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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 :

  • CHEK2 is not a Li-Fraumeni syndrome gene: time to update public resources (Contributed by Dr. Cristina Fortuno), Posted on August 7, 2023 by hqqu in Uncategorized
  • Prevalence and clinical implications of germline pathogenic variants in cancer predisposing genes in young patients across sarcoma subtypes (Contributed by Giovana Tardin Torrezan, PhD), Posted on August 7, 2023 by hqqu in Uncategorized
  • Integrating RNA-Seq into genome sequencing workflow enhances the analysis of structural variants causing neurodevelopmental disorders (Contributed by Kevin Riquin), Posted on July 27, 2023 by hqqu in Uncategorized
  • Clinical phenotype and genetic function analysis of a rare family with hereditary leiomyomatosis and renal cell carcinoma complicated with Birt–Hogg–Dubé syndrome (Contributed by Professor Jie-Wei Luo), Posted on July 20, 2023 by hqqu in Uncategorized
  • Performance of the eHealth decision support tool, MIPOGG, for recognising children with Li-Fraumeni, DICER1, Constitutional mismatch repair deficiency and Gorlin syndromes (Contributed by Dr. Catherine Goudie), Posted on July 17, 2023 by hqqu in Uncategorized
  • Exome sequencing links the SUMO protease SENP7 with fatal arthrogryposis multiplex congenita, early respiratory failure and neutropenia (Contributed by Dr. Karin Weiss), Posted on July 17, 2023 by hqqu in Uncategorized
  • Evaluation of European-based polygenic risk score for breast cancer in Ashkenazi Jewish women in Israel (Contributed by Prof. Rani Elkon), Posted on July 14, 2023 by hqqu in Uncategorized
  • Mutation in Mitral Valve Prolapse Susceptible Gene DCHS1 Causes Familial Mitral Annular Disjunction (Contributed by Nan ZHOU MD.,PhD.), Posted on July 1, 2023 by hqqu in Uncategorized
  • Evaluation of the clinical, biochemical, genotype and prognosis of mut-type methylmalonic acidemia in 365 Chinese cases (Contributed by Drs. Lili Liang and Lianshu Han), Posted on June 15, 2023 by hqqu in Uncategorized
  • Congenital mirror movements are associated with defective polymerisation of RAD51 (Contributed by Drs Caroline Dubacq and Oriane Trouillard), Posted on June 15, 2023 by hqqu in Uncategorized
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