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For: Meeks M, Walne A, Spiden S, Simpson H, Mussaffi-Georgy H, Hamam HD, Fehaid EL, Cheehab M, Al-Dabbagh M, Polak-Charcon S, Blau H, O'Rawe A, Mitchison HM, Gardiner RM, Chung E. A locus for primary ciliary dyskinesia maps to chromosome 19q. J Med Genet 2000;37:241-4. [PMID: 10745040 DOI: 10.1136/jmg.37.4.241] [Cited by in Crossref: 40] [Cited by in F6Publishing: 34] [Article Influence: 1.8] [Reference Citation Analysis]
Number Citing Articles
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2 Pazour GJ, Agrin N, Walker BL, Witman GB. Identification of predicted human outer dynein arm genes: candidates for primary ciliary dyskinesia genes. J Med Genet 2006;43:62-73. [PMID: 15937072 DOI: 10.1136/jmg.2005.033001] [Cited by in Crossref: 87] [Cited by in F6Publishing: 73] [Article Influence: 5.1] [Reference Citation Analysis]
3 Geremek M, Zietkiewicz E, Diehl SR, Alizadeh BZ, Wijmenga C, Witt M. Linkage analysis localises a Kartagener syndrome gene to a 3.5 cM region on chromosome 15q24-25. J Med Genet 2006;43:e1. [PMID: 16397065 DOI: 10.1136/jmg.2005.031526] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 0.5] [Reference Citation Analysis]
4 Tubbs RS, Wellons JC 3rd, Oakes WJ. Split cord malformation and situs inversus totalis: case report and review of the literature. Childs Nerv Syst 2004;20:131-4. [PMID: 14648098 DOI: 10.1007/s00381-003-0857-3] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.2] [Reference Citation Analysis]
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10 Pennarun G, Bridoux AM, Escudier E, Dastot-Le Moal F, Cacheux V, Amselem S, Duriez B. Isolation and expression of the human hPF20 gene orthologous to Chlamydomonas PF20: evaluation as a candidate for axonemal defects of respiratory cilia and sperm flagella. Am J Respir Cell Mol Biol 2002;26:362-70. [PMID: 11867345 DOI: 10.1165/ajrcmb.26.3.4738] [Cited by in Crossref: 32] [Cited by in F6Publishing: 26] [Article Influence: 1.6] [Reference Citation Analysis]
11 Omran H, Häffner K, Völkel A, Kuehr J, Ketelsen U, Ross U, Konietzko N, Wienker T, Brandis M, Hildebrandt F. Homozygosity Mapping of a Gene Locus for Primary Ciliary Dyskinesia on Chromosome 5p and Identification of the Heavy Dynein Chain DNAH5 as a Candidate Gene. Am J Respir Cell Mol Biol 2000;23:696-702. [DOI: 10.1165/ajrcmb.23.5.4257] [Cited by in Crossref: 84] [Cited by in F6Publishing: 68] [Article Influence: 3.8] [Reference Citation Analysis]
12 Ziętkiewicz E, Nitka B, Voelkel K, Skrzypczak U, Bukowy Z, Rutkiewicz E, Humińska K, Przystałowska H, Pogorzelski A, Witt M. Population specificity of the DNAI1 gene mutation spectrum in primary ciliary dyskinesia (PCD). Respir Res 2010;11:174. [PMID: 21143860 DOI: 10.1186/1465-9921-11-174] [Cited by in Crossref: 21] [Cited by in F6Publishing: 18] [Article Influence: 1.8] [Reference Citation Analysis]
13 Clark H, Clark LS. The genetics of neonatal respiratory disease. Seminars in Fetal and Neonatal Medicine 2005;10:271-82. [DOI: 10.1016/j.siny.2005.02.004] [Cited by in Crossref: 22] [Cited by in F6Publishing: 15] [Article Influence: 1.3] [Reference Citation Analysis]
14 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]
15 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]
16 Mur Sierra A, Viñolas Tolosa M, Sánchez García Vao C, García López A, Busquets Monge R, García Algar O, Lloreta Trull J, Bargués Cardelús R. Asociación entre el consumo de heroína durante la gestación y anomalías estructurales de los cilios respiratorios en el período neonatal. Anales de Pediatría 2001;55:335-8. [DOI: 10.1016/s1695-4033(01)77695-3] [Cited by in Crossref: 3] [Article Influence: 0.1] [Reference Citation Analysis]
17 Bartoloni L, Blouin JL, Maiti AK, Sainsbury A, Rossier C, Gehrig C, She JX, Marron MP, Lander ES, Meeks M, Chung E, Armengot M, Jorissen M, Scott HS, Delozier-Blanchet CD, Gardiner RM, Antonarakis SE. Axonemal beta heavy chain dynein DNAH9: cDNA sequence, genomic structure, and investigation of its role in primary ciliary dyskinesia. Genomics 2001;72:21-33. [PMID: 11247663 DOI: 10.1006/geno.2000.6462] [Cited by in Crossref: 32] [Cited by in F6Publishing: 28] [Article Influence: 1.5] [Reference Citation Analysis]
18 Chodhari R, Mitchison H, Meeks M. Cilia, primary ciliary dyskinesia and molecular genetics. Paediatric Respiratory Reviews 2004;5:69-76. [DOI: 10.1016/j.prrv.2003.09.005] [Cited by in Crossref: 43] [Cited by in F6Publishing: 35] [Article Influence: 2.4] [Reference Citation Analysis]
