| Year |
Citation |
Score |
| 2023 |
Wood EH, Moshfeghi DM, Capone A, Williams GA, Blumenkranz MS, Sieving PA, Harper CA, Hartnett ME, Drenser KA. A Literary Pediatric Retina Fellowship With Michael T. Trese, MD. Ophthalmic Surgery, Lasers & Imaging Retina. 54: 701-712. PMID 38113364 DOI: 10.3928/23258160-20231020-01 |
0.518 |
|
| 2023 |
Ku CA, Wei LW, Sieving PA. X-Linked Retinoschisis. Cold Spring Harbor Perspectives in Medicine. PMID 36690462 DOI: 10.1101/cshperspect.a041288 |
0.565 |
|
| 2023 |
Sin TN, Kim S, Li Y, Wang J, Chen R, Chung SH, Kim S, Casanova MI, Park S, Smit-McBride Z, Sun N, Pomerantz O, Roberts JA, Guan B, Hufnagel RB, ... Sieving PA, et al. A Spontaneous Nonhuman Primate Model of Myopic Foveoschisis. Investigative Ophthalmology & Visual Science. 64: 18. PMID 36689233 DOI: 10.1167/iovs.64.1.18 |
0.593 |
|
| 2022 |
Kiani AK, Pheby D, Henehan G, Brown R, Sieving P, Sykora P, Marks R, Falsini B, Capodicasa N, Miertus S, Lorusso L, Dondossola D, Tartaglia GM, Ergoren MC, Dundar M, et al. Ethical considerations regarding animal experimentation. Journal of Preventive Medicine and Hygiene. 63: E255-E266. PMID 36479489 DOI: 10.15167/2421-4248/jpmh2022.63.2S3.2768 |
0.434 |
|
| 2022 |
Kiani AK, Naureen Z, Pheby D, Henehan G, Brown R, Sieving P, Sykora P, Marks R, Falsini B, Capodicasa N, Miertus S, Lorusso L, Dondossola D, Tartaglia GM, Ergoren MC, et al. Methodology for clinical research. Journal of Preventive Medicine and Hygiene. 63: E267-E278. PMID 36479476 DOI: 10.15167/2421-4248/jpmh2022.63.2S3.2769 |
0.429 |
|
| 2022 |
Heymann JB, Vijayasarathy C, Fariss RN, Sieving PA. Advances in understanding the molecular structure of retinoschisin while questions remain of biological function. Progress in Retinal and Eye Research. 101147. PMID 36402656 DOI: 10.1016/j.preteyeres.2022.101147 |
0.542 |
|
| 2022 |
Ye EA, Zeng Y, Thomas S, Sun N, Smit-McBride Z, Sieving PA. XLRS Rat with Rs1 Exon-1-Del Shows Failure of Early Postnatal Outer Retina Development. Genes. 13. PMID 36360232 DOI: 10.3390/genes13111995 |
0.55 |
|
| 2022 |
Vijayasarathy C, Zeng Y, Marangoni D, Dong L, Pan ZH, Simpson EM, Fariss RN, Sieving PA. Targeted Expression of Retinoschisin by Retinal Bipolar Cells in XLRS Promotes Resolution of Retinoschisis Cysts Sans RS1 From Photoreceptors. Investigative Ophthalmology & Visual Science. 63: 8. PMID 36227606 DOI: 10.1167/iovs.63.11.8 |
0.554 |
|
| 2022 |
Bender C, Woo EG, Guan B, Ullah E, Feng E, Turriff A, Tumminia SJ, Sieving PA, Cukras CA, Hufnagel RB. Predominant Founder Effect among Recurrent Pathogenic Variants for an X-Linked Disorder. Genes. 13. PMID 35456481 DOI: 10.3390/genes13040675 |
0.503 |
|
| 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, ... Sieving PA, et al. Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia. Human Mutation. PMID 35332618 DOI: 10.1002/humu.24371 |
0.548 |
|
| 2021 |
Miyagishima KJ, Sharma R, Nimmagadda M, Clore-Gronenborn K, Qureshy Z, Ortolan D, Bose D, Farnoodian M, Zhang C, Fausey A, Sergeev YV, Abu-Asab M, Jun B, Do KV, Kautzman Guerin MA, ... Sieving PA, et al. AMPK modulation ameliorates dominant disease phenotypes of CTRP5 variant in retinal degeneration. Communications Biology. 4: 1360. PMID 34887495 DOI: 10.1038/s42003-021-02872-x |
0.538 |
|
| 2021 |
Biswas P, Villanueva AL, Soto-Hermida A, Duncan JL, Matsui H, Borooah S, Kumarov B, Richard G, Khan SY, Branham K, Huang B, Suk J, Bakall B, Goldberg JL, Gabriel L, ... Sieving PA, et al. Deciphering the genetic architecture and ethnographic distribution of IRD in three ethnic populations by whole genome sequence analysis. Plos Genetics. 17: e1009848. PMID 34662339 DOI: 10.1371/journal.pgen.1009848 |
0.541 |
|
| 2021 |
Hahn LC, van Schooneveld MJ, Wesseling NL, Florijn RJ, Ten Brink JB, Lissenberg-Witte BI, Strubbe I, Meester-Smoor MA, Thiadens AA, Diederen RM, van Cauwenbergh C, de Zaeytijd J, Walraedt S, de Baere E, Klaver CCW, ... Sieving PA, et al. X-linked Retinoschisis: Novel Clinical Observations and Genetic Spectrum in 340 Patients. Ophthalmology. PMID 34624300 DOI: 10.1016/j.ophtha.2021.09.021 |
0.472 |
|
| 2021 |
Mishra A, Sieving PA. X-linked Retinoschisis and Gene Therapy. International Ophthalmology Clinics. 61: 173-184. PMID 34584055 DOI: 10.1097/IIO.0000000000000373 |
0.461 |
|
| 2021 |
Zeng Y, Qian H, Campos MM, Li Y, Vijayasarathy C, Sieving PA. Rs1h exon 3-del rat model of X-linked retinoschisis with early onset and rapid phenotype is rescued by RS1 supplementation. Gene Therapy. PMID 34548657 DOI: 10.1038/s41434-021-00290-6 |
0.56 |
|
| 2021 |
Vijaysarathy C, Babu Sardar Pasha SP, Sieving PA. Of men and mice: Human X-linked retinoschisis and fidelity in mouse modeling. Progress in Retinal and Eye Research. 100999. PMID 34390869 DOI: 10.1016/j.preteyeres.2021.100999 |
0.614 |
|
| 2021 |
Keenan TDL, Vanderford EK, de Silva T, Sieving PA, Cukras CA. Massive advancing non-exudative type 1 choroidal neovascularization in CTRP5 Late Onset Retinal Degeneration: longitudinal findings on multimodal imaging and implications for age-related macular degeneration. Retina (Philadelphia, Pa.). PMID 33990119 DOI: 10.1097/IAE.0000000000003205 |
0.552 |
|
| 2021 |
Mishra A, Vijaysarathy C, Cukras CA, Wiley HE, Sen HN, Zeng Y, Wei L, Sieving PA. Immune function in X-linked retinoschisis (XLRS) subjects in an AAV8-RS1 Phase I/IIa gene therapy trial. Molecular Therapy : the Journal of the American Society of Gene Therapy. PMID 33601057 DOI: 10.1016/j.ymthe.2021.02.013 |
0.449 |
|
| 2021 |
Chung SH, Mollhoff IN, Mishra A, Sin TN, Ngo T, Ciulla T, Sieving PA, Thomasy S, Yiu G. Host immune responses after suprachoroidal delivery of AAV8 in nonhuman primate eyes. Human Gene Therapy. PMID 33446041 DOI: 10.1089/hum.2020.281 |
0.525 |
|
| 2020 |
Vijayasarathy C, Zeng Y, Brooks M, Fariss RN, Sieving PA. Genetic rescue of X-linked retinoschisis mouse (Rs1-/y) retina induces quiescence of the retinal microglial inflammatory state following AAV8-RS1 gene transfer and identifies gene networks underlying retinal recovery. Human Gene Therapy. PMID 33019822 DOI: 10.1089/hum.2020.213 |
0.561 |
|
| 2020 |
Song H, Zeng Y, Sardar Pasha SPB, Bush RA, Vijayasarathy C, Qian H, Wei L, Wiley HE, Wu Z, Sieving PA. Trans-Ocular Electric Current In Vivo Enhances AAV-Mediated Retinal Transduction in Large Animal Eye After Intravitreal Vector Administration. Translational Vision Science & Technology. 9: 28. PMID 32844051 DOI: 10.1167/Tvst.9.7.28 |
0.556 |
|
| 2020 |
Wright C, Mazzucco AE, Becker SM, Sieving PA, Tumminia SJ. NEI-Supported Age-Related Macular Degeneration Research: Past, Present, and Future. Translational Vision Science & Technology. 9: 49. PMID 32832254 DOI: 10.1167/tvst.9.7.49 |
0.495 |
|
| 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, ... Sieving PA, 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 |
0.488 |
|
| 2020 |
Zeng Y, Boyd R, Bartoe J, Wiley HE, Marangoni D, Wei LL, Sieving PA. "Para-retinal" Vector Administration into the Deep Vitreous Enhances Retinal Transgene Expression. Molecular Therapy. Methods & Clinical Development. 18: 422-427. PMID 32695844 DOI: 10.1016/j.omtm.2020.06.015 |
0.582 |
|
| 2019 |
Turriff A, Nolen R, D'Amanda C, Biesecker B, Cukras C, Sieving PA. "There are hills and valleys": Experiences of parenting a son with X-linked retinoschisis. American Journal of Ophthalmology. PMID 31765628 DOI: 10.1016/J.Ajo.2019.11.023 |
0.482 |
|
| 2019 |
Bush RA, Tanikawa A, Zeng Y, Sieving PA. Cone ERG Changes During Light Adaptation in Two All-Cone Mutant Mice: Implications for Rod-Cone Pathway Interactions. Investigative Ophthalmology & Visual Science. 60: 3680-3688. PMID 31469895 DOI: 10.1167/Iovs.19-27242 |
0.581 |
|
| 2019 |
Zeng Y, Qian H, Wu Z, Marangoni D, Sieving PA, Bush RA. AAVrh-10 transduces outer retinal cells in rodents and rabbits following intravitreal administration. Gene Therapy. PMID 31308478 DOI: 10.1038/S41434-019-0094-3 |
0.644 |
|
| 2019 |
Wright CB, Becker SM, Low LA, Tagle DA, Sieving PA. Improved Ocular Tissue Models and Eye-On-A-Chip Technologies Will Facilitate Ophthalmic Drug Development. Journal of Ocular Pharmacology and Therapeutics : the Official Journal of the Association For Ocular Pharmacology and Therapeutics. PMID 31166829 DOI: 10.1089/Jop.2018.0139 |
0.536 |
|
| 2019 |
Turriff A, Blain D, Similuk M, Biesecker B, Wiley H, Cukras C, Sieving PA. Motivations and Decision-Making Processes of Men with X-linked Retinoschisis Considering Participation in an Ocular Gene Therapy Trial. American Journal of Ophthalmology. PMID 30885710 DOI: 10.1016/J.Ajo.2019.03.009 |
0.51 |
|
| 2019 |
Song H, Bush RA, Zeng Y, Qian H, Wu Z, Sieving PA. Trans-ocular Electric Current Enhances AAV-Mediated Retinal Gene Transduction after Intravitreal Vector Administration. Molecular Therapy. Methods & Clinical Development. 13: 77-85. PMID 30719486 DOI: 10.1016/J.Omtm.2018.12.006 |
0.627 |
|
| 2019 |
Mott MC, Austin CP, Bianchi DW, Cashion AK, Gordon JA, Heemskerk JE, Hodes RJ, Koob GF, Riley WT, Sieving PA, Shurtleff D, Somerman MJ, Volkow ND, Anderson KC, Owens DF, et al. The NIH Blueprint for Neuroscience Research Seeks Community Input on Future Neuroscience Investments. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 39: 774-775. PMID 30700523 DOI: 10.1523/Jneurosci.2742-18.2018 |
