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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 :

  • Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresia (Contributed by Dr. Bruno Maranda), Posted on February 19, 2013 by hqqu in Uncategorized
  • TBC1D24 Truncating Mutation Resulting in Severe Neurodegeneration (Contributed by Dr. Asli Tolun), Posted on February 13, 2013 by hqqu in Uncategorized
  • Melanoma-prone families with CDK4 germline mutation: Phenotypic profile and associations with MC1R variants (Contributed by Dr. Hanne Eknes Puntervoll), Posted on February 5, 2013 by hqqu in Uncategorized
  • Mutations in POLR3A and POLR3B are a major cause of hypomyelinating leukodystrophies with or without dental abnormalities and/or hypogonadotropic hypogonadism (Contributed by Dr. Geneviève Bernard), Posted on January 25, 2013 by hqqu in Uncategorized
  • Whole Exome Sequencing Identifies a Mutation for a Novel Form of Corneal Intraepithelial Dyskeratosis (Contributed by Dr. Vincent Soler), Posted on January 24, 2013 by hqqu in Uncategorized
  • Mutations in TMEM231 cause Meckel–Gruber syndrome (Contributed by Dr. Fowzan S Alkuraya), Posted on January 24, 2013 by hqqu in Uncategorized
  • Role of PRRT2 in common paroxysmal neurological disorders: a gene with remarkable pleiotropy (Contributed by Dr. Sarah Heron), Posted on January 23, 2013 by hqqu in Uncategorized
  • Deletions in 16q24.2 are associated with autism spectrum disorder, intellectual disability and congenital renal malformation (Contributed by Dr. Gregory R. Handrigan), Posted on January 18, 2013 by hqqu in Uncategorized
  • High cumulative risks of cancer in patients with PTEN hamartoma tumour syndrome (Contributed by Dr. Virginie Bubien), Posted on January 18, 2013 by hqqu in Uncategorized
  • Heterogeneity of mutational mechanisms and modes of inheritance in auriculocondylar syndrome (Contributed by Dr. Chris Gordon), Posted on January 13, 2013 by hqqu in Uncategorized
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