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 :

  • Identification of a novel DLX5 mutation in a family with autosomal recessive split hand and foot malformation (Contributed by Dr. Fowzan S Alkuraya), Posted on November 27, 2011 by hqqu in Uncategorized
  • Defective NDUFA9 as a novel cause of neonatally fatal complex I disease (Contributed by Bianca J.C. van den Bosch, PhD), Posted on November 23, 2011 by hqqu in Uncategorized
  • Neonatal onset Autosomal Dominant Polycystic Kidney Disease (ADPKD) in a patient homozygous for a PKD2 missense mutation due to uniparental disomy (Contributed by Dr. Dorien Peters), Posted on November 23, 2011 by hqqu in Uncategorized
  • Linkage and association analyses of glaucoma related traits in a large pedigree from a Dutch genetically isolated population (Contributed by Prof. Tatiana I. Axenovich), Posted on November 5, 2011 by hqqu in Uncategorized
  • CHEK2*1100delC homozygosity is associated with a high breast cancer risk in women (Contributed by Quinten Waisfisz, PhD), Posted on November 5, 2011 by hqqu in Uncategorized
  • Genetic basis of pain variability: recent advances (Contributed by Erin Young), Posted on November 5, 2011 by hqqu in Uncategorized
  • Sex differences in reproductive fitness contribute to preferential maternal transmission of 22q11.2 deletions (Contributed by Dr Anne S Bassett), Posted on November 3, 2011 by hqqu in Uncategorized
  • Histone acetylation deficits in lymphoblastoid cell lines from patients with Rubinstein–Taybi syndrome (Contributed by Dr. Angel Barco), Posted on October 8, 2011 by hqqu in Uncategorized
  • Patients with a phenotype consistent with facioscapulohumeral muscular dystrophy display genetic and epigenetic heterogeneity (Contributed by Dr. Sabrina SACCONI), Posted on October 8, 2011 by hqqu in Uncategorized
  • Int22h-1/int22h-2-mediated Xq28 rearrangements: intellectual disability associated with duplications and in utero male lethality with deletions (Contributed by Ayman El-Hattab, M.D., F.A.A.P.), Posted on October 8, 2011 by hqqu in Uncategorized
  • «Previous page
  • 93
  • 94
  • 95
  • 96
  • 97
  • »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.