Analysis of short tandem repeats linked to polyglutamine diseases from whole-genome sequencing reveals intermediate alleles of HTT associated with an early disease onset in C9orf72 carriers.

Barbier M, Gareau T, Camuzat A, Guillaud-Bataille M, Boluda S, Clot F, Araktingi L, Borroni B, van der Zee J, Ghidoni R, Bellini S, Galimberti D, Rossi G, Nacmias B, De la Casa-Fages B, Pastor P, French Clinical and Genetic Research Network on FTD/FTD-ALS and PrevDemALS Study Groups, Latouche M, le Guern E, Durr A, Laquerrière A, Moccia R, Seilhean D, Alvarez V, Le Ber I

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DOI
10.1093/braincomms/fcaf220
Published
2025
Container
Brain communications
Publisher
Not recorded
Open access
yes

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BibTeX

@article{allodium:10.1093/braincomms/fcaf220,
  title = {Analysis of short tandem repeats linked to polyglutamine diseases from whole-genome sequencing reveals intermediate alleles of HTT associated with an early disease onset in C9orf72 carriers.},
  author = {Barbier M and Gareau T and Camuzat A and Guillaud-Bataille M and Boluda S and Clot F and Araktingi L and Borroni B and van der Zee J and Ghidoni R and Bellini S and Galimberti D and Rossi G and Nacmias B and De la Casa-Fages B and Pastor P and French Clinical and Genetic Research Network on FTD/FTD-ALS and PrevDemALS Study Groups and Latouche M and le Guern E and Durr A and Laquerrière A and Moccia R and Seilhean D and Alvarez V and Le Ber I},
  year = {2025},
  journal = {Brain communications},
  doi = {10.1093/braincomms/fcaf220},
  url = {https://doi.org/10.1093/braincomms/fcaf220}
}

RIS

TY  - JOUR
TI  - Analysis of short tandem repeats linked to polyglutamine diseases from whole-genome sequencing reveals intermediate alleles of HTT associated with an early disease onset in C9orf72 carriers.
AU  - Barbier M
AU  - Gareau T
AU  - Camuzat A
AU  - Guillaud-Bataille M
AU  - Boluda S
AU  - Clot F
AU  - Araktingi L
AU  - Borroni B
AU  - van der Zee J
AU  - Ghidoni R
AU  - Bellini S
AU  - Galimberti D
AU  - Rossi G
AU  - Nacmias B
AU  - De la Casa-Fages B
AU  - Pastor P
AU  - French Clinical and Genetic Research Network on FTD/FTD-ALS and PrevDemALS Study Groups
AU  - Latouche M
AU  - le Guern E
AU  - Durr A
AU  - Laquerrière A
AU  - Moccia R
AU  - Seilhean D
AU  - Alvarez V
AU  - Le Ber I
PY  - 2025
JO  - Brain communications
DO  - 10.1093/braincomms/fcaf220
UR  - https://doi.org/10.1093/braincomms/fcaf220
ER  - 

APA

M, B., T, G., A, C., M, G., S, B., F, C., L, A., B, B., J, V. D. Z., R, G., S, B., D, G., G, R., B, N., B, D. L. C., P, P., Groups, F. C. A. G. R. N. O. F. A. P. S., M, L., E, L. G., A, D., A, L., R, M., D, S., V, A., & I, L. B. (2025). Analysis of short tandem repeats linked to polyglutamine diseases from whole-genome sequencing reveals intermediate alleles of HTT associated with an early disease onset in C9orf72 carriers.. Brain communications. https://doi.org/10.1093/braincomms/fcaf220

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