BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: 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]
Number Citing Articles
1 Abdelhamed Z, Lukacs M, Cindric S, Ali S, Omran H, Stottmann RW. A novel hypomorphic allele of Spag17 causes primary ciliary dyskinesia phenotypes in mice. Dis Model Mech 2020;13:dmm045344. [PMID: 32988999 DOI: 10.1242/dmm.045344] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
2 Song Z, Zhang X, Jia S, Yelick PC, Zhao C. Zebrafish as a Model for Human Ciliopathies. Journal of Genetics and Genomics 2016;43:107-20. [DOI: 10.1016/j.jgg.2016.02.001] [Cited by in Crossref: 39] [Cited by in F6Publishing: 36] [Article Influence: 6.5] [Reference Citation Analysis]
3 Kouis P, Yiallouros PK, Middleton N, Evans JS, Kyriacou K, Papatheodorou SI. Prevalence of primary ciliary dyskinesia in consecutive referrals of suspect cases and the transmission electron microscopy detection rate: a systematic review and meta-analysis. Pediatr Res 2017;81:398-405. [DOI: 10.1038/pr.2016.263] [Cited by in Crossref: 24] [Cited by in F6Publishing: 23] [Article Influence: 4.0] [Reference Citation Analysis]
4 Ichikawa M, Saito K, Yanagisawa HA, Yagi T, Kamiya R, Yamaguchi S, Yajima J, Kushida Y, Nakano K, Numata O, Toyoshima YY. Axonemal dynein light chain-1 locates at the microtubule-binding domain of the γ heavy chain. Mol Biol Cell 2015;26:4236-47. [PMID: 26399296 DOI: 10.1091/mbc.E15-05-0289] [Cited by in Crossref: 19] [Cited by in F6Publishing: 12] [Article Influence: 2.7] [Reference Citation Analysis]
5 Frija-Masson J, Bassinet L, Honoré I, Dufeu N, Housset B, Coste A, Papon JF, Escudier E, Burgel PR, Maître B. Clinical characteristics, functional respiratory decline and follow-up in adult patients with primary ciliary dyskinesia. Thorax 2017;72:154-60. [PMID: 27382041 DOI: 10.1136/thoraxjnl-2015-207891] [Cited by in Crossref: 53] [Cited by in F6Publishing: 38] [Article Influence: 8.8] [Reference Citation Analysis]
6 Hamilton E, Cicuta P. Interpreting the synchronisation of driven colloidal oscillators via the mean pair interaction. New J Phys 2018;20:093028. [DOI: 10.1088/1367-2630/aae103] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 0.8] [Reference Citation Analysis]
7 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]
8 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]
9 Mcdonnell MJ, Rutherford RM. Other Predisposing Factors for Bronchiectasis. In: Chalmers J, Polverino E, Aliberti S, editors. Bronchiectasis. Cham: Springer International Publishing; 2018. pp. 129-45. [DOI: 10.1007/978-3-319-61452-6_10] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
10 Dubaissi E. A 'tad' of hope in the fight against airway disease. Biochem Soc Trans 2020;48:2347-57. [PMID: 33079166 DOI: 10.1042/BST20200745] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
11 Good M, Kolls JK, Empey KM. Neonatal Pulmonary Host Defense. Fetal and Neonatal Physiology. Elsevier; 2017. pp. 1262-1293.e12. [DOI: 10.1016/b978-0-323-35214-7.00130-x] [Cited by in Crossref: 1] [Article Influence: 0.2] [Reference Citation Analysis]
12 Bukowy-Bieryllo Z, Dabrowski M, Witt M, Zietkiewicz E. Aminoglycoside-stimulated readthrough of premature termination codons in selected genes involved in primary ciliary dyskinesia. RNA Biol 2016;13:1041-50. [PMID: 27618201 DOI: 10.1080/15476286.2016.1219832] [Cited by in Crossref: 19] [Cited by in F6Publishing: 17] [Article Influence: 3.2] [Reference Citation Analysis]
