| Year |
Citation |
Score |
| 2023 |
Birch DG, Cheetham JK, Daiger SP, Hoyng C, Kay C, MacDonald IM, Pennesi ME, Sullivan LS. Overcoming the Challenges to Clinical Development of X-Linked Retinitis Pigmentosa Therapies: Proceedings of an Expert Panel. Translational Vision Science & Technology. 12: 5. PMID 37294701 DOI: 10.1167/tvst.12.6.5 |
0.322 |
|
| 2023 |
Duncan JL, Cheng P, Maguire MG, Ayala AA, Birch DG, Cheetham JK, Durham TA, Fahim AT, Hoyng CB, Ishikawa H, Michaelides M, Pennesi ME, Alain-Sahel J, Stingl K, Weng CY. Static Perimetry in the Rate of Progression in USH2A-related Retinal Degeneration (RUSH2A) Study: Assessment through Two Years. American Journal of Ophthalmology. PMID 36764426 DOI: 10.1016/j.ajo.2023.02.002 |
0.372 |
|
| 2022 |
Conley SM, McClard CK, Mwoyosvi ML, Alkadhem N, Radojevic B, Klein M, Birch D, Ellis A, Icks SW, Guddanti T, Bennett LD. Delineating the Clinical Phenotype of Patients With the c.629C>G, p.Pro210Arg Mutation in Peripherin-2. Investigative Ophthalmology & Visual Science. 63: 19. PMID 35861669 DOI: 10.1167/iovs.63.8.19 |
0.381 |
|
| 2022 |
Solaki M, Baumann B, Reuter P, Andreasson S, Audo I, Ayuso C, Balousha G, Benedicenti F, Birch D, Bitoun P, Blain D, Bocquet B, Branham K, Català-Mora J, De Baere E, et al. Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia. Human Mutation. PMID 35332618 DOI: 10.1002/humu.24371 |
0.546 |
|
| 2022 |
Birch DG, Samarakoon L, Melia M, Duncan JL, Ayala AR, Audo I, Cheetham JK, Durham TA, Iannaccone A, Pennesi ME, Stingl K. The RUSH2A Study: Dark-Adapted Visual Fields in Patients With Retinal Degeneration Associated With Biallelic Variants in the USH2A Gene. Investigative Ophthalmology & Visual Science. 63: 17. PMID 35293952 DOI: 10.1167/iovs.63.3.17 |
0.348 |
|
| 2021 |
Schönbach EM, Janeschitz-Kriegl L, Strauss RW, Cattaneo MEGV, Fujinami K, Birch DG, Cideciyan AV, Sunness JS, Weleber RG, Ip MS, Sadda SR, Scholl HPN. The Progression of Stargardt Disease using Volumetric Hill of Vision Analyses Over 24 Months: ProgStar Report No.15. American Journal of Ophthalmology. PMID 33951446 DOI: 10.1016/j.ajo.2021.04.015 |
0.312 |
|
| 2021 |
Radojevic B, Jones K, Klein M, Mauro-Herrera M, Kingsley R, Birch DG, Bennett LD. Variable expressivity in patients with autosomal recessive retinitis pigmentosa associated with the gene . Ophthalmic Genetics. 42: 15-22. PMID 33465333 DOI: 10.1080/13816810.2020.1832532 |
0.389 |
|
| 2020 |
Zhai Y, Xu M, Dimopoulos IS, Birch DG, Bernstein PS, Holt J, Kirn D, Francis P, MacDonald IM. Quantification of RPE Changes in Choroideremia Using a Photoshop-Based Method. Translational Vision Science & Technology. 9: 21. PMID 32832227 DOI: 10.1167/Tvst.9.7.21 |
0.381 |
|
| 2020 |
Thompson DA, Iannaccone A, Ali RR, Arshavsky VY, Audo I, Bainbridge JWB, Besirli CG, Birch DG, Branham KE, Cideciyan AV, Daiger SP, Dalkara D, Duncan JL, Fahim AT, Flannery JG, et al. Advancing Clinical Trials for Inherited Retinal Diseases: Recommendations from the Second Monaciano Symposium. Translational Vision Science & Technology. 9: 2. PMID 32832209 DOI: 10.1167/Tvst.9.7.2 |
0.56 |
|
| 2020 |
Bennett LD, Klein M, John FT, Radojevic B, Jones K, Birch DG. Disease Progression in Patients with Autosomal Dominant Retinitis Pigmentosa due to a Mutation in Inosine Monophosphate Dehydrogenase 1 (IMPDH1). Translational Vision Science & Technology. 9: 14. PMID 32821486 DOI: 10.1167/Tvst.9.5.14 |
0.456 |
|
| 2020 |
Wang YZ, Galles D, Klein M, Locke KG, Birch DG. Application of a Deep Machine Learning Model for Automatic Measurement of EZ Width in SD-OCT Images of RP. Translational Vision Science & Technology. 9: 15. PMID 32818077 DOI: 10.1167/Tvst.9.2.15 |
0.314 |
|
| 2020 |
Schönbach EM, Strauss RW, Muñoz B, Wolfson Y, Ibrahim MA, Birch DG, Zrenner E, Sunness JS, Ip MS, Sadda SR, West SK, Scholl HPN. Longitudinal Microperimetric Changes of Macular Sensitivity in Stargardt Disease After 12 Months: ProgStar Report No. 13. Jama Ophthalmology. PMID 32463436 DOI: 10.1001/Jamaophthalmol.2020.1735 |
