| Year |
Citation |
Score |
| 2016 |
Birch DG, Bennett LD, Duncan JL, Weleber RG, Pennesi ME. Long-term follow-up of patients with retinitis pigmentosa (RP) receiving intraocular ciliary neurotrophic factor implants. American Journal of Ophthalmology. PMID 27457255 DOI: 10.1016/j.ajo.2016.07.013 |
0.76 |
|
| 2016 |
Carr BC, Emigh CE, Bennett LD, Pansick AD, Birch DG, Nguyen C. TOWARDS A TREATMENT FOR DIABETIC RETINOPATHY: Intravitreal Toxicity and Preclinical Safety Evaluation of Inducible Nitric Oxide Synthase Inhibitors. Retina (Philadelphia, Pa.). PMID 27380429 DOI: 10.1097/IAE.0000000000001133 |
0.68 |
|
| 2016 |
Ghodasra DH, Chen A, Arevalo JF, Birch DG, Branham K, Coley B, Dagnelie G, de Juan E, Devenyi RG, Dorn JD, Fisher A, Geruschat DR, Gregori NZ, Greenberg RJ, Hahn P, et al. Worldwide Argus II implantation: recommendations to optimize patient outcomes. Bmc Ophthalmology. 16: 52. PMID 27154461 DOI: 10.1186/s12886-016-0225-1 |
0.68 |
|
| 2016 |
Smith TB, Parker M, Steinkamp PN, Weleber RG, Smith N, Wilson DJ. Structure-Function Modeling of Optical Coherence Tomography and Standard Automated Perimetry in the Retina of Patients with Autosomal Dominant Retinitis Pigmentosa. Plos One. 11: e0148022. PMID 26845445 DOI: 10.1371/journal.pone.0148022 |
0.68 |
|
| 2016 |
Shankar SP, Hughbanks-Wheaton DK, Birch DG, Sullivan LS, Conneely KN, Bowne SJ, Stone EM, Daiger SP. Autosomal Dominant Retinal Dystrophies Caused by a Founder Splice Site Mutation, c.828+3A>T, in PRPH2 and Protein Haplotypes in trans as Modifiers. Investigative Ophthalmology & Visual Science. 57: 349-59. PMID 26842753 DOI: 10.1167/iovs.15-16965 |
0.68 |
|
| 2016 |
Bennett LD, Wang YZ, Klein M, Pennesi ME, Jayasundera T, Birch DG. Structure/Psychophysical Relationships in X-Linked Retinoschisis. Investigative Ophthalmology & Visual Science. 57: 332-7. PMID 26830370 DOI: 10.1167/iovs.15-18354 |
0.68 |
|
| 2016 |
Strauss RW, Ho A, Muñoz B, Cideciyan AV, Sahel JA, Sunness JS, Birch DG, Bernstein PS, Michaelides M, Traboulsi EI, Zrenner E, Sadda S, Ervin AM, West S, Scholl HP, et al. The Natural History of the Progression of Atrophy Secondary to Stargardt Disease (ProgStar) Studies: Design and Baseline Characteristics: ProgStar Report No. 1. Ophthalmology. 123: 817-28. PMID 26786511 DOI: 10.1016/j.ophtha.2015.12.009 |
0.68 |
|
| 2016 |
Weisschuh N, Mayer AK, Strom TM, Kohl S, Glöckle N, Schubach M, Andreasson S, Bernd A, Birch DG, Hamel CP, Heckenlively JR, Jacobson SG, Kamme C, Kellner U, Kunstmann E, et al. Mutation Detection in Patients with Retinal Dystrophies Using Targeted Next Generation Sequencing. Plos One. 11: e0145951. PMID 26766544 DOI: 10.1371/journal.pone.0145951 |
0.68 |
|
| 2016 |
Daiger SP, Sullivan LS, Bowne SJ, Koboldt DC, Blanton SH, Wheaton DK, Avery CE, Cadena ED, Koenekoop RK, Fulton RS, Wilson RK, Weinstock GM, Lewis RA, Birch DG. Identification of a Novel Gene on 10q22.1 Causing Autosomal Dominant Retinitis Pigmentosa (adRP). Advances in Experimental Medicine and Biology. 854: 193-200. PMID 26427411 DOI: 10.1007/978-3-319-17121-0_26 |
0.68 |
|
| 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, ... ... Birch DG, 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 |
0.68 |
|
| 2015 |
Hoffman DR, Hughbanks-Wheaton DK, Spencer R, Fish GE, Pearson NS, Wang YZ, Klein M, Takacs A, Locke KG, Birch DG. Docosahexaenoic Acid Slows Visual Field Progression in X-Linked Retinitis Pigmentosa: Ancillary Outcomes of the DHAX Trial. Investigative Ophthalmology & Visual Science. 56: 6646-6653. PMID 26469750 DOI: 10.1167/iovs.15-17786 |
0.76 |
|
| 2015 |
Shankar SP, Birch DG, Ruiz RS, Hughbanks-Wheaton DK, Sullivan LS, Bowne SJ, Stone EM, Daiger SP. Founder Effect of a c.828+3A>T Splice Site Mutation in Peripherin 2 (PRPH2) Causing Autosomal Dominant Retinal Dystrophies. Jama Ophthalmology. 133: 511-7. PMID 25675413 DOI: 10.1001/jamaophthalmol.2014.6115 |
0.76 |
|
| 2015 |
Birch DG, Locke KG, Felius J, Klein M, Wheaton DK, Hoffman DR, Hood DC. Rates of decline in regions of the visual field defined by frequency-domain optical coherence tomography in patients with RPGR-mediated X-linked retinitis pigmentosa. Ophthalmology. 122: 833-9. PMID 25556114 DOI: 10.1016/j.ophtha.2014.11.005 |
0.76 |
|
| 2015 |
Dugel PU, Novack RL, Csaky KG, Richmond PP, Birch DG, Kubota R. Phase II, randomized, placebo-controlled, 90-day study of emixustat hydrochloride in geographic atrophy associated with dry age-related macular degeneration Retina. 35: 1173-1183. DOI: 10.1097/IAE.0000000000000606 |
0.76 |
|
| 2015 |
Jung CC, Atan D, Ng D, Ploder L, Ross SE, Klein M, Birch DG, Diez E, McInnes RR. Transcription factor PRDM8 is required for rod bipolar and type 2 OFF-cone bipolar cell survival and amacrine subtype identity Proceedings of the National Academy of Sciences of the United States of America. 112: E3010-E3019. DOI: 10.1073/pnas.1505870112 |
0.76 |
|
| 2014 |
Cai CX, Locke KG, Ramachandran R, Birch DG, Hood DC. A comparison of progressive loss of the ellipsoid zone (EZ) band in autosomal dominant and x-linked retinitis pigmentosa. Investigative Ophthalmology & Visual Science. 55: 7417-22. PMID 25342618 DOI: 10.1167/iovs.14-15013 |
0.76 |
|
| 2014 |
Sullivan LS, Koboldt DC, Bowne SJ, Lang S, Blanton SH, Cadena E, Avery CE, Lewis RA, Webb-Jones K, Wheaton DH, Birch DG, Coussa R, Ren H, Lopez I, Chakarova C, et al. A dominant mutation in hexokinase 1 (HK1) causes retinitis pigmentosa. Investigative Ophthalmology & Visual Science. 55: 7147-58. PMID 25190649 DOI: 10.1167/iovs.14-15419 |
0.76 |
|
| 2014 |
Hughbanks-Wheaton DK, Birch DG, Fish GE, Spencer R, Pearson NS, Takacs A, Hoffman DR. Safety assessment of docosahexaenoic acid in X-linked retinitis pigmentosa: the 4-year DHAX trial. Investigative Ophthalmology & Visual Science. 55: 4958-66. PMID 25015354 DOI: 10.1167/iovs.14-14437 |
0.76 |
|
| 2014 |
Hoffman DR, Hughbanks-Wheaton DK, Pearson NS, Fish GE, Spencer R, Takacs A, Klein M, Locke KG, Birch DG. Four-year placebo-controlled trial of docosahexaenoic acid in X-linked retinitis pigmentosa (DHAX trial): a randomized clinical trial. Jama Ophthalmology. 132: 866-73. PMID 24805262 DOI: 10.1001/jamaophthalmol.2014.1634 |
0.76 |
|
| 2014 |
Wang F, Wang H, Tuan HF, Nguyen DH, Sun V, Keser V, Bowne SJ, Sullivan LS, Luo H, Zhao L, Wang X, Zaneveld JE, Salvo JS, Siddiqui S, Mao L, ... ... Birch DG, et al. Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinements. Human Genetics. 133: 331-45. PMID 24154662 DOI: 10.1007/s00439-013-1381-5 |
0.76 |
|
| 2013 |
Bowne SJ, Sullivan LS, Avery CE, Sasser EM, Roorda A, Duncan JL, Wheaton DH, Birch DG, Branham KE, Heckenlively JR, Sieving PA, Daiger SP. Mutations in the small nuclear riboprotein 200 kDa gene (SNRNP200) cause 1.6% of autosomal dominant retinitis pigmentosa. Molecular Vision. 19: 2407-17. PMID 24319334 |
