Deng H - Search Results

1

Identification of a novel collagen type IV alpha-4 (COL4A4) mutation in a Chinese family with autosomal dominant Alport syndrome using exome sequencing.

Deng S, Xu H, Yuan J, Xiao J, Yuan L, Deng X, Guan L, Zhu A, Rong P, Zhang J, Deng H. Deng S, et al. Among authors: deng x, deng h. Indian J Med Res. 2016 Aug;144(2):200-205. doi: 10.4103/0971-5916.195026. Indian J Med Res. 2016. PMID: 27934798 Free PMC article.

2

A novel PRPF31 splice-site mutation in a Chinese family with autosomal dominant retinitis pigmentosa.

Xia K, Zheng D, Pan Q, Liu Z, Xi X, Hu Z, Deng H, Liu X, Jiang D, Deng H, Xia J. Xia K, et al. Among authors: deng h. Mol Vis. 2004 May 20;10:361-5. Mol Vis. 2004. PMID: 15162096 Free article.

3

Genetic analysis of the NEUROG2 gene in patients with Parkinson's disease.

Deng S, Deng H, Le W, Xu H, Yang H, Deng X, Lv H, Xie W, Zhu S, Jankovic J. Deng S, et al. Among authors: deng h, deng x. Neurosci Lett. 2010 Jan 14;468(3):195-7. doi: 10.1016/j.neulet.2009.10.078. Epub 2009 Oct 29. Neurosci Lett. 2010. PMID: 19879328

4

Examination of the MASH1 gene in patients with Parkinson's disease.

Deng H, Yang H, Le W, Deng X, Xu H, Xiong W, Zhu S, Xie W, Song Z, Jankovic J. Deng H, et al. Among authors: deng x. Biochem Biophys Res Commun. 2010 Feb 19;392(4):548-50. doi: 10.1016/j.bbrc.2010.01.061. Epub 2010 Jan 25. Biochem Biophys Res Commun. 2010. PMID: 20097173

5

LINGO1 rs9652490 variant in Parkinson disease patients.

Guo Y, Jankovic J, Song Z, Yang H, Zheng W, Le W, Tang X, Deng X, Yang Y, Deng S, Luo Z, Deng H. Guo Y, et al. Among authors: deng x, deng h, deng s. Neurosci Lett. 2011 Jan 7;487(2):174-6. doi: 10.1016/j.neulet.2010.10.016. Epub 2010 Oct 15. Neurosci Lett. 2011. PMID: 20951767

6

Systematic genetic analysis of the PITX3 gene in patients with Parkinson disease.

Guo Y, Le WD, Jankovic J, Yang HR, Xu HB, Xie WJ, Song Z, Deng H. Guo Y, et al. Among authors: deng h. Mov Disord. 2011 Aug 1;26(9):1729-32. doi: 10.1002/mds.23693. Epub 2011 Apr 5. Mov Disord. 2011. PMID: 21469209

7

HLA rs3129882 variant in Chinese Han patients with late-onset sporadic Parkinson disease.

Guo Y, Deng X, Zheng W, Xu H, Song Z, Liang H, Lei J, Jiang X, Luo Z, Deng H. Guo Y, et al. Among authors: deng x, deng h. Neurosci Lett. 2011 Sep 1;501(3):185-7. doi: 10.1016/j.neulet.2011.05.245. Epub 2011 Jul 20. Neurosci Lett. 2011. PMID: 21791235

8

Genetic analysis of IREB2, FAM13A and XRCC5 variants in Chinese Han patients with chronic obstructive pulmonary disease.

Guo Y, Lin H, Gao K, Xu H, Deng X, Zhang Q, Luo Z, Sun S, Deng H. Guo Y, et al. Among authors: deng x, deng h. Biochem Biophys Res Commun. 2011 Nov 18;415(2):284-7. doi: 10.1016/j.bbrc.2011.10.042. Epub 2011 Oct 18. Biochem Biophys Res Commun. 2011. PMID: 22027142

9

Mutation screening of the HDC gene in Chinese Han patients with Tourette syndrome.

Lei J, Deng X, Zhang J, Su L, Xu H, Liang H, Huang X, Song Z, Deng H. Lei J, et al. Among authors: deng x, deng h. Am J Med Genet B Neuropsychiatr Genet. 2012 Jan;159B(1):72-6. doi: 10.1002/ajmg.b.32003. Epub 2011 Nov 16. Am J Med Genet B Neuropsychiatr Genet. 2012. PMID: 22095709

10

No evidence of association between the LINGO4 gene and essential tremor in Chinese Han patients.

Liang H, Zheng W, Xu H, Lei J, Song Z, Jiang X, Zeng Z, Deng H. Liang H, et al. Among authors: deng h. Parkinsonism Relat Disord. 2012 Mar;18(3):303-5. doi: 10.1016/j.parkreldis.2011.10.017. Epub 2011 Nov 21. Parkinsonism Relat Disord. 2012. PMID: 22104011

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