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For: Tan C, Meng L, Lv M, He X, Sha Y, Tang D, Tan Y, Hu T, He W, Tu C, Nie H, Zhang H, Du J, Lu G, Fan LQ, Cao Y, Lin G, Tan YQ. Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice. Am J Hum Genet 2022;109:157-71. [PMID: 34932939 DOI: 10.1016/j.ajhg.2021.11.022] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
Number Citing Articles
1 Liu S, Wei W, Wang P, Liu C, Jiang X, Li T, Li F, Wu Y, Chen S, Sun K, Xu R. LOF variants identifying candidate genes of laterality defects patients with congenital heart disease. PLoS Genet 2022;18:e1010530. [DOI: 10.1371/journal.pgen.1010530] [Reference Citation Analysis]
2 Wang J, Wang W, Shen L, Zheng A, Meng Q, Li H, Yang S. Clinical detection, diagnosis and treatment of morphological abnormalities of sperm flagella: A review of literature. Front Genet 2022;13. [DOI: 10.3389/fgene.2022.1034951] [Reference Citation Analysis]
3 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]
4 Shi X, Geng H, Yu H, Hu X, Wang G, Yang J, Zhao H, Bottillo I. Biallelic Variants in CCDC39 Gene Lead to Primary Ciliary Dyskinesia and Kartagener Syndrome. BioMed Research International 2022;2022:1-8. [DOI: 10.1155/2022/7130555] [Cited by in F6Publishing: 1] [Reference Citation Analysis]