0.473 |
|
| 2019 |
Heymann JB, Vijayasarathy C, Huang RK, Dearborn AD, Sieving PA, Steven AC. Cryo-EM of retinoschisin branched networks suggests an intercellular adhesive scaffold in the retina. The Journal of Cell Biology. PMID 30630865 DOI: 10.1083/Jcb.201806148 |
0.575 |
|
| 2019 |
Heymann JB, Bleck CKE, Fariss RN, Vijayasarathy C, Winkler DC, Huang R, Dearborn AD, Smirnov A, Sieving PA, Steven AC. Hunting for the Adhesion Molecule, Retinoschisin, in Retina using CEMOVIS Microscopy and Microanalysis. 25: 1308-1309. DOI: 10.1017/S143192761900727X |
0.539 |
|
| 2019 |
Heymann B, Bleck CK, Fariss RN, Smirnov A, Winkler DC, Vijayasarathy C, Huang R, Dearborn AD, Sieving PA, Steven AC. Hunting for the Adhesion Molecule, Retinoschisin, in Retina using Cemovis Biophysical Journal. 116: 574a. DOI: 10.1016/j.bpj.2018.11.3089 |
0.484 |
|
| 2018 |
Mazerik JN, Becker S, Sieving PA. 3-D retina organoids: Building platforms for therapies of the future. Cell Medicine. 10: 2155179018773758. PMID 32634188 DOI: 10.1177/2155179018773758 |
0.536 |
|
| 2018 |
Bianchi DW, Cooper JA, Gordon JA, Heemskerk J, Hodes R, Koob GF, Koroshetz WJ, Shurtleff D, Sieving PA, Volkow ND, Churchill JD, Ramos KM. Neuroethics for the National Institutes of Health BRAIN Initiative. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 38: 10583-10585. PMID 30541766 DOI: 10.1523/Jneurosci.2091-18.2018 |
0.469 |
|
| 2018 |
Burkard M, Kohl S, Krätzig T, Tanimoto N, Brennenstuhl C, Bausch AE, Junger K, Reuter P, Sothilingam V, Beck SC, Huber G, Ding XQ, Mayer AK, Baumann B, Weisschuh N, ... Sieving P, et al. Accessory heterozygous mutations in cone photoreceptor CNGA3 exacerbate CNG channel-associated retinopathy. The Journal of Clinical Investigation. PMID 30418171 DOI: 10.1172/Jci96098 |
0.631 |
|
| 2018 |
Agarwal N, Steinmetz MA, Sieving P. The National Eye Institute's Commitment to Career Development of Clinician-Scientists. Jama Ophthalmology. PMID 30267051 DOI: 10.1001/Jamaophthalmol.2018.3897 |
0.518 |
|
| 2018 |
Hardcastle AJ, Sieving PA, Sahel JA, Jacobson SG, Cideciyan AV, Flannery JG, Beltran WA, Aguirre GD. Translational Retinal Research and Therapies. Translational Vision Science & Technology. 7: 8. PMID 30225158 DOI: 10.1167/Tvst.7.5.8 |
0.585 |
|
| 2018 |
Cukras C, Wiley HE, Jeffrey BG, Sen HN, Turriff A, Zeng Y, Vijayasarathy C, Marangoni D, Ziccardi L, Kjellstrom S, Park TK, Hiriyanna S, Wright JF, Colosi P, Wu Z, ... Sieving PA, et al. Retinal AAV8-RS1 Gene Therapy for X-Linked Retinoschisis: Initial Findings from a Phase I/IIa Trial by Intravitreal Delivery. Molecular Therapy : the Journal of the American Society of Gene Therapy. 26: 2282-2294. PMID 30196853 DOI: 10.1016/J.Ymthe.2018.05.025 |
0.622 |
|
| 2018 |
Li L, Jiao X, D'Atri I, Ono F, Nelson R, Chan CC, Nakaya N, Ma Z, Ma Y, Cai X, Zhang L, Lin S, Hameed A, Chioza BA, Hardy H, ... ... Sieving PA, et al. Mutation in the intracellular chloride channel CLCC1 associated with autosomal recessive retinitis pigmentosa. Plos Genetics. 14: e1007504. PMID 30157172 DOI: 10.1371/Journal.Pgen.1007504 |
0.642 |
|
| 2018 |
Cukras CA, Huryn LA, Jeffrey BP, Turriff A, Sieving PA. Analysis of Anatomic and Functional Measures in X-Linked Retinoschisis. Investigative Ophthalmology & Visual Science. 59: 2841-2847. PMID 30025115 DOI: 10.1167/Iovs.17-23297 |
0.551 |
|
| 2018 |
Chekuri A, Guru AA, Biswas P, Branham K, Borooah S, Soto-Hermida A, Hicks M, Khan NW, Matsui H, Alapati A, Raghavendra PB, Roosing S, Sarangapani S, Mathavan S, Telenti A, ... Sieving PA, et al. IFT88 mutations identified in individuals with non-syndromic recessive retinal degeneration result in abnormal ciliogenesis. Human Genetics. PMID 29978320 DOI: 10.1007/S00439-018-1897-9 |
0.619 |
|
| 2018 |
MacDonald IM, Sieving PA. Investigation of the effect of dietary docosahexaenoic acid (DHA) supplementation on macular function in subjects with autosomal recessive Stargardt macular dystrophy. Ophthalmic Genetics. 1-10. PMID 29912604 DOI: 10.1080/13816810.2018.1484931 |
0.537 |
|
| 2018 |
Branham K, Guru AA, Kozak I, Biswas P, Othman M, Kishaba K, Mansoor H, Riazuddin S, Heckenlively JR, Riazuddin SA, Hejtmancik JF, Sieving PA, Ayyagari R. Identification of Novel Deletions as the Underlying Cause of Retinal Degeneration in Two Pedigrees. Advances in Experimental Medicine and Biology. 1074: 229-236. PMID 29721948 DOI: 10.1007/978-3-319-75402-4_28 |
0.609 |
|
| 2018 |
Allahdina AM, Stetson PF, Vitale S, Wong WT, Chew EY, Iii FLF, Sieving PA, Cukras C. Optical Coherence Tomography Minimum Intensity as an Objective Measure for the Detection of Hydroxychloroquine Toxicity. Investigative Ophthalmology & Visual Science. 59: 1953-1963. PMID 29677357 DOI: 10.1167/Iovs.17-22668 |
0.509 |
|
| 2017 |
Sieving PA. Tissue engineering: NIH competition to create 'eye in a dish'. Nature. 546: 352. PMID 28617468 DOI: 10.1038/546352B |
0.506 |
|
| 2017 |
Li L, Chen Y, Jiao X, Jin C, Jiang D, Tanwar M, Ma Z, Huang L, Ma X, Sun W, Chen J, Ma Y, M'hamdi O, Govindarajan G, Cabrera PE, ... ... Sieving PA, et al. Homozygosity Mapping and Genetic Analysis of Autosomal Recessive Retinal Dystrophies in 144 Consanguineous Pakistani Families. Investigative Ophthalmology & Visual Science. 58: 2218-2238. PMID 28418496 DOI: 10.1167/Iovs.17-21424 |
0.608 |
|
| 2017 |
Heymann JB, Vijayasarathy C, Huang R, Dearborn A, Sieving PA, Steven AC. Galactose Induces Formation of Chains of the Retinal Adhesion Protein, Retinoschisin Microscopy and Microanalysis. 23: 1112-1113. DOI: 10.1017/S1431927617006225 |
0.581 |
|
| 2016 |
Branham K, Matsui H, Biswas P, Guru AA, Hicks M, Suk JJ, Li H, Jakubosky D, Long T, Telenti A, Narai N, Heckenlively JR, Frazar KA, Sieving PA, Ayyagari R. Establishing the involvement of the novel gene AGBL5 in retinitis pigmentosa by whole genome sequencing. Physiological Genomics. physiolgenomics.0010. PMID 27764769 DOI: 10.1152/Physiolgenomics.00101.2016 |
0.622 |
|
| 2016 |
Marangoni D, Bush RA, Zeng Y, Wei LL, Ziccardi L, Vijayasarathy C, Bartoe JT, Palyada K, Santos M, Hiriyanna S, Wu Z, Colosi P, Sieving PA. Ocular and systemic safety of a recombinant AAV8 vector for X-linked retinoschisis gene therapy: GLP studies in rabbits and Rs1-KO mice. Molecular Therapy. Methods & Clinical Development. 5: 16011. PMID 27626041 DOI: 10.1038/Mtm.2016.11 |
0.592 |
|
| 2016 |
Zeng Y, Petralia RS, Vijayasarathy C, Wu Z, Hiriyanna S, Song H, Wang YX, Sieving PA, Bush RA. Retinal Structure and Gene Therapy Outcome in Retinoschisin-Deficient Mice Assessed by Spectral-Domain Optical Coherence Tomography. Investigative Ophthalmology & Visual Science. 57: OCT277-OCT287. PMID 27409484 DOI: 10.1167/Iovs.15-18920 |
0.59 |
|
| 2016 |
Cukras C, Flamendorf J, Wong WT, Ayyagari R, Cunningham D, Sieving PA. LONGITUDINAL STRUCTURAL CHANGES IN LATE-ONSET RETINAL DEGENERATION. Retina (Philadelphia, Pa.). PMID 27388725 DOI: 10.1097/Iae.0000000000001113 |
0.597 |
|
| 2016 |
Song H, Vijayasarathy C, Zeng Y, Marangoni D, Bush RA, Wu Z, Sieving PA. NADPH Oxidase Contributes to Photoreceptor Degeneration in Constitutively Active RAC1 Mice. Investigative Ophthalmology & Visual Science. 57: 2864-2875. PMID 27233035 DOI: 10.1167/Iovs.15-18974 |
0.528 |
|
| 2016 |
Tolun G, Vijayasarathy C, Huang R, Zeng Y, Li Y, Steven AC, Sieving PA, Heymann JB. Paired octamer rings of retinoschisin suggest a junctional model for cell-cell adhesion in the retina. Proceedings of the National Academy of Sciences of the United States of America. PMID 27114531 DOI: 10.1073/Pnas.1519048113 |
0.57 |
|
| 2016 |
Bush RA, Zeng Y, Colosi P, Kjellstrom S, Hiriyanna S, Vijayasarathy C, Santos M, Li J, Wu Z, Sieving PA. Preclinical Dose Escalation Study of Intravitreal AAV-RS1 Gene Therapy in a Mouse Model of X-linked Retinoschisis: Dose-Dependent Expression and Improved Retinal Structure and Function. Human Gene Therapy. PMID 27036983 DOI: 10.1089/Hum.2015.142 |
0.621 |
|
| 2016 |
Collins FS, Anderson JM, Austin CP, Battey JF, Birnbaum LS, Briggs JP, Clayton JA, Cuthbert B, Eisinger RW, Fauci AS, Gallin JI, Gibbons GH, Glass RI, Gottesman MM, Gray PA, ... Sieving PA, et al. Basic science: Bedrock of progress. Science (New York, N.Y.). 351: 1405. PMID 27013720 DOI: 10.1126/Science.351.6280.1405-A |
0.479 |
|
| 2016 |
Marangoni D, Bush RA, Zeng Y, Wei LL, Ziccardi L, Vijayasarathy C, Bartoe JT, Palyada K, Santos M, Hiriyanna S, Wu Z, Colosi P, Sieving PA. Ocular and systemic safety of a recombinant AAV8 vector for X-linked retinoschisis gene therapy: GLP studies in rabbits and Rs1-KO mice Molecular Therapy - Methods and Clinical Development. 5. DOI: 10.1038/mtm.2016.11 |
0.482 |
|
| 2016 |
Tolun G, Vijayasarathy C, Huang R, Zeng Y, Li Y, Sieving PA, Heymann JB, Steven AC. Retinoschisin at 4 Å Resolution from cryo-EM: A Junctional Model of Back-to-Back Octamers for Adhesion in the Retina Biophysical Journal. 110: 348a. DOI: 10.1016/J.Bpj.2015.11.1871 |
0.57 |
|
| 2015 |
