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For: Whitfield M, Thomas L, Bequignon E, Schmitt A, Stouvenel L, Montantin G, Tissier S, Duquesnoy P, Copin B, Chantot S, Dastot F, Faucon C, Barbotin AL, Loyens A, Siffroi JP, Papon JF, Escudier E, Amselem S, Mitchell V, Touré A, Legendre M. Mutations in DNAH17, Encoding a Sperm-Specific Axonemal Outer Dynein Arm Heavy Chain, Cause Isolated Male Infertility Due to Asthenozoospermia. Am J Hum Genet 2019;105:198-212. [PMID: 31178125 DOI: 10.1016/j.ajhg.2019.04.015] [Cited by in Crossref: 75] [Cited by in F6Publishing: 65] [Article Influence: 25.0] [Reference Citation Analysis]
Number Citing Articles
1 Oud MS, Houston BJ, Volozonoka L, Mastrorosa FK, Holt GS, Alobaidi BKS, deVries PF, Astuti G, Ramos L, Mclachlan RI, O'Bryan MK, Veltman JA, Chemes HE, Sheth H. Exome sequencing reveals variants in known and novel candidate genes for severe sperm motility disorders. Hum Reprod 2021:deab099. [PMID: 34089056 DOI: 10.1093/humrep/deab099] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
2 Legendre M, Zaragosi LE, Mitchison HM. Motile cilia and airway disease. Semin Cell Dev Biol 2021;110:19-33. [PMID: 33279404 DOI: 10.1016/j.semcdb.2020.11.007] [Cited by in Crossref: 15] [Cited by in F6Publishing: 11] [Article Influence: 7.5] [Reference Citation Analysis]
3 Yang Y, Jiang C, Zhang X, Liu X, Li J, Qiao X, Liu H, Shen Y. Loss-of-function mutation in DNAH8 induces asthenoteratospermia associated with multiple morphological abnormalities of the sperm flagella. Clin Genet 2020;98:396-401. [PMID: 32681648 DOI: 10.1111/cge.13815] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 4.5] [Reference Citation Analysis]
4 Xiong Y, Xia H, Yuan L, Deng S, Ding Z, Deng H. Identification of compound heterozygous DNAH11 variants in a Han-Chinese family with primary ciliary dyskinesia. J Cell Mol Med 2021;25:9028-37. [PMID: 34405951 DOI: 10.1111/jcmm.16866] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
5 Wang X, Yin L, Wen Y, Yuan S. Mitochondrial regulation during male germ cell development. Cell Mol Life Sci 2022;79. [DOI: 10.1007/s00018-022-04134-3] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 4.0] [Reference Citation Analysis]
6 Li B, Li S, Yan Z. Axonemal Dynein DNAH5 is Required for Sound Sensation in Drosophila Larvae. Neurosci Bull 2021;37:523-34. [PMID: 33570705 DOI: 10.1007/s12264-021-00631-w] [Reference Citation Analysis]
7 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] [Reference Citation Analysis]
8 Chen SY, Schenkel FS, Melo ALP, Oliveira HR, Pedrosa VB, Araujo AC, Melka MG, Brito LF. Identifying pleiotropic variants and candidate genes for fertility and reproduction traits in Holstein cattle via association studies based on imputed whole-genome sequence genotypes. BMC Genomics 2022;23:331. [PMID: 35484513 DOI: 10.1186/s12864-022-08555-z] [Reference Citation Analysis]
9 Pleuger C, Lehti MS, Dunleavy JE, Fietz D, O'Bryan MK. Haploid male germ cells-the Grand Central Station of protein transport. Hum Reprod Update 2020;26:474-500. [PMID: 32318721 DOI: 10.1093/humupd/dmaa004] [Cited by in Crossref: 20] [Cited by in F6Publishing: 16] [Article Influence: 10.0] [Reference Citation Analysis]