0.76 |
|
| 2013 |
Wang X, Wang H, Sun V, Tuan HF, Keser V, Wang K, Ren H, Lopez I, Zaneveld JE, Siddiqui S, Bowles S, Khan A, Salvo J, Jacobson SG, Iannaccone A, ... ... Birch D, et al. Comprehensive molecular diagnosis of 179 Leber congenital amaurosis and juvenile retinitis pigmentosa patients by targeted next generation sequencing. Journal of Medical Genetics. 50: 674-88. PMID 23847139 DOI: 10.1136/jmedgenet-2013-101558 |
0.76 |
|
| 2013 |
Birch DG, Locke KG, Wen Y, Locke KI, Hoffman DR, Hood DC. Spectral-domain optical coherence tomography measures of outer segment layer progression in patients with X-linked retinitis pigmentosa. Jama Ophthalmology. 131: 1143-50. PMID 23828615 DOI: 10.1001/jamaophthalmol.2013.4160 |
0.76 |
|
| 2013 |
Birch DG, Weleber RG, Duncan JL, Jaffe GJ, Tao W. Randomized trial of ciliary neurotrophic factor delivered by encapsulated cell intraocular implants for retinitis pigmentosa. American Journal of Ophthalmology. 156: 283-292.e1. PMID 23668681 DOI: 10.1016/j.ajo.2013.03.021 |
0.76 |
|
| 2013 |
Churchill JD, Bowne SJ, Sullivan LS, Lewis RA, Wheaton DK, Birch DG, Branham KE, Heckenlively JR, Daiger SP. Mutations in the X-linked retinitis pigmentosa genes RPGR and RP2 found in 8.5% of families with a provisional diagnosis of autosomal dominant retinitis pigmentosa. Investigative Ophthalmology & Visual Science. 54: 1411-6. PMID 23372056 DOI: 10.1167/iovs.12-11541 |
0.76 |
|
| 2013 |
Yanni SE, Wang J, Cheng CS, Locke KI, Wen Y, Birch DG, Birch EE. Normative reference ranges for the retinal nerve fiber layer, macula, and retinal layer thicknesses in children. American Journal of Ophthalmology. 155: 354-360.e1. PMID 23127751 DOI: 10.1016/j.ajo.2012.08.010 |
0.76 |
|
| 2012 |
Chen CJ, Scholl HP, Birch DG, Iwata T, Miller NR, Goldberg MF. Characterizing the phenotype and genotype of a family with occult macular dystrophy. Archives of Ophthalmology (Chicago, Ill. : 1960). 130: 1554-9. PMID 23229695 DOI: 10.1001/archophthalmol.2012.2683 |
0.76 |
|
| 2012 |
Branham K, Othman M, Brumm M, Karoukis AJ, Atmaca-Sonmez P, Yashar BM, Schwartz SB, Stover NB, Trzupek K, Wheaton D, Jennings B, Ciccarelli ML, Jayasundera KT, Lewis RA, Birch D, et al. Mutations in RPGR and RP2 account for 15% of males with simplex retinal degenerative disease. Investigative Ophthalmology & Visual Science. 53: 8232-7. PMID 23150612 DOI: 10.1167/iovs.12-11025 |
0.76 |
|
| 2012 |
Li X, McClellan ME, Tanito M, Garteiser P, Towner R, Bissig D, Berkowitz BA, Fliesler SJ, Woodruff ML, Fain GL, Birch DG, Khan MS, Ash JD, Elliott MH. Loss of caveolin-1 impairs retinal function due to disturbance of subretinal microenvironment. The Journal of Biological Chemistry. 287: 16424-34. PMID 22451674 DOI: 10.1074/jbc.M112.353763 |
0.76 |
|
| 2012 |
Peachey NS, Ray TA, Florijn R, Rowe LB, Sjoerdsma T, Contreras-Alcantara S, Baba K, Tosini G, Pozdeyev N, Iuvone PM, Bojang P, Pearring JN, Simonsz HJ, van Genderen M, Birch DG, et al. GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness. American Journal of Human Genetics. 90: 331-9. PMID 22325362 DOI: 10.1016/j.ajhg.2011.12.006 |
0.76 |
|
| 2012 |
Wen Y, Klein M, Hood DC, Birch DG. Relationships among multifocal electroretinogram amplitude, visual field sensitivity, and SD-OCT receptor layer thicknesses in patients with retinitis pigmentosa. Investigative Ophthalmology & Visual Science. 53: 833-40. PMID 22247460 DOI: 10.1167/iovs.11-8410 |
0.76 |
|
| 2012 |
Wen Y, Locke KG, Hood DC, Birch DG. Rod photoreceptor temporal properties in retinal degenerative diseases. Advances in Experimental Medicine and Biology. 723: 495-502. PMID 22183369 DOI: 10.1007/978-1-4614-0631-0_62 |
0.76 |
|
| 2012 |
Fahim AT, Bowne SJ, Sullivan LS, Webb KD, Williams JT, Wheaton DK, Birch DG, Daiger SP. Polymorphic variation of RPGRIP1L and IQCB1 as modifiers of X-linked retinitis pigmentosa caused by mutations in RPGR. Advances in Experimental Medicine and Biology. 723: 313-20. PMID 22183348 DOI: 10.1007/978-1-4614-0631-0_41 |
0.76 |
|
| 2012 |
Kubota R, Boman NL, David R, Mallikaarjun S, Patil S, Birch D. Safety and effect on rod function of ACU-4429, a novel small-molecule visual cycle modulator Retina. 32: 183-188. PMID 21519291 DOI: 10.1097/IAE.0b013e318217369e |
0.76 |
|
| 2011 |
Duncan JL, Ratnam K, Birch DG, Sundquist SM, Lucero AS, Zhang Y, Meltzer M, Smaoui N, Roorda A. Abnormal cone structure in foveal schisis cavities in X-linked retinoschisis from mutations in exon 6 of the RS1 gene. Investigative Ophthalmology & Visual Science. 52: 9614-23. PMID 22110067 DOI: 10.1167/iovs.11-8600 |
0.76 |
|
| 2011 |
Hood DC, Zhang X, Ramachandran R, Talamini CL, Raza A, Greenberg JP, Sherman J, Tsang SH, Birch DG. The inner segment/outer segment border seen on optical coherence tomography is less intense in patients with diminished cone function. Investigative Ophthalmology & Visual Science. 52: 9703-9. PMID 22110066 DOI: 10.1167/iovs.11-8650 |
0.76 |
|
| 2011 |
Wen Y, Locke KG, Klein M, Bowne SJ, Sullivan LS, Ray JW, Daiger SP, Birch DG, Hughbanks-Wheaton DK. Phenotypic characterization of 3 families with autosomal dominant retinitis pigmentosa due to mutations in KLHL7. Archives of Ophthalmology (Chicago, Ill. : 1960). 129: 1475-82. PMID 22084217 DOI: 10.1001/archophthalmol.2011.307 |
0.76 |
|
| 2011 |
Lazow MA, Hood DC, Ramachandran R, Burke TR, Wang YZ, Greenstein VC, Birch DG. Transition zones between healthy and diseased retina in choroideremia (CHM) and Stargardt disease (STGD) as compared to retinitis pigmentosa (RP). Investigative Ophthalmology & Visual Science. 52: 9581-90. PMID 22076985 DOI: 10.1167/iovs.11-8554 |
0.76 |
|
| 2011 |
Trotter JH, Klein M, Jinwal UK, Abisambra JF, Dickey CA, Tharkur J, Masiulis I, Ding J, Locke KG, Rickman CB, Birch DG, Weeber EJ, Herz J. ApoER2 function in the establishment and maintenance of retinal synaptic connectivity. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 14413-23. PMID 21976526 DOI: 10.1523/JNEUROSCI.3135-11.2011 |
0.76 |
|
| 2011 |
Fahim AT, Bowne SJ, Sullivan LS, Webb KD, Williams JT, Wheaton DK, Birch DG, Daiger SP. Allelic heterogeneity and genetic modifier loci contribute to clinical variation in males with X-linked retinitis pigmentosa due to RPGR mutations. Plos One. 6: e23021. PMID 21857984 DOI: 10.1371/journal.pone.0023021 |
0.76 |
|
| 2011 |
Birch DG, Wen Y, Locke K, Hood DC. Rod sensitivity, cone sensitivity, and photoreceptor layer thickness in retinal degenerative diseases. Investigative Ophthalmology & Visual Science. 52: 7141-7. PMID 21810977 DOI: 10.1167/iovs.11-7509 |
0.76 |
|
| 2011 |
