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For: Coutton C, Escoffier J, Martinez G, Arnoult C, Ray PF. Teratozoospermia: spotlight on the main genetic actors in the human. Hum Reprod Update 2015;21:455-85. [PMID: 25888788 DOI: 10.1093/humupd/dmv020] [Cited by in Crossref: 140] [Cited by in F6Publishing: 128] [Article Influence: 20.0] [Reference Citation Analysis]
Number Citing Articles
1 Elkina YL, Kuravsky ML, Bragina EE, Kurilo LF, Khayat SS, Sukhomlinova MY, Schmalhausen EV. Detection of a mutation in the intron of Sperm-specific glyceraldehyde-3-phosphate dehydrogenase gene in patients with fibrous sheath dysplasia of the sperm flagellum. Andrologia 2017;49. [PMID: 27135296 DOI: 10.1111/and.12606] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.7] [Reference Citation Analysis]
2 Alchinbayev MK, Aralbayeva AN, Tuleyeva LN, Duysenbayeva SM, Makazhanov MA. Aneuploidies level in sperm nuclei in patients with infertility. Mutagenesis 2016;31:559-65. [PMID: 27269280 DOI: 10.1093/mutage/gew020] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.7] [Reference Citation Analysis]
3 He X, Li W, Wu H, Lv M, Liu W, Liu C, Zhu F, Li C, Fang Y, Yang C, Cheng H, Zhang J, Tan J, Chen T, Tang D, Song B, Wang X, Zha X, Wang H, Wei Z, Yang S, Saiyin H, Zhou P, Jin L, Wang J, Zhang Z, Zhang F, Cao Y. Novel homozygous CFAP69 mutations in humans and mice cause severe asthenoteratospermia with multiple morphological abnormalities of the sperm flagella. J Med Genet 2019;56:96-103. [PMID: 30415212 DOI: 10.1136/jmedgenet-2018-105486] [Cited by in Crossref: 40] [Cited by in F6Publishing: 35] [Article Influence: 10.0] [Reference Citation Analysis]
4 Wang Y, Tu C, Nie H, Meng L, Li D, Wang W, Zhang H, Lu G, Lin G, Tan YQ, Du J. Novel DNAAF6 variants identified by whole-exome sequencing cause male infertility and primary ciliary dyskinesia. J Assist Reprod Genet 2020;37:811-20. [PMID: 32170493 DOI: 10.1007/s10815-020-01735-4] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
5 Mega OO, Edesiri TP, Victor E, Kingsley NE, Rume RA, Faith FY, Simon OI, Oghenetega BO, Agbonifo-Chijiokwu E. d-ribose- l-cysteine abrogates testicular maladaptive responses induced by polychlorinated bisphenol intoxication in rats via activation of the mTOR signaling pathway mediating inhibition of apoptosis, inflammation, and oxidonitrergic flux. J Biochem Mol Toxicol 2022;:e23161. [PMID: 35822628 DOI: 10.1002/jbt.23161] [Reference Citation Analysis]
6 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]
7 Coutton C, Martinez G, Kherraf ZE, Amiri-Yekta A, Boguenet M, Saut A, He X, Zhang F, Cristou-Kent M, Escoffier J, Bidart M, Satre V, Conne B, Fourati Ben Mustapha S, Halouani L, Marrakchi O, Makni M, Latrous H, Kharouf M, Pernet-Gallay K, Bonhivers M, Hennebicq S, Rives N, Dulioust E, Touré A, Gourabi H, Cao Y, Zouari R, Hosseini SH, Nef S, Thierry-Mieg N, Arnoult C, Ray PF. Bi-allelic Mutations in ARMC2 Lead to Severe Astheno-Teratozoospermia Due to Sperm Flagellum Malformations in Humans and Mice. Am J Hum Genet 2019;104:331-40. [PMID: 30686508 DOI: 10.1016/j.ajhg.2018.12.013] [Cited by in Crossref: 72] [Cited by in F6Publishing: 58] [Article Influence: 24.0] [Reference Citation Analysis]
