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For: Leigh MW, Pittman JE, Carson JL, Ferkol TW, Dell SD, Davis SD, Knowles MR, Zariwala MA. Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome. Genet Med 2009;11:473-87. [PMID: 19606528 DOI: 10.1097/GIM.0b013e3181a53562] [Cited by in Crossref: 246] [Cited by in F6Publishing: 138] [Article Influence: 18.9] [Reference Citation Analysis]
Number Citing Articles
1 Pereira R, Oliveira J, Ferraz L, Barros A, Santos R, Sousa M. Mutation analysis in patients with total sperm immotility. J Assist Reprod Genet 2015;32:893-902. [PMID: 25877373 DOI: 10.1007/s10815-015-0474-6] [Cited by in Crossref: 17] [Cited by in F6Publishing: 16] [Article Influence: 2.4] [Reference Citation Analysis]
2 Mali GR, Ali FA, Lau CK, Begum F, Boulanger J, Howe JD, Chen ZA, Rappsilber J, Skehel M, Carter AP. Shulin packages axonemal outer dynein arms for ciliary targeting. Science 2021;371:910-6. [PMID: 33632841 DOI: 10.1126/science.abe0526] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 6.0] [Reference Citation Analysis]
3 Solomon GM, Francis R, Chu KK, Birket SE, Gabriel G, Trombley JE, Lemke KL, Klena N, Turner B, Tearney GJ, Lo CW, Rowe SM. Assessment of ciliary phenotype in primary ciliary dyskinesia by micro-optical coherence tomography. JCI Insight 2017;2:e91702. [PMID: 28289722 DOI: 10.1172/jci.insight.91702] [Cited by in Crossref: 12] [Cited by in F6Publishing: 11] [Article Influence: 2.4] [Reference Citation Analysis]
4 Benjamens S, van den Berg TAJ, Lange JFM, Pol RA. Living donor hand-assisted laparoscopic nephrectomy in a healthy individual with situs inversus totalis: no need to turn down the donor. BMJ Case Rep 2020;13:e233523. [PMID: 31974263 DOI: 10.1136/bcr-2019-233523] [Reference Citation Analysis]
5 Daniels ML, Noone PG. Genetics, diagnosis, and future treatment strategies for primary ciliary dyskinesia. Expert Opin Orphan Drugs 2015;3:31-44. [PMID: 26998415 DOI: 10.1517/21678707.2015.989212] [Cited by in Crossref: 11] [Cited by in F6Publishing: 8] [Article Influence: 1.4] [Reference Citation Analysis]
6 Schwarzenbacher H, Burgstaller J, Seefried FR, Wurmser C, Hilbe M, Jung S, Fuerst C, Dinhopl N, Weissenböck H, Fuerst-Waltl B, Dolezal M, Winkler R, Grueter O, Bleul U, Wittek T, Fries R, Pausch H. A missense mutation in TUBD1 is associated with high juvenile mortality in Braunvieh and Fleckvieh cattle. BMC Genomics 2016;17:400. [PMID: 27225349 DOI: 10.1186/s12864-016-2742-y] [Cited by in Crossref: 33] [Cited by in F6Publishing: 28] [Article Influence: 5.5] [Reference Citation Analysis]
7 Knowles MR, Ostrowski LE, Loges NT, Hurd T, Leigh MW, Huang L, Wolf WE, Carson JL, Hazucha MJ, Yin W, Davis SD, Dell SD, Ferkol TW, Sagel SD, Olivier KN, Jahnke C, Olbrich H, Werner C, Raidt J, Wallmeier J, Pennekamp P, Dougherty GW, Hjeij R, Gee HY, Otto EA, Halbritter J, Chaki M, Diaz KA, Braun DA, Porath JD, Schueler M, Baktai G, Griese M, Turner EH, Lewis AP, Bamshad MJ, Nickerson DA, Hildebrandt F, Shendure J, Omran H, Zariwala MA. Mutations in SPAG1 cause primary ciliary dyskinesia associated with defective outer and inner dynein arms. Am J Hum Genet 2013;93:711-20. [PMID: 24055112 DOI: 10.1016/j.ajhg.2013.07.025] [Cited by in Crossref: 110] [Cited by in F6Publishing: 96] [Article Influence: 12.2] [Reference Citation Analysis]
8 Rubbo B, Behan L, Dehlink E, Goutaki M, Hogg C, Kouis P, Kuehni CE, Latzin P, Nielsen K, Norris D, Nyilas S, Price M, Lucas JS; BEAT-PCD. Proceedings of the COST action BM1407 inaugural conference BEAT-PCD: translational research in primary ciliary dyskinesia - bench, bedside, and population perspectives. BMC Proc 2016;10:66. [PMID: 28813544 DOI: 10.1186/s12919-016-0067-0] [Cited by in Crossref: 20] [Cited by in F6Publishing: 14] [Article Influence: 3.3] [Reference Citation Analysis]
9 Love D, Li FQ, Burke MC, Cyge B, Ohmitsu M, Cabello J, Larson JE, Brody SL, Cohen JC, Takemaru K. Altered lung morphogenesis, epithelial cell differentiation and mechanics in mice deficient in the Wnt/β-catenin antagonist Chibby. PLoS One 2010;5:e13600. [PMID: 21049041 DOI: 10.1371/journal.pone.0013600] [Cited by in Crossref: 28] [Cited by in F6Publishing: 27] [Article Influence: 2.3] [Reference Citation Analysis]
10 Tucker AS. Major evolutionary transitions and innovations: the tympanic middle ear. Philos Trans R Soc Lond B Biol Sci 2017;372:20150483. [PMID: 27994124 DOI: 10.1098/rstb.2015.0483] [Cited by in Crossref: 25] [Cited by in F6Publishing: 17] [Article Influence: 5.0] [Reference Citation Analysis]
11 Varagur K, Sanka SA, Strahle JM. Syndromic Hydrocephalus. Neurosurg Clin N Am 2022;33:67-79. [PMID: 34801143 DOI: 10.1016/j.nec.2021.09.006] [Reference Citation Analysis]
12 Ryu D, Ryu J, Lee C. Genome-wide association study reveals sex-specific selection signals against autosomal nucleotide variants. J Hum Genet 2016;61:423-6. [PMID: 26763874 DOI: 10.1038/jhg.2015.169] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 1.2] [Reference Citation Analysis]
13 Ostrowski LE, Yin W, Patel M, Sechelski J, Rogers T, Burns K, Grubb BR, Olsen JC. Restoring ciliary function to differentiated primary ciliary dyskinesia cells with a lentiviral vector. Gene Ther 2014;21:253-61. [PMID: 24451115 DOI: 10.1038/gt.2013.79] [Cited by in Crossref: 21] [Cited by in F6Publishing: 21] [Article Influence: 2.6] [Reference Citation Analysis]
14 Jain R, Javidan-Nejad C, Alexander-Brett J, Horani A, Cabellon MC, Walter MJ, Brody SL. Sensory functions of motile cilia and implication for bronchiectasis. Front Biosci (Schol Ed) 2012;4:1088-98. [PMID: 22202111 DOI: 10.2741/s320] [Cited by in Crossref: 6] [Cited by in F6Publishing: 24] [Article Influence: 0.6] [Reference Citation Analysis]
15 Rodriguez K, Gaston B, Wasman J, Marozkina N. Lessons From Unilateral Loss of Cilia: Early Nasal Nitric Oxide Gas Mixing and the Role of Sinus Patency in Determining Nasal Nitric Oxide. Clin Med Insights Ear Nose Throat 2017;10:1179550617746361. [PMID: 29276419 DOI: 10.1177/1179550617746361] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
16 Knowles MR, Leigh MW, Ostrowski LE, Huang L, Carson JL, Hazucha MJ, Yin W, Berg JS, Davis SD, Dell SD, Ferkol TW, Rosenfeld M, Sagel SD, Milla CE, Olivier KN, Turner EH, Lewis AP, Bamshad MJ, Nickerson DA, Shendure J, Zariwala MA; Genetic Disorders of Mucociliary Clearance Consortium. Exome sequencing identifies mutations in CCDC114 as a cause of primary ciliary dyskinesia. Am J Hum Genet 2013;92:99-106. [PMID: 23261302 DOI: 10.1016/j.ajhg.2012.11.003] [Cited by in Crossref: 108] [Cited by in F6Publishing: 90] [Article Influence: 12.0] [Reference Citation Analysis]
17 Horani A, Brody SL, Ferkol TW. Picking up speed: advances in the genetics of primary ciliary dyskinesia. Pediatr Res 2014;75:158-64. [PMID: 24192704 DOI: 10.1038/pr.2013.200] [Cited by in Crossref: 50] [Cited by in F6Publishing: 43] [Article Influence: 5.6] [Reference Citation Analysis]
