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For: Yuan P, Liang ZK, Liang H, Zheng LY, Li D, Li J, Zhang J, Tian J, Lai LH, Zhang K, He ZY, Zhang QX, Wang WJ. Expanding the phenotypic and genetic spectrum of Chinese patients with congenital absence of vas deferens bearing CFTR and ADGRG 2 alleles. Andrology 2019;7:329-40. [DOI: 10.1111/andr.12592] [Cited by in Crossref: 25] [Cited by in F6Publishing: 25] [Article Influence: 8.3] [Reference Citation Analysis]
Number Citing Articles
1 Feng J, Zhang Y, Yang X, Zhang Y. Heterogeneous spectrum of CFTR gene mutations in Chinese patients with CAVD and the dilemma of genetic blocking strategy. Reproduction 2022:REP-21-0315. [PMID: 35913788 DOI: 10.1530/REP-21-0315] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
2 Cai Z, Li H. Congenital Bilateral Absence of the Vas Deferens. Front Genet 2022;13:775123. [DOI: 10.3389/fgene.2022.775123] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Cheng H, Yang S, Meng Q, Zheng B, Gu Y, Wang L, Song T, Xu C, Wang G, Han M, Shen L, Ding J, Li H, Ouyang J. Genetic analysis and intracytoplasmic sperm injection outcomes of Chinese patients with congenital bilateral absence of vas deferens. J Assist Reprod Genet 2022. [PMID: 35119551 DOI: 10.1007/s10815-022-02417-z] [Reference Citation Analysis]
4 Zou C, Yu D, Geng H, Lan X, Sun W. A patient with 47, XYY mosaic karyotype and congenital absence of bilateral vas deferens: a case report and literature review. BMC Urol 2022;22:16. [PMID: 35109852 DOI: 10.1186/s12894-022-00965-1] [Reference Citation Analysis]
5 Krausz C, Rosta V, Swerdloff RS, Wang C. Genetics of Male Infertility. Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics 2022. [DOI: 10.1016/b978-0-12-815236-2.00010-2] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
6 Li Q, Shen Y, Zhao LJ, Wang JB, Huang X. Mutations in CFTR genes are associated with oligoasthenospermia in infertile men undergoing IVF. Andrologia 2021;:e14355. [PMID: 34931337 DOI: 10.1111/and.14355] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
7 Tan MQ, Huang WJ, Lan FH, Xu YJ, Zheng MY, Tang Y. Genetic mutation analysis of 22 patients with congenital absence of vas deferens: A single-center study†. Biol Reprod 2021:ioab194. [PMID: 34673937 DOI: 10.1093/biolre/ioab194] [Reference Citation Analysis]
8 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]
9 Wong R, Gu K, Ko Y, Patel P. Congenital absence of the vas deferens: Cystic fibrosis transmembrane regulatory gene mutations. Best Pract Res Clin Endocrinol Metab 2020;34:101476. [PMID: 33353780 DOI: 10.1016/j.beem.2020.101476] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
10 Sedova AO, Shtaut MI, Bragina EE, Repina SA, Sorokina TM, Kurilo LF, Chernykh VB. Comprehensive semen examination in cystic fibrosis patients without seminal ducts obstruction. Androl genit hir 2020;21:44-55. [DOI: 10.17650/2070-9781-2020-21-3-44-55] [Reference Citation Analysis]
11 Zhang D, Wang Y, Lin H, Sun Y, Wang M, Jia Y, Yu X, Jiang H, Xu W, Sun JP, Xu Z. Function and therapeutic potential of G protein-coupled receptors in epididymis. Br J Pharmacol 2020;177:5489-508. [PMID: 32901914 DOI: 10.1111/bph.15252] [Cited by in Crossref: 8] [Cited by in F6Publishing: 10] [Article Influence: 4.0] [Reference Citation Analysis]
12 Karavolos S, Panagiotopoulou N, Alahwany H, Martins da Silva S. An update on the management of male infertility. Obstet Gynecol 2020;22:267-74. [DOI: 10.1111/tog.12688] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
13 Ma C, Wang R, Li T, Li H, Wang B. Analysis of CNVs of CFTR gene in Chinese Han population with CBAVD. Mol Genet Genomic Med 2020;8:e1506. [PMID: 32951344 DOI: 10.1002/mgg3.1506] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
