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David G. Birch, PhD - Publications

Affiliations: 
Retina Foundation of the Southwest, Dallas, TX, United States 
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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
Low-probability matches (unlikely to be authored by this person)
2018 Abalem MF, Musch DC, Birch DG, Pennesi ME, Heckenlively JR, Jayasundera T. Diurnal variations of foveoschisis by optical coherence tomography in patients with RS1 X-linked juvenile retinoschisis. Ophthalmic Genetics. 1-6. PMID 29902095 DOI: 10.1080/13816810.2018.1466340  0.3
1993 Birch E, Birch D, Hoffman D, Hale L, Everett M, Uauy R. Breast-Feeding and Optimal Visual Development Journal of Pediatric Ophthalmology and Strabismus. 30: 33-38. DOI: 10.3928/0191-3913-19930101-09  0.299
2017 Jones KD, Wheaton DK, Bowne SJ, Sullivan LS, Birch DG, Chen R, Daiger SP. Next-generation sequencing to solve complex inherited retinal dystrophy: A case series of multiple genes contributing to disease in extended families. Molecular Vision. 23: 470-481. PMID 28761320  0.299
2018 Strauss RW, Kong X, Bittencourt MG, Ho A, Jha A, Schönbach EM, Ahmed MI, Muñoz B, Ervin AM, Michaelides M, Birch DG, Sahel JA, Sunness JS, Zrenner E, Bagheri S, et al. Scotopic Microperimetric Assessment of Rod Function in Stargardt Disease (SMART) Study: Design and Baseline Characteristics (Report No. 1). Ophthalmic Research. 1-8. PMID 29940588 DOI: 10.1159/000488711  0.299
1992 Snyder WB, Bloome MA, Birch DG. Pneumatic retinopexy versus scleral buckle. Preferences of Vitreous Society members, 1990. Retina-the Journal of Retinal and Vitreous Diseases. 12: 43-45. DOI: 10.1097/00006982-199212010-00009  0.298
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. Erratum to: Worldwide Argus II implantation: recommendations to optimize patient outcomes. Bmc Ophthalmology. 16: 129. PMID 27473341 DOI: 10.1186/S12886-016-0259-4  0.297
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  0.297
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  0.296
1996 Uauy R, Peirano P, Hoffman D, Mena P, Birch D, Birch E. Role of essential fatty acids in the function of the developing nervous system. Lipids. S167-76. PMID 8729114 DOI: 10.1007/Bf02637071  0.296
2018 Fujinami K, Strauss RW, Chiang JP, Audo IS, Bernstein PS, Birch DG, Bomotti SM, Cideciyan AV, Ervin AM, Marino MJ, Sahel JA, Mohand-Said S, Sunness JS, Traboulsi EI, West S, et al. Detailed genetic characteristics of an international large cohort of patients with Stargardt disease: ProgStar study report 8. The British Journal of Ophthalmology. PMID 29925512 DOI: 10.1136/Bjophthalmol-2018-312064  0.295
1987 Birch E, Hale L, Stager D, Fuller D, Birch D. Operant acuity of toddlers and developmentally delayed children with low vision. Journal of Pediatric Ophthalmology & Strabismus. 24: 64-69. DOI: 10.3928/0191-3913-19870301-04  0.295
2017 Schönbach EM, Ibrahim MA, Kong X, Strauss RW, Muñoz B, Birch DG, Sunness JS, West SK, Scholl HPN. Metrics and Acquisition Modes for Fixation Stability as a Visual Function Biomarker. Investigative Ophthalmology & Visual Science. 58: BIO268-BIO276. PMID 28973313 DOI: 10.1167/Iovs.17-21710  0.295
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  0.293
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  0.293
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 DOI: 10.1093/Ajcn/81.4.871  0.292
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.  0.289