8 Han Y, Liang C, Yu Y, Manthari RK, Cheng C, Tan Y, Li X, Tian X, Fu W, Yang J, Yang W, Xing Y, Wang J, Zhang J. Chronic arsenic exposure lowered sperm motility via impairing ultra-microstructure and key proteins expressions of sperm acrosome and flagellum formation during spermiogenesis in male mice. Sci Total Environ 2020;734:139233. [PMID: 32460071 DOI: 10.1016/j.scitotenv.2020.139233] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Zhang G, Li D, Tu C, Meng L, Tan Y, Ji Z, Cheng J, Lu G, Lin G, Zhang H, Sun J, Wang M, Du J, Xu W. Loss-of-function missense variant of AKAP4 induced male infertility through reduced interaction with QRICH2 during sperm flagella development. Hum Mol Genet 2021:ddab234. [PMID: 34415320 DOI: 10.1093/hmg/ddab234] [Reference Citation Analysis]
10 Sha YW, Wang X, Su ZY, Wang C, Ji ZY, Mei LB, Zhang L, Deng BB, Huang XJ, Yan W, Chen J, Li P, Cui YQ, Qu QL, Yin C, He XM. TDRD6 is associated with oligoasthenoteratozoospermia by sequencing the patient from a consanguineous family. Gene 2018;659:84-8. [PMID: 29551503 DOI: 10.1016/j.gene.2018.03.040] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 2.3] [Reference Citation Analysis]
11 Li Y, Sha Y, Wang X, Ding L, Liu W, Ji Z, Mei L, Huang X, Lin S, Kong S, Lu J, Qin W, Zhang X, Zhuang J, Tang Y, Lu Z. DNAH2 is a novel candidate gene associated with multiple morphological abnormalities of the sperm flagella. Clin Genet 2019;95:590-600. [PMID: 30811583 DOI: 10.1111/cge.13525] [Cited by in Crossref: 33] [Cited by in F6Publishing: 28] [Article Influence: 11.0] [Reference Citation Analysis]
12 Auger J, Jouannet P, Eustache F. Another look at human sperm morphology. Hum Reprod 2015;31:10-23. [DOI: 10.1093/humrep/dev251] [Cited by in Crossref: 66] [Cited by in F6Publishing: 60] [Article Influence: 9.4] [Reference Citation Analysis]
13 Krausz C, Riera-Escamilla A. Genetics of male infertility. Nat Rev Urol 2018;15:369-84. [PMID: 29622783 DOI: 10.1038/s41585-018-0003-3] [Cited by in Crossref: 165] [Cited by in F6Publishing: 154] [Article Influence: 55.0] [Reference Citation Analysis]
14 Hu J, Lessard C, Longstaff C, O'Brien M, Palmer K, Reinholdt L, Eppig J, Schimenti J, Handel MA. ENU-induced mutant allele of Dnah1, ferf1, causes abnormal sperm behavior and fertilization failure in mice. Mol Reprod Dev 2019;86:416-25. [PMID: 30734403 DOI: 10.1002/mrd.23120] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
15 Tavalaee M, Nasr-esfahani MH. Expression profile of PLC ζ, PAWP, and TR-KIT in association with fertilization potential, embryo development, and pregnancy outcomes in globozoospermic candidates for intra-cytoplasmic sperm injection and artificial oocyte activation. Andrology 2016;4:850-6. [DOI: 10.1111/andr.12179] [Cited by in Crossref: 19] [Cited by in F6Publishing: 20] [Article Influence: 3.2] [Reference Citation Analysis]
16 Fahmy MA, Abd-Alla HI, Hassan EE, Hassan ZM, Sweelam HM. Genotoxicity and sperm defects induced by 5-FU in male mice and the possible protective role of Pentas lanceolata-iridoids. Mutat Res 2020;850-851:503145. [PMID: 32247555 DOI: 10.1016/j.mrgentox.2020.503145] [Reference Citation Analysis]
17 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] [Reference Citation Analysis]
18 Touré A, Martinez G, Kherraf ZE, Cazin C, Beurois J, Arnoult C, Ray PF, Coutton C. The genetic architecture of morphological abnormalities of the sperm tail. Hum Genet 2021;140:21-42. [PMID: 31950240 DOI: 10.1007/s00439-020-02113-x] [Cited by in Crossref: 29] [Cited by in F6Publishing: 30] [Article Influence: 14.5] [Reference Citation Analysis]