Marangoni D, Vijayasarathy C, Bush RA, Wei LL, Wen R, Sieving PA. Intravitreal Ciliary Neurotrophic Factor Transiently Improves Cone-Mediated Function in a CNGB3-/- Mouse Model of Achromatopsia. Investigative Ophthalmology & Visual Science. 56: 6810-6822. PMID 26567794 DOI: 10.1167/Iovs.15-16866 |
0.58 |
|
| 2015 |
Bush RA, Wei LL, Sieving PA. Convergence of Human Genetics and Animal Studies: Gene Therapy for X-Linked Retinoschisis. Cold Spring Harbor Perspectives in Medicine. PMID 26101206 DOI: 10.1101/Cshperspect.A017368 |
0.619 |
|
| 2015 |
Ou J, Vijayasarathy C, Ziccardi L, Chen S, Zeng Y, Marangoni D, Pope JG, Bush RA, Wu Z, Li W, Sieving PA. Synaptic pathology and therapeutic repair in adult retinoschisis mouse by AAV-RS1 transfer. The Journal of Clinical Investigation. PMID 26098217 DOI: 10.1172/Jci81380 |
0.578 |
|
| 2015 |
Wu Z, Hiriyanna S, Qian H, Mookherjee S, Campos MM, Gao C, Fariss R, Sieving PA, Li T, Colosi P, Swaroop A. A long-term efficacy study of gene replacement therapy for RPGR-associated retinal degeneration. Human Molecular Genetics. 24: 3956-70. PMID 25877300 DOI: 10.1093/Hmg/Ddv134 |
0.631 |
|
| 2015 |
Veleri S, Lazar CH, Chang B, Sieving PA, Banin E, Swaroop A. Biology and therapy of inherited retinal degenerative disease: insights from mouse models. Disease Models & Mechanisms. 8: 109-29. PMID 25650393 DOI: 10.1242/Dmm.017913 |
0.646 |
|
| 2015 |
Cukras C, Huynh N, Vitale S, Wong WT, Ferris FL, Sieving PA. Subjective and objective screening tests for hydroxychloroquine toxicity. Ophthalmology. 122: 356-66. PMID 25444344 DOI: 10.1016/J.Ophtha.2014.07.056 |
0.516 |
|
| 2015 |
Zein WM, Falsini B, Tsilou ET, Turriff AE, Schultz JM, Friedman TB, Brewer CC, Zalewski CK, King KA, Muskett JA, Rehman AU, Morell RJ, Griffith AJ, Sieving PA. Cone responses in Usher syndrome types 1 and 2 by microvolt electroretinography. Investigative Ophthalmology & Visual Science. 56: 107-14. PMID 25425308 DOI: 10.1167/Iovs.14-15355 |
0.541 |
|
| 2015 |
Sieving PA, Vijayasarathy C, Ou J, Ziccardi L, Chen S, Zeng Y, Marangoni D, Li W, Wu Z, Wei LL, Bush RA. 600. Human Gene Therapy for a Synaptic Disease: X-Linked Retinoschisis (XLRS) Molecular Therapy. 23: S238. DOI: 10.1016/S1525-0016(16)34209-5 |
0.601 |
|
| 2014 |
Jeffrey BG, Cukras CA, Vitale S, Turriff A, Bowles K, Sieving PA. Test-Retest Intervisit Variability of Functional and Structural Parameters in X-Linked Retinoschisis. Translational Vision Science & Technology. 3: 5. PMID 25346871 DOI: 10.1167/Tvst.3.5.5 |
0.494 |
|
| 2014 |
Marangoni D, Wu Z, Wiley HE, Zeiss CJ, Vijayasarathy C, Zeng Y, Hiriyanna S, Bush RA, Wei LL, Colosi P, Sieving PA. Preclinical safety evaluation of a recombinant AAV8 vector for X-linked retinoschisis after intravitreal administration in rabbits. Human Gene Therapy. Clinical Development. 25: 202-11. PMID 25211193 DOI: 10.1089/Humc.2014.067 |
0.607 |
|
| 2014 |
Zein WM, Jeffrey BG, Wiley HE, Turriff AE, Tumminia SJ, Tao W, Bush RA, Marangoni D, Wen R, Wei LL, Sieving PA. CNGB3-achromatopsia clinical trial with CNTF: diminished rod pathway responses with no evidence of improvement in cone function. Investigative Ophthalmology & Visual Science. 55: 6301-8. PMID 25205868 DOI: 10.1167/Iovs.14-14860 |
0.621 |
|
| 2014 |
Ziccardi L, Vijayasarathy C, Bush RA, Sieving PA. Photoreceptor pathology in the X-linked retinoschisis (XLRS) mouse results in delayed rod maturation and impaired light driven transducin translocation. Advances in Experimental Medicine and Biology. 801: 559-66. PMID 24664744 DOI: 10.1007/978-1-4614-3209-8_71 |
0.579 |
|
| 2014 |
Song H, Bush RA, Vijayasarathy C, Fariss RN, Kjellstrom S, Sieving PA. Transgenic expression of constitutively active RAC1 disrupts mouse rod morphogenesis. Investigative Ophthalmology & Visual Science. 55: 2659-68. PMID 24651551 DOI: 10.1167/Iovs.13-13649 |
0.537 |
|
| 2014 |
Li D, Jin C, Jiao X, Li L, Bushra T, Naeem MA, Butt NH, Husnain T, Sieving PA, Riazuddin S, Riazuddin SA, Hejtmancik JF. AIPL1 implicated in the pathogenesis of two cases of autosomal recessive retinal degeneration. Molecular Vision. 20: 1-14. PMID 24426771 |
0.619 |
|
| 2014 |
Huynh N, Jeffrey BG, Turriff A, Sieving PA, Cukras CA. Sorting out co-occurrence of rare monogenic retinopathies: Stargardt disease co-existing with congenital stationary night blindness. Ophthalmic Genetics. 35: 51-6. PMID 24397708 DOI: 10.3109/13816810.2013.865762 |
0.623 |
|
| 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 |
0.587 |
|
| 2013 |
D'Souza L, Cukras C, Antolik C, Craig C, Lee JY, He H, Li S, Smaoui N, Hejtmancik JF, Sieving PA, Wang X. Characterization of novel RS1 exonic deletions in juvenile X-linked retinoschisis. Molecular Vision. 19: 2209-16. PMID 24227916 |
0.548 |
|
| 2013 |
Kabir F, Naz S, Riazuddin SA, Naeem MA, Khan SN, Husnain T, Akram J, Sieving PA, Hejtmancik JF, Riazuddin S. Novel mutations in RPE65 identified in consanguineous Pakistani families with retinal dystrophy. Molecular Vision. 19: 1554-64. PMID 23878505 |
0.588 |
|
| 2013 |
Sergeev YV, Vitale S, Sieving PA, Vincent A, Robson AG, Moore AT, Webster AR, Holder GE. Molecular modeling indicates distinct classes of missense variants with mild and severe XLRS phenotypes. Human Molecular Genetics. 22: 4756-67. PMID 23847049 DOI: 10.1093/Hmg/Ddt329 |
0.628 |
|
| 2013 |
Swaroop A, Sieving PA. The golden era of ocular disease gene discovery: Race to the finish Clinical Genetics. 84: 99-101. PMID 23713688 DOI: 10.1111/Cge.12204 |
0.537 |
|
| 2013 |
Zahid S, Khan N, Branham K, Othman M, Karoukis AJ, Sharma N, Moncrief A, Mahmood MN, Sieving PA, Swaroop A, Heckenlively JR, Jayasundera T. Phenotypic conservation in patients with X-linked retinitis pigmentosa caused by RPGR mutations. Jama Ophthalmology. 131: 1016-25. PMID 23681342 DOI: 10.1001/Jamaophthalmol.2013.120 |
0.627 |
|
| 2012 |
Cukras CA, Wong WT, Caruso R, Cunningham D, Zein W, Sieving P. Fundus autofluorescence patterns in stargardt disease over time-reply. Archives of Ophthalmology (Chicago, Ill. : 1960). 130: 1354-5. PMID 23753838 DOI: 10.1001/Archophthalmol.2012.2008 |
0.492 |
|
| 2012 |
Cukras C, Gaasterland T, Lee P, Gudiseva HV, Chavali VR, Pullakhandam R, Maranhao B, Edsall L, Soares S, Reddy GB, Sieving PA, Ayyagari R. Exome analysis identified a novel mutation in the RBP4 gene in a consanguineous pedigree with retinal dystrophy and developmental abnormalities. Plos One. 7: e50205. PMID 23189188 DOI: 10.1371/Journal.Pone.0050205 |
0.656 |
|
| 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, ... Sieving PA, 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 |
0.634 |
|
| 2012 |
Sieving PA. NEI audacious goals initiative to catalyze innovation. Investigative Ophthalmology & Visual Science. 53: 7149-50. PMID 23047720 DOI: 10.1167/Iovs.12-11069 |
0.466 |
|
| 2012 |
Ziccardi L, Vijayasarathy C, Bush RA, Sieving PA. Loss of retinoschisin (RS1) cell surface protein in maturing mouse rod photoreceptors elevates the luminance threshold for light-driven translocation of transducin but not arrestin. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 13010-21. PMID 22993419 DOI: 10.1523/Jneurosci.1913-12.2012 |
0.572 |
|
| 2012 |
Naeem MA, Chavali VR, Ali S, Iqbal M, Riazuddin S, Khan SN, Husnain T, Sieving PA, Ayyagari R, Riazuddin S, Hejtmancik JF, Riazuddin SA. GNAT1 associated with autosomal recessive congenital stationary night blindness. Investigative Ophthalmology & Visual Science. 53: 1353-61. PMID 22190596 DOI: 10.1167/Iovs.11-8026 |
0.598 |
|
| 2012 |
Vijayasarathy C, Ziccardi L, Sieving PA. Biology of retinoschisin. Advances in Experimental Medicine and Biology. 723: 513-8. PMID 22183371 DOI: 10.1007/978-1-4614-0631-0_64 |
0.637 |
|
| 2012 |
Wen R, Tao W, Li Y, Sieving PA. CNTF and retina. Progress in Retinal and Eye Research. 31: 136-51. PMID 22182585 DOI: 10.1016/J.Preteyeres.2011.11.005 |
0.623 |
|
| 2012 |
Cukras CA, Wong WT, Caruso R, Cunningham D, Zein W, Sieving PA. Centrifugal expansion of fundus autofluorescence patterns in Stargardt disease over time. Archives of Ophthalmology (Chicago, Ill. : 1960). 130: 171-9. PMID 21987580 DOI: 10.1001/Archophthalmol.2011.332 |
0.554 |
|
| 2012 |
Falsini B, Bush RA, Sieving PA. Neuroprotection Retina Fifth Edition. 1: 716-733. DOI: 10.1016/B978-1-4557-0737-9.00037-0 |
0.427 |
|
| 2011 |
Bowles K, Cukras C, Turriff A, Sergeev Y, Vitale S, Bush RA, Sieving PA. X-linked retinoschisis: RS1 mutation severity and age affect the ERG phenotype in a cohort of 68 affected male subjects. Investigative Ophthalmology & Visual Science. 52: 9250-6. PMID 22039241 DOI: 10.1167/Iovs.11-8115 |
0.574 |
|
| 2011 |
Iqbal M, Naeem MA, Riazuddin SA, Ali S, Farooq T, Qazi ZA, Khan SN, Husnain T, Riazuddin S, Sieving PA, Hejtmancik JF, Riazuddin S. Association of pathogenic mutations in TULP1 with retinitis pigmentosa in consanguineous Pakistani families. Archives of Ophthalmology (Chicago, Ill. : 1960). 129: 1351-7. PMID 21987678 DOI: 10.1001/Archophthalmol.2011.267 |
0.63 |
|
| 2011 |
