| Year |
Citation |
Score |
| 2022 |
Oh JK, Vargas Del Valle JG, Lima de Carvalho JR, Sun YJ, Levi SR, Ryu J, Yang J, Nagasaki T, Emanuelli A, Rasool N, Allikmets R, Sparrow JR, Izquierdo NJ, Duncan JL, Mahajan VB, et al. Expanding the phenotype of TTLL5-associated retinal dystrophy: a case series. Orphanet Journal of Rare Diseases. 17: 146. PMID 35365235 DOI: 10.1186/s13023-022-02295-9 |
0.324 |
|
| 2020 |
Oh JK, Ryu J, Lima de Carvalho JR, Levi SR, Lee W, Tsamis E, Greenstein VC, Mahajan VB, Allikmets R, Tsang SH. Optical Gap Biomarker in Cone-Dominant Retinal Dystrophy. American Journal of Ophthalmology. PMID 32445700 DOI: 10.1016/J.Ajo.2020.05.016 |
0.303 |
|
| 2020 |
Tang PH, Chemudupati T, Wert KJ, Folk JC, Mahajan M, Tsang SH, Bassuk AG, Mahajan VB. Phenotypic variance in Calpain-5 retinal degeneration. American Journal of Ophthalmology Case Reports. 18: 100627. PMID 32274441 DOI: 10.1016/J.Ajoc.2020.100627 |
0.384 |
|
| 2020 |
Evans LP, Woll AW, Wu S, Todd BP, Hehr NN, Hedberg-Buenz A, Anderson MG, Newell EA, Ferguson PJ, Mahajan VB, Harper MM, Bassuk AG. Modulation of post-traumatic immune response using the IL-1 receptor antagonist anakinra for improved visual outcomes. Journal of Neurotrauma. PMID 32056479 DOI: 10.1089/Neu.2019.6725 |
0.301 |
|
| 2020 |
Wert KJ, Velez G, Kanchustambham VL, Shankar V, Evans LP, Sengillo JD, Zare RN, Bassuk AG, Tsang SH, Mahajan VB. Metabolite therapy guided by liquid biopsy proteomics delays retinal neurodegeneration. Ebiomedicine. 52: 102636. PMID 32028070 DOI: 10.1016/J.Ebiom.2020.102636 |
0.368 |
|
| 2020 |
Velez G, Sun YJ, Khan S, Yang J, Herrmann J, Chemudupati T, MacLaren RE, Gakhar L, Wakatsuki S, Bassuk AG, Mahajan VB. Structural Insights into the Unique Activation Mechanisms of a Non-classical Calpain and Its Disease-Causing Variants. Cell Reports. 30: 881-892.e5. PMID 31968260 DOI: 10.1016/J.Celrep.2019.12.077 |
0.644 |
|
| 2019 |
Oh JK, Lima de Carvalho JR, Sun YJ, Ragi S, Yang J, Levi SR, Ryu J, Bassuk AG, Mahajan VB, Tsang SH. Novel mutations in the 3-box motif of the BACK domain of KLHL7 associated with nonsyndromic autosomal dominant retinitis pigmentosa. Orphanet Journal of Rare Diseases. 14: 295. PMID 31856884 DOI: 10.1186/S13023-019-1275-2 |
0.431 |
|
| 2019 |
Ragi SD, Lima de Carvalho JR, Tanaka AJ, Park KS, Mahajan VB, Maumenee IH, Tsang SH. Compound heterozygous novel frameshift variants in the gene result in Leber congenital amaurosis. Cold Spring Harbor Molecular Case Studies. 5. PMID 31836589 DOI: 10.1101/mcs.a004481 |
0.321 |
|
| 2019 |
Zhang J, Fang F, Li L, Huang H, Webber HC, Sun Y, Mahajan VB, Hu Y. A Reversible Silicon Oil-Induced Ocular Hypertension Model in Mice. Journal of Visualized Experiments : Jove. PMID 31789319 DOI: 10.3791/60409 |
0.331 |
|
| 2019 |
Lin Y, Xu CL, Velez G, Yang J, Tanaka AJ, Breazzano MP, Mahajan VB, Sparrow JR, Tsang SH. Novel REEP6 gene mutation associated with autosomal recessive retinitis pigmentosa. Documenta Ophthalmologica. Advances in Ophthalmology. PMID 31538292 DOI: 10.1007/S10633-019-09719-1 |
0.427 |
|
| 2019 |
Zhang L, Cui X, Han Y, Park KS, Gao X, Zhang X, Yuan Z, Hu Y, Hsu CW, Li X, Bassuk AG, Mahajan VB, Wang NK, Tsang SH. Hypoxic drive caused Type 3 neovascularization in a preclinical model of exudative age-related macular degeneration. Human Molecular Genetics. PMID 31518400 DOI: 10.1093/Hmg/Ddz159 |
0.364 |
|
| 2019 |
