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For: Lucas JS, Paff T, Goggin P, Haarman E. Diagnostic Methods in Primary Ciliary Dyskinesia. Paediatric Respiratory Reviews 2016;18:8-17. [DOI: 10.1016/j.prrv.2015.07.017] [Cited by in Crossref: 9] [Cited by in F6Publishing: 12] [Article Influence: 1.5] [Reference Citation Analysis]
Number Citing Articles
1 Fitzgerald DA, Shapiro AJ. Primary Ciliary Dyskinesia. Paediatr Respir Rev 2016;18:1-2. [PMID: 26826908 DOI: 10.1016/j.prrv.2015.11.010] [Cited by in Crossref: 1] [Article Influence: 0.2] [Reference Citation Analysis]
2 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]
3 Ascari G, Peelman F, Farinelli P, Rosseel T, Lambrechts N, Wunderlich KA, Wagner M, Nikopoulos K, Martens P, Balikova I, Derycke L, Holtappels G, Krysko O, Van Laethem T, De Jaegere S, Guillemyn B, De Rycke R, De Bleecker J, Creytens D, Van Dorpe J, Gerris J, Bachert C, Neuhofer C, Walraedt S, Bischoff A, Pedersen LB, Klopstock T, Rivolta C, Leroy BP, De Baere E, Coppieters F. Functional characterization of the first missense variant in CEP78, a founder allele associated with cone-rod dystrophy, hearing loss, and reduced male fertility. Hum Mutat 2020;41:998-1011. [PMID: 31999394 DOI: 10.1002/humu.23993] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
4 Kempeneers C, Seaton C, Garcia Espinosa B, Chilvers MA. Ciliary functional analysis: Beating a path towards standardization. Pediatr Pulmonol 2019;54:1627-38. [PMID: 31313529 DOI: 10.1002/ppul.24439] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 3.0] [Reference Citation Analysis]
5 Dong S, Bei F, Yu T, Sun L, Chen X, Yan H. A Novel Compound Heterozygous Mutation in the DNAH11 Gene Found in Neonatal Twins With Primary Ciliary Dyskinesis. Front Genet 2022;13:814511. [PMID: 35295944 DOI: 10.3389/fgene.2022.814511] [Reference Citation Analysis]
6 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]
7 Halbeisen FS, Jose A, de Jong C, Nyilas S, Latzin P, Kuehni CE, Goutaki M. Spirometric indices in primary ciliary dyskinesia: systematic review and meta-analysis. ERJ Open Res 2019;5:00231-2018. [PMID: 31111042 DOI: 10.1183/23120541.00231-2018] [Cited by in Crossref: 11] [Cited by in F6Publishing: 10] [Article Influence: 3.7] [Reference Citation Analysis]
8 Behan L, Dunn Galvin A, Rubbo B, Masefield S, Copeland F, Manion M, Rindlisbacher B, Redfern B, Lucas JS. Diagnosing primary ciliary dyskinesia: an international patient perspective. Eur Respir J 2016;48:1096-107. [PMID: 27492837 DOI: 10.1183/13993003.02018-2015] [Cited by in Crossref: 32] [Cited by in F6Publishing: 29] [Article Influence: 5.3] [Reference Citation Analysis]
9 Paff T, Kooi IE, Moutaouakil Y, Riesebos E, Sistermans EA, Daniels HJMA, Weiss JMM, Niessen HHWM, Haarman EG, Pals G, Micha D. Diagnostic yield of a targeted gene panel in primary ciliary dyskinesia patients. Hum Mutat 2018;39:653-65. [PMID: 29363216 DOI: 10.1002/humu.23403] [Cited by in Crossref: 20] [Cited by in F6Publishing: 17] [Article Influence: 5.0] [Reference Citation Analysis]
10 Ong HX, Jackson CL, Cole JL, Lackie PM, Traini D, Young PM, Lucas J, Conway J. Primary Air–Liquid Interface Culture of Nasal Epithelium for Nasal Drug Delivery. Mol Pharmaceutics 2016;13:2242-52. [DOI: 10.1021/acs.molpharmaceut.5b00852] [Cited by in Crossref: 22] [Cited by in F6Publishing: 22] [Article Influence: 3.7] [Reference Citation Analysis]
11 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]
12 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]
13 Poprzeczko M, Bicka M, Farahat H, Bazan R, Osinka A, Fabczak H, Joachimiak E, Wloga D. Rare Human Diseases: Model Organisms in Deciphering the Molecular Basis of Primary Ciliary Dyskinesia. Cells 2019;8:E1614. [PMID: 31835861 DOI: 10.3390/cells8121614] [Cited by in Crossref: 11] [Cited by in F6Publishing: 8] [Article Influence: 3.7] [Reference Citation Analysis]
14 Li Y, Jiang C, Zhang X, Liu M, Sun Y, Yang Y, Shen Y. The effect of a novel LRRC6 mutation on the flagellar ultrastructure in a primary ciliary dyskinesia patient. J Assist Reprod Genet 2021;38:689-96. [PMID: 33403504 DOI: 10.1007/s10815-020-02036-6] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]