Ali S, Riazuddin SA, Shahzadi A, Nasir IA, Khan SN, Husnain T, Akram J, Sieving PA, Hejtmancik JF, Riazuddin S. Mutations in the β-subunit of rod phosphodiesterase identified in consanguineous Pakistani families with autosomal recessive retinitis pigmentosa. Molecular Vision. 17: 1373-80. PMID 21655355 |
0.582 |
|
| 2011 |
Naz S, Ali S, Riazuddin SA, Farooq T, Butt NH, Zafar AU, Khan SN, Husnain T, Macdonald IM, Sieving PA, Hejtmancik JF, Riazuddin S. Mutations in RLBP1 associated with fundus albipunctatus in consanguineous Pakistani families. The British Journal of Ophthalmology. 95: 1019-24. PMID 21447491 DOI: 10.1136/Bjo.2010.189076 |
0.567 |
|
| 2010 |
Riazuddin SA, Shahzadi A, Zeitz C, Ahmed ZM, Ayyagari R, Chavali VR, Ponferrada VG, Audo I, Michiels C, Lancelot ME, Nasir IA, Zafar AU, Khan SN, Husnain T, Jiao X, ... Sieving PA, et al. A mutation in SLC24A1 implicated in autosomal-recessive congenital stationary night blindness. American Journal of Human Genetics. 87: 523-31. PMID 20850105 DOI: 10.1016/J.Ajhg.2010.08.013 |
0.647 |
|
| 2010 |
Vijayasarathy C, Sui R, Zeng Y, Yang G, Xu F, Caruso RC, Lewis RA, Ziccardi L, Sieving PA. Molecular mechanisms leading to null-protein product from retinoschisin (RS1) signal-sequence mutants in X-linked retinoschisis (XLRS) disease. Human Mutation. 31: 1251-60. PMID 20809529 DOI: 10.1002/Humu.21350 |
0.6 |
|
| 2010 |
Li L, Nakaya N, Chavali VR, Ma Z, Jiao X, Sieving PA, Riazuddin S, Tomarev SI, Ayyagari R, Riazuddin SA, Hejtmancik JF. A mutation in ZNF513, a putative regulator of photoreceptor development, causes autosomal-recessive retinitis pigmentosa. American Journal of Human Genetics. 87: 400-9. PMID 20797688 DOI: 10.1016/J.Ajhg.2010.08.003 |
0.654 |
|
| 2010 |
Kotova S, Vijayasarathy C, Dimitriadis EK, Ikonomou L, Jaffe H, Sieving PA. Retinoschisin (RS1) interacts with negatively charged lipid bilayers in the presence of Ca2+: an atomic force microscopy study. Biochemistry. 49: 7023-32. PMID 20677810 DOI: 10.1021/Bi1007029 |
0.552 |
|
| 2010 |
Raz-Prag D, Grimes WN, Fariss RN, Vijayasarathy C, Campos MM, Bush RA, Diamond JS, Sieving PA. Probing potassium channel function in vivo by intracellular delivery of antibodies in a rat model of retinal neurodegeneration. Proceedings of the National Academy of Sciences of the United States of America. 107: 12710-5. PMID 20616020 DOI: 10.1073/Pnas.0913472107 |
0.591 |
|
| 2010 |
Kjellström S, Vijayasarathy C, Ponjavic V, Sieving PA, Andréasson S. Long-term 12 year follow-up of X-linked congenital retinoschisis. Ophthalmic Genetics. 31: 114-25. PMID 20569020 DOI: 10.3109/13816810.2010.482555 |
0.572 |
|
| 2010 |
Shahzadi A, Riazuddin SA, Ali S, Li D, Khan SN, Husnain T, Akram J, Sieving PA, Hejtmancik JF, Riazuddin S. Nonsense mutation in MERTK causes autosomal recessive retinitis pigmentosa in a consanguineous Pakistani family. The British Journal of Ophthalmology. 94: 1094-9. PMID 20538656 DOI: 10.1136/Bjo.2009.171892 |
0.63 |
|
| 2010 |
Riazuddin SA, Iqbal M, Wang Y, Masuda T, Chen Y, Bowne S, Sullivan LS, Waseem NH, Bhattacharya S, Daiger SP, Zhang K, Khan SN, Riazuddin S, Hejtmancik JF, Sieving PA, et al. A splice-site mutation in a retina-specific exon of BBS8 causes nonsyndromic retinitis pigmentosa. American Journal of Human Genetics. 86: 805-12. PMID 20451172 DOI: 10.1016/J.Ajhg.2010.04.001 |
0.632 |
|
| 2010 |
Naz S, Riazuddin SA, Li L, Shahid M, Kousar S, Sieving PA, Hejtmancik JF, Riazuddin S. A novel locus for autosomal recessive retinitis pigmentosa in a consanguineous Pakistani family maps to chromosome 2p. American Journal of Ophthalmology. 149: 861-6. PMID 20227676 DOI: 10.1016/J.Ajo.2009.12.034 |
0.613 |
|
| 2010 |
Sieving PA. At the frontier of vision research: the National Eye Institute celebrates 40 years. American Journal of Ophthalmology. 149: 179-81. PMID 20103048 DOI: 10.1016/J.Ajo.2009.10.016 |
0.547 |
|
| 2010 |
Sergeev YV, Caruso RC, Meltzer MR, Smaoui N, MacDonald IM, Sieving PA. Molecular modeling of retinoschisin with functional analysis of pathogenic mutations from human X-linked retinoschisis Human Molecular Genetics. 19: 1302-1313. PMID 20061330 DOI: 10.1093/Hmg/Ddq006 |
0.626 |
|
| 2010 |
Wu DM, Khanna H, Atmaca-Sonmez P, Sieving PA, Branham K, Othman M, Swaroop A, Daiger SP, Heckenlively JR. Long-term follow-up of a family with dominant X-linked retinitis pigmentosa. Eye (London, England). 24: 764-74. PMID 19893586 DOI: 10.1038/Eye.2009.270 |
0.618 |
|
| 2009 |
Vijayasarathy C, Ziccardi L, Zeng Y, Smaoui N, Caruso RC, Sieving PA. Null retinoschisin-protein expression from an RS1 c354del1-ins18 mutation causing progressive and severe XLRS in a cross-sectional family study. Investigative Ophthalmology & Visual Science. 50: 5375-83. PMID 19474399 DOI: 10.1167/Iovs.09-3839 |
0.579 |
|
| 2009 |
Haruta M, Bush RA, Kjellstrom S, Vijayasarathy C, Zeng Y, Le YZ, Sieving PA. Depleting Rac1 in mouse rod photoreceptors protects them from photo-oxidative stress without affecting their structure or function Proceedings of the National Academy of Sciences of the United States of America. 106: 9397-9402. PMID 19470639 DOI: 10.1073/Pnas.0808940106 |
0.615 |
|
| 2009 |
Park TK, Wu Z, Kjellstrom S, Zeng Y, Bush RA, Sieving PA, Colosi P. Intravitreal delivery of AAV8 retinoschisin results in cell type-specific gene expression and retinal rescue in the Rs1-KO mouse. Gene Therapy. 16: 916-26. PMID 19458650 DOI: 10.1038/Gt.2009.61 |
0.645 |
|
| 2009 |
Luna G, Kjellstrom S, Verardo MR, Lewis GP, Byun J, Sieving PA, Fisher SK. The effects of transient retinal detachment on cavity size and glial and neural remodeling in a mouse model of X-linked retinoschisis. Investigative Ophthalmology & Visual Science. 50: 3977-84. PMID 19387072 DOI: 10.1167/Iovs.08-2910 |
0.635 |
|
| 2009 |
Raz-Prag D, Zeng Y, Sieving PA, Bush RA. Photoreceptor protection by adeno-associated virus-mediated LEDGF expression in the RCS rat model of retinal degeneration: probing the mechanism. Investigative Ophthalmology & Visual Science. 50: 3897-906. PMID 19324854 DOI: 10.1167/Iovs.08-3153 |
0.586 |
|
| 2008 |
Ahmed ZM, Kjellstrom S, Haywood-Watson RJ, Bush RA, Hampton LL, Battey JF, Riazuddin S, Frolenkov G, Sieving PA, Friedman TB. Double homozygous waltzer and Ames waltzer mice provide no evidence of retinal degeneration. Molecular Vision. 14: 2227-36. PMID 19057657 |
0.601 |
|
| 2008 |
Dizhoor AM, Woodruff ML, Olshevskaya EV, Cilluffo MC, Cornwall MC, Sieving PA, Fain GL. Night blindness and the mechanism of constitutive signaling of mutant G90D rhodopsin. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 28: 11662-72. PMID 18987202 DOI: 10.1523/Jneurosci.4006-08.2008 |
0.588 |
|
| 2008 |
Takada Y, Vijayasarathy C, Zeng Y, Kjellstrom S, Bush RA, Sieving PA. Synaptic pathology in retinoschisis knockout (Rs1-/y) mouse retina and modification by rAAV-Rs1 gene delivery. Investigative Ophthalmology & Visual Science. 49: 3677-86. PMID 18660429 DOI: 10.1167/Iovs.07-1071 |
0.581 |
|
| 2008 |
Brooks BP, Macdonald IM, Tumminia SJ, Smaoui N, Blain D, Nezhuvingal AA, Sieving PA. Genomics in the era of molecular ophthalmology: reflections on the National Ophthalmic Disease Genotyping Network (eyeGENE). Archives of Ophthalmology (Chicago, Ill. : 1960). 126: 424-5. PMID 18332328 DOI: 10.1001/Archopht.126.3.424 |
0.522 |
|
| 2008 |
Vijayasarathy C, Takada Y, Zeng Y, Bush RA, Sieving PA. Organization and molecular interactions of retinoschisin in photoreceptors. Advances in Experimental Medicine and Biology. 613: 291-7. PMID 18188957 DOI: 10.1007/978-0-387-74904-4_34 |
0.541 |
|
| 2008 |
Machida S, Raz-Prag D, Fariss RN, Sieving PA, Bush RA. Photopic ERG negative response from amacrine cell signaling in RCS rat retinal degeneration. Investigative Ophthalmology & Visual Science. 49: 442-52. PMID 18172124 DOI: 10.1167/Iovs.07-0291 |
0.563 |
|
| 2007 |
MacDonald IM, Brooks BP, Sieving PA. Eyeing a new network. Science (New York, N.Y.). 318: 1068. PMID 18006726 DOI: 10.1126/Science.318.5853.1068 |
0.524 |
|
| 2007 |
Woodruff ML, Olshevskaya EV, Savchenko AB, Peshenko IV, Barrett R, Bush RA, Sieving PA, Fain GL, Dizhoor AM. Constitutive excitation by Gly90Asp rhodopsin rescues rods from degeneration caused by elevated production of cGMP in the dark. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 8805-15. PMID 17699662 DOI: 10.1523/Jneurosci.2751-07.2007 |
0.62 |
|
| 2007 |
Khan NW, Wissinger B, Kohl S, Sieving PA. CNGB3 achromatopsia with progressive loss of residual cone function and impaired rod-mediated function. Investigative Ophthalmology & Visual Science. 48: 3864-71. PMID 17652762 DOI: 10.1167/Iovs.06-1521 |
0.586 |
|
| 2007 |
Kjellstrom S, Bush RA, Zeng Y, Takada Y, Sieving PA. Retinoschisin gene therapy and natural history in the Rs1h-KO mouse: long-term rescue from retinal degeneration. Investigative Ophthalmology & Visual Science. 48: 3837-45. PMID 17652759 DOI: 10.1167/Iovs.07-0203 |
0.599 |
|
| 2007 |
Zhang Q, Zulfiqar F, Xiao X, Riazuddin SA, Ahmad Z, Caruso R, MacDonald I, Sieving P, Hejtmancik JF. Severe retinitis pigmentosa mapped to 4p15 and associated with a novel mutation in the PROM1 gene Human Genetics. 122: 293-299. PMID 17605048 DOI: 10.1007/S00439-007-0395-2 |
0.649 |
|
| 2007 |