18 Yuan S, Sun Z. Expanding horizons: ciliary proteins reach beyond cilia. Annu Rev Genet 2013;47:353-76. [PMID: 24016188 DOI: 10.1146/annurev-genet-111212-133243] [Cited by in Crossref: 55] [Cited by in F6Publishing: 58] [Article Influence: 6.1] [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 Horani A, Ferkol TW. Advances in the Genetics of Primary Ciliary Dyskinesia: Clinical Implications. Chest 2018;154:645-52. [PMID: 29800551 DOI: 10.1016/j.chest.2018.05.007] [Cited by in Crossref: 52] [Cited by in F6Publishing: 40] [Article Influence: 13.0] [Reference Citation Analysis]
21 Horani A, Brody SL, Ferkol TW, Shoseyov D, Wasserman MG, Ta-shma A, Wilson KS, Bayly PV, Amirav I, Cohen-Cymberknoh M, Dutcher SK, Elpeleg O, Kerem E. CCDC65 mutation causes primary ciliary dyskinesia with normal ultrastructure and hyperkinetic cilia. PLoS One 2013;8:e72299. [PMID: 23991085 DOI: 10.1371/journal.pone.0072299] [Cited by in Crossref: 77] [Cited by in F6Publishing: 69] [Article Influence: 8.6] [Reference Citation Analysis]
22 Nakhleh N, Francis R, Giese RA, Tian X, Li Y, Zariwala MA, Yagi H, Khalifa O, Kureshi S, Chatterjee B, Sabol SL, Swisher M, Connelly PS, Daniels MP, Srinivasan A, Kuehl K, Kravitz N, Burns K, Sami I, Omran H, Barmada M, Olivier K, Chawla KK, Leigh M, Jonas R, Knowles M, Leatherbury L, Lo CW. High prevalence of respiratory ciliary dysfunction in congenital heart disease patients with heterotaxy. Circulation 2012;125:2232-42. [PMID: 22499950 DOI: 10.1161/CIRCULATIONAHA.111.079780] [Cited by in Crossref: 117] [Cited by in F6Publishing: 65] [Article Influence: 11.7] [Reference Citation Analysis]
23 Yaghi A, Dolovich MB. Airway Epithelial Cell Cilia and Obstructive Lung Disease. Cells 2016;5:E40. [PMID: 27845721 DOI: 10.3390/cells5040040] [Cited by in Crossref: 72] [Cited by in F6Publishing: 57] [Article Influence: 12.0] [Reference Citation Analysis]
24 Quintanilha JCF, Wang J, Sibley AB, Jiang C, Etheridge AS, Shen F, Jiang G, Mulkey F, Patel JN, Hertz DL, Dees EC, McLeod HL, Bertagnolli M, Rugo H, Kindler HL, Kelly WK, Ratain MJ, Kroetz DL, Owzar K, Schneider BP, Lin D, Innocenti F. Bevacizumab-induced hypertension and proteinuria: a genome-wide study of more than 1000 patients. Br J Cancer 2021. [PMID: 34616010 DOI: 10.1038/s41416-021-01557-w] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
25 Zhang B, Ma H, Khan T, Ma A, Li T, Zhang H, Gao J, Zhou J, Li Y, Yu C, Bao J, Ali A, Murtaza G, Yin H, Gao Q, Jiang X, Zhang F, Liu C, Khan I, Zubair M, Hussain HMJ, Khan R, Yousaf A, Yuan L, Lu Y, Xu X, Wang Y, Tao Q, Hao Q, Fang H, Cheng H, Zhang Y, Shi Q. A DNAH17 missense variant causes flagella destabilization and asthenozoospermia. J Exp Med 2020;217:e20182365. [PMID: 31658987 DOI: 10.1084/jem.20182365] [Cited by in Crossref: 26] [Cited by in F6Publishing: 25] [Article Influence: 13.0] [Reference Citation Analysis]
26 Huang C, Liu NC, Wang XB, Gu BH, Zhang JX, Li-Zhang, Li Z. Novel deletion mutations of the PIH1D3 gene in an infertile young man with primary ciliary dyskinesia and his cousin with Kartagener's syndrome. Asian J Androl 2021;23:330-2. [PMID: 33106461 DOI: 10.4103/aja.aja_43_20] [Reference Citation Analysis]
27 Lee JH, McDonald ML, Cho MH, Wan ES, Castaldi PJ, Hunninghake GM, Marchetti N, Lynch DA, Crapo JD, Lomas DA, Coxson HO, Bakke PS, Silverman EK, Hersh CP; COPDGene and ECLIPSE Investigators. DNAH5 is associated with total lung capacity in chronic obstructive pulmonary disease. Respir Res 2014;15:97. [PMID: 25134640 DOI: 10.1186/s12931-014-0097-y] [Cited by in Crossref: 15] [Cited by in F6Publishing: 16] [Article Influence: 1.9] [Reference Citation Analysis]
28 Horani A, Druley TE, Zariwala MA, Patel AC, Levinson BT, Van Arendonk LG, Thornton KC, Giacalone JC, Albee AJ, Wilson KS, Turner EH, Nickerson DA, Shendure J, Bayly PV, Leigh MW, Knowles MR, Brody SL, Dutcher SK, Ferkol TW. Whole-exome capture and sequencing identifies HEATR2 mutation as a cause of primary ciliary dyskinesia. Am J Hum Genet 2012;91:685-93. [PMID: 23040496 DOI: 10.1016/j.ajhg.2012.08.022] [Cited by in Crossref: 130] [Cited by in F6Publishing: 115] [Article Influence: 13.0] [Reference Citation Analysis]
29 Gabriel GC, Lo CW. Left-right patterning in congenital heart disease beyond heterotaxy. Am J Med Genet C Semin Med Genet 2020;184:90-6. [PMID: 31999049 DOI: 10.1002/ajmg.c.31768] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 3.0] [Reference Citation Analysis]
30 Burvill A, Blackham R, Hamdorf J. Laparoscopic sleeve gastrectomy in a patient with situs inversus totalis and Kartagener syndrome: an unusual surgical conundrum. BMJ Case Rep 2019;12:e229550. [PMID: 31345831 DOI: 10.1136/bcr-2019-229550] [Cited by in Crossref: 2] [Article Influence: 0.7] [Reference Citation Analysis]
31 Hoque M, Kim EN, Chen D, Li F, Takemaru K. Essential Roles of Efferent Duct Multicilia in Male Fertility. Cells 2022;11:341. [DOI: 10.3390/cells11030341] [Reference Citation Analysis]
32 Knowles MR, Daniels LA, Davis SD, Zariwala MA, Leigh MW. Primary ciliary dyskinesia. Recent advances in diagnostics, genetics, and characterization of clinical disease. Am J Respir Crit Care Med. 2013;188:913-922. [PMID: 23796196 DOI: 10.1164/rccm.201301-0059ci] [Cited by in Crossref: 288] [Cited by in F6Publishing: 150] [Article Influence: 32.0] [Reference Citation Analysis]
33 Teves ME, Zhang Z, Costanzo RM, Henderson SC, Corwin FD, Zweit J, Sundaresan G, Subler M, Salloum FN, Rubin BK, Strauss JF 3rd. Sperm-associated antigen-17 gene is essential for motile cilia function and neonatal survival. Am J Respir Cell Mol Biol 2013;48:765-72. [PMID: 23418344 DOI: 10.1165/rcmb.2012-0362OC] [Cited by in Crossref: 31] [Cited by in F6Publishing: 27] [Article Influence: 3.4] [Reference Citation Analysis]
34 Moye AR, Bedoni N, Cunningham JG, Sanzhaeva U, Tucker ES, Mathers P, Peter VG, Quinodoz M, Paris LP, Coutinho-Santos L, Camacho P, Purcell MG, Winkelmann AC, Foster JA, Pugacheva EN, Rivolta C, Ramamurthy V. Mutations in ARL2BP, a protein required for ciliary microtubule structure, cause syndromic male infertility in humans and mice. PLoS Genet 2019;15:e1008315. [PMID: 31425546 DOI: 10.1371/journal.pgen.1008315] [Cited by in Crossref: 12] [Cited by in F6Publishing: 11] [Article Influence: 4.0] [Reference Citation Analysis]
35 Falkenberg LG, Beckman SA, Ravisankar P, Dohn TE, Waxman JS. Ccdc103 promotes myeloid cell proliferation and migration independent of motile cilia. Dis Model Mech 2021;14:dmm048439. [PMID: 34028558 DOI: 10.1242/dmm.048439] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
36 McEvoy MJ. Cyanotic episodes in an infant with known situs inversus: indications for an apparent life-threatening event evaluation. J Pediatr Health Care 2012;26:364-9. [PMID: 22410196 DOI: 10.1016/j.pedhc.2012.02.001] [Reference Citation Analysis]
