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lei li - Publications

Affiliations: 
Peking University, Beijing, Beijing Shi, China 
Area:
polymer chemistry
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8 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
2013 Liu W, Liu W, Hu D, Zhu T, Ma Z, Yang J, Xie W, Li C, Li L, Yang J, Li T, Bian H, Tong Q. Mutation spectrum in a large cohort of unrelated Chinese patients with hypertrophic cardiomyopathy. The American Journal of Cardiology. 112: 585-9. PMID 23711808 DOI: 10.1016/J.Amjcard.2013.04.021  0.333
2013 Liu W, Hu D, Zhu T, Ma Z, Yang J, Xie W, Li C, Li L, Yang J, Li T, Bian H, Tong Q, Liu W. GW24-e1791 Mutation spectrum in a large cohort of unrelated Chinese patients with hypertrophic cardiomyopathy Heart. 99: A33.3-A33. DOI: 10.1136/Heartjnl-2013-304613.87  0.333
2012 Ge Q, Li C, Yuan Y, Liu W, Gao Y, Li L, Hu D. A Hotspot Mutation Ryr2-R169Q For Chinese Patients With Catecholaminergic Polymorphic Ventricular Tachycardia Heart. 98. DOI: 10.1136/Heartjnl-2012-302920A.65  0.318
2012 Gao Y, Li C, Liang L, Li Y, Liu W, Ma J, Li L, Hu D. Novel Mutations On Scn5A Caused Fatal Arrhythmia Syndrome In Chinese1 Heart. 98. DOI: 10.1136/Heartjnl-2012-302920A.49  0.311
2012 Liu W, Liu W, Qiu X, Hu D, Zhu T, Li C, Li L, Liu W. PHENOTYPE DIFFERENCE BETWEEN GENOTYPE OF PLAKOPHILIN-2 MUTATION AND DESMOGLEIN-2 MUTATION IN SYMPTOMATIC CHINESE PATIENTS WITH ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA/CARDIOMYOPATHY-A REPORT FROM CHINESE ARVD REGISTRY Heart. 98: E95.3-E95. DOI: 10.1136/Heartjnl-2012-302920A.255  0.309
2012 Gao Y, Li C, Liu W, Yuan Y, Li L, Hu D. The Mosaicism Genetic Pattern For Timothy Syndrome With Cacna1C Mutation G406R Heart. 98. DOI: 10.1136/Heartjnl-2012-302920A.108  0.309
2009 Qiu X, Liu W, Hu D, Zhu T, Li C, Li L, Guo C, Liu X, Wang L, Zheng H, Wang C, Diao Q, Shi D, Zhan P, Deng Y, et al. Mutations of plakophilin-2 in Chinese with arrhythmogenic right ventricular dysplasia/cardiomyopathy. The American Journal of Cardiology. 103: 1439-44. PMID 19427443 DOI: 10.1016/J.Amjcard.2009.01.356  0.314
2006 Pan G, Liu W, Hu D, Xie W, Zhu T, Li L, Li C, Bian H. Comparative study of gene mutation between Chinese patients with familial and sporadic hypertrophic cardiomyopathy National Medical Journal of China. 86: 2998-3001. DOI: 10.3760/J:Issn:0376-2491.2006.42.013  0.313
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