Hufnagel, R. ., Zimmerman, S. ., Krueger, L. ., Bender, P. ., Ahmed, Z. ., & Saal, H. . (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
LA Krueger
First name:
LA
Last name:
Krueger
Mizutani, T. ., Fowler, B. ., Kim, Y. ., Yasuma, R. ., Krueger, L. ., Gelfand, B. ., & 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. ., Hufnagel, R. ., Rebelo, A. ., Zanna, C. ., Patel, N. ., Gonzalez, M. ., … Dallman, J. . (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. ., Arno, G. ., Hein, N. ., Hersheson, J. ., Prasad, M. ., Anderson, Y. ., … Ahmed, Z. . (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. ., Wilson, S. ., Titialii-Torres, K. ., Bills, J. ., Krueger, L. ., Petersen, R. ., … Morris, A. . (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. ., Wilson, S. ., Titialii-Torres, K. ., Bills, J. ., Krueger, L. ., Petersen, R. ., … Morris, A. . (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. ., & Morris, A. . (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. ., Sethna, S. ., Krueger, L. ., Yang, M. ., & Hufnagel, R. . (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. ., & Morris, A. . 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)