Exploring genetic variants in premature ovarian insufficiency: a cohort-based investigation of monogenic etiologies.

Sassi A, Peyrassol X, Marangoni M, Gheldof A, Van Dooren S, Alvaro Mercadal B, Pintiaux A, Antoine C, Abramowicz M, Désir J, Delbaere A.

Open source

DOI: 10.1210/jendso/bvag215
Published: 2026-10-28
Container: J Endocr Soc
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1210/jendso/bvag215,
  title = {Exploring genetic variants in premature ovarian insufficiency: a cohort-based investigation of monogenic etiologies.},
  author = {Sassi A and  Peyrassol X and  Marangoni M and  Gheldof A and  Van Dooren S and  Alvaro Mercadal B and  Pintiaux A and  Antoine C and  Abramowicz M and  Désir J and  Delbaere A.},
  year = {2026},
  journal = {J Endocr Soc},
  doi = {10.1210/jendso/bvag215},
  url = {https://doi.org/10.1210/jendso/bvag215}
}

RIS

TY  - JOUR
TI  - Exploring genetic variants in premature ovarian insufficiency: a cohort-based investigation of monogenic etiologies.
AU  - Sassi A
AU  -  Peyrassol X
AU  -  Marangoni M
AU  -  Gheldof A
AU  -  Van Dooren S
AU  -  Alvaro Mercadal B
AU  -  Pintiaux A
AU  -  Antoine C
AU  -  Abramowicz M
AU  -  Désir J
AU  -  Delbaere A.
PY  - 2026
JO  - J Endocr Soc
DO  - 10.1210/jendso/bvag215
UR  - https://doi.org/10.1210/jendso/bvag215
ER  -

APA

A, S., X, P., M, M., A, G., S, V. D., B, A. M., A, P., C, A., M, A., J, D., & A., D. (2026). Exploring genetic variants in premature ovarian insufficiency: a cohort-based investigation of monogenic etiologies.. J Endocr Soc. https://doi.org/10.1210/jendso/bvag215

Source records

europe-pmc · retrieved 2026-11-10T09:59:10.161Z