0.322 |
|
| 2020 |
Duncan JL, Liang W, Maguire MG, Audo I, Ayala AR, Birch DG, Carroll J, Cheetham JK, Esposti SD, Durham TA, Erker L, Farsiu S, Ferris FL, Heon E, Hufnagel RB, et al. Baseline Visual Field Findings in the RUSH2A Study: Associated Factors and Correlation with Other Measures of Disease Severity. American Journal of Ophthalmology. PMID 32446738 DOI: 10.1016/J.Ajo.2020.05.024 |
0.395 |
|
| 2020 |
Jones KD, Radziwon A, Birch DG, MacDonald IM. A novel SVA retrotransposon insertion in the gene results in loss of REP-1 causing choroideremia. Ophthalmic Genetics. 1-4. PMID 32441177 DOI: 10.1080/13816810.2020.1768557 |
0.465 |
|
| 2020 |
Schönbach EM, Strauss RW, Ahmed MI, Janes JL, Cideciyan AV, Birch DG, Sunness JS, Zrenner E, Ip MS, Kong X, Sadda SR, Scholl HPN. The Effect of Attention on Fixation Stability during Dynamic Fixation Testing in Stargardt Disease. American Journal of Ophthalmology. PMID 32422174 DOI: 10.1016/J.Ajo.2020.05.002 |
0.301 |
|
| 2020 |
Schönbach EM, Strauss RW, Ibrahim MA, Janes JL, Birch DG, Cideciyan AV, Sunness JS, Muñoz B, Ip MS, Sadda SR, Scholl HPN. Faster Sensitivity Loss around Dense Scotomas than for Overall Macular Sensitivity in Stargardt Disease: ProgStar Report No. 14. American Journal of Ophthalmology. PMID 32222369 DOI: 10.1016/J.Ajo.2020.03.020 |
0.366 |
|
| 2020 |
Bennett LD, Klein M, John FT, Radojevic B, Jones K, Birch DG. Disease Progression in Patients with Autosomal Dominant Retinitis Pigmentosa due to a Mutation in Inosine Monophosphate Dehydrogenase 1 (IMPDH1) Translational Vision Science & Technology. 9: 14. DOI: 10.1167/tvst.9.5.14 |
0.38 |
|
| 2019 |
Fahim AT, Sullivan LS, Bowne SJ, Jones KD, Wheaton DKH, Khan NW, Heckenlively JR, Jayasundera KT, Branham KH, Andrews CA, Othman MI, Karoukis AJ, Birch DG, Daiger SP. X-Chromosome Inactivation Is a Biomarker of Clinical Severity in Female Carriers of RPGR-Associated X-Linked Retinitis Pigmentosa. Ophthalmology. Retina. PMID 31953110 DOI: 10.1016/J.Oret.2019.11.010 |
0.345 |
|
| 2019 |
Nittala MG, Velaga SB, Hariri A, Pfau M, Birch DG, Haines J, Pericak-Vance MA, Stambolian D, Sadda SR. Retinal Sensitivity Using Microperimetry in Age-Related Macular Degeneration in an Amish Population. Ophthalmic Surgery, Lasers & Imaging Retina. 50: e236-e241. PMID 31589764 DOI: 10.3928/23258160-20190905-15 |
0.384 |
|
| 2019 |
Strauss RW, Kong X, Ho A, Jha A, West S, Ip M, Bernstein PS, Birch DG, Cideciyan AV, Michaelides M, Sahel JA, Sunness JS, Traboulsi EI, Zrenner E, Pitetta S, et al. Progression of Stargardt Disease as Determined by Fundus Autofluorescence Over a 12-Month Period: ProgStar Report No. 11. Jama Ophthalmology. PMID 31369039 DOI: 10.1001/Jamaophthalmol.2019.2885 |
0.321 |
|
| 2019 |
Barnes CS, Schuchard RA, Birch DG, Dagnelie G, Wood L, Koenekoop RK, Bittner AK. Reliability of Semiautomated Kinetic Perimetry (SKP) and Goldmann Kinetic Perimetry in Children and Adults With Retinal Dystrophies. Translational Vision Science & Technology. 8: 36. PMID 31211001 DOI: 10.1167/Tvst.8.3.36 |
0.376 |
|
| 2019 |
Lin TC, Wang LC, Yue L, Zhang Y, Falabella P, Zhu D, Hinton DR, Rao NA, Birch DG, Spencer R, Dorn JD, Humayun MS. Histopathologic Assessment of Optic Nerves and Retina From a Patient With Chronically Implanted Argus II Retinal Prosthesis System. Translational Vision Science & Technology. 8: 31. PMID 31171998 DOI: 10.1167/Tvst.8.3.31 |
0.385 |
|
| 2019 |
Pennesi ME, Birch DG, Duncan JL, Bennett J, Girach A. CHOROIDEREMIA: Retinal Degeneration With an Unmet Need. Retina (Philadelphia, Pa.). PMID 31021898 DOI: 10.1097/Iae.0000000000002553 |
0.516 |
|
| 2019 |
Ervin AM, Strauss RW, Ahmed MI, Birch D, Cheetham J, Ferris FL, Ip MS, Jaffe GJ, Maguire MG, Schönbach EM, Sadda SR, West SK, Scholl HPN. A Workshop on Measuring the Progression of Atrophy Secondary to Stargardt Disease in the ProgStar Studies: Findings and Lessons Learned. Translational Vision Science & Technology. 8: 16. PMID 31019847 DOI: 10.1167/Tvst.8.2.16 |
