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About:hqqu

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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 :

  • Current novel-gene-finding strategy for autosomal-dominant hypercholesterolaemia needs refinement (Contributed by Dr. Sigrid Fouchier), Posted on November 21, 2014 by hqqu in Uncategorized
  • Exhaustive methylation analysis revealed uneven profiles of methylation at IGF2/ICR1/H19 11p15 loci in Russell Silver syndrome (Contributed by Dr. Salah Azzi), Posted on November 13, 2014 by hqqu in Uncategorized
  • Next-generation sequencing of nine atrial fibrillation candidate genes identified novel de novo mutations in patients with extreme trait of atrial fibrillation (Contributed by Dr. Chia-Ti Tsai), Posted on November 12, 2014 by hqqu in Uncategorized
  • Pseudogene in Cancer: Real Functions and Promising Signature (Contributed by Dr. Lu Xiao-Jie), Posted on November 12, 2014 by hqqu in Uncategorized
  • Differential increase of specific FMR1 mRNA isoforms in premutation carriers (Contributed by Dr. Dalyir Pretto), Posted on October 30, 2014 by hqqu in Uncategorized
  • MUTATIONS IN THE TRICARBOXYLIC ACID CYCLE ENZYME, ACONITASE 2, CAUSE EITHER ISOLATED OR SYNDROMIC OPTIC NEUROPATHY WITH ENCEPHALOPATHY AND CEREBELLAR ATROPHY (Contributed by Dr. Agnès Rötig), Posted on October 29, 2014 by hqqu in Uncategorized
  • International requirements for consent in biobank research. Qualitative review of research guidelines (Contributed by Dr. Daniel Strech), Posted on October 29, 2014 by hqqu in Uncategorized
  • Recent advances in primary ciliary dyskinesia genetics (Contributed by Dr. Małgorzata Kurkowiak), Posted on October 29, 2014 by hqqu in Uncategorized
  • Clinical, histological and genetic characterization of patients with tubular aggregate myopathy caused by mutations in STIM1 (Contributed by Dr. Johann Böhm), Posted on October 18, 2014 by hqqu in Uncategorized
  • OTX2 mutations cause autosomal dominant pattern dystrophy of the retinal pigment epithelium (Contributed by Dr. Ajoy Vincent), Posted on October 8, 2014 by hqqu in Uncategorized
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