Wert KJ, Koch SF, Velez G, Hsu CW, Mahajan M, Bassuk AG, Tsang SH, Mahajan VB. CAPN5 genetic inactivation phenotype supports therapeutic inhibition trials. Human Mutation. PMID 31403230 DOI: 10.1002/Humu.23894 |
0.366 |
|
| 2019 |
Takahashi VKL, Xu CL, Takiuti JT, Apatoff MBL, Duong JK, Mahajan VB, Tsang SH. Comparison of structural progression between ciliopathy and non-ciliopathy associated with autosomal recessive retinitis pigmentosa. Orphanet Journal of Rare Diseases. 14: 187. PMID 31370859 DOI: 10.1186/S13023-019-1163-9 |
0.361 |
|
| 2019 |
Chang YJ, Xu CL, Cui X, Bassuk AG, Mahajan VB, Tsai YT, Tsang SH. CRISPR Base Editing in Induced Pluripotent Stem Cells. Methods in Molecular Biology (Clifton, N.J.). PMID 31250381 DOI: 10.1007/7651_2019_243 |
0.308 |
|
| 2019 |
Abe K, Cox A, Takamatsu N, Velez G, Laxer RM, Tse SML, Mahajan VB, Bassuk AG, Fuchs H, Ferguson PJ, Hrabe de Angelis M. Gain-of-function mutations in a member of the Src family kinases cause autoinflammatory bone disease in mice and humans. Proceedings of the National Academy of Sciences of the United States of America. PMID 31138708 DOI: 10.1073/Pnas.1819825116 |
0.358 |
|
| 2019 |
Velez G, Yang J, Li AS, Tsang SH, Bassuk AG, Mahajan VB. Proteomic insight into the pathogenesis of CAPN5-vitreoretinopathy. Scientific Reports. 9: 7608. PMID 31110225 DOI: 10.1038/S41598-019-44031-7 |
0.346 |
|
| 2019 |
Wert KJ, Bakall B, Bassuk AG, Tsang SH, Mahajan VB. Insights into Retinal Development Using Live Imaging in Female Carriers of Choroideremia. Ophthalmic Surgery, Lasers & Imaging Retina. 50: e158-e162. PMID 31100169 DOI: 10.3928/23258160-20190503-15 |
0.362 |
|
| 2019 |
Zhang J, Li L, Huang H, Fang F, Webber HC, Zhuang P, Liu L, Dalal R, Tang PH, Mahajan VB, Sun Y, Li S, Zhang M, Goldberg JL, Hu Y. Silicone oil-induced ocular hypertension and glaucomatous neurodegeneration in mouse. Elife. 8. PMID 31090540 DOI: 10.7554/Elife.45881 |
0.312 |
|
| 2019 |
Wang NK, Mahajan VB, Tsang SH. Therapeutic Window for Phosphodiesterase 6-Related Retinitis Pigmentosa. Jama Ophthalmology. PMID 30998807 DOI: 10.1001/Jamaophthalmol.2018.6381 |
0.348 |
|
| 2019 |
O'Keefe G, Hanif AM, Mahajan VB, Jain N. Early Onset Neovascular Inflammatory Vitreoretinopathy Due to a De Novo CAPN5 Mutation: Report of a Case. Ocular Immunology and Inflammation. 1-3. PMID 30986125 DOI: 10.1080/09273948.2019.1582783 |
0.343 |
|
| 2019 |
Sancho-Pelluz J, Cui X, Lee W, Tsai YT, Wu WH, Justus S, Washington I, Hsu CW, Park KS, Koch S, Velez G, Bassuk AG, Mahajan VB, Lin CS, Tsang SH. Mechanisms of neurodegeneration in a preclinical autosomal dominant retinitis pigmentosa knock-in model with a Rho mutation. Cellular and Molecular Life Sciences : Cmls. PMID 30976840 DOI: 10.1007/S00018-019-03090-9 |
0.411 |
|
| 2019 |
Tang PH, Jauregui R, Tsang SH, Bassuk AG, Mahajan VB. Optical Coherence Tomography Angiography of RPGR-Associated Retinitis Pigmentosa Suggests Foveal Avascular Zone is a Biomarker for Vision Loss. Ophthalmic Surgery, Lasers & Imaging Retina. 50: e44-e48. PMID 30768229 DOI: 10.3928/23258160-20190129-18 |
0.348 |
|
| 2019 |
Tang PH, Velez G, Tsang SH, Bassuk AG, Mahajan VB. VCAN Canonical Splice Site Mutation is Associated With Vitreoretinal Degeneration and Disrupts an MMP Proteolytic Site. Investigative Ophthalmology & Visual Science. 60: 282-293. PMID 30657523 DOI: 10.1167/Iovs.18-25624 |
0.333 |
|
| 2019 |
