Jill M. Weimer, Ph.D.

2006 University of Rochester, Rochester, NY 
Neuroscience Biology
"Jill Weimer"
Mean distance: 17.71 (cluster 11)


Sign in to add mentor
Eva Anton grad student
Howard J. Federoff grad student 2006 Rochester
 (Systematic analysis of cellular and behavioural changes in the Cln3-/- mouse model of Batten disease.)
BETA: Related publications


You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Moutal A, White KA, Chefdeville A, et al. (2019) Dysregulation of CRMP2 Post-Translational Modifications Drive Its Pathological Functions. Molecular Neurobiology
Johnson TB, Cain JT, White KA, et al. (2019) Therapeutic landscape for Batten disease: current treatments and future prospects. Nature Reviews. Neurology
Poppens MJ, Cain JT, Johnson TB, et al. (2019) Tracking sex-dependent differences in a mouse model of CLN6-Batten disease. Orphanet Journal of Rare Diseases. 14: 19
Johnson TB, Mechels K, Anderson RE, et al. (2018) Characterization of a recurrent missense mutation in the forkhead DNA-binding domain of FOXP1. Scientific Reports. 8: 16161
Madeo M, Colbert PL, Vermeer DW, et al. (2018) Cancer exosomes induce tumor innervation. Nature Communications. 9: 4284
Timm D, Cain JT, Geraets RD, et al. (2018) Searching for novel biomarkers using a mouse model of CLN3-Batten disease. Plos One. 13: e0201470
White KA, Swier VJ, Cain JT, et al. (2018) A porcine model of neurofibromatosis type 1 that mimics the human disease. Jci Insight. 3
Beraldi R, Meyerholz DK, Savinov A, et al. (2017) Genetic Ataxia Telangiectasia porcine model phenocopies the multisystemic features of the human disease. Biochimica Et Biophysica Acta
Geraets RD, Langin LM, Cain JT, et al. (2017) A tailored mouse model of CLN2 disease: A nonsense mutant for testing personalized therapies. Plos One. 12: e0176526
Cain JT, Kim DI, Quast M, et al. (2017) Nonsense pathogenic variants in exon 1 of PHOX2B lead to translational reinitiation in congenital central hypoventilation syndrome. American Journal of Medical Genetics. Part A
See more...