These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
148 related articles for article (PubMed ID: 35973810)
1. Sequencing of the Wen Y; Wang X; Zheng R; Dai S; Li J; Yang Y; Shen Y J Med Genet; 2023 Apr; 60(4):380-390. PubMed ID: 35973810 [TBL] [Abstract][Full Text] [Related]
2. Novel homozygous truncating variants in ZMYND15 causing severe oligozoospermia and their implications for male infertility. Hu TY; Zhang H; Meng LL; Yuan SM; Tu CF; Du J; Lu GX; Lin G; Nie HC; Tan YQ Hum Mutat; 2021 Jan; 42(1):31-36. PubMed ID: 33169450 [TBL] [Abstract][Full Text] [Related]
3. Whole-exome sequencing identifies mutations in FSIP2 as a recurrent cause of multiple morphological abnormalities of the sperm flagella. Martinez G; Kherraf ZE; Zouari R; Fourati Ben Mustapha S; Saut A; Pernet-Gallay K; Bertrand A; Bidart M; Hograindleur JP; Amiri-Yekta A; Kharouf M; Karaouzène T; Thierry-Mieg N; Dacheux-Deschamps D; Satre V; Bonhivers M; Touré A; Arnoult C; Ray PF; Coutton C Hum Reprod; 2018 Oct; 33(10):1973-1984. PubMed ID: 30137358 [TBL] [Abstract][Full Text] [Related]
4. Whole-exome sequencing of a cohort of infertile men reveals novel causative genes in teratozoospermia that are chiefly related to sperm head defects. Li Y; Wang Y; Wen Y; Zhang T; Wang X; Jiang C; Zheng R; Zhou F; Chen D; Yang Y; Shen Y Hum Reprod; 2021 Dec; 37(1):152-177. PubMed ID: 34791246 [TBL] [Abstract][Full Text] [Related]
5. Exome sequencing reveals novel causes as well as new candidate genes for human globozoospermia. Oud MS; Okutman Ö; Hendricks LAJ; de Vries PF; Houston BJ; Vissers LELM; O'Bryan MK; Ramos L; Chemes HE; Viville S; Veltman JA Hum Reprod; 2020 Jan; 35(1):240-252. PubMed ID: 31985809 [TBL] [Abstract][Full Text] [Related]
6. From azoospermia to macrozoospermia, a phenotypic continuum due to mutations in the Kherraf ZE; Cazin C; Lestrade F; Muronova J; Coutton C; Arnoult C; Thierry-Mieg N; Ray PF Asian J Androl; 2022; 24(3):243-247. PubMed ID: 35017390 [TBL] [Abstract][Full Text] [Related]
7. A novel homozygous mutation in DNAJB13-a gene associated with the sperm axoneme-leads to teratozoospermia. Liu M; Li J; Jiang C; Zhou Y; Sun Y; Yang Y; Shen Y J Assist Reprod Genet; 2022 Mar; 39(3):757-764. PubMed ID: 35166991 [TBL] [Abstract][Full Text] [Related]
8. Biallelic variants in KCTD19 associated with male factor infertility and oligoasthenoteratozoospermia. Wang W; Su L; Meng L; He J; Tan C; Yi D; Cheng D; Zhang H; Lu G; Du J; Lin G; Zhang Q; Tu C; Tan YQ Hum Reprod; 2023 Jul; 38(7):1399-1411. PubMed ID: 37192818 [TBL] [Abstract][Full Text] [Related]
9. Population-based genetic analysis in infertile men reveals novel mutations of ADAD family members in patients with impaired spermatogenesis. Dai S; Liu M; Liu M; Jiang C; Yang Y; Han H; Yang Y; Jiang X; Shen Y Hum Mol Genet; 2023 May; 32(11):1814-1825. PubMed ID: 36708028 [TBL] [Abstract][Full Text] [Related]