Takahashi VKL, Takiuti JT, Carvalho-Jr JRL, Xu CL, Duong JK, Mahajan VB, Tsang SH. Fundus autofluorescence and ellipsoid zone (EZ) line width can be an outcome measurement in RHO-associated autosomal dominant retinitis pigmentosa. Graefe's Archive For Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie. PMID 30635721 DOI: 10.1007/S00417-018-04234-6 |
0.356 |
|
| 2019 |
Wert KJ, Mahajan VB. In Vivo Expression of Mutant Calpains in the Eye Using Lentivirus. Methods in Molecular Biology (Clifton, N.J.). 1915: 233-247. PMID 30617808 DOI: 10.1007/978-1-4939-8988-1_18 |
0.4 |
|
| 2018 |
Jauregui R, Thomas AL, Liechty B, Velez G, Mahajan VB, Clark L, Tsang SH. SCAPER-associated nonsyndromic autosomal recessive retinitis pigmentosa. American Journal of Medical Genetics. Part A. PMID 30561111 DOI: 10.1002/Ajmg.A.61001 |
0.389 |
|
| 2018 |
Wang SF, Kowal TJ, Ning K, Koo EB, Wu AY, Mahajan VB, Sun Y. Review of Ocular Manifestations of Joubert Syndrome. Genes. 9. PMID 30518138 DOI: 10.3390/Genes9120605 |
0.363 |
|
| 2018 |
Takahashi VKL, Takiuti JT, Jauregui R, Mahajan VB, Tsang SH. Rates of Bone Spicule Pigment Appearance in patients with Retinitis Pigmentosa Sine Pigmento. American Journal of Ophthalmology. PMID 30081015 DOI: 10.1016/J.Ajo.2018.07.036 |
0.304 |
|
| 2018 |
Xu CL, Cho GY, Sengillo JD, Park KS, Mahajan VB, Tsang SH. Translation of CRISPR Genome Surgery to the Bedside for Retinal Diseases. Frontiers in Cell and Developmental Biology. 6: 46. PMID 29876348 DOI: 10.3389/Fcell.2018.00046 |
0.306 |
|
| 2018 |
DiCarlo JE, Mahajan VB, Tsang SH. Gene therapy and genome surgery in the retina. The Journal of Clinical Investigation. 128: 2177-2188. PMID 29856367 DOI: 10.1172/Jci120429 |
0.356 |
|
| 2018 |
Lin MK, Yang J, Hsu CW, Gore A, Bassuk AG, Brown LM, Colligan R, Sengillo JD, Mahajan VB, Tsang SH. HTRA1, an age-related macular degeneration protease, processes extracellular matrix proteins EFEMP1 and TSP1. Aging Cell. e12710. PMID 29730901 DOI: 10.1111/Acel.12710 |
0.384 |
|
| 2018 |
Jauregui R, Cho GY, Takahashi VKL, Takiuti JT, Bassuk AG, Mahajan VB, Tsang SH. Caring for Hereditary Childhood Retinal Blindness. Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.). PMID 29536675 DOI: 10.22608/Apo.201851 |
0.307 |
|
| 2018 |
Velez G, Bassuk AG, Schaefer KA, Brooks B, Gakhar L, Mahajan M, Kahn P, Tsang SH, Ferguson PJ, Mahajan VB. A novel de novo CAPN5 mutation in a patient with inflammatory vitreoretinopathy, hearing loss, and developmental delay. Cold Spring Harbor Molecular Case Studies. PMID 29472286 DOI: 10.1101/mcs.a002519 |
0.648 |
|
| 2018 |
Velez G, Machlab DA, Tang PH, Sun Y, Tsang SH, Bassuk AG, Mahajan VB. Proteomic analysis of the human retina reveals region-specific susceptibilities to metabolic- and oxidative stress-related diseases. Plos One. 13: e0193250. PMID 29466423 DOI: 10.1371/Journal.Pone.0193250 |
0.354 |
|
| 2018 |
Cabral T, Lima LH, Mello LGM, Polido J, Correa ÉP, Oshima A, Duong J, Serracarbassa P, Regatieri CV, Mahajan VB, Belfort R. Bevacizumab Injection in Patients with Neovascular Age-Related Macular Degeneration Increases Angiogenic Biomarkers. Ophthalmology Retina. 2: 31-37. PMID 29376143 DOI: 10.1016/J.Oret.2017.04.004 |
0.309 |
|
| 2018 |
Apatoff MBL, Sengillo JD, White EC, Bakhoum MF, Bassuk AG, Mahajan VB, Tsang SH. Autologous stem cell therapy for inherited and acquired retinal disease. Regenerative Medicine. PMID 29360008 DOI: 10.2217/Rme-2017-0089 |
0.354 |
|
| 2018 |
