All Stories

  1. The association of renin–angiotensinogen system genes polymorphisms and idiopathic recurrent pregnancy loss

    Article • Human Fertility, October 2017, Taylor & Francis

    Mehri Khatami

  2. Association of MTHFD1, eNOS, CBS and ACE Polymorphisms with CHD

    Article • The Kaohsiung Journal of Medical Sciences, July 2017, Elsevier

    Mehri Khatami

  3. NKX2.5 gene mutations in congenital hypothyroidism

    Article • Journal of Pediatric Endocrinology and Metabolism, January 2017, De Gruyter

    Mehri Khatami

  4. Upregulation of miR-222 in gastric cancer patients

    Article • Journal of Genetics, December 2016, Springer Science + Business Media

    Mehri Khatami

  5. rs5918 (PlA1/A2) polymorphism in the ITGB3 gene and risk of coronary artery disease

    Article • Archives of Medical Science - Atherosclerotic Diseases, January 2016, Termedia Sp. z.o.o.

    Mehri Khatami

  6. Polymorphisms in NOS3, MTHFR, APOB and TNF-α Genes in Coronary Atherosclerotic Lesions

    Article • Research in Cardiovascular Medicine, December 2015, Kowsar Medical Institute

    Mehri Khatami

  7. mitochondrial genome variations in Persian LQTS patients

    Article • Cardiovascular Pathology, March 2010, Elsevier

    Mehri Khatami

  8. Complex I and ATP Content Deficiency in Friedreich's Ataxia

    Article • Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques, January 2009, Cambridge University Press

    Professor Saman Hosseinkhani, Mehri Khatami

  9. trinucleotide CAG repeats of the DNA polymerase gene (POLG) in Friedreich’s ataxia patients

    Article • Neurological Sciences, November 2008, Springer Science + Business Media

    Professor Saman Hosseinkhani, Mehri Khatami

  10. Novel Heteroplasmic C13806A Mutation in Friedreich’s Ataxia

    Article • Cellular and Molecular Neurobiology, September 2008, Springer Science + Business Media

    Professor Saman Hosseinkhani, Mehri Khatami