37 Juárez OE, Arreola-meraz L, Sánchez-castrejón E, Avila-poveda OH, López-galindo LL, Rosas C, Galindo-sánchez CE. Oviducal gland transcriptomics of Octopus maya through physiological stages and the negative effects of temperature on fertilization. PeerJ 2022;10:e12895. [DOI: 10.7717/peerj.12895] [Reference Citation Analysis]
38 Xu G, Wilson KS, Okamoto RJ, Shao JY, Dutcher SK, Bayly PV. Flexural Rigidity and Shear Stiffness of Flagella Estimated from Induced Bends and Counterbends. Biophys J 2016;110:2759-68. [PMID: 27332134 DOI: 10.1016/j.bpj.2016.05.017] [Cited by in Crossref: 25] [Cited by in F6Publishing: 18] [Article Influence: 5.0] [Reference Citation Analysis]
39 Shapiro AJ, Zariwala MA, Ferkol T, Davis SD, Sagel SD, Dell SD, Rosenfeld M, Olivier KN, Milla C, Daniel SJ, Kimple AJ, Manion M, Knowles MR, Leigh MW; Genetic Disorders of Mucociliary Clearance Consortium. Diagnosis, monitoring, and treatment of primary ciliary dyskinesia: PCD foundation consensus recommendations based on state of the art review. Pediatr Pulmonol 2016;51:115-32. [PMID: 26418604 DOI: 10.1002/ppul.23304] [Cited by in Crossref: 170] [Cited by in F6Publishing: 138] [Article Influence: 24.3] [Reference Citation Analysis]
40 Yashiro K, Miyagawa S, Sawa Y. Molecular Mechanism Underlying Heterotaxy and Cardiac Isomerism. Ped Cardiol Card Surg 2017;33:349-61. [DOI: 10.9794/jspccs.33.349] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
41 Kim RH, A Hall D, Cutz E, Knowles MR, Nelligan KA, Nykamp K, Zariwala MA, Dell SD. The role of molecular genetic analysis in the diagnosis of primary ciliary dyskinesia. Ann Am Thorac Soc 2014;11:351-9. [PMID: 24498942 DOI: 10.1513/AnnalsATS.201306-194OC] [Cited by in Crossref: 38] [Cited by in F6Publishing: 18] [Article Influence: 4.8] [Reference Citation Analysis]
42 Cho EH, Ki CS, Yun SA, Kim SY, Jhun BW, Koh WJ, Huh HJ, Lee NY. Genetic Analysis of Korean Adult Patients with Nontuberculous Mycobacteria Suspected of Primary Ciliary Dyskinesia Using Whole Exome Sequencing. Yonsei Med J 2021;62:224-30. [PMID: 33635012 DOI: 10.3349/ymj.2021.62.3.224] [Reference Citation Analysis]
43 Guerri G, Maniscalchi T, Barati S, Dhuli K, Busetto GM, Del Giudice F, De Berardinis E, De Antoni L, Miertus J, Bertelli M. Syndromic infertility. Acta Biomed 2019;90:75-82. [PMID: 31577259 DOI: 10.23750/abm.v90i10-S.8764] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
44 Cakmak A, Inal-Ince D, Sonbahar-Ulu H, Bozdemir-Ozel C, Tekerlek H, Saglam M, Calik-Kutukcu E, Vardar-Yagli N, Yalcin EE, Ozcelik U, Arikan H. Aerobic exercise training in Kartagener's syndrome: case report. J Exerc Rehabil 2019;15:468-71. [PMID: 31316943 DOI: 10.12965/jer.1938144.072] [Reference Citation Analysis]
45 Precone V, Cannarella R, Paolacci S, Busetto GM, Beccari T, Stuppia L, Tonini G, Zulian A, Marceddu G, Calogero AE, Bertelli M. Male Infertility Diagnosis: Improvement of Genetic Analysis Performance by the Introduction of Pre-Diagnostic Genes in a Next-Generation Sequencing Custom-Made Panel. Front Endocrinol (Lausanne) 2020;11:605237. [PMID: 33574797 DOI: 10.3389/fendo.2020.605237] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
46 Michalik M, Samet A, Dmowska-Koroblewska A, Podbielska-Kubera A, Waszczuk-Jankowska M, Struck-Lewicka W, Markuszewski MJ. An Overview of the Application of Systems Biology in an Understanding of Chronic Rhinosinusitis (CRS) Development. J Pers Med 2020;10:E245. [PMID: 33255995 DOI: 10.3390/jpm10040245] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
47 McManus IC, Davison A, Armour JA. Multilocus genetic models of handedness closely resemble single-locus models in explaining family data and are compatible with genome-wide association studies. Ann N Y Acad Sci 2013;1288:48-58. [PMID: 23631511 DOI: 10.1111/nyas.12102] [Cited by in Crossref: 103] [Cited by in F6Publishing: 79] [Article Influence: 11.4] [Reference Citation Analysis]
48 Sedaghat MH, George UZ, Abouali O. A nonlinear viscoelastic model of mucociliary clearance. Rheol Acta 2021;60:371-84. [DOI: 10.1007/s00397-021-01274-4] [Reference Citation Analysis]
49 Boon M, Jorissen M, Proesmans M, De Boeck K. Primary ciliary dyskinesia, an orphan disease. Eur J Pediatr. 2013;172:151-162. [PMID: 22777640 DOI: 10.1007/s00431-012-1785-6] [Cited by in Crossref: 55] [Cited by in F6Publishing: 55] [Article Influence: 5.5] [Reference Citation Analysis]
50 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: 138] [Cited by in F6Publishing: 124] [Article Influence: 15.3] [Reference Citation Analysis]
51 Giridhar PV, Bell SM, Sridharan A, Rajavelu P, Kitzmiller JA, Na CL, Kofron M, Brandt EB, Ericksen M, Naren AP, Moon C, Khurana Hershey GK, Whitsett JA. Airway Epithelial KIF3A Regulates Th2 Responses to Aeroallergens. J Immunol 2016;197:4228-39. [PMID: 27794000 DOI: 10.4049/jimmunol.1600926] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 1.2] [Reference Citation Analysis]
52 Zariwala MA, Omran H, Ferkol TW. The emerging genetics of primary ciliary dyskinesia. Proc Am Thorac Soc 2011;8:430-3. [PMID: 21926394 DOI: 10.1513/pats.201103-023SD] [Cited by in Crossref: 70] [Cited by in F6Publishing: 40] [Article Influence: 7.0] [Reference Citation Analysis]
53 Vacaru AM, Unlu G, Spitzner M, Mione M, Knapik EW, Sadler KC. In vivo cell biology in zebrafish - providing insights into vertebrate development and disease. J Cell Sci 2014;127:485-95. [PMID: 24481493 DOI: 10.1242/jcs.140194] [Cited by in Crossref: 45] [Cited by in F6Publishing: 41] [Article Influence: 5.6] [Reference Citation Analysis]
54 Coppieters F, Casteels I, Meire F, De Jaegere S, Hooghe S, van Regemorter N, Van Esch H, Matuleviciene A, Nunes L, Meersschaut V, Walraedt S, Standaert L, Coucke P, Hoeben H, Kroes HY, Vande Walle J, de Ravel T, Leroy BP, De Baere E. Genetic screening of LCA in Belgium: predominance of CEP290 and identification of potential modifier alleles in AHI1 of CEP290-related phenotypes. Hum Mutat 2010;31:E1709-66. [PMID: 20683928 DOI: 10.1002/humu.21336] [Cited by in Crossref: 84] [Cited by in F6Publishing: 77] [Article Influence: 7.6] [Reference Citation Analysis]
55 Amack JD. Salient features of the ciliated organ of asymmetry. Bioarchitecture 2014;4:6-15. [PMID: 24481178 DOI: 10.4161/bioa.28014] [Cited by in Crossref: 17] [Cited by in F6Publishing: 16] [Article Influence: 2.1] [Reference Citation Analysis]
56 McKenzie CW, Klonoski JM, Maier T, Trujillo G, Vitiello PF, Huber VC, Lee L. Enhanced response to pulmonary Streptococcus pneumoniae infection is associated with primary ciliary dyskinesia in mice lacking Pcdp1 and Spef2. Cilia 2013;2:18. [PMID: 24360193 DOI: 10.1186/2046-2530-2-18] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 1.2] [Reference Citation Analysis]
