Xuan Yuan

Research Associate

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  • 8 Similar Profiles
Glioma Medicine & Life Sciences
Glycosylphosphatidylinositols Medicine & Life Sciences
Idoxuridine Medicine & Life Sciences
Paroxysmal Hemoglobinuria Medicine & Life Sciences
tirapazamine Medicine & Life Sciences
Polymers Medicine & Life Sciences
Induced Pluripotent Stem Cells Medicine & Life Sciences
Alternative Complement Pathway Medicine & Life Sciences

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Research Output 1998 2019

Rare Germline Mutations in Complement Regulatory Genes Make the Antiphospholipid Syndrome Catastrophic

Chaturvedi, S., Braunstein, E. M., Yuan, X., Chen, H., Alluri, R. K., Streiff, M. B., Petri, M., Crowther, M., McCrae, K. R. & Brodsky, R. A., Nov 13 2019, In : Blood. 134, 1, 1 p.

Research output: Contribution to journalArticle

Antiphospholipid Syndrome
Germ-Line Mutation
Regulator Genes
Advisory Committees

Germline mutations in the alternative pathway of complement predispose to HELLP syndrome

Vaught, A., Braunstein, E., Jasem, J., Yuan, X., Makhlin, I., Eloundou, S., Baines, A. C., Merrill, S., Chaturvedi, S., Blakemore, K., Sperati, C. J. & Brodsky, R. A., Mar 22 2018, In : JCI insight. 3, 6

Research output: Contribution to journalArticle

Open Access
Alternative Complement Pathway
Germ-Line Mutation
Blood Platelets

A hypomorphic PIGA gene mutation causes severe defects in neuron development and susceptibility to complement-mediated toxicity in a human iPSC model

Yuan, X., Li, Z., Baines, A. C., Gavriilaki, E., Ye, Z., Wen, Z., Braunstein, E., Biesecker, L. G., Cheng, L., Dong, X. & Brodsky, R. A., Apr 1 2017, In : PLoS One. 12, 4, e0174074.

Research output: Contribution to journalArticle


Eculizumab cessation in atypical hemolytic uremic syndrome

Merrill, S., Brittingham, Z. D., Yuan, X., Moliterno, A. R., Sperati, C. J. & Brodsky, R. A., Jul 20 2017, In : Blood. 130, 3, p. 368-372 5 p.

Research output: Contribution to journalLetter

Antibodies, Monoclonal, Humanized

Hypotonia and intellectual disability without dysmorphic features in a patient with PIGN-related disease

Thiffault, I., Zuccarelli, B., Welsh, H., Yuan, X., Farrow, E., Zellmer, L., Miller, N., Soden, S., Abdelmoity, A., Brodsky, R. A. & Saunders, C., Nov 2 2017, In : BMC Medical Genetics. 18, 1, 124.

Research output: Contribution to journalArticle

Muscle Hypotonia
Intellectual Disability