Xi Wu, Ph.D.
Affiliations: | 2000 | University of Illinois at Chicago, Chicago, IL, United States |
Area:
MathematicsGoogle:
"Xi Wu"Parents
Sign in to add mentor| Stephen S. Yau | grad student | 2000 | University of Illinois, Chicago | |
| (Topics in the nonlinear filtering theory.) | ||||
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Publications
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| Zhang H, Chen C, Wu X, et al. (2022) Effects of 14 F9 synonymous codon variants on hemophilia B expression: alteration of splicing along with protein expression. Human Mutation |
| Liang Q, Lin X, Wu X, et al. (2021) Unraveling the molecular basis underlying nine putative splice site variants of von Willebrand factor. Human Mutation |
| Ma S, Chen C, Liang Q, et al. (2019) Phenotype and genotype of FXIII deficiency in two unrelated probands: identification of a novel F13A1 large deletion mediated by complex rearrangement. Orphanet Journal of Rare Diseases. 14: 182 |
| Xie X, Chen C, Liang Q, et al. (2019) Characterization of two large duplications of F9 associated with mild and severe haemophilia B, respectively. Haemophilia : the Official Journal of the World Federation of Hemophilia |
| Zhou J, Ding Q, Wu W, et al. (2016) Dysfibrinogenemia-associated novel heterozygous mutation, Shanghai (FGA c.169_180+2 del), leads to N-terminal truncation of fibrinogen Aα chain and impairs fibrin polymerization. Journal of Clinical Pathology |
| Zhou J, Xin Y, Ding Q, et al. (2015) Thromboelastography predicts risks of obstetric complication occurrence in (hypo)dysfibrinogenemia patients under non-pregnant state. Clinical and Experimental Pharmacology & Physiology |
| Zhou J, Ding Q, Chen Y, et al. (2015) Clinical features and molecular basis of 102 Chinese patients with congenital dysfibrinogenemia. Blood Cells, Molecules & Diseases. 55: 308-15 |