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For: Kasak L, Laan M. Monogenic causes of non-obstructive azoospermia: challenges, established knowledge, limitations and perspectives. Hum Genet 2021;140:135-54. [DOI: 10.1007/s00439-020-02112-y] [Cited by in Crossref: 18] [Cited by in F6Publishing: 23] [Article Influence: 9.0] [Reference Citation Analysis]
Number Citing Articles
1 Wang X, Li Z, Qu M, Xiong C, Li H. A homozygous PIWIL2 frameshift variant affects the formation and maintenance of human-induced pluripotent stem cell-derived spermatogonial stem cells and causes Sertoli cell-only syndrome. Stem Cell Res Ther 2022;13. [DOI: 10.1186/s13287-022-03175-6] [Reference Citation Analysis]
2 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]
3 Akbari A, Zoha Tabatabaei S, Salehi N, Padidar K, Almadani N, Ali Sadighi Gilani M, Mashayekhi M, Motevaseli E, Totonchi M. Novel STAG3 variant associated with primary ovarian insufficiency and non-obstructive azoospermia in an Iranian consanguineous family. Gene 2022;821:146281. [PMID: 35176428 DOI: 10.1016/j.gene.2022.146281] [Reference Citation Analysis]
4 Tang D, Li K, Geng H, Xu C, Lv M, Gao Y, Wang G, Yu H, Shao Z, Shen Q, Jiang H, Zhang X, He X, Cao Y. Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia. Reprod Biol Endocrinol 2022;20. [DOI: 10.1186/s12958-022-00936-z] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
5 Oud MS, Smits RM, Smith HE, Mastrorosa FK, Holt GS, Houston BJ, de Vries PF, Alobaidi BKS, Batty LE, Ismail H, Greenwood J, Sheth H, Mikulasova A, Astuti GDN, Gilissen C, McEleny K, Turner H, Coxhead J, Cockell S, Braat DDM, Fleischer K, D'Hauwers KWM, Schaafsma E, Nagirnaja L, Conrad DF, Friedrich C, Kliesch S, Aston KI, Riera-Escamilla A, Krausz C, Gonzaga-Jauregui C, Santibanez-Koref M, Elliott DJ, Vissers LELM, Tüttelmann F, O'Bryan MK, Ramos L, Xavier MJ, van der Heijden GW, Veltman JA; Genetics of Male Infertility Initiative (GEMINI) consortium. A de novo paradigm for male infertility. Nat Commun 2022;13:154. [PMID: 35013161 DOI: 10.1038/s41467-021-27132-8] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 5.0] [Reference Citation Analysis]
6 Skakkebæk NE, Lindahl-Jacobsen R, Levine H, Andersson AM, Jørgensen N, Main KM, Lidegaard Ø, Priskorn L, Holmboe SA, Bräuner EV, Almstrup K, Franca LR, Znaor A, Kortenkamp A, Hart RJ, Juul A. Environmental factors in declining human fertility. Nat Rev Endocrinol 2021. [PMID: 34912078 DOI: 10.1038/s41574-021-00598-8] [Cited by in Crossref: 12] [Cited by in F6Publishing: 11] [Article Influence: 12.0] [Reference Citation Analysis]
7 Laan M, Kasak L, Punab M. Translational aspects of novel findings in genetics of male infertility-status quo 2021. Br Med Bull 2021:ldab025. [PMID: 34755838 DOI: 10.1093/bmb/ldab025] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
8 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 F6Publishing: 2] [Reference Citation Analysis]
9 Krausz C, Cioppi F. Genetic Factors of Non-Obstructive Azoospermia: Consequences on Patients' and Offspring Health. J Clin Med 2021;10:4009. [PMID: 34501457 DOI: 10.3390/jcm10174009] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
10 Cao D, Shi F, Guo C, Liu Y, Lin Z, Zhang J, Li RHW, Yao Y, Liu K, Ng EHY, Yeung WSB, Wang T. A pathogenic DMC1 frameshift mutation causes nonobstructive azoospermia but not primary ovarian insufficiency in humans. Mol Hum Reprod 2021;27:gaab058. [PMID: 34515795 DOI: 10.1093/molehr/gaab058] [Reference Citation Analysis]
