Wren, Georgina, O'Callaghan, Peter, Zaidi, Abbas, Thompson, Andrew  ORCID: https://orcid.org/0000-0001-6788-7222, Humby, Trevor  ORCID: https://orcid.org/0000-0002-1840-1799 and Davies, William  ORCID: https://orcid.org/0000-0002-7714-2440
      2025.
      
      Monitoring heart rhythms in adult males with X-linked ichthyosis using wearable technology: a feasibility study.
      Archives of Dermatological Research
      317
      
      
      , 351.
      10.1007/s00403-025-03884-x
    
  
    
    
       
    
  
  
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      Wren, Georgina H. and Davies, William  ORCID: https://orcid.org/0000-0002-7714-2440
      2024.
      
      Cardiac arrhythmia in individuals with steroid sulfatase deficiency (X linked ichthyosis): candidate anatomical and biochemical pathways.
      Essays in Biochemistry
      68
      
        (4)
      
      , pp. 423-429.
      
      10.1042/EBC20230098
    
  
    
    
       
    
  
  
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      Wren, Georgina
      2024.
      Exploring the psychological and physiological issues associated with X-linked ichthyosis.
      PhD Thesis,
      Cardiff University.
    
  
    
       
    
    
  
  
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      Wren, Georgina H. and Davies, William  ORCID: https://orcid.org/0000-0002-7714-2440
      2022.
      
      X-linked ichthyosis: New insights into a multi-system disorder.
      Skin Health and Disease
      2
      
        (4)
      
      
      , e179.
      10.1002/ski2.179
    
  
    
    
       
    
  
  
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      Wren, Georgina and Mercer, Jenny
      2022.
      
      Dismissal, distrust, and dismay: a phenomenological exploration of young women’s diagnostic experiences with endometriosis and subsequent support.
      Journal of Health Psychology
      27
      
        (11)
      
      , pp. 2549-2565.
      
      10.1177/13591053211059387
    
  
    
       
    
    
  
  
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      Wren, Georgina and Davies, William  ORCID: https://orcid.org/0000-0002-7714-2440
      2022.
      
      Sex-linked genetic mechanisms and atrial fibrillation risk.
      European Journal of Medical Genetics
      65
      
        (4)
      
      
      , 104459.
      10.1016/j.ejmg.2022.104459
    
  
    
    
       
    
  
  
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