0.331 |
|
| 2019 |
Bennett LD, Metz G, Klein M, Locke KG, Khwaja A, Birch DG. Regional Variations and Intra-/Intersession Repeatability for Scotopic Sensitivity in Normal Controls and Patients With Inherited Retinal Degenerations. Investigative Ophthalmology & Visual Science. 60: 1122-1131. PMID 30901388 DOI: 10.1167/Iovs.18-25473 |
0.47 |
|
| 2019 |
Csaky KG, Patel PJ, Sepah YJ, Birch DG, Do DV, Ip MS, Guymer RH, Luu CD, Gune S, Lin H, Ferrara D. Microperimetry for Geographic Atrophy Secondary to Age-Related Macular Degeneration. Survey of Ophthalmology. PMID 30703401 DOI: 10.1016/J.Survophthal.2019.01.014 |
0.358 |
|
| 2019 |
Ong T, Pennesi ME, Birch DG, Lam BL, Tsang SH. Adeno-Associated Viral Gene Therapy for Inherited Retinal Disease. Pharmaceutical Research. 36: 34. PMID 30617669 DOI: 10.1007/S11095-018-2564-5 |
0.5 |
|
| 2018 |
Kiser K, Webb-Jones KD, Bowne SJ, Sullivan LS, Daiger SP, Birch DG. Time Course of Disease Progression of PRPF31-mediated Retinitis Pigmentosa. American Journal of Ophthalmology. PMID 30582903 DOI: 10.1016/J.Ajo.2018.12.009 |
0.481 |
|
| 2018 |
Duncan JL, Pierce EA, Laster AM, Daiger SP, Birch DG, Ash JD, Iannaccone A, Flannery JG, Sahel JA, Zack DJ, Zarbin MA. Inherited Retinal Degenerations: Current Landscape and Knowledge Gaps. Translational Vision Science & Technology. 7: 6. PMID 30034950 DOI: 10.1167/Tvst.7.4.6 |
0.396 |
|
| 2018 |
Gregori NZ, Callaway NF, Hoeppner C, Yuan A, Rachitskaya A, Feuer W, Ameri H, Arevalo JF, Augustin AJ, Birch DG, Dagnelie G, Grisanti S, Davis JL, Hahn P, Handa JT, et al. Retinal Anatomy and Electrode Array Position in Retinitis Pigmentosa Patients after Argus II Implantation: an International Study. American Journal of Ophthalmology. PMID 29940167 DOI: 10.1016/J.Ajo.2018.06.012 |
0.414 |
|
| 2018 |
Birch DG, Bernstein PS, Iannacone A, Pennesi ME, Lam BL, Heckenlively J, Csaky K, Hartnett ME, Winthrop KL, Jayasundera T, Hughbanks-Wheaton DK, Warner J, Yang P, Fish GE, Teske MP, et al. Effect of Oral Valproic Acid vs Placebo for Vision Loss in Patients With Autosomal Dominant Retinitis Pigmentosa: A Randomized Phase 2 Multicenter Placebo-Controlled Clinical Trial. Jama Ophthalmology. PMID 29879277 DOI: 10.1001/Jamaophthalmol.2018.1171 |
0.426 |
|
| 2018 |
Daiger SP, Bowne SJ, Sullivan LS, Branham K, Wheaton DK, Jones KD, Avery CE, Cadena ED, Heckenlively JR, Birch DG. Molecular Findings in Families with an Initial Diagnose of Autosomal Dominant Retinitis Pigmentosa (adRP). Advances in Experimental Medicine and Biology. 1074: 237-245. PMID 29721949 DOI: 10.1007/978-3-319-75402-4_29 |
0.375 |
|
| 2018 |
Täger J, Kohl S, Birch DG, Wheaton DKH, Wissinger B, Reuter P. An early nonsense mutation facilitates the expression of a short isoform of CNGA3 by alternative translation initiation. Experimental Eye Research. 171: 48-53. PMID 29499183 DOI: 10.1016/J.Exer.2018.02.027 |
0.412 |
|
| 2017 |
Schönbach EM, Ibrahim MA, Strauss RW, Birch DG, Cideciyan AV, Hahn GA, Ho A, Kong X, Nasser F, Sunness JS, Zrenner E, Sadda SR, West SK, Scholl HPN. Fixation Location and Stability Using the MP-1 Microperimeter in Stargardt Disease: ProgStar Report No. 3. Ophthalmology. Retina. 1: 68-76. PMID 31047397 DOI: 10.1016/J.Oret.2016.08.009 |
0.309 |
|
| 2017 |
Strauss RW, Muñoz B, Ho A, Jha A, Michaelides M, Cideciyan AV, Audo I, Birch DG, Hariri AH, Nittala MG, Sadda S, West S, Scholl HPN. Progression of Stargardt Disease as Determined by Fundus Autofluorescence in the Retrospective Progression of Stargardt Disease Study (ProgStar Report No. 9). Jama Ophthalmology. PMID 29049437 DOI: 10.1001/Jamaophthalmol.2017.4152 |
0.313 |
|
| 2017 |
Bennett LD, Klein M, Locke KG, Kiser K, Birch DG. Dark-Adapted Chromatic Perimetry for Measuring Rod Visual Fields in Patients with Retinitis Pigmentosa. Translational Vision Science & Technology. 6: 15. PMID 28798898 DOI: 10.1167/Tvst.6.4.15 |
