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Cited by in F6Publishing
For: Yao C, Yang C, Zhao L, Li P, Tian R, Chen H, Guo Y, Huang Y, Zhi E, Zhai J, Sun H, Zhang J, Hong Y, Zhang L, Ji Z, Zhang F, Zhou Z, Li Z. Bi-allelic SHOC1 loss-of-function mutations cause meiotic arrest and non-obstructive azoospermia. J Med Genet 2020:jmedgenet-2020-107042. [PMID: 32900840 DOI: 10.1136/jmedgenet-2020-107042] [Cited by in Crossref: 12] [Cited by in F6Publishing: 13] [Article Influence: 6.0] [Reference Citation Analysis]
Number Citing Articles
1 Huang S, Huang Y, Li S, He Y. Chromosome 17 translocation affects sperm morphology: Two case studies and literature review. Andrologia 2022;:e14620. [PMID: 36270636 DOI: 10.1111/and.14620] [Reference Citation Analysis]
2 Huang Y, Tian R, Xu J, Ji Z, Zhang Y, Zhao L, Yang C, Li P, Zhi E, Bai H, Han S, Luo J, Zhao J, Zhang J, Zhou Z, Li Z, Yao C. Novel copy number variations within SYCE1 caused meiotic arrest and non-obstructive azoospermia. BMC Med Genomics 2022;15:137. [PMID: 35718780 DOI: 10.1186/s12920-022-01288-8] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
3 Zhang Y, Li P, Liu N, Jing T, Ji Z, Yang C, Zhao L, Tian R, Chen H, Huang Y, Zhi E, Ou N, Bai H, Zhou Y, Li Z, Yao C. Novel Bi-Allelic Variants of FANCM Cause Sertoli Cell-Only Syndrome and Non-Obstructive Azoospermia. Front Genet 2021;12:799886. [PMID: 34976027 DOI: 10.3389/fgene.2021.799886] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
4 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: 4.0] [Reference Citation Analysis]
5 Ji Z, Yao C, Yang C, Huang C, Zhao L, Han X, Zhu Z, Zhi E, Liu N, Zhou Z, Li Z. Novel Hemizygous Mutations of TEX11 Cause Meiotic Arrest and Non-obstructive Azoospermia in Chinese Han Population. Front Genet 2021;12:741355. [PMID: 34621296 DOI: 10.3389/fgene.2021.741355] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Cioppi F, Rosta V, Krausz C. Genetics of Azoospermia. Int J Mol Sci 2021;22:3264. [PMID: 33806855 DOI: 10.3390/ijms22063264] [Cited by in Crossref: 22] [Cited by in F6Publishing: 24] [Article Influence: 22.0] [Reference Citation Analysis]
7 Fan S, Jiao Y, Khan R, Jiang X, Javed AR, Ali A, Zhang H, Zhou J, Naeem M, Murtaza G, Li Y, Yang G, Zaman Q, Zubair M, Guan H, Zhang X, Ma H, Jiang H, Ali H, Dil S, Shah W, Ahmad N, Zhang Y, Shi Q. Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humans. Am J Hum Genet 2021;108:324-36. [PMID: 33508233 DOI: 10.1016/j.ajhg.2021.01.010] [Cited by in Crossref: 25] [Cited by in F6Publishing: 27] [Article Influence: 25.0] [Reference Citation Analysis]