All Stories

  1. Micromolar Zinc in Annexin A5 Anticoagulation as a Potential Remedy for RPRGL3-Associated Recurrent Pregnancy Loss

    Article • Reproductive Sciences, May 2018, SAGE Publications

    Dr Arseni Markoff

  2. Lessons From the EThIGII Trial

    Article • Clinical and Applied Thrombosis/Hemostasis, July 2016, SAGE Publications

    Dr Arseni Markoff

  3. Haplotypes and polymorphisms of the ANXA5 nontranslated region in Japanese and European women with recurrent miscarriage and in controls

    Article • Fertility and Sterility, January 2014, Elsevier

    Dr Arseni Markoff

  4. Further insights into the role of the annexin A5 M2 haplotype as recurrent pregnancy loss factor, assessing timing of miscarriage and partner risk

    Article • Fertility and Sterility, November 2013, Elsevier

    Dr Arseni Markoff, Professor Regina Komsa-Penkova

  5. Independent association of the M2/ANXA5 haplotype with recurrent pregnancy loss (RPL) in PCOS patients

    Article • Metabolism, August 2013, Elsevier

    Dr Arseni Markoff

  6. Functional Characterisation of Alpha-Galactosidase A Mutations as a Basis for a New Classification System in Fabry Disease

    Article • PLoS Genetics, August 2013, PLOS

    Dr Arseni Markoff

  7. The haplotype M2 of the ANXA5 gene is not associated with antitrophoblast antibodies

    Article • Journal of Assisted Reproduction and Genetics, March 2013, Springer Science + Business Media

    Dr Arseni Markoff

  8. Hereditary Thrombophilic Risk Factors for Recurrent Pregnancy Loss

    Article • Hereditary Genetics, January 2013, OMICS Publishing Group

    Dr Arseni Markoff

  9. Paternal and maternal carriage of the annexin A5 M2 haplotype are equal risk factors for recurrent pregnancy loss: a pilot study

    Article • Fertility and Sterility, August 2012, Elsevier

    Dr Arseni Markoff

  10. Hereditary thrombophilic risk factors for recurrent pregnancy loss

    Article • Journal of Community Genetics, June 2010, Springer Science + Business Media

    Dr Arseni Markoff

  11. Erratum to: Chromosomal evolution of the PKD1gene family in primates

    Article • BMC Evolutionary Biology, January 2009, Springer Science + Business Media

    Dr Arseni Markoff

  12. Annexin A5 Interacts with Polycystin-1 and Interferes with the Polycystin-1 Stimulated Recruitment of E-cadherin into Adherens Junctions

    Article • Journal of Molecular Biology, June 2007, Elsevier

    Dr Arseni Markoff

  13. Spectrum of molecular defects and mutation detection rate in patients with mild and moderate hemophilia A

    Article • Human Mutation, January 2007, Hindawi Publishing Corporation

    Dr Arseni Markoff

  14. Spectrum of molecular defects and mutation detection rate in patients with severe hemophilia A

    Article • Human Mutation, September 2005, Hindawi Publishing Corporation

    Dr Arseni Markoff

  15. Structural and functional characterisation of the mouse annexin A9 promoter

    Article • Biochimica et Biophysica Acta (BBA) - Molecular Cell Research, December 2004, Elsevier

    Dr Arseni Markoff

  16. Structure and Expression of the Murine Annexin A9 Gene

    Article • Genome Letters, December 2002, American Scientific Publishers

    Dr Arseni Markoff

  17. Prevalence of small rearrangements in the factor VIII gene F8C among patients with severe hemophilia A

    Article • Human Mutation, August 2002, Hindawi Publishing Corporation

    Dr Arseni Markoff

  18. Mutation detection in the duplicated region of the polycystic kidney disease 1 (PKD1) gene in PKD1-linked Australian families

    Article • Human Mutation, February 2002, Hindawi Publishing Corporation

    Dr Arseni Markoff

  19. Autosomal Dominant Polycystic Kidney Disease – Clinical and Genetic Aspects

    Article • Kidney and Blood Pressure Research, January 2002, Karger Publishers

    Dr Arseni Markoff

  20. Homologues to the First Gene for Autosomal Dominant Polycystic Kidney Disease Are Pseudogenes

    Article • Genomics, June 2001, Elsevier

    Dr Arseni Markoff

  21. Seven novel and four recurrent point mutations in the factor VIII (F8C) gene

    Article • Human Mutation, January 2001, Hindawi Publishing Corporation

    Dr Arseni Markoff

  22. Screening the 3? region of the polycystic kidney disease 1 (PKD1) gene in 41 Bulgarian and Australian kindreds reveals a prevalence of protein truncating mutations

    Article • Human Mutation, January 2000, Hindawi Publishing Corporation

    Dr Arseni Markoff

  23. Comparison of conformation-sensitive gel electrophoresis and single-strand conformation polymorphism analysis for detection of mutations in the BRCA1 gene using optimized conformation analysis protocols

    Article • European Journal of Human Genetics, March 1998, Springer Science + Business Media

    Dr Arseni Markoff