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Cited by in F6Publishing
For: Guo T, Tu CF, Yang DH, Ding SZ, Lei C, Wang RC, Liu L, Kang X, Shen XQ, Yang YF, Tan ZP, Tan YQ, Luo H. Bi-allelic BRWD1 variants cause male infertility with asthenoteratozoospermia and likely primary ciliary dyskinesia. Hum Genet 2021;140:761-73. [PMID: 33389130 DOI: 10.1007/s00439-020-02241-4] [Cited by in Crossref: 1] [Cited by in F6Publishing: 10] [Article Influence: 1.0] [Reference Citation Analysis]
Number Citing Articles
1 Liu Y, Lei C, Wang R, Yang D, Yang B, Xu Y, Lu C, Wang L, Ding S, Guo T, Liu S, Luo H. Case Report: Whole-Exome Sequencing-Based Copy Number Variation Analysis Identified a Novel DRC1 Homozygous Exon Deletion in a Patient With Primary Ciliary Dyskinesia. Front Genet 2022;13:940292. [PMID: 35873463 DOI: 10.3389/fgene.2022.940292] [Reference Citation Analysis]
2 Guo T, Lu C, Yang D, Lei C, Liu Y, Xu Y, Yang B, Wang R, Luo H. Case Report: DNAAF4 Variants Cause Primary Ciliary Dyskinesia and Infertility in Two Han Chinese Families. Front Genet 2022;13:934920. [DOI: 10.3389/fgene.2022.934920] [Reference Citation Analysis]
3 Hou M, Xi Q, Zhu L, Jia W, Liu Z, Wang C, Zhou X, Zhang D, Xing C, Peng X, Luo Y, Jin L, Li Z, Zhang X. Novel Compound Heterozygous Mutation in FSIP2 Causes Multiple Morphological Abnormalities of the Sperm Flagella (MMAF) and Male Infertility. Reprod Sci . [DOI: 10.1007/s43032-022-00965-4] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Yu X, Yuan L, Deng S, Xia H, Tu X, Deng X, Huang X, Cao X, Deng H. Identification of DNAH17 Variants in Han-Chinese Patients With Left–Right Asymmetry Disorders. Front Genet 2022;13:862292. [DOI: 10.3389/fgene.2022.862292] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Hu T, Meng L, Tan C, Luo C, He WB, Tu C, Zhang H, Du J, Nie H, Lu GX, Lin G, Tan YQ. Biallelic CFAP61 variants cause male infertility in humans and mice with severe oligoasthenoteratozoospermia. J Med Genet 2022:jmedgenet-2021-108249. [PMID: 35387802 DOI: 10.1136/jmedgenet-2021-108249] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Xu Y, Yang B, Lei C, Yang D, Ding S, Lu C, Wang L, Guo T, Wang R, Luo H. Novel Compound Heterozygous Variants in CCDC40 Associated with Primary Ciliary Dyskinesia and Multiple Morphological Abnormalities of the Sperm Flagella. PGPM 2022;Volume 15:341-50. [DOI: 10.2147/pgpm.s359821] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
7 Ma A, Zeb A, Ali I, Zhao D, Khan A, Zhang B, Zhou J, Khan R, Zhang H, Zhang Y, Khan I, Shah W, Ali H, Javed AR, Ma H, Shi Q. Biallelic Variants in CFAP61 Cause Multiple Morphological Abnormalities of the Flagella and Male Infertility. Front Cell Dev Biol 2022;9:803818. [DOI: 10.3389/fcell.2021.803818] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Lei C, Yang D, Wang R, Ding S, Wang L, Guo T, Luo H. DRC1 deficiency caused primary ciliary dyskinesia and MMAF in a Chinese patient. J Hum Genet 2021. [PMID: 34815526 DOI: 10.1038/s10038-021-00985-z] [Cited by in F6Publishing: 4] [Reference Citation Analysis]
9 Ma H, Zhang B, Khan A, Zhao D, Ma A, Jianteng Z, Khan I, Khan K, Zhang H, Zhang Y, Xiaohua J, Dil S, Zeb A, Rahim F, Shi Q. Novel frameshift mutation in STK33 is associated with asthenozoospermia and multiple morphological abnormality of the flagella. Hum Mol Genet 2021:ddab165. [PMID: 34155512 DOI: 10.1093/hmg/ddab165] [Cited by in F6Publishing: 5] [Reference Citation Analysis]
10 Azhar M, Altaf S, Uddin I, Cheng J, Wu L, Tong X, Qin W, Bao J. Towards Post-Meiotic Sperm Production: Genetic Insight into Human Infertility from Mouse Models. Int J Biol Sci 2021;17:2487-503. [PMID: 34326689 DOI: 10.7150/ijbs.60384] [Cited by in F6Publishing: 1] [Reference Citation Analysis]