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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 :

  • Genotype-phenotype correlations for pancreatic cancer risk in Dutch melanoma families with pathogenic CDKN2A variants (Contributed by Dr. Kasper Overbeek), Posted on June 1, 2020 by hqqu in Uncategorized
  • Prevalence of BRCA1/BRCA2 pathogenic variation in Chinese Han population (Contributed by Dr. San Ming Wang), Posted on June 1, 2020 by hqqu in Uncategorized
  • Paternal 132 bp deletion affecting KCNQ1OT1 in 11p15.5 is associated with growth retardation but does not affect imprinting (Contributed by Prof. Thomas Eggermann), Posted on May 25, 2020 by hqqu in Uncategorized
  • Hypomethylation of a centromeric block of ICR1 is sufficient to cause Silver-Russell syndrome (Contributed by Dr. Hidenobu Soejima), Posted on May 25, 2020 by hqqu in Uncategorized
  • Bi-allelic TTC5 variants cause delayed developmental milestones and intellectual disability (Contributed by Dr. Ashleigh E Schaffer), Posted on May 22, 2020 by hqqu in Uncategorized
  • A component of MICOS (APOO/MIC26) associated with a new X-linked mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features (Contributed by Dr. Cristiane Benincá), Posted on May 22, 2020 by hqqu in Uncategorized
  • ‘Kinesinopathies’: emerging role of the kinesin family member genes in birth defects (Contributed by Silvia Kalantari and Isabel Filges), Posted on May 20, 2020 by hqqu in Uncategorized
  • Evidence for polygenic and oligogenic basis of Australian sporadic amyotrophic lateral sclerosis (Contributed by Dr. Emily McCann), Posted on May 15, 2020 by hqqu in Uncategorized
  • Update and audit of the St George’s classification algorithm of primary lymphatic anomalies: a clinical and molecular approach to diagnosis (Contributed by Professor Sahar Mansour), Posted on May 15, 2020 by hqqu in Uncategorized
  • Prevalence and associated phenotypes of DUSP6, IL17RD and SPRY4 variants in a large Chinese cohort with isolated hypogonadotropic hypogonadism (Contributed by Meichao Men), Posted on May 12, 2020 by hqqu in Uncategorized
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