57 Fujita S, Matsuo T, Ishiura M, Kikkawa M. High-throughput phenotyping of chlamydomonas swimming mutants based on nanoscale video analysis. Biophys J 2014;107:336-45. [PMID: 25028875 DOI: 10.1016/j.bpj.2014.05.033] [Cited by in Crossref: 9] [Cited by in F6Publishing: 6] [Article Influence: 1.3] [Reference Citation Analysis]
58 Peabody JE, Shei RJ, Bermingham BM, Phillips SE, Turner B, Rowe SM, Solomon GM. Seeing cilia: imaging modalities for ciliary motion and clinical connections. Am J Physiol Lung Cell Mol Physiol 2018;314:L909-21. [PMID: 29493257 DOI: 10.1152/ajplung.00556.2017] [Cited by in Crossref: 11] [Cited by in F6Publishing: 10] [Article Influence: 2.8] [Reference Citation Analysis]
59 Knowles MR, Ostrowski LE, Leigh MW, Sears PR, Davis SD, Wolf WE, Hazucha MJ, Carson JL, Olivier KN, Sagel SD. Mutations in RSPH1 cause primary ciliary dyskinesia with a unique clinical and ciliary phenotype. Am J Respir Crit Care Med. 2014;189:707-717. [PMID: 24568568 DOI: 10.1164/rccm.201311-2047oc] [Cited by in Crossref: 131] [Cited by in F6Publishing: 69] [Article Influence: 16.4] [Reference Citation Analysis]
60 Svobodová T, Djakow J, Zemková D, Cipra A, Pohunek P, Lebl J. Impaired Growth during Childhood in Patients with Primary Ciliary Dyskinesia. Int J Endocrinol 2013;2013:731423. [PMID: 24454367 DOI: 10.1155/2013/731423] [Cited by in Crossref: 9] [Cited by in F6Publishing: 11] [Article Influence: 1.0] [Reference Citation Analysis]
61 El-Radaideh K, Al-Qudah M, Alali M, Alhowary AA. Anesthesia During Functional Endoscopic Sinus Surgery for Kartagener's Syndrome: A Case Report and Literature Review. Int J Gen Med 2020;13:157-61. [PMID: 32431532 DOI: 10.2147/IJGM.S251060] [Reference Citation Analysis]
62 Olm MA, Kögler JE Jr, Macchione M, Shoemark A, Saldiva PH, Rodrigues JC. Primary ciliary dyskinesia: evaluation using cilia beat frequency assessment via spectral analysis of digital microscopy images. J Appl Physiol (1985) 2011;111:295-302. [PMID: 21551013 DOI: 10.1152/japplphysiol.00629.2010] [Cited by in Crossref: 26] [Cited by in F6Publishing: 24] [Article Influence: 2.4] [Reference Citation Analysis]
63 Feldman KS, Zahid M. In vivo Evaluation of Mucociliary Clearance in Mice. J Vis Exp 2020. [PMID: 33393517 DOI: 10.3791/61929] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
64 Basten SG, Giles RH. Functional aspects of primary cilia in signaling, cell cycle and tumorigenesis. Cilia 2013;2:6. [PMID: 23628112 DOI: 10.1186/2046-2530-2-6] [Cited by in Crossref: 120] [Cited by in F6Publishing: 114] [Article Influence: 13.3] [Reference Citation Analysis]
65 Ostrowski LE, Dutcher SK, Lo CW. Cilia and models for studying structure and function. Proc Am Thorac Soc 2011;8:423-9. [PMID: 21926393 DOI: 10.1513/pats.201103-027SD] [Cited by in Crossref: 31] [Cited by in F6Publishing: 18] [Article Influence: 3.1] [Reference Citation Analysis]
66 Wang B, Zhang X, Jiang W, Huang J, Chen J, Kreisel D, Danguilan JLJ, Hsin M, Lin H. Double lung transplantation for end-stage Kartagener syndrome: a case report and literature review. J Thorac Dis 2020;12:1588-94. [PMID: 32395296 DOI: 10.21037/jtd.2020.02.28] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
67 Sedykh I, TeSlaa JJ, Tatarsky RL, Keller AN, Toops KA, Lakkaraju A, Nyholm MK, Wolman MA, Grinblat Y. Novel roles for the radial spoke head protein 9 in neural and neurosensory cilia. Sci Rep 2016;6:34437. [PMID: 27687975 DOI: 10.1038/srep34437] [Cited by in Crossref: 11] [Cited by in F6Publishing: 10] [Article Influence: 1.8] [Reference Citation Analysis]
68 Lin AE, Krikov S, Riehle-Colarusso T, Frías JL, Belmont J, Anderka M, Geva T, Getz KD, Botto LD; National Birth Defects Prevention Study. Laterality defects in the national birth defects prevention study (1998-2007): birth prevalence and descriptive epidemiology. Am J Med Genet A 2014;164A:2581-91. [PMID: 25099286 DOI: 10.1002/ajmg.a.36695] [Cited by in Crossref: 84] [Cited by in F6Publishing: 71] [Article Influence: 10.5] [Reference Citation Analysis]
69 Li Y, Klena NT, Gabriel GC, Liu X, Kim AJ, Lemke K, Chen Y, Chatterjee B, Devine W, Damerla RR, Chang C, Yagi H, San Agustin JT, Thahir M, Anderton S, Lawhead C, Vescovi A, Pratt H, Morgan J, Haynes L, Smith CL, Eppig JT, Reinholdt L, Francis R, Leatherbury L, Ganapathiraju MK, Tobita K, Pazour GJ, Lo CW. Global genetic analysis in mice unveils central role for cilia in congenital heart disease. Nature 2015;521:520-4. [PMID: 25807483 DOI: 10.1038/nature14269] [Cited by in Crossref: 239] [Cited by in F6Publishing: 218] [Article Influence: 34.1] [Reference Citation Analysis]
70 Olm MA, Caldini EG, Mauad T. Diagnosis of primary ciliary dyskinesia. J Bras Pneumol 2015;41:251-63. [PMID: 26176524 DOI: 10.1590/S1806-37132015000004447] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
71 Jayathilake P, Le D, Tan Z, Lee H, Khoo B. A numerical study of muco-ciliary transport under the condition of diseased cilia. Computer Methods in Biomechanics and Biomedical Engineering 2013;18:944-51. [DOI: 10.1080/10255842.2013.864285] [Cited by in Crossref: 16] [Article Influence: 2.0] [Reference Citation Analysis]
72 Guan Y, Yang H, Yao X, Xu H, Liu H, Tang X, Hao C, Zhang X, Zhao S, Ge W, Ni X. Clinical and Genetic Spectrum of Children With Primary Ciliary Dyskinesia in China. Chest 2021;159:1768-81. [PMID: 33577779 DOI: 10.1016/j.chest.2021.02.006] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
73 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]
74 Sehgal IS, Dhooria S, Bal A, Agarwal R. Allergic bronchopulmonary aspergillosis in an adult with Kartagener syndrome. BMJ Case Rep 2015;2015:bcr2015211493. [PMID: 26250371 DOI: 10.1136/bcr-2015-211493] [Cited by in Crossref: 7] [Cited by in F6Publishing: 9] [Article Influence: 1.0] [Reference Citation Analysis]
75 Liu M, Huang S, Zhao X, Wu F, Zhu D, Zhai X, Wang A. Successful Live Birth Following Natural Cycle Oocyte Retrieval in a Woman with Primary Infertility and Atypical Primary Ovarian Insufficiency with a DNAH1 Gene Deletion Mutation. Genet Test Mol Biomarkers 2021;25:668-73. [PMID: 34672773 DOI: 10.1089/gtmb.2020.0303] [Reference Citation Analysis]
76 Schumann M, Freitag N, Haag E, Bloch W. Individualized physical training in the therapy of Primary Ciliary Dyskinesia - A case report. Respir Med Case Rep 2019;28:100925. [PMID: 31463189 DOI: 10.1016/j.rmcr.2019.100925] [Reference Citation Analysis]
77 Schmidt H, Gleave ES, Carter AP. Insights into dynein motor domain function from a 3.3-Å crystal structure. Nat Struct Mol Biol 2012;19:492-7, S1. [PMID: 22426545 DOI: 10.1038/nsmb.2272] [Cited by in Crossref: 138] [Cited by in F6Publishing: 118] [Article Influence: 13.8] [Reference Citation Analysis]
78 Eitler K, Bibok A, Telkes G. Situs Inversus Totalis: A Clinical Review. IJGM 2022;Volume 15:2437-49. [DOI: 10.2147/ijgm.s295444] [Reference Citation Analysis]