13 Stevanovic N, Skakic A, Minic P, Sovtic A, Stojiljkovic M, Pavlovic S, Andjelkovic M. Identification and Classification of Novel Genetic Variants: En Route to the Diagnosis of Primary Ciliary Dyskinesia. Int J Mol Sci 2021;22:8821. [PMID: 34445527 DOI: 10.3390/ijms22168821] [Reference Citation Analysis]
14 Šedová L, Buková I, Bažantová P, Petrezsélyová S, Prochazka J, Školníková E, Zudová D, Včelák J, Makovický P, Bendlová B, Šeda O, Sedlacek R. Semi-Lethal Primary Ciliary Dyskinesia in Rats Lacking the Nme7 Gene. Int J Mol Sci 2021;22:3810. [PMID: 33916973 DOI: 10.3390/ijms22083810] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
15 Hagen EM, Sicko RJ, Kay DM, Rigler SL, Dimopoulos A, Ahmad S, Doleman MH, Fan R, Romitti PA, Browne ML, Caggana M, Brody LC, Shaw GM, Jelliffe-Pawlowski LL, Mills JL. Copy-number variant analysis of classic heterotaxy highlights the importance of body patterning pathways. Hum Genet 2016;135:1355-64. [PMID: 27637763 DOI: 10.1007/s00439-016-1727-x] [Cited by in Crossref: 11] [Cited by in F6Publishing: 10] [Article Influence: 1.8] [Reference Citation Analysis]
16 Kobayashi D, Asano-Hoshino A, Nakakura T, Nishimaki T, Ansai S, Kinoshita M, Ogawa M, Hagiwara H, Yokoyama T. Loss of zinc finger MYND-type containing 10 (zmynd10) affects cilia integrity and axonemal localization of dynein arms, resulting in ciliary dysmotility, polycystic kidney and scoliosis in medaka (Oryzias latipes). Dev Biol 2017;430:69-79. [PMID: 28823919 DOI: 10.1016/j.ydbio.2017.08.016] [Cited by in Crossref: 11] [Cited by in F6Publishing: 10] [Article Influence: 2.2] [Reference Citation Analysis]
17 Gunes S, Sengupta P, Henkel R, Alguraigari A, Sinigaglia MM, Kayal M, Joumah A, Agarwal A. Microtubular Dysfunction and Male Infertility. World J Mens Health 2020;38:9-23. [PMID: 30350487 DOI: 10.5534/wjmh.180066] [Cited by in Crossref: 11] [Cited by in F6Publishing: 7] [Article Influence: 2.8] [Reference Citation Analysis]
18 Kurkowiak M, Ziętkiewicz E, Greber A, Voelkel K, Wojda A, Pogorzelski A, Witt M. ZMYND10--Mutation Analysis in Slavic Patients with Primary Ciliary Dyskinesia. PLoS One 2016;11:e0148067. [PMID: 26824761 DOI: 10.1371/journal.pone.0148067] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 1.3] [Reference Citation Analysis]
19 Asmanov AI, Zlobina NV, Radtsig EY, Polev GA, Sorokina EV. [Polypous pansinusitis with the deformation of the external nose in a 8 year-old child presenting with the primary ciliary dyskinesia syndrome]. Vestn Otorinolaringol 2017;82:61-3. [PMID: 29072668 DOI: 10.17116/otorino201782561-63] [Reference Citation Analysis]
20 Marshall CR, Scherer SW, Zariwala MA, Lau L, Paton TA, Stockley T, Jobling RK, Ray PN, Knowles MR, Hall DA, Dell SD, Kim RH; FORGE Canada Consortium. Whole-Exome Sequencing and Targeted Copy Number Analysis in Primary Ciliary Dyskinesia. G3 (Bethesda) 2015;5:1775-81. [PMID: 26139845 DOI: 10.1534/g3.115.019851] [Cited by in Crossref: 38] [Cited by in F6Publishing: 39] [Article Influence: 5.4] [Reference Citation Analysis]
21 Ciancio N, de Santi MM, Campisi R, Amato L, Di Martino G, Di Maria G. Kartagener's syndrome: review of a case series. Multidiscip Respir Med 2015;10:18. [PMID: 26075070 DOI: 10.1186/s40248-015-0015-2] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 0.4] [Reference Citation Analysis]