11 Pantos K, Grigoriadis S, Tomara P, Louka I, Maziotis E, Pantou A, Nitsos N, Vaxevanoglou T, Kokkali G, Agarwal A, Sfakianoudis K, Simopoulou M. Investigating the Role of the microRNA-34/449 Family in Male Infertility: A Critical Analysis and Review of the Literature. Front Endocrinol (Lausanne) 2021;12:709943. [PMID: 34276570 DOI: 10.3389/fendo.2021.709943] [Cited by in F6Publishing: 3] [Reference Citation Analysis]
12 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] [Reference Citation Analysis]
13 Liu W, Gao X, Zhang H, Liu R, Cao Y, Yu R, Fang G, Ma J, Zhao S. Analysis of STAG3 variants in Chinese non-obstructive azoospermia patients with germ cell maturation arrest. Sci Rep 2021;11:10077. [PMID: 33980954 DOI: 10.1038/s41598-021-89559-9] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
14 Khosravi A, Hasani A, Behnam P, Piryaei A, Pirani M, Aliaghaei A, Raee P, Abdi S, Fathabadi FF, Abdollahifar MA. An effective method for establishing animal models of azoospermia and oligospermia. Andrologia 2021;53:e14095. [PMID: 33961697 DOI: 10.1111/and.14095] [Cited by in F6Publishing: 1] [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: 4] [Cited by in F6Publishing: 15] [Article Influence: 4.0] [Reference Citation Analysis]
16 Chen G, Zheng B. Effect of macrophages in semen on sperm quality. Reprod Biol Endocrinol 2021;19:38. [PMID: 33663557 DOI: 10.1186/s12958-021-00724-1] [Reference Citation Analysis]
17 Laan M, Kasak L, Timinskas K, Grigorova M, Venclovas Č, Renaux A, Lenaerts T, Punab M. NR5A1 c.991-1G > C splice-site variant causes familial 46,XY partial gonadal dysgenesis with incomplete penetrance. Clin Endocrinol (Oxf) 2021;94:656-66. [PMID: 33296094 DOI: 10.1111/cen.14381] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
18 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: 3] [Cited by in F6Publishing: 11] [Article Influence: 1.5] [Reference Citation Analysis]
19 Aitken RJ, Baker MA. The Role of Genetics and Oxidative Stress in the Etiology of Male Infertility-A Unifying Hypothesis? Front Endocrinol (Lausanne) 2020;11:581838. [PMID: 33101214 DOI: 10.3389/fendo.2020.581838] [Cited by in Crossref: 9] [Cited by in F6Publishing: 19] [Article Influence: 4.5] [Reference Citation Analysis]
20 Yao C, Yang C, Zhao L, Li P, Tian R, Chen H, Guo Y, Huang Y, Zhi E, Zhai J, Sun H, Zhang J, Hong Y, Zhang L, Ji Z, Zhang F, Zhou Z, Li Z. Bi-allelic SHOC1 loss-of-function mutations cause meiotic arrest and non-obstructive azoospermia. J Med Genet 2020:jmedgenet-2020-107042. [PMID: 32900840 DOI: 10.1136/jmedgenet-2020-107042] [Cited by in Crossref: 2] [Cited by in F6Publishing: 6] [Article Influence: 1.0] [Reference Citation Analysis]
21 Ge R, Feng G, Jing X, Zhang R, Wang P, Wu Q. EnACP: An Ensemble Learning Model for Identification of Anticancer Peptides. Front Genet 2020;11:760. [PMID: 32903636 DOI: 10.3389/fgene.2020.00760] [Cited by in Crossref: 5] [Cited by in F6Publishing: 9] [Article Influence: 2.5] [Reference Citation Analysis]
22 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: 13] [Cited by in F6Publishing: 17] [Article Influence: 6.5] [Reference Citation Analysis]
23 Soraggi S, Riera M, Rajpert-De Meyts E, Schierup MH, Almstrup K. Evaluating genetic causes of azoospermia: What can we learn from a complex cellular structure and single-cell transcriptomics of the human testis? Hum Genet 2021;140:183-201. [PMID: 31950241 DOI: 10.1007/s00439-020-02116-8] [Cited by in Crossref: 14] [Cited by in F6Publishing: 13] [Article Influence: 7.0] [Reference Citation Analysis]