0.451 |
|
| 2017 |
Soens ZT, Branch J, Wu S, Yuan Z, Li Y, Li H, Wang K, Xu M, Rajan L, Motta FL, Simões RT, Lopez-Solache I, Ajlan R, Birch DG, Zhao P, et al. Leveraging splice-affecting variant predictors and a minigene validation system to identify Mendelian disease-causing variants amongst exon-captured variants of uncertain significance. Human Mutation. PMID 28714225 DOI: 10.1002/Humu.23294 |
0.352 |
|
| 2017 |
Sullivan LS, Bowne SJ, Koboldt DC, Cadena EL, Heckenlively JR, Branham KE, Wheaton DH, Jones KD, Ruiz RS, Pennesi ME, Yang P, Davis-Boozer D, Northrup H, Gurevich VV, Chen R, ... ... Birch DG, et al. A Novel Dominant Mutation in SAG, the Arrestin-1 Gene, Is a Common Cause of Retinitis Pigmentosa in Hispanic Families in the Southwestern United States. Investigative Ophthalmology & Visual Science. 58: 2774-2784. PMID 28549094 DOI: 10.1167/Iovs.16-21341 |
0.432 |
|
| 2017 |
Strauss RW, Muñoz B, Ho A, Jha A, Michaelides M, Mohand-Said S, Cideciyan AV, Birch D, Hariri AH, Nittala MG, Sadda S, Scholl HPN. Incidence of Atrophic Lesions in Stargardt Disease in the Progression of Atrophy Secondary to Stargardt Disease (ProgStar) Study: Report No. 5. Jama Ophthalmology. PMID 28542697 DOI: 10.1001/Jamaophthalmol.2017.1121 |
0.306 |
|
| 2017 |
Schönbach EM, Wolfson Y, Strauss RW, Ibrahim MA, Kong X, Muñoz B, Birch DG, Cideciyan AV, Hahn GA, Nittala M, Sunness JS, Sadda SR, West SK, Scholl HPN. Macular Sensitivity Measured With Microperimetry in Stargardt Disease in the Progression of Atrophy Secondary to Stargardt Disease (ProgStar) Study: Report No. 7. Jama Ophthalmology. PMID 28542693 DOI: 10.1001/Jamaophthalmol.2017.1162 |
0.376 |
|
| 2017 |
Hariri AH, Velaga SB, Girach A, Ip MS, Le PV, Lam BL, Fischer MD, Sankila EM, Pennesi M, Holz FG, MacLaren RE, Birch DG, Hoyng CB, MacDonald IM, Black GC, et al. Measurement and Reproducibility of Preserved Ellipsoid Zone Area and Preserved RPE Area in a Cohort of Eyes with Choroideremia. American Journal of Ophthalmology. PMID 28499705 DOI: 10.1016/J.Ajo.2017.05.002 |
0.311 |
|
| 2017 |
Radziwon A, Arno G, Wheaton D, McDonagh EM, Baple EL, Webb-Jones K, Birch D, Webster AR, MacDonald IM. Single base substitutions in the CHM promoter as a cause of choroideremia. Human Mutation. PMID 28271586 DOI: 10.1002/Humu.23212 |
0.356 |
|
| 2017 |
Birch DG, Benz MS, Miller DM, Antoszyk AN, Markoff J, Kozma P, Meunier E, Sergott RC. EVALUATION OF FULL-FIELD ELECTRORETINOGRAM REDUCTIONS AFTER OCRIPLASMIN TREATMENT: Results of the OASIS Trial ERG Substudy. Retina (Philadelphia, Pa.). PMID 28198785 DOI: 10.1097/Iae.0000000000001536 |
0.322 |
|
| 2016 |
Ventura MJ, Wheaton D, Xu M, Birch D, Bowne SJ, Sullivan LS, Daiger SP, Whitney AE, Jones RO, Moser AB, Chen R, Wangler MF. Diagnosis of a mild peroxisomal phenotype with next-generation sequencing. Molecular Genetics and Metabolism Reports. 9: 75-78. PMID 27872819 DOI: 10.1016/J.Ymgmr.2016.10.006 |
0.326 |
|
| 2016 |
Sadda SR, Chakravarthy U, Birch DG, Staurenghi G, Henry EC, Brittain C. CLINICAL ENDPOINTS FOR THE STUDY OF GEOGRAPHIC ATROPHY SECONDARY TO AGE-RELATED MACULAR DEGENERATION. Retina (Philadelphia, Pa.). 36: 1806-1822. PMID 27652913 DOI: 10.1097/Iae.0000000000001283 |
0.303 |
|
| 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 |
0.363 |
|
| 2016 |
da Cruz L, Dorn JD, Humayun MS, Dagnelie G, Handa J, Barale PO, Sahel JA, Stanga PE, Hafezi F, Safran AB, Salzmann J, Santos A, Birch D, Spencer R, Cideciyan AV, et al. Five-Year Safety and Performance Results from the Argus II Retinal Prosthesis System Clinical Trial. Ophthalmology. PMID 27453256 DOI: 10.1016/J.Ophtha.2016.06.049 |
0.422 |
|
| 2016 |
Buena-Atienza E, Rüther K, Baumann B, Bergholz R, Birch D, De Baere E, Dollfus H, Greally MT, Gustavsson P, Hamel CP, Heckenlively JR, Leroy BP, Plomp AS, Pott JW, Rose K, et al. De novo intrachromosomal gene conversion from OPN1MW to OPN1LW in the male germline results in Blue Cone Monochromacy. Scientific Reports. 6: 28253. PMID 27339364 DOI: 10.1038/Srep28253 |
