Skip to content
JMG Blog logo
  • Home
  • Journal

About:hqqu

Profile
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 :

  • Clinical exome sequencing data reveal high diagnostic yields for congenital diaphragmatic hernia plus (CDH+) and new phenotypic expansions involving CDH (Contributed by Dr. Daryl A Scott), Posted on January 21, 2021 by hqqu in Uncategorized
  • Unexpected role of SIX1 variants in craniosynostosis: expanding the phenotype of SIX1-related disorders (Contributed by Eduardo Calpena), Posted on January 12, 2021 by hqqu in Uncategorized
  • Calibration of polygenic risk scores is required prior to clinical implementation: results of three common cancers in UKB (Contributed by W Kyle Resurreccion), Posted on December 22, 2020 by hqqu in Uncategorized
  • Deep exploration of a CDKN1C mutation causing a mixture of Beckwith-Wiedemann and IMAGe syndromes revealed a novel transcript associated with developmental delay (Contributed by Dr. Siren Berland), Posted on December 22, 2020 by hqqu in Uncategorized
  • Phenotype and genotype spectra of a Chinese cohort with nephronophthisis-related ciliopathy (Contributed by Dr. Xiaoshan Tang), Posted on December 15, 2020 by hqqu in Uncategorized
  • Dysfunction of VIPR2 leads to myopia in humans and mice (Contributed by Dr. Xiangtian Zhou), Posted on December 15, 2020 by hqqu in Uncategorized
  • Linkage analysis identifies an isolated strabismus locus at 14q12 overlapping with FOXG1 syndrome region (Contributed by Cynthia Ye), Posted on December 2, 2020 by hqqu in Uncategorized
  • Combining evidence for and against pathogenicity for variants in cancer susceptibility genes: CanVIG-UK consensus recommendations (Contributed by Dr. Alice Garrett), Posted on November 21, 2020 by hqqu in Uncategorized
  • MELAS-associated m.5541C>T mutation caused instability of mitochondrial tRNATrp and remarkable mitochondrial dysfunction (Contributed by Professor Chuanzhu Yan), Posted on November 21, 2020 by hqqu in Uncategorized
  • Canadian College of Medical Geneticists (CCMG) points to consider: resuming genetic services in a pandemic—a summary (Contributed by Dr. Elaine Suk-Ying Goh), Posted on November 17, 2020 by hqqu in Uncategorized
  • «Previous page
  • 35
  • 36
  • 37
  • 38
  • 39
  • »Next page
  • 103

BMJ Careers

BMJ Blogs

Comment and Opinion | Open Debate

The views and opinions expressed on this site are solely those of the original authors. They do not necessarily represent the views of BMJ and should not be used to replace medical advice. Please see our full website terms and conditions.

All BMJ blog posts are posted under a CC-BY-NC licence

BMJ Journals

© BMJ Publishing Group Limited 2026. All rights reserved.