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 :

  • Bi-allelic variants in MAATS1 encoding CFAP91, a calmodulin- and spoke-associated complex protein, cause severe astheno-teratozoospermia and male infertility (Contributed by Prof. Charles COUTTON), Posted on March 14, 2020 by hqqu in Uncategorized
  • Pathogenic variants in TNRC6B cause a genetic disorder characterised by developmental delay/intellectual disability and a spectrum of neurobehavioural phenotypes including autism and ADHD (Contributed by Dr. Marwan Shinawi), Posted on March 10, 2020 by hqqu in Uncategorized
  • Severity of oro-dental anomalies in Loeys-Dietz syndrome segregates by gene mutation (Contributed by Dr. Priyam Jani), Posted on March 9, 2020 by hqqu in Uncategorized
  • Association between genetic polymorphisms and endometrial cancer risk: a systematic review (Contributed by Dr. Emma Crosbie), Posted on February 18, 2020 by hqqu in Uncategorized
  • RE-DEFINITION OF FAMILIAL INTESTINAL GASTRIC CANCER: CLINICAL AND GENETIC PERSPECTIVES (Contributed by Dr. Carla Oliveira), Posted on February 18, 2020 by hqqu in Uncategorized
  • MicroRNA-4516-mediated regulation of MAPK10 relies on 3’UTR cis-acting variants and contributes to the altered risk of Hirschsprung disease (Contributed by Dr. Yang Wang), Posted on February 18, 2020 by hqqu in Uncategorized
  • Investigating the genetic susceptibility to exertional heat illness (Contributed by Professor PM Hopkins), Posted on February 14, 2020 by hqqu in Uncategorized
  • Phenotype of genetically confirmed Silver-Russell syndrome beyond childhood (Contributed by Dr. Karen Temple), Posted on February 14, 2020 by hqqu in Uncategorized
  • Excess of singleton loss-of-function variants in Parkinson’s disease contributes to genetic risk (Contributed by Dr. Patrick May), Posted on February 14, 2020 by hqqu in Uncategorized
  • CDK5RAP2 primary microcephaly is associated with hypothalamic, retinal and cochlear developmental defects (Contributed by Dr Sandrine Passemard), Posted on February 6, 2020 by hqqu in Uncategorized
  • «Previous page
  • 42
  • 43
  • 44
  • 45
  • 46
  • »Next page
  • 102

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.