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Wang, L., Wu, M., Wen, Z., Xia, Q.P., Yan, H.F., and Luo, Z.Y. (2012). Isolation and characterization of microsatellite loci in the endangered tree Diplopanax stachyanthus (Araliaceae). Am J Bot, 99: e167-9.

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 Luo, C., Yang, Y.F., Yin, B.L., Chen, J.L., Huang, C., Zhang, W.Z., Wang, J., Zhang, H., Yang, J.F., and Tan, Z.P. (2012). Microduplication of 3p25.2 encompassing RAF1 associated with congenital heart disease suggestive of Noonan syndrome. Am J Med Genet A, 158A: 1918-23.

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 Chen, J.L., Yang, Y.F., Huang, C., Wang, J., Yang, J.F., and Tan, Z.P. (2012). Clinical and molecular delineation of 16p13.3 duplication in a patient with congenital heart defect and multiple congenital anomalies. Am J Med Genet A, 158A: 685-8.

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 Wu, R.R., Jin, H., Gao, K., Twamley, E.W., Ou, J.J., Shao, P., Wang, J., Guo, X.F., Davis, J.M., Chan, P.K., and Zhao, J.P. (2012). Metformin for treatment of antipsychotic-induced amenorrhea and weight gain in women with first-episode schizophrenia: a double-blind, randomized, placebo-controlled study. Am J Psychiatry, 169: 813-21.

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Ma, C., Yeung, E.S., Qi, S., and Han, R. (2012). Highly sensitive detection of microRNA by chemiluminescence based on enzymatic polymerization. Anal Bioanal Chem, 402: 2217-20.

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Ma, C., Chen, H., Han, R., He, H., and Zeng, W. (2012). Fluorescence detection of adenosine triphosphate using smart probe. Anal Biochem, 429: 8-10.

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Liu, Q.P., Wu, L.S., Li, F.F., Liu, S., Su, J., Kuang, Y.H., Chen, C., Xie, X.Y., Jiang, M.H., Zhao, S., Chen, M.L., and Chen, X. (2012). The association between GJB2 gene polymorphism and psoriasis: a verification study.Arch Dermatol Res, 304: 769-72.

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 Lu, J.H., Tan, J.Q., Durairajan, S.S., Liu, L.F., Zhang, Z.H., Ma, L., Shen, H.M., Chan, H.Y., and Li, M. (2012). Isorhynchophylline, a natural alkaloid, promotes the degradation of alpha-synuclein in neuronal cells via inducing autophagy. Autophagy, 8: 98-108.

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Zheng, X.R., Zhang, S.S., Yin, F., Tang, J.L., Yang, Y.J., Wang, X., and Zhong, L. (2012). Neuroprotection of VEGF-expression neural stem cells in neonatal cerebral palsy rats. Behav Brain Res, 230: 108-15.

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 Kuang, Y.H., Patel, J.P., Sodani, K., Wu, C.P., Liao, L.Q., Patel, A., Tiwari, A.K., Dai, C.L., Chen, X., Fu, L.W., Ambudkar, S.V., Korlipara, V.L., and Chen, Z.S. (2012). OSI-930 analogues as novel reversal agents for ABCG2-mediated multidrug resistance. Biochem Pharmacol, 84: 766-74.

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 Liang, D., Zhou, Z., Meng, D., Du, J., Wen, J., Niikawa, N., and Wu, L. (2012). Three patients with Wolf-Hirschhorn syndrome carrying a satellited chromosome 4p. Birth Defects Res A Clin Mol Teratol, 94: 549-52.

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Qin, B., Xiao, B., Liang, D., Li, Y., Jiang, T., and Yang, H. (2012). MicroRNA let-7c inhibits Bcl-xl expression and regulates ox-LDL-induced endothelial apoptosis. BMB Rep, 45: 464-9.

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 Liu, J.P., Zhan, X.Q., Li, M.Y., Li, G.Q., Zhang, P.F., Xiao, Z.F., Shao, M.Y., Peng, F., Hu, R., and Chen, Z.C. (2012). Mitochondrial proteomics of nasopharyngeal carcinoma metastasis. BMC Medical Genomics, 5: 62.