Wu WH, Tsai YT, Justus S, Cho GY, Sengillo JD, Xu Y, Cabral T, Lin CS, Bassuk AG, Mahajan VB, Tsang SH. CRISPR Repair Reveals Causative Mutation in a Preclinical Model of Retinitis Pigmentosa: A Brief Methodology. Methods in Molecular Biology (Clifton, N.J.). 1715: 191-205. PMID 29188514 DOI: 10.1007/978-1-4939-7522-8_13 |
0.372 |
|
| 2018 |
Schaefer KA, Wu W, Colgan DF, Tsang SH, Bassuk AG, Mahajan VB. Correction: Retraction: Unexpected mutations after CRISPR–Cas9 editing in vivo Nature Methods. 15: 394-394. DOI: 10.1038/Nmeth0518-394A |
0.301 |
|
| 2017 |
Velez G, Tsang SH, Tsai YT, Hsu CW, Gore A, Abdelhakim AH, Mahajan M, Silverman RH, Sparrow JR, Bassuk AG, Mahajan VB. Gene Therapy Restores Mfrp and Corrects Axial Eye Length. Scientific Reports. 7: 16151. PMID 29170418 DOI: 10.1038/S41598-017-16275-8 |
0.4 |
|
| 2017 |
Cabral T, Toral MA, Velez G, DiCarlo JE, Gore AM, Mahajan M, Tsang SH, Bassuk AG, Mahajan VB. Dissection of Human Retina and RPE-Choroid for Proteomic Analysis. Journal of Visualized Experiments : Jove. PMID 29155757 DOI: 10.3791/56203 |
0.351 |
|
| 2017 |
Sengillo JD, Cabral T, Schuerch K, Duong J, Lee W, Boudreault K, Xu Y, Justus S, Sparrow JR, Mahajan VB, Tsang SH. Electroretinography Reveals Difference in Cone Function between Syndromic and Nonsyndromic USH2A Patients. Scientific Reports. 7: 11170. PMID 28894305 DOI: 10.1038/S41598-017-11679-Y |
0.385 |
|
| 2017 |
Cabral T, Sengillo JD, Duong JK, Justus S, Boudreault K, Schuerch K, Belfort R, Mahajan VB, Sparrow JR, Tsang SH. Retrospective Analysis of Structural Disease Progression in Retinitis Pigmentosa Utilizing Multimodal Imaging. Scientific Reports. 7: 10347. PMID 28871101 DOI: 10.1038/S41598-017-10473-0 |
0.327 |
|
| 2017 |
Velez G, Roybal CN, Binkley E, Bassuk AG, Tsang SH, Mahajan VB. Proteomic Analysis of Elevated Intraocular Pressure with Retinal Detachment. American Journal of Ophthalmology Case Reports. 5: 107-110. PMID 28825049 DOI: 10.1016/J.Ajoc.2016.12.023 |
0.312 |
|
| 2017 |
Russell S, Bennett J, Wellman JA, Chung DC, Yu ZF, Tillman A, Wittes J, Pappas J, Elci O, McCague S, Cross D, Marshall KA, Walshire J, Kehoe TL, Reichert H, ... ... Mahajan VB, et al. Efficacy and safety of voretigene neparvovec (AAV2-hRPE65v2) in patients with RPE65-mediated inherited retinal dystrophy: a randomised, controlled, open-label, phase 3 trial. Lancet (London, England). PMID 28712537 DOI: 10.1016/S0140-6736(17)31868-8 |
0.318 |
|
| 2017 |
DiCarlo JE, Sengillo JD, Justus S, Cabral T, Tsang SH, Mahajan VB. CRISPR-Cas Genome Surgery in Ophthalmology. Translational Vision Science & Technology. 6: 13. PMID 28573077 DOI: 10.1167/Tvst.6.3.13 |
0.323 |
|
| 2017 |
Schaefer KA, Wu WH, Colgan DF, Tsang SH, Bassuk AG, Mahajan VB. Unexpected mutations after CRISPR-Cas9 editing in vivo. Nature Methods. 14: 547-548. PMID 28557981 DOI: 10.1038/Nmeth.4293 |
0.331 |
|
| 2017 |
Toral MA, Velez G, Boudreault K, Schaefer KA, Xu Y, Saffra N, Bassuk AG, Tsang SH, Mahajan VB. Structural modeling of a novel SLC38A8 mutation that causes foveal hypoplasia. Molecular Genetics & Genomic Medicine. 5: 202-209. PMID 28546991 DOI: 10.1002/Mgg3.266 |
0.399 |
|
| 2017 |
Cox AJ, Darbro BW, Laxer RM, Velez G, Bing X, Finer AL, Erives A, Mahajan VB, Bassuk AG, Ferguson PJ. Recessive coding and regulatory mutations in FBLIM1 underlie the pathogenesis of chronic recurrent multifocal osteomyelitis (CRMO). Plos One. 12: e0169687. PMID 28301468 DOI: 10.1371/Journal.Pone.0169687 |
0.342 |
|
