Parkinson's Disease || Public Health Genomics Knowledge Base (v1.0)

Public Health Genomics Knowledge Base (v1.0)





Parkinson's Disease

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Last Updated: Feb 12, 2016

• Parkinsonism in a pair of monozygotic CADASIL twins sharing the R1006C mutation: a transcranial sonography study.
  Ragno Michele, et al. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2016 2 (From HuGE Literature Finder)
• Lack of association between IL-10 and IL-18 gene promoter polymorphisms and Parkinson's disease with cognitive impairment in a Chinese population.
  Liu Zhenhua, et al. Scientific reports 2016 0 19021 (From HuGE Literature Finder)
• Functional Genomics of Candidate Genes Derived from Genome-Wide Association Studies for Five Common Neurological Diseases.
  Guio-Vega Gina P, et al. The International journal of neuroscience 2016 2 1-25 (From HuGE Literature Finder)
• An Alzheimer's Disease-Derived Biomarker Signature Identifies Parkinson's Disease Patients with Dementia.
  Berlyand Yosef, et al. PloS one 2016 0 (1) e0147319 (From HuGE Literature Finder)
• Serum Levels of Coenzyme Q10 in Patients with Multiple System Atrophy.
  Kasai Takashi, et al. PloS one 2016 0 (1) e0147574 (From HuGE Literature Finder)
• Supine hypertension in Parkinson's disease and multiple system atrophy.
  Fanciulli Alessandra, et al. Clinical autonomic research : official journal of the Clinical Autonomic Research Society 2016 1 (From HuGE Literature Finder)
• Association of a BACE1 Gene Polymorphism with Parkinson's Disease in a Norwegian Population.
  Lange Johannes, et al. Parkinson's disease 2015 0 973298 (From HuGE Literature Finder)
• Variants in the SNCA gene associate with motor progression while variants in the MAPT gene associate with the severity of Parkinson's disease.
  Wang Gang, et al. Parkinsonism & related disorders 2015 12 (From HuGE Literature Finder)
• Mutation analyses and association studies to assess the role of the presenilin-associated rhomboid-like gene in Parkinson's disease.
  Wüst Richard, et al. Neurobiology of aging 2015 12 (From HuGE Literature Finder)
• Association study of TREM2 polymorphism rs75932628 with leucoaraiosis or Parkinson's disease in the Han Chinese population.
  Li Zhiming, et al. BMJ open 2016 0 (1) e009499 (From HuGE Literature Finder)
• Systematic Review of the Relationship between Vitamin D and Parkinson's Disease.
  Rimmelzwaan Lisanne M, et al. Journal of Parkinson's disease 2016 1 (From HuGE Literature Finder)
• Associations between TOMM40 Poly-T Repeat Variants and Dementia in Cases with Parkinsonism.
  Lindqvist Daniel, et al. Journal of Parkinson's disease 2016 1 (From HuGE Literature Finder)
• The analysis of association between SNCA, HUSEYO and CSMD1 gene variants and Parkinson's disease in Iranian population.
  Shahmohammadibeni Neda, et al. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2016 1 (From HuGE Literature Finder)
• Relationship between Alzheimer's disease GWAS-linked top hits and risk of Parkinson's disease with or without cognitive decline: a Chinese population-based study.
  Wang Ya-Qin, et al. Neurobiology of aging 2015 12 (From HuGE Literature Finder)
• Lack of CHCHD2 mutations in Parkinson's disease in a Taiwanese population.
  Fan Tian-Sin, et al. Neurobiology of aging 2015 12 (From HuGE Literature Finder)
• Genetic association of cyclooxygenase-2 gene polymorphisms with Parkinson's disease susceptibility in Chinese Han population.
  Dai Yi, et al. International journal of clinical and experimental pathology 2015 0 (10) 13495-9 (From HuGE Literature Finder)
• Genetic analysis of TREM2 variants in Chinese Han patients with sporadic Parkinson's disease.
  Tan Ting, et al. Neuroscience letters 2015 12 189-192 (From HuGE Literature Finder)
• CHCHD2 gene mutations in familial and sporadic Parkinson's disease.
  Shi Chang-He, et al. Neurobiology of aging 2015 11 (From HuGE Literature Finder)
• DAT imaging and clinical biomarkers in relatives at genetic risk for LRRK2?R1441G Parkinson's disease.
  Bergareche Alberto, et al. Movement disorders : official journal of the Movement Disorder Society 2015 12 (From HuGE Literature Finder)
• Linking a genome-wide association study signal to a LRRK2 coding variant in Parkinson's disease.
  Foo Jia Nee, et al. Movement disorders : official journal of the Movement Disorder Society 2015 12 (From HuGE Literature Finder)