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Gong, Z.C., Huang, Q., Dai, X.P., Lei, G.H., Lu, H.B., Yin, J.Y., Xu, X.J., Qu, J., Pei, Q., Dong, M., Zhou, B.T., Shen, J., Zhou, G., Zhou, H.H., and Liu, Z.Q. (2012). NeuroD1 A45T and PAX4 R121W polymorphisms are associated with plasma glucose level of repaglinide monotherapy in Chinese patients with type 2 diabetes. Br J Clin Pharmacol, 74: 501-9.

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 Li, L., Dai, H.J., Ye, M., Wang, S.L., Xiao, X.J., Zheng, J., Chen, H.Y., Luo, Y.H., and Liu, J. (2012). Lycorine induces cell-cycle arrest in the G0/G1 phase in K562 cells via HDAC inhibition. Cancer Cell Int, 12: 49.

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Omran, A., Peng, J., Shrestha, B., Ashhab, M.U., and Yin, F. (2012). Male Child with Van Wyk-Grumbach's Syndrome and Other Complications of Long-Standing Primary Hypothyroidism: A Case Report. Case Rep Pediatr, 2012: 352751.

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Chen, Y., Bates, D.L., Dey, R., Chen, P.H., Machado, A.C., Laird-Offringa, I.A., Rohs, R., and Chen, L. (2012). DNA Binding by GATA Transcription Factor Suggests Mechanisms of DNA Looping and Long-Range Gene Regulation. Cell Rep, 2: 1197-206.

18

Pan, Y., Hu, M., Liang, H., Wang, J.J., and Tang, L.J. (2012). The expression of the PIWI family members miwi and mili in mice testis is negatively affected by estrogen. Cell Tissue Res, 350: 177-81.

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Peng, J., Deng, X., He, F., Omran, A., Zhang, C., Yin, F., and Liu, J. (2012). Role of ventriculoperitoneal shunt surgery in grade IV tubercular meningitis with hydrocephalus. Childs Nerv Syst, 28: 209-15.

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Xiong, Z., Luo, S., Xu, X., Zhang, L., Peng, H., Li, W., Xue, J., Chen, X., Hu, Z., and Xia, K. (2012). Novel FLG mutations associated with ichthyosis vulgaris in the Chinese population. Clin Exp Dermatol, 37: 177-80.

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Liu, L., Xie, H., Chen, X., Shi, W., Xiao, X., Lei, D., and Li, J. (2012). Differential response of normal human epidermal keratinocytes and HaCaT cells to hydrogen peroxide-induced oxidative stress. Clin Exp Dermatol,37: 772-80.

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Li, M., Li, C., Li, D., Xie, Y., Shi, J., Li, G., Guan, Y., Zhang, P., Peng, F., Xiao, Z., and Chen, Z. (2012). Periostin, a stroma-associated protein, correlates with tumor invasiveness and progression in nasopharyngeal carcinoma.Clin Exp Metastasis, 29: 865-77.

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Zhou, B.T., Zhou, Q.H., Yin, J.Y., Li, G.L., Xu, X.J., Qu, J., Liu, D., Zhou, H.H., and Liu, Z.Q. (2012). Comprehensive analysis of the association of SCN1A gene polymorphisms with the retention rate of carbamazepine following monotherapy for new-onset focal seizures in the Chinese Han population. Clin Exp Pharmacol Physiol, 39: 379-84.

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Dai, X.P., Huang, Q., Yin, J.Y., Guo, Y., Gong, Z.C., Lei, M.X., Jiang, T.J., Zhou, H.H., and Liu, Z.Q. (2012). KCNQ1 gene polymorphisms are associated with the therapeutic efficacy of repaglinide in Chinese type 2 diabetic patients. Clin Exp Pharmacol Physiol, 39: 462-8.

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Xu, X., Duan, L., Zhou, B., Ma, R., Zhou, H., and Liu, Z. (2012). Genetic polymorphism of copper transporter protein 1 is related to platinum resistance in Chinese non-small cell lung carcinoma patients. Clin Exp Pharmacol Physiol, 39: 786-92.

