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 :

  • Their loss is our gain: regressive evolution in vertebrates provides genomic models for uncovering human disease loci (Contributed by Dr. Christopher A Emerling), Posted on August 16, 2017 by hqqu in Uncategorized
  • Mutations in SCAPER cause autosomal recessive retinitis pigmentosa with intellectual disability (Contributed by Dr. Tamar Ben-Yosef), Posted on August 9, 2017 by hqqu in Uncategorized
  • Heterogeneous clinical spectrum of DNAJC12-deficient hyperphenylalaninemia: from attention deficit to severe dystonia and intellectual disability (Contributed by Prof. Dr. Beat Thöny), Posted on August 9, 2017 by hqqu in Uncategorized
  • A common SLC26A4-linked haplotype underlying non-syndromic hearing loss with enlargement of the vestibular aqueduct (Contributed by Dr. Andrew J Griffith), Posted on August 5, 2017 by hqqu in Uncategorized
  • Increased Breast Cancer Risk in MSH2 Carriers from a Large Canadian Familial Cancer Registry (Contributed by Dr. Mira Goldberg), Posted on August 4, 2017 by hqqu in Uncategorized
  • Segregation of mitochondrial DNA mutations in the human placenta: implication for prenatal diagnosis of mtDNA disorders (Contributed by Drs. Julie Steffann and Jean-Paul Bonnefont), Posted on July 28, 2017 by hqqu in Uncategorized
  • A germline deletion of 9p21.3 presenting as familial melanoma, astrocytoma and breast cancer: clinical and genetic counselling challenges (Contributed by Dr. Jaime Vengoechea and Christine Tallo, MMSc, CGC), Posted on July 28, 2017 by hqqu in Uncategorized
  • Identification of the first dominant mutation of LAMA5 gene causing a complex multisystem syndrome due to dysfunction of the extracellular matrix (Contributed by Dr. Teresa Esposito), Posted on July 22, 2017 by hqqu in Uncategorized
  • Assessing genome-wide copy number variation in the Han Chinese population (Contributed by Prof. Dr. Shuhua Xu), Posted on July 13, 2017 by hqqu in Uncategorized
  • The focal facial dermal dysplasias: phenotypic spectrum and molecular genetic heterogeneity (Contributed by Brenden Chen), Posted on June 29, 2017 by hqqu in Uncategorized
  • «Previous page
  • 59
  • 60
  • 61
  • 62
  • 63
  • »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.