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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 :

  • GERMLINE MUTATIONS IN WNK2 COULD BE ASSOCIATED WITH SERRATED POLYPOSIS SYNDROME, Soares de Lima et al. (Contributed by Dr. Sergi Castellví-Bel), Posted on October 30, 2022 by hqqu in Uncategorized
  • The clinical, neuroimaging, and molecular characteristics of PPP2R5D related neurodevelopmental disorders: an expanded series with functional characterization and genotype-phenotype correlation (Contributed by Nora M Oyama, Pieter Vaneynde, Sara Reynhout, Emily C Pao, Andrew Timms, Xiao Fan, Kimberly Foss, Rita Derua, Veerle Janssens, Wendy K Chung and Ghayda M Mirzaa), Posted on October 11, 2022 by hqqu in Uncategorized
  • Identifying the molecular drivers of ALS-implicated missense mutations (Contributed by Dr. David Ascher), Posted on October 3, 2022 by hqqu in Uncategorized
  • Prospective validation of the BOADICEA multifactorial breast cancer risk prediction model in a large prospective cohort study (Contributed by Xin Yang), Posted on September 27, 2022 by hqqu in Uncategorized
  • Enhancing the BOADICEA cancer risk prediction model to incorporate new data on RAD51C, RAD51D, BARD1 updates to tumour pathology and cancer incidence (Contributed by Dr. Antonis Antoniou), Posted on September 27, 2022 by hqqu in Uncategorized
  • Clinical applicability of the Polygenic Risk Score for breast cancer risk prediction in familial cases (Contributed by Dr. Inge M M Lakeman), Posted on September 23, 2022 by hqqu in Uncategorized
  • Patient-facing Digital Tools for Delivering Genetic Services: A Systematic Review (Contributed by Stephanie Luca, HBSc, MA, PMP), Posted on September 23, 2022 by hqqu in Uncategorized
  • Systems approach to enhance Lynch syndrome diagnosis through tumour testing (Contributed by Dr. Xavier Llor), Posted on September 20, 2022 by hqqu in Uncategorized
  • Clinical diversity and molecular mechanism of VPS35L-associated Ritscher-Schinzel syndrome (Contributed by Dr. Shiomi Otsuji), Posted on September 20, 2022 by hqqu in Uncategorized
  • Advancing in Schaaf-Yang syndrome pathophysiology: from bedside to subcellular analyses of truncated MAGEL2 (Contributed by Dr. Roser Urreizti), Posted on September 8, 2022 by hqqu in Uncategorized
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