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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 :

  • The UCL Low-Density Lipoprotein Receptor Gene Variant Database: Pathogenicity Update, Posted on November 7, 2016 by hqqu in Uncategorized
  • The cerebellum and embodied semantics: Evidence from a case of genetic ataxia due to STUB1 mutations, Posted on November 3, 2016 by hqqu in Uncategorized
  • AMMECR1: a single point mutation causes developmental delay, midface hypoplasia and elliptocytosis, Posted on November 3, 2016 by hqqu in Uncategorized
  • ACBD5 deficiency causes a defect in peroxisomal very long-chain fatty acid metabolism, Posted on October 31, 2016 by hqqu in Uncategorized
  • A de novo missense mutation of GABRB2 causes early myoclonic encephalopathy, Posted on October 28, 2016 by hqqu in Uncategorized
  • Impact of subsidies on cancer genetic testing uptake in Singapore, Posted on October 27, 2016 by hqqu in Uncategorized
  • Chitayat syndrome: hyperphalangism, characteristic facies, hallux valgus and bronchomalacia results from a recurrent c.266A>G p.(Tyr89Cys) variant in the ERF gene, Posted on October 13, 2016 by hqqu in Uncategorized
  • Genotype–phenotype correlation and functional studies in patients with cystic fibrosis bearing CFTR complex alleles, Posted on October 13, 2016 by hqqu in Uncategorized
  • A novel TRAPPC11 mutation in two Turkish families associated with cerebral atrophy, global retardation, scoliosis, achalasia, and alacrima, Posted on October 5, 2016 by hqqu in Uncategorized
  • CEP78 is mutated in a distinct type of Usher syndrome, Posted on September 21, 2016 by hqqu in Uncategorized
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