79 Ferkol TW, Puffenberger EG, Lie H, Helms C, Strauss KA, Bowcock A, Carson JL, Hazucha M, Morton DH, Patel AC, Leigh MW, Knowles MR, Zariwala MA. Primary ciliary dyskinesia-causing mutations in Amish and Mennonite communities. J Pediatr 2013;163:383-7. [PMID: 23477994 DOI: 10.1016/j.jpeds.2013.01.061] [Cited by in Crossref: 12] [Cited by in F6Publishing: 9] [Article Influence: 1.3] [Reference Citation Analysis]
80 Davis SD, Ferkol TW, Rosenfeld M, Lee HS, Dell SD, Sagel SD, Milla C, Zariwala MA, Pittman JE, Shapiro AJ, Carson JL, Krischer JP, Hazucha MJ, Cooper ML, Knowles MR, Leigh MW. Clinical features of childhood primary ciliary dyskinesia by genotype and ultrastructural phenotype. Am J Respir Crit Care Med 2015;191:316-24. [PMID: 25493340 DOI: 10.1164/rccm.201409-1672OC] [Cited by in Crossref: 142] [Cited by in F6Publishing: 67] [Article Influence: 20.3] [Reference Citation Analysis]
81 Werner C, Onnebrink JG, Omran H. Diagnosis and management of primary ciliary dyskinesia. Cilia 2015;4:2. [PMID: 25610612 DOI: 10.1186/s13630-014-0011-8] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
82 Ibrahim R, Daood H. Kartagener syndrome: A case report. Can J Respir Ther 2021;57:44-8. [PMID: 33912655 DOI: 10.29390/cjrt-2020-064] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
83 Khalid A, Khan AR. Video-Assisted Thoracoscopic Decortication of Left Lung Empyema in a Patient With Kartagener's Syndrome. Cureus 2021;13:e19281. [PMID: 34877223 DOI: 10.7759/cureus.19281] [Reference Citation Analysis]
84 Mata M, Milian L, Armengot M, Carda C. Gene mutations in primary ciliary dyskinesia related to otitis media. Curr Allergy Asthma Rep 2014;14:420. [PMID: 24459089 DOI: 10.1007/s11882-014-0420-1] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 1.3] [Reference Citation Analysis]
85 Boerwinkle C, Marshall JD, Bryant J, Gahl WA, Olivier KN, Gunay-Aygun M. Respiratory manifestations in 38 patients with Alström syndrome. Pediatr Pulmonol 2017;52:487-93. [PMID: 28029746 DOI: 10.1002/ppul.23607] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 1.7] [Reference Citation Analysis]
86 Knowles MR, Leigh MW, Carson JL, Davis SD, Dell SD, Ferkol TW, Olivier KN, Sagel SD, Rosenfeld M, Burns KA, Minnix SL, Armstrong MC, Lori A, Hazucha MJ, Loges NT, Olbrich H, Becker-Heck A, Schmidts M, Werner C, Omran H, Zariwala MA; Genetic Disorders of Mucociliary Clearance Consortium. Mutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructure. Thorax 2012;67:433-41. [PMID: 22184204 DOI: 10.1136/thoraxjnl-2011-200301] [Cited by in Crossref: 138] [Cited by in F6Publishing: 122] [Article Influence: 12.5] [Reference Citation Analysis]
87 Feldman KS, Kim E, Czachowski MJ, Wu Y, Lo CW, Zahid M. Differential effect of anesthetics on mucociliary clearance in vivo in mice. Sci Rep 2021;11:4896. [PMID: 33649513 DOI: 10.1038/s41598-021-84605-y] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
88 Alcorn MR, Callander DC, López-Santos A, Torres Cleuren YN, Birsoy B, Joshi PM, Santure AW, Rothman JH. Heterotaxy in Caenorhabditis: widespread natural variation in left-right arrangement of the major organs. Philos Trans R Soc Lond B Biol Sci 2016;371:20150404. [PMID: 27821534 DOI: 10.1098/rstb.2015.0404] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 1.4] [Reference Citation Analysis]
89 Rademacher J, Dettmer S, Fuge J, Vogel-Claussen J, Shin HO, Shah A, Pedro PI, Wilson R, Welte T, Wacker F, Loebinger MR, Ringshausen FC. The Primary Ciliary Dyskinesia Computed Tomography Score in Adults with Bronchiectasis: A Derivation und Validation Study. Respiration 2021;100:499-509. [PMID: 33895745 DOI: 10.1159/000514927] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
90 Chen W, Zhang Y, Shen L, Zhu J, Cai K, Lu Z, Zeng W, Zhao J, Zhou X. Biallelic DNAH9 mutations are identified in Chinese patients with defective left-right patterning and cilia-related complex congenital heart disease. Hum Genet 2022. [PMID: 35050399 DOI: 10.1007/s00439-021-02426-5] [Reference Citation Analysis]
91 Daniels ML, Leigh MW, Davis SD, Armstrong MC, Carson JL, Hazucha M, Dell SD, Eriksson M, Collins FS, Knowles MR, Zariwala MA. Founder mutation in RSPH4A identified in patients of Hispanic descent with primary ciliary dyskinesia. Hum Mutat 2013;34:1352-6. [PMID: 23798057 DOI: 10.1002/humu.22371] [Cited by in Crossref: 34] [Cited by in F6Publishing: 31] [Article Influence: 3.8] [Reference Citation Analysis]
92 Saransh J, Vikas DM. Auditory processing disorders associated with a case of Kartagner's syndrome. Intractable Rare Dis Res 2014;3:19-24. [PMID: 25343122 DOI: 10.5582/irdr.3.19] [Cited by in Crossref: 2] [Article Influence: 0.3] [Reference Citation Analysis]
93 Zariwala MA, Gee HY, Kurkowiak M, Al-Mutairi DA, Leigh MW, Hurd TW, Hjeij R, Dell SD, Chaki M, Dougherty GW, Adan M, Spear PC, Esteve-Rudd J, Loges NT, Rosenfeld M, Diaz KA, Olbrich H, Wolf WE, Sheridan E, Batten TF, Halbritter J, Porath JD, Kohl S, Lovric S, Hwang DY, Pittman JE, Burns KA, Ferkol TW, Sagel SD, Olivier KN, Morgan LC, Werner C, Raidt J, Pennekamp P, Sun Z, Zhou W, Airik R, Natarajan S, Allen SJ, Amirav I, Wieczorek D, Landwehr K, Nielsen K, Schwerk N, Sertic J, Köhler G, Washburn J, Levy S, Fan S, Koerner-Rettberg C, Amselem S, Williams DS, Mitchell BJ, Drummond IA, Otto EA, Omran H, Knowles MR, Hildebrandt F. ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6. Am J Hum Genet 2013;93:336-45. [PMID: 23891469 DOI: 10.1016/j.ajhg.2013.06.007] [Cited by in Crossref: 142] [Cited by in F6Publishing: 118] [Article Influence: 15.8] [Reference Citation Analysis]
94 Collins SA, Walker WT, Lucas JS. Genetic Testing in the Diagnosis of Primary Ciliary Dyskinesia: State-of-the-Art and Future Perspectives. J Clin Med 2014;3:491-503. [PMID: 26237387 DOI: 10.3390/jcm3020491] [Cited by in Crossref: 13] [Cited by in F6Publishing: 11] [Article Influence: 1.6] [Reference Citation Analysis]
95 Werner C, Onnebrink JG, Omran H. Diagnosis and management of primary ciliary dyskinesia. Cilia 2015;4:2. [PMID: 25610612 DOI: 10.1186/s13630-014-0011-8] [Cited by in Crossref: 94] [Cited by in F6Publishing: 74] [Article Influence: 13.4] [Reference Citation Analysis]
96 Papon JF, Bassinet L, Cariou-Patron G, Zerah-Lancner F, Vojtek AM, Blanchon S, Crestani B, Amselem S, Coste A, Housset B, Escudier E, Louis B. Quantitative analysis of ciliary beating in primary ciliary dyskinesia: a pilot study. Orphanet J Rare Dis 2012;7:78. [PMID: 23057704 DOI: 10.1186/1750-1172-7-78] [Cited by in Crossref: 47] [Cited by in F6Publishing: 39] [Article Influence: 4.7] [Reference Citation Analysis]
97 Toba S, Fox LA, Sakakibara H, Porter ME, Oiwa K, Sale WS. Distinct roles of 1alpha and 1beta heavy chains of the inner arm dynein I1 of Chlamydomonas flagella. Mol Biol Cell 2011;22:342-53. [PMID: 21148301 DOI: 10.1091/mbc.E10-10-0806] [Cited by in Crossref: 30] [Cited by in F6Publishing: 18] [Article Influence: 2.5] [Reference Citation Analysis]
