James J. Fink
Affiliations: | 2013- | University of Connecticut Health Center, Farmington, CT, United States |
Area:
iPSC physiology and plasticityGoogle:
"James Fink"Mean distance: 16.94 (cluster 6) | S | N | B | C | P |
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Publications
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| Fink JJ, Delaney-Busch N, Dawes R, et al. (2024) Deep functional measurements of Fragile X syndrome human neurons reveal multiparametric electrophysiological disease phenotype. Communications Biology. 7: 1447 |
| Fink JJ, Schreiner JD, Bloom JE, et al. (2021) Hyperexcitable Phenotypes in Induced Pluripotent Stem Cell-Derived Neurons From Patients With 15q11-q13 Duplication Syndrome, a Genetic Form of Autism. Biological Psychiatry |
| Sirois CL, Bloom JE, Fink JJ, et al. (2020) Abundance and localization of human UBE3A protein isoforms. Human Molecular Genetics |
| Germain N, Sirois C, Fink J, et al. (2019) CELLULAR PHENOTYPES OF ANGELMAN AND DUP15Q SYNDROME INDUCED PLURIPOTENT STEM CELL-DERIVED NEURONS European Neuropsychopharmacology. 29: S1060 |
| Fink JJ, Levine ES. (2018) Uncovering True Cellular Phenotypes: Using Induced Pluripotent Stem Cell-Derived Neurons to Study Early Insults in Neurodevelopmental Disorders. Frontiers in Neurology. 9: 237 |
| Fink JJ, Robinson TM, Germain ND, et al. (2017) Disrupted neuronal maturation in Angelman syndrome-derived induced pluripotent stem cells. Nature Communications. 8: 15038 |
| Germain ND, Chen PF, Plocik AM, et al. (2014) Gene expression analysis of human induced pluripotent stem cell-derived neurons carrying copy number variants of chromosome 15q11-q13.1. Molecular Autism. 5: 44 |