19 Wu H, Wang J, Cheng H, Gao Y, Liu W, Zhang Z, Jiang H, Li W, Zhu F, Lv M, Liu C, Tan Q, Zhang X, Wang C, Ni X, Chen Y, Song B, Zhou P, Wei Z, Zhang F, He X, Cao Y. Patients with severe asthenoteratospermia carrying SPAG6 or RSPH3 mutations have a positive pregnancy outcome following intracytoplasmic sperm injection. J Assist Reprod Genet 2020;37:829-40. [PMID: 32124190 DOI: 10.1007/s10815-020-01721-w] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 2.5] [Reference Citation Analysis]
20 Jiang C, Zhang X, Zhang H, Guo J, Zhang C, Li J, Yang Y. Novel bi-allelic mutations in DNAH1 cause multiple morphological abnormalities of the sperm flagella resulting in male infertility. Transl Androl Urol 2021;10:1656-64. [PMID: 33968654 DOI: 10.21037/tau-20-1434] [Reference Citation Analysis]
21 Faja F, Pallotti F, Cargnelutti F, Senofonte G, Carlini T, Lenzi A, Lombardo F, Paoli D. Molecular Analysis of DPY19L2, PICK1 and SPATA16 in Italian Unrelated Globozoospermic Men. Life (Basel) 2021;11:641. [PMID: 34209343 DOI: 10.3390/life11070641] [Reference Citation Analysis]
22 Barratt CL, Wang C, Baldi E, Toskin I, Kiarie J, Lamb DJ. What advances may the future bring to the diagnosis, treatment, and care of male sexual and reproductive health? Fertility and Sterility 2022;117:258-67. [DOI: 10.1016/j.fertnstert.2021.12.013] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
23 Liu S, Zhang J, Kherraf ZE, Sun S, Zhang X, Cazin C, Coutton C, Zouari R, Zhao S, Hu F, Fourati Ben Mustapha S, Arnoult C, Ray PF, Liu M. CFAP61 is required for sperm flagellum formation and male fertility in human and mouse. Development 2021;148:dev199805. [PMID: 34792097 DOI: 10.1242/dev.199805] [Reference Citation Analysis]
24 Collodel G, Ferretti F, Masini M, Gualtieri G, Moretti E. Influence of age on sperm characteristics evaluated by light and electron microscopies. Sci Rep 2021;11:4989. [PMID: 33654135 DOI: 10.1038/s41598-021-84051-w] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
25 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. Homozygous mutations in CCDC34 cause male infertility with oligoasthenoteratozoospermia in humans and mice. J Med Genet 2021:jmedgenet-2021-107919. [PMID: 34348960 DOI: 10.1136/jmedgenet-2021-107919] [Reference Citation Analysis]
26 Bracke A, Peeters K, Punjabi U, Hoogewijs D, Dewilde S. A search for molecular mechanisms underlying male idiopathic infertility. Reproductive BioMedicine Online 2018;36:327-39. [DOI: 10.1016/j.rbmo.2017.12.005] [Cited by in Crossref: 65] [Cited by in F6Publishing: 64] [Article Influence: 16.3] [Reference Citation Analysis]
27 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. Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF. Reprod Biol Endocrinol 2022;20. [DOI: 10.1186/s12958-022-00916-3] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
28 Tu C, Wang W, Hu T, Lu G, Lin G, Tan YQ. Genetic underpinnings of asthenozoospermia. Best Pract Res Clin Endocrinol Metab 2020;34:101472. [PMID: 33191078 DOI: 10.1016/j.beem.2020.101472] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
29 Gunes S, Sengupta P, Henkel R, Alguraigari A, Sinigaglia MM, Kayal M, Joumah A, Agarwal A. Microtubular Dysfunction and Male Infertility. World J Mens Health 2020;38:9-23. [PMID: 30350487 DOI: 10.5534/wjmh.180066] [Cited by in Crossref: 11] [Cited by in F6Publishing: 7] [Article Influence: 2.8] [Reference Citation Analysis]
