Skip to content
JMG Blog logo
  • Home
  • Journal

About:hqqu

Profile
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 :

  • 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
  • Sweating ability and genotype in individuals with X-linked hypohidrotic ectodermal dysplasia, Posted on February 26, 2011 by hqqu in Uncategorized
  • Melanoma risk for CDKN2A mutation carriers who are relatives of population-based case carriers in Australia and the UK, Posted on February 15, 2011 by hqqu in Uncategorized
  • A homozygous nonsense mutation (c.214C>A) in biliverdin reductase alpha gene (BLVRA) results in accumulation of biliverdin during episodes of cholestasis, Posted on January 30, 2011 by hqqu in Uncategorized
  • A molecular analysis of individuals with neurofibromatosis type 1 (NF1) and optic pathway gliomas (OPGs), and an assessment of genotype–phenotype correlations, Posted on January 30, 2011 by hqqu in Uncategorized
  • Cranial meningiomas in 411 neurofibromatosis type 2 (NF2) patients with proven gene mutations: clear positional effect of mutations, but absence of female severity effect on age at onset, Posted on January 30, 2011 by hqqu in Uncategorized
  • DICER1 syndrome – clarifying the diagnosis, clinical features and management implications of a pleiotropic tumor predisposition syndrome, Posted on January 25, 2011 by hqqu in Uncategorized
  • «Previous page
  • 95
  • 96
  • 97
  • 98
  • 99
  • »Next page

BMJ Careers

BMJ Blogs

Comment and Opinion | Open Debate

The views and opinions expressed on this site are solely those of the original authors. They do not necessarily represent the views of BMJ and should not be used to replace medical advice. Please see our full website terms and conditions.

All BMJ blog posts are posted under a CC-BY-NC licence

BMJ Journals

© BMJ Publishing Group Limited 2025. All rights reserved.