19 Ji ZY, Sha YW, Ding L, Li P. Genetic factors contributing to human primary ciliary dyskinesia and male infertility. Asian J Androl 2017;19:515-20. [PMID: 27270341 DOI: 10.4103/1008-682X.181227] [Cited by in Crossref: 18] [Cited by in F6Publishing: 9] [Article Influence: 4.5] [Reference Citation Analysis]
20 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]
21 Tubbs RS, Wellons JC 3rd, Oakes WJ. Split cord malformation and situs inversus totalis: case report and review of the literature. Childs Nerv Syst 2005;21:161-4. [PMID: 14745579 DOI: 10.1007/s00381-003-0895-x] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 0.3] [Reference Citation Analysis]
22 Eriksson M, Ansved T, Anvret M, Carey N. A mammalian radial spokehead-like gene, RSHL1, at the myotonic dystrophy-1 locus. Biochem Biophys Res Commun 2001;281:835-41. [PMID: 11237735 DOI: 10.1006/bbrc.2001.4465] [Cited by in Crossref: 13] [Cited by in F6Publishing: 12] [Article Influence: 0.6] [Reference Citation Analysis]
23 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]
24 Failly M, Saitta A, Muñoz A, Falconnet E, Rossier C, Santamaria F, de Santi MM, Lazor R, DeLozier-Blanchet CD, Bartoloni L, Blouin JL. DNAI1 mutations explain only 2% of primary ciliary dykinesia. Respiration 2008;76:198-204. [PMID: 18434704 DOI: 10.1159/000128567] [Cited by in Crossref: 31] [Cited by in F6Publishing: 31] [Article Influence: 2.2] [Reference Citation Analysis]
25 Skrzypczak U, Rutkiewicz E, Pogorzelski A, Witt M, Zietkiewicz E. Carrier status for 3 most frequent CFTR mutations in Polish PCD/KS patients: lack of association with the primary ciliary dyskinesia phenotype. J Appl Genet 2007;48:85-8. [PMID: 17272866 DOI: 10.1007/BF03194662] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.2] [Reference Citation Analysis]
26 Zariwala M, Noone PG, Sannuti A, Minnix S, Zhou Z, Leigh MW, Hazucha M, Carson JL, Knowles MR. Germline Mutations in an Intermediate Chain Dynein Cause Primary Ciliary Dyskinesia. Am J Respir Cell Mol Biol 2001;25:577-83. [DOI: 10.1165/ajrcmb.25.5.4619] [Cited by in Crossref: 80] [Cited by in F6Publishing: 68] [Article Influence: 3.8] [Reference Citation Analysis]
27 Pennarun G, Chapelin C, Escudier E, Bridoux A, Dastot F, Cacheux V, Goossens M, Amselem S, Duriez B. The human dynein intermediate chain 2 gene (DNAI2): cloning, mapping, expression pattern, and evaluation as a candidate for primary ciliary dyskinesia. Hum Genet 2000;107:642-9. [DOI: 10.1007/s004390000427] [Cited by in Crossref: 28] [Cited by in F6Publishing: 27] [Article Influence: 1.3] [Reference Citation Analysis]
28 Roomans GM, Ivanovs A, Shebani EB, Johannesson M. Transmission electron microscopy in the diagnosis of primary ciliary dyskinesia. Ups J Med Sci 2006;111:155-68. [PMID: 16553254 DOI: 10.3109/2000-1967-010] [Cited by in Crossref: 18] [Cited by in F6Publishing: 16] [Article Influence: 1.1] [Reference Citation Analysis]
29 Santos JWAD, Waldow A, Figueiredo CWCD, Kleinubing DR, Barros SSD. Discinesia ciliar primária. J Pneumologia 2001;27:262-8. [DOI: 10.1590/s0102-35862001000500006] [Cited by in Crossref: 4] [Article Influence: 0.2] [Reference Citation Analysis]
30 Geremek M, Bruinenberg M, Ziętkiewicz E, Pogorzelski A, Witt M, Wijmenga C. Gene expression studies in cells from primary ciliary dyskinesia patients identify 208 potential ciliary genes. Hum Genet 2011;129:283-93. [PMID: 21136274 DOI: 10.1007/s00439-010-0922-4] [Cited by in Crossref: 25] [Cited by in F6Publishing: 21] [Article Influence: 2.1] [Reference Citation Analysis]
31 Takada S, Wilkerson CG, Wakabayashi K, Kamiya R, Witman GB. The outer dynein arm-docking complex: composition and characterization of a subunit (oda1) necessary for outer arm assembly. Mol Biol Cell 2002;13:1015-29. [PMID: 11907279 DOI: 10.1091/mbc.01-04-0201] [Cited by in Crossref: 93] [Cited by in F6Publishing: 74] [Article Influence: 4.7] [Reference Citation Analysis]
32 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]
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34 Kurima K, Yang Y, Sorber K, Griffith AJ. Characterization of the transmembrane channel-like (TMC) gene family: functional clues from hearing loss and epidermodysplasia verruciformis. Genomics 2003;82:300-8. [PMID: 12906855 DOI: 10.1016/s0888-7543(03)00154-x] [Cited by in Crossref: 93] [Cited by in F6Publishing: 57] [Article Influence: 5.2] [Reference Citation Analysis]