Hood DC, Ramachandran R, Holopigian K, Lazow M, Birch DG, Greenstein VC. Method for deriving visual field boundaries from OCT scans of patients with retinitis pigmentosa. Biomedical Optics Express. 2: 1106-14. PMID 21559123 DOI: 10.1364/BOE.2.001106 |
0.76 |
|
| 2011 |
Zhang K, Hopkins JJ, Heier JS, Birch DG, Halperin LS, Albini TA, Brown DM, Jaffe GJ, Tao W, Williams GA. Ciliary neurotrophic factor delivered by encapsulated cell intraocular implants for treatment of geographic atrophy in age-related macular degeneration. Proceedings of the National Academy of Sciences of the United States of America. 108: 6241-5. PMID 21444807 DOI: 10.1073/pnas.1018987108 |
0.76 |
|
| 2011 |
Wen Y, Locke KG, Hood DC, Birch DG. Rod photoreceptor temporal properties in retinitis pigmentosa. Experimental Eye Research. 92: 202-8. PMID 21219898 DOI: 10.1016/j.exer.2010.12.014 |
0.76 |
|
| 2011 |
Bowne SJ, Sullivan LS, Koboldt DC, Ding L, Fulton R, Abbott RM, Sodergren EJ, Birch DG, Wheaton DH, Heckenlively JR, Liu Q, Pierce EA, Weinstock GM, Daiger SP. Identification of disease-causing mutations in autosomal dominant retinitis pigmentosa (adRP) using next-generation DNA sequencing. Investigative Ophthalmology & Visual Science. 52: 494-503. PMID 20861475 DOI: 10.1167/iovs.10-6180 |
0.76 |
|
| 2011 |
Hood DC, Lazow MA, Locke KG, Greenstein VC, Birch DG. The transition zone between healthy and diseased retina in patients with retinitis pigmentosa. Investigative Ophthalmology & Visual Science. 52: 101-8. PMID 20720228 DOI: 10.1167/iovs.10-5799 |
0.76 |
|
| 2011 |
Birch DG, Birch EE, Spencer R. Electroretinographic testing in infants and children Pediatric Retina. 67-84. DOI: 10.1007/978-3-642-12041-1_3 |
0.76 |
|
| 2011 |
Sullivan JM, Birch DG, Spencer R. Pediatric hereditary macular degenerations Pediatric Retina. 245-294. DOI: 10.1007/978-3-642-12041-1_11 |
0.76 |
|
| 2010 |
Daiger SP, Sullivan LS, Bowne SJ, Birch DG, Heckenlively JR, Pierce EA, Weinstock GM. Targeted high-throughput DNA sequencing for gene discovery in retinitis pigmentosa. Advances in Experimental Medicine and Biology. 664: 325-31. PMID 20238032 DOI: 10.1007/978-1-4419-1399-9_37 |
0.76 |
|
| 2010 |
Rangaswamy NV, Patel HM, Locke KG, Hood DC, Birch DG. A comparison of visual field sensitivity to photoreceptor thickness in retinitis pigmentosa. Investigative Ophthalmology & Visual Science. 51: 4213-9. PMID 20220048 DOI: 10.1167/iovs.09-4945 |
0.76 |
|
| 2010 |
Birch DG, Williams PD, Callanan D, Wang R, Locke KG, Hood DC. Macular atrophy in birdshot retinochoroidopathy: an optical coherence tomography and multifocal electroretinography analysis. Retina (Philadelphia, Pa.). 30: 930-7. PMID 20098346 DOI: 10.1097/IAE.0b013e3181c720b4 |
0.76 |
|
| 2009 |
Klein M, Birch DG. Psychophysical assessment of low visual function in patients with retinal degenerative diseases (RDDs) with the Diagnosys full-field stimulus threshold (D-FST). Documenta Ophthalmologica. Advances in Ophthalmology. 119: 217-24. PMID 19885692 DOI: 10.1007/s10633-009-9204-7 |
0.76 |
|
| 2009 |
Friedman JS, Ray JW, Waseem N, Johnson K, Brooks MJ, Hugosson T, Breuer D, Branham KE, Krauth DS, Bowne SJ, Sullivan LS, Ponjavic V, Gränse L, Khanna R, Trager EH, ... ... Birch DG, et al. Mutations in a BTB-Kelch protein, KLHL7, cause autosomal-dominant retinitis pigmentosa. American Journal of Human Genetics. 84: 792-800. PMID 19520207 DOI: 10.1016/j.ajhg.2009.05.007 |
0.76 |
|
| 2009 |
Hood DC, Lin CE, Lazow MA, Locke KG, Zhang X, Birch DG. Thickness of receptor and post-receptor retinal layers in patients with retinitis pigmentosa measured with frequency-domain optical coherence tomography. Investigative Ophthalmology & Visual Science. 50: 2328-36. PMID 19011017 DOI: 10.1167/iovs.08-2936 |
0.76 |
|
| 2009 |
Yang Z, Chen Y, Lillo C, Chien J, Yu Z, Michaelides M, Klein M, Howes KA, Li Y, Kaminoh Y, Chen H, Zhao C, Al-Sheikh YT, Karan G, Corbeil D, ... ... Birch DG, et al. Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice (Journal of Clinical Investigation (2008) 118, (2908-2916) DOI: 10.1172/JCI35891) Journal of Clinical Investigation. 119: 1396. DOI: 10.1172/JCI35891C1 |
0.76 |
|
| 2008 |
Jiang L, Wheaton D, Bereta G, Zhang K, Palczewski K, Birch DG, Baehr W. A novel GCAP1(N104K) mutation in EF-hand 3 (EF3) linked to autosomal dominant cone dystrophy. Vision Research. 48: 2425-32. PMID 18706439 DOI: 10.1016/j.visres.2008.07.016 |
0.76 |
|
| 2008 |
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, ... ... Birch DG, et al. Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice. The Journal of Clinical Investigation. 118: 2908-16. PMID 18654668 DOI: 10.1172/JCI35891 |
0.76 |
|
| 2008 |
Bowne SJ, Sullivan LS, Gire AI, Birch DG, Hughbanks-Wheaton D, Heckenlively JR, Daiger SP. Mutations in the TOPORS gene cause 1% of autosomal dominant retinitis pigmentosa. Molecular Vision. 14: 922-7. PMID 18509552 |
0.76 |
|
| 2008 |
Daiger SP, Sullivan LS, Gire AI, Birch DG, Heckenlively JR, Bowne SJ. Mutations in known genes account for 58% of autosomal dominant retinitis pigmentosa (adRP). Advances in Experimental Medicine and Biology. 613: 203-9. PMID 18188946 DOI: 10.1007/978-0-387-74904-4_23 |
0.76 |
|
| 2007 |
Gire AI, Sullivan LS, Bowne SJ, Birch DG, Hughbanks-Wheaton D, Heckenlively JR, Daiger SP. The Gly56Arg mutation in NR2E3 accounts for 1-2% of autosomal dominant retinitis pigmentosa. Molecular Vision. 13: 1970-5. PMID 17982421 |
0.76 |
|
| 2007 |
McMahon A, Butovich IA, Mata NL, Klein M, Ritter R, Richardson J, Birch DG, Edwards AO, Kedzierski W. Retinal pathology and skin barrier defect in mice carrying a Stargardt disease-3 mutation in elongase of very long chain fatty acids-4. Molecular Vision. 13: 258-72. PMID 17356513 |
0.76 |
|
| 2007 |
Kozma P, Locke KG, Wang YZ, Birch DG, Edwards AO. Persistent cone dysfunction in acute exudative polymorphous vitelliform maculopathy. Retina (Philadelphia, Pa.). 27: 109-13. PMID 17218925 DOI: 10.1097/01.iae.0000226537.95346.ca |
0.76 |
|
| 2006 |
Kasus-Jacobi A, Birch DG, Anderson RE. Photoreceptor retinol dehydrogenases. An attempt to characterize the function of Rdh11. Advances in Experimental Medicine and Biology. 572: 505-11. PMID 17249616 DOI: 10.1007/0-387-32442-9_70 |
0.76 |
|
| 2006 |
Sullivan LS, Bowne SJ, Seaman CR, Blanton SH, Lewis RA, Heckenlively JR, Birch DG, Hughbanks-Wheaton D, Daiger SP. Genomic rearrangements of the PRPF31 gene account for 2.5% of autosomal dominant retinitis pigmentosa. Investigative Ophthalmology & Visual Science. 47: 4579-88. PMID 17003455 DOI: 10.1167/iovs.06-0440 |
0.76 |
|
| 2006 |