22 Shoemark A, Boon M, Brochhausen C, Bukowy-Bieryllo Z, De Santi MM, Goggin P, Griffin P, Hegele RG, Hirst RA, Leigh MW, Lupton A, MacKenney K, Omran H, Pache JC, Pinto A, Reinholt FP, Schroeder J, Yiallouros P, Escudier E; representing the BEAT-PCD Network Guideline Development Group. International consensus guideline for reporting transmission electron microscopy results in the diagnosis of primary ciliary dyskinesia (BEAT PCD TEM Criteria). Eur Respir J 2020;55:1900725. [PMID: 32060067 DOI: 10.1183/13993003.00725-2019] [Cited by in Crossref: 19] [Cited by in F6Publishing: 21] [Article Influence: 9.5] [Reference Citation Analysis]
23 Cao Y, Shao C, Song Y, Bai C, He L. Clinical analysis of patients with primary ciliary dyskinesia in mainland China. Clin Respir J 2016;10:765-71. [PMID: 25764361 DOI: 10.1111/crj.12284] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.4] [Reference Citation Analysis]
24 Dahlmann J, Sahabian A, Drick N, Haase A, Göhring G, Lachmann N, Ringshausen FC, Welte T, Martin U, Olmer R. Generation of two hiPSC lines (MHHi016-A, MHHi016-B) from a primary ciliary dyskinesia patient carrying a homozygous 5 bp duplication (c.248_252dup (p.Gly85Cysfs*11)) in exon 1 of the CCNO gene. Stem Cell Res 2020;46:101850. [PMID: 32464346 DOI: 10.1016/j.scr.2020.101850] [Reference Citation Analysis]
25 Yue Y, Huang Q, Zhu P, Zhao P, Tan X, Liu S, Li S, Han X, Cheng L, Li B, Fu Y. Identification of Pathogenic Mutations and Investigation of the NOTCH Pathway Activation in Kartagener Syndrome. Front Genet 2019;10:749. [PMID: 31507630 DOI: 10.3389/fgene.2019.00749] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
26 Milla CE. The evolving spectrum of ciliopathies and respiratory disease. Curr Opin Pediatr 2016;28:339-47. [PMID: 27070443 DOI: 10.1097/MOP.0000000000000358] [Cited by in Crossref: 8] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
27 Subaran RL, Stewart WCL. FREQMAX provides an alternative approach for determining high-resolution allele frequency thresholds in carrier screening. Hum Mutat 2020;41:2078-86. [PMID: 33032373 DOI: 10.1002/humu.24123] [Reference Citation Analysis]
28 Cockx M, Gouwy M, Ruytinx P, Lodewijckx I, Van Hout A, Knoops S, Pörtner N, Ronsse I, Vanbrabant L, Godding V, De Boeck K, Van Damme J, Boon M, Struyf S. Monocytes from patients with Primary Ciliary Dyskinesia show enhanced inflammatory properties and produce higher levels of pro-inflammatory cytokines. Sci Rep 2017;7:14657. [PMID: 29116124 DOI: 10.1038/s41598-017-15027-y] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 1.6] [Reference Citation Analysis]
29 Zhao Y, Pinskey J, Lin J, Yin W, Sears PR, Daniels LA, Zariwala MA, Knowles MR, Ostrowski LE, Nicastro D. Structural insights into the cause of human RSPH4A primary ciliary dyskinesia. Mol Biol Cell 2021;32:1202-9. [PMID: 33852348 DOI: 10.1091/mbc.E20-12-0806] [Reference Citation Analysis]
30 Xu X, Dong L, Ma C, Xu X, Wu H, Wang J, Zhou P, Cao Y, Wei Z. Establishment of an induced pluripotent stem cell line from a patient with primary ciliary dyskinesia carrying biallelic mutations in CCNO. Stem Cell Res 2021;53:102372. [PMID: 34088001 DOI: 10.1016/j.scr.2021.102372] [Reference Citation Analysis]
31 Silva E, Betleja E, John E, Spear P, Moresco JJ, Zhang S, Yates JR 3rd, Mitchell BJ, Mahjoub MR. Ccdc11 is a novel centriolar satellite protein essential for ciliogenesis and establishment of left-right asymmetry. Mol Biol Cell 2016;27:48-63. [PMID: 26538025 DOI: 10.1091/mbc.E15-07-0474] [Cited by in Crossref: 23] [Cited by in F6Publishing: 12] [Article Influence: 3.3] [Reference Citation Analysis]
