Feng G - Search Results

1

Polymorphisms in microRNA target sites influence susceptibility to schizophrenia by altering the binding of miRNAs to their targets.

Gong Y, Wu CN, Xu J, Feng G, Xing QH, Fu W, Li C, He L, Zhao XZ. Gong Y, et al. Among authors: feng g. Eur Neuropsychopharmacol. 2013 Oct;23(10):1182-9. doi: 10.1016/j.euroneuro.2012.12.002. Epub 2013 Jan 16. Eur Neuropsychopharmacol. 2013. PMID: 23332465

2

Polymorphisms of chromogranin B gene associated with schizophrenia in Chinese Han population.

Zhang B, Tan Z, Zhang C, Shi Y, Lin Z, Gu N, Feng G, He L. Zhang B, et al. Among authors: feng g. Neurosci Lett. 2002 May 3;323(3):229-33. doi: 10.1016/s0304-3940(02)00145-3. Neurosci Lett. 2002. PMID: 11959426

3

A locus for congenital preauricular fistula maps to chromosome 8q11.1-q13.3.

Zou F, Peng Y, Wang X, Sun A, Liu W, Bai S, Zhu H, Gao B, Feng G, He L. Zou F, et al. Among authors: feng g. J Hum Genet. 2003;48(3):155-8. doi: 10.1007/s100380300024. J Hum Genet. 2003. PMID: 12624728

4

A novel insertion mutation in spastin gene is the cause of spastic paraplegia in a Chinese family.

Qin W, Zhang T, Han J, Tang L, Li X, Feng G, Liu W, He L. Qin W, et al. Among authors: feng g. J Neurol Sci. 2003 Jun 15;210(1-2):35-9. doi: 10.1016/s0022-510x(03)00011-x. J Neurol Sci. 2003. PMID: 12736085

5

A gene locus responsible for dyschromatosis symmetrica hereditaria (DSH) maps to chromosome 6q24.2-q25.2.

Xing QH, Wang MT, Chen XD, Feng GY, Ji HY, Yang JD, Gao JJ, Qin W, Qian XQ, Wu SN, He L. Xing QH, et al. Am J Hum Genet. 2003 Aug;73(2):377-82. doi: 10.1086/377007. Epub 2003 Jun 12. Am J Hum Genet. 2003. PMID: 12815562 Free PMC article.

6

Association of APOE gene with schizophrenia in Chinese: a possible risk factor in times of malnutrition.

Liu W, Breen G, Zhang J, Li S, Gu N, Feng G, Bai S, Shen T, Yu A, Xue H, St Clair D, He L. Liu W, et al. Among authors: feng g. Schizophr Res. 2003 Aug 1;62(3):225-30. doi: 10.1016/s0920-9964(02)00384-5. Schizophr Res. 2003. PMID: 12837518

7

Evidence for a major susceptibility locus at 11q22.1-23.3 has been detected in a large Chinese family with pure grand mal epilepsy.

Yang MS, Wang XF, Qin W, Feng GY, He L. Yang MS, et al. Neurosci Lett. 2003 Aug 7;346(3):133-6. doi: 10.1016/s0304-3940(03)00500-7. Neurosci Lett. 2003. PMID: 12853102

8

[Transmission disequilibrium test of polymorphisms of serotonin transporter gene and schizophrenia based on family trios].

Sun WW, Fan JB, Qian XQ, Tang JX, Xing YL, Shi JG, Zhu SM, Liu HJ, Gu NF, Feng GY, He L. Sun WW, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Aug;20(4):342-4. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003. PMID: 12903048 Chinese.

9

Association analysis of polymorphisms in the upstream region of the human dopamine D4 receptor gene in schizophrenia.

Xing QH, Wu SN, Lin ZG, Li HF, Yang JD, Feng GY, Wang MT, Yang WW, He L. Xing QH, et al. Schizophr Res. 2003 Dec 1;65(1):9-14. doi: 10.1016/s0920-9964(03)00064-1. Schizophr Res. 2003. PMID: 14623368

10

[Genetic analysis of a Chinese pedigree with congenital synpolydactyly].

Qin W, Shu AL, Xing QH, Yang MS, Feng GY, He L. Qin W, et al. Yi Chuan Xue Bao. 2003 Oct;30(10):973-7. Yi Chuan Xue Bao. 2003. PMID: 14669516 Chinese.

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