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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 :

  • Stay at home: Implementation and impact of virtualizing cancer genetic services during COVID-19 (Contributed by Maia Norman), Posted on October 18, 2020 by hqqu in Uncategorized
  • A blood functional assay for clinical interpretation of germline TP53 variants (Contributed by Dr Isabelle Tournier), Posted on October 14, 2020 by hqqu in Uncategorized
  • Molecular landscape of CAPN3 mutations in limb-girdle muscular dystrophy type R1: from a Chinese multicentre analysis to a worldwide perspective (Contributed by Dr. Sushan Luo), Posted on September 29, 2020 by hqqu in Uncategorized
  • A practical approach to the genetic diagnosis of unsolved dystrophinopathies: a stepwise strategy in the genomic era (Contributed by Dr. Zhiying Xie), Posted on September 28, 2020 by hqqu in Uncategorized
  • Biallelic variant in cyclin B3 is associated with failure of maternal meiosis II and recurrent digynic triploidy (Contributed by Dr. Andrea Riccio), Posted on September 24, 2020 by hqqu in Uncategorized
  • Systematic evaluation of olfaction in patients with hereditary cystic kidney diseases/renal ciliopathies (Contributed by Dr. Jens König), Posted on September 24, 2020 by hqqu in Uncategorized
  • Sporadic vestibular schwannoma: a molecular testing summary (Contributed by Katie Sadler), Posted on September 24, 2020 by hqqu in Uncategorized
  • TMEM16A deficiency: a potentially fatal neonatal disease resulting from impaired chloride currents (Contributed by Dr. med. Julien H. Park), Posted on September 24, 2020 by hqqu in Uncategorized
  • Description of a multidisciplinary model of care in a French cohort of adult patients with tuberous sclerosis complex (Contributed by Dr Pierre Pfirmann), Posted on September 24, 2020 by hqqu in Uncategorized
  • Ethnic-specific BRCA1/2 variation within Asia population: evidence from over 78 000 cancer and 40 000 non-cancer cases of Indian, Chinese, Korean and Japanese populations (Contributed by Dr. San Ming Wang), Posted on September 24, 2020 by hqqu in Uncategorized
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