10. PRSS55 is a novel potential causative gene for human male infertility. Liu M; Jiang C; Zhang X; Zhang G; Liu M; Zheng R; Yang Y; Shen Y Reprod Biomed Online; 2022 Sep; 45(3):553-562. PubMed ID: 35821214 [TBL] [Abstract][Full Text] [Related]
11. Loss of SPACA1 function causes autosomal recessive globozoospermia by damaging the acrosome-acroplaxome complex. Chen P; Saiyin H; Shi R; Liu B; Han X; Gao Y; Ye X; Zhang X; Sun Y Hum Reprod; 2021 Aug; 36(9):2587-2596. PubMed ID: 34172998 [TBL] [Abstract][Full Text] [Related]
12. Novel variations in TENT5D lead to teratozoospermia in infertile patients. Zhang YT; Shen G; Zhuo LC; Yang X; Wang SY; Ruan TC; Jiang C; Wang X; Wang Y; Yang YH; Shen Y Andrology; 2024 Sep; 12(6):1336-1346. PubMed ID: 38228861 [TBL] [Abstract][Full Text] [Related]
13. A novel homozygous missense mutation of PMFBP1 causes acephalic spermatozoa syndrome. Lu M; Kong S; Xiang M; Wang Y; Zhang J; Duan Z; Zha X; Wang F; Cao Y; Zhu F J Assist Reprod Genet; 2021 Apr; 38(4):949-955. PubMed ID: 33484382 [TBL] [Abstract][Full Text] [Related]
14. Homozygous mutations in Cong J; Wang X; Amiri-Yekta A; Wang L; Kherraf ZE; Liu C; Cazin C; Tang S; Hosseini SH; Tian S; Daneshipour A; Wang J; Zhou Y; Zeng Y; Yang S; He X; Li J; Cao Y; Jin L; Ray PF; Zhang F J Med Genet; 2022 Jul; 59(7):710-718. PubMed ID: 34348960 [TBL] [Abstract][Full Text] [Related]
15. Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF. Xu C; Tang D; Shao Z; Geng H; Gao Y; Li K; Tan Q; Wang G; Wang C; Wu H; Li G; Lv M; He X; Cao Y Reprod Biol Endocrinol; 2022 Mar; 20(1):41. PubMed ID: 35232447 [TBL] [Abstract][Full Text] [Related]
16. Correlation among isolated teratozoospermia, sperm DNA fragmentation and markers of systemic inflammation in primary infertile men. Candela L; Boeri L; Capogrosso P; Cazzaniga W; Pozzi E; Belladelli F; Baudo A; Ravizzoli A; Ventimiglia E; Viganò P; Alfano M; Abbate C; Cornelius J; Mattei A; Montorsi F; Salonia A PLoS One; 2021; 16(6):e0251608. PubMed ID: 34097690 [TBL] [Abstract][Full Text] [Related]
17. A loss-of-function variant in ZCWPW1 causes human male infertility with sperm head defect and high DNA fragmentation. Song Y; Guo J; Zhou Y; Wei X; Li J; Zhang G; Wang H Reprod Health; 2024 Feb; 21(1):18. PubMed ID: 38310235 [TBL] [Abstract][Full Text] [Related]
18. Identification of genomic variants causing sperm abnormalities and reduced male fertility. Taylor JF; Schnabel RD; Sutovsky P Anim Reprod Sci; 2018 Jul; 194():57-62. PubMed ID: 29454799 [TBL] [Abstract][Full Text] [Related]
19. Biallelic mutations in Hua J; Guo L; Yao Y; Hu W; Wan YY; Xu B Asian J Androl; 2023; 25(3):398-403. PubMed ID: 36178131 [TBL] [Abstract][Full Text] [Related]
20. Loss-of-function mutations in centrosomal protein 112 is associated with human acephalic spermatozoa phenotype. Sha Y; Wang X; Yuan J; Zhu X; Su Z; Zhang X; Xu X; Wei X Clin Genet; 2020 Feb; 97(2):321-328. PubMed ID: 31654588 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]