0.33 |
|
| 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 |
0.365 |
|
| 2016 |
Hariri AH, Zhang HY, Ho A, Francis P, Weleber RG, Birch DG, Ferris FL, Sadda SR. Quantification of Ellipsoid Zone Changes in Retinitis Pigmentosa Using en Face Spectral Domain-Optical Coherence Tomography. Jama Ophthalmology. PMID 27031504 DOI: 10.1001/Jamaophthalmol.2016.0502 |
0.359 |
|
| 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 |
0.396 |
|
| 2016 |
Ghazi NG, Abboud EB, Nowilaty SR, Alkuraya H, Alhommadi A, Cai H, Hou R, Deng WT, Boye SL, Almaghamsi A, Al Saikhan F, Al-Dhibi H, Birch D, Chung C, Colak D, et al. Treatment of retinitis pigmentosa due to MERTK mutations by ocular subretinal injection of adeno-associated virus gene vector: results of a phase I trial. Human Genetics. PMID 26825853 DOI: 10.1007/S00439-016-1637-Y |
0.426 |
|
| 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 |
0.303 |
|
| 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 |
0.398 |
|
| 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 |
0.394 |
|
| 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 |
0.446 |
|
| 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 |
0.38 |
|
| 2015 |
Wen Y, Birch DG. Outer Segment Thickness Predicts Visual Field Response to QLT091001 in Patients with RPE65 or LRAT Mutations. Translational Vision Science & Technology. 4: 8. PMID 26448901 DOI: 10.1167/Tvst.4.5.8 |
0.439 |
|
| 2015 |
Ho AC, Humayun MS, Dorn JD, da Cruz L, Dagnelie G, Handa J, Barale PO, Sahel JA, Stanga PE, Hafezi F, Safran AB, Salzmann J, Santos A, Birch D, Spencer R, et al. Long-Term Results from an Epiretinal Prosthesis to Restore Sight to the Blind. Ophthalmology. 122: 1547-54. PMID 26162233 DOI: 10.1016/J.Ophtha.2015.04.032 |
0.394 |
|
| 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: E3010-9. PMID 26023183 DOI: 10.1073/Pnas.1505870112 |
0.363 |
|
| 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 (Philadelphia, Pa.). 35: 1173-83. PMID 25932553 DOI: 10.1097/Iae.0000000000000606 |
0.304 |
|
| 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 |
0.379 |
|
| 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 |
0.354 |
|
| 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 |
0.419 |
|
| 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 |
0.494 |
|
| 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 |
0.365 |
|
| 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 |
0.422 |
|
| 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 |
0.48 |
|
| 2013 |
Ramachandran R, Zhou L, Locke KG, Birch DG, Hood DC. A Comparison of Methods for Tracking Progression in X-Linked Retinitis Pigmentosa Using Frequency Domain OCT. Translational Vision Science & Technology. 2: 5. PMID 24349883 DOI: 10.1167/Tvst.2.7.5 |
0.421 |
|
| 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 |
0.579 |
|
| 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 |
0.46 |
|
| 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 |
0.404 |
|
| 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 |
0.384 |
|
| 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 |
0.494 |
|
| 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 |
0.377 |
|
| 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 |
0.428 |
|
| 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 |
0.636 |
|
| 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 |
0.452 |
|
| 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 |
0.403 |
|
| 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 |
0.432 |
|
| 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 |
0.371 |
|
| 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 |
0.457 |
|
| 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 |
0.324 |
|
| 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 |
0.36 |
|
| 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 |
0.377 |
|
| 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 |
0.473 |
