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Public Health Genomics Knowledge Base (v1.0)

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Last Updated: Dec 14, 2015

• USAT: A Unified Score-Based Association Test for Multiple Phenotype-Genotype Analysis.
  Ray Debashree, et al. Genetic epidemiology 2015 12
[Entered on Dec 13, 2015 in HuGE Database]
• Mutation analysis of CHCHD2 in Canadian patients with familial Parkinson's disease.
  Zhang Ming, et al. Neurobiology of aging 2015 11
[Entered on Dec 13, 2015 in HuGE Database]
• Somatic mtDNA variation is an important component of Parkinson's disease.
  Coxhead Jonathan, et al. Neurobiology of aging 2015 11
[Entered on Dec 13, 2015 in HuGE Database]
• Two distinct clinical features and cognitive impairment in amyotrophic lateral sclerosis patients with TARDBP gene mutations in the Chinese population.
  Ju XiaoDong, et al. Neurobiology of aging 2015 11
[Entered on Dec 13, 2015 in HuGE Database]
• Prognostic significance of the Musashi-2 (MSI2) gene in childhood acute lymphoblastic leukemia.
  Zhao H Z, et al. Neoplasma 2015 12
[Entered on Dec 13, 2015 in HuGE Database]
• CYP2C19 drug-drug and drug-gene interactions in ED patients.
  Flaten Hanna K, et al. The American journal of emergency medicine 2015 11
[Entered on Dec 13, 2015 in HuGE Database]
• ABCB1 polymorphism and acenocoumarol safety in patients with valvular atrial fibrillation.
  Rozhkov A, et al. The International journal of risk & safety in medicine 2015 11 S15-6
[Entered on Dec 13, 2015 in HuGE Database]
• VKORC1 polymorphisms and warfarin maintenance dose in population of Sakha (Yakuts).
  Chertovskikh Y V, et al. The International journal of risk & safety in medicine 2015 11 S17-8
[Entered on Dec 13, 2015 in HuGE Database]
• Pharmacogenetic testing in population of South Ural.
  Barysheva V O, et al. The International journal of risk & safety in medicine 2015 11 S25-6
[Entered on Dec 13, 2015 in HuGE Database]
• HTR1B gene variants associate with the susceptibility of Raynauds' phenomenon in workers exposed hand-arm vibration.
  Chen Qingsong, et al. Clinical hemorheology and microcirculation 2015 11
[Entered on Dec 13, 2015 in HuGE Database]
• Subjective Memory Complaints in APOE?4 Carriers are Associated with High Amyloid-? Burden.
  Zwan Marissa D, et al. Journal of Alzheimer's disease : JAD 2015 11
[Entered on Dec 13, 2015 in HuGE Database]
• Vascular Health Indices and Cognitive Domain Function: Singapore Longitudinal Ageing Studies.
  Lim Shir Lynn, et al. Journal of Alzheimer's disease : JAD 2015 11
[Entered on Dec 13, 2015 in HuGE Database]
• Shared Genetic Etiology between Type 2 Diabetes and Alzheimer's Disease Identified by Bioinformatics Analysis.
  Gao Lei, et al. Journal of Alzheimer's disease : JAD 2015 11
[Entered on Dec 13, 2015 in HuGE Database]
• Heterozygous PALB2 c.1592delT mutation channels DNA double-strand break repair into error-prone pathways in breast cancer patients.
  Obermeier K, et al. Oncogene 2015 12
[Entered on Dec 13, 2015 in HuGE Database]
• Association study of polymorphisms in miRNAs with T2DM in Chinese population.
  Li Yiping, et al. International journal of medical sciences 2015 0 (11) 875-80
[Entered on Dec 13, 2015 in HuGE Database]
• Effects of mitochondrial haplogroup N9a on type 2 diabetes mellitus and its associated complications.
  Niu Qing, et al. Experimental and therapeutic medicine 2015 11 (5) 1918-1924
[Entered on Dec 13, 2015 in HuGE Database]
• Association between PTPN22 C1858T polymorphism and alopecia areata risk.
  Salinas-Santander Mauricio, et al. Experimental and therapeutic medicine 2015 11 (5) 1953-1958
[Entered on Dec 13, 2015 in HuGE Database]
• Association between polymorphisms of estrogen receptor 2 and benign prostatic hyperplasia.
  Kim Su Kang, et al. Experimental and therapeutic medicine 2015 11 (5) 1990-1994
[Entered on Dec 13, 2015 in HuGE Database]
• Very Long Term Stability of Mixed Chimerism after Allogeneic Hematopoietic Stem Cell Transplantation in Patients with Hematologic Malignancies.
  Levrat Emmanuel, et al. Bone marrow research 0 0 176526
[Entered on Dec 13, 2015 in HuGE Database]
• Analysis of a Functional IL-6 Gene Polymorphism in HLAB27 Associated and Intermediate Uveitis Gives New Insight in Disease Pathogenesis and Commonality with Other Autoimmune Diseases.
  Ewald Lindner, et al. Journal of immunology research 2015 0 174062
[Entered on Dec 13, 2015 in HuGE Database]