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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 :

  • De novo copy number variants are associated with congenital diaphragmatic hernia (Contributed by Dr. Lan Yu), Posted on October 10, 2012 by hqqu in Uncategorized
  • Use of targeted exome sequencing as a diagnostic tool for Familial Hypercholesterolaemia (Contributed by Marta Futema), Posted on October 10, 2012 by hqqu in Uncategorized
  • Study of autosomal recessive osteogenesis imperfecta in Arabia reveals a novel locus defined by TMEM38B mutation (Contributed by Dr Fowzan S Alkuraya), Posted on October 10, 2012 by hqqu in Uncategorized
  • A balanced translocation truncates Neurotrimin in a family with intracranial and thoracic aortic aneurysm (Contributed by Teppo Varilo M.D., Ph.D.), Posted on October 10, 2012 by hqqu in Uncategorized
  • Distinct and replicable genetic risk factors for acute respiratory distress syndrome of pulmonary or extrapulmonary origin (Contributed by Dr. Paula Tejera), Posted on October 9, 2012 by hqqu in Uncategorized
  • Epigenetic state and expression of imprinted genes in umbilical cord correlates with growth parameters in human pregnancy (Contributed by Dr. Anne Ferguson-Smith), Posted on October 5, 2012 by hqqu in Uncategorized
  • Co-occurrence of recurrent duplications of the DiGeorge syndrome region on both chromosome 22 homologues due to inherited and de novo events (Contributed by Dr. Weimin Bi), Posted on October 5, 2012 by hqqu in Uncategorized
  • The speech gene FOXP2 is not imprinted (Contributed by Dr. Philip Stanier), Posted on October 2, 2012 by hqqu in Uncategorized
  • Prediction of breast cancer risk by genetic risk factors, overall and by hormone receptor status (Contributed by Dr. Anika Hüsing), Posted on September 12, 2012 by hqqu in Uncategorized
  • Deletion of the 3q26 region including the EVI1 and MDS1 genes in a neonate with congenital thrombocytopenia and subsequent aplastic anaemia (Contributed by Maartje Nielsen), Posted on September 12, 2012 by hqqu in Uncategorized
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