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  0.288
2018 Strauss RW, Muñoz B, Ahmed MI, Bittencourt M, Schönbach EM, Michaelides M, Birch D, Zrenner E, Ervin AM, Charbel Issa P, Kong J, Wolfson Y, Shah M, Bagheri S, West S, et al. The Progression of the Stargardt Disease Type 4 (ProgStar-4) Study: Design and Baseline Characteristics (ProgStar-4 Report No. 1). Ophthalmic Research. 1-10. PMID 30110705 DOI: 10.1159/000491791  0.286
2020 Kubota R, Birch DG, Gregory JK, Koester JM. Randomised study evaluating the pharmacodynamics of emixustat hydrochloride in subjects with macular atrophy secondary to Stargardt disease. The British Journal of Ophthalmology. PMID 33214244 DOI: 10.1136/bjophthalmol-2020-317712  0.285
2018 Hariri AH, Ip MS, Girach A, Lam BL, Fischer MD, Sankila EM, Pennesi ME, Holz FG, Maclaren RE, Birch DG, Hoyng CB, MacDonald IM, Black GC, Tsang SH, Bressler NM, et al. Macular spatial distribution of preserved autofluorescence in patients with choroideremia. The British Journal of Ophthalmology. PMID 30297337 DOI: 10.1136/Bjophthalmol-2018-312620  0.285
2021 Chung DC, Birch DG, MacLaren RE. Endpoints for Measuring Efficacy in Clinical Trials for Inherited Retinal Disease. International Ophthalmology Clinics. 61: 63-78. PMID 34584045 DOI: 10.1097/IIO.0000000000000388  0.284
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  0.284
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 DOI: 10.1093/Ajcn/75.3.570  0.282
2020 Nittala MG, Uji A, Velaga SB, Hariri AH, Naor J, Birch DG, Spencer R, Leng T, Capela A, Tsukamoto A, Ip M, Sadda SR. Effect of Human Central Nervous System Stem Cell Subretinal Transplantation on Progression of Geographic Atrophy Secondary to Non Neovascular Age-Related Macular Degeneration. Ophthalmology. Retina. PMID 32562884 DOI: 10.1016/J.Oret.2020.06.012  0.282
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  0.281
2021 Durham TA, Duncan JL, Ayala AR, Birch DG, Cheetham JK, Ferris FL, Hoyng CB, Pennesi ME, Sahel JA. Tackling the Challenges of Product Development Through a Collaborative Rare Disease Network: The Foundation Fighting Blindness Consortium. Translational Vision Science & Technology. 10: 23. PMID 34004001 DOI: 10.1167/tvst.10.4.23  0.281
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 DOI: 10.1364/Josaa.13.000623  0.28
2023 Wang YZ, Juroch K, Chen Y, Ying GS, Birch DG. Deep Learning-Facilitated Study of the Rate of Change in Photoreceptor Outer Segment Metrics in RPGR-Related X-Linked Retinitis Pigmentosa. Investigative Ophthalmology & Visual Science. 64: 31. PMID 37988107 DOI: 10.1167/iovs.64.14.31  0.28
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  0.278
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  0.278
1980 Enoch JM, Birch DG, Birch EE, Benedetto MD. Alteration in directional sensitivity of the retina by monocular occlusion. Vision Research. 20: 1185-9. PMID 7269275 DOI: 10.1016/0042-6989(80)90058-9  0.277
2021 Leroy BP, Birch DG, Duncan JL, Lam BL, Koenekoop RK, Porto FBO, Russell SR, Girach A. Leber Congenital Amaurosis Due to CEP290 Mutations - Severe Vision Impairment with a High Unmet Medical Need: A Review. Retina (Philadelphia, Pa.). PMID 33595255 DOI: 10.1097/IAE.0000000000003133  0.276
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  0.276
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 9648504 DOI: 10.1159/000059653  0.276
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  0.275
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  0.274