|
| 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 |
0.447 |
|
| 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 |
0.394 |
|
| 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 |
0.41 |
|
| 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 |
0.458 |
|
| 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 |
0.415 |
|
| 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 |
0.309 |
|
| 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 |
0.406 |
|
| 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 |
0.43 |
|
| 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 |
0.378 |
|
| 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 |
0.396 |
|
| 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 |
0.423 |
|
| 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 |
0.407 |
|
| 2010 |
Birch DG. The role of electrophysiology in detecting and following retinal dystrophies Journal of Vision. 8: 38-38. DOI: 10.1167/8.17.38 |
0.423 |
|
| 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 |
0.35 |
|
| 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 |
0.436 |
|
| 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 |
0.392 |
|
| 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 |
0.347 |
|
| 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 |
0.386 |
|
| 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 |
0.413 |
|
| 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 |
0.343 |
|
| 2008 |
Kitiratschky VB, Wilke R, Renner AB, Kellner U, Vadalà M, Birch DG, Wissinger B, Zrenner E, Kohl S. Mutation analysis identifies GUCY2D as the major gene responsible for autosomal dominant progressive cone degeneration. Investigative Ophthalmology & Visual Science. 49: 5015-23. PMID 18487367 DOI: 10.1167/Iovs.08-1901 |
0.441 |
|
| 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 |
0.401 |
|
| 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 |
0.34 |
|
| 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 |
0.435 |
|
| 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 |
0.424 |
|
| 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 |
0.442 |
|
| 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 |
0.414 |
|
| 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 DOI: 10.1097/00006982-200512001-00023 |
0.359 |
|
| 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 |
0.451 |
|
| 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 |
0.377 |
|
| 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 |
0.368 |
|
| 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 |
0.428 |
|
| 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 |
0.388 |
|
| 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 |
0.363 |
|
| 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 |
0.418 |
|
| 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 |
0.436 |
|
| 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 |
0.402 |
|
| 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 DOI: 10.1007/978-1-4615-0067-4_1 |
0.375 |
|
| 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 |
0.337 |
|
| 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 |
0.395 |
|
| 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 |
0.401 |
|
| 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 |
0.357 |
|
| 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 |
0.344 |
|
| 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 DOI: 10.1001/Archopht.120.8.1045 |
0.361 |
|
| 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 |
0.318 |
|
| 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 |
0.612 |
|
| 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 DOI: 10.1093/Hmg/11.5.559 |
0.462 |
|
| 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 |
0.395 |
|
| 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 |
0.468 |
|
| 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 DOI: 10.1007/S11745-001-0798-1 |
0.334 |
|