MacDonald IM, Sauvé Y, Sieving PA. Preventing blindness in retinal disease: ciliary neurotrophic factor intraocular implants. Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie. 42: 399-402. PMID 17508034 DOI: 10.3129/Can.J.Ophthalmol.I07-039 |
0.583 |
|
| 2007 |
Vijayasarathy C, Takada Y, Zeng Y, Bush RA, Sieving PA. Retinoschisin is a peripheral membrane protein with affinity for anionic phospholipids and affected by divalent cations. Investigative Ophthalmology & Visual Science. 48: 991-1000. PMID 17325137 DOI: 10.1167/Iovs.06-0915 |
0.585 |
|
| 2007 |
Sieving PA, Collins FS. Genetic ophthalmology and the era of clinical care. Jama. 297: 733-6. PMID 17315303 DOI: 10.1001/Jama.297.7.733 |
0.485 |
|
| 2007 |
Downs K, Zacks DN, Caruso R, Karoukis AJ, Branham K, Yashar BM, Haimann MH, Trzupek K, Meltzer M, Blain D, Richards JE, Weleber RG, Heckenlively JR, Sieving PA, Ayyagari R. Molecular testing for hereditary retinal disease as part of clinical care. Archives of Ophthalmology (Chicago, Ill. : 1960). 125: 252-8. PMID 17296903 DOI: 10.1001/Archopht.125.2.252 |
0.593 |
|
| 2006 |
Wen R, Song Y, Kjellstrom S, Tanikawa A, Liu Y, Li Y, Zhao L, Bush RA, Laties AM, Sieving PA. Regulation of rod phototransduction machinery by ciliary neurotrophic factor. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 13523-30. PMID 17192435 DOI: 10.1523/Jneurosci.4021-06.2006 |
0.6 |
|
| 2006 |
Riazuddin SA, Zulfiqar F, Zhang Q, Yao W, Li S, Jiao X, Shahzadi A, Amer M, Iqbal M, Hussnain T, Sieving PA, Riazuddin S, Hejtmancik JF. Mutations in the gene encoding the alpha-subunit of rod phosphodiesterase in consanguineous Pakistani families. Molecular Vision. 12: 1283-91. PMID 17110911 |
0.562 |
|
| 2006 |
Takada Y, Fariss RN, Muller M, Bush RA, Rushing EJ, Sieving PA. Retinoschisin expression and localization in rodent and human pineal and consequences of mouse RS1 gene knockout. Molecular Vision. 12: 1108-16. PMID 17093404 |
0.58 |
|
| 2006 |
Aslanukov A, Bhowmick R, Guruju M, Oswald J, Raz D, Bush RA, Sieving PA, Lu X, Bock CB, Ferreira PA. RanBP2 modulates Cox11 and hexokinase I activities and haploinsufficiency of RanBP2 causes deficits in glucose metabolism. Plos Genetics. 2: e177. PMID 17069463 DOI: 10.1371/Journal.Pgen.0020177 |
0.516 |
|
| 2006 |
Vasireddy V, Jablonski MM, Mandal MN, Raz-Prag D, Wang XF, Nizol L, Iannaccone A, Musch DC, Bush RA, Salem N, Sieving PA, Ayyagari R. Elovl4 5-bp-deletion knock-in mice develop progressive photoreceptor degeneration. Investigative Ophthalmology & Visual Science. 47: 4558-68. PMID 17003453 DOI: 10.1167/Iovs.06-0353 |
0.573 |
|
| 2006 |
Prenner JL, Capone A, Ciaccia S, Takada Y, Sieving PA, Trese MT. Congenital X-linked retinoschisis classification system. Retina (Philadelphia, Pa.). 26: S61-4. PMID 16946682 DOI: 10.1097/01.Iae.0000244290.09499.C1 |
0.527 |
|
| 2006 |
Vijayasarathy C, Gawinowicz MA, Zeng Y, Takada Y, Bush RA, Sieving PA. Identification and characterization of two mature isoforms of retinoschisin in murine retina. Biochemical and Biophysical Research Communications. 349: 99-105. PMID 16930543 DOI: 10.1016/J.Bbrc.2006.07.202 |
0.55 |
|
| 2006 |
Raz-Prag D, Ayyagari R, Fariss RN, Mandal MN, Vasireddy V, Majchrzak S, Webber AL, Bush RA, Salem N, Petrukhin K, Sieving PA. Haploinsufficiency is not the key mechanism of pathogenesis in a heterozygous Elovl4 knockout mouse model of STGD3 disease. Investigative Ophthalmology & Visual Science. 47: 3603-11. PMID 16877435 DOI: 10.1167/Iovs.05-1527 |
0.612 |
|
| 2006 |
Haywood-Watson RJ, Ahmed ZM, Kjellstrom S, Bush RA, Takada Y, Hampton LL, Battey JF, Sieving PA, Friedman TB. Ames Waltzer deaf mice have reduced electroretinogram amplitudes and complex alternative splicing of Pcdh15 transcripts. Investigative Ophthalmology & Visual Science. 47: 3074-84. PMID 16799054 DOI: 10.1167/Iovs.06-0108 |
0.587 |
|
| 2006 |
Alexander DF, Alving BM, Battey JF, Berg JM, Collins FS, Fauci AS, Gallin JI, Grady PA, Hodes RJ, Hrynkow SH, Insel TR, Jones JF, Katz SI, Landis SC, Li TK, ... Sieving PA, et al. Response to: "Rescuing the NIH before it is too late". The Journal of Clinical Investigation. 116: 1462-3. PMID 16648877 DOI: 10.1172/Jci28894 |
0.487 |
|
| 2006 |
Sieving PA, Caruso RC, Tao W, Coleman HR, Thompson DJ, Fullmer KR, Bush RA. Ciliary neurotrophic factor (CNTF) for human retinal degeneration: phase I trial of CNTF delivered by encapsulated cell intraocular implants. Proceedings of the National Academy of Sciences of the United States of America. 103: 3896-901. PMID 16505355 DOI: 10.1073/Pnas.0600236103 |
0.607 |
|
| 2006 |
Thompson DA, Janecke AR, Lange J, Feathers KL, Hübner CA, McHenry CL, Stockton DW, Rammesmayer G, Lupski JR, Antinolo G, Ayuso C, Baiget M, Gouras P, Heckenlively JR, Hollander Ad, ... Sieving PA, et al. Erratum: Retinal degeneration associated with RDH12 mutations results from decreased 11-cis retinal synthesis due to disruption of the visual cycle (Human Molecular Genetics (2005) vol. 14 (3865-3875) 10.1093/hmg/ ddi411) Human Molecular Genetics. 15. DOI: 10.1093/Hmg/Ddl079 |
0.638 |
|
| 2005 |
Sieving PA. Fostering partnerships: The National Institutes of Health (NIH) Mission. Retina (Philadelphia, Pa.). 25: S84-S85. PMID 16374355 DOI: 10.1097/00006982-200512001-00041 |
0.463 |
|
| 2005 |
Sieving PA. The national eye institute: translational clinical research initiatives on inherited and orphan retinal diseases: personal observations. Retina (Philadelphia, Pa.). 25: S8-S9. PMID 16374351 DOI: 10.1097/00006982-200512001-00003 |
0.591 |
|
| 2005 |
Zhang Q, Zulfiqar F, Riazuddin SA, Xiao X, Yasmeen A, Rogan PK, Caruso R, Sieving PA, Riazuddin S, Hejtmancik JF. A variant form of Oguchi disease mapped to 13q34 associated with partial deletion of GRK1 gene. Molecular Vision. 11: 977-85. PMID 16319817 |
0.508 |
|
| 2005 |
Thompson DA, Janecke AR, Lange J, Feathers KL, Hübner CA, McHenry CL, Stockton DW, Rammesmayer G, Lupski JR, Antinolo G, Ayuso C, Baiget M, Gouras P, Heckenlively JR, den Hollander A, ... Sieving PA, et al. Retinal degeneration associated with RDH12 mutations results from decreased 11-cis retinal synthesis due to disruption of the visual cycle. Human Molecular Genetics. 14: 3865-75. PMID 16269441 DOI: 10.1093/Hmg/Ddi411 |
0.658 |
|
| 2005 |
Zhang Q, Zulfiqar F, Xiao X, Riazuddin SA, Ayyagari R, Sabar F, Caruso R, Sieving PA, Riazuddin S, Hejtmancik JF. Severe autosomal recessive retinitis pigmentosa maps to chromosome 1p13.3-p21.2 between D1S2896 and D1S457 but outside ABCA4. Human Genetics. 118: 356-65. PMID 16189710 DOI: 10.1007/S00439-005-0054-4 |
0.592 |
|
| 2005 |
Vasireddy V, Vijayasarathy C, Huang J, Wang XF, Jablonski MM, Petty HR, Sieving PA, Ayyagari R. Stargardt-like macular dystrophy protein ELOVL4 exerts a dominant negative effect by recruiting wild-type protein into aggresomes. Molecular Vision. 11: 665-76. PMID 16163264 |
0.515 |
|
| 2005 |
Ayyagari R, Mandal MN, Karoukis AJ, Chen L, McLaren NC, Lichter M, Wong DT, Hitchcock PF, Caruso RC, Moroi SE, Maumenee IH, Sieving PA. Late-onset macular degeneration and long anterior lens zonules result from a CTRP5 gene mutation. Investigative Ophthalmology & Visual Science. 46: 3363-71. PMID 16123441 DOI: 10.1167/Iovs.05-0159 |
0.628 |
|
| 2005 |
Mandal MN, Heckenlively JR, Burch T, Chen L, Vasireddy V, Koenekoop RK, Sieving PA, Ayyagari R. Sequencing arrays for screening multiple genes associated with early-onset human retinal degenerations on a high-throughput platform. Investigative Ophthalmology & Visual Science. 46: 3355-62. PMID 16123440 DOI: 10.1167/Iovs.05-0007 |
0.601 |
|
| 2005 |
Brzezinski JA, Brown NL, Tanikawa A, Bush RA, Sieving PA, Vitaterna MH, Takahashi JS, Glaser T. Loss of circadian photoentrainment and abnormal retinal electrophysiology in Math5 mutant mice. Investigative Ophthalmology & Visual Science. 46: 2540-51. PMID 15980246 DOI: 10.1167/Iovs.04-1123 |
0.597 |
|
| 2005 |
Riazuddin SA, Zulfiqar F, Zhang Q, Sergeev YV, Qazi ZA, Husnain T, Caruso R, Riazuddin S, Sieving PA, Hejtmancik JF. Autosomal recessive retinitis pigmentosa is associated with mutations in RP1 in three consanguineous Pakistani families. Investigative Ophthalmology & Visual Science. 46: 2264-70. PMID 15980210 DOI: 10.1167/Iovs.04-1280 |
0.64 |
|
| 2005 |
Kohl S, Varsanyi B, Antunes GA, Baumann B, Hoyng CB, Jägle H, Rosenberg T, Kellner U, Lorenz B, Salati R, Jurklies B, Farkas A, Andreasson S, Weleber RG, Jacobson SG, ... Sieving PA, et al. CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia. European Journal of Human Genetics : Ejhg. 13: 302-8. PMID 15657609 DOI: 10.1038/Sj.Ejhg.5201269 |
0.574 |
|
| 2005 |
Khan NW, Kondo M, Hiriyanna KT, Jamison JA, Bush RA, Sieving PA. Primate Retinal Signaling Pathways: Suppressing ON-Pathway Activity in Monkey With Glutamate Analogues Mimics Human CSNB1-NYX Genetic Night Blindness. Journal of Neurophysiology. 93: 481-92. PMID 15331616 DOI: 10.1152/Jn.00365.2004 |
0.786 |
|
| 2005 |
Aslanukov A, Bhowmick R, Guruju M, Oswald J, Raz D, Bush RA, Sieving P, Lu X, Bock CB, Ferreira PA. RanBP2 Modulates Cox11 and Hexokinase I Activities and Haploinsufficiency of RanBP2 Causes Deficits in Hexokinase I and Glucose Metabolism Plos Genetics. DOI: 10.1371/Journal.Pgen.0020177.Eor |