1980 Enoch JM, Birch DG. Evidence for alteration in photoreceptor orientation. Ophthalmology. 87: 821-34. PMID 7053161  0.273
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 DOI: 10.1093/Ajcn/57.5.807S  0.273
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  0.271
2018 Schönbach EM, Strauss RW, Kong X, Muñoz B, Ibrahim MA, Sunness JS, Birch DG, Hahn GA, Nasser F, Zrenner E, Sadda SR, West SK, Scholl HPN. Longitudinal Changes of Fixation Location and Stability within 12 Months in Stargardt Disease: ProgStar Report No. 12. American Journal of Ophthalmology. PMID 29890160 DOI: 10.1016/J.Ajo.2018.06.003  0.271
2021 Kong X, Ibrahim-Ahmed M, Bittencourt MG, Strauss RW, Birch DG, Cideciyan AV, Ervin AM, Ho A, Sunness JS, Audo IS, Michaelides M, Zrenner E, Sadda S, Ip MS, West S, et al. Longitudinal Changes in Scotopic and Mesopic Macular Function as Assessed with Microperimetry in Patients with Stargardt Disease: SMART Study Report No. 2: Short Title: Scotopic and Mesopic Macular Functions in Stargardt Disease. American Journal of Ophthalmology. PMID 34695402 DOI: 10.1016/j.ajo.2021.10.014  0.269
2011 Sullivan JM, Birch DG, Spencer R. Pediatric hereditary macular degenerations Pediatric Retina. 245-294. DOI: 10.1007/978-3-642-12041-1_11  0.269
2022 Girach A, Audo I, Birch DG, Huckfeldt RM, Lam BL, Leroy BP, Michaelides M, Russell SR, Sallum JMF, Stingl K, Tsang SH, Yang P. RNA-based therapies in inherited retinal diseases. Therapeutic Advances in Ophthalmology. 14: 25158414221134602. PMID 36388727 DOI: 10.1177/25158414221134602  0.269
2022 Lad EM, Duncan JL, Liang W, Maguire MG, Ayala AR, Audo I, Birch DG, Carroll J, Cheetham JK, Durham TA, Fahim AT, Loo J, Deng Z, Mukherjee D, Heon E, et al. Baseline Microperimetry and OCT in the RUSH2A Study: Structure-Function Association and Correlation with Disease Severity. American Journal of Ophthalmology. PMID 36007554 DOI: 10.1016/j.ajo.2022.08.013  0.268
2023 Grosspoetzl M, Riedl R, Schliessleder G, Hu ZJ, Michaelides M, Sadda S, Birch D, Issa PC, Wedrich A, Seidel G, Scholl HPN, Strauss RW. The Progression of PROM1-associated retinal degeneration as determined by spectral-domain optical coherence tomography over a 24-months period. American Journal of Ophthalmology. PMID 37979600 DOI: 10.1016/j.ajo.2023.11.010  0.267
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  0.266
2021 Qian X, Wang J, Wang M, Igelman AD, Jones KD, Li Y, Wang K, Goetz KE, Birch DG, Yang P, Pennesi ME, Chen R. Identification of Deep-Intronic Splice Mutations in a Large Cohort of Patients With Inherited Retinal Diseases. Frontiers in Genetics. 12: 647400. PMID 33737949 DOI: 10.3389/fgene.2021.647400  0.266
1989 Fish GE, Birch DG. The focal electroretinogram in the clinical assessment of macular disease Ophthalmology. 96: 109-114. PMID 2645549  0.264
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  0.263
2018 Pennesi ME, Birch DG, Jayasundera KT, Parker M, Tan O, Gurses-Ozden R, Reichley C, Beasley KN, Yang P, Weleber RG, Bennett LD, Heckenlively JR, Kothapalli K, Chulay JD, For The Xlrs-Study Group. Prospective Evaluation of Patients With X-Linked Retinoschisis During 18 Months. Investigative Ophthalmology & Visual Science. 59: 5941-5956. PMID 30551202 DOI: 10.1167/Iovs.18-24565  0.263
2016 Bowne SJ, Sullivan LS, Wheaton DK, Locke KG, Jones KD, Koboldt DC, Fulton RS, Wilson RK, Blanton SH, Birch DG, Daiger SP. North Carolina macular dystrophy (MCDR1) caused by a novel tandem duplication of the PRDM13 gene. Molecular Vision. 22: 1239-1247. PMID 27777503  0.262