Sullivan LS, Bowne SJ, Birch DG, Hughbanks-Wheaton D, Heckenlively JR, Lewis RA, Garcia CA, Ruiz RS, Blanton SH, Northrup H, Gire AI, Seaman R, Duzkale H, Spellicy CJ, Zhu J, et al. Prevalence of disease-causing mutations in families with autosomal dominant retinitis pigmentosa: a screen of known genes in 200 families. Investigative Ophthalmology & Visual Science. 47: 3052-64. PMID 16799052 DOI: 10.1167/iovs.05-1443 |
0.76 |
|
| 2006 |
McGee J, Goodyear RJ, McMillan DR, Stauffer EA, Holt JR, Locke KG, Birch DG, Legan PK, White PC, Walsh EJ, Richardson GP. The very large G-protein-coupled receptor VLGR1: a component of the ankle link complex required for the normal development of auditory hair bundles. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 6543-53. PMID 16775142 DOI: 10.1523/JNEUROSCI.0693-06.2006 |
0.76 |
|
| 2006 |
Bowne SJ, Sullivan LS, Mortimer SE, Hedstrom L, Zhu J, Spellicy CJ, Gire AI, Hughbanks-Wheaton D, Birch DG, Lewis RA, Heckenlively JR, Daiger SP. Spectrum and frequency of mutations in IMPDH1 associated with autosomal dominant retinitis pigmentosa and leber congenital amaurosis. Investigative Ophthalmology & Visual Science. 47: 34-42. PMID 16384941 DOI: 10.1167/iovs.05-0868 |
0.76 |
|
| 2005 |
Birch DG. A randomized placebo-controlled clinical trial of docosahexaenoic acid (DHA) supplementation for X-linked retinitis pigmentosa. Retina (Philadelphia, Pa.). 25: S52-S54. PMID 16374336 |
0.76 |
|
| 2005 |
Kozma P, Hughbanks-Wheaton DK, Locke KG, Fish GE, Gire AI, Spellicy CJ, Sullivan LS, Bowne SJ, Daiger SP, Birch DG. Phenotypic characterization of a large family with RP10 autosomal-dominant retinitis pigmentosa: an Asp226Asn mutation in the IMPDH1 gene. American Journal of Ophthalmology. 140: 858-867. PMID 16214101 DOI: 10.1016/j.ajo.2005.05.027 |
0.76 |
|
| 2005 |
Cheng CW, Chow RL, Lebel M, Sakuma R, Cheung HO, Thanabalasingham V, Zhang X, Bruneau BG, Birch DG, Hui CC, McInnes RR, Cheng SH. The Iroquois homeobox gene, Irx5, is required for retinal cone bipolar cell development. Developmental Biology. 287: 48-60. PMID 16182275 DOI: 10.1016/j.ydbio.2005.08.029 |
0.76 |
|
| 2005 |
Fishman GA, Jacobson SG, Alexander KR, Cideciyan AV, Birch DG, Weleber RG, Hood DC. Outcome measures and their application in clinical trials for retinal degenerative diseases: outline, review, and perspective. Retina (Philadelphia, Pa.). 25: 772-7. PMID 16141867 DOI: 10.1097/00006982-200509000-00014 |
0.76 |
|
| 2005 |
Birch EE, Castañeda YS, Wheaton DH, Birch DG, Uauy RD, Hoffman DR. Visual maturation of term infants fed long-chain polyunsaturated fatty acid-supplemented or control formula for 12 mo. The American Journal of Clinical Nutrition. 81: 871-9. PMID 15817866 |
0.76 |
|
| 2005 |
Kasus-Jacobi A, Ou J, Birch DG, Locke KG, Shelton JM, Richardson JA, Murphy AJ, Valenzuela DM, Yancopoulos GD, Edwards AO. Functional characterization of mouse RDH11 as a retinol dehydrogenase involved in dark adaptation in vivo. The Journal of Biological Chemistry. 280: 20413-20. PMID 15790565 DOI: 10.1074/jbc.M413789200 |
0.76 |
|
| 2005 |
Karan G, Lillo C, Yang Z, Cameron DJ, Locke KG, Zhao Y, Thirumalaichary S, Li C, Birch DG, Vollmer-Snarr HR, Williams DS, Zhang K. Lipofuscin accumulation, abnormal electrophysiology, and photoreceptor degeneration in mutant ELOVL4 transgenic mice: a model for macular degeneration. Proceedings of the National Academy of Sciences of the United States of America. 102: 4164-9. PMID 15749821 DOI: 10.1073/pnas.0407698102 |
0.76 |
|
| 2005 |
Ding K, Scortegagna M, Seaman R, Birch DG, Garcia JA. Retinal disease in mice lacking hypoxia-inducible transcription factor-2alpha. Investigative Ophthalmology & Visual Science. 46: 1010-6. PMID 15728559 DOI: 10.1167/iovs.04-0788 |
0.76 |
|
| 2004 |
Birch DG. Surrogate electroretinographic markers for assessing therapeutic efficacy in the retina. Expert Review of Molecular Diagnostics. 4: 693-703. PMID 15347262 DOI: 10.1586/14737159.4.5.693 |
0.76 |
|
| 2004 |
Dharmaraj S, Leroy BP, Sohocki MM, Koenekoop RK, Perrault I, Anwar K, Khaliq S, Devi RS, Birch DG, De Pool E, Izquierdo N, Van Maldergem L, Ismail M, Payne AM, Holder GE, et al. The phenotype of Leber congenital amaurosis in patients with AIPL1 mutations. Archives of Ophthalmology (Chicago, Ill. : 1960). 122: 1029-37. PMID 15249368 DOI: 10.1001/archopht.122.7.1029 |
0.76 |
|
| 2004 |
Kang Derwent JJ, Derlacki DJ, Hetling JR, Fishman GA, Birch DG, Grover S, Stone EM, Pepperberg DR. Dark adaptation of rod photoreceptors in normal subjects, and in patients with Stargardt disease and an ABCA4 mutation. Investigative Ophthalmology & Visual Science. 45: 2447-56. PMID 15223829 DOI: 10.1167/iovs.03-1178 |
0.76 |
|
| 2004 |
Hoffman DR, Locke KG, Wheaton DH, Fish GE, Spencer R, Birch DG. A randomized, placebo-controlled clinical trial of docosahexaenoic acid supplementation for X-linked retinitis pigmentosa. American Journal of Ophthalmology. 137: 704-18. PMID 15059710 DOI: 10.1016/j.ajo.2003.10.045 |
0.76 |
|
| 2004 |
Chow RL, Volgyi B, Szilard RK, Ng D, McKerlie C, Bloomfield SA, Birch DG, McInnes RR. Control of late off-center cone bipolar cell differentiation and visual signaling by the homeobox gene Vsx1. Proceedings of the National Academy of Sciences of the United States of America. 101: 1754-9. PMID 14745032 DOI: 10.1073/pnas.0306520101 |
0.76 |
|
| 2003 |
Daiger SP, Sullivan LS, Bowne SJ, Kennan A, Humphries P, Birch DG, Heckenlively JR. Identification of the RP1 and RP10 (IMPDH1) genes causing autosomal dominant RP. Advances in Experimental Medicine and Biology. 533: 1-11. PMID 15180241 |
0.76 |
|
| 2003 |
Rotenstreich Y, Fishman GA, Anderson RJ, Birch DG. Interocular amplitude differences of the full field electroretinogram in normal subjects. The British Journal of Ophthalmology. 87: 1268-71. PMID 14507764 DOI: 10.1136/bjo.87.10.1268 |
0.76 |
|
| 2003 |
Wheaton DH, Hoffman DR, Locke KG, Watkins RB, Birch DG. Biological safety assessment of docosahexaenoic acid supplementation in a randomized clinical trial for X-linked retinitis pigmentosa. Archives of Ophthalmology (Chicago, Ill. : 1960). 121: 1269-78. PMID 12963609 DOI: 10.1001/archopht.121.9.1269 |
0.76 |
|
| 2003 |
Tzekov RT, Locke KG, Hood DC, Birch DG. Cone and rod ERG phototransduction parameters in retinitis pigmentosa. Investigative Ophthalmology & Visual Science. 44: 3993-4000. PMID 12939320 DOI: 10.1167/iovs.02-1104 |
0.76 |
|
| 2003 |
Hoffman DR, Birch EE, Castañeda YS, Fawcett SL, Wheaton DH, Birch DG, Uauy R. Visual function in breast-fed term infants weaned to formula with or without long-chain polyunsaturates at 4 to 6 months: a randomized clinical trial. The Journal of Pediatrics. 142: 669-77. PMID 12838196 DOI: 10.1067/mpd.2003.213 |
0.76 |
|
| 2003 |