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Xu, X., Zhang, L., Tong, P., Xun, G., Su, W., Xiong, Z., Zhu, T., Zheng, Y., Luo, S., Pan, Y., Xia, K., and Hu, Z. (2012). Exome sequencing identifies UPF3B as the causative gene for a Chinese non-syndrome mental retardation pedigree. Clin Genet, doi:10.1111/cge.12014.

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Qiao, G., Yang, L., Li, Z., Ying, H., Hassen, Y., Yin, F., and Zhang, J. (2012). Program death-1 regulates peripheral T cell tolerance via an anergy-independent mechanism. Clin Immunol, 143: 128-33.

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Sun, Z., Yang, X., Ye, H., Zhou, G., and Jiang, H. (2012). Delayed encephalopathy with movement disorder and catatonia: A rare combination after wasp stings. Clin Neurol Neurosurg, doi:10.1016/j.clineuro.2012.11.030.

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Qu, J., Zhou, B.T., Yin, J.Y., Xu, X.J., Zhao, Y.C., Lei, G.H., Tang, Q., Zhou, H.H., and Liu, Z.Q. (2012). ABCC2 polymorphisms and haplotype are associated with drug resistance in Chinese epileptic patients. CNS Neurosci Ther, 18: 647-51.

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Zhou, B.T., Zhou, Q.H., Yin, J.Y., Li, G.L., Qu, J., Xu, X.J., Liu, D., Zhou, H.H., and Liu, Z.Q. (2012). Effects of SCN1A and GABA receptor genetic polymorphisms on carbamazepine tolerability and efficacy in Chinese patients with partial seizures: 2-year longitudinal clinical follow-up. CNS Neurosci Ther, 18: 566-72.

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 He, F., Peng, J., Deng, X.L., Yang, L.F., Camara, A.D., Omran, A., Wang, G.L., Wu, L.W., Zhang, C.L., and Yin, F. (2012). Mechanisms of tumor necrosis factor-alpha-induced leaks in intestine epithelial barrier. Cytokine, 59: 264-72.

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Omran, A., Peng, J., Zhang, C., Xiang, Q.L., Xue, J., Gan, N., Kong, H., and Yin, F. (2012). Interleukin-1beta and microRNA-146a in an immature rat model and children with mesial temporal lobe epilepsy. Epilepsia, 53: 1215-24.

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Luo, H., Xie, L., Wang, S.Z., Chen, J.L., Huang, C., Wang, J., Yang, J.F., Zhang, W.Z., Yang, Y.F., and Tan, Z.P. (2012). Duplication of 8q12 encompassing CHD7 is associated with a distinct phenotype but without duane anomaly. Eur J Med Genet, 55: 646-9.

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Ge, S., Mao, Y., Yi, Y., Xie, D., Chen, Z., and Xiao, Z. (2012). Comparative proteomic analysis of secreted proteins from nasopharyngeal carcinoma-associated stromal fibroblasts and normal fibroblasts. Exp Ther Med,3: 857-60.

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Zhang, H., Luo, H., Chen, H., Mei, L., He, C., Jiang, L., Li, J.D., and Feng, Y. (2012). Functional analysis of MITF gene mutations associated with Waardenburg syndrome type 2. FEBS Lett, 586: 4126-31.

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Peng, J., Deng, X., Wang, G., Duan, Y., and Yin, F. (2012). A retrospective analysis of pathological and clinical diagnoses: report of 240 pediatric autopsies. Fetal Pediatr Pathol, 31: 63-73.

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Deng, G., Jiang, C., and Li, Y.X. (2012). Clinical utility of the mood and anxiety symptom questionnaire in a chinese sample of patients with pancreatic cancer. Gastroenterol Nurs, 35: 193-8.

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Peng, H., Zhang, Y., Long, Z., Zhao, D., Guo, Z., Xue, J., Xie, Z., Xiong, Z., Xu, X., Su, W., Wang, B., Xia, K., and Hu, Z. (2012). A novel splicing mutation in COL1A1 gene caused type I osteogenesis imperfecta in a Chinese family. Gene, 502: 168-71.

