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Cited by in F6Publishing
For: Geremek M, Schoenmaker F, Zietkiewicz E, Pogorzelski A, Diehl S, Wijmenga C, Witt M. Sequence analysis of 21 genes located in the Kartagener syndrome linkage region on chromosome 15q. Eur J Hum Genet 2008;16:688-95. [DOI: 10.1038/ejhg.2008.5] [Cited by in Crossref: 12] [Cited by in F6Publishing: 10] [Article Influence: 0.9] [Reference Citation Analysis]
Number Citing Articles
1 Xu X, Gong P, Wen J. Clinical and genetic analysis of a family with Kartagener syndrome caused by novel DNAH5 mutations. J Assist Reprod Genet 2017;34:275-81. [PMID: 27988889 DOI: 10.1007/s10815-016-0849-3] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 1.2] [Reference Citation Analysis]
2 Austin-Tse C, Halbritter J, Zariwala MA, Gilberti RM, Gee HY, Hellman N, Pathak N, Liu Y, Panizzi JR, Patel-King RS, Tritschler D, Bower R, O'Toole E, Porath JD, Hurd TW, Chaki M, Diaz KA, Kohl S, Lovric S, Hwang DY, Braun DA, Schueler M, Airik R, Otto EA, Leigh MW, Noone PG, Carson JL, Davis SD, Pittman JE, Ferkol TW, Atkinson JJ, Olivier KN, Sagel SD, Dell SD, Rosenfeld M, Milla CE, Loges NT, Omran H, Porter ME, King SM, Knowles MR, Drummond IA, Hildebrandt F. Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia. Am J Hum Genet 2013;93:672-86. [PMID: 24094744 DOI: 10.1016/j.ajhg.2013.08.015] [Cited by in Crossref: 127] [Cited by in F6Publishing: 117] [Article Influence: 15.9] [Reference Citation Analysis]
3 Charlier P, Costea G, Huynh-Charlier I, Brun L, de la Grandmaison GL. Diagnosis of aortic dextroposition on human skeletal remains. Leg Med (Tokyo) 2012;14:101-4. [PMID: 22284940 DOI: 10.1016/j.legalmed.2011.12.006] [Cited by in Crossref: 1] [Article Influence: 0.1] [Reference Citation Analysis]
4 Beckers A, Fuhl F, Ott T, Boldt K, Brislinger MM, Walentek P, Schuster-Gossler K, Hegermann J, Alten L, Kremmer E, Przykopanski A, Serth K, Ueffing M, Blum M, Gossler A. The highly conserved FOXJ1 target CFAP161 is dispensable for motile ciliary function in mouse and Xenopus. Sci Rep 2021;11:13333. [PMID: 34172766 DOI: 10.1038/s41598-021-92495-3] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
5 Sha YW, Ding L, Li P. Management of primary ciliary dyskinesia/Kartagener's syndrome in infertile male patients and current progress in defining the underlying genetic mechanism. Asian J Androl 2014;16:101-6. [PMID: 24369140 DOI: 10.4103/1008-682X.122192] [Cited by in Crossref: 29] [Cited by in F6Publishing: 13] [Article Influence: 3.6] [Reference Citation Analysis]
6 Ma M, Stoyanova M, Rademacher G, Dutcher SK, Brown A, Zhang R. Structure of the Decorated Ciliary Doublet Microtubule. Cell 2019;179:909-922.e12. [PMID: 31668805 DOI: 10.1016/j.cell.2019.09.030] [Cited by in Crossref: 44] [Cited by in F6Publishing: 37] [Article Influence: 14.7] [Reference Citation Analysis]
7 Castleman VH, Romio L, Chodhari R, Hirst RA, de Castro SC, Parker KA, Ybot-Gonzalez P, Emes RD, Wilson SW, Wallis C, Johnson CA, Herrera RJ, Rutman A, Dixon M, Shoemark A, Bush A, Hogg C, Gardiner RM, Reish O, Greene ND, O'Callaghan C, Purton S, Chung EM, Mitchison HM. Mutations in radial spoke head protein genes RSPH9 and RSPH4A cause primary ciliary dyskinesia with central-microtubular-pair abnormalities. Am J Hum Genet 2009;84:197-209. [PMID: 19200523 DOI: 10.1016/j.ajhg.2009.01.011] [Cited by in Crossref: 219] [Cited by in F6Publishing: 197] [Article Influence: 16.8] [Reference Citation Analysis]
8 Andjelkovic M, Minic P, Vreca M, Stojiljkovic M, Skakic A, Sovtic A, Rodic M, Skodric-Trifunovic V, Maric N, Visekruna J, Spasovski V, Pavlovic S. Genomic profiling supports the diagnosis of primary ciliary dyskinesia and reveals novel candidate genes and genetic variants. PLoS One 2018;13:e0205422. [PMID: 30300419 DOI: 10.1371/journal.pone.0205422] [Cited by in Crossref: 16] [Cited by in F6Publishing: 12] [Article Influence: 4.0] [Reference Citation Analysis]
9 Escudier E, Duquesnoy P, Papon JF, Amselem S. Ciliary defects and genetics of primary ciliary dyskinesia. Paediatr Respir Rev 2009;10:51-4. [PMID: 19410201 DOI: 10.1016/j.prrv.2009.02.001] [Cited by in Crossref: 56] [Cited by in F6Publishing: 53] [Article Influence: 4.3] [Reference Citation Analysis]
10 Türkoğlu K, Orhan K, Demir P, Karabulut B, Can-Karabulut DC. Primary ciliary dyskinesia: Kartagener syndrome with central giant cell granuloma. A case report. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2010;110:e49-56. [PMID: 20868986 DOI: 10.1016/j.tripleo.2010.05.054] [Cited by in F6Publishing: 1] [Reference Citation Analysis]