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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 :

  • Psychosocial effects of whole-body MRI screening in adult high-risk pathogenic TP53 mutation carriers: a case-controlled study (SIGNIFY) (Contributed by Dr Elizabeth K Bancroft), Posted on November 13, 2019 by hqqu in Uncategorized
  • NEK11 as a candidate high-penetrance melanoma susceptibility gene (Contributed by Eirini Christodoulou), Posted on November 13, 2019 by hqqu in Uncategorized
  • Cornelia de Lange syndrome: from molecular diagnosis to therapeutic approach (Contributed by Dr Antonio Musio), Posted on November 13, 2019 by hqqu in Uncategorized
  • Homozygous mutations in REC114 cause female infertility characterised by multiple pronuclei formation and early embryonic arrest (Contributed by Dr. Lei Wang), Posted on November 13, 2019 by hqqu in Uncategorized
  • Intronic SMCHD1 variants in FSHD: testing the potential for CRISPR-Cas9 genome editing (Contributed by Remko Goossens), Posted on November 5, 2019 by hqqu in Uncategorized
  • Gastric polyposis and desmoid tumours as a new familial adenomatous polyposis clinical variant associated with APC mutation at the extreme 3′-end (Contributed by Prof. Cristiano Simone), Posted on October 8, 2019 by hqqu in Uncategorized
  • Complete loss of KCNA1 activity causes neonatal epileptic encephalopathy and dyskinesia (Contributed by Dr. Edgard Verdura), Posted on October 8, 2019 by hqqu in Uncategorized
  • Increasing knowledge in IGF1R defects: lessons from 35 new patients (Contributed by Dr Eloïse Giabicani), Posted on October 8, 2019 by hqqu in Uncategorized
  • Paediatric systemic lupus erythematosus as a manifestation of constitutional mismatch repair deficiency (Contributed by Dr. Yael Goldberg), Posted on September 25, 2019 by hqqu in Uncategorized
  • Biallelic Mutations in CFAP65 Cause Male Infertility with Multiple Morphological Abnormalities of the Sperm Flagella in Humans and Mice (Contributed by Prof. Feng Zhang), Posted on September 25, 2019 by hqqu in Uncategorized
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