Deep functional measurements of Fragile X syndrome human neurons reveal multiparametric electrophysiological disease phenotype.

Fink JJ, Delaney-Busch N, Dawes R, Nanou E, Folts C, Harikrishnan K, Hempel C, Upadhyay H, Nguyen T, Shroff H, Stoppel D, Ryan SJ, Jacques J, Grooms J, Berry-Kravis E, Bear MF, Williams LA, Gerber D, Bunnage M, Furey B, Dempsey GT.

Open source

DOI
10.1038/s42003-024-07120-6
Published
2024-11-06
Container
Commun Biol
Publisher
Not recorded
Open access
yes

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BibTeX

@article{allodium:10.1038/s42003-024-07120-6,
  title = {Deep functional measurements of Fragile X syndrome human neurons reveal multiparametric electrophysiological disease phenotype.},
  author = {Fink JJ and  Delaney-Busch N and  Dawes R and  Nanou E and  Folts C and  Harikrishnan K and  Hempel C and  Upadhyay H and  Nguyen T and  Shroff H and  Stoppel D and  Ryan SJ and  Jacques J and  Grooms J and  Berry-Kravis E and  Bear MF and  Williams LA and  Gerber D and  Bunnage M and  Furey B and  Dempsey GT.},
  year = {2024},
  journal = {Commun Biol},
  doi = {10.1038/s42003-024-07120-6},
  url = {https://doi.org/10.1038/s42003-024-07120-6}
}

RIS

TY  - JOUR
TI  - Deep functional measurements of Fragile X syndrome human neurons reveal multiparametric electrophysiological disease phenotype.
AU  - Fink JJ
AU  -  Delaney-Busch N
AU  -  Dawes R
AU  -  Nanou E
AU  -  Folts C
AU  -  Harikrishnan K
AU  -  Hempel C
AU  -  Upadhyay H
AU  -  Nguyen T
AU  -  Shroff H
AU  -  Stoppel D
AU  -  Ryan SJ
AU  -  Jacques J
AU  -  Grooms J
AU  -  Berry-Kravis E
AU  -  Bear MF
AU  -  Williams LA
AU  -  Gerber D
AU  -  Bunnage M
AU  -  Furey B
AU  -  Dempsey GT.
PY  - 2024
JO  - Commun Biol
DO  - 10.1038/s42003-024-07120-6
UR  - https://doi.org/10.1038/s42003-024-07120-6
ER  - 

APA

JJ, F., N, D., R, D., E, N., C, F., K, H., C, H., H, U., T, N., H, S., D, S., SJ, R., J, J., J, G., E, B., MF, B., LA, W., D, G., M, B., B, F., & GT., D. (2024). Deep functional measurements of Fragile X syndrome human neurons reveal multiparametric electrophysiological disease phenotype.. Commun Biol. https://doi.org/10.1038/s42003-024-07120-6

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