98 Li X, Xu L, Li J, Li B, Bai X, Strauss JF 3rd, Zhang Z, Wang H. Otitis media in sperm-associated antigen 6 (Spag6)-deficient mice. PLoS One 2014;9:e112879. [PMID: 25393619 DOI: 10.1371/journal.pone.0112879] [Cited by in Crossref: 17] [Cited by in F6Publishing: 20] [Article Influence: 2.1] [Reference Citation Analysis]
99 Lie H, Zariwala MA, Helms C, Bowcock AM, Carson JL, Brown DE 3rd, Hazucha MJ, Forsen J, Molter D, Knowles MR, Leigh MW, Ferkol TW. Primary ciliary dyskinesia in Amish communities. J Pediatr 2010;156:1023-5. [PMID: 20350728 DOI: 10.1016/j.jpeds.2010.01.054] [Cited by in Crossref: 9] [Cited by in F6Publishing: 7] [Article Influence: 0.8] [Reference Citation Analysis]
100 Ryu H, Lee H, Lee J, Noh H, Shin M, Kumar V, Hong S, Kim J, Park S. The molecular dynamics of subdistal appendages in multi-ciliated cells. Nat Commun 2021;12:612. [PMID: 33504787 DOI: 10.1038/s41467-021-20902-4] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
101 Horani A, Ferkol TW, Shoseyov D, Wasserman MG, Oren YS, Kerem B, Amirav I, Cohen-Cymberknoh M, Dutcher SK, Brody SL, Elpeleg O, Kerem E. LRRC6 mutation causes primary ciliary dyskinesia with dynein arm defects. PLoS One 2013;8:e59436. [PMID: 23527195 DOI: 10.1371/journal.pone.0059436] [Cited by in Crossref: 60] [Cited by in F6Publishing: 55] [Article Influence: 6.7] [Reference Citation Analysis]
102 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: 1] [Article Influence: 1.5] [Reference Citation Analysis]
103 Funkhouser WK 3rd, Niethammer M, Carson JL, Burns KA, Knowles MR, Leigh MW, Zariwala MA, Funkhouser WK Jr. A new tool improves diagnostic test performance for transmission em evaluation of axonemal dynein arms. Ultrastruct Pathol 2014;38:248-55. [PMID: 23957500 DOI: 10.3109/01913123.2013.815081] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 0.9] [Reference Citation Analysis]
104 Sironen A, Kotaja N, Mulhern H, Wyatt TA, Sisson JH, Pavlik JA, Miiluniemi M, Fleming MD, Lee L. Loss of SPEF2 function in mice results in spermatogenesis defects and primary ciliary dyskinesia. Biol Reprod 2011;85:690-701. [PMID: 21715716 DOI: 10.1095/biolreprod.111.091132] [Cited by in Crossref: 81] [Cited by in F6Publishing: 75] [Article Influence: 7.4] [Reference Citation Analysis]
105 Kouis P, Papatheodorou SI, Yiallouros PK. Diagnostic accuracy of nasal nitric oxide for establishing diagnosis of primary ciliary dyskinesia: a meta-analysis. BMC Pulm Med 2015;15:153. [PMID: 26634346 DOI: 10.1186/s12890-015-0147-3] [Cited by in Crossref: 18] [Cited by in F6Publishing: 17] [Article Influence: 2.6] [Reference Citation Analysis]
106 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]
107 Basten SG, Davis EE, Gillis AJ, van Rooijen E, Stoop H, Babala N, Logister I, Heath ZG, Jonges TN, Katsanis N, Voest EE, van Eeden FJ, Medema RH, Ketting RF, Schulte-Merker S, Looijenga LH, Giles RH. Mutations in LRRC50 predispose zebrafish and humans to seminomas. PLoS Genet 2013;9:e1003384. [PMID: 23599692 DOI: 10.1371/journal.pgen.1003384] [Cited by in Crossref: 32] [Cited by in F6Publishing: 27] [Article Influence: 3.6] [Reference Citation Analysis]
108 Quinn SP, Zahid MJ, Durkin JR, Francis RJ, Lo CW, Chennubhotla SC. Automated identification of abnormal respiratory ciliary motion in nasal biopsies. Sci Transl Med 2015;7:299ra124. [PMID: 26246169 DOI: 10.1126/scitranslmed.aaa1233] [Cited by in Crossref: 26] [Cited by in F6Publishing: 20] [Article Influence: 4.3] [Reference Citation Analysis]
109 Sears PR, Yin WN, Ostrowski LE. Continuous mucociliary transport by primary human airway epithelial cells in vitro. Am J Physiol Lung Cell Mol Physiol 2015;309:L99-108. [PMID: 25979076 DOI: 10.1152/ajplung.00024.2015] [Cited by in Crossref: 35] [Cited by in F6Publishing: 35] [Article Influence: 5.0] [Reference Citation Analysis]
110 Elam CA, Wirschell M, Yamamoto R, Fox LA, York K, Kamiya R, Dutcher SK, Sale WS. An axonemal PP2A B-subunit is required for PP2A localization and flagellar motility. Cytoskeleton (Hoboken) 2011;68:363-72. [PMID: 21692192 DOI: 10.1002/cm.20519] [Cited by in Crossref: 17] [Cited by in F6Publishing: 17] [Article Influence: 1.5] [Reference Citation Analysis]
111 Cyge B, Fischer V, Takemaru K, Li FQ. Generation and characterization of monoclonal antibodies against human Chibby protein. Hybridoma (Larchmt) 2011;30:163-8. [PMID: 21529289 DOI: 10.1089/hyb.2010.0098] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 0.5] [Reference Citation Analysis]
112 Cyge B, Voronina V, Hoque M, Kim EN, Hall J, Bailey-Lundberg JM, Pazour GJ, Crawford HC, Moon RT, Li FQ, Takemaru KI. Loss of the ciliary protein Chibby1 in mice leads to exocrine pancreatic degeneration and pancreatitis. Sci Rep 2021;11:17220. [PMID: 34446743 DOI: 10.1038/s41598-021-96597-w] [Reference Citation Analysis]
113 Zi XX, Guan WJ, Peng Y, Tan KS, Liu J, He TT, Ong YK, Thong M, Shi L, Wang DY. An Integrated Analysis of Radial Spoke Head and Outer Dynein Arm Protein Defects and Ciliogenesis Abnormality in Nasal Polyps. Front Genet 2019;10:1083. [PMID: 31798623 DOI: 10.3389/fgene.2019.01083] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
114 Nawa T, Yokozawa M, Takamuro M, Kasuga A. Plastic bronchitis developing 5 years after Fontan procedure in a girl with Kartagener's syndrome. Pediatr Cardiol 2012;33:846-9. [PMID: 22331057 DOI: 10.1007/s00246-012-0235-6] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
115 Young LR, Trapnell BC, Mandl KD, Swarr DT, Wambach JA, Blaisdell CJ. Accelerating Scientific Advancement for Pediatric Rare Lung Disease Research. Report from a National Institutes of Health-NHLBI Workshop, September 3 and 4, 2015. Ann Am Thorac Soc 2016;13:385-93. [PMID: 27925785 DOI: 10.1513/AnnalsATS.201605-402OT] [Cited by in Crossref: 7] [Cited by in F6Publishing: 3] [Article Influence: 1.8] [Reference Citation Analysis]
116 Wang S, Burton JC, Behringer RR, Larina IV. In vivo micro-scale tomography of ciliary behavior in the mammalian oviduct. Sci Rep 2015;5:13216. [PMID: 26279472 DOI: 10.1038/srep13216] [Cited by in Crossref: 22] [Cited by in F6Publishing: 18] [Article Influence: 3.1] [Reference Citation Analysis]
117 Vingerhoets G, Gerrits R, Verhelst H. Atypical Brain Asymmetry in Human Situs Inversus: Gut Feeling or Real Evidence? Symmetry 2021;13:695. [DOI: 10.3390/sym13040695] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
118 Shi X, Geng H, Yu H, Hu X, Wang G, Yang J, Zhao H, Bottillo I. Biallelic Variants in CCDC39 Gene Lead to Primary Ciliary Dyskinesia and Kartagener Syndrome. BioMed Research International 2022;2022:1-8. [DOI: 10.1155/2022/7130555] [Reference Citation Analysis]