32 Schroeder JA. Application of laboratory and digital techniques for visual enhancement during the ultrastructural assessment of cilia. Ultrastructural Pathology 2017;41:399-407. [DOI: 10.1080/01913123.2017.1363335] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
33 Hyland RM, Brody SL. Impact of Motile Ciliopathies on Human Development and Clinical Consequences in the Newborn. Cells 2021;11:125. [PMID: 35011687 DOI: 10.3390/cells11010125] [Reference Citation Analysis]
34 Ha S, Lindsay AM, Timms AE, Beier DR. Mutations in Dnaaf1 and Lrrc48 Cause Hydrocephalus, Laterality Defects, and Sinusitis in Mice. G3 (Bethesda) 2016;6:2479-87. [PMID: 27261005 DOI: 10.1534/g3.116.030791] [Cited by in Crossref: 19] [Cited by in F6Publishing: 17] [Article Influence: 3.2] [Reference Citation Analysis]
35 Lorès P, Coutton C, El Khouri E, Stouvenel L, Givelet M, Thomas L, Rode B, Schmitt A, Louis B, Sakheli Z, Chaudhry M, Fernandez-Gonzales A, Mitsialis A, Dacheux D, Wolf JP, Papon JF, Gacon G, Escudier E, Arnoult C, Bonhivers M, Savinov SN, Amselem S, Ray PF, Dulioust E, Touré A. Homozygous missense mutation L673P in adenylate kinase 7 (AK7) leads to primary male infertility and multiple morphological anomalies of the flagella but not to primary ciliary dyskinesia. Hum Mol Genet 2018;27:1196-211. [PMID: 29365104 DOI: 10.1093/hmg/ddy034] [Cited by in Crossref: 50] [Cited by in F6Publishing: 52] [Article Influence: 16.7] [Reference Citation Analysis]
36 Haarman EG, Schmidts M. Accuracy of diagnostic testing in primary ciliary dyskinesia: are we there yet? Eur Respir J 2016;47:699-701. [DOI: 10.1183/13993003.01914-2015] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 0.8] [Reference Citation Analysis]
37 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]
38 Gu H, Yuan ZZ, Xie XH, Yang YF, Tan ZP. A novel nonsense PKD1L1 variant cause heterotaxy syndrome with congenital asplenia in a Han Chinese patient. J Hum Genet 2022. [PMID: 35691949 DOI: 10.1038/s10038-022-01053-w] [Reference Citation Analysis]
39 LeBlanc S, Allain EP, Girouard G, Mallet M, Amor MB. Expanded phenotype of primary ciliary dyskinesia related to DRC1 pathogenic variant with dysmorphisms and vascular anomalies. Am J Med Genet A 2021. [PMID: 34851034 DOI: 10.1002/ajmg.a.62586] [Reference Citation Analysis]
40 Goutaki M, Maurer E, Halbeisen FS, Amirav I, Barbato A, Behan L, Boon M, Casaulta C, Clement A, Crowley S, Haarman E, Hogg C, Karadag B, Koerner-Rettberg C, Leigh MW, Loebinger MR, Mazurek H, Morgan L, Nielsen KG, Omran H, Schwerk N, Scigliano S, Werner C, Yiallouros P, Zivkovic Z, Lucas JS, Kuehni CE; PCD Italian Consortium., Swiss PCD Group., French Reference Centre for Rare Lung Diseases., Genetic Disorders of Mucociliary Clearance Consortium. The international primary ciliary dyskinesia cohort (iPCD Cohort): methods and first results. Eur Respir J 2017;49:1601181. [PMID: 28052956 DOI: 10.1183/13993003.01181-2016] [Cited by in Crossref: 55] [Cited by in F6Publishing: 46] [Article Influence: 11.0] [Reference Citation Analysis]
41 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]
42 Conduit PT, Wainman A, Raff JW. Centrosome function and assembly in animal cells. Nat Rev Mol Cell Biol 2015;16:611-24. [PMID: 26373263 DOI: 10.1038/nrm4062] [Cited by in Crossref: 302] [Cited by in F6Publishing: 263] [Article Influence: 43.1] [Reference Citation Analysis]
