☰

You Li, Ph.D. - Publications

Affiliations: 
University of Pittsburgh, Pittsburgh, PA, United States 
Area:
biochemistry, genetics
Tree Info Grants Similar researchers PubMed Report error

6 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

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  0.32
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  0.309
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  0.309
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  0.309
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  0.321
2013 Hjeij R, Lindstrand A, Francis R, Zariwala MA, Liu X, Li Y, Damerla R, Dougherty GW, Abouhamed M, Olbrich H, Loges NT, Pennekamp P, Davis EE, Carvalho CM, Pehlivan D, et al. ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetry. American Journal of Human Genetics. 93: 357-67. PMID 23849778 DOI: 10.1016/J.Ajhg.2013.06.009  0.305
Show low-probability matches.