YONG YANG

Main Publications:

1. Y Yang, Y Wang, S Li, Z Xu, H Li, L Ma, J Fan, D Bu, B Liu, Z Fan, G Wu, J Jin, B Ding, X Zhu, Y Shen, Mutations in SCN9A, encoding a sodium channel alpha subunit, in patients with primary erythermalgia. JOURNAL OF MEDICAL GENETICS, 41(3): 171-4, 2004. (cited by Cell, Nature and Science papers)
2. L Wang, D Bu, Y Yang, X Chen, X Zhu, Castleman's tumours and production of autoantibody in paraneoplastic pemphigus. LANCET, 363: 525-31, 2004.
3. C Han, AM Rush, SD Dib-Hajj, S Li, Z Xu, Y Wang, L Tyrrell, X Wang, Y Yang*, SG Waxman*, Sporadic onset of erythermalgia: a gain-of-function mutation in Nav1.7. ANNALS OF NEUROLOGY, 59(3): 553-8, 2006. 
4. C Han, SD Dib-Hajj, Z Lin, Y Li, EM Eastman, L Tyrrell, X Cao, Y Yang*, SG Waxman*, Early- and late-onset inherited erythromelalgia: genotype–phenotype correlation. BRAIN, 132(7): 1711-22, 2009.
5. Z Lin, Q Chen, M Lee, X Cao, J Zhang, D Ma, L Chen, X Hu, H Wang,1 X Wang, P Zhang, X Liu, L Guan, Y Tang, H Yang, P Tu, D Bu, X Zhu, K Wang, R Li*, Y Yang*, Exome Sequencing Reveals Mutations in TRPV3 as a Cause of Olmsted Syndrome. AMERICAN JOURNAL OF HUMAN GENETICS, 90(3): 558-64, 2012.