| 2017 |
Velez G, Gakhar L, Khan S, Koster HJ, Yang J, Tsang SH, Bassuk AG, Mahajan VB. Crystal structure of the human calpain-5 catalytic core Acta Crystallographica Section a Foundations and Advances. 73: a31-a32. DOI: 10.1107/S0108767317099688 |
0.58 |
|
| 2016 |
Zhang L, Du J, Justus S, Hsu CW, Bonet-Ponce L, Wu WH, Tsai YT, Wu WP, Jia Y, Duong JK, Mahajan VB, Lin CS, Wang S, Hurley JB, Tsang SH. Reprogramming metabolism by targeting sirtuin 6 attenuates retinal degeneration. The Journal of Clinical Investigation. 126: 4659-4673. PMID 27841758 DOI: 10.1172/Jci86905 |
0.394 |
|
| 2016 |
Zhang L, Justus S, Xu Y, Pluchenik T, Hsu CW, Yang J, Duong JK, Lin CS, Jia Y, Bassuk AG, Mahajan VB, Tsang SH. Reprogramming toward anabolism impedes degeneration in a preclinical model of retinitis pigmentosa. Human Molecular Genetics. PMID 27516389 DOI: 10.1093/Hmg/Ddw256 |
0.373 |
|
| 2016 |
Gakhar L, Bassuk AG, Velez G, Khan S, Yang J, Tsang SH, Mahajan VB. Small-angle x-ray scattering of calpain-5 reveals a highly open conformation among calpains. Journal of Structural Biology. PMID 27474374 DOI: 10.1016/J.Jsb.2016.07.017 |
0.618 |
|
| 2016 |
Xu K, Chin EK, Mahajan VB, Almeida DR. Intravitreal Foscarnet With Concurrent Silicone Oil Tamponade for Rhegmatogenous Retinal Detachment Secondary to Viral Retinitis. Retina (Philadelphia, Pa.). PMID 27429388 DOI: 10.1097/Iae.0000000000001174 |
0.321 |
|
| 2016 |
Cham A, Bansal M, Banda HK, Kwon Y, Tlucek PS, Bassuk AG, Tsang SH, Sobol WM, Folk JC, Yeh S, Mahajan VB. Secondary glaucoma in CAPN5-associated neovascular inflammatory vitreoretinopathy. Clinical Ophthalmology (Auckland, N.Z.). 10: 1187-97. PMID 27390515 DOI: 10.2147/Opth.S103324 |
0.329 |
|
| 2016 |
Wu WH, Tsai YT, Justus S, Lee T, Zhang L, Lin CS, Bassuk AG, Mahajan VB, Tsang SH. CRISPR repair reveals causative mutation in a preclinical model of retinitis pigmentosa. Molecular Therapy : the Journal of the American Society of Gene Therapy. PMID 27203441 DOI: 10.1038/Mt.2016.107 |
0.418 |
|
| 2016 |
Wert KJ, Mahajan VB, Zhang L, Yan Y, Li Y, Tosi J, Hsu CW, Nagasaki T, Janisch KM, Grant MB, Mahajan M, Bassuk AG, Tsang SH. Neuroretinal hypoxic signaling in a new preclinical murine model for proliferative diabetic retinopathy. Signal Transduction and Targeted Therapy. 1. PMID 27195131 DOI: 10.1038/Sigtrans.2016.5 |
0.34 |
|
| 2016 |
Moshfegh Y, Velez G, Li Y, Bassuk AG, Mahajan VB, Tsang SH. BESTROPHIN1 mutations cause defective chloride conductance in patient stem cell-derived RPE. Human Molecular Genetics. PMID 27193166 DOI: 10.1093/Hmg/Ddw126 |
0.371 |
|
| 2016 |
Schaefer KA, Toral MA, Velez G, Cox AJ, Baker SA, Borcherding NC, Colgan DF, Bondada V, Mashburn CB, Yu CG, Geddes JW, Tsang SH, Bassuk AG, Mahajan VB. Calpain-5 Expression in the Retina Localizes to Photoreceptor Synapses. Investigative Ophthalmology & Visual Science. 57: 2509-2521. PMID 27152965 DOI: 10.1167/Iovs.15-18680 |
0.304 |
|
| 2016 |
Mammo Z, Almeida DR, Cunningham MA, Chin EK, Mahajan VB. ACANTHAMOEBA ENDOPHTHALMITIS AFTER RECURRENT KERATITIS AND NODULAR SCLERITIS. Retinal Cases & Brief Reports. PMID 27152698 DOI: 10.1097/Icb.0000000000000323 |
0.328 |
|
| 2016 |
Chin EK, Almeida DR, Mahajan VB. Chronic Recurrent Pseudophakic Endophthalmitis. Jama Ophthalmology. 134: 455-6. PMID 26868359 DOI: 10.1001/Jamaophthalmol.2015.3638 |
0.308 |
|
| 2016 |
