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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 :

  • Setleis Syndrome in Mexican-Nahua Sibs Due to a Homozygous TWIST2 Frameshift Mutation and Partial Expression in Heterozygotes: Review of the Focal Facial Dermal Dysplasias and Subtype Reclassification (Contributed by Amy Yang, MD), Posted on March 5, 2012 by hqqu in Uncategorized
  • AKAP9-rs6964587 and breast cancer risk: an extended case-control study by the Breast Cancer Association Consortium (Contributed by Dr Roger L Milne), Posted on March 5, 2012 by hqqu in Uncategorized
  • A role for XRCC2 gene polymorphisms in breast cancer risk and survival (Contributed by Dr Angela Cox), Posted on March 5, 2012 by hqqu in Uncategorized
  • Variants in or near KITLG, BAK1, DMRT1, and TERT-CLPTM1L predispose to familial testicular germ cell tumour (Contributed by Christian P. Kratz, M.D.), Posted on March 5, 2012 by hqqu in Uncategorized
  • Chromosome fragility in Fanconi anemia patients: diagnostic implications and clinical impact (Contributed by Professor Jordi Surrallés), Posted on March 5, 2012 by hqqu in Uncategorized
  • Maternally transmitted late-onset nonsyndromic deafness is associated with the novel heteroplasmic T12201C mutation in the mitochondrial tRNAHis gene (Contributed by Prof. Min-Xin Guan), Posted on March 5, 2012 by hqqu in Uncategorized
  • Exome sequencing reveals a novel Fanconi group defined by XRCC2 mutation (Contributed by Prof. Fowzan S Alkuraya), Posted on January 10, 2012 by hqqu in Uncategorized
  • Facioscapulohumeral muscular dystrophy: new insights from compound heterozygotes and implication for prenatal genetic counselling (Contributed by Prof. Rossella Tupler), Posted on January 4, 2012 by hqqu in Uncategorized
  • Mutations in PRRT2 result in paroxysmal dyskinesias with marked variability in clinical expression (Contributed by Dr. Qing Liu), Posted on December 30, 2011 by hqqu in Uncategorized
  • Complete loss of expression of the ANT1 gene causing cardiomyopathy and myopathy (Contributed by Andoni Echaniz-Laguna), Posted on December 20, 2011 by hqqu in Uncategorized
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