E Blennow
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    Explore the profile of E Blennow including associated specialties, affiliations and a list of published articles.
          
  Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
  
  
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          Snapshot
              Articles
              62
            
            
              Citations
              652
            
            
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          Related Specialties
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  Recent Articles
          1.
        
    
    Haapaniemi Kouru K, Malmgren H, Nordenskjold M, Fridstrom M, Csemiczky G, Blennow E
  
  
    Hum Reprod
    . 2012 Jun;
          27(9):2843-9.
    
    PMID: 22736325
  
  
          Study Question: What are the significant factors that influence the outcome of a PGD treatment? Summary Answer: The age of the woman and the number of biopsied cells per embryo...
      
2.
        
    
    Zachariadis V, Gauffin F, Kuchinskaya E, Heyman M, Schoumans J, Blennow E, et al.
  
  
    Leukemia
    . 2011 Jan;
          25(4):622-8.
    
    PMID: 21242996
  
  
          The dic(9;20)(p13.2;q11.2) is reported to be present in ∼2% of childhood B-cell precursor acute lymphoblastic leukemia (BCP ALL). However, it easily escapes detection by G-banding analysis and its true prevalence...
      
3.
        
    
    Iwarsson E, Malmgren H, Blennow E
  
  
    Semin Fetal Neonatal Med
    . 2010 Dec;
          16(2):74-80.
    
    PMID: 21176890
  
  
          More than two decades after the first clinical application, preimplantation genetic diagnosis (PGD) is an established medical procedure and an accepted alternative to conventional prenatal diagnosis for patients at high...
      
4.
        
    
    Lindstrand A, Schoumans J, Gustavsson P, Hanemaaijer N, Malmgren H, Blennow E
  
  
    Clin Genet
    . 2010 Mar;
          77(6):552-62.
    
    PMID: 20236111
  
  
          Array-CGH is a powerful tool for the rapid detection of genomic imbalances. By customizing the array it is possible to increase the resolution in a targeted genomic region of interest...
      
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    Lindstrand A, Malmgren H, Sahlen S, Schoumans J, Nordgren A, Ergander U, et al.
  
  
    Clin Genet
    . 2009 Oct;
          77(2):145-54.
    
    PMID: 19863549
  
  
          We have investigated three patients with 21q deletions, two with developmental delay, dysmorphic features and internal organ malformations, and one with cognitive function within the normal range but with some...
      
6.
        
    
    Lindstrand A, Malmgren H, Sahlen S, Xin H, Schoumans J, Blennow E
  
  
    Am J Med Genet A
    . 2008 Nov;
          146A(24):3217-22.
    
    PMID: 19006217
  
  
          No abstract available.
      
7.
        
    
    Blennow E, Lagerstedt K, Malmgren H, Sahlen S, Schoumans J, Anderlid B
  
  
    Clin Genet
    . 2008 May;
          74(1):61-7.
    
    PMID: 18445048
  
  
          Microduplication of 22q11.2 has been reported in fewer than 40 cases, all of them including the DiGeorge critical region (DGCR). We here present the characterization of a new duplication that...
      
8.
        
    
    Kuchinskaya E, Nordgren A, Heyman M, Schoumans J, Corcoran M, Staaf J, et al.
  
  
    Leukemia
    . 2007 Feb;
          21(6):1327-30.
    
    PMID: 17315016
  
  
          No abstract available.
      
9.
        
    
    Imreh M, Gertow K, Cedervall J, Unger C, Holmberg K, Szoke K, et al.
  
  
    J Cell Biochem
    . 2006 Apr;
          99(2):508-16.
    
    PMID: 16622834
  
  
          Previous studies in several laboratories have demonstrated inadvertent chromosomal abnormalities in long-term cultured human embryonic stem cells (HESC). Here, using a two-step selection process we report a functional adaptation of...
      
10.
        
    
    Kuchinskaya E, Heyman M, Grander D, Linderholm M, Soderhall S, Zaritskey A, et al.
  
  
    Eur J Haematol
    . 2005 May;
          74(6):466-80.
    
    PMID: 15876250
  
  
          Objectives: To compare the gene expression pattern in children and adults with acute lymphoblastic leukaemia (ALL) in order to improve our understanding of the difference in disease biology and prognosis....