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 :

  • The speech gene FOXP2 is not imprinted (Contributed by Dr. Philip Stanier), Posted on October 2, 2012 by hqqu in Uncategorized
  • Prediction of breast cancer risk by genetic risk factors, overall and by hormone receptor status (Contributed by Dr. Anika Hüsing), Posted on September 12, 2012 by hqqu in Uncategorized
  • Deletion of the 3q26 region including the EVI1 and MDS1 genes in a neonate with congenital thrombocytopenia and subsequent aplastic anaemia (Contributed by Maartje Nielsen), Posted on September 12, 2012 by hqqu in Uncategorized
  • Complex I deficiency: clinical features, biochemistry and molecular genetics (Contributed by Shamima Rahman FRCP FRCPCH PhD), Posted on September 12, 2012 by hqqu in Uncategorized
  • Recessive germline SDHA and SDHB mutations causing leukodystrophy and isolated mitochondrial complex II deficiency (Contributed by R.W. Taylor PhD, DSc, FRCPath), Posted on September 12, 2012 by hqqu in Uncategorized
  • Exome sequencing identifies a COL14A1 mutation in a large Chinese pedigree with punctate palmoplantar keratoderma (Contributed by Xuejun Zhang M.D. Ph.D.), Posted on September 12, 2012 by hqqu in Uncategorized
  • Dominantly inherited diabetes mellitus caused by GATA6 haploinsufficiency: variable intrafamilial presentation (Contributed by Dr. Tohru Yorifuji), Posted on September 7, 2012 by hqqu in Uncategorized
  • Quantitative trait locus analysis for next-generation sequencing with the functional linear models (Contributed by Dr. Momiao Xiong), Posted on August 13, 2012 by hqqu in Uncategorized
  • Neurofibromatosis type 1: from genotype to phenotype (Contributed by Dr. Eric Pasmant), Posted on August 13, 2012 by hqqu in Uncategorized
  • A systematic review of associated structural and chromosomal defects in oral clefts: when is prenatal genetic analysis indicated? (Contributed by Dr. AM Rozendaal), Posted on August 13, 2012 by hqqu in Uncategorized
  • «Previous page
  • 90
  • 91
  • 92
  • 93
  • 94
  • »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.