| The gene history of zebrafish tlr4a and tlr4b is predictive of their divergent functions C Sullivan, J Charette, J Catchen, CR Lage, G Giasson, JH Postlethwait, ... The Journal of Immunology 183 (9), 5896-5908, 2009 | 178 | 2009 |
| Study of host–microbe interactions in zebrafish K Milligan-Myhre, JR Charette, RT Phennicie, WZ Stephens, JF Rawls, ... Methods in cell biology 105, 87-116, 2011 | 126 | 2011 |
| Disruption of murine Adamtsl4 results in zonular fiber detachment from the lens and in retinal pigment epithelium dedifferentiation GB Collin, D Hubmacher, JR Charette, WL Hicks, L Stone, M Yu, ... Human molecular genetics 24 (24), 6958-6974, 2015 | 58 | 2015 |
| Mutations in CTNNA1 cause butterfly-shaped pigment dystrophy and perturbed retinal pigment epithelium integrity NTM Saksens, MP Krebs, FE Schoenmaker-Koller, W Hicks, M Yu, L Shi, ... Nature genetics 48 (2), 144-151, 2016 | 56 | 2016 |
| Mouse models of NMNAT1-leber congenital amaurosis (LCA9) recapitulate key features of the human disease SH Greenwald, JR Charette, M Staniszewska, LY Shi, SDM Brown, ... The American journal of pathology 186 (7), 1925-1938, 2016 | 47 | 2016 |
| Mouse models of human ocular disease for translational research MP Krebs, GB Collin, WL Hicks, M Yu, JR Charette, LY Shi, J Wang, ... PLoS One 12 (8), e0183837, 2017 | 45 | 2017 |
| Gene Profiling of Postnatal Mfrprd6 Mutant Eyes Reveals Differential Accumulation of Prss56, Visual Cycle and Phototransduction mRNAs R Soundararajan, J Won, TM Stearns, JR Charette, WL Hicks, GB Collin, ... PloS one 9 (10), e110299, 2014 | 25 | 2014 |
| Disruption in murine Eml1 perturbs retinal lamination during early development GB Collin, J Won, MP Krebs, WJ Hicks, JR Charette, JK Naggert, ... Scientific reports 10 (1), 5647, 2020 | 15 | 2020 |
| A chemical mutagenesis screen identifies mouse models with ERG defects JR Charette, IS Samuels, M Yu, L Stone, W Hicks, LY Shi, MP Krebs, ... Retinal Degenerative Diseases: Mechanisms and Experimental Therapy, 177-183, 2016 | 15 | 2016 |
| A DN-mda5 transgenic zebrafish model demonstrates that Mda5 plays an important role in snakehead rhabdovirus resistance KA Gabor, JR Charette, MJ Pietraszewski, DJ Wingfield, JS Shim, ... Developmental & Comparative Immunology 51 (2), 298-304, 2015 | 13 | 2015 |
| A mutagenesis-derived Lrp5 mouse mutant with abnormal retinal vasculature and low bone mineral density JR Charette, SE Earp, BA Bell, CL Ackert-Bicknell, DA Godfrey, S Rao, ... Molecular Vision 23, 140, 2017 | 12 | 2017 |
| An FRMD4B variant suppresses dysplastic photoreceptor lesions in models of enhanced S-cone syndrome and of Nrl deficiency Y Kong, L Zhao, JR Charette, WL Hicks, L Stone, PM Nishina, JK Naggert Human Molecular Genetics 27 (19), 3340-3352, 2018 | 9 | 2018 |
| Genetic modifier loci of mouse Mfrprd6 identified by quantitative trait locus analysis J Won, JR Charette, VM Philip, TM Stearns, W Zhang, JK Naggert, ... Experimental eye research 118, 30-35, 2014 | 9 | 2014 |
| Single-Cell RNA Sequencing Reveals Molecular Features of Heterogeneity in the Murine Retinal Pigment Epithelium RS Pandey, MP Krebs, MT Bolisetty, JR Charette, JK Naggert, P Robson, ... International Journal of Molecular Sciences 23 (18), 10419, 2022 | 6 | 2022 |
| Identification of Arhgef12 and Prkci as genetic modifiers of retinal dysplasia in the Crb1rd8 mouse model SM Weatherly, GB Collin, JR Charette, L Stone, N Damkham, LF Hyde, ... PLoS Genetics 18 (6), e1009798, 2022 | 5 | 2022 |
| A Splicing Mutation in Slc4a5 Results in Retinal Detachment and Retinal Pigment Epithelium Dysfunction GB Collin, L Shi, M Yu, N Akturk, JR Charette, LF Hyde, SM Weatherly, ... International Journal of Molecular Sciences 23 (4), 2220, 2022 | 5 | 2022 |
| Taxonomic assessment of two wild house mouse subspecies using whole-genome sequencing RA Lawal, VL Mathis, ME Barter, JR Charette, A Garretson, BL Dumont Scientific Reports 12 (1), 20866, 2022 | 3 | 2022 |
| Single-cell RNA sequencing reveals molecular features of postnatal maturation in the murine retinal pigment epithelium RS Pandey, MP Krebs, MT Bolisetty, JR Charette, JK Naggert, P Robson, ... bioRxiv, 2022.05. 07.491046, 2022 | | 2022 |
| Mutation of differentiation genes Prkci or Foxo3 modifies the retinal dysplastic phenotype of Crb1rd8 mice MP Krebs, W Hicks, L Stone, J Charette, J Naggert, P Nishina Investigative Ophthalmology & Visual Science 58 (8), 4523-4523, 2017 | | 2017 |
| Mouse models of NMNAT1-Leber congenital amaurosis recapitulate key features of the human disease SH Greenwald, JR Charette, M Staniszewska, LY Shi, SDM Brown, ... Investigative Ophthalmology & Visual Science 57 (12), 2255-2255, 2016 | | 2016 |