30 Lei C, Yang D, Wang R, Ding S, Wang L, Guo T, Luo H. DRC1 deficiency caused primary ciliary dyskinesia and MMAF in a Chinese patient. J Hum Genet 2021. [PMID: 34815526 DOI: 10.1038/s10038-021-00985-z] [Reference Citation Analysis]
31 Gioria M, Pasini ME, Berruti G. Dynamic of contribution of UBPy-sorted cargo to acrosome biogenesis: effects of its derailment in a mouse model of globozoospermia, the infertile Vps54 (L967Q) mutant. Cell Tissue Res 2017;369:413-27. [DOI: 10.1007/s00441-017-2592-1] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 1.6] [Reference Citation Analysis]
32 Tu C, Nie H, Meng L, Yuan S, He W, Luo A, Li H, Li W, Du J, Lu G, Lin G, Tan YQ. Identification of DNAH6 mutations in infertile men with multiple morphological abnormalities of the sperm flagella. Sci Rep 2019;9:15864. [PMID: 31676830 DOI: 10.1038/s41598-019-52436-7] [Cited by in Crossref: 19] [Cited by in F6Publishing: 17] [Article Influence: 6.3] [Reference Citation Analysis]
33 Lin YH, Huang CY, Ke CC, Wang YY, Lai TH, Liu HC, Ku WC, Chan CC, Lin YH. ACTN4 Mediates SEPT14 Mutation-Induced Sperm Head Defects. Biomedicines 2020;8:E518. [PMID: 33228246 DOI: 10.3390/biomedicines8110518] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
34 Alimohammadi F, Ebrahimi Nasab M, Rafaee A, Hashemi M, Totonchi M, Mohseni Meybodi A, Sadighi Gilani MA, Sabbaghian M. Deletion of dpy-19 like 2 (DPY19L2) gene is associated with total but not partial globozoospermia. Reprod Fertil Dev 2020;32:727. [DOI: 10.1071/rd19025] [Cited by in Crossref: 2] [Article Influence: 1.0] [Reference Citation Analysis]
35 Guidi LG, Holloway ZG, Arnoult C, Ray PF, Monaco AP, Molnár Z, Velayos-Baeza A. AU040320 deficiency leads to disruption of acrosome biogenesis and infertility in homozygous mutant mice. Sci Rep 2018;8:10379. [PMID: 29991750 DOI: 10.1038/s41598-018-28666-6] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 1.8] [Reference Citation Analysis]
36 Escoffier J, Lee HC, Yassine S, Zouari R, Martinez G, Karaouzène T, Coutton C, Kherraf ZE, Halouani L, Triki C, Nef S, Thierry-Mieg N, Savinov SN, Fissore R, Ray PF, Arnoult C. Homozygous mutation of PLCZ1 leads to defective human oocyte activation and infertility that is not rescued by the WW-binding protein PAWP. Hum Mol Genet 2016;25:878-91. [PMID: 26721930 DOI: 10.1093/hmg/ddv617] [Cited by in Crossref: 71] [Cited by in F6Publishing: 64] [Article Influence: 10.1] [Reference Citation Analysis]
37 Hamza L, Gaitch N, Sallem A, Boucekkine N, Girodon E, Oumeziane A, Attal N, Wolf JP, Bienvenu T. Two frequent loss-of-function mutations in Aurora Kinase C gene in Algerian infertile men with macrozoospermia. Andrologia 2020;52:e13868. [PMID: 33118205 DOI: 10.1111/and.13868] [Reference Citation Analysis]
38 Hu HY, Wei TY, Feng ZK, Li SJ, Zhao R, Yi XL, Hu TL, Zhao H, Li CX, Liu ZG. Novel Biallelic DNAH1 Variations Cause Multiple Morphological Abnormalities of the Sperm Flagella. DNA Cell Biol 2021;40:833-40. [PMID: 33989052 DOI: 10.1089/dna.2021.0097] [Reference Citation Analysis]