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 DOI: 10.1364/Josaa.13.000586  0.261
2021 Wang YZ, Wu W, Birch DG. A Hybrid Model Composed of Two Convolutional Neural Networks (CNNs) for Automatic Retinal Layer Segmentation of OCT Images in Retinitis Pigmentosa (RP). Translational Vision Science & Technology. 10: 9. PMID 34751740 DOI: 10.1167/tvst.10.13.9  0.26
1979 Enoch JM, Birch DG, Birch EE. Monocular light exclusion for a period of days reduces directional sensitivity of the human retina. Science (New York, N.Y.). 206: 705-7. PMID 493976  0.259
2015 Batabyal S, Cervenka G, Birch D, Kim YT, Mohanty S. Broadband activation by white-opsin lowers intensity threshold for cellular stimulation. Scientific Reports. 5: 17857. PMID 26658483 DOI: 10.1038/srep17857  0.257
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.  0.256
1982 Stromeyer CF, Mulligan JB, Birch DG, Dawson BM. Adaptation to polarized light in humans. Vision Research. 22: 217-23. PMID 7101757 DOI: 10.1016/0042-6989(82)90121-3  0.255
2022 Wissinger B, Baumann B, Buena-Atienza E, Ravesh Z, Cideciyan AV, Stingl K, Audo I, Meunier I, Bocquet B, Traboulsi EI, Hardcastle AJ, Gardner JC, Michaelides M, Branham KE, Rosenberg T, ... ... Birch D, et al. The landscape of submicroscopic structural variants at the gene cluster on Xq28 underlying blue cone monochromacy. Proceedings of the National Academy of Sciences of the United States of America. 119: e2115538119. PMID 35759666 DOI: 10.1073/pnas.2115538119  0.254
1980 Birch DG, Birch EE, Enoch JM. Visual sensitivity, resolution, and Rayleigh matches following monocular occlusion for one week. Journal of the Optical Society of America. 70: 954-8. PMID 7411267  0.254
2020 Birch DG, Cheng P, Duncan JL, Ayala AR, Maguire MG, Audo I, Cheetham JK, Durham TA, Fahim AT, Ferris FL, Heon E, Huckfeldt RM, Iannaccone A, Khan NW, Lad EM, et al. The RUSH2A Study: Best-Corrected Visual Acuity, Full-Field Electroretinography Amplitudes, and Full-Field Stimulus Thresholds at Baseline. Translational Vision Science & Technology. 9: 9. PMID 33133772 DOI: 10.1167/tvst.9.11.9  0.252
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  0.25
2021 Patel P, Jones K, Friedman DI, Birch DG, Ufret-Vincenty RL. Unexpected Etiology in a Case of Bilateral Maculopathy. Case Reports in Ophthalmology. 12: 622-628. PMID 34326763 DOI: 10.1159/000514705  0.249
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  0.248
1985 Enoch JM, Birch DG, Birch EE. Photoreceptor alignment. Science (New York, N.Y.). 229: 708. PMID 17841482 DOI: 10.1126/science.229.4715.708  0.248
1985 Enoch JM, Birch DG, Birch EE. Photoreceptor alignment [4] Science. 229: 708.  0.248
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  0.247
2022 Wang YZ, Birch DG. Performance of Deep Learning Models in Automatic Measurement of Ellipsoid Zone Area on Baseline Optical Coherence Tomography (OCT) Images From the Rate of Progression of USH2A-Related Retinal Degeneration (RUSH2A) Study. Frontiers in Medicine. 9: 932498. PMID 35865175 DOI: 10.3389/fmed.2022.932498  0.245
2023 Wang YZ, Juroch K, Birch DG. Deep Learning-Assisted Measurements of Photoreceptor Ellipsoid Zone Area and Outer Segment Volume as Biomarkers for Retinitis Pigmentosa. Bioengineering (Basel, Switzerland). 10. PMID 38135984 DOI: 10.3390/bioengineering10121394  0.243
2023 Chang DS, Callaway NF, Steffen V, Csaky K, Guymer RH, Birch DG, Patel PJ, Ip M, Gao SS, Briggs J, Honigberg L, Lai P, Ferrara D, Sepah YJ. Macular Sensitivity Endpoints in Geographic Atrophy: Exploratory Analysis of Chroma and Spectri Clinical Trials. Ophthalmology Science. 4: 100351. PMID 37869030 DOI: 10.1016/j.xops.2023.100351  0.24
