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For: 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]
Number Citing Articles
1 Xiang W, Zur Lage P, Newton FG, Qiu G, Jarman AP. The dynamics of protein localisation to restricted zones within Drosophila mechanosensory cilia. Sci Rep 2022;12:13338. [PMID: 35922464 DOI: 10.1038/s41598-022-17189-w] [Reference Citation Analysis]
2 Lynham J, Houry WA. The Role of Hsp90-R2TP in Macromolecular Complex Assembly and Stabilization. Biomolecules 2022;12:1045. [DOI: 10.3390/biom12081045] [Reference Citation Analysis]
3 Yu X, Yuan L, Deng S, Xia H, Tu X, Deng X, Huang X, Cao X, Deng H. Identification of DNAH17 Variants in Han-Chinese Patients With Left–Right Asymmetry Disorders. Front Genet 2022;13:862292. [DOI: 10.3389/fgene.2022.862292] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Bukowy-Bieryllo Z, Witt M, Zietkiewicz E. Perspectives for Primary Ciliary Dyskinesia. Int J Mol Sci 2022;23:4122. [PMID: 35456939 DOI: 10.3390/ijms23084122] [Reference Citation Analysis]
5 Bouhouche K, Valentine MS, Le Borgne P, Lemullois M, Yano J, Lodh S, Nabi A, Tassin AM, Van Houten JL. Paramecium, a Model to Study Ciliary Beating and Ciliogenesis: Insights From Cutting-Edge Approaches. Front Cell Dev Biol 2022;10:847908. [DOI: 10.3389/fcell.2022.847908] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 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]
7 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] [Reference Citation Analysis]
8 Amselem S, Gueguen S, Weinbach J, Clement A, Landais P; RaDiCo Program. RaDiCo, the French national research program on rare disease cohorts. Orphanet J Rare Dis 2021;16:454. [PMID: 34715889 DOI: 10.1186/s13023-021-02089-5] [Reference Citation Analysis]
9 Zhang X, Sun J, Lu Y, Zhang J, Shimada K, Noda T, Zhao S, Koyano T, Matsuyama M, Zhou S, Wu J, Ikawa M, Liu M. LRRC23 is a conserved component of the radial spoke that is necessary for sperm motility and male fertility in mice. J Cell Sci 2021;134:jcs259381. [PMID: 34585727 DOI: 10.1242/jcs.259381] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
10 Valentine M, Van Houten J. Using Paramecium as a Model for Ciliopathies. Genes (Basel) 2021;12:1493. [PMID: 34680887 DOI: 10.3390/genes12101493] [Reference Citation Analysis]
11 Jayasena CN, Sironen A. Diagnostics and Management of Male Infertility in Primary Ciliary Dyskinesia. Diagnostics (Basel) 2021;11:1550. [PMID: 34573892 DOI: 10.3390/diagnostics11091550] [Reference Citation Analysis]
12 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]
13 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]
14 O'Connor MG, Horani A, Shapiro AJ. Progress in Diagnosing Primary Ciliary Dyskinesia: The North American Perspective. Diagnostics (Basel) 2021;11:1278. [PMID: 34359360 DOI: 10.3390/diagnostics11071278] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
15 Bouhouche K, Le Borgne P, Lemullois M, Tassin AM. [Paramecium, a model organism to study ciliogenesis and ciliopathies]. Med Sci (Paris) 2021;37:632-8. [PMID: 34180823 DOI: 10.1051/medsci/2021087] [Reference Citation Analysis]
16 El Khouri E, Ghoumid J, Haye D, Giuliano F, Drevillon L, Briand-Suleau A, De La Grange P, Nau V, Gaillon T, Bienvenu T, Jacquemin-Sablon H, Goossens M, Amselem S, Giurgea I. Wnt/β-catenin pathway and cell adhesion deregulation in CSDE1-related intellectual disability and autism spectrum disorders. Mol Psychiatry 2021. [PMID: 33867523 DOI: 10.1038/s41380-021-01072-7] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
17 Yiallouros PK, Kouis P, Kyriacou K, Evriviadou A, Anagnostopoulou P, Matthaiou A, Tsiolakis I, Pirpa P, Michailidou K, Potamiti L, Loizidou MA, Hadjisavvas A. Implementation of multigene panel NGS diagnosis in the national primary ciliary dyskinesia cohort of Cyprus: An island with a high disease prevalence. Hum Mutat 2021;42:e62-77. [PMID: 33715250 DOI: 10.1002/humu.24196] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
18 Duong Phu M, Bross S, Burkhalter MD, Philipp M. Limitations and opportunities in the pharmacotherapy of ciliopathies. Pharmacol Ther 2021;225:107841. [PMID: 33771583 DOI: 10.1016/j.pharmthera.2021.107841] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
19 Aprea I, Raidt J, Höben IM, Loges NT, Nöthe-Menchen T, Pennekamp P, Olbrich H, Kaiser T, Biebach L, Tüttelmann F, Horvath J, Schubert M, Krallmann C, Kliesch S, Omran H. Defects in the cytoplasmic assembly of axonemal dynein arms cause morphological abnormalities and dysmotility in sperm cells leading to male infertility. PLoS Genet 2021;17:e1009306. [PMID: 33635866 DOI: 10.1371/journal.pgen.1009306] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 4.0] [Reference Citation Analysis]
20 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]
21 Brennan SK, Molter D, Menezes M, Dunsky K, Leonard D, Lieu J, Hirose K, Hazan G, Horani A, Ferkol T, Brody SL. Implementation of a screening tool for primary ciliary dyskinesia (PCD) in a pediatric otolaryngology clinic. Int J Pediatr Otorhinolaryngol 2021;142:110586. [PMID: 33388601 DOI: 10.1016/j.ijporl.2020.110586] [Reference Citation Analysis]
22 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]
23 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]
24 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]
25 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: 10] [Article Influence: 4.5] [Reference Citation Analysis]
26 Bhatt R, Hogg C. Primary ciliary dyskinesia: a major player in a bigger game. Breathe (Sheff) 2020;16:200047. [PMID: 33304404 DOI: 10.1183/20734735.0047-2020] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
27 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: 63] [Article Influence: 17.5] [Reference Citation Analysis]