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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 57 kb deletion in cystinosis patients extends into TRPV1 causing dysregulation of transcription in peripheral blood mononuclear cells, Posted on May 6, 2011 by hqqu in Uncategorized
  • FOXN1 mutation abrogates prenatal T-cell development in humans, Posted on April 23, 2011 by hqqu in Uncategorized
  • Hearing function and thresholds: a genome-wide association study in European isolated populations identifies new loci and pathways, Posted on April 15, 2011 by hqqu in Uncategorized
  • Unexpected findings in cancer predisposition genes detected by array comparative genomic hybridisation: what are the issues?, Posted on March 23, 2011 by hqqu in Uncategorized
  • Germline PALB2 mutation analysis in breast–pancreas cancer families, Posted on March 18, 2011 by hqqu in Uncategorized
  • Call for Abstracts/Papers, Fourth Summit on Systems Biology, June 15-17, Richmond, Virginia, USA, Posted on March 11, 2011 by hqqu in Uncategorized
  • Kearns-Sayre syndrome caused by defective R1/p53R2 assembly, Posted on March 5, 2011 by hqqu in Uncategorized
  • C14ORF179 encoding IFT43 is mutated in Sensenbrenner syndrome, Posted on March 5, 2011 by hqqu in Uncategorized
  • CHD7 mutations and CHARGE syndrome: the clinical implications of an expanding phenotype, Posted on March 5, 2011 by hqqu in Uncategorized
  • A 4.6kb genomic duplication on 20p12.2-12.3 is associated with brachydactyly type A2 in a Chinese family, Posted on February 26, 2011 by hqqu in Uncategorized
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