43 Lai M, Pifferi M, Bush A, Piras M, Michelucci A, Di Cicco M, del Grosso A, Quaranta P, Cursi C, Tantillo E, Franceschi S, Mazzanti MC, Simi P, Saggese G, Boner A, Pistello M. Gene editing of DNAH11 restores normal cilia motility in primary ciliary dyskinesia. J Med Genet 2016;53:242-9. [DOI: 10.1136/jmedgenet-2015-103539] [Cited by in Crossref: 28] [Cited by in F6Publishing: 25] [Article Influence: 4.7] [Reference Citation Analysis]
44 Hammoudeh S, Gadelhak W, Janahi IA. Primary ciliary dyskinesia among Arabs: Where do we go from here? Paediatr Respir Rev 2019;29:19-22. [PMID: 30792130 DOI: 10.1016/j.prrv.2018.09.002] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
45 Hart RJ. Physiological Aspects of Female Fertility: Role of the Environment, Modern Lifestyle, and Genetics. Physiological Reviews 2016;96:873-909. [DOI: 10.1152/physrev.00023.2015] [Cited by in Crossref: 66] [Cited by in F6Publishing: 52] [Article Influence: 11.0] [Reference Citation Analysis]
46 Boaretto F, Snijders D, Salvoro C, Spalletta A, Mostacciuolo ML, Collura M, Cazzato S, Girosi D, Silvestri M, Rossi GA, Barbato A, Vazza G. Diagnosis of Primary Ciliary Dyskinesia by a Targeted Next-Generation Sequencing Panel: Molecular and Clinical Findings in Italian Patients. J Mol Diagn 2016;18:912-22. [PMID: 27637300 DOI: 10.1016/j.jmoldx.2016.07.002] [Cited by in Crossref: 27] [Cited by in F6Publishing: 25] [Article Influence: 4.5] [Reference Citation Analysis]
47 LaDuca H, Farwell KD, Vuong H, Lu HM, Mu W, Shahmirzadi L, Tang S, Chen J, Bhide S, Chao EC. Exome sequencing covers >98% of mutations identified on targeted next generation sequencing panels. PLoS One 2017;12:e0170843. [PMID: 28152038 DOI: 10.1371/journal.pone.0170843] [Cited by in Crossref: 47] [Cited by in F6Publishing: 43] [Article Influence: 9.4] [Reference Citation Analysis]
48 Gitman L, Peña M. Pathogenesis of Pediatric Rhinosinusitis. In: Ramadan HH, Baroody FM, editors. Pediatric Rhinosinusitis. Cham: Springer International Publishing; 2020. pp. 17-40. [DOI: 10.1007/978-3-030-22891-0_3] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
49 Amorim A, Gamboa F, Sucena M, Cunha K, Anciães M, Lopes S, Pereira S, Ferreira R, Azevedo P, Costeira J, Monteiro R, da Costa J, Pires S, Nunes C. Recommendations for aetiological diagnosis of bronchiectasis. Revista Portuguesa de Pneumologia (English Edition) 2016;22:222-35. [DOI: 10.1016/j.rppnen.2016.03.004] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.3] [Reference Citation Analysis]
50 Cannarella R, Maniscalchi ET, Condorelli RA, Scalia M, Guerri G, La Vignera S, Bertelli M, Calogero AE. Ultrastructural Sperm Flagellum Defects in a Patient With CCDC39 Compound Heterozygous Mutations and Primary Ciliary Dyskinesia/Situs Viscerum Inversus. Front Genet 2020;11:974. [PMID: 33005176 DOI: 10.3389/fgene.2020.00974] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
51 Bragina EE, Arifulin EA, Senchenkov EP. Genetically determined and functional human sperm motility decrease. Russ J Dev Biol 2016;47:239-53. [DOI: 10.1134/s1062360416050027] [Cited by in Crossref: 4] [Article Influence: 0.7] [Reference Citation Analysis]
52 Narasimhan V, Roy S. Cilia: Organelles at the Heart of Heart Disease. Curr Biol 2015;25:R559-62. [PMID: 26126281 DOI: 10.1016/j.cub.2015.05.005] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
53 Nizami MI, Narahari NK, Paramjyothi GK, Sharma A. An unusual cause of simultaneous bilateral spontaneous pneumothorax. World J Emerg Med 2017;8:74-6. [PMID: 28123627 DOI: 10.5847/wjem.j.1920-8642.2017.01.015] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
