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For: Hou D, Yao C, Xu B, Luo W, Ke H, Li Z, Qin Y, Guo T. Variations of C14ORF39 and SYCE1 identified in idiopathic premature ovarian insufficiency and nonobstructive azoospermia. J Clin Endocrinol Metab 2021:dgab777. [PMID: 34718620 DOI: 10.1210/clinem/dgab777] [Cited by in Crossref: 4] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Zeng Y, Li L, Li Q, Hu J, Zhang N, Wu L, Yan Z, Qu R, Dong J, Liu R, Choy KW, Wang L, Sang Q, Guan Y, Chen B. Genetic screening in patients with ovarian dysfunction. Clin Genet 2023;103:352-7. [PMID: 36373164 DOI: 10.1111/cge.14267] [Reference Citation Analysis]
2 Willems M, Olsen C, Caljon B, Vloeberghs V, De Schepper J, Tournaye H, Van Saen D, Goossens E. Transcriptomic differences between fibrotic and non-fibrotic testicular tissue reveal possible key players in Klinefelter syndrome-related testicular fibrosis. Sci Rep 2022;12:21518. [PMID: 36513788 DOI: 10.1038/s41598-022-26011-6] [Reference Citation Analysis]
3 Xu B, Li Z, Li S, Ke H, Zhang Q, Qin Y, Guo T. Pathogenic variants in TSC2 might cause premature ovarian insufficiency through activated mTOR induced hyperactivation of primordial follicles. Fertil Steril 2022;118:1139-49. [PMID: 36229297 DOI: 10.1016/j.fertnstert.2022.08.853] [Reference Citation Analysis]
4 Czukiewska SM, Chuva de Sousa Lopes SM. Fetal germ cell development in humans, a link with infertility. Semin Cell Dev Biol 2022;131:58-65. [PMID: 35431137 DOI: 10.1016/j.semcdb.2022.03.035] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
5 Wang Y, Yang Y, Li Y, Chen M. Identification of sex determination locus in sea cucumber Apostichopus japonicus using genome-wide association study. BMC Genomics 2022;23:391. [PMID: 35606723 DOI: 10.1186/s12864-022-08632-3] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
6 Wu H, Zhang X, Hua R, Li Y, Cheng L, Li K, Liu Y, Gao Y, Shen Q, Wang G, Lv M, Xu Y, He X, Cao Y, Liu M. Homozygous missense mutation in CCDC155 disrupts the transmembrane distribution of CCDC155 and SUN1, resulting in non-obstructive azoospermia and premature ovarian insufficiency in humans. Hum Genet 2022. [PMID: 35587281 DOI: 10.1007/s00439-022-02459-4] [Reference Citation Analysis]
7 Kherraf ZE, Cazin C, Bouker A, Fourati Ben Mustapha S, Hennebicq S, Septier A, Coutton C, Raymond L, Nouchy M, Thierry-Mieg N, Zouari R, Arnoult C, Ray PF. Whole-exome sequencing improves the diagnosis and care of men with non-obstructive azoospermia. Am J Hum Genet 2022;109:508-17. [PMID: 35172124 DOI: 10.1016/j.ajhg.2022.01.011] [Cited by in Crossref: 9] [Cited by in F6Publishing: 8] [Article Influence: 9.0] [Reference Citation Analysis]