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For: Salas-Huetos A, Tüttelmann F, Wyrwoll MJ, Kliesch S, Lopes AM, Goncalves J, Boyden SE, Wöste M, Hotaling JM, Nagirnaja L, Conrad DF, Carrell DT, Aston KI; GEMINI Consortium. Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermia. Hum Genet 2021;140:217-27. [PMID: 33211200 DOI: 10.1007/s00439-020-02236-1] [Cited by in Crossref: 18] [Cited by in F6Publishing: 19] [Article Influence: 9.0] [Reference Citation Analysis]
Number Citing Articles
1 Siebert-kuss LM, Krenz H, Tekath T, Wöste M, Di Persio S, Terwort N, Wyrwoll MJ, Cremers J, Wistuba J, Dugas M, Kliesch S, Schlatt S, Tüttelmann F, Gromoll J, Neuhaus N, Laurentino S. Transcriptome analyses in infertile men reveal germ cell–specific expression and splicing patterns. Life Sci Alliance 2023;6:e202201633. [DOI: 10.26508/lsa.202201633] [Reference Citation Analysis]
2 Kang C, Bertolla R, Pagani R. The '-ics' of male reproduction: genomics, epigenetics, proteomics, metabolomics, and microbiomics. Curr Opin Urol 2022. [PMID: 36210759 DOI: 10.1097/MOU.0000000000001052] [Reference Citation Analysis]
3 Wyrwoll MJ, Gaasbeek CM, Golubickaite I, Stakaitis R, Oud MS, Nagirnaja L, Dion C, Sindi EB, Leitch HG, Jayasena CN, Sironen A, Dicke AK, Rotte N, Stallmeyer B, Kliesch S, Grangeiro CHP, Araujo TF, Lasko P, D'Hauwers K, Smits RM, Ramos L, Xavier MJ, Conrad DF, Almstrup K, Veltman JA, Tüttelmann F, van der Heijden GW; Genetics of Male Infertility Initiative (GEMINI) consortium. The piRNA-pathway factor FKBP6 is essential for spermatogenesis but dispensable for control of meiotic LINE-1 expression in humans. Am J Hum Genet 2022:S0002-9297(22)00405-0. [PMID: 36150389 DOI: 10.1016/j.ajhg.2022.09.002] [Reference Citation Analysis]
4 Jensen CFS, Wang D, Mamsen LS, Giwercman A, Jørgensen N, Fode M, Ohl D, Dong L, Hildorf SE, Pors SE, Fedder J, Ntemou E, Andersen CY, Sønksen J. Sertoli and Germ Cells Within Atrophic Seminiferous Tubules of Men With Non-Obstructive Azoospermia. Front Endocrinol (Lausanne) 2022;13:825904. [PMID: 35721721 DOI: 10.3389/fendo.2022.825904] [Reference Citation Analysis]
5 Zhang Q, Tao C, Gao S, Li S, Xu B, Ke H, Wang Y, Zhang F, Qin Y, Zhang L, Guo T. Homozygous variant in KASH5 causes premature ovarian insufficiency by disordered meiotic homologous pairing. J Clin Endocrinol Metab 2022:dgac368. [PMID: 35708642 DOI: 10.1210/clinem/dgac368] [Reference Citation Analysis]
6 Tang X, Xiao Q, Wang X, He Y, Tian Y, Xia B, Guo Y, Huang J, Duan P, Tan Y. Single-Cell Transcriptomics-Based Study of Transcriptional Regulatory Features in the Non-Obstructive Azoospermia Testis. Front Genet 2022;13:875762. [DOI: 10.3389/fgene.2022.875762] [Reference Citation Analysis]
7 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]
8 Harmak H, Charoute H, Redouane S, Filali OA, Barakat A, Rouba H, Harrison P. Computational Analysis of the Potential Impact of MTC Complex Missenses SNPs Associated with Male Infertility. BioMed Research International 2022;2022:1-18. [DOI: 10.1155/2022/1664825] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
9 Zhang K, Tarczykowska A, Gupta DK, Pendlebury DF, Zuckerman C, Nandakumar J, Shibuya H. The TERB1 MYB domain suppresses telomere erosion in meiotic prophase I. Cell Rep 2022;38:110289. [PMID: 35081355 DOI: 10.1016/j.celrep.2021.110289] [Reference Citation Analysis]
10 Cannarella R, Bertelli M, Condorelli RA, Vilaj M, La Vignera S, Jezek D, Calogero AE. Analysis of 29 Targeted Genes for Non-Obstructive Azoospermia: The Relationship between Genetic Testing and Testicular Histology. World J Mens Health 2022;40:e51. [DOI: 10.5534/wjmh.220009] [Reference Citation Analysis]
11 Anifandis G, Samara M, Simopoulou M, Messini CI, Chatzimeletiou K, Thodou E, Daponte A, Georgiou I. Insights into the Role of Telomeres in Human Embryological Parameters. Opinions Regarding IVF. J Dev Biol 2021;9:49. [PMID: 34842724 DOI: 10.3390/jdb9040049] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
12 Wu H, Zhang X, Shen Q, Liu Y, Gao Y, Wang G, Lv M, Hua R, Xu Y, Zhou P, Wei Z, Tao F, He X, Cao Y, Liu M. A homozygous loss-of-function mutation in FBXO43 causes human non-obstructive azoospermia. Clin Genet 2021. [PMID: 34595750 DOI: 10.1111/cge.14069] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
13 Sha Y, Liu W, Wei X, Zhu X, Tang B, Zhang X, Yang X, Wang Y, Wang X. Pathogenic variants of ATG4D in infertile men with non-obstructive azoospermia identified using whole-exome sequencing. Clin Genet 2021;100:280-91. [PMID: 33988247 DOI: 10.1111/cge.13995] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
14 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]