Bassuk AG, Zheng A, Li Y, Tsang SH, Mahajan VB. Precision Medicine: Genetic Repair of Retinitis Pigmentosa in Patient-Derived Stem Cells. Scientific Reports. 6: 19969. PMID 26814166 DOI: 10.1038/Srep19969 |
0.395 |
|
| 2015 |
Almeida DR, Chin EK, Tarantola RM, Tegins EO, Lopez CA, Boldt HC, Gehrs KM, Sohn EH, Russell SR, Folk JC, Mahajan VB. Long-term outcomes in patients undergoing vitrectomy for retinal detachment due to viral retinitis. Clinical Ophthalmology (Auckland, N.Z.). 9: 1307-14. PMID 26229423 DOI: 10.2147/Opth.S87644 |
0.36 |
|
| 2015 |
Skeie JM, Roybal CN, Mahajan VB. Proteomic insight into the molecular function of the vitreous. Plos One. 10: e0127567. PMID 26020955 DOI: 10.1371/Journal.Pone.0127567 |
0.304 |
|
| 2015 |
Wert KJ, Bassuk AG, Wu WH, Gakhar L, Coglan D, Mahajan M, Wu S, Yang J, Lin CS, Tsang SH, Mahajan VB. CAPN5 mutation in hereditary uveitis: the R243L mutation increases calpain catalytic activity and triggers intraocular inflammation in a mouse model. Human Molecular Genetics. 24: 4584-98. PMID 25994508 DOI: 10.1093/Hmg/Ddv189 |
0.695 |
|
| 2015 |
Bassuk AG, Yeh S, Wu S, Martin DF, Tsang SH, Gakhar L, Mahajan VB. Structural modeling of a novel CAPN5 mutation that causes uveitis and neovascular retinal detachment. Plos One. 10: e0122352. PMID 25856303 DOI: 10.1371/Journal.Pone.0122352 |
0.687 |
|
| 2015 |
Marsiglia M, Lee W, Mahajan VB, Zernant J, Delori FC, Tsang SH, Sparrow JR. Quantitative autofluorescence as a clinical tool for expedited differential diagnosis of retinal degeneration. Jama Ophthalmology. 133: 219-20. PMID 25375877 DOI: 10.1001/Jamaophthalmol.2014.4507 |
0.437 |
|
| 2015 |
Wert KJ, Bassuk AG, Wu WH, Gakhar L, Coglan D, Mahajan M, Wu S, Yang J, Lin CS, Tsang SH, Mahajan VB. CAPN5 mutation in hereditary uveitis: The R243L mutation increases calpain catalytic activity and triggers intraocular inflammation in a mouse model Human Molecular Genetics. 24: 4584-4598. DOI: 10.1093/hmg/ddv189 |
0.622 |
|
| 2014 |
Chen J, Ingham N, Kelly J, Jadeja S, Goulding D, Pass J, Mahajan VB, Tsang SH, Nijnik A, Jackson IJ, White JK, Forge A, Jagger D, Steel KP. Spinster homolog 2 (spns2) deficiency causes early onset progressive hearing loss. Plos Genetics. 10: e1004688. PMID 25356849 DOI: 10.1371/Journal.Pgen.1004688 |
0.353 |
|
| 2014 |
Skeie JM, Mahajan VB. Proteomic landscape of the human choroid-retinal pigment epithelial complex. Jama Ophthalmology. 132: 1271-81. PMID 25058583 DOI: 10.1001/Jamaophthalmol.2014.2065 |
0.357 |
|
| 2014 |
Bassuk AG, Sujirakul T, Tsang SH, Mahajan VB. A novel RPGR mutation masquerading as Stargardt disease. The British Journal of Ophthalmology. 98: 709-11. PMID 24489377 DOI: 10.1136/Bjophthalmol-2013-304822 |
0.382 |
|
| 2014 |
Wert KJ, Skeie JM, Bassuk AG, Olivier AK, Tsang SH, Mahajan VB. Functional validation of a human CAPN5 exome variant by lentiviral transduction into mouse retina. Human Molecular Genetics. 23: 2665-77. PMID 24381307 DOI: 10.1093/Hmg/Ddt661 |
0.392 |
|
| 2013 |
Paemka L, Mahajan VB, Skeie JM, Sowers LP, Ehaideb SN, Gonzalez-Alegre P, Sasaoka T, Tao H, Miyagi A, Ueno N, Takao K, Miyakawa T, Wu S, Darbro BW, Ferguson PJ, et al. PRICKLE1 interaction with SYNAPSIN I reveals a role in autism spectrum disorders. Plos One. 8: e80737. PMID 24312498 DOI: 10.1371/Journal.Pone.0080737 |
0.33 |
|
| 2013 |
Skeie JM, Mahajan VB. Proteomic interactions in the mouse vitreous-retina complex. Plos One. 8: e82140. PMID 24312404 DOI: 10.1371/Journal.Pone.0082140 |
0.363 |
|
