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

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)