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About:hqqu

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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 :

  • Mutation in MPDZ causes severe congenital hydrocephalus (Contributed by Fowzan S Alkuraya, MD FAAP FACMG), Posted on December 15, 2012 by hqqu in Uncategorized
  • IL12B SNPs and Copy number variation in IL23R gene associate with susceptibility to leprosy (Contributed by Prof. R.N.K.Bamezai), Posted on December 15, 2012 by hqqu in Uncategorized
  • EFTUD2 haploinsufficiency leads to syndromic oesophageal atresia (Contributed by Muriel Holder), Posted on November 28, 2012 by hqqu in Uncategorized
  • Whole exome sequencing identified a novel zinc-finger gene ZNF141 associated with autosomal recessive postaxial polydactyly type A (Contributed by Dr. Wasim Ahmad), Posted on November 17, 2012 by hqqu in Uncategorized
  • Identification of a functional variant in the KIF5A- CYP27B1- METTL1- FAM119B locus associated with Multiple Sclerosis (Contributed by Dr Antonio Alcina), Posted on November 17, 2012 by hqqu in Uncategorized
  • An Italian association study and meta-analysis with previous GWAS confirm WNT4, CDKN2BAS and FN1 as the first identified susceptibility loci for endometriosis (Contributed by Luca Pagliardini), Posted on November 11, 2012 by hqqu in Uncategorized
  • Two novel CCDC88C mutations confirm the role of DAPLE in autosomal recessive congenital hydrocephalus (Contributed by Drielsma Anaïs), Posted on November 2, 2012 by hqqu in Uncategorized
  • Risk of malignant paraganglioma in SDHB-mutation and SDHD-mutation carriers: a systematic review and meta-analysis (Contributed by Dr. Leonie van Hulsteijn), Posted on October 25, 2012 by hqqu in Uncategorized
  • Exome sequencing identified a missense mutation of EPS8L3 in Marie Unna Hereditary Hypotrichosis (Contributed by Dr. Xuejun Zhang), Posted on October 25, 2012 by hqqu in Uncategorized
  • A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders (Contributed by Sébastien Jacquemont), Posted on October 10, 2012 by hqqu in Uncategorized
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