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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 :

  • Pulmonary function and structure abnormalities in children and young adults with osteogenesis imperfecta point to intrinsic and extrinsic lung abnormalities (Contributed by Dr. Joan Marini), Posted on May 18, 2023 by hqqu in Uncategorized
  • The phenotypic differences of C9ORF72 gene positive and negative amyotrophic lateral sclerosis: A comparative case series (Contributed by Dr Laura White), Posted on May 13, 2023 by hqqu in Uncategorized
  • Variants in the gene DNA2 causes Rothmund-Thomson syndrome-like presentation (Contributed by Dr. Debora Romeo Bertola), Posted on April 19, 2023 by hqqu in Uncategorized
  • Early breast cancer risk detection: a novel framework leveraging polygenic risk scores and machine learning (Contributed by Dr. Lynn Rose Tao), Posted on April 19, 2023 by hqqu in Uncategorized
  • Strategic validation of variants of uncertain significance in ECHS1 genetic testing (Contributed by Dr. Yasushi Okazaki), Posted on April 19, 2023 by hqqu in Uncategorized
  • Germline (epi)genetics reveals high predisposition in females: a 5-year, nationwide, prospective Wilms tumour cohort (Contributed by Dr. Ulrik Kristoffer Stoltze), Posted on April 6, 2023 by hqqu in Uncategorized
  • Validation and depth evaluation of low-pass genome sequencing in prenatal diagnosis using 387 amniotic fluid samples (Contributed by Prof. Minyue Dong), Posted on April 4, 2023 by hqqu in Uncategorized
  • The crucial role of titin in fetal development: recurrent miscarriages and bone, heart and muscle anomalies characterise the severe end of titinopathies spectrum (Contributed by Dr Maria Francesca Di Feo), Posted on March 29, 2023 by hqqu in Uncategorized
  • PSMD3 gene mutations cause pathological myopia (Contributed by Dr. Jing Chen), Posted on March 26, 2023 by hqqu in Uncategorized
  • MSH2 is the very young onset ovarian cancer predisposition gene, not BRCA1 (Contributed by Dr Niki Flaum), Posted on March 10, 2023 by hqqu in Uncategorized
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