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For: Ziętkiewicz E, Nitka B, Voelkel K, Skrzypczak U, Bukowy Z, Rutkiewicz E, Humińska K, Przystałowska H, Pogorzelski A, Witt M. Population specificity of the DNAI1 gene mutation spectrum in primary ciliary dyskinesia (PCD). Respir Res 2010;11:174. [PMID: 21143860 DOI: 10.1186/1465-9921-11-174] [Cited by in Crossref: 21] [Cited by in F6Publishing: 18] [Article Influence: 1.8] [Reference Citation Analysis]
Number Citing Articles
1 Xu K, Wen M, Duan W, Ren L, Hu F, Xiao J, Wang J, Tao M, Zhang C, Wang J, Zhou Y, Zhang Y, Liu Y, Liu S. Comparative Analysis of Testis Transcriptomes from Triploid and Fertile Diploid Cyprinid Fish1. Biology of Reproduction 2015;92. [DOI: 10.1095/biolreprod.114.125609] [Cited by in Crossref: 18] [Cited by in F6Publishing: 18] [Article Influence: 2.6] [Reference Citation Analysis]
2 Amirav I, Roduta Roberts M, Mussaffi H, Mandelberg A, Roth Y, Abitbul R, Luder A, Blau H, Alkrinawi S, Aviram M, Ben-Ami M, Rotschild M, Bentur L, Shoseyov D, Cohen-Cymberknoh M, Kerem E, Avital A, Springer C, Hevroni A, Dabbah H, Elizur A, Picard E, Goldberg S, Rivlin J, Livnat G, Lavie M, Alias N, Soferman R, Olbrich H, Raidt J, Wallmeier J, Werner C, Loges NT, Omran H. Collecting clinical data in primary ciliary dyskinesia- challenges and opportunities. F1000Res 2016;5:2031. [PMID: 27781089 DOI: 10.12688/f1000research.9323.2] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
3 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]
4 Bukowy-bieryłło Z, Ziętkiewicz E, Loges NT, Wittmer M, Geremek M, Olbrich H, Fliegauf M, Voelkel K, Rutkiewicz E, Rutland J, Morgan L, Pogorzelski A, Martin J, Haan E, Berger W, Omran H, Witt M. RPGR mutations might cause reduced orientation of respiratory cilia. Pediatr Pulmonol 2013;48:352-63. [DOI: 10.1002/ppul.22632] [Cited by in Crossref: 57] [Cited by in F6Publishing: 54] [Article Influence: 5.7] [Reference Citation Analysis]
5 Li W, Tan H, Liu J, Hu J, Cui J, Wang S, Liu Q, Hu F, Ren L, Tao M, Zhao R, Yang C, Qin Q, Liu S. Comparative analysis of testis transcriptomes associated with male infertility in triploid cyprinid fish. Reprod Fertil Dev 2019;31:248-60. [PMID: 30086823 DOI: 10.1071/RD18034] [Cited by in Crossref: 6] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
6 Djakow J, Kramná L, Dušátková L, Uhlík J, Pursiheimo JP, Svobodová T, Pohunek P, Cinek O. An effective combination of sanger and next generation sequencing in diagnostics of primary ciliary dyskinesia. Pediatr Pulmonol 2016;51:498-509. [PMID: 26228299 DOI: 10.1002/ppul.23261] [Cited by in Crossref: 17] [Cited by in F6Publishing: 15] [Article Influence: 2.4] [Reference Citation Analysis]
7 Bush A, Hogg C. Primary ciliary dyskinesia: recent advances in epidemiology, diagnosis, management and relationship with the expanding spectrum of ciliopathy. Expert Review of Respiratory Medicine 2014;6:663-82. [DOI: 10.1586/ers.12.60] [Cited by in Crossref: 32] [Cited by in F6Publishing: 30] [Article Influence: 4.0] [Reference Citation Analysis]
8 Kobayashi D, Takeda H. Ciliary motility: the components and cytoplasmic preassembly mechanisms of the axonemal dyneins. Differentiation 2012;83:S23-9. [PMID: 22154137 DOI: 10.1016/j.diff.2011.11.009] [Cited by in Crossref: 45] [Cited by in F6Publishing: 40] [Article Influence: 4.1] [Reference Citation Analysis]
9 Kurkowiak M, Ziętkiewicz E, Witt M. Recent advances in primary ciliary dyskinesia genetics. J Med Genet 2015;52:1-9. [PMID: 25351953 DOI: 10.1136/jmedgenet-2014-102755] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
10 Takeuchi K, Kitano M, Kiyotoshi H, Ikegami K, Ogawa S, Ikejiri M, Nagao M, Fujisawa T, Nakatani K. A targeted next-generation sequencing panel reveals novel mutations in Japanese patients with primary ciliary dyskinesia. Auris Nasus Larynx 2018;45:585-91. [PMID: 28939216 DOI: 10.1016/j.anl.2017.09.007] [Cited by in Crossref: 18] [Cited by in F6Publishing: 16] [Article Influence: 3.6] [Reference Citation Analysis]
