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Experimental Neurology|September 24, 2025
Animal models of Chiari malformation types 1 and 2: Mechanistic insights and translational challengesWilliam Davalan, Qiang Li, Andrew T Hale, et al.Journal of Neurosurgery. Pediatrics|May 2, 2025
Clinical phenotypes among patients with familial forms of Chiari malformation type 1Kedous Y Mekbib, William Muñoz, Garrett Allington, et al.The Journal of Clinical Investigation|May 15, 2026
Towards precision medicine for brain arteriovenous malformationsAndrew T Hale, Adam J Kundishora, Pazhanichamy Kalailingam, et al.Ophthalmology|January 15, 2022
Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its DevelopmentMark J Simcoe, Ameet Shah, Baojian Fan, et al.Proceedings of the National Academy of Sciences of the United States of America|May 5, 2025
Single-cell elderly blood-CSF atlas implicates peripherally influenced immune dysregulation in normal pressure hydrocephalusPhan Q Duy, Emre Kiziltug, Ana B W Greenberg, et al.Human Molecular Genetics|December 19, 2018
Non-Synonymous variants in premelanosome protein (PMEL) cause ocular pigment dispersion and pigmentary glaucomaAdrian A Lahola-Chomiak, Tim Footz, Kim Nguyen-Phuoc, et al.Brain : a Journal of Neurology|December 16, 2024
De novo variants disrupt an LDB1-regulated transcriptional network in congenital ventriculomegalyGarrett Allington, Neel H Mehta, Evan Dennis, et al.Human Mutation|December 19, 2021
EFEMP1 rare variants cause familial juvenile-onset open-angle glaucomaEdward Ryan A Collantes, Manuel S Delfin, Baojian Fan, et al.Science Translational Medicine|July 8, 2026
Developmental genetic determinants of the human cerebrospinal fluid-ventricular systemGarrett Allington, Evan Dennis, Qiang Li, et al.Pageof 2