10 He Z, Mei L, Connell M, Maxwell CA. Hyaluronan Mediated Motility Receptor (HMMR) Encodes an Evolutionarily Conserved Homeostasis, Mitosis, and Meiosis Regulator Rather than a Hyaluronan Receptor. Cells 2020;9:E819. [PMID: 32231069 DOI: 10.3390/cells9040819] [Cited by in Crossref: 8] [Cited by in F6Publishing: 10] [Article Influence: 4.0] [Reference Citation Analysis]
11 Brennan SK, Ferkol TW, Davis SD. Emerging Genotype-Phenotype Relationships in Primary Ciliary Dyskinesia. Int J Mol Sci 2021;22:8272. [PMID: 34361034 DOI: 10.3390/ijms22158272] [Reference Citation Analysis]
12 Dougherty GW, Mizuno K, Nöthe-Menchen T, Ikawa Y, Boldt K, Ta-Shma A, Aprea I, Minegishi K, Pang YP, Pennekamp P, Loges NT, Raidt J, Hjeij R, Wallmeier J, Mussaffi H, Perles Z, Elpeleg O, Rabert F, Shiratori H, Letteboer SJ, Horn N, Young S, Strünker T, Stumme F, Werner C, Olbrich H, Takaoka K, Ide T, Twan WK, Biebach L, Große-Onnebrink J, Klinkenbusch JA, Praveen K, Bracht DC, Höben IM, Junger K, Gützlaff J, Cindrić S, Aviram M, Kaiser T, Memari Y, Dzeja PP, Dworniczak B, Ueffing M, Roepman R, Bartscherer K, Katsanis N, Davis EE, Amirav I, Hamada H, Omran H. CFAP45 deficiency causes situs abnormalities and asthenospermia by disrupting an axonemal adenine nucleotide homeostasis module. Nat Commun 2020;11:5520. [PMID: 33139725 DOI: 10.1038/s41467-020-19113-0] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
13 Wallmeier J, Nielsen KG, Kuehni CE, Lucas JS, Leigh MW, Zariwala MA, Omran H. Motile ciliopathies. Nat Rev Dis Primers 2020;6:77. [PMID: 32943623 DOI: 10.1038/s41572-020-0209-6] [Cited by in Crossref: 35] [Cited by in F6Publishing: 26] [Article Influence: 17.5] [Reference Citation Analysis]
14 Wang C, Xue W, Zhang H, Fu Y. Identification of candidate genes encoding tumor-specific neoantigens in early- and late-stage colon adenocarcinoma. Aging (Albany NY) 2021;13:4024-44. [PMID: 33428592 DOI: 10.18632/aging.202370] [Reference Citation Analysis]
15 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]
16 Hao X, Wang H, Cui F, Yang Z, Ye L, Huang R, Meng J. Reduction of SLC7A11 and GPX4 Contributing to Ferroptosis in Sperm from Asthenozoospermia Individuals. Reprod Sci 2022. [PMID: 35729458 DOI: 10.1007/s43032-022-01004-y] [Reference Citation Analysis]
17 Zhou Z, Mao X, Chen B, Mu J, Wang W, Li B, Yan Z, Dong J, Li Q, Kuang Y, Wang L, Wu L, Sang Q. A novel splicing variant in DNAH8 causes asthenozoospermia. J Assist Reprod Genet 2021;38:1545-50. [PMID: 33611675 DOI: 10.1007/s10815-021-02116-1] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
18 Zheng R, Sun Y, Jiang C, Chen D, Yang Y, Shen Y. A novel mutation in DNAH17 is present in a patient with multiple morphological abnormalities of the flagella. Reprod Biomed Online 2021:S1472-6483(21)00240-6. [PMID: 34373205 DOI: 10.1016/j.rbmo.2021.05.009] [Reference Citation Analysis]
19 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]
20 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]