| 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 Mã©Dicas E Biolã³Gicas / Sociedade Brasileira De BiofãSica ... [Et Al.]. 34: 1037-40. PMID 11471043 DOI: 10.1590/S0100-879X2001000800010 |
0.309 |
|
| 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 |
0.483 |
|
| 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 |
0.384 |
|
| 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 DOI: 10.1002/1098-1004(200102)17:2<151::Aid-Humu7>3.0.Co;2-W |
0.422 |
|
| 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 |
0.424 |
|
| 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 |
0.396 |
|
| 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 |
0.51 |
|
| 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 |
0.426 |
|
| 2000 |
Sohoki MM, Browne SJ, Sullivan LS, Blackshaw S, Cepko CL, Payne AM, Bhattacharya SS, Khaliq S, Mehdi SQ, Birch DG, Harrison WR, Elder FF, Heckenlively JR, Daiger SP. Mutations in a new photoreceptor-pineal gene on 17p cause leber congenital amaurosis. Nat gen 2000;24:79-83 American Journal of Ophthalmology. 129: 834-5. PMID 10927016 DOI: 10.1016/S0002-9394(00)00517-1 |
0.356 |
|
| 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 DOI: 10.1076/1381-6810(200006)2121-8Ft089 |
0.443 |
|
| 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 |
0.481 |
|
| 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 |
0.389 |
|
| 2000 |
Pepperberg DR, Birch DG, Hood DC. Electroretinographic determination of human rod flash response in vivo. Methods in Enzymology. 316: 202-23. PMID 10800677 DOI: 10.1016/S0076-6879(00)16725-4 |
0.359 |
|
| 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 |
0.405 |
|
| 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 |
0.432 |
|
| 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 |
0.417 |
|
| 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 DOI: 10.1523/Jneurosci.19-14-05889.1999 |
0.403 |
|
| 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 DOI: 10.1097/00006982-199903000-00010 |
0.413 |
|
| 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 |
0.507 |
|
| 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 DOI: 10.1016/S0161-6420(99)90064-7 |
0.449 |
|
| 1999 |
Yang R, Robinson SW, Xiong W, Yau K, Birch DG, Garbers DL. Disruption of a Retinal Guanylyl Cyclase Gene Leads to Cone-Specific Dystrophy and Paradoxical Rod Behavior The Journal of Neuroscience. 19: 5889-5897. DOI: 10.1523/JNEUROSCI.19-14-05889.1999 |
0.306 |
|
| 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 |
0.387 |
|
| 1998 |
Sohocki MM, Sullivan LS, Mintz-Hittner HA, Birch D, Heckenlively JR, Freund CL, Mclnnes RR, Daiger SP. A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene American Journal of Human Genetics. 63: 1307-1315. PMID 9792858 DOI: 10.1086/302101 |
0.504 |
|
| 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 |
0.305 |
|
| 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 |
0.354 |
|
| 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 |
0.611 |
|
| 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 DOI: 10.1136/Fn.76.3.F168 |
0.333 |
|
| 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 DOI: 10.1017/S0952523800008774 |
0.316 |
|
| 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 |
0.312 |
|
| 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. |
0.327 |
|
| 1996 |
Birch DG, Sandberg MA. Submicrovolt full-field cone electroretinograms: Artifacts and reproducibility Documenta Ophthalmologica. 92: 269-280. PMID 9476594 DOI: 10.1007/Bf02584081 |
0.385 |
|
| 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 |
0.312 |
|
| 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 |
0.45 |
|
| 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. |
0.335 |
|
| 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 |
0.348 |
|
| 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 |
0.345 |
|
| 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 |
0.309 |
|
| 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 DOI: 10.1364/Josaa.12.002259 |
