| Year |
Citation |
Score |
| 2016 |
Li Y, Yagi H, Onuoha EO, Damerla RR, Francis R, Furutani Y, Tariq M, King SM, Hendricks G, Cui C, Saydmohammed M, Lee DM, Zahid M, Sami I, Leatherbury L, et al. DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia. Plos Genetics. 12: e1005821. PMID 26918822 DOI: 10.1371/Journal.Pgen.1005821 |
0.313 |
|
| 2015 |
Li Y, Garrod AS, Madan-Khetarpal S, Sreedher G, McGuire M, Yagi H, Klena NT, Gabriel GC, Khalifa O, Zahid M, Panigrahy A, Weiner DJ, Lo CW. Respiratory motile cilia dysfunction in a patient with cranioectodermal dysplasia. American Journal of Medical Genetics. Part A. 167: 2188-96. PMID 25914204 DOI: 10.1002/Ajmg.A.37133 |
0.303 |
|
| 2015 |
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, et al. Global genetic analysis in mice unveils central role for cilia in congenital heart disease. Nature. 521: 520-4. PMID 25807483 DOI: 10.1038/Nature14269 |
0.304 |
|
| 2015 |
Onoufriadis A, Hjeij R, Watson CM, Slagle CE, Klena NT, Dougherty GW, Kurkowiak M, Loges NT, Diggle CP, Morante NF, Gabriel GC, Lemke KL, Li Y, Pennekamp P, Menchen T, et al. Gene discovery for motile cilia disorders: mutation spectrum in primary ciliary dyskinesia and discovery of mutations in CCDC151 Cilia. 4: 30. DOI: 10.1186/2046-2530-4-S1-P30 |
0.303 |
|
| 2014 |
Rao Damerla R, Gabriel GC, Li Y, Klena NT, Liu X, Chen Y, Cui C, Pazour GJ, Lo CW. Role of cilia in structural birth defects: insights from ciliopathy mutant mouse models. Birth Defects Research. Part C, Embryo Today : Reviews. 102: 115-25. PMID 24975753 DOI: 10.1002/Bdrc.21067 |
0.316 |
|
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