39 Coutton C, Vargas AS, Amiri-Yekta A, Kherraf ZE, Ben Mustapha SF, Le Tanno P, Wambergue-Legrand C, Karaouzène T, Martinez G, Crouzy S, Daneshipour A, Hosseini SH, Mitchell V, Halouani L, Marrakchi O, Makni M, Latrous H, Kharouf M, Deleuze JF, Boland A, Hennebicq S, Satre V, Jouk PS, Thierry-Mieg N, Conne B, Dacheux D, Landrein N, Schmitt A, Stouvenel L, Lorès P, El Khouri E, Bottari SP, Fauré J, Wolf JP, Pernet-Gallay K, Escoffier J, Gourabi H, Robinson DR, Nef S, Dulioust E, Zouari R, Bonhivers M, Touré A, Arnoult C, Ray PF. Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human. Nat Commun 2018;9:686. [PMID: 29449551 DOI: 10.1038/s41467-017-02792-7] [Cited by in Crossref: 91] [Cited by in F6Publishing: 83] [Article Influence: 22.8] [Reference Citation Analysis]
40 Wei X, Sha Y, Wei Z, Zhu X, He F, Zhang X, Liu W, Wang Y, Lu Z. Bi-allelic mutations in DNAH7 cause asthenozoospermia by impairing the integrality of axoneme structure. Acta Biochim Biophys Sin (Shanghai) 2021;53:1300-9. [PMID: 34476482 DOI: 10.1093/abbs/gmab113] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
41 Bronson R, Mikhailik A, Schwedes J, Gnatenko D, Hatchwell E. Detection of candidate nectin gene mutations in infertile men with severe teratospermia. J Assist Reprod Genet 2017;34:1295-302. [PMID: 28689229 DOI: 10.1007/s10815-017-0985-4] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
42 Krausz C, Cioppi F, Riera-Escamilla A. Testing for genetic contributions to infertility: potential clinical impact. Expert Rev Mol Diagn 2018;18:331-46. [PMID: 29540081 DOI: 10.1080/14737159.2018.1453358] [Cited by in Crossref: 28] [Cited by in F6Publishing: 25] [Article Influence: 7.0] [Reference Citation Analysis]
43 Li K, Li R, Ni Y, Sun P, Liu Y, Zhang D, Huang H. Novel distance-progesterone-combined selection approach improves human sperm quality. J Transl Med 2018;16:203. [PMID: 30029659 DOI: 10.1186/s12967-018-1575-7] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
44 Bai S, Hu X, Zhao Y, Li W, Wan Y, Jin R, Wang Y, Guo T, Tong X, Xu B. Compound heterozygosity for novel AURKC mutations in an infertile man with macrozoospermia. Andrologia 2020;52:e13663. [PMID: 32478938 DOI: 10.1111/and.13663] [Reference Citation Analysis]
45 Moretti E, Gambera L, Stendardi A, Belmonte G, Salvatici MC, Collodel G. Characterisation of three systematic sperm tail defects and their influence on ICSI outcome. Andrologia 2018;50:e13128. [PMID: 30132935 DOI: 10.1111/and.13128] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.8] [Reference Citation Analysis]
46 Fujihara Y, Oji A, Larasati T, Kojima-Kita K, Ikawa M. Human Globozoospermia-Related Gene Spata16 Is Required for Sperm Formation Revealed by CRISPR/Cas9-Mediated Mouse Models. Int J Mol Sci 2017;18:E2208. [PMID: 29065458 DOI: 10.3390/ijms18102208] [Cited by in Crossref: 23] [Cited by in F6Publishing: 19] [Article Influence: 4.6] [Reference Citation Analysis]
47 Celse T, Cazin C, Mietton F, Martinez G, Martinez D, Thierry-Mieg N, Septier A, Guillemain C, Beurois J, Clergeau A, Mustapha SFB, Kharouf M, Zoghmar A, Chargui A, Papaxanthos A, Dorphin B, Foliguet B, Triki C, Sifer C, Lauton D, Tachdjian G, Schuler G, Lejeune H, Puechberty J, Bessonnat J, Pasquier L, Mery L, Poulain M, Chaabouni M, Sermondade N, Cabry R, Benbouhadja S, Veau S, Frapsauce C, Mitchell V, Achard V, Satre V, Hennebicq S, Zouari R, Arnoult C, Kherraf ZE, Coutton C, Ray PF. Genetic analyses of a large cohort of infertile patients with globozoospermia, DPY19L2 still the main actor, GGN confirmed as a guest player. Hum Genet 2021;140:43-57. [PMID: 33108537 DOI: 10.1007/s00439-020-02229-0] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 2.5] [Reference Citation Analysis]
