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About:hqqu

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Huiqi Qu’s research interest is the genetics and functional genomics of human complex diseases (e.g. tuberculosis, obesity, and diabetes). He is working on the genetics and functional genomics of tuberculosis and diabetes. By integrating proteomics, genomics, and GWAS study, they are trying to clarify the molecular mechanisms of tuberculosis susceptibility, and develop genetic markers for diabetes risk prediction.

Posts by hqqu :

  • Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresia, Posted on February 19, 2013 by hqqu in Uncategorized
  • TBC1D24 Truncating Mutation Resulting in Severe Neurodegeneration, Posted on February 13, 2013 by hqqu in Uncategorized
  • Melanoma-prone families with CDK4 germline mutation: Phenotypic profile and associations with MC1R variants, Posted on February 5, 2013 by hqqu in Uncategorized
  • Mutations in POLR3A and POLR3B are a major cause of hypomyelinating leukodystrophies with or without dental abnormalities and/or hypogonadotropic hypogonadism, Posted on January 25, 2013 by hqqu in Uncategorized
  • Whole Exome Sequencing Identifies a Mutation for a Novel Form of Corneal Intraepithelial Dyskeratosis, Posted on January 24, 2013 by hqqu in Uncategorized
  • Mutations in TMEM231 cause Meckel–Gruber syndrome, Posted on January 24, 2013 by hqqu in Uncategorized
  • Role of PRRT2 in common paroxysmal neurological disorders: a gene with remarkable pleiotropy, Posted on January 23, 2013 by hqqu in Uncategorized
  • Deletions in 16q24.2 are associated with autism spectrum disorder, intellectual disability and congenital renal malformation, Posted on January 18, 2013 by hqqu in Uncategorized
  • High cumulative risks of cancer in patients with PTEN hamartoma tumour syndrome, Posted on January 18, 2013 by hqqu in Uncategorized
  • Heterogeneity of mutational mechanisms and modes of inheritance in auriculocondylar syndrome, Posted on January 13, 2013 by hqqu in Uncategorized
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