| 2013 |
White JK, Gerdin AK, Karp NA, Ryder E, Buljan M, Bussell JN, Salisbury J, Clare S, Ingham NJ, Podrini C, Houghton R, Estabel J, Bottomley JR, Melvin DG, Sunter D, ... ... Mahajan VB, et al. Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes. Cell. 154: 452-64. PMID 23870131 DOI: 10.1016/J.Cell.2013.06.022 |
0.302 |
|
| 2013 |
Mahajan VB, Lin JH. Lymphocyte infiltration in CAPN5 autosomal dominant neovascular inflammatory vitreoretinopathy. Clinical Ophthalmology (Auckland, N.Z.). 7: 1339-45. PMID 23861576 DOI: 10.2147/Opth.S46450 |
0.369 |
|
| 2013 |
Bakall B, Folk JC, Boldt HC, Sohn EH, Stone EM, Russell SR, Mahajan VB. Aflibercept therapy for exudative age-related macular degeneration resistant to bevacizumab and ranibizumab. American Journal of Ophthalmology. 156: 15-22.e1. PMID 23706500 DOI: 10.1016/J.Ajo.2013.02.017 |
0.332 |
|
| 2013 |
Darbro BW, Mahajan VB, Gakhar L, Skeie JM, Campbell E, Wu S, Bing X, Millen KJ, Dobyns WB, Kessler JA, Jalali A, Cremer J, Segre A, Manak JR, Aldinger KA, et al. Mutations in extracellular matrix genes NID1 and LAMC1 cause autosomal dominant Dandy-Walker malformation and occipital cephaloceles. Human Mutation. 34: 1075-9. PMID 23674478 DOI: 10.1002/Humu.22351 |
0.646 |
|
| 2013 |
Cunningham MA, Tarantola RM, Folk JC, Sohn EH, Boldt HC, Graff JA, Elkins K, Russell SR, Mahajan VB. Proliferative vitreoretinopathy may be a risk factor in combined macular hole retinal detachment cases Retina. 33: 579-585. PMID 23222494 DOI: 10.1097/Iae.0B013E31826B0C41 |
0.331 |
|
| 2013 |
Tarantola RM, Tsui JY, Graff JM, Russell SR, Boldt HC, Folk JC, Mahajan VB. Intraoperative sclerotomy-related retinal breaks during 23-gauge pars plana vitrectomy. Retina (Philadelphia, Pa.). 33: 136-42. PMID 22791174 DOI: 10.1097/Iae.0B013E31825E1D62 |
0.341 |
|
| 2012 |
Wert KJ, Skeie JM, Davis RJ, Tsang SH, Mahajan VB. Subretinal injection of gene therapy vectors and stem cells in the perinatal mouse eye. Journal of Visualized Experiments : Jove. PMID 23207897 DOI: 10.3791/4286 |
0.314 |
|
| 2012 |
McIntyre RE, Lakshminarasimhan Chavali P, Ismail O, Carragher DM, Sanchez-Andrade G, Forment JV, Fu B, Del Castillo Velasco-Herrera M, Edwards A, van der Weyden L, Yang F, Ramirez-Solis R, Estabel J, Gallagher FA, ... ... Mahajan VB, et al. Disruption of mouse Cenpj, a regulator of centriole biogenesis, phenocopies Seckel syndrome. Plos Genetics. 8: e1003022. PMID 23166506 DOI: 10.1371/Journal.Pgen.1003022 |
0.307 |
|
| 2012 |
Mahajan VB, Skeie JM, Bassuk AG, Fingert JH, Braun TA, Daggett HT, Folk JC, Sheffield VC, Stone EM. Calpain-5 mutations cause autoimmune uveitis, retinal neovascularization, and photoreceptor degeneration. Plos Genetics. 8: e1003001. PMID 23055945 DOI: 10.1371/Journal.Pgen.1003001 |
0.445 |
|
| 2012 |
Tlucek PS, Folk JC, Orien JA, Stone EM, Mahajan VB. Inhibition of neovascularization but not fibrosis with the fluocinolone acetonide implant in autosomal dominant neovascular inflammatory vitreoretinopathy. Archives of Ophthalmology (Chicago, Ill. : 1960). 130: 1395-401. PMID 22777573 DOI: 10.1001/Archophthalmol.2012.1971 |
0.342 |
|
| 2011 |
Mahajan VB, Skeie JM, Assefnia AH, Mahajan M, Tsang SH. Mouse eye enucleation for remote high-throughput phenotyping. Journal of Visualized Experiments : Jove. PMID 22126835 DOI: 10.3791/3184 |
0.349 |
|
| 2011 |