48 Kherraf ZE, Conne B, Amiri-Yekta A, Kent MC, Coutton C, Escoffier J, Nef S, Arnoult C, Ray PF. Creation of knock out and knock in mice by CRISPR/Cas9 to validate candidate genes for human male infertility, interest, difficulties and feasibility. Mol Cell Endocrinol 2018;468:70-80. [PMID: 29522859 DOI: 10.1016/j.mce.2018.03.002] [Cited by in Crossref: 13] [Cited by in F6Publishing: 11] [Article Influence: 3.3] [Reference Citation Analysis]
49 Linck RW, Chemes H, Albertini DF. The axoneme: the propulsive engine of spermatozoa and cilia and associated ciliopathies leading to infertility. J Assist Reprod Genet 2016;33:141-56. [PMID: 26825807 DOI: 10.1007/s10815-016-0652-1] [Cited by in Crossref: 45] [Cited by in F6Publishing: 38] [Article Influence: 7.5] [Reference Citation Analysis]
50 Chylíková B, Hrdlička I, Veselá K, Řežábek K, Liška F. Recurrent Microdeletions at Xq27.3-Xq28 and Male Infertility: A Study in the Czech Population. PLoS One 2016;11:e0156102. [PMID: 27257673 DOI: 10.1371/journal.pone.0156102] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
51 Liu M, Li J, Jiang C, Zhou Y, Sun Y, Yang Y, Shen Y. A novel homozygous mutation in DNAJB13-a gene associated with the sperm axoneme-leads to teratozoospermia. J Assist Reprod Genet 2022. [PMID: 35166991 DOI: 10.1007/s10815-022-02431-1] [Reference Citation Analysis]
52 Paci M, Elkhatib R, Longepied G, Bourgeois P, Ray PF, Levy N, Mitchell MJ, Metzler-Guillemain C. The involvement of the nuclear lamina in human and rodent spermiogenesis: a systematic review. Basic Clin Androl 2018;28:7. [PMID: 29946470 DOI: 10.1186/s12610-018-0072-4] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.8] [Reference Citation Analysis]
53 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] [Reference Citation Analysis]
54 Oura S, Kazi S, Savolainen A, Nozawa K, Castañeda J, Yu Z, Miyata H, Matzuk RM, Hansen JN, Wachten D, Matzuk MM, Prunskaite-Hyyryläinen R. Cfap97d1 is important for flagellar axoneme maintenance and male mouse fertility. PLoS Genet 2020;16:e1008954. [PMID: 32785227 DOI: 10.1371/journal.pgen.1008954] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
55 Moretti E, Collodel G, Salvatici MC, Belmonte G, Signorini C. New insights into sperm with total globozoospermia: Increased fatty acid oxidation and centrin1 alteration. Systems Biology in Reproductive Medicine 2019;65:390-9. [DOI: 10.1080/19396368.2019.1626934] [Cited by in Crossref: 12] [Cited by in F6Publishing: 11] [Article Influence: 4.0] [Reference Citation Analysis]
56 Akbari A, Pipitone GB, Anvar Z, Jaafarinia M, Ferrari M, Carrera P, Totonchi M. ADCY10 frameshift variant leading to severe recessive asthenozoospermia and segregating with absorptive hypercalciuria. Hum Reprod 2019;34:1155-64. [PMID: 31119281 DOI: 10.1093/humrep/dez048] [Cited by in Crossref: 14] [Cited by in F6Publishing: 14] [Article Influence: 7.0] [Reference Citation Analysis]
57 Song B, Liu C, Gao Y, Marley JL, Li W, Ni X, Liu W, Chen Y, Wang J, Wang C, Zhou P, Wei Z, He X, Zhang F, Cao Y. Novel compound heterozygous variants in dynein axonemal heavy chain 17 cause asthenoteratospermia with sperm flagellar defects. J Genet Genomics 2020;47:713-7. [PMID: 33423959 DOI: 10.1016/j.jgg.2020.07.004] [Reference Citation Analysis]
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