Associated Papers
Primary ovarian insufficiency due to homozygous variants in the homeobox transcription factor NOBOX.
Zidoune H et al.
Molecular Biology Reports, 2025
Reclassifying NOBOX variants in primary ovarian insufficiency cases with a corrected gene model and a novel quantitative framework.
Veitia RA et al.
Human Reproduction (oxford, England), 2025
40246288 (PubMed )
Supplement: deaf058_supplementary_table_s2.docx
NOBOX gene variants in premature ovarian insufficiency: ethnicity-dependent insights.
Jordan P et al.
Journal of Assisted Reproduction and Genetics, 2024
Sumoylation regulates functional properties of the oocyte transcription factors SOHLH1 and NOBOX.
Patton BK et al.
Faseb Journal : Official Publication of the Federation of American Societies for Experimental Biology, 2023
Compound heterozygous null mutations of NOBOX in sisters with delayed puberty and primary amenorrhea.
Sassi A et al.
Molecular Genetics & Genomic Medicine, 2021
Molecular genetics of infertility: loss-of-function mutations in humans and corresponding knockout/mutated mice.
Jiao SY et al.
Human Reproduction Update, 2021
The GenomeAsia 100K Project enables genetic discoveries across Asia.
Unknown Author
Nature, 2019
31802016 (PubMed )
Supplement: 41586_2019_1793_MOESM3_ESM.xlsx › S4b_-_Disease_Var
A novel homozygous 1-bp deletion in the NOBOX gene in two Brazilian sisters with primary ovarian failure.
França MM et al.
Endocrine, 2017
R-spondin2, a novel target of NOBOX: identification of variants in a cohort of women with primary ovarian insufficiency.
Bouilly J et al.
Journal of Ovarian Research, 2017
Aetiological coding sequence variants in non-syndromic premature ovarian failure: From genetic linkage analysis to next generation sequencing.
Laissue P
Molecular and Cellular Endocrinology, 2015
Genetics of premature ovarian failure.
Bilgin EM et al.
Current Opinion in Obstetrics & Gynecology, 2015
Ethnic specificity of variants of the ESR1, HK3, BRSK1 genes and the 8q22.3 locus: no association with premature ovarian failure (POF) in Serbian women.
Qin Y et al.
Maturitas, 2014
Novel NOBOX loss-of-function mutations account for 6.2% of cases in a large primary ovarian insufficiency cohort.
Bouilly J et al.
Human Mutation, 2011
Genetics of Female Infertility: Molecular Study of Newborn Ovary Homeobox Gene in Poor Ovarian Responders.
Batiha O et al.
Journal of Human Reproductive Sciences, 0
Select a paper to view details