1999 Peña M, Birch D, Uauy R, Peirano P. The effect of sleep state on electroretinographic (ERG) activity during early human development Early Human Development. 55: 51-62. PMID 10367982 DOI: 10.1016/S0378-3782(99)00006-7  0.234
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  0.234
2022 Pennesi ME, Yang P, Birch DG, Weng CY, Moore AT, Iannaccone A, Comander JI, Jayasundera T, Chulay J. Intravitreal Delivery of rAAV2tYF-CB-hRS1 Vector for Gene Augmentation Therapy in X-linked Retinoschisis - 1 Year Clinical Results. Ophthalmology. Retina. PMID 35781068 DOI: 10.1016/j.oret.2022.06.013  0.233
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  0.232
2023 Greenstein VC, Castillejos DS, Tsang SH, Lee W, Sparrow JR, Allikmets R, Birch DG, Hood DC. Monitoring Lesion Area Progression in Stargardt Disease: A Comparison of En Face Optical Coherence Tomography and Fundus Autofluorescence. Translational Vision Science & Technology. 12: 2. PMID 37126335 DOI: 10.1167/tvst.12.5.2  0.224
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.  0.219
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  0.212
2021 Schönbach EM, Strauss RW, Cattaneo MEGV, Fujinami K, Birch DG, Cideciyan AV, Sunness JS, Zrenner E, Sadda SR, Scholl HPN. Longitudinal Changes of Fixation Stability and Location within 24 Months in Stargardt Disease: ProgStar Report No. 16: Short title: Longitudinal Changes of Fixation in Stargardt Disease. American Journal of Ophthalmology. PMID 34298008 DOI: 10.1016/j.ajo.2021.07.013  0.209
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  0.209
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.  0.209
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  0.208
1981 Enoch JM, Birch DG. Inferred positive phototropic activity in human photoreceptors. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 291: 323-51. PMID 6111095  0.206
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.  0.188
2008 Birch D. F.G. Holz, S. Schmitz-Valckenbergm, R.F. Spaide, A.C. Bird (eds): Atlas of Fundus Autofluorescence Imaging Documenta Ophthalmologica. 117: 267-268. DOI: 10.1007/S10633-008-9134-9  0.187
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.  0.186
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  0.186
1999 Benson WE, Chan P, Sharma S, Snyder WB, Bloome MA, Birch DG. Survey: Current Popularity of Pneumatic Retinopexy Retina-the Journal of Retinal and Vitreous Diseases. 19: 238. DOI: 10.1097/00006982-199905000-00010  0.181
2024 MacLaren RE, Lam BL, Fischer MD, Holz FG, Pennesi ME, Birch DG, Sankila EM, Meunier IA, Stepien KE, Sallum JMF, Li J, Yoon D, Panda S, Gow JA. A Prospective, Observational, Non-Interventional Clinical Study of Participants With Choroideremia: The NIGHT Study. American Journal of Ophthalmology. PMID 38311152 DOI: 10.1016/j.ajo.2024.01.022  0.18
2023 Strauss RW, Ho A, Jha A, Fujinami K, Michaelides M, Cideciyan AV, Audo I, Birch DG, Sadda S, Ip M, West S, Schönbach EM, Kong X, Scholl HPN. The progression of Stargardt Disease as determined by fundus autofluorescence over a 24-month period (ProgStar Report No. 17). American Journal of Ophthalmology. PMID 36764427 DOI: 10.1016/j.ajo.2023.02.003  0.168
1992 Snyder WB, Bloome MA, Birch DG. Pneumatic retinopexy versus scleral buckle Retina. 12: 43-45. PMID 1565870  0.162
