Baiba Alksere
Overview
    Explore the profile of Baiba Alksere 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
  
  
  Snapshot
          Snapshot
              Articles
              6
            
            
              Citations
              18
            
            
              Followers
              0
            
  
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          Related Specialties
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  Recent Articles
          1.
        
    
    Alksere B, Kornejeva L, Grinfelde I, Dzalbs A, Enkure D, Conka U, et al.
  
  
    Mol Genet Metab Rep
    . 2021 Sep;
          29:100796.
    
    PMID: 34584847
  
  
          Hereditary ectodermal dysplasias are a complex group of inherited disorders characterised by abnormalities in two or more ectodermal derivatives (skin, nails, sweat glands, ). There are two main types of...
      
2.
        
    
    Puzuka A, Alksere B, Gailite L, Erenpreiss J
  
  
    Life (Basel)
    . 2021 Jul;
          11(7).
    
    PMID: 34209597
  
  
          Genome instability may play a role in severe cases of male infertility, with disrupted spermatogenesis being just one manifestation of decreased general health and increased morbidity. Here, we review the...
      
3.
        
    
    Alksere B, Grinfelde I, Kornejeva L, Dzalbs A, Vedmedovska N, Kovalova I, et al.
  
  
    Gynecol Endocrinol
    . 2020 Dec;
          36(sup1):53-57.
    
    PMID: 33305664
  
  
           The aim of this study is to summarize the outcomes of transfers of mosaic embryos, which were classified according to guidelines and in strong collaboration of reproductologists, clinical geneticists and...
      
4.
        
    
    Alksere B, Berzina D, Dudorova A, Conka U, Andersone S, Pimane E, et al.
  
  
    Case Rep Genet
    . 2019 Nov;
          2019:3802613.
    
    PMID: 31781421
  
  
          Male factor infertility accounts for 40-50% of all infertility cases. Deletions of one or more AZF region parts in chromosome Y are one of the most common genetic causes of...
      
5.
        
    
    Fodina V, Dudorova A, Alksere B, Dzalbs A, Vedmedovska N, Andersone S, et al.
  
  
    Gynecol Endocrinol
    . 2019 Sep;
          35(sup1):18-23.
    
    PMID: 31532310
  
  
          The aim of this study was to analyze differences in chromosomal aberrations and euploidy in embryos of each translocation type and gender of carrier in the case series of 10...
      
6.
        
    
    Volozonoka L, Perminov D, Kornejeva L, Alksere B, Novikova N, Pimane E, et al.
  
  
    J Assist Reprod Genet
    . 2018 Apr;
          35(8):1457-1472.
    
    PMID: 29687370
  
  
          Purpose: To compare multiple displacement amplification and OmniPlex whole genome amplification technique performance during array comparative genome hybridization (aCGH), Sanger sequencing, SNaPshot and fragment size analysis downstream applications in frame...