Tucker, EJ, Gutfreund, N, Belaud‐Rotureau, M, Gilot, D, Brun, T, Kline, BL, Bell, KM, Domin‐Bernhard, M, Théard, C, Touraine, P, et al.
Dominant TP63 missense variants lead to constitutive activation and premature ovarian insufficiency.
Human Mutation
43(10)
:
1443 -1453
2022
view publication
Marzouni, ET, Stern, C, Sinclair, AH, Tucker, EJ.
Stem Cells and Organs-on-chips: New Promising Technologies for Human Infertility Treatment.
Endocrine Reviews
43(5)
:
878 -906
2022
view publication
Nakagawa, R, Takasawa, K, Gau, M, Tsuji-Hosokawa, A, Kawaji, H, Murakawa, Y, Takada, S, Mikami, M, Narumi, S, Fukami, M, et al.
Two ovarian candidate enhancers, identified by time series enhancer RNA analyses, harbor rare genetic variations identified in ovarian insufficiency..
Human Molecular Genetics
31(13)
:
2223 -2235
2022
view publication
Sreenivasan, R, Bell, K, van den Bergen, J, Robevska, G, Belluoccio, D, Dahiya, R, Leong, GM, Dulon, J, Touraine, P, Tucker, EJ, et al.
Whole exome sequencing reveals copy number variants in individuals with disorders of sex development.
Molecular and Cellular Endocrinology
546:
111570
2022
view publication
Tucker, EJ, Bell, KM, Robevska, G, van den Bergen, J, Ayers, KL, Listyasari, N, Faradz, SM, Dulon, J, Bakhshalizadeh, S, Sreenivasan, R, et al.
Meiotic genes in premature ovarian insufficiency: variants in HROB and REC8 as likely genetic causes.
European Journal of Human Genetics
30(2)
:
219 -228
2022
view publication