2022 Loo J, Jaffe GJ, Duncan JL, Birch DG, Farsiu S. Validation of a deep learning-based algorithm for segmentation of the ellipsoid zone on optical coherence tomography images of an USH2A-related retinal degeneration clinical trial. Retina (Philadelphia, Pa.). PMID 35174801 DOI: 10.1097/IAE.0000000000003448  0.15
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  0.144
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.  0.144
2021 da Palma MM, Igelman AD, Ku C, Burr A, You JY, Place EM, Wang NK, Oh JK, Branham KE, Zhang X, Ahn J, Gorin MB, Lam BL, Ronquillo CC, Bernstein PS, ... ... Birch DG, et al. Characterization of the Spectrum of Ophthalmic Changes in Patients With Alagille Syndrome. Investigative Ophthalmology & Visual Science. 62: 27. PMID 34185059 DOI: 10.1167/iovs.62.7.27  0.139
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  0.138
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  0.135
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  0.122
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.  0.119
2007 Birch DG, Liang FQ. Age-related macular degeneration: a target for nanotechnology derived medicines. International Journal of Nanomedicine. 2: 65-77. PMID 17722514  0.119
2020 Xu S, Coku A, Muraleedharan CK, Harajli A, Mishulin E, Dahabra C, Choi J, Garcia WJ, Webb K, Birch D, Goetz K, Li W. Mutation Screening in the miR-183/96/182 Cluster in Patients With Inherited Retinal Dystrophy. Frontiers in Cell and Developmental Biology. 8: 619641. PMID 33425925 DOI: 10.3389/fcell.2020.619641  0.119
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  0.118
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  0.117
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.  0.116
1996 Berezovsky A, Middendorf RC, Birch DG. Electroretinographic findings in patients treated with tamoxifen Investigative Ophthalmology and Visual Science. 37: S345.  0.112
2016 McGinn D, Birch D, Akroyd D, Molina-Solana M, Guo Y, Knottenbelt WJ. Visualizing Dynamic Bitcoin Transaction Patterns. Big Data. 4: 109-119. PMID 27441715 DOI: 10.1089/big.2015.0056  0.111
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  0.109
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. DOI: 10.1016/j.ophtha.2015.04.032  0.082
2021 Richter AG, Shields AM, Karim A, Birch D, Faustini SE, Steadman L, Ward K, Plant T, Reynolds G, Veenith T, Cunningham AF, Drayson MT, Wraith DC. Establishing the prevalence of common tissue-specific autoantibodies following severe acute respiratory syndrome coronavirus 2 infection. Clinical and Experimental Immunology. PMID 34082475 DOI: 10.1111/cei.13623  0.08
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  0.076
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.  0.076
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.  0.074
2016 Wall MB, Birch D, Yong MY. Opportunities and considerations for visualising neuroimaging data on very large displays. F1000research. 5: 2157. PMID 27703670 DOI: 10.12688/f1000research.9522.1  0.072
2015 Cameron M, Janakan G, Birch D, Nazir S. A closed loop obstruction caused by entrapment of the fallopian tube and herniation through the broad ligament. International Journal of Surgery Case Reports. 12: 57-9. PMID 26011802 DOI: 10.1016/j.ijscr.2015.02.010  0.066
2003 Hill RR, Birch D, Jeffs GE, North M. Enantioselection in peptide bond formation. Organic & Biomolecular Chemistry. 1: 965-72. PMID 12929635 DOI: 10.1039/b211914e  0.063
