H Deng

Summary

Publications

  1. doi The molecular biology of genetic-based epilepsies
    Hao Deng
    Center for Experimental Medicine, The Third Xiangya Hospital, Central South University, Tongzipo Road 138, Changsha, Hunan, 410013, People s Republic of China
    Mol Neurobiol 49:352-67. 2014
  2. pmc Genetic analysis of the FBXO42 gene in Chinese Han patients with Parkinson's disease
    Kai Gao
    Center for Experimental Medicine, The Third Xiangya Hospital, Central South University, 138 Tongzipo Road, Changsha, Hunan 410013, China
    BMC Neurol 13:125. 2013
  3. doi The VPS35 gene and Parkinson's disease
    Hao Deng
    Center for Experimental Medicine, The Third Xiangya Hospital, Central South University, Changsha, China
    Mov Disord 28:569-75. 2013
  4. doi F-box only protein 7 gene in parkinsonian-pyramidal disease
    Hao Deng
    Center for Experimental Medicine, Third Xiangya Hospital, Central South University, Changsha, Hunan, China
    JAMA Neurol 70:20-4. 2013
  5. doi The genetics of Tourette syndrome
    Hao Deng
    Center for Experimental Medicine, The Third Xiangya Hospital, Central South University, 138 Tongzipo Road, Changsha, Hunan 410013, China
    Nat Rev Neurol 8:203-13. 2012
  6. doi LINGO1 variants in essential tremor and Parkinson's disease
    H Deng
    Center for Experimental Medicine, Department of Neurology, The Third Xiangya Hospital, Central South University, Changsha, HN, China
    Acta Neurol Scand 125:1-7. 2012
  7. ncbi Confirmation and refinement of a genetic locus for disseminated superficial actinic porokeratosis (DSAP1) at 12q23.2-24.1
    L Q Wu
    National Laboratory of Medical Genetics, Xiangya Second Hospital, Central South University, Changsha, Hunan 410078, China
    Br J Dermatol 150:999-1004. 2004
  8. doi Examination of the MSX1 gene in patients with Parkinson's disease
    H Deng
    Center for Experimental Medicine, The Third Xiangya Hospital, Central South University, China
    Acta Neurol Scand 120:442-4. 2009
  9. ncbi [Gly40Ser mutation of glucagon receptor gene and NIDDM in Han nationality]
    H Deng
    National Lab of Medical Genetics of China, Central South University, Changsha 410078, China
    Hunan Yi Ke Da Xue Xue Bao 26:291-3. 2001
  10. ncbi A novel locus (DSAP2) for disseminated superficial actinic porokeratosis maps to chromosome 15q25.1-26.1
    K Xia
    National Laboratory of Medical Genetics, Department of Dermatology, Xiangya Hospital, Changsha, Hunan 410078, China
    Br J Dermatol 147:650-4. 2002

Collaborators

  • Joseph Jankovic
  • Kai Gao
  • K Xia
  • L Q Wu
  • Y F Yang
  • Z G Long
  • Q Pan
  • J H Xia
  • D Zheng
  • H P Dai
  • Xiaofei Xiu
  • Xiong Deng
  • Zhi Song
  • Anding Zhu
  • Wen Zheng
  • B S Tang
  • Y J Yang
  • Y Feng
  • F Cai
  • T L Zhao
  • C Y Lu
  • H L Zhang
  • C Q Li

Detail Information

Publications10

  1. doi The molecular biology of genetic-based epilepsies
    Hao Deng
    Center for Experimental Medicine, The Third Xiangya Hospital, Central South University, Tongzipo Road 138, Changsha, Hunan, 410013, People s Republic of China
    Mol Neurobiol 49:352-67. 2014
    ..These progresses have improved our understanding of the complex neurological disorder. ..
  2. pmc Genetic analysis of the FBXO42 gene in Chinese Han patients with Parkinson's disease
    Kai Gao
    Center for Experimental Medicine, The Third Xiangya Hospital, Central South University, 138 Tongzipo Road, Changsha, Hunan 410013, China
    BMC Neurol 13:125. 2013
    ..The F-box protein 42 gene (FBXO42), a paralog of the FBXO7 gene, is involved in the ubiquitin-proteasome system that may play a role in the pathogenesis of PD...
  3. doi The VPS35 gene and Parkinson's disease
    Hao Deng
    Center for Experimental Medicine, The Third Xiangya Hospital, Central South University, Changsha, China
    Mov Disord 28:569-75. 2013
    ..Further understanding of these mechanisms will undoubtedly provide new insights into the pathogenic mechanisms of PD and may lead to prevention and better treatment of the disorder...
  4. doi F-box only protein 7 gene in parkinsonian-pyramidal disease
    Hao Deng
    Center for Experimental Medicine, Third Xiangya Hospital, Central South University, Changsha, Hunan, China
    JAMA Neurol 70:20-4. 2013
    ....
  5. doi The genetics of Tourette syndrome
    Hao Deng
    Center for Experimental Medicine, The Third Xiangya Hospital, Central South University, 138 Tongzipo Road, Changsha, Hunan 410013, China
    Nat Rev Neurol 8:203-13. 2012
    ..In this Review, we provide an overview of the genetics of Tourette syndrome and highlight how this knowledge has improved our understanding of the possible pathogenic mechanisms of this neurological disorder...
  6. doi LINGO1 variants in essential tremor and Parkinson's disease
    H Deng
    Center for Experimental Medicine, Department of Neurology, The Third Xiangya Hospital, Central South University, Changsha, HN, China
    Acta Neurol Scand 125:1-7. 2012
    ..Here, we review published reports of the LINGO1 variants in ET and PD in an attempt to better understand the molecular and pathogenic relationship of LINGO1 to the two disorders...
  7. ncbi Confirmation and refinement of a genetic locus for disseminated superficial actinic porokeratosis (DSAP1) at 12q23.2-24.1
    L Q Wu
    National Laboratory of Medical Genetics, Xiangya Second Hospital, Central South University, Changsha, Hunan 410078, China
    Br J Dermatol 150:999-1004. 2004
    ..Our previous study has identified two loci for disseminated superficial actinic porokeratosis (DSAP), but the genes responsible are still unknown...
  8. doi Examination of the MSX1 gene in patients with Parkinson's disease
    H Deng
    Center for Experimental Medicine, The Third Xiangya Hospital, Central South University, China
    Acta Neurol Scand 120:442-4. 2009
    ..The muscle segment homeobox drosophila homolog of 1 gene (MSX1) is a major upstream regulator of the dopaminergic neuronal subtype specification...
  9. ncbi [Gly40Ser mutation of glucagon receptor gene and NIDDM in Han nationality]
    H Deng
    National Lab of Medical Genetics of China, Central South University, Changsha 410078, China
    Hunan Yi Ke Da Xue Xue Bao 26:291-3. 2001
    ..To ascertain whether Gly40Ser mutation in exon 2 of glucagon receptor (GCG-R) gene is associated with late-onset non-insulin-dependent diabetes millitus (NIDDM) in Chinese...
  10. ncbi A novel locus (DSAP2) for disseminated superficial actinic porokeratosis maps to chromosome 15q25.1-26.1
    K Xia
    National Laboratory of Medical Genetics, Department of Dermatology, Xiangya Hospital, Changsha, Hunan 410078, China
    Br J Dermatol 147:650-4. 2002
    ..The first locus for DSAP was localized to chromosome 12q23.2-24.1, but no gene responsible for porokeratosis has been identified to date...