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For: Xavier MJ, Salas-Huetos A, Oud MS, Aston KI, Veltman JA. Disease gene discovery in male infertility: past, present and future. Hum Genet 2021;140:7-19. [PMID: 32638125 DOI: 10.1007/s00439-020-02202-x] [Cited by in Crossref: 24] [Cited by in F6Publishing: 26] [Article Influence: 12.0] [Reference Citation Analysis]
Number Citing Articles
1 Eggermann T. Imprinting Disorders in Humans. Handbook of Epigenetics 2023. [DOI: 10.1016/b978-0-323-91909-8.00001-3] [Reference Citation Analysis]
2 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]
3 Hardy J, Pollock N, Gingrich T, Sweet P, Ramesh A, Kuong J, Basar A, Jiang H, Hwang K, Vukina J, Jaffe T, Olszewska M, Kurpisz M, Yatsenko AN. Genomic testing for copy number and single nucleotide variants in spermatogenic failure. J Assist Reprod Genet 2022. [PMID: 35849255 DOI: 10.1007/s10815-022-02538-5] [Reference Citation Analysis]
4 Kamel A, Saberiyan M, Mirfakhraie R, Teimori H. Reduced expression of CFAP44 and CFAP44-AS1 may affect sperm motility and morphology. Andrologia 2022;:e14447. [PMID: 35470451 DOI: 10.1111/and.14447] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
5 Zhang X, Wang L, Ma Y, Wang Y, Liu H, Liu M, Qin L, Li J, Jiang C, Zhang X, Shan X, Liu Y, Li J, Li Y, Zheng R, Sun Y, Sun J, Leng X, Liang Y, Zhang F, Jiang X, Yang Y, Shen Y. CEP128 is involved in spermatogenesis in humans and mice. Nat Commun 2022;13:1395. [PMID: 35296684 DOI: 10.1038/s41467-022-29109-7] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
6 Moshkivskaya VA. Comparative analysis of the subjective perception of oneself as a future parent among married couples with different reproductive history. Vestn Mininskogo univ 2021;9. [DOI: 10.26795/2307-1281-2021-9-4-8] [Reference Citation Analysis]
7 Wang X, Qu M, Li Z, Long Y, Hong K, Li H. Valproic acid promotes the in vitro differentiation of human pluripotent stem cells into spermatogonial stem cell-like cells. Stem Cell Res Ther 2021;12:553. [PMID: 34715904 DOI: 10.1186/s13287-021-02621-1] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
8 Salehi N, Karimi-Jafari MH, Totonchi M, Amiri-Yekta A. Integration and gene co-expression network analysis of scRNA-seq transcriptomes reveal heterogeneity and key functional genes in human spermatogenesis. Sci Rep 2021;11:19089. [PMID: 34580317 DOI: 10.1038/s41598-021-98267-3] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
9 Nosková A, Hiltpold M, Janett F, Echtermann T, Fang ZH, Sidler X, Selige C, Hofer A, Neuenschwander S, Pausch H. Infertility due to defective sperm flagella caused by an intronic deletion in DNAH17 that perturbs splicing. Genetics 2021;217:iyaa033. [PMID: 33724408 DOI: 10.1093/genetics/iyaa033] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
10 Pacchierotti F, Ardoino L, Benassi B, Consales C, Cordelli E, Eleuteri P, Marino C, Sciortino M, Brinkworth MH, Chen G, McNamee JP, Wood AW, Hooijmans CR, de Vries RBM. Effects of Radiofrequency Electromagnetic Field (RF-EMF) exposure on male fertility and pregnancy and birth outcomes: Protocols for a systematic review of experimental studies in non-human mammals and in human sperm exposed in vitro. Environ Int 2021;157:106806. [PMID: 34454359 DOI: 10.1016/j.envint.2021.106806] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
11 Zhang X, Li M, Jiang X, Ma H, Fan S, Li Y, Yu C, Xu J, Khan R, Jiang H, Shi Q. Nuclear translocation of MTL5 from cytoplasm requires its direct interaction with LIN9 and is essential for male meiosis and fertility. PLoS Genet 2021;17:e1009753. [PMID: 34388164 DOI: 10.1371/journal.pgen.1009753] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
12 Eggermann T. Maternal Effect Mutations: A Novel Cause for Human Reproductive Failure. Geburtshilfe Frauenheilkd 2021;81:780-8. [PMID: 34294945 DOI: 10.1055/a-1396-4390] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [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 Hardy JJ, Wyrwoll MJ, Mcfadden W, Malcher A, Rotte N, Pollock NC, Munyoki S, Veroli MV, Houston BJ, Xavier MJ, Kasak L, Punab M, Laan M, Kliesch S, Schlegel P, Jaffe T, Hwang K, Vukina J, Brieño-Enríquez MA, Orwig K, Yanowitz J, Buszczak M, Veltman JA, Oud M, Nagirnaja L, Olszewska M, O'Bryan MK, Conrad DF, Kurpisz M, Tüttelmann F, Yatsenko AN; GEMINI Consortium. Variants in GCNA, X-linked germ-cell genome integrity gene, identified in men with primary spermatogenic failure. Hum Genet 2021;140:1169-82. [PMID: 33963445 DOI: 10.1007/s00439-021-02287-y] [Cited by in Crossref: 10] [Cited by in F6Publishing: 6] [Article Influence: 10.0] [Reference Citation Analysis]
15 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]
16 Pini T, Raubenheimer D, Simpson SJ, Crean AJ. Obesity and Male Reproduction; Placing the Western Diet in Context. Front Endocrinol (Lausanne) 2021;12:622292. [PMID: 33776921 DOI: 10.3389/fendo.2021.622292] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
17 La H, Yoo H, Lee EJ, Thang NX, Choi HJ, Oh J, Park JH, Hong K. Insights from the Applications of Single-Cell Transcriptomic Analysis in Germ Cell Development and Reproductive Medicine. Int J Mol Sci 2021;22:E823. [PMID: 33467661 DOI: 10.3390/ijms22020823] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
18 Singh NN, Hoffman S, Reddi PP, Singh RN. Spinal muscular atrophy: Broad disease spectrum and sex-specific phenotypes. Biochim Biophys Acta Mol Basis Dis 2021;1867:166063. [PMID: 33412266 DOI: 10.1016/j.bbadis.2020.166063] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 10.0] [Reference Citation Analysis]
19 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]
20 Nosková A, Hiltpold M, Janett F, Echtermann T, Fang Z, Sidler X, Selige C, Hofer A, Neuenschwander S, Pausch H. Infertility due to defective sperm flagella caused by an intronic deletion in DNAH17 that perturbs splicing.. [DOI: 10.1101/2020.10.16.333344] [Reference Citation Analysis]
21 Cannarella R, Precone V, Guerri G, Busetto GM, Di Renzo GC, Gerli S, Manara E, Dautaj A, Bertelli M, Calogero AE. Clinical Evaluation of a Custom Gene Panel as a Tool for Precision Male Infertility Diagnosis by Next-Generation Sequencing. Life (Basel) 2020;10:E242. [PMID: 33076341 DOI: 10.3390/life10100242] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 3.0] [Reference Citation Analysis]