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Dive into the research topics where Erika Finanger is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Collaborations and top research areas from the last five years
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Long-Term Evaluation of Givinostat in Duchenne Muscular Dystrophy, and Natural History Comparisons
the Givinostat Study 51 Investigators, the Cooperative International Neuromuscular Research Group (CINRG) Duchenne Natural History Study (DNHS) Investigators & the ImagingDMD Investigators, Nov 1 2025, In: Annals of Clinical and Translational Neurology. 12, 11, p. 2335-2348 14 p.Research output: Contribution to journal › Article › peer-review
Open Access5 Link opens in a new tab Scopus citations -
New hope for older SMA patients with next-generation self-complementary AAV gene therapy
Nakai, H., Finanger, E. L. & Samulski, R. J., Oct 1 2025, In: Molecular Therapy. 33, 10, p. 4662-4664 3 p.Research output: Contribution to journal › Comment/debate › peer-review
Open Access -
Characterization of severe COL6-related dystrophy due to the recurrent variant COL6A1 c.930+189C>T
Foley, A. R., Bolduc, V., Guirguis, F., Donkervoort, S., Hu, Y., Orbach, R., Mccarty, R. M., Sarathy, A., Norato, G., Cummings, B. B., Lek, M., Sarkozy, A., Butterfield, R. J., Kirschner, J., Nascimento, A., Natera-De Benito, D., Quijano-Roy, S., Stojkovic, T., Merlini, L. & Comi, G. & 49 others, , Sep 1 2025, In: Brain. 148, 9, p. 3215-3227 13 p.Research output: Contribution to journal › Article › peer-review
Open Access1 Link opens in a new tab Scopus citations -
Meaningful changes in motor function in Duchenne muscular dystrophy (DMD): A multi-center study
PRO-DMD-01 study investigators, Association Française contre les Myopathies, The UK NorthStar Clinical Network, ImagingDMD investigators & cTAP, Jul 1 2024, In: PloS one. 19, 7 July, e0304984.Research output: Contribution to journal › Article › peer-review
Open Access9 Link opens in a new tab Scopus citations -
Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections
Deciphering Developmental Disorders, Genomics England Research Consortium & Undiagnosed Disease Network, Feb 1 2024, In: Genetics in Medicine. 26, 2, 101023.Research output: Contribution to journal › Article › peer-review
Open Access4 Link opens in a new tab Scopus citations