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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 :

  • Specifying the ovarian cancer risk threshold of ‘premenopausal risk-reducing salpingo-oophorectomy’ for ovarian cancer prevention: a cost-effectiveness analysis (Contributed by Dr Ranjit Manchanda), Posted on June 29, 2016 by hqqu in Uncategorized
  • Identification of bi-allelicLRRK1mutations inosteosclerotic metaphyseal dysplasiaand evidence for locus heterogeneity (Contributed by Dr. Aritoshi Iida), Posted on June 22, 2016 by hqqu in Uncategorized
  • Gain-of-function mutation in TRPV4 identified in patients with osteonecrosis of the femoral head (Contributed by Dr Chantal Séguin), Posted on June 21, 2016 by hqqu in Uncategorized
  • Mutations in TUBB8 cause a multiplicity of phenotypes in human oocytes and early embryos (Contributed by Dr. Lei Wang), Posted on June 6, 2016 by hqqu in Uncategorized
  • Genes associated with common variable immunodeficiency: one diagnosis to rule them all? (Contributed by Delfien Bogaert on behalf of all authors), Posted on June 1, 2016 by hqqu in Uncategorized
  • A Splicing Mutation in VPS4B Causes Dentin Dysplasia I (Contributed by Prof. Fu Xiong), Posted on May 31, 2016 by hqqu in Uncategorized
  • GATOR1 complex: the common genetic actor in focal epilepsies (Contributed by Sara Baldassari), Posted on May 19, 2016 by hqqu in Uncategorized
  • New paradigms for BRCA1/BRCA2 testing in women with ovarian cancer: results of the Genetic Testing in Epithelial Ovarian Cancer (GTEOC) study (Contributed by Dr. Marc Tischkowitz), Posted on May 12, 2016 by hqqu in Uncategorized
  • Mutations in CEP120 cause Joubert syndrome as well as complex ciliopathy phenotypes (Contributed by Dr. Susanne Roosing), Posted on May 6, 2016 by hqqu in Uncategorized
  • When chromatin organisation floats astray: the Srcap gene and Floating–Harbor syndrome (Contributed by Professor Patrizio Dimitri), Posted on April 26, 2016 by hqqu in Uncategorized
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