Quellec G, Russell SR, Seddon JM, Reynolds R, Scheetz T, Mahajan VB, Stone EM, Abrà moff MD. Automated discovery and quantification of image-based complex phenotypes: a twin study of drusen phenotypes in age-related macular degeneration. Investigative Ophthalmology & Visual Science. 52: 9195-206. PMID 22039249 DOI: 10.1167/Iovs.10-6793 |
0.307 |
|
| 2011 |
Kay CN, Tarantola RM, Gehrs KM, Folk JC, Mahajan VB, Boldt HC, Syed NA, Russell SR. Uveitis following intravitreal bevacizumab: A non-infectious cluster Ophthalmic Surgery Lasers and Imaging. 42: 292-296. PMID 21800802 DOI: 10.3928/15428877-20110603-04 |
0.314 |
|
| 2011 |
Roller AB, Folk JC, Patel NM, Boldt HC, Russell SR, Abramoff MD, Mahajan VB. Intravitreal bevacizumab for treatment of proliferative and nonproliferative type 2 idiopathic macular telangiectasia. Retina (Philadelphia, Pa.). 31: 1848-55. PMID 21610563 DOI: 10.1097/Iae.0B013E31820D3Feb |
0.342 |
|
| 2011 |
Skeie JM, Tsang SH, Mahajan VB. Evisceration of mouse vitreous and retina for proteomic analyses. Journal of Visualized Experiments : Jove. PMID 21490583 DOI: 10.3791/2795 |
0.394 |
|
| 2011 |
Ko AC, Brinton JP, Mahajan VB, Zimmerman B, Brinton GS, Stone EM, Folk JC, Mullins RF. Seroreactivity against aqueous-soluble and detergent-soluble retinal proteins in posterior uveitis. Archives of Ophthalmology (Chicago, Ill. : 1960). 129: 415-20. PMID 21482867 DOI: 10.1001/Archophthalmol.2011.65 |
0.354 |
|
| 2011 |
Skeie JM, Mahajan VB. Dissection of human vitreous body elements for proteomic analysis. Journal of Visualized Experiments : Jove. PMID 21304469 DOI: 10.3791/2455 |
0.368 |
|
| 2011 |
Tao H, Manak JR, Sowers L, Mei X, Kiyonari H, Abe T, Dahdaleh NS, Yang T, Wu S, Chen S, Fox MH, Gurnett C, Montine T, Bird T, Shaffer LG, ... ... Mahajan VB, et al. Mutations in prickle orthologs cause seizures in flies, mice, and humans. American Journal of Human Genetics. 88: 138-49. PMID 21276947 DOI: 10.1016/J.Ajhg.2010.12.012 |
0.315 |
|
| 2010 |
Mahajan VB, Olney AH, Garrett P, Chary A, Dragan E, Lerner G, Murray J, Bassuk AG. Collagen XVIII mutation in Knobloch syndrome with acute lymphoblastic leukemia American Journal of Medical Genetics, Part A. 152: 2875-2879. PMID 20799329 DOI: 10.1002/Ajmg.A.33621 |
0.343 |
|
| 2010 |
Roller AB, Mahajan VB, Boldt HC, Abramoff MD, Russell SR, Folk JC. Effects of vitrectomy on age-related macular degeneration. Ophthalmology. 117: 1381-6. PMID 20176401 DOI: 10.1016/J.Ophtha.2009.11.007 |
0.342 |
|
| 2009 |
Shah SS, Tsang SH, Mahajan VB. Erythropoetin receptor expression in the human diabetic retina. Bmc Research Notes. 2: 234. PMID 19930719 DOI: 10.1186/1756-0500-2-234 |
0.313 |
|
| 2009 |
Mahajan VB, Russell SR, Stone EM. A new macular dystrophy with anomalous vascular development, pigment spots, cystic spaces, and neovascularization. Archives of Ophthalmology (Chicago, Ill. : 1960). 127: 1449-57. PMID 19901210 DOI: 10.1001/Archophthalmol.2009.210 |
0.307 |
|
| 2001 |
Pai KS, Mahajan VB, Lau A, Cunningham DD. Thrombin receptor signaling to cytoskeleton requires Hsp90. The Journal of Biological Chemistry. 276: 32642-7. PMID 11413145 DOI: 10.1074/Jbc.M104212200 |
0.578 |
|
| 2000 |
Mahajan VB, Pai KS, Lau A, Cunningham DD. Creatine kinase, an ATP-generating enzyme, is required for thrombin receptor signaling to the cytoskeleton. Proceedings of the National Academy of Sciences of the United States of America. 97: 12062-7. PMID 11050237 DOI: 10.1073/Pnas.97.22.12062 |
0.583 |
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