Skip to content
JMG Blog logo
  • Home
  • Journal

About:hqqu

Profile
Huiqi Qu has a background as a physician trained in internal medicine and a PhD in Experimental Medicine (Endocrinology). His research applies human genetics and multi-omics to complex and pediatric diseases, including GWAS, polygenic risk scores (PRS), single-cell transcriptomics, and integrative genomics to support precision medicine and clinical translation.

Posts by hqqu :

  • Germline PALB2 mutation analysis in breast–pancreas cancer families (Contributed by Zsofia K. Stadler, MD), 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 (Contributed by Dr Robert Pitceathly), Posted on March 5, 2011 by hqqu in Uncategorized
  • C14ORF179 encoding IFT43 is mutated in Sensenbrenner syndrome (Contributed by Heleen Arts, PhD), Posted on March 5, 2011 by hqqu in Uncategorized
  • CHD7 mutations and CHARGE syndrome: the clinical implications of an expanding phenotype (Contributed by Jorieke EH Bergman, MD), 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 (Contributed by Professor Yiming Wang), Posted on February 26, 2011 by hqqu in Uncategorized
  • Sweating ability and genotype in individuals with X-linked hypohidrotic ectodermal dysplasia (Contributed by Dr. Holm Schneider), 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 (Contributed by Dr. Anne E Cust), 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 (Contributed by Dr. Jose J. G. Marin), 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 (Contributed by Dr. Saba Sharif), Posted on January 30, 2011 by hqqu in Uncategorized
  • «Previous page
  • 97
  • 98
  • 99
  • 100
  • 101
  • »Next page
  • 102

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 2026. All rights reserved.