14 Oates RD. Commentary on: A novel hemizygous loss-of-function mutation in ADGRG2 causes male infertility with congenital bilateral absence of the vas deferens. J Assist Reprod Genet 2020;37:1327-1328. [DOI: 10.1007/s10815-020-01834-2] [Reference Citation Analysis]
15 Wu H, Gao Y, Ma C, Shen Q, Wang J, Lv M, Liu C, Cheng H, Zhu F, Tian S, Elshewy N, Ni X, Tan Q, Xu X, Zhou P, Wei Z, Zhang F, He X, Cao Y. A novel hemizygous loss-of-function mutation in ADGRG2 causes male infertility with congenital bilateral absence of the vas deferens. J Assist Reprod Genet 2020;37:1421-9. [PMID: 32314195 DOI: 10.1007/s10815-020-01779-6] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 3.5] [Reference Citation Analysis]
16 Wang H, An M, Liu Y, Hu K, Jin Y, Xu S, Chen B, Lu M. Genetic diagnosis and sperm retrieval outcomes for Chinese patients with congenital bilateral absence of vas deferens. Andrology 2020;8:1064-9. [PMID: 32020786 DOI: 10.1111/andr.12769] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
17 Bieth E, Hamdi SM, Mieusset R. Genetics of the congenital absence of the vas deferens. Hum Genet 2021;140:59-76. [PMID: 32025909 DOI: 10.1007/s00439-020-02122-w] [Cited by in Crossref: 25] [Cited by in F6Publishing: 21] [Article Influence: 12.5] [Reference Citation Analysis]
18 Sharma S, Kumaran GK, Hanukoglu I. High-resolution imaging of the actin cytoskeleton and epithelial sodium channel, CFTR, and aquaporin-9 localization in the vas deferens. Mol Reprod Dev 2020;87:305-19. [PMID: 31950584 DOI: 10.1002/mrd.23317] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
19 Pagin A, Bergougnoux A, Girodon E, Reboul MP, Willoquaux C, Kesteloot M, Raynal C, Bienvenu T, Humbert M, Lalau G, Bieth E. Novel ADGRG2 truncating variants in patients with X-linked congenital absence of vas deferens. Andrology 2020;8:618-24. [PMID: 31845523 DOI: 10.1111/andr.12744] [Cited by in Crossref: 14] [Cited by in F6Publishing: 15] [Article Influence: 4.7] [Reference Citation Analysis]
20 Vockel M, Riera-Escamilla A, Tüttelmann F, Krausz C. The X chromosome and male infertility. Hum Genet 2021;140:203-15. [PMID: 31875237 DOI: 10.1007/s00439-019-02101-w] [Cited by in Crossref: 24] [Cited by in F6Publishing: 16] [Article Influence: 8.0] [Reference Citation Analysis]
21 Ferlin A, Stuppia L. Diagnostics of CFTR-negative patients with congenital bilateral absence of vas deferens: which mutations are of most interest? Expert Rev Mol Diagn 2020;20:265-7. [PMID: 31854215 DOI: 10.1080/14737159.2020.1707081] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
22 Ge B, Zhang M, Wang R, Wang D, Li T, Li H, Wang B. A rare frameshift variant in trans with the IVS9-5T allele of CFTR in a Chinese pedigree with congenital aplasia of vas deferens. J Assist Reprod Genet 2019;36:2541-5. [PMID: 31709488 DOI: 10.1007/s10815-019-01617-4] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.7] [Reference Citation Analysis]
23 Thirumavalavan N, Gabrielsen JS, Lamb DJ. Where are we going with gene screening for male infertility? Fertil Steril 2019;111:842-50. [PMID: 31029238 DOI: 10.1016/j.fertnstert.2019.03.036] [Cited by in Crossref: 28] [Cited by in F6Publishing: 23] [Article Influence: 9.3] [Reference Citation Analysis]
24 Bassilana F, Nash M, Ludwig MG. Adhesion G protein-coupled receptors: opportunities for drug discovery. Nat Rev Drug Discov 2019;18:869-84. [PMID: 31462748 DOI: 10.1038/s41573-019-0039-y] [Cited by in Crossref: 39] [Cited by in F6Publishing: 40] [Article Influence: 13.0] [Reference Citation Analysis]