0.466 |
|
| 2004 |
Takada Y, Fariss RN, Tanikawa A, Zeng Y, Carper D, Bush R, Sieving PA. A retinal neuronal developmental wave of retinoschisin expression begins in ganglion cells during layer formation. Investigative Ophthalmology & Visual Science. 45: 3302-12. PMID 15326155 DOI: 10.1167/Iovs.04-0156 |
0.645 |
|
| 2004 |
Zeng Y, Takada Y, Kjellstrom S, Hiriyanna K, Tanikawa A, Wawrousek E, Smaoui N, Caruso R, Bush RA, Sieving PA. RS-1 Gene Delivery to an Adult Rs1h Knockout Mouse Model Restores ERG b-Wave with Reversal of the Electronegative Waveform of X-Linked Retinoschisis. Investigative Ophthalmology & Visual Science. 45: 3279-85. PMID 15326152 DOI: 10.1167/Iovs.04-0576 |
0.606 |
|
| 2004 |
Bush RA, Lei B, Tao W, Raz D, Chan CC, Cox TA, Santos-Muffley M, Sieving PA. Encapsulated cell-based intraocular delivery of ciliary neurotrophic factor in normal rabbit: dose-dependent effects on ERG and retinal histology. Investigative Ophthalmology & Visual Science. 45: 2420-30. PMID 15223826 DOI: 10.1167/Iovs.03-1342 |
0.554 |
|
| 2004 |
Sieving PA. Healthy Vision Month--May 2004: focus is on diabetic retinopathy. Optometry (St. Louis, Mo.). 75: 271-3. PMID 15141816 |
0.426 |
|
| 2004 |
Insel TR, Volkow ND, Landis SC, Li TK, Battey JF, Sieving P. Limits to growth: why neuroscience needs large-scale science. Nature Neuroscience. 7: 426-7. PMID 15114352 DOI: 10.1038/Nn0504-426 |
0.454 |
|
| 2004 |
McHenry CL, Liu Y, Feng W, Nair AR, Feathers KL, Ding X, Gal A, Vollrath D, Sieving PA, Thompson DA. MERTK arginine-844-cysteine in a patient with severe rod-cone dystrophy: loss of mutant protein function in transfected cells. Investigative Ophthalmology & Visual Science. 45: 1456-63. PMID 15111602 DOI: 10.1167/Iovs.03-0909 |
0.653 |
|
| 2004 |
Mandal MN, Ambasudhan R, Wong PW, Gage PJ, Sieving PA, Ayyagari R. Characterization of mouse orthologue of ELOVL4: genomic organization and spatial and temporal expression. Genomics. 83: 626-35. PMID 15028285 DOI: 10.1016/J.Ygeno.2003.09.020 |
0.571 |
|
| 2004 |
Ambasudhan R, Wang X, Jablonski MM, Thompson DA, Lagali PS, Wong PW, Sieving PA, Ayyagari R. Atrophic macular degeneration mutations in ELOVL4 result in the intracellular misrouting of the protein. Genomics. 83: 615-25. PMID 15028284 DOI: 10.1016/J.Ygeno.2003.10.004 |
0.566 |
|
| 2004 |
Abecasis GR, Yashar BM, Zhao Y, Ghiasvand NM, Zareparsi S, Branham KE, Reddick AC, Trager EH, Yoshida S, Bahling J, Filippova E, Elner S, Johnson MW, Vine AK, Sieving PA, et al. Age-related macular degeneration: a high-resolution genome scan for susceptibility loci in a population enriched for late-stage disease. American Journal of Human Genetics. 74: 482-94. PMID 14968411 DOI: 10.1086/382786 |
0.547 |
|
| 2004 |
Abecasis G, Yashar B, Zhao Y, Ghiavand N, Zareparsi S, Branham E, Reddick A, Trager E, Yoshida S, Bahling J, Filippova E, Elner S, Johnson M, Vine A, Sieving P, et al. Age-related macular degeneration: a high-resolution genome scan for susceptibility loci in a population enriched for late stage disease American Journal of Ophthalmology. 138: 515. DOI: 10.1016/j.ajo.2004.07.009 |
0.464 |
|
| 2003 |
Moroi SE, Lark KK, Sieving PA, Nouri-Mahdavi K, Schlötzer-Schrehardt U, Katz GJ, Ritch R. Long anterior zonules and pigment dispersion. American Journal of Ophthalmology. 136: 1176-8. PMID 14644241 DOI: 10.1016/S0002-9394(03)00657-3 |
0.504 |
|
| 2003 |
Ahmed ZM, Riazuddin S, Ahmad J, Bernstein SL, Guo Y, Sabar MF, Sieving P, Riazuddin S, Griffith AJ, Friedman TB, Belyantseva IA, Wilcox ER. PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23. Human Molecular Genetics. 12: 3215-23. PMID 14570705 DOI: 10.1093/Hmg/Ddg358 |
0.641 |
|
| 2003 |
Schimmenti LA, Manligas GS, Sieving PA. Optic nerve dysplasia and renal insufficiency in a family with a novel PAX2 mutation, Arg115X: further ophthalmologic delineation of the renal-coloboma syndrome. Ophthalmic Genetics. 24: 191-202. PMID 14566649 DOI: 10.1076/Opge.24.4.191.17229 |
0.536 |
|
| 2003 |
Lee TK, McTaggart KE, Sieving PA, Heckenlively JR, Levin AV, Greenberg J, Weleber RG, Tong PY, Anhalt EF, Powell BR, MacDonald IM. Clinical diagnoses that overlap with choroideremia. Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie. 38: 364-72; quiz 372. PMID 12956277 DOI: 10.1016/S0008-4182(03)80047-9 |
0.481 |
|
| 2003 |
Radu RA, Mata NL, Nusinowitz S, Liu X, Sieving PA, Travis GH. Treatment with isotretinoin inhibits lipofuscin accumulation in a mouse model of recessive Stargardt's macular degeneration. Proceedings of the National Academy of Sciences of the United States of America. 100: 4742-7. PMID 12671074 DOI: 10.1073/Pnas.0737855100 |
0.601 |
|
| 2003 |
Rivolta C, Ayyagari R, Sieving PA, Berson EL, Dryja TP. Evaluation of the ELOVL4 gene in patients with autosomal recessive retinitis pigmentosa and Leber congenital amaurosis. Molecular Vision. 9: 49-51. PMID 12592226 |
0.611 |
|
| 2003 |
Acar C, Mears AJ, Yashar BM, Maheshwary AS, Andreasson S, Baldi A, Sieving PA, Iannaccone A, Musarella MA, Jacobson SG, Swaroop A. Mutation screening of patients with Leber Congenital Amaurosis or the enhanced S-Cone Syndrome reveals a lack of sequence variations in the NRL gene. Molecular Vision. 9: 14-7. PMID 12552256 |
0.598 |
|
| 2002 |
Ayyagari R, Demirci FY, Liu J, Bingham EL, Stringham H, Kakuk LE, Boehnke M, Gorin MB, Richards JE, Sieving PA. X-linked recessive atrophic macular degeneration from RPGR mutation. Genomics. 80: 166-71. PMID 12160730 DOI: 10.1006/Geno.2002.6815 |
0.667 |
|
| 2002 |
Kondo M, Sieving PA. Post-photoreceptoral activity dominates primate photopic 32-Hz ERG for sine-, square-, and pulsed stimuli. Investigative Ophthalmology & Visual Science. 43: 2500-7. PMID 12091456 |
0.466 |
|
| 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, ... ... Sieving PA, 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 |
0.625 |
|
| 2002 |
Traverso V, Bush RA, Sieving PA, Deretic D. Retinal cAMP levels during the progression of retinal degeneration in rhodopsin P23H and S334ter transgenic rats. Investigative Ophthalmology & Visual Science. 43: 1655-61. PMID 11980887 |
0.578 |
|
| 2002 |
Felius J, Thompson DA, Khan NW, Bingham EL, Jamison JA, Kemp JA, Sieving PA. Clinical course and visual function in a family with mutations in the RPE65 gene. Archives of Ophthalmology (Chicago, Ill. : 1960). 120: 55-61. PMID 11786058 DOI: 10.1001/Archopht.120.1.55 |
0.802 |
|
| 2001 |
Ayyagari R, Zhang K, Hutchinson A, Yu Z, Swaroop A, Kakuk LE, Seddon JM, Bernstein PS, Lewis RA, Tammur J, Yang Z, Li Y, Zhang H, Yashar BM, Liu J, ... Sieving PA, et al. Evaluation of the ELOVL4 gene in patients with age-related macular degeneration. Ophthalmic Genetics. 22: 233-9. PMID 11803489 DOI: 10.1076/Opge.22.4.233.2219 |
0.533 |
|
| 2001 |
Khan NW, Jamison JA, Kemp JA, Sieving PA. Analysis of photoreceptor function and inner retinal activity in juvenile X-linked retinoschisis. Vision Research. 41: 3931-42. PMID 11738458 DOI: 10.1016/S0042-6989(01)00188-2 |
0.783 |
|
| 2001 |
Mears AJ, Kondo M, Swain PK, Takada Y, Bush RA, Saunders TL, Sieving PA, Swaroop A. Nrl is required for rod photoreceptor development Nature Genetics. 29: 447-452. PMID 11694879 DOI: 10.1038/Ng774 |
0.653 |
|
| 2001 |
Jamison JA, Bush RA, Lei B, Sieving PA. Characterization of the rod photoresponse isolated from the dark-adapted primate ERG. Visual Neuroscience. 18: 445-55. PMID 11497421 DOI: 10.1017/S0952523801183112 |
0.772 |
|
| 2001 |
Humphries MM, Kiang S, McNally N, Donovan MA, Sieving PA, Bush RA, Machida S, Cotter T, Hobson A, Farrar J, Humphries P, Kenna P. Comparative structural and functional analysis of photoreceptor neurons of Rho-/- mice reveal increased survival on C57BL/6J in comparison to 129Sv genetic background. Visual Neuroscience. 18: 437-43. PMID 11497420 DOI: 10.1017/S0952523801183100 |
0.588 |
|
| 2001 |
Sieving PA, Fowler ML, Bush RA, Machida S, Calvert PD, Green DG, Makino CL, McHenry CL. Constitutive "light" adaptation in rods from G90D rhodopsin: a mechanism for human congenital nightblindness without rod cell loss. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 21: 5449-60. PMID 11466416 DOI: 10.1523/Jneurosci.21-15-05449.2001 |
0.616 |
|
| 2001 |
Sieving PA. Fifteen years of work: The COMS outcomes for medium-sized choroidal melanoma Archives of Ophthalmology. 119: 1067-1068. PMID 11448330 DOI: 10.1001/Archopht.119.7.1067 |
0.469 |
|
| 2001 |
Thompson DA, Li Y, McHenry CL, Carlson TJ, Ding X, Sieving PA, Apfelstedt-Sylla E, Gal A. Mutations in the gene encoding lecithin retinol acyltransferase are associated with early-onset severe retinal dystrophy. Nature Genetics. 28: 123-4. PMID 11381255 DOI: 10.1038/88828 |
0.653 |
|
| 2001 |
Sieving PA, Chaudhry P, Kondo M, Provenzano M, Wu D, Carlson TJ, Bush RA, Thompson DA. Inhibition of the visual cycle in vivo by 13-cis retinoic acid protects from light damage and provides a mechanism for night blindness in isotretinoin therapy. Proceedings of the National Academy of Sciences of the United States of America. 98: 1835-40. PMID 11172037 DOI: 10.1073/Pnas.98.4.1835 |