119 Tilley AE, Walters MS, Shaykhiev R, Crystal RG. Cilia dysfunction in lung disease. Annu Rev Physiol. 2015;77:379-406. [PMID: 25386990 DOI: 10.1146/annurev-physiol-021014-071931] [Cited by in Crossref: 161] [Cited by in F6Publishing: 144] [Article Influence: 20.1] [Reference Citation Analysis]
120 Zhang Y, Chen W, Zeng W, Lu Z, Zhou X. Biallelic loss of function NEK3 mutations deacetylate α-tubulin and downregulate NUP205 that predispose individuals to cilia-related abnormal cardiac left-right patterning. Cell Death Dis 2020;11:1005. [PMID: 33230144 DOI: 10.1038/s41419-020-03214-1] [Reference Citation Analysis]
121 Knowles MR, Daniels LA, Davis SD, Zariwala MA, Leigh MW. Primary ciliary dyskinesia. Recent advances in diagnostics, genetics, and characterization of clinical disease. Am J Respir Crit Care Med 2013;188:913-22. [PMID: 23796196 DOI: 10.1164/rccm.201301-0059CI] [Reference Citation Analysis]
122 O'Toole ET, Giddings TH Jr, Porter ME, Ostrowski LE. Computer-assisted image analysis of human cilia and Chlamydomonas flagella reveals both similarities and differences in axoneme structure. Cytoskeleton (Hoboken) 2012;69:577-90. [PMID: 22573610 DOI: 10.1002/cm.21035] [Cited by in Crossref: 35] [Cited by in F6Publishing: 30] [Article Influence: 3.5] [Reference Citation Analysis]
123 Saeed M. Locus and gene-based GWAS meta-analysis identifies new diabetic nephropathy genes. Immunogenetics 2018;70:347-53. [PMID: 29147756 DOI: 10.1007/s00251-017-1044-0] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.6] [Reference Citation Analysis]
124 Maggi F, Pifferi M, Michelucci A, Albani M, Sbranti S, Lanini L, Simi P, Macchia P, Pistello M, Bendinelli M. Torque teno virus viremia load size in patients with selected congenital defects of innate immunity. Clin Vaccine Immunol 2011;18:692-4. [PMID: 21325487 DOI: 10.1128/CVI.00466-10] [Cited by in Crossref: 20] [Cited by in F6Publishing: 7] [Article Influence: 1.8] [Reference Citation Analysis]
125 Hoque M, Chen D, Hess RA, Li FQ, Takemaru KI. CEP164 is essential for efferent duct multiciliogenesis and male fertility. Reproduction 2021;162:129-39. [PMID: 34085951 DOI: 10.1530/REP-21-0042] [Reference Citation Analysis]
126 Hartill VL, van de Hoek G, Patel MP, Little R, Watson CM, Berry IR, Shoemark A, Abdelmottaleb D, Parkes E, Bacchelli C, Szymanska K, Knoers NV, Scambler PJ, Ueffing M, Boldt K, Yates R, Winyard PJ, Adler B, Moya E, Hattingh L, Shenoy A, Hogg C, Sheridan E, Roepman R, Norris D, Mitchison HM, Giles RH, Johnson CA. DNAAF1 links heart laterality with the AAA+ ATPase RUVBL1 and ciliary intraflagellar transport. Hum Mol Genet 2018;27:529-45. [PMID: 29228333 DOI: 10.1093/hmg/ddx422] [Cited by in Crossref: 19] [Cited by in F6Publishing: 17] [Article Influence: 6.3] [Reference Citation Analysis]
127 Ilian A, Motoc A, Balulescu L, Secosan C, Grigoras D, Pirtea L. A Case Report of Left Atrial Isomerism in a Syndromic Context. Genes (Basel) 2020;11:E1211. [PMID: 33081203 DOI: 10.3390/genes11101211] [Reference Citation Analysis]
128 Séguéla PE, Pierrat-Bonnefois G, Paul JF. A dextrocardia in a foetal Egyptian mummy? Cardiol Young 2013;23:287-90. [PMID: 22814111 DOI: 10.1017/S1047951112001011] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
129 Lo JC, Jamsai D, O'Connor AE, Borg C, Clark BJ, Whisstock JC, Field MC, Adams V, Ishikawa T, Aitken RJ, Whittle B, Goodnow CC, Ormandy CJ, O'Bryan MK. RAB-like 2 has an essential role in male fertility, sperm intra-flagellar transport, and tail assembly. PLoS Genet 2012;8:e1002969. [PMID: 23055941 DOI: 10.1371/journal.pgen.1002969] [Cited by in Crossref: 47] [Cited by in F6Publishing: 46] [Article Influence: 4.7] [Reference Citation Analysis]
130 Shamoto N, Narita K, Kubo T, Oda T, Takeda S. CFAP70 Is a Novel Axoneme-Binding Protein That Localizes at the Base of the Outer Dynein Arm and Regulates Ciliary Motility. Cells 2018;7:E124. [PMID: 30158508 DOI: 10.3390/cells7090124] [Cited by in Crossref: 19] [Cited by in F6Publishing: 15] [Article Influence: 4.8] [Reference Citation Analysis]
131 Hessel J, Heldrich J, Fuller J, Staudt MR, Radisch S, Hollmann C, Harvey BG, Kaner RJ, Salit J, Yee-Levin J, Sridhar S, Pillai S, Hilton H, Wolff G, Bitter H, Visvanathan S, Fine J, Stevenson CS, Crystal RG, Tilley AE. Intraflagellar transport gene expression associated with short cilia in smoking and COPD. PLoS One 2014;9:e85453. [PMID: 24465567 DOI: 10.1371/journal.pone.0085453] [Cited by in Crossref: 52] [Cited by in F6Publishing: 43] [Article Influence: 6.5] [Reference Citation Analysis]
132 Suzaki I, Hirano K, Arai S, Maruyama Y, Mizuyoshi T, Tokudome T, Fujii N, Kobayashi H. Primary Ciliary Dyskinesia with Refractory Chronic Rhinosinusitis. Am J Case Rep 2020;21:e923270. [PMID: 32862191 DOI: 10.12659/AJCR.923270] [Reference Citation Analysis]
133 Finn R, Evans CC, Lee L. Strain-dependent brain defects in mouse models of primary ciliary dyskinesia with mutations in Pcdp1 and Spef2. Neuroscience 2014;277:552-67. [PMID: 25073043 DOI: 10.1016/j.neuroscience.2014.07.029] [Cited by in Crossref: 16] [Cited by in F6Publishing: 14] [Article Influence: 2.0] [Reference Citation Analysis]
134 Sakamoto K, Nakajima M, Kawamura K, Nakamura E, Tada N, Kondo A, Arai H, Miyajima M. Ependymal ciliary motion and their role in congenital hydrocephalus. Childs Nerv Syst 2021. [PMID: 33999288 DOI: 10.1007/s00381-021-05194-9] [Reference Citation Analysis]
135 Patir A, Fraser AM, Barnett MW, McTeir L, Rainger J, Davey MG, Freeman TC. The transcriptional signature associated with human motile cilia. Sci Rep 2020;10:10814. [PMID: 32616903 DOI: 10.1038/s41598-020-66453-4] [Cited by in Crossref: 9] [Cited by in F6Publishing: 6] [Article Influence: 4.5] [Reference Citation Analysis]
136 Gabriel GC, Pazour GJ, Lo CW. Congenital Heart Defects and Ciliopathies Associated With Renal Phenotypes. Front Pediatr 2018;6:175. [PMID: 29963541 DOI: 10.3389/fped.2018.00175] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 0.8] [Reference Citation Analysis]
137 Inaba A, Furuhata M, Morimoto K, Rahman M, Takahashi O, Hijikata M, Knowles MR, Keicho N. Primary ciliary dyskinesia in Japan: systematic review and meta-analysis. BMC Pulm Med 2019;19:135. [PMID: 31345208 DOI: 10.1186/s12890-019-0897-4] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
138 Laudien M. Orphan diseases of the nose and paranasal sinuses: Pathogenesis - clinic - therapy. GMS Curr Top Otorhinolaryngol Head Neck Surg 2015;14:Doc04. [PMID: 26770278 DOI: 10.3205/cto000119] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
139 Ta CM, Vien TN, Ng LCT, DeCaen PG. Structure and function of polycystin channels in primary cilia. Cell Signal 2020;72:109626. [PMID: 32251715 DOI: 10.1016/j.cellsig.2020.109626] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 3.0] [Reference Citation Analysis]
