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For: Jiao SY, Yang YH, Chen SR. Molecular genetics of infertility: loss-of-function mutations in humans and corresponding knockout/mutated mice. Hum Reprod Update 2021;27:154-89. [PMID: 33118031 DOI: 10.1093/humupd/dmaa034] [Cited by in Crossref: 7] [Cited by in F6Publishing: 31] [Article Influence: 3.5] [Reference Citation Analysis]
Number Citing Articles
1 Zhao L, Li Q, Kuang Y, Xu P, Sun X, Meng Q, Wang W, Zeng Y, Chen B, Fu J, Dong J, Zhu J, Luo Y, Gu H, Li C, Li C, Wu L, Mao X, Fan H, Liu R, Zhang Z, Li Q, Du J, He L, Jin L, Wang L, Sang Q. Heterozygous loss-of-function variants in LHX8 cause female infertility characterized by oocyte maturation arrest. Genet Med 2022:S1098-3600(22)00873-5. [PMID: 36029299 DOI: 10.1016/j.gim.2022.07.027] [Reference Citation Analysis]
2 Shang L, Ren S, Yang X, Zhang F, Jin L, Zhang X, Wu Y. EIF4ENIF1 variants in two patients with non-syndromic premature ovarian insufficiency. Eur J Med Genet 2022;:104597. [PMID: 36030004 DOI: 10.1016/j.ejmg.2022.104597] [Reference Citation Analysis]
3 Wu J, Liu Y, Song Y, Wang L, Ai J, Li K. Aging conundrum: A perspective for ovarian aging. Front Endocrinol 2022;13:952471. [DOI: 10.3389/fendo.2022.952471] [Reference Citation Analysis]
4 Guo T, Lu C, Yang D, Lei C, Liu Y, Xu Y, Yang B, Wang R, Luo H. Case Report: DNAAF4 Variants Cause Primary Ciliary Dyskinesia and Infertility in Two Han Chinese Families. Front Genet 2022;13:934920. [DOI: 10.3389/fgene.2022.934920] [Reference Citation Analysis]
5 Zhang XZ, Wei LL, Jin HJ, Zhang XH, Chen SR. The perinuclear theca protein Calicin helps shape the sperm head and maintain the nuclear structure in mice. Cell Rep 2022;40:111049. [PMID: 35793634 DOI: 10.1016/j.celrep.2022.111049] [Reference Citation Analysis]
6 Jin ZR, Cao YL, Luo ZC, Zhao QC, Xi Y, Weng JM, Zhang Z, Jiang H. Therapeutic Effects of Xianlu Oral Solution on Rats with Oligoasthenozoospermia through Alleviating Apoptosis and Oxidative Stress. Evid Based Complement Alternat Med 2022;2022:1269530. [PMID: 35761898 DOI: 10.1155/2022/1269530] [Reference Citation Analysis]
7 Yang D, Yang H, Yang B, Wang K, Zhu Q, Wang J, Ding F, Rao B, Xue R, Peng J, Wang Q, Cao Y, Zou W, Chen B, Zhang Z. Embryological Characteristics of Human Oocytes With Agar-Like Zona Pellucida and Its Clinical Treatment Strategy. Front Endocrinol 2022;13:859361. [DOI: 10.3389/fendo.2022.859361] [Reference Citation Analysis]
8 Cao N, Hu C, Xia B, He Y, Huang J, Yuan Z, Deng J, Duan P. The Activated AMPK/mTORC2 Signaling Pathway Associated with Oxidative Stress in Seminal Plasma Contributes to Idiopathic Asthenozoospermia. Oxid Med Cell Longev 2022;2022:4240490. [PMID: 35720189 DOI: 10.1155/2022/4240490] [Reference Citation Analysis]
9 Song H, Chen D, Bai R, Feng Y, Wu S, Wang T, Xia X, Li J, Miao YL, Zuo B, Li F. BCL2-associated athanogene 6 exon24 contributes to testosterone synthesis and male fertility in mammals. Cell Prolif 2022;:e13281. [PMID: 35688694 DOI: 10.1111/cpr.13281] [Reference Citation Analysis]