0.588 |
|
| 2001 |
Zhang K, Kniazeva M, Han M, Li W, Yu Z, Yang Z, Li Y, Metzker ML, Allikmets R, Zack DJ, Kakuk LE, Lagali PS, Wong PW, MacDonald IM, Sieving PA, et al. A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy. Nature Genetics. 27: 89-93. PMID 11138005 DOI: 10.1038/83817 |
0.631 |
|
| 2000 |
Thompson DA, Gyürüs P, Fleischer LL, Bingham EL, McHenry CL, Apfelstedt-Sylla E, Zrenner E, Lorenz B, Richards JE, Jacobson SG, Sieving PA, Gal A. Genetics and phenotypes of RPE65 mutations in inherited retinal degeneration. Investigative Ophthalmology & Visual Science. 41: 4293-9. PMID 11095629 |
0.311 |
|
| 2000 |
Ayyagari R, Kakuk LE, Bingham EL, Szczesny JJ, Kemp J, Toda Y, Felius J, Sieving PA. Spectrum of color gene deletions and phenotype in patients with blue cone monochromacy. Human Genetics. 107: 75-82. PMID 10982039 DOI: 10.1007/S004390000338 |
0.603 |
|
| 2000 |
Mears AJ, Hiriyanna S, Vervoort R, Yashar B, Gieser L, Fahrner S, Daiger SP, Heckenlively JR, Sieving PA, Wright AF, Swaroop A. Remapping of the RP15 locus for X-linked cone-rod degeneration to Xp11.4-p21.1, and identification of a de novo insertion in the RPGR exon ORF15. American Journal of Human Genetics. 67: 1000-3. PMID 10970770 DOI: 10.1086/303091 |
0.611 |
|
| 2000 |
Machida S, Kondo M, Jamison JA, Khan NW, Kononen LT, Sugawara T, Bush RA, Sieving PA. P23H rhodopsin transgenic rat: correlation of retinal function with histopathology. Investigative Ophthalmology & Visual Science. 41: 3200-9. PMID 10967084 |
0.775 |
|
| 2000 |
Kohl S, Baumann B, Broghammer M, Jägle H, Sieving P, Kellner U, Spegal R, Anastasi M, Zrenner E, Sharpe LT, Wissinger B. Mutations in the CNGB3 gene encoding the beta-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21. Human Molecular Genetics. 9: 2107-16. PMID 10958649 DOI: 10.1093/Hmg/9.14.2107 |
0.585 |
|
| 2000 |
Sieving PA, Yashar BM, Ayyagari R. Juvenile retinoschisis: a model for diagnostic testing of x-linked ophthalmic disease. Trans Am ophthalmol soc 1999;97:451-464 American Journal of Ophthalmology. 129: 833. PMID 10927013 DOI: 10.1016/S0002-9394(00)00512-2 |
0.513 |
|
| 2000 |
Eksandh LC, Ponjavic V, Ayyagari R, Bingham EL, Hiriyanna KT, Andréasson S, Ehinger B, Sieving PA. Phenotypic expression of juvenile X-linked retinoschisis in Swedish families with different mutations in the XLRS1 gene. Archives of Ophthalmology (Chicago, Ill. : 1960). 118: 1098-104. PMID 10922205 DOI: 10.1001/Archopht.118.8.1098 |
0.581 |
|
| 2000 |
Sugawara T, Sieving PA, Bush RA. Quantitative relationship of the scotopic and photopic ERG to photoreceptor cell loss in light damaged rats Experimental Eye Research. 70: 693-705. PMID 10870528 DOI: 10.1006/Exer.2000.0842 |
0.571 |
|
| 2000 |
Hrach CJ, Johnson MW, Hassan AS, Lei B, Sieving PA, Elner VM. Retinal toxicity of commercial intravitreal tissue plasminogen activator solution in cat eyes Archives of Ophthalmology. 118: 659-663. PMID 10815158 DOI: 10.1001/Archopht.118.5.659 |
0.58 |
|
| 2000 |
Ayyagari R, Griesinger IB, Bingham E, Lark KK, Moroi SE, Sieving PA. Autosomal dominant hemorrhagic macular dystrophy not associated with the TIMP3 gene. Archives of Ophthalmology (Chicago, Ill. : 1960). 118: 85-92. PMID 10636420 DOI: 10.1001/Archopht.118.1.85 |
0.576 |
|
| 2000 |
Lei B, Bush RA, Milam AH, Sieving PA. Human melanoma-associated retinopathy (MAR) antibodies alter the retinal ON-response of the monkey ERG in vivo Investigative Ophthalmology and Visual Science. 41: 262-266. PMID 10634629 |
0.315 |
|
| 1999 |
Hiriyanna KT, Bingham EL, Yashar BM, Ayyagari R, Fishman G, Small KW, Weinberg DV, Weleber RG, Lewis RA, Andreasson S, Richards JE, Sieving PA. Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence change. Human Mutation. 14: 423-7. PMID 10533068 DOI: 10.1002/(Sici)1098-1004(199911)14:5<423::Aid-Humu8>3.0.Co;2-D |
0.572 |
|
| 1999 |
Sieving PA, Bingham EL, Kemp J, Richards J, Hiriyanna K. Juvenile X-linked retinoschisis from XLRS1 Arg213Trp mutation with preservation of the electroretinogram scotopic b-wave American Journal of Ophthalmology. 128: 179-184. PMID 10458173 DOI: 10.1016/S0002-9394(99)00144-0 |
0.609 |
|
| 1999 |
Mendoza-Londono R, Hiriyanna KT, Bingham EL, Rodriguez F, Shastry BS, Rodriguez A, Sieving PA, Tamayo ML. A Colombian family with X-linked juvenile retinoschisis with three affected females finding of a frameshift mutation. Ophthalmic Genetics. 20: 37-43. PMID 10415464 DOI: 10.1076/Opge.20.1.37.2299 |
0.59 |
|
| 1999 |
McNally N, Kenna P, Humphries MM, Hobson AH, Khan NW, Bush RA, Sieving PA, Humphries P, Farrar GJ. Structural and functional rescue of murine rod photoreceptors by human rhodopsin transgene Human Molecular Genetics. 8: 1309-1312. PMID 10369877 DOI: 10.1093/Hmg/8.7.1309 |
0.599 |
|
| 1999 |
Toda K, Bush RA, Humphries P, Sieving PA. The electroretinogram of the rhodopsin knockout mouse Visual Neuroscience. 16: 391-398. PMID 10367972 DOI: 10.1017/S0952523899162187 |
0.576 |
|
| 1999 |
Caldwell GM, Kakuk LE, Griesinger IB, Simpson SA, Nowak NJ, Small KW, Maumenee IH, Rosenfeld PJ, Sieving PA, Shows TB, Ayyagari R. Bestrophin gene mutations in patients with Best vitelliform macular dystrophy. Genomics. 58: 98-101. PMID 10331951 DOI: 10.1006/Geno.1999.5808 |
0.589 |
|
| 1999 |
Mears AJ, Gieser L, Yan D, Chen C, Fahrner S, Hiriyanna S, Fujita R, Jacobson SG, Sieving PA, Swaroop A. Protein-truncation mutations in the RP2 gene in a North American cohort of families with X-linked retinitis pigmentosa. American Journal of Human Genetics. 64: 897-900. PMID 10053026 DOI: 10.1086/302298 |
0.569 |
|
| 1999 |
Walpole SM, Hiriyana KT, Nicolaou A, Bingham EL, Durham J, Vaudin M, Ross MT, Yates JR, Sieving PA, Trump D. Identification and characterization of the human homologue (RAI2) of a mouse retinoic acid-induced gene in Xp22. Genomics. 55: 275-83. PMID 10049581 DOI: 10.1006/Geno.1998.5667 |
0.533 |
|
| 1999 |
Swaroop A, Wang QL, Wu W, Cook J, Coats C, Xu S, Chen S, Zack DJ, Sieving PA. Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the development of photoreceptor function. Human Molecular Genetics. 8: 299-305. PMID 9931337 DOI: 10.1093/Hmg/8.2.299 |
0.623 |
|
| 1998 |
Den Dunnen JT, Kraayenbrink T, Van Schooneveld M, Van Vosse ED, De Jong PTVM, Ten Brink JB, Schuurman E, Tijmes N, Van Ommen GJB, Bergen AAB, Andolfi G, Montini E, Li Y, Oudet C, Bolz H, ... Sieving PA, et al. Functional implications of the spectrum of mutations found in 234 cases with X-linked juvenile retinoschisis (XLRS) Human Molecular Genetics. 7: 1185-1192. PMID 9618178 DOI: 10.1093/Hmg/7.7.1185 |
0.579 |
|
| 1998 |
Innis JW, Sieving PA, McMillan P, Weatherly RA. Apparently new syndrome of sensorineural hearing loss, retinal pigment epithelium lesions, and discolored teeth. American Journal of Medical Genetics. 75: 13-7. PMID 9450850 DOI: 10.1002/(Sici)1096-8628(19980106)75:1<13::Aid-Ajmg4>3.0.Co;2-R |
0.564 |
|
| 1997 |
Swain PK, Chen S, Wang QL, Affatigato LM, Coats CL, Brady KD, Fishman GA, Jacobson SG, Swaroop A, Stone E, Sieving PA, Zack DJ. Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degeneration. Neuron. 19: 1329-36. PMID 9427255 DOI: 10.1016/S0896-6273(00)80423-7 |
0.641 |
|
| 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 |
0.627 |
|
| 1997 |
Kim SH, Bush RA, Sieving PA. Increased phase lag of the fundamental harmonic component of the 30 Hz flicker ERG in Schubert-Bornschein complete type CSNB Vision Research. 37: 2471-2475. PMID 9381682 DOI: 10.1016/S0042-6989(97)00035-7 |
0.573 |
|
| 1997 |
Farjo Q, Jackson A, Pieke-Dahl S, Scott K, Kimberling WJ, Sieving PA, Richards JE, Swaroop A. Human bZIP transcription factor gene NRL: Structure, genomic sequence, and fine linkage mapping at 14q11.2 and negative mutation analysis in patients with retinal degeneration Genomics. 45: 395-401. PMID 9344665 DOI: 10.1006/Geno.1997.4964 |
0.625 |
|
| 1997 |
Fujita R, Buraczynska M, Gieser L, Wu W, Forsythe P, Abrahamson M, Jacobson SG, Sieving PA, Andréasson S, Swaroop A. Analysis of the RPGR gene in 11 pedigrees with the retinitis pigmentosa type 3 genotype: Paucity of mutations in the coding region but splice defects in two families American Journal of Human Genetics. 61: 571-580. PMID 9326322 DOI: 10.1086/515523 |
0.642 |
|
| 1997 |
Humphries MM, Rancourt D, Farrar GJ, Kenna P, Hazel M, Bush RA, Sieving PA, Sheils DM, McNally N, Creighton P, Erven A, Boros A, Gulya K, Capecchi MR, Humphries P. Retinopathy induced in mice by targeted disruption of the rhodopsin gene. Nature Genetics. 15: 216-9. PMID 9020854 DOI: 10.1038/ng0297-216 |
0.616 |
|
| 1996 |
Pawar H, Bingham EL, Hiriyanna K, Segal M, Richards JE, Sieving PA. X-linked juvenile retinoschisis: Localization between (DXS1195, DXS418) and AFM291wf5 on a single YAC Human Heredity. 46: 329-335. PMID 8956029 DOI: 10.1159/000154373 |
0.531 |
|
| 1996 |
Naarendorp F, Rice KS, Sieving PA. Summation of rod and S cone signals at threshold in human observers Vision Research. 36: 2681-2688. PMID 8917755 DOI: 10.1016/0042-6989(96)00023-5 |
0.564 |
|
| 1996 |
