Xing QH - Search Results

1

Association of DRD2 polymorphisms and chlorpromazine-induced extrapyramidal syndrome in Chinese schizophrenic patients.

Wu SN, Gao R, Xing QH, Li HF, Shen YF, Gu NF, Feng GY, He L. Wu SN, et al. Among authors: xing qh. Acta Pharmacol Sin. 2006 Aug;27(8):966-70. doi: 10.1111/j.1745-7254.2006.00355.x. Acta Pharmacol Sin. 2006. PMID: 16867246

2

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.

3

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

4

[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. Among authors: xing qh. Yi Chuan Xue Bao. 2003 Oct;30(10):973-7. Yi Chuan Xue Bao. 2003. PMID: 14669516 Chinese.

5

A novel insertion mutation in the FOXL2 gene is detected in a big Chinese family with blepharophimosis-ptosis-epicanthus inversus.

Qian X, Shu A, Qin W, Xing Q, Gao J, Yang J, Feng G, He L. Qian X, et al. Mutat Res. 2004 Oct 4;554(1-2):19-22. doi: 10.1016/j.mrfmmm.2004.02.014. Mutat Res. 2004. PMID: 15450400

6

A family-based association study of PLP1 and schizophrenia.

Qin W, Gao J, Xing Q, Yang J, Qian X, Li X, Guo Z, Chen H, Wang L, Huang X, Gu N, Feng G, He L. Qin W, et al. Neurosci Lett. 2005 Mar 3;375(3):207-10. doi: 10.1016/j.neulet.2004.11.013. Epub 2004 Dec 2. Neurosci Lett. 2005. PMID: 15694262

7

Response to chlorpromazine treatment may be associated with polymorphisms of the DRD2 gene in Chinese schizophrenic patients.

Wu S, Xing Q, Gao R, Li X, Gu N, Feng G, He L. Wu S, et al. Neurosci Lett. 2005 Mar 7;376(1):1-4. doi: 10.1016/j.neulet.2004.11.014. Epub 2004 Dec 2. Neurosci Lett. 2005. PMID: 15694263

8

A family-based association study of schizophrenia with polymorphisms at three candidate genes.

Duan S, Gao R, Xing Q, Du J, Liu Z, Chen Q, Wang H, Feng G, He L. Duan S, et al. Neurosci Lett. 2005 Apr 29;379(1):32-6. doi: 10.1016/j.neulet.2004.12.040. Epub 2005 Jan 12. Neurosci Lett. 2005. PMID: 15814194

9

A locus for familial generalized lentiginosis without systemic involvement maps to chromosome 4q21.1-q22.3.

Xing Q, Chen X, Wang M, Bai W, Peng X, Gao R, Wu S, Qian X, Qin W, Gao J, Feng G, He L. Xing Q, et al. Hum Genet. 2005 Jul;117(2-3):154-9. doi: 10.1007/s00439-005-1284-1. Epub 2005 Apr 20. Hum Genet. 2005. PMID: 15841387

10

[Mutation detection of COL1A1 gene in a pedigree with osteogenesis imperfecta].

Qin W, He JX, Shi J, Xing QH, Gao JJ, He L, Qian XQ, Liu ZJ, Shu AL, He L. Qin W, et al. Among authors: xing qh. Yi Chuan Xue Bao. 2005 Mar;32(3):248-52. Yi Chuan Xue Bao. 2005. PMID: 15931785 Chinese.

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