Grover S, Fishman GA, Birch DG, Locke KG, Rosner B. Variability of full-field electroretinogram responses in subjects without diffuse photoreceptor cell disease. Ophthalmology. 110: 1159-63. PMID 12799241 DOI: 10.1016/S0161-6420(03)00253-7 |
0.76 |
|
| 2003 |
Bowne SJ, Daiger SP, Malone KA, Heckenlively JR, Kennan A, Humphries P, Hughbanks-Wheaton D, Birch DG, Liu Q, Pierce EA, Zuo J, Huang Q, Donovan DD, Sullivan LS. Characterization of RP1L1, a highly polymorphic paralog of the retinitis pigmentosa 1 (RP1) gene. Molecular Vision. 9: 129-37. PMID 12724644 |
0.76 |
|
| 2003 |
Cideciyan AV, Jacobson SG, Gupta N, Osawa S, Locke KG, Weiss ER, Wright AF, Birch DG, Milam AH. Cone deactivation kinetics and GRK1/GRK7 expression in enhanced S cone syndrome caused by mutations in NR2E3. Investigative Ophthalmology & Visual Science. 44: 1268-74. PMID 12601058 DOI: 10.1167/iovs.02-0494 |
0.76 |
|
| 2003 |
Birch DG, Toler SM, Swanson WH, Fish GE, Laties AM, Benson W. Double-blind placebo-controlled evaluation of the acute effects of sildenafil citrate (Viagra; Pfizer) on visual function in subjects with early-stage age-related macular degeneration Evidence-Based Eye Care. 4: 34-35. DOI: 10.1097/00132578-200301000-00016 |
0.76 |
|
| 2002 |
Birch DG, Hood DC, Locke KG, Hoffman DR, Tzekov RT. Quantitative electroretinogram measures of phototransduction in cone and rod photoreceptors: normal aging, progression with disease, and test-retest variability. Archives of Ophthalmology (Chicago, Ill. : 1960). 120: 1045-51. PMID 12149058 |
0.76 |
|
| 2002 |
Birch DG, Toler SM, Swanson WH, Fish GE, Laties AM. A double-blind placebo-controlled evaluation of the acute effects of sildenafil citrate (Viagra) on visual function in subjects with early-stage age-related macular degeneration. American Journal of Ophthalmology. 133: 665-72. PMID 11992864 DOI: 10.1016/S0002-9394(02)01338-7 |
0.76 |
|
| 2002 |
Breuer DK, Yashar BM, Filippova E, Hiriyanna S, Lyons RH, Mears AJ, Asaye B, Acar C, Vervoort R, Wright AF, Musarella MA, Wheeler P, MacDonald I, Iannaccone A, Birch D, et al. A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosa. American Journal of Human Genetics. 70: 1545-54. PMID 11992260 DOI: 10.1086/340848 |
0.76 |
|
| 2002 |
Bowne SJ, Sullivan LS, Blanton SH, Cepko CL, Blackshaw S, Birch DG, Hughbanks-Wheaton D, Heckenlively JR, Daiger SP. Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa. Human Molecular Genetics. 11: 559-68. PMID 11875050 |
0.76 |
|
| 2002 |
Birch EE, Hoffman DR, Castañeda YS, Fawcett SL, Birch DG, Uauy RD. A randomized controlled trial of long-chain polyunsaturated fatty acid supplementation of formula in term infants after weaning at 6 wk of age. The American Journal of Clinical Nutrition. 75: 570-80. PMID 11864865 |
0.76 |
|
| 2002 |
Birch DG, Hood DC. The full-field ERG as an outcome measure for treatment trials in hereditary retinal diseases Journal of Vision. 2: 107a. DOI: 10.1167/2.10.107 |
0.76 |
|
| 2002 |
Derwent JJK, Grover S, Hetling JR, Birch DG, Stone EM, Fishman GA, Pepperberg DR. Paired-flash electroretinography: A new tool to examine rod function in patients with Stargardt disease Annual International Conference of the Ieee Engineering in Medicine and Biology - Proceedings. 3: 2129-2130. |
0.76 |
|
| 2001 |
Birch DG, Peters AY, Locke KL, Spencer R, Megarity CF, Travis GH. Visual function in patients with cone-rod dystrophy (CRD) associated with mutations in the ABCA4(ABCR) gene. Experimental Eye Research. 73: 877-86. PMID 11846518 DOI: 10.1006/exer.2001.1093 |
0.76 |
|
| 2001 |
Uauy R, Hoffman DR, Peirano P, Birch DG, Birch EE. Essential fatty acids in visual and brain development. Lipids. 36: 885-95. PMID 11724460 |
0.76 |
|
| 2001 |
Hoffman DR, DeMar JC, Heird WC, Birch DG, Anderson RE. Impaired synthesis of DHA in patients with X-linked retinitis pigmentosa. Journal of Lipid Research. 42: 1395-401. PMID 11518758 |
0.76 |
|
| 2001 |
Berezovsky A, Salomão SR, Birch DG. Pupil size following dark adaptation in patients with retinitis pigmentosa. Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas MéDicas E BiolóGicas / Sociedade Brasileira De BiofÃSica ... [Et Al.]. 34: 1037-40. PMID 11471043 |
0.76 |
|
| 2001 |
Mata NL, Tzekov RT, Liu X, Weng J, Birch DG, Travis GH. Delayed dark-adaptation and lipofuscin accumulation in abcr+/- mice: implications for involvement of ABCR in age-related macular degeneration. Investigative Ophthalmology & Visual Science. 42: 1685-90. PMID 11431429 |
0.76 |
|
| 2001 |
Kedzierski W, Nusinowitz S, Birch D, Clarke G, McInnes RR, Bok D, Travis GH. Deficiency of rds/peripherin causes photoreceptor death in mouse models of digenic and dominant retinitis pigmentosa Proceedings of the National Academy of Sciences of the United States of America. 98: 7718-7723. PMID 11427722 DOI: 10.1073/pnas.141124198 |
0.76 |
|
| 2001 |
Tzekov RT, Liu Y, Sohocki MM, Zack DJ, Daiger SP, Heckenlively JR, Birch DG. Autosomal dominant retinal degeneration and bone loss in patients with a 12-bp deletion in the CRX gene. Investigative Ophthalmology & Visual Science. 42: 1319-27. PMID 11328746 |
0.76 |
|
| 2001 |
Guevara-Fujita M, Fahrner S, Buraczynska K, Cook J, Wheaton D, Cortes F, Vicencio C, Pena M, Fishman G, Mintz-Hittner H, Birch D, Hoffman D, Mears A, Fujita R, Swaroop A. Five novel RPGR mutations in families with X-linked retinitis pigmentosa Human Mutation. 17: 151. PMID 11180598 |
0.76 |
|
| 2001 |
Sohocki MM, Daiger SP, Bowne SJ, Rodriquez JA, Northrup H, Heckenlively JR, Birch DG, Mintz-Hittner H, Ruiz RS, Lewis RA, Saperstein DA, Sullivan LS. Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies. Human Mutation. 17: 42-51. PMID 11139241 DOI: 10.1002/1098-1004(2001)17:1<42::AID-HUMU5>3.0.CO;2-K |
0.76 |
|
| 2000 |
Hoffman DR, Birch EE, Birch DG, Uauy R, Castañeda YS, Lapus MG, Wheaton DH. Impact of early dietary intake and blood lipid composition of long-chain polyunsaturated fatty acids on later visual development. Journal of Pediatric Gastroenterology and Nutrition. 31: 540-53. PMID 11144440 DOI: 10.1097/00005176-200011000-00016 |
0.76 |
|
| 2000 |
Peters AY, Locke KG, Birch DG. Comparison of the Goldmann-Weekers dark adaptometer and LKC Technologies Scotopic Sensitivity tester-1. Documenta Ophthalmologica. Advances in Ophthalmology. 101: 1-9. PMID 11128963 DOI: 10.1023/A:1002765024774 |
0.76 |
|
| 2000 |
Bech-Hansen NT, Naylor MJ, Maybaum TA, Sparkes RL, Koop B, Birch DG, Bergen AA, Prinsen CF, Polomeno RC, Gal A, Drack AV, Musarella MA, Jacobson SG, Young RS, Weleber RG. Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness. Nature Genetics. 26: 319-23. PMID 11062471 DOI: 10.1038/81619 |
0.76 |
|
| 2000 |
Swanson WH, Felius J, Birch DG. Effect of stimulus size on static visual fields in patients with retinitis pigmentosa. Ophthalmology. 107: 1950-4. PMID 11013205 DOI: 10.1016/S0161-6420(00)00356-0 |
