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LA Krueger

First name:
LA
Last name:
Krueger
Hufnagel, R. B., Zimmerman, S. L., Krueger, L. A., Bender, P. L., Ahmed, Z. M., & Saal, H. M. (2016). A new frontonasal dysplasia syndrome associated with deletion of the SIX2 gene. American Journal Of Medical Genetics. Part A, 170A(2), 487-491. https://doi.org/10.1002/ajmg.a.37441
Mizutani, T., Fowler, B. J., Kim, Y., Yasuma, R., Krueger, L. A., Gelfand, B. D., & Ambati, J. (2015). Nucleoside Reverse Transcriptase Inhibitors Suppress Laser-Induced Choroidal Neovascularization in Mice. Investigative Ophthalmology & Visual Science, 56(12), 7122-9. https://doi.org/10.1167/iovs.15-17440
Abrams, A. J., Hufnagel, R. B., Rebelo, A., Zanna, C., Patel, N., Gonzalez, M. A., et al. (2015). Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder. Nature Genetics, 47(8), 926-32. https://doi.org/10.1038/ng.3354
Hufnagel, R. B., Arno, G., Hein, N. D., Hersheson, J., Prasad, M., Anderson, Y., et al. (2015). Neuropathy target esterase impairments cause Oliver-McFarlane and Laurence-Moon syndromes. Journal Of Medical Genetics, 52(2), 85-94. https://doi.org/10.1136/jmedgenet-2014-102856
Coomer, C. E., Wilson, S. G., Titialii-Torres, K. F., Bills, J. D., Krueger, L. A., Petersen, R. A., et al. (2020). Her9/Hes4 is required for retinal photoreceptor development, maintenance, and survival. Scientific Reports, 10(1), 11316. https://doi.org/10.1038/s41598-020-68172-2 (Original work published 2020)
Coomer, C. E., Wilson, S. G., Titialii-Torres, K. F., Bills, J. D., Krueger, L. A., Petersen, R. A., et al. (2020). Author Correction: Her9/Hes4 is required for retinal photoreceptor development, maintenance, and survival. Scientific Reports, 10(1), 14843. https://doi.org/10.1038/s41598-020-72314-x (Original work published 2020)
Krueger, L. A., & Morris, A. C. (2022). Generation of a zebrafish knock-in line expressing MYC-tagged Sox11a using CRISPR/Cas9 genome editing. Biochemical And Biophysical Research Communications, 608, 8-13. https://doi.org/10.1016/j.bbrc.2022.03.103 (Original work published 2022)
Ahmed, M. R., Sethna, S., Krueger, L. A., Yang, M. B., & Hufnagel, R. B. (2022). Variable Anterior Segment Dysgenesis and Cardiac Anomalies Caused by a Novel Truncating Variant of FOXC1. Genes, 13(3). https://doi.org/10.3390/genes13030411 (Original work published 2022)
Krueger, L. A., & Morris, A. C. Eyes on CHARGE syndrome: Roles of CHD7 in ocular development. Frontiers In Cell And Developmental Biology, 10, 994412. https://doi.org/10.3389/fcell.2022.994412 (Original work published 2022)