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For: Reish O, Slatkin M, Chapman-Shimshoni D, Elizur A, Chioza B, Castleman V, Mitchison HM. Founder mutation(s) in the RSPH9 gene leading to primary ciliary dyskinesia in two inbred Bedouin families. Ann Hum Genet 2010;74:117-25. [PMID: 20070851 DOI: 10.1111/j.1469-1809.2009.00559.x] [Cited by in Crossref: 12] [Cited by in F6Publishing: 10] [Article Influence: 1.0] [Reference Citation Analysis]
Number Citing Articles
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2 Alsaadi MM, Gaunt TR, Boustred CR, Guthrie PA, Liu X, Lenzi L, Rainbow L, Hall N, Alharbi KK, Day IN. From a single whole exome read to notions of clinical screening: primary ciliary dyskinesia and RSPH9 p.Lys268del in the Arabian Peninsula. Ann Hum Genet 2012;76:211-20. [PMID: 22384920 DOI: 10.1111/j.1469-1809.2012.00704.x] [Cited by in Crossref: 14] [Cited by in F6Publishing: 13] [Article Influence: 1.4] [Reference Citation Analysis]
3 Garcia CHS, Depoix D, Carvalho PC, Bastos IMD, Ricart CAO, de Sousa MV, Ferguson DJP, Santana JM, Grellier P, Charneau S. Comparative proteomic analysis of kinesin-8B deficient Plasmodium berghei during gametogenesis. J Proteomics 2021;236:104118. [PMID: 33486016 DOI: 10.1016/j.jprot.2021.104118] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Harrison MJ, Shapiro AJ, Kennedy MP. Congenital Heart Disease and Primary Ciliary Dyskinesia. Paediatr Respir Rev 2016;18:25-32. [PMID: 26545972 DOI: 10.1016/j.prrv.2015.09.003] [Cited by in Crossref: 9] [Cited by in F6Publishing: 14] [Article Influence: 1.3] [Reference Citation Analysis]
5 Leigh MW. Primary Ciliary Dyskinesia. Kendig & Chernick’s Disorders of the Respiratory Tract in Children. Elsevier; 2012. pp. 995-1002. [DOI: 10.1016/b978-1-4377-1984-0.00071-1] [Cited by in Crossref: 2] [Article Influence: 0.2] [Reference Citation Analysis]
6 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]
7 Zlotogora J. The molecular basis of autosomal recessive diseases among the Arabs and Druze in Israel. Hum Genet 2010;128:473-9. [PMID: 20852892 DOI: 10.1007/s00439-010-0890-8] [Cited by in Crossref: 24] [Cited by in F6Publishing: 21] [Article Influence: 2.0] [Reference Citation Analysis]
8 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]
9 Alsafwani RS, Nasser KK, Shinawi T, Banaganapalli B, ElSokary HA, Zaher ZF, Shaik NA, Abdelmohsen G, Al-Aama JY, Shapiro AJ, O Al-Radi O, Elango R, Alahmadi T. Novel MYO1D Missense Variant Identified Through Whole Exome Sequencing and Computational Biology Analysis Expands the Spectrum of Causal Genes of Laterality Defects. Front Med (Lausanne) 2021;8:724826. [PMID: 34589502 DOI: 10.3389/fmed.2021.724826] [Reference Citation Analysis]
10 Lee L. Mechanisms of mammalian ciliary motility: Insights from primary ciliary dyskinesia genetics. Gene 2011;473:57-66. [PMID: 21111794 DOI: 10.1016/j.gene.2010.11.006] [Cited by in Crossref: 50] [Cited by in F6Publishing: 48] [Article Influence: 4.2] [Reference Citation Analysis]
11 Mabrouk I, Al-harthi N, Mani R, Montantin G, Tissier S, Lagha R, Ben Abdallah F, Hassan MM, Alhomrani M, Gaber A, Alsanie WF, Ouali H, Jambi FA, Almaghamsi TM, Alqarni NA, Alfarsi NA, Kashgari K, Al-zahrani HJ, Al-shamary ZA, Al-harbi A, Amselem S, Escudier E, Legendre M. Combining RSPH9 founder mutation screening and next-generation sequencing analysis is efficient for primary ciliary dyskinesia diagnosis in Saudi patients. J Hum Genet. [DOI: 10.1038/s10038-021-01006-9] [Reference Citation Analysis]
12 Lindahl P, Säll T, Bjartell A, Johansson AM, Lilja H, Halldén C. Copy number variants in the kallikrein gene cluster. PLoS One 2013;8:e69097. [PMID: 23894413 DOI: 10.1371/journal.pone.0069097] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.2] [Reference Citation Analysis]
13 Fassad MR, Shoman WI, Morsy H, Patel MP, Radwan N, Jenkins L, Cullup T, Fouda E, Mitchison HM, Fasseeh N. Clinical and genetic spectrum in 33 Egyptian families with suspected primary ciliary dyskinesia. Clin Genet 2020;97:509-15. [PMID: 31650533 DOI: 10.1111/cge.13661] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]