21 Oud MS, Okutman Ö, Hendricks LAJ, de Vries PF, Houston BJ, Vissers LELM, O'Bryan MK, Ramos L, Chemes HE, Viville S, Veltman JA. Exome sequencing reveals novel causes as well as new candidate genes for human globozoospermia. Hum Reprod 2020;35:240-52. [PMID: 31985809 DOI: 10.1093/humrep/dez246] [Cited by in Crossref: 12] [Cited by in F6Publishing: 11] [Article Influence: 12.0] [Reference Citation Analysis]
22 Walton T, Wu H, Brown A. Structure of a microtubule-bound axonemal dynein. Nat Commun 2021;12:477. [PMID: 33473120 DOI: 10.1038/s41467-020-20735-7] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 5.0] [Reference Citation Analysis]
23 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] [Reference Citation Analysis]
24 Sironen A, Shoemark A, Patel M, Loebinger MR, Mitchison HM. Sperm defects in primary ciliary dyskinesia and related causes of male infertility. Cell Mol Life Sci 2020;77:2029-48. [PMID: 31781811 DOI: 10.1007/s00018-019-03389-7] [Cited by in Crossref: 41] [Cited by in F6Publishing: 40] [Article Influence: 13.7] [Reference Citation Analysis]
25 Aitken RJ. The Male Is Significantly Implicated as the Cause of Unexplained Infertility. Semin Reprod Med 2020;38:3-20. [PMID: 33086406 DOI: 10.1055/s-0040-1718941] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
26 Dai H, Wang D, Guang X, Zhang W. Pulmonary Hypertension in a Patient With Kartagener’s Syndrome and a Novel Homozygous Nonsense Mutation in CCDC40 Gene: A Case Report. Front Med 2022;9:860684. [DOI: 10.3389/fmed.2022.860684] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
27 Schultz R, Elenius V, Lukkarinen H, Saarela T. Two novel mutations in the DNAH11 gene in primary ciliary dyskinesia (CILD7) with considerable variety in the clinical and beating cilia phenotype. BMC Med Genet 2020;21:237. [PMID: 33243178 DOI: 10.1186/s12881-020-01171-2] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
28 Liu C, Tu C, Wang L, Wu H, Houston BJ, Mastrorosa FK, Zhang W, Shen Y, Wang J, Tian S, Meng L, Cong J, Yang S, Jiang Y, Tang S, Zeng Y, Lv M, Lin G, Li J, Saiyin H, He X, Jin L, Touré A, Ray PF, Veltman JA, Shi Q, O'Bryan MK, Cao Y, Tan YQ, Zhang F. Deleterious variants in X-linked CFAP47 induce asthenoteratozoospermia and primary male infertility. Am J Hum Genet 2021;108:309-23. [PMID: 33472045 DOI: 10.1016/j.ajhg.2021.01.002] [Cited by in Crossref: 20] [Cited by in F6Publishing: 16] [Article Influence: 20.0] [Reference Citation Analysis]
29 Sha Y, Sha Y, Liu W, Zhu X, Weng M, Zhang X, Wang Y, Zhou H. Biallelic mutations of CFAP58 are associated with multiple morphological abnormalities of the sperm flagella. Clin Genet 2021;99:443-8. [PMID: 33314088 DOI: 10.1111/cge.13898] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
30 Ferreux L, Bourdon M, Chargui A, Schmitt A, Stouvenel L, Lorès P, Ray P, Lousqui J, Pocate-Cheriet K, Santulli P, Dulioust E, Toure A, Patrat C. Genetic diagnosis, sperm phenotype and ICSI outcome in case of severe asthenozoospermia with multiple morphological abnormalities of the flagellum. Hum Reprod 2021;36:2848-60. [PMID: 34529793 DOI: 10.1093/humrep/deab200] [Reference Citation Analysis]