10 Yang C, Lin X, Ji Z, Huang Y, Zhang L, Luo J, Chen H, Li P, Tian R, Zhi E, Hong Y, Zhou Z, Zhang F, Li Z, Yao C. Novel bi-allelic variants in KASH5 are associated with meiotic arrest and non-obstructive azoospermia. Mol Hum Reprod 2022:gaac021. [PMID: 35674372 DOI: 10.1093/molehr/gaac021] [Reference Citation Analysis]
11 Zheng R, Wang Y, Li Y, Guo J, Wen Y, Jiang C, Yang Y, Shen Y. FSIP2 plays a role in the acrosome development during spermiogenesis. J Med Genet 2022:jmedgenet-2021-108406. [PMID: 35654582 DOI: 10.1136/jmedgenet-2021-108406] [Reference Citation Analysis]
12 Saulnier J, Chalmel F, Delessard M, Moutard L, Pereira T, Fraissinet F, Dumont L, Rives-Feraille A, Rondanino C, Rives N. Understanding the Underlying Molecular Mechanisms of Meiotic Arrest during In Vitro Spermatogenesis in Rat Prepubertal Testicular Tissue. Int J Mol Sci 2022;23:5893. [PMID: 35682573 DOI: 10.3390/ijms23115893] [Reference Citation Analysis]
13 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]
14 Cavarocchi E, Whitfield M, Saez F, Touré A. Sperm Ion Transporters and Channels in Human Asthenozoospermia: Genetic Etiology, Lessons from Animal Models, and Clinical Perspectives. Int J Mol Sci 2022;23:3926. [PMID: 35409285 DOI: 10.3390/ijms23073926] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
15 Yang J, Lin D, Yao W, Yun D, Zhou L, Gao S, Sun F. NBMA Promotes Spermatogenesis by Mediating Oct4 Pathway. ChemistryOpen 2022;:e202100219. [PMID: 35142088 DOI: 10.1002/open.202100219] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
16 Niziolek M, Bicka M, Osinka A, Samsel Z, Sekretarska J, Poprzeczko M, Bazan R, Fabczak H, Joachimiak E, Wloga D. PCD Genes-From Patients to Model Organisms and Back to Humans. Int J Mol Sci 2022;23:1749. [PMID: 35163666 DOI: 10.3390/ijms23031749] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
17 Ma A, Zeb A, Ali I, Zhao D, Khan A, Zhang B, Zhou J, Khan R, Zhang H, Zhang Y, Khan I, Shah W, Ali H, Javed AR, Ma H, Shi Q. Biallelic Variants in CFAP61 Cause Multiple Morphological Abnormalities of the Flagella and Male Infertility. Front Cell Dev Biol 2022;9:803818. [DOI: 10.3389/fcell.2021.803818] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
18 Mitchell LE. Maternal effect genes: Update and review of evidence for a link with birth defects. HGG Adv 2022;3:100067. [PMID: 35047854 DOI: 10.1016/j.xhgg.2021.100067] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
19 Wang Y, Chen Q, Zhang F, Yang X, Shang L, Ren S, Pan Y, Zhou Z, Li G, Fang Y, Jin L, Wu Y, Zhang X. Whole exome sequencing identified a rare WT1 loss-of-function variant in a non-syndromic POI patient. Mol Genet Genomic Med 2021;:e1820. [PMID: 34845858 DOI: 10.1002/mgg3.1820] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
20 Li Y, Wang Y, Wen Y, Zhang T, Wang X, Jiang C, Zheng R, Zhou F, Chen D, Yang Y, Shen Y. Whole-exome sequencing of a cohort of infertile men reveals novel causative genes in teratozoospermia that are chiefly related to sperm head defects. Hum Reprod 2021:deab229. [PMID: 34791246 DOI: 10.1093/humrep/deab229] [Cited by in F6Publishing: 3] [Reference Citation Analysis]