0.76 |
|
| 2000 |
Tzekov RT, Sohocki MM, Daiger SP, Birch DG. Visual phenotype in patients with Arg41Gln and ala196+1bp mutations in the CRX gene. Ophthalmic Genetics. 21: 89-99. PMID 10916183 |
0.76 |
|
| 2000 |
Sohocki MM, Perrault I, Leroy BP, Payne AM, Dharmaraj S, Bhattacharya SS, Kaplan J, Maumenee IH, Koenekoop R, Meire FM, Birch DG, Heckenlively JR, Daiger SP. Prevalence of AIPL1 mutations in inherited retinal degenerative disease. Molecular Genetics and Metabolism. 70: 142-50. PMID 10873396 DOI: 10.1006/mgme.2000.3001 |
0.76 |
|
| 2000 |
Clarke G, Goldberg AF, Vidgen D, Collins L, Ploder L, Schwarz L, Molday LL, Rossant J, Szél A, Molday RS, Birch DG, McInnes RR. Rom-1 is required for rod photoreceptor viability and the regulation of disk morphogenesis. Nature Genetics. 25: 67-73. PMID 10802659 DOI: 10.1038/75621 |
0.76 |
|
| 2000 |
Pepperberg DR, Birch DG, Hood DC. Electroretinographic determination of human rod flash response in vivo. Methods in Enzymology. 316: 202-23. PMID 10800677 |
0.76 |
|
| 2000 |
Birch EE, Garfield S, Hoffman DR, Uauy R, Birch DG. A randomized controlled trial of early dietary supply of long-chain polyunsaturated fatty acids and mental development in term infants. Developmental Medicine and Child Neurology. 42: 174-81. PMID 10755457 DOI: 10.1017/S0012162200000311 |
0.76 |
|
| 2000 |
Bowne SJ, Sullivan LS, Ding L, Traer E, Prescott SM, Birch DG, Kennan A, Humphries P, Daiger SP. Evaluation of human diacylglycerol kinase(iota), DGKI, a homolog of Drosophila rdgA, in inherited retinopathy mapping to 7q. Molecular Vision. 6: 6-9. PMID 10706894 |
0.76 |
|
| 2000 |
Sohocki MM, Bowne SJ, Sullivan LS, Blackshaw S, Cepko CL, Payne AM, Bhattacharya SS, Khaliq S, Qasim Mehdi S, Birch DG, Harrison WR, Elder FF, Heckenlively JR, Daiger SP. Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis. Nature Genetics. 24: 79-83. PMID 10615133 DOI: 10.1038/71732 |
0.76 |
|
| 1999 |
Bowne SJ, Daiger SP, Hims MM, Sohocki MM, Malone KA, McKie AB, Heckenlively JR, Birch DG, Inglehearn CF, Bhattacharya SS, Bird A, Sullivan LS. Mutations in the RP1 gene causing autosomal dominant retinitis pigmentosa. Human Molecular Genetics. 8: 2121-8. PMID 10484783 DOI: 10.1093/hmg/8.11.2121 |
0.76 |
|
| 1999 |
Hoffman DR, Birch EE, Birch DG, Uauy R. Fatty acid profile of buccal cheek cell phospholipids as an index for dietary intake of docosahexaenoic acid in preterm infants. Lipids. 34: 337-42. PMID 10443966 DOI: 10.1007/s11745-999-0371-y |
0.76 |
|
| 1999 |
Weng J, Mata NL, Azarian SM, Tzekov RT, Birch DG, Travis GH. Insights into the function of Rim protein in photoreceptors and etiology of Stargardt's disease from the phenotype in abcr knockout mice. Cell. 98: 13-23. PMID 10412977 DOI: 10.1016/S0092-8674(00)80602-9 |
0.76 |
|
| 1999 |
Yang RB, Robinson SW, Xiong WH, Yau KW, Birch DG, Garbers DL. Disruption of a retinal guanylyl cyclase gene leads to cone-specific dystrophy and paradoxical rod behavior. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 19: 5889-97. PMID 10407028 |
0.76 |
|
| 1999 |
Benson WE, Chan P, Sharma S, Snyder WB, Bloome MA, Birch DG. Current popularity of pneumatic retinopexy. Retina (Philadelphia, Pa.). 19: 238-41. PMID 10380030 |
0.76 |
|
| 1999 |
Birch DG. Retinal degeneration in retinitis pigmentosa and neuronal ceroid lipofuscinosis: An overview Molecular Genetics and Metabolism. 66: 356-366. PMID 10191129 DOI: 10.1006/mgme.1999.2829 |
0.76 |
|
| 1999 |
Birch DG, Anderson JL, Fish GE. Yearly rates of rod and cone functional loss in retinitis pigmentosa and cone-rod dystrophy Ophthalmology. 106: 258-268. PMID 9951474 |
0.76 |
|
| 1998 |
Hoffman DR, Birch DG. Omega 3 fatty acid status in patients with retinitis pigmentosa World Review of Nutrition and Dietetics. 83: 52-60. PMID 1998128409 |
0.76 |
|
| 1998 |
Gieser L, Fujita R, Göring HHH, Ott J, Hoffman DR, Cideciyan AV, Birch DG, Jacobson SG, Swaroop A. A novel locus (RP24) for X-linked retinitis pigmentosa maps to Xq26-27 American Journal of Human Genetics. 63: 1439-1447. PMID 9792872 DOI: 10.1086/302121 |
0.76 |
|
| 1998 |
Birch EE, Hoffman DR, Uauy R, Birch DG, Prestidge C. Visual acuity and the essentiality of docosahexaenoic acid and arachidonic acid in the diet of term infants. Pediatric Research. 44: 201-9. PMID 9702915 DOI: 10.1203/00006450-199808000-00011 |
0.76 |
|
| 1998 |
Nusinowitz S, Birch DG, Birch EE. Rod photoresponses in 6-week and 4-month-old human infants. Vision Research. 38: 627-35. PMID 9604094 DOI: 10.1016/S0042-6989(97)00286-1 |
0.76 |
|
| 1998 |
Boycott KM, Pearce WG, Musarella MA, Weleber RG, Maybaum TA, Birch DG, Miyake Y, Young RSL, Bech-Hansen NT. Evidence for genetic heterogeneity in X-linked congenital stationary night blindness American Journal of Human Genetics. 62: 865-875. PMID 9529339 DOI: 10.1086/301781 |
0.76 |
|
| 1997 |
Buraczynska M, Wu W, Fujita R, Buraczynska K, Phelps E, Andréasson S, Bennett J, Birch DG, Fishman GA, Hoffman DR, Inana G, Jacobson SG, Musarella MA, Sieving PA, Swaroop A. Spectrum of mutations in the RPGR gene that are identified in 20% of families with X-linked retinitis pigmentosa. American Journal of Human Genetics. 61: 1287-92. PMID 9399904 DOI: 10.1086/301646 |
0.76 |
|
| 1997 |
Kennedy KA, Ipson MA, Birch DG, Tyson JE, Anderson JL, Nusinowitz S, West L, Spencer R, Birch EE. Light reduction and the electroretinogram of preterm infants. Archives of Disease in Childhood. Fetal and Neonatal Edition. 76: F168-73. PMID 9175946 |
0.76 |
|
| 1997 |
Bennett MJ, Boriack RL, Birch DG. In-utero and post-delivery supplementation of motor neuron degeneration mutant mice with polyunsaturated fatty acids does not alter the clinical or pathological course Neuropediatrics. 28: 82-84. PMID 9151333 |
0.76 |
|
| 1997 |
Pepperberg DR, Birch DG, Hood DC. Photoresponses of human rods in vivo derived from paired-flash electroretinograms. Visual Neuroscience. 14: 73-82. PMID 9057270 |
0.76 |
|
| 1997 |
Kedzierski W, Lloyd M, Birch DG, Bok D, Travis GH. Generation and analysis of transgenic mice expressing P216L-substituted rds/peripherin in rod photoreceptors Investigative Ophthalmology and Visual Science. 38: 498-509. PMID 9040483 |
0.76 |
|
| 1997 |
Berezovsky A, Salomäo SR, Birch DG. Pupillometric measures in patients with retinitis pigmentosa (RP): An evaluation of the equivalent light hypothesis Investigative Ophthalmology and Visual Science. 38: S310. |
0.76 |
|
| 1996 |
Birch DG, Sandberg MA. Submicrovolt full-field cone electroretinograms: Artifacts and reproducibility Documenta Ophthalmologica. 92: 269-280. PMID 9476594 DOI: 10.1007/BF02584081 |
0.68 |
|
| 1996 |