11 Zietkiewicz E, Bukowy-Bieryllo Z, Rabiasz A, Daca-Roszak P, Wojda A, Voelkel K, Rutkiewicz E, Pogorzelski A, Rasteiro M, Witt M. CFAP300: Mutations in Slavic Patients with Primary Ciliary Dyskinesia and a Role in Ciliary Dynein Arms Trafficking. Am J Respir Cell Mol Biol 2019;61:440-9. [PMID: 30916986 DOI: 10.1165/rcmb.2018-0260OC] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
12 Djakow J, Svobodová T, Hrach K, Uhlík J, Cinek O, Pohunek P. Effectiveness of sequencing selected exons of DNAH5 and DNAI1 in diagnosis of primary ciliary dyskinesia. Pediatr Pulmonol 2012;47:864-75. [PMID: 22416021 DOI: 10.1002/ppul.22520] [Cited by in Crossref: 23] [Cited by in F6Publishing: 22] [Article Influence: 2.3] [Reference Citation Analysis]
13 Bukowy Z, Ziętkiewicz E, Witt M. In vitro culturing of ciliary respiratory cells--a model for studies of genetic diseases. J Appl Genet 2011;52:39-51. [PMID: 21125367 DOI: 10.1007/s13353-010-0005-1] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 0.8] [Reference Citation Analysis]
14 Ziętkiewicz E, Bukowy-Bieryłło Z, Voelkel K, Klimek B, Dmeńska H, Pogorzelski A, Sulikowska-Rowińska A, Rutkiewicz E, Witt M. Mutations in radial spoke head genes and ultrastructural cilia defects in East-European cohort of primary ciliary dyskinesia patients. PLoS One 2012;7:e33667. [PMID: 22448264 DOI: 10.1371/journal.pone.0033667] [Cited by in Crossref: 45] [Cited by in F6Publishing: 39] [Article Influence: 4.5] [Reference Citation Analysis]
15 Guo T, Tan ZP, Chen HM, Zheng DY, Liu L, Huang XG, Chen P, Luo H, Yang YF. An effective combination of whole-exome sequencing and runs of homozygosity for the diagnosis of primary ciliary dyskinesia in consanguineous families. Sci Rep 2017;7:7905. [PMID: 28801648 DOI: 10.1038/s41598-017-08510-z] [Cited by in Crossref: 16] [Cited by in F6Publishing: 15] [Article Influence: 3.2] [Reference Citation Analysis]
16 Kurkowiak M, Ziętkiewicz E, Witt M. Recent advances in primary ciliary dyskinesia genetics. J Med Genet 2015;52:1-9. [PMID: 25351953 DOI: 10.1136/jmedgenet-2014-102755] [Cited by in Crossref: 63] [Cited by in F6Publishing: 55] [Article Influence: 7.9] [Reference Citation Analysis]
17 Reula A, Lucas J, Moreno-galdó A, Romero T, Milara X, Carda C, Mata-roig M, Escribano A, Dasi F, Armengot-carceller M. New insights in primary ciliary dyskinesia. Expert Opinion on Orphan Drugs 2017;5:537-48. [DOI: 10.1080/21678707.2017.1324780] [Cited by in Crossref: 11] [Cited by in F6Publishing: 3] [Article Influence: 2.2] [Reference Citation Analysis]
18 Amirav I, Roduta Roberts M, Mussaffi H, Mandelberg A, Roth Y, Abitbul R, Luder A, Blau H, Alkrinawi S, Aviram M, Ben-ami M, Rotschild M, Bentur L, Shoseyov D, Cohen-cymberknoh M, Kerem E, Avital A, Springer C, Hevroni A, Dabbah H, Elizur A, Picard E, Goldberg S, Rivlin J, Livnat G, Lavie M, Alias N, Soferman R, Olbrich H, Raidt J, Wallmeier J, Werner C, Loges NT, Omran H. Collecting clinical data in primary ciliary dyskinesia- challenges and opportunities. F1000Res 2016;5:2031. [DOI: 10.12688/f1000research.9323.1] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 0.7] [Reference Citation Analysis]
19 Catana A, Apostu AP. The determination factors of left-right asymmetry disorders- a short review. Clujul Med 2017;90:139-46. [PMID: 28559696 DOI: 10.15386/cjmed-701] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 0.4] [Reference Citation Analysis]
20 Ziętkiewicz E, Rutkiewicz E, Pogorzelski A, Klimek B, Voelkel K, Witt M. CFTR mutations spectrum and the efficiency of molecular diagnostics in Polish cystic fibrosis patients. PLoS One 2014;9:e89094. [PMID: 24586523 DOI: 10.1371/journal.pone.0089094] [Cited by in Crossref: 8] [Cited by in F6Publishing: 10] [Article Influence: 1.0] [Reference Citation Analysis]
21 Wan Y, Qu N, Yang Y, Ma J, Li Z, Zhang Z. Identification of a 3-gene signature based on differentially expressed invasion genes related to cancer molecular subtypes to predict the prognosis of osteosarcoma patients. Bioengineered 2021;12:5916-31. [PMID: 34488541 DOI: 10.1080/21655979.2021.1971919] [Reference Citation Analysis]