| Year |
Citation |
Score |
| 2020 |
Uyhazi KE, Aravand P, Bell BA, Wei Z, Leo L, Serrano LW, Pearson DJ, Shpylchak I, Pham J, Vasireddy V, Bennett J, Aleman TS. Treatment Potential for LCA5-Associated Leber Congenital Amaurosis. Investigative Ophthalmology & Visual Science. 61: 30. PMID 32428231 DOI: 10.1167/Iovs.61.5.30 |
0.661 |
|
| 2019 |
Duong TT, Lim J, Vasireddy V, Papp T, Nguyen H, Leo L, Pan J, Zhou S, Chen HI, Bennett J, Mills JA. Comparative AAV-eGFP Transgene Expression Using Vector Serotypes 1-9, 7m8, and 8b in Human Pluripotent Stem Cells, RPEs, and Human and Rat Cortical Neurons. Stem Cells International. 2019: 7281912. PMID 30800164 DOI: 10.1155/2019/7281912 |
0.656 |
|
| 2018 |
Qiang L, Piermarini E, Muralidharan H, Yu W, Leo L, Hennessy LE, Fernandes S, Connors T, Yates PL, Swift M, Zholudeva LV, Lane MA, Morfini G, Alexander GM, Heiman-Patterson TD, et al. Hereditary Spastic Paraplegia: gain-of-function mechanisms revealed by new transgenic mouse. Human Molecular Genetics. PMID 30520996 DOI: 10.1093/Hmg/Ddy419 |
0.404 |
|
| 2018 |
Song JY, Aravand P, Nikonov S, Leo L, Lyubarsky A, Bennicelli JL, Pan J, Wei Z, Shpylchak I, Herrera P, Bennett DJ, Commins N, Maguire AM, Pham J, den Hollander AI, et al. Amelioration of Neurosensory Structure and Function in Animal and Cellular Models of a Congenital Blindness. Molecular Therapy : the Journal of the American Society of Gene Therapy. PMID 29673930 DOI: 10.1016/J.Ymthe.2018.03.015 |
0.706 |
|
| 2018 |
Duong TT, Vasireddy V, Ramachandran P, Herrera PS, Leo L, Merkel C, Bennett J, Mills JA. Use of induced pluripotent stem cell models to probe the pathogenesis of Choroideremia and to develop a potential treatment. Stem Cell Research. 27: 140-150. PMID 29414605 DOI: 10.1016/J.Scr.2018.01.009 |
0.549 |
|
| 2018 |
Mills JA, Herrera PS, Kaur M, Leo L, McEldrew D, Tintos-Hernandez JA, Rajagopalan R, Gagne A, Zhang Z, Ortiz-Gonzalez XR, Krantz ID. NIPBL+/- haploinsufficiency reveals a constellation of transcriptome disruptions in the pluripotent and cardiac states. Scientific Reports. 8: 1056. PMID 29348408 DOI: 10.1038/S41598-018-19173-9 |
0.602 |
|
| 2017 |
Leo L, Weissmann C, Burns M, Kang M, Song Y, Qiang L, Brady ST, Baas PW, Morfini G. Mutant spastin proteins promote deficits in axonal transport through an isoform-specific mechanism involving casein kinase 2 activation. Human Molecular Genetics. PMID 28398512 DOI: 10.1093/Hmg/Ddx125 |
0.338 |
|
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