0.307 |
|
| 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 |
0.329 |
|
| 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 |
0.333 |
|
| 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 DOI: 10.1159/000423551 |
0.311 |
|
| 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 DOI: 10.1002/Humu.1380020309 |
0.387 |
|
| 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 DOI: 10.1016/S0002-9394(14)71278-4 |
0.361 |
|
| 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 DOI: 10.1364/Josaa.10.001624 |
0.361 |
|
| 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 |
0.317 |
|
| 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 DOI: 10.1017/S0952523800006076 |
0.322 |
|
| 1992 |
Uauy R, Birch E, Birch D, Peirano P. Visual and brain function measurements in studies of n-3 fatty acid requirements of infants. The Journal of Pediatrics. 120: S168-80. PMID 1560326 DOI: 10.1016/S0022-3476(05)81252-1 |
0.325 |
|
| 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 |
0.319 |
|
| 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 |
0.32 |
|
| 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 DOI: 10.1016/S0161-6420(91)32242-5 |
0.343 |
|
| 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 |
0.45 |
|
| 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 DOI: 10.1016/S0161-6420(90)32493-4 |
0.35 |
|
| 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 DOI: 10.1017/S0952523800000468 |
0.327 |
|
| 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 |
0.368 |
|
| 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 |
0.378 |
|
| 1988 |
Birch DG, Fish GE. Focal cone electroretinograms: Aging and macular disease Documenta Ophthalmologica. 69: 211-220. PMID 3168723 DOI: 10.1007/Bf00154401 |
0.391 |
|
| 1987 |
Birch DG, Fish GE. Rod ERGs in retinitis pigmentosa and cone-rod degeneration Investigative Ophthalmology and Visual Science. 28: 140-150. PMID 3804644 |
0.372 |
|
| 1987 |
Birch DG. Diurnal rhythm in the human rod ERG: Retinitis pigmentosa Investigative Ophthalmology and Visual Science. 28: 2042-2048. PMID 3679752 |
0.345 |
|
| 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 |
0.383 |
|
| 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 |
0.309 |
|
| 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 |
0.3 |
|
| 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 |
0.302 |
|
| 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 |
0.478 |
|
| 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 DOI: 10.1016/S0161-6420(86)33598-X |
0.406 |
|
| 1986 |
Birch DG, Fish GE. Rod ERGs in children with hereditary retinal degeneration Journal of Pediatric Ophthalmology and Strabismus. 23: 227-232. PMID 3772690 DOI: 10.3928/0191-3913-19860901-07 |
0.446 |
|
| 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 DOI: 10.1016/0002-9394(85)90351-4 |
0.593 |
|
| 1984 |
Birch DG, Berson EL, Sandberg MA. Diurnal rhythm in the human rod ERG. Investigative Ophthalmology & Visual Science. 25: 236-8. PMID 6538188 |
0.509 |
|
| 1983 |
Marmor MF, Aguirre G, Arden G, Berson E, Birch DG, Boughman JA, Carr R, Chatrian GE, Del Monte M, Dowling J, Enoch J, Fishman GA, Fulton AB, Garcia CA, Gouras P, et al. Retinitis Pigmentosa Ophthalmology. 90: 126-131. DOI: 10.1016/S0161-6420(83)34587-5 |
0.635 |
|
| 1982 |
Birch DG, Sandberg MA. Psychophysical studies of cone optical bandwidth in patients with retinitis pigmentosa Vision Research. 22: 1113-1117. PMID 7147721 DOI: 10.1016/0042-6989(82)90075-X |
0.43 |
|
| 1982 |
Birch DG, Sandberg MA, Berson EL. The Stiles-Crawford effect in retinitis pigmentosa. Investigative Ophthalmology & Visual Science. 22: 157-64. PMID 7056630 |
0.603 |
|
| 1980 |
Fitzgerald CR, Birch DG, Enoch JM. Functional analysis of vision in patients after retinal detachment repair. Archives of Ophthalmology (Chicago, Ill. : 1960). 98: 1237-44. PMID 7396776 DOI: 10.1001/Archopht.1980.01020040089012 |
0.429 |
|
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