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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 :

  • Identification of chromosome 3q28 and ALPK1 as susceptibility loci for chronic kidney disease in Japanese individuals by a genome-wide association study (Contributed by Dr. Yoshiji Yamada), Posted on March 28, 2013 by hqqu in Uncategorized
  • Ovarian cancer among 8005 women from a breast cancer family history clinic: No increased risk of invasive ovarian cancer in families testing negative for BRCA1 and BRCA2 (Contributed by Dr. Sarah Ingham), Posted on March 28, 2013 by hqqu in Uncategorized
  • Recent Advances in the Genetics of Sarcoidosis (Contributed by Dr. Paolo Spagnolo), Posted on March 22, 2013 by hqqu in Uncategorized
  • Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci (Contributed by Dr. Daphna Weissglas-Volkov), Posted on March 15, 2013 by hqqu in Uncategorized
  • Recent advances in the molecular genetics of epilepsy (Contributed by Drs. Sam Berkovic and Michael Hildebrand), Posted on March 6, 2013 by hqqu in Uncategorized
  • ARHGDIA: a novel gene implicated in nephrotic syndrome (Contributed by Dr. Indra Gupta), Posted on February 22, 2013 by hqqu in Uncategorized
  • Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresia (Contributed by Dr. Bruno Maranda), Posted on February 19, 2013 by hqqu in Uncategorized
  • TBC1D24 Truncating Mutation Resulting in Severe Neurodegeneration (Contributed by Dr. Asli Tolun), Posted on February 13, 2013 by hqqu in Uncategorized
  • Melanoma-prone families with CDK4 germline mutation: Phenotypic profile and associations with MC1R variants (Contributed by Dr. Hanne Eknes Puntervoll), Posted on February 5, 2013 by hqqu in Uncategorized
  • Mutations in POLR3A and POLR3B are a major cause of hypomyelinating leukodystrophies with or without dental abnormalities and/or hypogonadotropic hypogonadism (Contributed by Dr. Geneviève Bernard), Posted on January 25, 2013 by hqqu in Uncategorized
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