2003 Billard I, Ansoborlo E, Apperson K, Arpigny S, Azenha ME, Birch D, Bros P, Burrows HD, Choppin G, Couston L, Dubois V, Fanghänel T, Geipel G, Hubert S, Kim JI, et al. Aqueous solutions of uranium(VI) as studied by time-resolved emission spectroscopy: A round-robin test Applied Spectroscopy. 57: 1027-1038. PMID 14661847 DOI: 10.1366/000370203322259002  0.057
2010 Karolin J, Pánek D, MacMillan A, Rolinski O, Birch D. Fluorescence biosensing in nanopores. Annual International Conference of the Ieee Engineering in Medicine and Biology Society. Ieee Engineering in Medicine and Biology Society. Annual International Conference. 2009: 4154-7. PMID 19964618 DOI: 10.1109/IEMBS.2009.5333940  0.053
2021 Schneider L, Guo YK, Birch D, Sarkies P. Network-based visualisation reveals new insights into transposable element diversity. Molecular Systems Biology. 17: e9600. PMID 34169647 DOI: 10.15252/msb.20209600  0.052
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  0.048
2015 Birch D, Mely Y, Wolfbeis O. A journal in ascendancy. Methods and Applications in Fluorescence. 3: 040203. PMID 29148502 DOI: 10.1088/2050-6120/3/4/040203  0.044
2007 Brown S, Birch D, Thyagaraj S, Teufel J, Phillips C. Effects of a single-lesson tobacco prevention curriculum on knowledge, skill identification and smoking intention. Journal of Drug Education. 37: 55-69. PMID 17982935 DOI: 10.2190/638J-J7G2-4T58-28JU  0.041
2010 Durai R, Birch D. QUIZ HQ 56. A rare cause of acute abdomen. Journal of Gastrointestinal and Liver Diseases : Jgld. 19: 203, 212. PMID 20593057  0.034
2013 Birch D, Mély Y, Wolfbeis OS. Celebrating our first year. Methods and Applications in Fluorescence. 1: 040201. PMID 29148450 DOI: 10.1088/2050-6120/1/4/040201  0.034
2011 Saxl T, Khan F, Ferla M, Birch D, Pickup J. A fluorescence lifetime-based fibre-optic glucose sensor using glucose/ galactose-binding protein Analyst. 136: 968-972. PMID 21165474 DOI: 10.1039/C0An00430H  0.033
2012 Chaney BH, Chavarria E, Stellefson ML, Birch D, Spear C. American Association for Health Education (AAHE) 2011 Membership Survey: Summary of Findings. American Journal of Health Education / American Alliance For Health, Physical Education, Recreation, and Dance. 43: 322-326. PMID 24133673 DOI: 10.1080/19325037.2012.10598862  0.026
2013 Birch D, Mély Y, Wolfbeis OS. Welcome to Methods and Applications in Fluorescence. Methods and Applications in Fluorescence. 1: 010201. PMID 29148440 DOI: 10.1088/2050-6120/1/1/010201  0.025
2016 Birch D, Mely Y, Wolfbeis O. Building a quality home for fluorescence. Methods and Applications in Fluorescence. 4: 040401. PMID 28192288 DOI: 10.1088/2050-6120/4/4/040401  0.025
2012 Lee YJ, Basu NN, Parampalli U, Birch D. An unusual case of rectal perforation resulting in extensive surgical emphysema Bmj Case Reports. 2012. PMID 22665399 DOI: 10.1136/bcr.09.2011.4822  0.019
2017 Wilroy J, Turner L, Birch D, Leaver-Dunn D, Hibberd E, Leeper J. Development and evaluation of a social cognitive theory-based instrument to assess correlations for physical activity among people with spinal cord injury. Disability and Health Journal. PMID 28359637 DOI: 10.1016/J.Dhjo.2017.03.010  0.01
2014 Birch D, Mely Y, Wolfbeis O. Creating a high impact journal for research in fluorescence. Methods and Applications in Fluorescence. 2: 040201. PMID 29148474 DOI: 10.1088/2050-6120/2/4/040201  0.01
1988 Turpin DH, Elrifi IR, Birch DG, Weger HG, Holmes JJ. Interactions between photosynthesis, respiration, and nitrogen assimilation in microalgae Canadian Journal of Botany. 66: 2083-2097.  0.01
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