Hou YC, Richards JE, Bingham EL, Pawar H, Scott K, Segal M, Lunetta KL, Boehnke M, Sieving PA. Linkage study of Best's vitelliform macular dystrophy (VMD2) in a large North American family Human Heredity. 46: 211-220. PMID 8807324 DOI: 10.1159/000154356 |
0.582 |
|
| 1996 |
Bush RA, Sieving PA. Inner retinal contributions to the primate photopic fast flicker electroretinogram Journal of the Optical Society of America a: Optics and Image Science, and Vision. 13: 557-565. PMID 8627412 DOI: 10.1364/Josaa.13.000557 |
0.579 |
|
| 1996 |
Jaquish CE, Blangero J, Haffner SM, Stern MP, Maccluer JW, Witt M, Reis A, Cichy W, Dziechciowska K, Lin S, Speed TP, Guerra DCd, Arvelo H, Larralde AR, Salzano FM, ... Sieving PA, et al. Subject Index Vol. 46, 1996 Human Heredity. 46: 347-348. DOI: 10.1159/000154380 |
0.458 |
|
| 1996 |
Jaquish CE, Blangero J, Haffner SM, Stern MP, Maccluer JW, Witt M, Reis A, Cichy W, Dziechciowska K, Lin S, Speed TP, Guerra DCd, Arvelo H, Larralde AR, Salzano FM, ... Sieving PA, et al. Acknowledgement to the Reviewers, Vol. 46, 1996 Human Heredity. 46: 344-344. DOI: 10.1159/000154378 |
0.457 |
|
| 1996 |
Jaquish CE, Blangero J, Haffner SM, Stern MP, Maccluer JW, Witt M, Reis A, Cichy W, Dziechciowska K, Lin S, Speed TP, Guerra DCd, Arvelo H, Larralde AR, Salzano FM, ... Sieving PA, et al. Contents, Vol. 46, 1996 Human Heredity. 46. DOI: 10.1159/000154367 |
0.443 |
|
| 1996 |
Jamison JA, Bush RA, Sieving PA. Effects of APB and PDA on the phototransduction modeling of the dark adapted primate a-wave Investigative Ophthalmology and Visual Science. 37. |
0.702 |
|
| 1995 |
Sieving PA. Diagnostic issues with inherited retinal and macular dystrophies Seminars in Ophthalmology. 10: 279-294. PMID 10160215 DOI: 10.3109/08820539509063799 |
0.634 |
|
| 1995 |
Frishman LJ, Sieving PA. Evidence for two sites of adaptation affecting the dark-adapted ERG of cats and primates. Vision Research. 35: 435-42. PMID 7892737 DOI: 10.1016/0042-6989(94)00165-I |
0.575 |
|
| 1995 |
Sieving PA, Richards JE, Naarendorp F, Bingham EL, Scott K, Alpern M. Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutation. Proceedings of the National Academy of Sciences of the United States of America. 92: 880-4. PMID 7846071 DOI: 10.1073/Pnas.92.3.880 |
0.652 |
|
| 1995 |
Richards JE, Scott KM, Sieving PA. Disruption of conserved rhodopsin disulfide bond by Cys187Tyr mutation causes early and severe autosomal dominant retinitis pigmentosa Ophthalmology. 102: 669-677. PMID 7724183 DOI: 10.1016/S0161-6420(95)30972-4 |
0.637 |
|
| 1995 |
Pawar H, Bingham EL, Lunetta KL, Segal M, Richards JE, Boehnke M, Sieving PA. Refined genetic mapping of juvenile X-linked retinoschisis Human Heredity. 45: 206-210. PMID 7558052 DOI: 10.1159/000154290 |
0.564 |
|
| 1994 |
Sieving PA, Murayama K, Naarendorp F. Push-pull model of the primate photopic electroretinogram: A role for hyperpolarizing neurons in shaping the b-wave Visual Neuroscience. 11: 519-532. PMID 8038126 DOI: 10.1017/S0952523800002431 |
0.564 |
|
| 1994 |
Yan D, Wong D, Zheng K, Thiselton D, Fujita R, Sieving PA, Bhattacharya SS, Yang-feng TL, Richards JE, Swaroop A. Dinucleotide repeat polymorphism at the DXS977 locus Human Molecular Genetics. 3: 1030. PMID 7951222 DOI: 10.1093/Hmg/3.6.1030 |
0.503 |
|
| 1993 |
Geller AM, Sieving PA. Assessment of foveal cone photoreceptors in Stargardt's macular dystrophy using a small dot detection task Vision Research. 33: 1509-1524. PMID 8351823 DOI: 10.1016/0042-6989(93)90144-L |
0.544 |
|
| 1993 |
Naarendorp F, Hitchcock PF, Sieving PA. Dopaminergic modulation of rod pathway signals does not affect the scotopic ERG of cat at dark-adapted threshold Journal of Neurophysiology. 70: 1681-1691. PMID 8283223 DOI: 10.1152/Jn.1993.70.4.1681 |
0.563 |
|
| 1993 |
Sieving PA. Photopic on- and off-pathway abnormalities in retinal dystrophies Transactions of the American Ophthalmological Society. 91: 701-775. PMID 8140708 |
0.319 |
|
| 1992 |
Geller AM, Sieving PA, Green DG. Effect on grating identification of sampling with degenerate arrays Journal of the Optical Society of America a: Optics and Image Science, and Vision. 9: 472-477. PMID 1548555 DOI: 10.1364/Josaa.9.000472 |
0.54 |
|
| 1991 |
Naarendorp F, Sieving PA. The scotopic threshold response of the cat erg is suppressed selectively by GABA and glycine Vision Research. 31: 1-15. PMID 2006543 DOI: 10.1016/0042-6989(91)90068-G |
0.535 |
|
| 1991 |
Sneed SR, Sieving PA. Fenestrated sheen macular dystrophy American Journal of Ophthalmology. 112: 1-7. PMID 1882912 DOI: 10.1016/S0002-9394(14)76204-X |
0.637 |
|
| 1991 |
Arrindell EL, Trobe JD, Sieving PA, Barnett JL. Pupillary and Electroretinographic Abnormalities in a Family With Neuronal Intranuclear Hyaline Inclusion Disease Archives of Ophthalmology. 109: 373-378. PMID 1848426 DOI: 10.1001/Archopht.1991.01080030075043 |
0.529 |
|
| 1991 |
Richards JE, Kuo CY, Boehnke M, Sieving PA. Rhodopsin Thr58Arg mutation in a family with autosomal dominant retinitis pigmentosa Ophthalmology. 98: 1797-1805. PMID 1775313 DOI: 10.1016/S0161-6420(91)32047-5 |
0.599 |
|
| 1991 |
Steinberg RH, Frishman LJ, Sieving PA. Chapter 6 Negative components of the electroretinogram from proximal retina and photoreceptor Progress in Retinal Research. 10: 121-160. DOI: 10.1016/0278-4327(91)90011-P |
0.588 |
|
| 1990 |
Rowe SE, Trobe JD, Sieving PA. Idiopathic photoreceptor dysfunction causes unexplained visual acuity loss in later adulthood. Ophthalmology. 97: 1632-7. PMID 2087294 DOI: 10.1016/S0161-6420(90)32366-7 |
0.615 |
|
| 1989 |
Ticho B, Sieving PA. Leber's congenital amaurosis with marbelized fundus and juvenile nephronophthisis. American Journal of Ophthalmology. 107: 426-8. PMID 2929712 DOI: 10.1016/0002-9394(89)90670-3 |
0.516 |
|
| 1988 |
Han DP, Sieving PA, Johnson MW, Martonyi CL. Foveal retinoschisis associated with senile retinoschisis in a woman. American Journal of Ophthalmology. 106: 107-9. PMID 3394761 DOI: 10.1016/S0002-9394(14)76406-2 |
0.49 |
|
| 1988 |
Frishman LJ, Sieving PA, Steinberg RH. Contributions to the electroretinogram of currents originating in proximal retina. Visual Neuroscience. 1: 307-15. PMID 3154802 DOI: 10.1017/S0952523800001966 |
0.571 |
|
| 1987 |
Sieving PA, Steinberg RH. Proximal retinal contribution to the intraretinal 8-Hz pattern ERG of cat. Journal of Neurophysiology. 57: 104-20. PMID 3559667 DOI: 10.1152/jn.1987.57.1.104 |
0.538 |
|
| 1987 |
Sieving P. Synthesis of methyl 3-oxo-4,4-dimethylpentanoate-1,3-14C Journal of Labelled Compounds and Radiopharmaceuticals. 24: 753-758. DOI: 10.1002/jlcr.2580240704 |
0.38 |
|
| 1986 |
Sieving PA, Niffenegger JH, Berson EL. Electroretinographic findings in selected pedigrees with choroideremia. American Journal of Ophthalmology. 101: 361-7. PMID 3953730 DOI: 10.1016/0002-9394(86)90832-9 |
0.453 |
|
| 1986 |
Sieving PA, Frishman LJ, Steinberg RH. Scotopic threshold response of proximal retina in cat. Journal of Neurophysiology. 56: 1049-61. PMID 3783228 DOI: 10.1152/Jn.1986.56.4.1049 |
0.599 |
|
| 1986 |
Sieving PA, Frishman LJ, Steinberg RH. M-wave of proximal retina in cat. Journal of Neurophysiology. 56: 1039-48. PMID 3783227 DOI: 10.1152/jn.1986.56.4.1039 |
0.531 |
|
| 1984 |
Sieving PA, Fishman GA, Jampol LM, Pugh D. Multiple evanescent white dot syndrome. II. Electrophysiology of the photoreceptors during retinal pigment epithelial disease. Archives of Ophthalmology (Chicago, Ill. : 1960). 102: 675-9. PMID 6721750 DOI: 10.1001/archopht.1984.01040030531009 |
0.559 |
|
| 1984 |
Jampol LM, Sieving PA, Pugh D, Fishman GA, Gilbert H. Multiple evanescent white dot syndrome. I. Clinical findings. Archives of Ophthalmology (Chicago, Ill. : 1960). 102: 671-4. PMID 6721749 DOI: 10.1001/Archopht.1984.01040030527008 |
0.611 |
|
| 1984 |
Sieving PA, Fishman GA, Salzano T, Rabb MF. Acute macular neuroretinopathy: early receptor potential change suggests photoreceptor pathology. The British Journal of Ophthalmology. 68: 229-34. PMID 6704358 DOI: 10.1136/bjo.68.4.229 |
0.565 |
|
| 1984 |
Sieving P. Cone and rod ERGs in degenerations of central retina Survey of Ophthalmology. 29: 235-236. DOI: 10.1016/0039-6257(84)90219-4 |
0.581 |
|
| 1983 |
Sieving PA, Fishman GA, Alexander KR, Goldberg MF. Early receptor potential measurements in human ocular siderosis. Archives of Ophthalmology (Chicago, Ill. : 1960). 101: 1716-20. PMID 6639427 DOI: 10.1001/Archopht.1983.01040020718010 |
0.576 |
|
| 1978 |
Maggiano JM, Fishman GA, Evans LS, Sieving P, Goldbaum M. Calibration error in dark adaptometer. Archives of Ophthalmology (Chicago, Ill. : 1960). 96: 1082-3. PMID 655945 DOI: 10.1001/Archopht.1978.03910050602024 |
0.559 |
|
| 1978 |
Sieving PA, Fishman GA, Maggiano JM. Corneal wick electrode for recording bright flash electroretinograms and early receptor potentials. Archives of Ophthalmology (Chicago, Ill. : 1960). 96: 899-900. PMID 655931 DOI: 10.1001/Archopht.1978.03910050501024 |
0.507 |
|
| 1978 |
Sieving PA, Fishman GA. Refractive errors of retinitis pigmentosa patients. The British Journal of Ophthalmology. 62: 163-7. PMID 638108 DOI: 10.1136/bjo.62.3.163 |
0.492 |
|
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