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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 :

  • Large-scale genotyping identifies a new locus at 22q13.2 associated with female breast size, Posted on July 3, 2013 by hqqu in Uncategorized
  • Comparison of the clinical scoring systems in Silver–Russell syndrome and development of modified diagnostic criteria to guide molecular genetic testing, Posted on June 29, 2013 by hqqu in Uncategorized
  • Can the diagnosis of NF1 be excluded clinically? A lack of pigmentary findings in families with spinal neurofibromatosis demonstrates a limitation of clinical diagnosis, Posted on June 29, 2013 by hqqu in Uncategorized
  • West syndrome, microcephaly, grey matter heterotopia and hypoplasia of corpus callosum due to a novel ARFGEF2 mutation, Posted on June 29, 2013 by hqqu in Uncategorized
  • Associations of common variants in HFE and TMPRSS6 with iron parameters are independent of serum hepcidin in a general population: a replication study, Posted on June 22, 2013 by hqqu in Uncategorized
  • Digenic inheritance in medical genetics, Posted on June 19, 2013 by hqqu in Uncategorized
  • Genome-wide association study identifies ephrin type A receptors implicated in paclitaxel induced peripheral sensory neuropathy, Posted on June 17, 2013 by hqqu in Uncategorized
  • Meta-Analysis of Genome-Wide Studies Identifies MEF2C SNPs Associated with Bone Mineral Density at Forearm, Posted on June 11, 2013 by hqqu in Uncategorized
  • Recessive truncating NALCN mutation in infantile neuroaxonal dystrophy with facial dysmorphism, Posted on June 7, 2013 by hqqu in Uncategorized
  • A de novo X;8 translocation creates a PTK2-THOC2 gene fusion with THOC2 expression knockdown in a patient with psychomotor retardation and congenital cerebellar hypoplasia, Posted on June 7, 2013 by hqqu in Uncategorized
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