Skip to content
JMG Blog logo
  • Home
  • Journal

About:hqqu

Profile
Huiqi Qu’s research interest is the genetics and functional genomics of human complex diseases (e.g. tuberculosis, obesity, and diabetes). He is working on the genetics and functional genomics of tuberculosis and diabetes. By integrating proteomics, genomics, and GWAS study, they are trying to clarify the molecular mechanisms of tuberculosis susceptibility, and develop genetic markers for diabetes risk prediction.

Posts by hqqu :

  • Differential disruption of autoinhibition and defect in assembly of cytoskeleton during cell division decide the fate of human DIAPH1-related cytoskeletopathy, Posted on September 2, 2019 by hqqu in Uncategorized
  • De novo SCAMP5 mutation causes a neurodevelopmental disorder with autistic features and seizures, Posted on August 27, 2019 by hqqu in Uncategorized
  • New insights into 5α-reductase type 2 deficiency based on a multi-centre study: regional distribution and genotype–phenotype profiling of SRD5A2 in 190 Chinese patients, Posted on August 20, 2019 by hqqu in Uncategorized
  • Addition of a 161-SNP polygenic risk score to family history-based risk prediction: impact on clinical management in non-BRCA1/2 breast cancer families, Posted on August 20, 2019 by hqqu in Uncategorized
  • Genetic factors contributing to autism spectrum disorder in Williams-Beuren syndrome, Posted on August 20, 2019 by hqqu in Uncategorized
  • ‘Metaphyseal dysplasia without hypotrichosis’ can present with late-onset extraskeletal manifestations, Posted on August 20, 2019 by hqqu in Uncategorized
  • Biallelic mutations in CFAP65 lead to severe asthenoteratospermia due to acrosome hypoplasia and flagellum malformations, Posted on August 20, 2019 by hqqu in Uncategorized
  • Long-read sequencing identified repeat expansions in the 5′UTR of the NOTCH2NLC gene from Chinese patients with neuronal intranuclear inclusion disease, Posted on August 20, 2019 by hqqu in Uncategorized
  • Hypolipidaemia among patients with PMM2-CDG is associated with low circulating PCSK9 levels: a case report followed by observational and experimental studies, Posted on August 10, 2019 by hqqu in Uncategorized
  • Truncating mutations in exons 20 and 21 of OFD1 can cause primary ciliary dyskinesia without associated syndromic symptoms, Posted on August 4, 2019 by hqqu in Uncategorized
  • «Previous page
  • 42
  • 43
  • 44
  • 45
  • 46
  • »Next page
  • 98

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 2025. All rights reserved.