31 Houston BJ, Riera-Escamilla A, Wyrwoll MJ, Salas-Huetos A, Xavier MJ, Nagirnaja L, Friedrich C, Conrad DF, Aston KI, Krausz C, Tüttelmann F, O'Bryan MK, Veltman JA, Oud MS. A systematic review of the validated monogenic causes of human male infertility: 2020 update and a discussion of emerging gene-disease relationships. Hum Reprod Update 2021:dmab030. [PMID: 34498060 DOI: 10.1093/humupd/dmab030] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
32 Yogo K. Molecular basis of the morphogenesis of sperm head and tail in mice. Reprod Med Biol 2022;21:e12466. [PMID: 35619659 DOI: 10.1002/rmb2.12466] [Reference Citation Analysis]
33 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]
34 Jia M, Shi R, Xue X. Novel DNAH17 mutations associated with fertilization failures after ICSI. Gynecol Endocrinol 2021;37:769-71. [PMID: 34126833 DOI: 10.1080/09513590.2021.1937979] [Reference Citation Analysis]
35 He X, Liu C, Yang X, Lv M, Ni X, Li Q, Cheng H, Liu W, Tian S, Wu H, Gao Y, Yang C, Tan Q, Cong J, Tang D, Zhang J, Song B, Zhong Y, Li H, Zhi W, Mao X, Fu F, Ge L, Shen Q, Zhang M, Saiyin H, Jin L, Xu Y, Zhou P, Wei Z, Zhang F, Cao Y. Bi-allelic Loss-of-function Variants in CFAP58 Cause Flagellar Axoneme and Mitochondrial Sheath Defects and Asthenoteratozoospermia in Humans and Mice. Am J Hum Genet 2020;107:514-26. [PMID: 32791035 DOI: 10.1016/j.ajhg.2020.07.010] [Cited by in Crossref: 38] [Cited by in F6Publishing: 34] [Article Influence: 19.0] [Reference Citation Analysis]
36 Liu Z, Wang C, Ni F, Yang F, Wei H, Li T, Wang J, Wang B. Novel compound heterozygous variants of DNAH17 in a Chinese infertile man with multiple morphological abnormalities of sperm flagella. Andrologia 2022;:e14553. [PMID: 35932098 DOI: 10.1111/and.14553] [Reference Citation Analysis]
37 Štiavnická M, Chaulot-Talmon A, Perrier JP, Hošek P, Kenny DA, Lonergan P, Kiefer H, Fair S. Sperm DNA methylation patterns at discrete CpGs and genes involved in embryonic development are related to bull fertility. BMC Genomics 2022;23:379. [PMID: 35585482 DOI: 10.1186/s12864-022-08614-5] [Reference Citation Analysis]
38 Koay TW, Osterhof C, Orlando IMC, Keppner A, Andre D, Yousefian S, Suárez Alonso M, Correia M, Markworth R, Schödel J, Hankeln T, Hoogewijs D. Androglobin gene expression patterns and FOXJ1-dependent regulation indicate its functional association with ciliogenesis. J Biol Chem 2021;296:100291. [PMID: 33453283 DOI: 10.1016/j.jbc.2021.100291] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
39 Gu L, Liu X, Yang J, Bai J. A new hemizygous missense mutation, c.454T>C (p.S152P), in AKAP4 gene is associated with asthenozoospermia. Mol Reprod Dev 2021;88:587-97. [PMID: 34409659 DOI: 10.1002/mrd.23529] [Reference Citation Analysis]
40 Tu C, Cong J, Zhang Q, He X, Zheng R, Yang X, Gao Y, Wu H, Lv M, Gu Y, Lu S, Liu C, Tian S, Meng L, Wang W, Tan C, Nie H, Li D, Zhang H, Gong F, Hu L, Lu G, Xu W, Lin G, Zhang F, Cao Y, Tan YQ. Bi-allelic mutations of DNAH10 cause primary male infertility with asthenoteratozoospermia in humans and mice. Am J Hum Genet 2021;108:1466-77. [PMID: 34237282 DOI: 10.1016/j.ajhg.2021.06.010] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 10.0] [Reference Citation Analysis]
41 Li L, Feng F, Wang Y, Guo J, Yue W. Mutational effect of human CFAP43 splice-site variant causing multiple morphological abnormalities of the sperm flagella. Andrologia 2020;52:e13575. [PMID: 32207550 DOI: 10.1111/and.13575] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
