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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 :

  • Comparison of the clinical scoring systems in Silver–Russell syndrome and development of modified diagnostic criteria to guide molecular genetic testing (Contributed by Dr Renuka Dias), Posted on June 29, 2013 by hqqu in Uncategorized
  • Can the diagnosis of NF1 be excluded clinically? A lack of pigmentary findings in families with spinal neurofibromatosis demonstrates a limitation of clinical diagnosis (Contributed by Dr Emma MM Burkitt Wright), Posted on June 29, 2013 by hqqu in Uncategorized
  • West syndrome, microcephaly, grey matter heterotopia and hypoplasia of corpus callosum due to a novel ARFGEF2 mutation (Contributed by Simon Edvardson MD), Posted on June 29, 2013 by hqqu in Uncategorized
  • Associations of common variants in HFE and TMPRSS6 with iron parameters are independent of serum hepcidin in a general population: a replication study (Contributed by Miss Tessel Galesloot), Posted on June 22, 2013 by hqqu in Uncategorized
  • Digenic inheritance in medical genetics (Contributed by Dr. Alejandro Schaffer), Posted on June 19, 2013 by hqqu in Uncategorized
  • Genome-wide association study identifies ephrin type A receptors implicated in paclitaxel induced peripheral sensory neuropathy (Contributed by Luis Javier Leandro García), Posted on June 17, 2013 by hqqu in Uncategorized
  • Meta-Analysis of Genome-Wide Studies Identifies MEF2C SNPs Associated with Bone Mineral Density at Forearm (Contributed by Dr. Hou-Feng Zheng), Posted on June 11, 2013 by hqqu in Uncategorized
  • Recessive truncating NALCN mutation in infantile neuroaxonal dystrophy with facial dysmorphism (Contributed by Prof. Asli Tolun), Posted on June 7, 2013 by hqqu in Uncategorized
  • A de novo X;8 translocation creates a PTK2-THOC2 gene fusion with THOC2 expression knockdown in a patient with psychomotor retardation and congenital cerebellar hypoplasia (Contributed by Dr. Alfredo Brusco), Posted on June 7, 2013 by hqqu in Uncategorized
  • Identification of well-differentiated gene expressions between Han Chinese and Japanese using genome-wide microarray data analysis (Contributed by Dr. Shuhua Xu), Posted on June 4, 2013 by hqqu in Uncategorized
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