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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 :

  • Bacteria-free minicircle DNA system to generate integration-free CAR-T cells (Contributed by Chen Cheng), Posted on July 20, 2018 by hqqu in Uncategorized
  • Paternal uniparental disomy of chromosome 19 in a pair of monochorionic diamniotic twins with dysmorphic features and developmental delay (Contributed by Kit San Yeung), Posted on July 14, 2018 by hqqu in Uncategorized
  • Fine mapping MHC associations in Graves’ disease and its clinical subtypes in Han Chinese (Contributed by Dr. Xun Chu), Posted on July 9, 2018 by hqqu in Uncategorized
  • Applications and advances of CRISPR-Cas9 in cancer immunotherapy (Contributed by An-Liang Xia), Posted on July 3, 2018 by hqqu in Uncategorized
  • Genetic obesity: next-generation sequencing results of 1230 patients with obesity (Contributed by Dr. Lotte Kleinendorst), Posted on July 3, 2018 by hqqu in Uncategorized
  • Hereditary lobular breast cancer with an emphasis on E-cadherin genetic defect (Contributed by Dr. Giovanni Corso), Posted on June 21, 2018 by hqqu in Uncategorized
  • Identification of new risk factors for rolandic epilepsy: CNV at Xp22.31 and alterations at cholinergic synapses (Contributed by Dr. Laura Addis), Posted on May 22, 2018 by hqqu in Uncategorized
  • Molecular genetic classification in Prader-Willi syndrome: a multisite cohort study (Contributed by Professor Merlin G. Butler), Posted on May 6, 2018 by hqqu in Uncategorized
  • Evaluation of polygenic risk scores for ovarian cancer risk prediction in a prospective cohort study (Contributed by Xin Yang and Prof Antonis C Antoniou), Posted on May 6, 2018 by hqqu in Uncategorized
  • Old gene, new phenotype: Splicing altering variants in CEACAM16 cause recessive non-syndromic hearing impairment (Contributed by Kevin T Booth), Posted on April 27, 2018 by hqqu in Uncategorized
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