140 Cho KJ, Noh SH, Han SM, Choi WI, Kim HY, Yu S, Lee JS, Rim JH, Lee MG, Hildebrandt F, Gee HY. ZMYND10 stabilizes intermediate chain proteins in the cytoplasmic pre-assembly of dynein arms. PLoS Genet 2018;14:e1007316. [PMID: 29601588 DOI: 10.1371/journal.pgen.1007316] [Cited by in Crossref: 21] [Cited by in F6Publishing: 19] [Article Influence: 5.3] [Reference Citation Analysis]
141 Kariya S, Okano M, Nishizaki K. Relationship between chronic rhinosinusitis and lower airway diseases: An extensive review. World J Otorhinolaryngol 2015; 5(2): 44-52 [DOI: 10.5319/wjo.v5.i2.44] [Cited by in CrossRef: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]
142 Sharbidre K, Zahid M, Venkatesh SK, Bhati C, Lalwani N. Imaging of fibropolycystic liver disease. Abdom Radiol (NY) 2022. [PMID: 35670875 DOI: 10.1007/s00261-022-03565-7] [Reference Citation Analysis]
143 Zhang X, Wang X, Li H, Wang W, Zhao S. The value of nasal nitric oxide measurement in the diagnosis of primary ciliary dyskinesia. Pediatr Investig 2019;3:209-13. [PMID: 32851324 DOI: 10.1002/ped4.12160] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
144 Braun DA, Hildebrandt F. Ciliopathies. Cold Spring Harb Perspect Biol 2017;9:a028191. [PMID: 27793968 DOI: 10.1101/cshperspect.a028191] [Cited by in Crossref: 182] [Cited by in F6Publishing: 174] [Article Influence: 36.4] [Reference Citation Analysis]
145 Ferkol TW, Leigh MW. Ciliopathies: the central role of cilia in a spectrum of pediatric disorders. J Pediatr 2012;160:366-71. [PMID: 22177992 DOI: 10.1016/j.jpeds.2011.11.024] [Cited by in Crossref: 57] [Cited by in F6Publishing: 48] [Article Influence: 5.2] [Reference Citation Analysis]
146 Pariz JR, Rané C, Drevet J, Hallak J. Dysplasia of the fibrous sheath with axonemal and centriolar defects combined with lack of mitochondrial activity as associated factors of ICSI failure in primary ciliary dyskinesia syndrome. Int Braz J Urol 2021;47:617-26. [PMID: 33621011 DOI: 10.1590/S1677-5538.IBJU.2019.0362] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
147 Shimizu Y, Sakakibara H, Kojima H, Oiwa K. Slow axonemal dynein e facilitates the motility of faster dynein c. Biophys J 2014;106:2157-65. [PMID: 24853744 DOI: 10.1016/j.bpj.2014.04.009] [Cited by in Crossref: 15] [Cited by in F6Publishing: 10] [Article Influence: 1.9] [Reference Citation Analysis]
148 Hoegger MJ, Awadalla M, Namati E, Itani OA, Fischer AJ, Tucker AJ, Adam RJ, McLennan G, Hoffman EA, Stoltz DA, Welsh MJ. Assessing mucociliary transport of single particles in vivo shows variable speed and preference for the ventral trachea in newborn pigs. Proc Natl Acad Sci U S A 2014;111:2355-60. [PMID: 24474805 DOI: 10.1073/pnas.1323633111] [Cited by in Crossref: 44] [Cited by in F6Publishing: 42] [Article Influence: 5.5] [Reference Citation Analysis]
149 Raoufi M, Sator H, Lahma J, El Ayoubi A, Nitassi S, Oujilal A, Benbouzid MA, Essakalli L, Elouazzani H, Rhorfi IA, Abid A. A case of Kartagener syndrome with rhinolalia clausa. Pan Afr Med J 2016;23:159. [PMID: 27375831 DOI: 10.11604/pamj.2016.23.159.8664] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
150 Dcunha R, Hussein RS, Ananda H, Kumari S, Adiga SK, Kannan N, Zhao Y, Kalthur G. Current Insights and Latest Updates in Sperm Motility and Associated Applications in Assisted Reproduction. Reprod Sci 2020. [PMID: 33289064 DOI: 10.1007/s43032-020-00408-y] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 2.5] [Reference Citation Analysis]
151 Cooper JL, Quinton PM, Ballard ST. Mucociliary transport in porcine trachea: differential effects of inhibiting chloride and bicarbonate secretion. Am J Physiol Lung Cell Mol Physiol 2013;304:L184-90. [PMID: 23204069 DOI: 10.1152/ajplung.00143.2012] [Cited by in Crossref: 37] [Cited by in F6Publishing: 36] [Article Influence: 3.7] [Reference Citation Analysis]
152 Baek H, Shin HJ, Kim JJ, Shin N, Kim S, Yi MH, Zhang E, Hong J, Kang JW, Kim Y, Kim CS, Kim DW. Primary cilia modulate TLR4-mediated inflammatory responses in hippocampal neurons. J Neuroinflammation 2017;14:189. [PMID: 28927423 DOI: 10.1186/s12974-017-0958-7] [Cited by in Crossref: 12] [Cited by in F6Publishing: 11] [Article Influence: 2.4] [Reference Citation Analysis]
153 Ledda RE, Balbi M, Milone F, Ciuni A, Silva M, Sverzellati N, Milanese G. Imaging in non-cystic fibrosis bronchiectasis and current limitations. BJR Open 2021;3:20210026. [PMID: 34381953 DOI: 10.1259/bjro.20210026] [Reference Citation Analysis]
154 Postema MC, Carrion-Castillo A, Fisher SE, Vingerhoets G, Francks C. The genetics of situs inversus without primary ciliary dyskinesia. Sci Rep 2020;10:3677. [PMID: 32111882 DOI: 10.1038/s41598-020-60589-z] [Cited by in Crossref: 12] [Cited by in F6Publishing: 3] [Article Influence: 6.0] [Reference Citation Analysis]
155 Ostrowski LE, Stewart D, Hazucha M. Interferon γ stimulates accumulation of gas phase nitric oxide in differentiated cultures of normal and cystic fibrosis airway epithelial cells. Lung 2012;190:563-71. [PMID: 22729230 DOI: 10.1007/s00408-012-9395-7] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 0.7] [Reference Citation Analysis]
156 Leigh MW, Pittman JE, Carson JL, Ferkol TW, Dell SD, Davis SD, Knowles MR, Zariwala MA. Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome. Genet Med 2009;11:473-87. [PMID: 19606528 DOI: 10.1097/GIM.0b013e3181a53562] [Cited by in Crossref: 246] [Cited by in F6Publishing: 138] [Article Influence: 18.9] [Reference Citation Analysis]
157 Pereira R, Oliveira ME, Santos R, Oliveira E, Barbosa T, Santos T, Gonçalves P, Ferraz L, Pinto S, Barros A, Oliveira J, Sousa M. Characterization of CCDC103 expression profiles: further insights in primary ciliary dyskinesia and in human reproduction. J Assist Reprod Genet 2019;36:1683-700. [PMID: 31273583 DOI: 10.1007/s10815-019-01509-7] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 2.7] [Reference Citation Analysis]
158 Bougioukas I, Mikroulis D, Danner B, Lawal L, Eleftheriadis S, Bougioukas G, Didilis V. Coronary artery bypass surgery in a patient with Kartagener syndrome: a case report and literature review. J Cardiothorac Surg 2010;5:68. [PMID: 20796272 DOI: 10.1186/1749-8090-5-68] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
159 Boon M, Jorissen M, Proesmans M, De Boeck K. Primary ciliary dyskinesia, an orphan disease. Eur J Pediatr 2013;172:151-62. [PMID: 22777640 DOI: 10.1007/s00431-012-1785-6] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
160 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]
161 Berg JS, Evans JP, Leigh MW, Omran H, Bizon C, Mane K, Knowles MR, Weck KE, Zariwala MA. Next generation massively parallel sequencing of targeted exomes to identify genetic mutations in primary ciliary dyskinesia: implications for application to clinical testing. Genet Med 2011;13:218-29. [PMID: 21270641 DOI: 10.1097/GIM.0b013e318203cff2] [Cited by in Crossref: 47] [Cited by in F6Publishing: 22] [Article Influence: 4.3] [Reference Citation Analysis]