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 :

  • 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
  • Genetic diagnosis of Duchenne muscular dystrophy using next-generation sequencing technology: comprehensive mutational search in a single platform (Contributed by Byung Chan Lim MD), Posted on October 4, 2011 by hqqu in Uncategorized
  • Germline BAP1 mutation predisposes to uveal melanoma, lung adenocarcinoma, meningioma, and other cancers (Contributed by Mohamed H. Abdel-Rahman, MD, PhD), Posted on September 23, 2011 by hqqu in Uncategorized
  • New findings for phenotype–genotype correlations in a large European series of holoprosencephaly cases (Contributed by Sandra MERCIER), Posted on September 23, 2011 by hqqu in Uncategorized
  • «Previous page
  • 95
  • 96
  • 97
  • 98
  • 99
  • »Next page
  • 103

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.