Hood DC, Birch DG. Assessing abnormal rod photoreceptor activity with the a-wave of the electroretinogram: applications and methods. Documenta Ophthalmologica. Advances in Ophthalmology. 92: 253-67. PMID 9476593 DOI: 10.1007/BF02584080 |
0.68 |
|
| 1996 |
Hood DC, Birch DG. Abnormalities of the retinal cone system in retinitis pigmentosa. Vision Research. 36: 1699-709. PMID 8759470 DOI: 10.1016/0042-6989(95)00246-4 |
0.76 |
|
| 1996 |
Hood DC, Birch DG. Beta wave of the scotopic (rod) electroretinogram as a measure of the activity of human on-bipolar cells. Journal of the Optical Society of America. a, Optics, Image Science, and Vision. 13: 623-33. PMID 8627419 |
0.76 |
|
| 1996 |
Pepperberg DR, Birch DG, Hofmann KP, Hood DC. Recovery kinetics of human rod phototransduction inferred from the two-branched alpha-wave saturation function. Journal of the Optical Society of America. a, Optics, Image Science, and Vision. 13: 586-600. PMID 8627416 |
0.76 |
|
| 1996 |
Huffman DR, Birch EE, Birch DG, Uauy R. Dietary long-chain polyunsaturates (LCPs) for preterm and term infants? Controversies in visual function outcomes International Congress and Symposium Series - Royal Society of Medicine. 45-55. |
0.76 |
|
| 1996 |
Daiger SP, Sullivan LS, Blanton SH, Garcia CA, Birch DG, Heckenlively JR. Model system for linkage testing in families with autosomal dominant retinitis pigmentosa Investigative Ophthalmology and Visual Science. 37: S666. |
0.76 |
|
| 1996 |
Shady S, Hood DC, Birch DG. The effect of RP on the rod-driven oscillatory potentials of the ERG Investigative Ophthalmology and Visual Science. 37: S341. |
0.76 |
|
| 1996 |
Birch DG, Pepperberg DR, Hood DC. Recovery of dark- and light-adapted flash responses of human rods and cones Investigative Ophthalmology and Visual Science. 37: S811. |
0.76 |
|
| 1996 |
Berezovsky A, Middendorf RC, Birch DG. Electroretinographic findings in patients treated with tamoxifen Investigative Ophthalmology and Visual Science. 37: S345. |
0.76 |
|
| 1996 |
Hoffman DR, Birch EE, Birch DG, Uauy R, Castañeda YC, Wheaton D. Red Blood Cell (RBC) fatty acid profiles in term infants fed formulas enriched with Long-Chain Polyunsaturates (LCP) Investigative Ophthalmology and Visual Science. 37: S802. |
0.76 |
|
| 1996 |
Birch EE, Birch DG, Hoffman DR, Uauy R, Bane MC, Castañeda YS, Wheaton D, Prestidge CB. Visual maturation of term infants fed ω3 long chain polyunsaturated fatty acid (LCPUFA) supplemented formula Investigative Ophthalmology and Visual Science. 37: S1112. |
0.76 |
|
| 1996 |
Sullivan LS, Guilford SR, Birch DG, Daiger SP. A novel splice site mutation in the gene for peripherin/RDS causing dominant retinal degeneration Investigative Ophthalmology and Visual Science. 37: S1145. |
0.76 |
|
| 1996 |
Pepperberg DR, Birch DG, Hood DC. Flash responses of human rods in vivo derived from paired-flash ERGs Investigative Ophthalmology and Visual Science. 37: S5. |
0.76 |
|
| 1995 |
Hood DC, Birch DG. Phototransduction in human cones measured using the alpha-wave of the ERG. Vision Research. 35: 2801-10. PMID 8533321 DOI: 10.1016/0042-6989(95)00034-W |
0.76 |
|
| 1995 |
Hoffman DR, Uauy R, Birch DG. Metabolism of omega-3 fatty acids in patients with autosomal dominant retinitis pigmentosa Experimental Eye Research. 60: 279-289. PMID 7789408 DOI: 10.1016/S0014-4835(05)80110-1 |
0.76 |
|
| 1995 |
Shady S, Hood DC, Birch DG. Rod phototransduction in retinitis pigmentosa. Distinguishing alternative mechanisms of degeneration. Investigative Ophthalmology & Visual Science. 36: 1027-37. PMID 7730012 |
0.76 |
|
| 1995 |
Hoffman DR, Birch DG. Docosahexaenoic acid in red blood cells of patients with X-linked retinitis pigmentosa Investigative Ophthalmology and Visual Science. 36: 1009-1018. PMID 7730010 |
0.76 |
|
| 1995 |
Birch DG, Hood DC, Nusinowitz S, Pepperberg DR. Abnormal activation and inactivation mechanisms of rod transduction in patients with autosomal dominant retinitis pigmentosa and the pro-23-his mutation. Investigative Ophthalmology & Visual Science. 36: 1603-14. PMID 7601641 |
0.76 |
|
| 1995 |
Nusinowitz S, Hood DC, Birch DG. Rod transduction parameters from the a wave of local receptor populations. Journal of the Optical Society of America. a, Optics, Image Science, and Vision. 12: 2259-66. PMID 7500207 |
0.76 |
|
| 1995 |
Hood DC, Birch DG. Computational Models of Rod-Driven Retinal Activity Ieee Engineering in Medicine and Biology Magazine. 14: 59-66. DOI: 10.1109/51.340750 |
0.76 |
|
| 1994 |
Hood DC, Birch DG. Rod phototransduction in retinitis pigmentosa: estimation and interpretation of parameters derived from the rod a-wave. Investigative Ophthalmology & Visual Science. 35: 2948-61. PMID 8206712 |
0.76 |
|
| 1994 |
Hood DC, Shady S, Birch DG. Understanding changes in the b-wave of the ERG caused by heterogeneous receptor damage. Investigative Ophthalmology & Visual Science. 35: 2477-88. PMID 8163337 |
0.76 |
|
| 1994 |
Gouras P, MacKay CJ, Swanson WH, Birch DG, Anderson JL. S-cone function in patients with retinitis pigmentosa [1] Investigative Ophthalmology and Visual Science. 35: 781-783. PMID 8125738 |
0.76 |
|
| 1994 |
Uauy R, Hoffman DR, Birch EE, Birch DG, Jameson DM, Tyson J. Safety and efficacy of omega-3 fatty acids in the nutrition of very low birth weight infants: soy oil and marine oil supplementation of formula. The Journal of Pediatrics. 124: 612-20. PMID 7908693 DOI: 10.1016/S0022-3476(05)83144-0 |
0.76 |
|
| 1994 |
Uauy-Dagach R, Birch EE, Birch DG, Hoffman DR. Significance of omega 3 fatty acids for retinal and brain development of preterm and term infants. World Review of Nutrition and Dietetics. 75: 52-62. PMID 7871833 |
0.76 |
|
| 1993 |
Hoffman DR, Birch EE, Birch DG, Uauy RD. Effects of supplementation with omega 3 long-chain polyunsaturated fatty acids on retinal and cortical development in premature infants. The American Journal of Clinical Nutrition. 57: 807S-812S. PMID 8475899 |
0.76 |
|
| 1993 |
Rodriguez JA, Herrera CA, Birch DG, Daiger SP. A leucine to arginine amino acid substitution at codon 46 of rhodopsin is responsible for a severe form of autosomal dominant retinitis pigmentosa Human Mutation. 2: 205-213. PMID 8364589 |
0.76 |
|
| 1993 |
Birch DG, Anderson JL, Fish GE, Jost BF. Pattern-reversal electroretinographic follow-up of laser photocoagulation for subfoveal neovascular lesions in age-related macular degeneration American Journal of Ophthalmology. 116: 148-155. PMID 8352298 |
0.76 |
|
| 1993 |
Hood DC, Shady S, Birch DG. Heterogeneity in retinal disease and the computational model of the human-rod response. Journal of the Optical Society of America. a, Optics and Image Science. 10: 1624-30. PMID 8350151 |
0.76 |
|
| 1993 |