21 Li K, Wang G, Lv M, Wang J, Gao Y, Tang F, Xu C, Yang W, Yu H, Shao Z, Geng H, Tan Q, Shen Q, Tang D, Ni X, Wang T, Song B, Wu H, Huo R, Zhang Z, Xu Y, Zhou P, Tao F, Wei Z, He X, Cao Y. Bi-allelic variants in DNAH10 cause asthenoteratozoospermia and male infertility. J Assist Reprod Genet 2021. [PMID: 34657236 DOI: 10.1007/s10815-021-02306-x] [Cited by in F6Publishing: 4] [Reference Citation Analysis]
22 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 F6Publishing: 3] [Reference Citation Analysis]
23 Ji C, Wang Y, Wei X, Zhang X, Cong R, Yao L, Qin C, Song N. Potential of testis-derived circular RNAs in seminal plasma to predict the outcome of microdissection testicular sperm extraction in patients with idiopathic non-obstructive azoospermia. Hum Reprod 2021;36:2649-60. [PMID: 34477868 DOI: 10.1093/humrep/deab196] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
24 Lu Q, Zhang X, Cao Q, Wang C, Ding J, Zhao C, Zhang J, Ling X, Meng Q, Huo R, Li H. Expanding the Genetic and Phenotypic Spectrum of Female Infertility Caused by TUBB8 Mutations. Reprod Sci 2021. [PMID: 34494234 DOI: 10.1007/s43032-021-00694-0] [Reference Citation Analysis]
25 Sha Y, Liu W, Li L, Serafimovski M, Isachenko V, Li Y, Chen J, Zhao B, Wang Y, Wei X. Pathogenic Variants in ACTRT1 Cause Acephalic Spermatozoa Syndrome. Front Cell Dev Biol 2021;9:676246. [PMID: 34422805 DOI: 10.3389/fcell.2021.676246] [Reference Citation Analysis]
26 Zhou Z, Yang X, Pan Y, Shang L, Chen S, Yang J, Jin L, Zhang F, Wu Y. Temporal transcriptomic landscape of postnatal mouse ovaries reveals dynamic gene signatures associated with ovarian aging. Hum Mol Genet 2021:ddab163. [PMID: 34137841 DOI: 10.1093/hmg/ddab163] [Reference Citation Analysis]
27 Azhar M, Altaf S, Uddin I, Cheng J, Wu L, Tong X, Qin W, Bao J. Towards Post-Meiotic Sperm Production: Genetic Insight into Human Infertility from Mouse Models. Int J Biol Sci 2021;17:2487-503. [PMID: 34326689 DOI: 10.7150/ijbs.60384] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
28 Morciano P, Di Giorgio ML, Tullo L, Cenci G. The Organization of the Golgi Structures during Drosophila Male Meiosis Requires the Citrate Lyase ATPCL. Int J Mol Sci 2021;22:5745. [PMID: 34072207 DOI: 10.3390/ijms22115745] [Reference Citation Analysis]
29 Zhang H, Chen T, Wu K, Hou Z, Zhao S, Zhang C, Gao Y, Gao M, Chen ZJ, Zhao H. Dominant mutations in CHK1 cause pronuclear fusion failure and zygote arrest that can be rescued by CHK1 inhibitor. Cell Res 2021;31:814-7. [PMID: 33953335 DOI: 10.1038/s41422-021-00507-8] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
30 Sang Q, Zhou Z, Mu J, Wang L. Genetic factors as potential molecular markers of human oocyte and embryo quality. J Assist Reprod Genet 2021;38:993-1002. [PMID: 33895934 DOI: 10.1007/s10815-021-02196-z] [Cited by in Crossref: 1] [Cited by in F6Publishing: 12] [Article Influence: 1.0] [Reference Citation Analysis]
31 Wang X, Wu D, Li W, Yang L. Emerging biomaterials for reproductive medicine. Engineered Regeneration 2021;2:230-45. [DOI: 10.1016/j.engreg.2021.11.006] [Cited by in F6Publishing: 2] [Reference Citation Analysis]