42 Houston BJ, Conrad DF, O'Bryan MK. A framework for high-resolution phenotyping of candidate male infertility mutants: from human to mouse. Hum Genet 2021;140:155-82. [PMID: 32248361 DOI: 10.1007/s00439-020-02159-x] [Cited by in Crossref: 6] [Cited by in F6Publishing: 8] [Article Influence: 3.0] [Reference Citation Analysis]
43 Breuer K, Riedhammer KM, Müller N, Schaidinger B, Dombrowsky G, Dittrich S, Zeidler S, Bauer UMM, Westphal DS, Meitinger T, Dakal TC, Hitz MP, Breuer J, Reutter H, Hilger AC, Hoefele J. Exome sequencing in individuals with cardiovascular laterality defects identifies potential candidate genes. Eur J Hum Genet 2022. [PMID: 35474353 DOI: 10.1038/s41431-022-01100-2] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
44 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: 8] [Article Influence: 3.5] [Reference Citation Analysis]
45 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: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
46 Kumar N, Singh AK. The anatomy, movement, and functions of human sperm tail: an evolving mystery. Biol Reprod 2021;104:508-20. [PMID: 33238303 DOI: 10.1093/biolre/ioaa213] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
47 Sha Y, Wei X, Ding L, Mei L, Huang X, Lin S, Su Z, Kong L, Zhang Y, Ji Z. DNAH17 is associated with asthenozoospermia and multiple morphological abnormalities of sperm flagella. Ann Hum Genet 2020;84:271-9. [PMID: 31841227 DOI: 10.1111/ahg.12369] [Cited by in Crossref: 14] [Cited by in F6Publishing: 11] [Article Influence: 4.7] [Reference Citation Analysis]
48 Pilot M, Moura AE, Okhlopkov IM, Mamaev NV, Manaseryan NH, Hayrapetyan V, Kopaliani N, Tsingarska E, Alagaili AN, Mohammed OB, Ostrander EA, Bogdanowicz W. Human-modified canids in human-modified landscapes: The evolutionary consequences of hybridization for grey wolves and free-ranging domestic dogs. Evol Appl 2021;14:2433-56. [PMID: 34745336 DOI: 10.1111/eva.13257] [Reference Citation Analysis]
49 Du L, Chen W, Cheng Z, Wu S, He J, Han L, He Z, Qin W. Novel Gene Regulation in Normal and Abnormal Spermatogenesis. Cells 2021;10:666. [PMID: 33802813 DOI: 10.3390/cells10030666] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
50 Thomas L, Bouhouche K, Whitfield M, Thouvenin G, Coste A, Louis B, Szymanski C, Bequignon E, Papon JF, Castelli M, Lemullois M, Dhalluin X, Drouin-Garraud V, Montantin G, Tissier S, Duquesnoy P, Copin B, Dastot F, Couvet S, Barbotin AL, Faucon C, Honore I, Maitre B, Beydon N, Tamalet A, Rives N, Koll F, Escudier E, Tassin AM, Touré A, Mitchell V, Amselem S, Legendre M. TTC12 Loss-of-Function Mutations Cause Primary Ciliary Dyskinesia and Unveil Distinct Dynein Assembly Mechanisms in Motile Cilia Versus Flagella. Am J Hum Genet 2020;106:153-69. [PMID: 31978331 DOI: 10.1016/j.ajhg.2019.12.010] [Cited by in Crossref: 27] [Cited by in F6Publishing: 23] [Article Influence: 13.5] [Reference Citation Analysis]