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Huang, C., Yang, Y.F., Yin, N., Chen, J.L., Wang, J., Zhang, H., and Tan, Z.P. (2012). Congenital heart defect and mental retardation in a patient with a 13q33.1-34 deletion. Gene, 498: 308-10.

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Guo, H., Xun, G., Peng, Y., Xiang, X., Xiong, Z., Zhang, L., He, Y., Xu, X., Liu, Y., Lu, L., Long, Z., Pan, Q., Hu, Z., Zhao, J., and Xia, K. (2012). Disruption of Contactin 4 in two subjects with autism in Chinese population. Gene,505: 201-5.

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Huang, C., Yang, Y.F., Zhang, H., Xie, L., Chen, J.L., Wang, J., Tan, Z.P., and Luo, H. (2012). Microdeletion on 17p11.2 in a Smith-Magenis syndrome patient with mental retardation and congenital heart defect: first report from China. Genet Mol Res, 11: 2321-7.

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Zhong, Q., Liang, D., Liu, J., Xue, J., and Wu, L. (2012). Mutation analysis in Chinese patients with Cornelia de Lange syndrome. Genet Test Mol Biomarkers, 16: 1130-4.

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Hu, Z., Xiong, Z., Xu, X., Li, F., Lu, L., Li, W., Su, J., Liu, Y., Liu, D., Xie, Z., Peng, Y., Kuang, Y., Wu, L., Zhang, J., Pan, Q., Tang, B., Chen, X., and Xia, K. (2012). Loss-of-function mutations in filaggrin gene associate with psoriasis vulgaris in Chinese population. Hum Genet, 131: 1269-74.

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Zhang, H., Chen, H., Luo, H., An, J., Sun, L., Mei, L., He, C., Jiang, L., Jiang, W., Xia, K., Li, J.D., and Feng, Y. (2012). Functional analysis of Waardenburg syndrome-associated PAX3 and SOX10 mutations: report of a dominant-negative SOX10 mutation in Waardenburg syndrome type II. Hum Genet, 131: 491-503.

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Choo, Y.S., Vogler, G., Wang, D., Kalvakuri, S., Iliuk, A., Tao, W.A., Bodmer, R., and Zhang, Z. (2012). Regulation of parkin and PINK1 by neddylation. Hum Mol Genet, 21: 2514-23.

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Qurashi, A., Liu, H., Ray, L., Nelson, D.L., Duan, R., and Jin, P. (2012). Chemical screen reveals small molecules suppressing fragile X premutation rCGG repeat-mediated neurodegeneration in Drosophila. Hum Mol Genet, 21: 2068-75.

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Wang, T., Pan, Q., Lin, L., Szulwach, K.E., Song, C.X., He, C., Wu, H., Warren, S.T., Jin, P., Duan, R., and Li, X. (2012). Genome-wide DNA hydroxymethylation changes are associated with neurodevelopmental genes in the developing human cerebellum. Hum Mol Genet, 21: 5500-10.

48

 Zhu, L., Li, Y., and Xu, A. (2012). Influence of controlled ovarian hyperstimulation on uterine peristalsis in infertile women. Hum Reprod, 27: 2684-9.

49

Ramkalawan, H., Wang, Y.Z., Hurbungs, A., Yang, Y.F., Tian, F.F., Zhou, W.B., Li, J., Yang, H., Xiao, B., and Zhang, W. (2012). Pioglitazone, PPARgamma agonist, attenuates experimental autoimmune neuritis.Inflammation, 35: 1338-47.

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Fang, M., Chen, H., Li, L.H., Wu, R., Li, Y., Liu, L., Ye, M., Huang, J., Zhu, S., Wang, G., Zhang, Q., Zheng, H., Zhang, L., Wang, B., Zhou, J., and Zhao, J.P. (2012). Comparison of risperidone oral solution and intramuscular haloperidol with the latter shifting to oral therapy for the treatment of acute agitation in patients with schizophrenia.Int Clin Psychopharmacol, 27: 107-13.