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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 :

  • A genome-wide association study of serum levels of prostate-specific antigen in the Japanese population (Contributed by Chikashi Terao), Posted on June 11, 2014 by hqqu in Uncategorized
  • Prediction of the age at onset in spinocerebellar ataxia type 1, 2, 3 and 6 (Contributed by Sophie Tézenas du Montcel, MD, PhD), Posted on April 29, 2014 by hqqu in Uncategorized
  • Pathogenic mutations in GLI2 cause a specific phenotype that is distinct from holoprosencephaly (Contributed by Kelly Bear), Posted on April 18, 2014 by hqqu in Uncategorized
  • A missense mutation in the splicing factor gene DHX38 is associated with early-onset retinitis pigmentosa with macular coloboma (Contributed by Prof. dr. Frans P.M. Cremers), Posted on April 15, 2014 by hqqu in Uncategorized
  • A familial disorder of altered DNA-methylation (Contributed by Dr. med. Almuth Caliebe), Posted on April 10, 2014 by hqqu in Uncategorized
  • A meta-analysis identifies adolescent idiopathic scoliosis association with LBX1 locus in multiple ethnic groups (Contributed by Dr. Carol Wise), Posted on April 10, 2014 by hqqu in Uncategorized
  • ADAP2 in heart development: a candidate gene for the occurrence of Cardiovascular Malformations in NF1 Microdeletion Syndrome (Contributed by Dr. Marco Venturin), Posted on April 7, 2014 by hqqu in Uncategorized
  • Mutations in the enzyme glutathione peroxidase 4 cause Sedaghatian-type spondylometaphyseal dysplasia (Contributed by Dr. Kym Boycott), Posted on April 4, 2014 by hqqu in Uncategorized
  • RB1 mutation spectrum in a comprehensive nationwide cohort of retinoblastoma patients (Contributed by Berber Mol), Posted on April 1, 2014 by hqqu in Uncategorized
  • Mutation in KANK2, encoding a sequestering protein for steroid receptor coactivators, causes keratoderma and woolly hair (Contributed by Dr. Yuval Ramot), Posted on March 26, 2014 by hqqu in Uncategorized
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