51 Zhao Y, Wang LK, Eskin A, Kang X, Fajardo VM, Mehta Z, Pineles S, Schmidt RJ, Nagiel A, Satou G, Garg M, Federman M, Reardon LC, Lee SL, Biniwale R, Grody WW, Halnon N, Khanlou N, Quintero-Rivera F, Alejos JC, Nakano A, Fishbein GA, Van Arsdell GS, Nelson SF, Touma M. Recessive ciliopathy mutations in primary endocardial fibroelastosis: a rare neonatal cardiomyopathy in a case of Alstrom syndrome. J Mol Med (Berl) 2021. [PMID: 34387706 DOI: 10.1007/s00109-021-02112-z] [Reference Citation Analysis]
52 Yu W, An M, Xu Y, Gao Q, Lu M, Li Y, Zhang L, Wang H, Xu Z. Mutational landscape of DNAH1 in Chinese patients with multiple morphological abnormalities of the sperm flagella: cohort study and literature review. J Assist Reprod Genet 2021;38:2031-8. [PMID: 33929677 DOI: 10.1007/s10815-021-02201-5] [Reference Citation Analysis]
53 Liu C, Miyata H, Gao Y, Sha Y, Tang S, Xu Z, Whitfield M, Patrat C, Wu H, Dulioust E, Tian S, Shimada K, Cong J, Noda T, Li H, Morohoshi A, Cazin C, Kherraf ZE, Arnoult C, Jin L, He X, Ray PF, Cao Y, Touré A, Zhang F, Ikawa M. Bi-allelic DNAH8 Variants Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Primary Male Infertility. Am J Hum Genet 2020;107:330-41. [PMID: 32619401 DOI: 10.1016/j.ajhg.2020.06.004] [Cited by in Crossref: 56] [Cited by in F6Publishing: 43] [Article Influence: 28.0] [Reference Citation Analysis]
54 Aprea I, Nöthe-Menchen T, Dougherty GW, Raidt J, Loges NT, Kaiser T, Wallmeier J, Olbrich H, Strünker T, Kliesch S, Pennekamp P, Omran H. Motility of efferent duct cilia aids passage of sperm cells through the male reproductive system. Mol Hum Reprod 2021;27:gaab009. [PMID: 33561200 DOI: 10.1093/molehr/gaab009] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
55 Guo T, Tu CF, Yang DH, Ding SZ, Lei C, Wang RC, Liu L, Kang X, Shen XQ, Yang YF, Tan ZP, Tan YQ, Luo H. Bi-allelic BRWD1 variants cause male infertility with asthenoteratozoospermia and likely primary ciliary dyskinesia. Hum Genet 2021;140:761-73. [PMID: 33389130 DOI: 10.1007/s00439-020-02241-4] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
56 Gao Y, Tian S, Sha Y, Zha X, Cheng H, Wang A, Liu C, Lv M, Ni X, Li Q, Wu H, Tan Q, Tang D, Song B, Ding D, Cong J, Xu Y, Zhou P, Wei Z, Cao Y, Xu Y, Zhang F, He X. Novel bi-allelic variants in DNAH2 cause severe asthenoteratozoospermia with multiple morphological abnormalities of the flagella. Reprod Biomed Online 2021;42:963-72. [PMID: 33771466 DOI: 10.1016/j.rbmo.2021.01.011] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
57 Hwang JY, Nawaz S, Choi J, Wang H, Hussain S, Nawaz M, Lopez-Giraldez F, Jeong K, Dong W, Oh JN, Bilguvar K, Mane S, Lee CK, Bystroff C, Lifton RP, Ahmad W, Chung JJ. Genetic Defects in DNAH2 Underlie Male Infertility With Multiple Morphological Abnormalities of the Sperm Flagella in Humans and Mice. Front Cell Dev Biol 2021;9:662903. [PMID: 33968937 DOI: 10.3389/fcell.2021.662903] [Reference Citation Analysis]
58 Weng M, Sha Y, Zeng YU, Huang N, Liu W, Zhang X, Zhou H. Mutations in DNAH8 contribute to multiple morphological abnormalities of sperm flagella and male infertility. Acta Biochim Biophys Sin (Shanghai) 2021;53:472-80. [PMID: 33704367 DOI: 10.1093/abbs/gmab013] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
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