 2011;155(1):22-32.

123. Muhammad E, Leventhal N, Parvari G, Hanukoglu A, Hanukoglu I, Chalifa-Caspi V, et al. Autosomal recessive hyponatremia due to isolated salt wasting in sweat associated with a mutation in the active site of Carbonic Anhydrase 12. Hum Genet. 2011;129(4):397-405.

124. Mullins RF, Dewald AD, Streb LM, Wang K, Kuehn MH, Stone EM. Elevated membrane attack complex in human choroid with high risk complement factor H genotypes. Exp Eye Res. 2011;93(4):565-567.

125. Mullins RF, Skeie JM, Folk JC, Solivan-Timpe FM, Oetting TA, Huang J, et al. Evaluation of variants in the selectin genes in age-related macular degeneration. BMC medical genetics. 2011;12(1):58.

126. Niemeijer M, Xu X, Dumitrescu A, Gupta P, van Ginneken B, Folk J, et al. Automated Measurement of the Arteriolar-To-Venular Width Ratio in Digital Color Fundus Photographs. IEEE Trans Med Imaging. 2011;30(11):1941-1950.

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last updated: 12/28/2011