He L - Search Results

1

Promoter hypomethylation of COMT in human placenta is not associated with the development of pre-eclampsia.

Zhao A, Cheng Y, Li X, Li Q, Wang L, Xu J, Xiang Y, Xing Q, He L, Zhao X. Zhao A, et al. Among authors: he l. Mol Hum Reprod. 2011 Mar;17(3):199-206. doi: 10.1093/molehr/gaq092. Epub 2010 Nov 3. Mol Hum Reprod. 2011. PMID: 21047975

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

5

An association between polymorphisms of the interleukin-10 gene promoter and schizophrenia in the Chinese population.

Yu L, Yang MS, Zhao J, Shi YY, Zhao XZ, Yang JD, Liu ZJ, Gu NF, Feng GY, He L. Yu L, et al. Among authors: he l. Schizophr Res. 2004 Nov 1;71(1):179-83. doi: 10.1016/j.schres.2004.01.001. Schizophr Res. 2004. PMID: 15374585

6

Family-based association study of synapsin II and schizophrenia.

Chen Q, He G, Qin W, Chen QY, Zhao XZ, Duan SW, Liu XM, Feng GY, Xu YF, St Clair D, Li M, Wang JH, Xing YL, Shi JG, He L. Chen Q, et al. Among authors: he g, he l. Am J Hum Genet. 2004 Nov;75(5):873-7. doi: 10.1086/425588. Epub 2004 Sep 24. Am J Hum Genet. 2004. PMID: 15449241 Free PMC article.

7

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. Among authors: he l. Mutat Res. 2004 Oct 4;554(1-2):19-22. doi: 10.1016/j.mrfmmm.2004.02.014. Mutat Res. 2004. PMID: 15450400

8

No genetic association between polymorphisms in the AMPA receptor subunit GluR4 gene (GRIA4) and schizophrenia in the Chinese population.

Guo S, Shi Y, Zhao X, Duan S, Zhou J, Meng J, Yang Y, Gu N, Feng G, Liu H, Zhu S, He L. Guo S, et al. Among authors: he l. Neurosci Lett. 2004 Oct 14;369(2):168-72. doi: 10.1016/j.neulet.2004.07.079. Neurosci Lett. 2004. PMID: 15450689

9

Case-control study and transmission disequilibrium test provide consistent evidence for association between schizophrenia and genetic variation in the 22q11 gene ZDHHC8.

Chen WY, Shi YY, Zheng YL, Zhao XZ, Zhang GJ, Chen SQ, Yang PD, He L. Chen WY, et al. Among authors: he l. Hum Mol Genet. 2004 Dec 1;13(23):2991-5. doi: 10.1093/hmg/ddh322. Epub 2004 Oct 15. Hum Mol Genet. 2004. PMID: 15489219

10

SNPs and haplotypes in the S100B gene reveal association with schizophrenia.

Liu J, Shi Y, Tang J, Guo T, Li X, Yang Y, Chen Q, Zhao X, He G, Feng G, Gu N, Zhu S, Liu H, He L. Liu J, et al. Among authors: he g, he l. Biochem Biophys Res Commun. 2005 Mar 4;328(1):335-41. doi: 10.1016/j.bbrc.2004.12.175. Biochem Biophys Res Commun. 2005. PMID: 15670788 Clinical Trial.

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