Douglas Vollrath
Affiliations: | Stanford University, Palo Alto, CA |
Area:
GeneticsGoogle:
"Douglas Vollrath"Mean distance: 106866
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Publications
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| Liu B, Calton MA, Abell NS, et al. (2019) Genetic analyses of human fetal retinal pigment epithelium gene expression suggest ocular disease mechanisms. Communications Biology. 2: 186 |
| Huang J, Gu S, Chen M, et al. (2019) Abnormal mTORC1 signaling leads to retinal pigment epithelium degeneration. Theranostics. 9: 1170-1180 |
| Bailey JNC, Gharahkhani P, Kang JH, et al. (2018) Testosterone Pathway Genetic Polymorphisms in Relation to Primary Open-Angle Glaucoma: An Analysis in Two Large Datasets. Investigative Ophthalmology & Visual Science. 59: 629-636 |
| Aschard H, Kang JH, Iglesias AI, et al. (2017) Genetic correlations between intraocular pressure, blood pressure and primary open-angle glaucoma: a multi-cohort analysis. European Journal of Human Genetics : Ejhg |
| Khawaja AP, Cooke Bailey JN, Kang JH, et al. (2016) Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses. Investigative Ophthalmology & Visual Science. 57: 5046-5052 |
| Ghazi NG, Abboud EB, Nowilaty SR, et al. (2016) Treatment of retinitis pigmentosa due to MERTK mutations by ocular subretinal injection of adeno-associated virus gene vector: results of a phase I trial. Human Genetics |
| Bailey JN, Loomis SJ, Kang JH, et al. (2016) Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma. Nature Genetics |
| LaVail MM, Yasumura D, Matthes MT, et al. (2016) Gene Therapy for MERTK-Associated Retinal Degenerations. Advances in Experimental Medicine and Biology. 854: 487-93 |
| Vollrath D, Yasumura D, Benchorin G, et al. (2015) Tyro3 Modulates Mertk-Associated Retinal Degeneration. Plos Genetics. 11: e1005723 |
| Liu Y, Chen X, Xu Q, et al. (2015) SPP2 Mutations Cause Autosomal Dominant Retinitis Pigmentosa. Scientific Reports. 5: 14867 |