54 Szymanski EP, Leung JM, Fowler CJ, Haney C, Hsu AP, Chen F, Duggal P, Oler AJ, McCormack R, Podack E, Drummond RA, Lionakis MS, Browne SK, Prevots DR, Knowles M, Cutting G, Liu X, Devine SE, Fraser CM, Tettelin H, Olivier KN, Holland SM. Pulmonary Nontuberculous Mycobacterial Infection. A Multisystem, Multigenic Disease. Am J Respir Crit Care Med 2015;192:618-28. [PMID: 26038974 DOI: 10.1164/rccm.201502-0387OC] [Cited by in Crossref: 93] [Cited by in F6Publishing: 45] [Article Influence: 13.3] [Reference Citation Analysis]
55 Munye MM, Tagalakis AD, Barnes JL, Brown RE, McAnulty RJ, Howe SJ, Hart SL. Minicircle DNA Provides Enhanced and Prolonged Transgene Expression Following Airway Gene Transfer. Sci Rep 2016;6:23125. [PMID: 26975732 DOI: 10.1038/srep23125] [Cited by in Crossref: 38] [Cited by in F6Publishing: 33] [Article Influence: 6.3] [Reference Citation Analysis]
56 Kouis P, Papatheodorou SI, Middleton N, Giallouros G, Kyriacou K, Cohen JT, Evans JS, Yiallouros PK. Cost-effectiveness analysis of three algorithms for diagnosing primary ciliary dyskinesia: a simulation study. Orphanet J Rare Dis 2019;14:142. [PMID: 31196140 DOI: 10.1186/s13023-019-1116-3] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
57 Alsamri MT, Alabdouli A, Iram D, Alkalbani AM, Almarzooqi AS, Souid AK, Vijayan R. A Study on the Genetics of Primary Ciliary Dyskinesia. J Clin Med 2021;10:5102. [PMID: 34768622 DOI: 10.3390/jcm10215102] [Reference Citation Analysis]
58 Ghosh S, Das PJ, McQueen CM, Gerber V, Swiderski CE, Lavoie JP, Chowdhary BP, Raudsepp T. Analysis of genomic copy number variation in equine recurrent airway obstruction (heaves). Anim Genet 2016;47:334-44. [PMID: 26932307 DOI: 10.1111/age.12426] [Cited by in Crossref: 10] [Cited by in F6Publishing: 9] [Article Influence: 1.7] [Reference Citation Analysis]
59 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]
60 Morris-Rosendahl DJ, Kaindl AM. What next-generation sequencing (NGS) technology has enabled us to learn about primary autosomal recessive microcephaly (MCPH). Mol Cell Probes 2015;29:271-81. [PMID: 26050940 DOI: 10.1016/j.mcp.2015.05.015] [Cited by in Crossref: 49] [Cited by in F6Publishing: 40] [Article Influence: 7.0] [Reference Citation Analysis]
61 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]
62 Xu J, Li L, Ren J, Zhong X, Xie C, Zheng A, Abudukadier A, Tuerxun M, Zhang S, Tang L, Hairoula D, Zou X. Whole-Exome Sequencing Implicates the USP34 rs777591A > G Intron Variant in Chronic Obstructive Pulmonary Disease in a Kashi Cohort. Front Cell Dev Biol 2022;9:792027. [DOI: 10.3389/fcell.2021.792027] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
63 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]
64 Damseh N, Quercia N, Rumman N, Dell SD, Kim RH. Primary ciliary dyskinesia: mechanisms and management. Appl Clin Genet 2017;10:67-74. [PMID: 29033599 DOI: 10.2147/TACG.S127129] [Cited by in Crossref: 35] [Cited by in F6Publishing: 17] [Article Influence: 7.0] [Reference Citation Analysis]
65 Sahabian A, von Schlehdorn L, Drick N, Pink I, Dahlmann J, Haase A, Göhring G, Welte T, Martin U, Ringshausen FC, Olmer R. Generation of two hiPSC clones (MHHi019-A, MHHi019-B) from a primary ciliary dyskinesia patient carrying a homozygous deletion in the NME5 gene (c.415delA (p.Ile139Tyrfs*8)). Stem Cell Res 2020;48:101988. [PMID: 32950024 DOI: 10.1016/j.scr.2020.101988] [Reference Citation Analysis]