Hood DC, Birch DG. Light adaptation of human rod receptors: the leading edge of the human a-wave and models of rod receptor activity. Vision Research. 33: 1605-18. PMID 8236849 DOI: 10.1016/0042-6989(93)90027-T |
0.76 |
|
| 1993 |
Hoffman DR, Uauy R, Birch DG. Red Blood Cell Fatty Acid Levels in Patients with Autosomal Dominant Retinitis Pigmentosa Experimental Eye Research. 57: 359-368. PMID 8224023 DOI: 10.1006/exer.1993.1135 |
0.76 |
|
| 1993 |
Hood DC, Birch DG. Human cone receptor activity: the leading edge of the a-wave and models of receptor activity. Visual Neuroscience. 10: 857-71. PMID 8217936 |
0.76 |
|
| 1993 |
Birch DG, Anderson JL, Birch EE. Early abnormalities of rod function in children with X-linked retinitis pigmentosa Clinical Vision Sciences. 8: 329-335. |
0.76 |
|
| 1992 |
Snyder WB, Bloome MA, Birch DG. Pneumatic retinopexy versus scleral buckle Retina. 12: 43-45. PMID 1565870 |
0.76 |
|
| 1992 |
Hood DC, Birch DG. A computational model of the amplitude and implicit time of the b-wave of the human ERG. Visual Neuroscience. 8: 107-26. PMID 1558823 DOI: 10.1017/S0952523800009275 |
0.76 |
|
| 1992 |
Birch DG, Anderson JL. Standardized Full-Field Electroretinography: Normal Values and Their Variation with Age Archives of Ophthalmology. 110: 1571-1576. PMID 1444914 DOI: 10.1001/archopht.1992.01080230071024 |
0.76 |
|
| 1992 |
Birch EE, Birch DG, Hoffman DR, Uauy R. Dietary essential fatty acid supply and visual acuity development. Investigative Ophthalmology & Visual Science. 33: 3242-53. PMID 1399429 |
0.76 |
|
| 1992 |
Birch DG, Birch EE, Hoffman DR, Uauy RD. Retinal development in very-low-birth-weight infants fed diets differing in omega-3 fatty acids. Investigative Ophthalmology & Visual Science. 33: 2365-76. PMID 1386065 |
0.76 |
|
| 1992 |
Birch DG, Anderson JL, Fish GE, Jost BF. Pattern-reversal electroretinographic acuity in untreated eyes with subfoveal neovascular membranes Investigative Ophthalmology and Visual Science. 33: 2097-2104. PMID 1376721 |
0.76 |
|
| 1991 |
Fish GE, Jost BF, Snyder WB, Fuller DG, Birch DG. Cataract extraction after brachytherapy for malignant melanoma of the choroid Ophthalmology. 98: 619-622. PMID 2062493 |
0.76 |
|
| 1991 |
Birch DG, Anderson JL, Fish GE. Longitudinal measures in children receiving ENCAD for hereditary retinal degeneration Documenta Ophthalmologica. 77: 185-192. PMID 1760967 DOI: 10.1007/BF00161366 |
0.76 |
|
| 1990 |
Jost BF, Hutton WL, Fuller DG, Vaiser A, Snyder WB, Fish GE, Spencer R, Birch DG. Vitrectomy in eyes at risk for macular hole formation Ophthalmology. 97: 843-847. PMID 2381695 |
0.76 |
|
| 1990 |
Hood DC, Birch DG. A quantitative measure of the electrical activity of human rod photoreceptors using electroretinography. Visual Neuroscience. 5: 379-87. PMID 2265151 |
0.76 |
|
| 1990 |
Uauy RD, Birch DG, Birch EE, Tyson JE, Hoffman DR. Effect of dietary omega-3 fatty acids on retinal function of very-low-birth-weight neonates. Pediatric Research. 28: 485-92. PMID 2255573 DOI: 10.1203/00006450-199011000-00014 |
0.76 |
|
| 1990 |
Birch DG, Anderson JL. Rod visual fields in cone-rod degeneration: Comparisons to retinitis pigmentosa Investigative Ophthalmology and Visual Science. 31: 2288-2299. PMID 2242994 |
0.76 |
|
| 1990 |
Birch EE, Birch DG, Petrig B, Uauy R. Retinal and cortical function of very low birthweight infants at 36 and 57 weeks postconception Clinical Vision Sciences. 5: 363-373. |
0.76 |
|
| 1990 |
Hood DC, Birch DG. The relationship between models of receptor activity and the a-wave of the human erg Clinical Vision Sciences. 5: 293-297. |
0.76 |
|
| 1989 |
Fish GE, Birch DG. The focal electroretinogram in the clinical assessment of macular disease Ophthalmology. 96: 109-114. PMID 2645549 |
0.76 |
|
| 1988 |
Birch DG, Jost BF, Fish GE. The Focal Electroretinogram in Fellow Eyes of Patients with Idiopathic Macular Holes Archives of Ophthalmology. 106: 1558-1563. PMID 3190541 DOI: 10.1001/archopht.1988.01060140726043 |
0.76 |
|
| 1988 |
Birch DG, Fish GE. Focal cone electroretinograms: Aging and macular disease Documenta Ophthalmologica. 69: 211-220. PMID 3168723 DOI: 10.1007/BF00154401 |
0.76 |
|
| 1987 |
Birch DG, Fish GE. Rod ERGs in retinitis pigmentosa and cone-rod degeneration Investigative Ophthalmology and Visual Science. 28: 140-150. PMID 3804644 |
0.76 |
|
| 1987 |
Birch DG. Diurnal rhythm in the human rod ERG: Retinitis pigmentosa Investigative Ophthalmology and Visual Science. 28: 2042-2048. PMID 3679752 |
0.76 |
|
| 1987 |
Birch DG, Sandberg MA. Dependence of cone b-wave implicit time on rod amplitude in retinitis pigmentosa Vision Research. 27: 1105-1112. PMID 3660664 DOI: 10.1016/0042-6989(87)90025-3 |
0.76 |
|
| 1987 |
Enoch JM, Hamer RD, Lakshminarayanan V, Yasuma T, Birch DG, Yamade S. Effect of monocular light exclusion on the Stiles-Crawford function. Vision Research. 27: 507-10. PMID 3660611 DOI: 10.1016/0042-6989(87)90035-6 |
0.76 |
|
| 1987 |
Birch EE, Birch DG. Pupillometric measures of retinal sensitivity in infants and adults with retinitis pigmentosa. Vision Research. 27: 499-505. PMID 3660610 DOI: 10.1016/0042-6989(87)90034-4 |
0.76 |
|
| 1987 |
Birch DG, Herman WK, deFaller JM, Disbrow DT, Birch EE. The relationship between rod perimetric thresholds and full-field rod ERGs in retinitis pigmentosa. Investigative Ophthalmology & Visual Science. 28: 954-65. PMID 3583634 |
0.76 |
|
| 1986 |
Birch DG, Sandberg MA, Berson EL. Diurnal rhythm in the human rod ERG. Relationship to cyclic lighting. Investigative Ophthalmology & Visual Science. 27: 268-70. PMID 3943951 |
0.76 |
|
| 1986 |
Fish GE, Birch DG, Fuller DG, Straach R. A comparison of visual function tests in eyes with maculopathy Ophthalmology. 93: 1177-1182. PMID 3808628 |
0.76 |
|
| 1986 |
Birch DG, Fish GE. Rod ERGs in children with hereditary retinal degeneration Journal of Pediatric Ophthalmology and Strabismus. 23: 227-232. PMID 3772690 |
0.76 |
|
| 1985 |
Berson EL, Sandberg MA, Rosner B, Birch DG, Hanson AH. Natural course of retinitis pigmentosa over a three-year interval. American Journal of Ophthalmology. 99: 240-51. PMID 3976802 |
0.76 |
|
| 1985 |
Enoch JM, Birch DG. Comment on inferred positive phototropic activity in human photoreceptors. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 309: 611-3. PMID 2861610 |
0.76 |
|
| 1985 |
Enoch JM, Birch DG, Birch EE. Photoreceptor alignment [4] Science. 229: 708. |
0.76 |
|
| 1984 |
Birch DG, Berson EL, Sandberg MA. Diurnal rhythm in the human rod ERG. Investigative Ophthalmology & Visual Science. 25: 236-8. PMID 6538188 |
0.88 |
|
| 1982 |
Birch DG, Sandberg MA, Berson EL. The Stiles-Crawford effect in retinitis pigmentosa. Investigative Ophthalmology & Visual Science. 22: 157-64. PMID 7056630 |
0.88 |
|
| Show low-probability matches. |