All Stories

  1. Incomplete penetrance of CRX gene for autosomal dominant form of cone-rod dystrophy

    Article • Ophthalmic Genetics, May 2019, Taylor & Francis

    Mr Javad Jamshidi, Dr Hamid Ahmadieh

  2. A novel mutation in SMOC1 and variable phenotypic expression in two patients with Waardenburg anophthalmia syndrome

    Article • European Journal of Medical Genetics, November 2017, Elsevier

    Mr Javad Jamshidi

  3. Genetic analysis of SNCA gene polymorphisms in Parkinson’s disease in an Iranian population

    Article • Basal Ganglia, November 2017, Elsevier

    Mr Javad Jamshidi

  4. Support for “Disease-Only” Genotypes and Excess of Homozygosity at the CYTH4 Primate-Specific GTTT-Repeat in Schizophrenia

    Article • Genetic Testing and Molecular Biomarkers, August 2017, Mary Ann Liebert Inc

    Mr Javad Jamshidi

  5. Association of renin–angiotensin–aldosterone system gene polymorphisms with left ventricular hypertrophy in patients with heart failure with preserved ejection fraction: A case–control study

    Article • Clinical and Experimental Hypertension, May 2017, Taylor & Francis

    Mr Javad Jamshidi

  6. A Clinical and Molecular Genetic Study of 50 Families with Autosomal Recessive Parkinsonism Revealed Known and Novel Gene Mutations

    Article • Molecular Neurobiology, May 2017, Springer Science + Business Media

    Mr Javad Jamshidi

  7. Association of β-Secretase Functional Polymorphism with Risk of Schizophrenia

    Article • Genetic Testing and Molecular Biomarkers, April 2017, Mary Ann Liebert Inc

    Dr, Reza Mirfakhraie , Mr Javad Jamshidi

  8. Bioinformatic tools to determine the pathogenicity of a missense mutation in PKHD1 in autosomal recessive polycystic kidney disease

    Article • Nephrology, March 2017, Wiley

    Mr Javad Jamshidi

  9. Omentin Val109Asp polymorphism and risk of coronary artery disease

    Article • Asian Cardiovascular and Thoracic Annals, March 2017, SAGE Publications

    Mr Javad Jamshidi

  10. RAB7L1 promoter polymorphism and risk of Parkinson’s disease; a case-control study

    Article • Neurological Research, February 2017, Taylor & Francis

    Mr Javad Jamshidi

  11. A genetic variant in miRNA binding site of glutamate receptor 4, metabotropic (GRM4) is associated with increased risk of major depressive disorder

    Article • Journal of Affective Disorders, January 2017, Elsevier

    Mr Javad Jamshidi

  12. PTRHD1(C2orf79) mutations lead to autosomal-recessive intellectual disability and parkinsonism

    Article • Movement Disorders, October 2016, Wiley

    Mr Javad Jamshidi

  13. SIPA1L2, MIR4697, GCH1 and VPS13C loci and risk of Parkinson's diseases in Iranian population: A case-control study

    Article • Journal of the Neurological Sciences, October 2016, Elsevier

    Mr Javad Jamshidi

  14. Genetic Analysis of the ZNF512B , SLC41A1, and ALDH2 Polymorphisms in Parkinson's Disease in the Iranian Population

    Article • Genetic Testing and Molecular Biomarkers, October 2016, Mary Ann Liebert Inc

    Mr Javad Jamshidi

  15. SNAP-25 gene variations and attention-deficit hyperactivity disorder in Iranian population

    Article • Neurological Research, September 2016, Taylor & Francis

    Mr Javad Jamshidi

  16. Vitamin D receptor gene rs4334089 polymorphism and Parkinson’s disease in Iranian population

    Article • Basal Ganglia, August 2016, Elsevier

    Mr Javad Jamshidi

  17. A novel mutation and variable phenotypic expression in a large consanguineous pedigree with Jalili syndrome

    Article • Eye, July 2016, Nature

    Mr Javad Jamshidi

  18. Functional Genetic Variants of FOXP3 and Risk of Multiple Sclerosis

    Article • Iranian Red Crescent Medical Journal, May 2016, Kowsar Medical Institute

    Mr Javad Jamshidi

  19. RIT2 Polymorphisms: Is There a Differential Association?

    Article • Molecular Neurobiology, March 2016, Springer Science + Business Media

    Mr Javad Jamshidi

  20. c.376G>A mutation in WFS1 gene causes Wolfram syndrome without deafness

    Article • European Journal of Medical Genetics, February 2016, Elsevier

    Mr Javad Jamshidi

  21. Association of ACE gene D polymorphism with left ventricular hypertrophy in patients with diastolic heart failure: a case–control study

    Article • BMJ Open, February 2016, BMJ

    Mr Javad Jamshidi

  22. The analysis of association between SNCA, HUSEYO and CSMD1 gene variants and Parkinson’s disease in Iranian population

    Article • Neurological Sciences, January 2016, Springer Science + Business Media

    Mr Javad Jamshidi

  23. A genetic variant in CAMKK2 gene is possibly associated with increased risk of bipolar disorder

    Article • Journal of Neural Transmission, September 2015, Springer Science + Business Media

    Mr Javad Jamshidi

  24. Variation in the miRNA-433 binding site of FGF20 is a risk factor for Parkinson's disease in Iranian population

    Article • Journal of the Neurological Sciences, August 2015, Elsevier

    Mr Javad Jamshidi

  25. HLA-DRAis associated with Parkinson's disease in Iranian population

    Article • International Journal of Immunogenetics, October 2014, Wiley

    Mr Javad Jamshidi

  26. Detection of copy number changes in genes associated with Parkinson's disease in Iranian patients

    Article • Neuroscience Letters, September 2013, Elsevier

    Mr Javad Jamshidi

  27. Biased Homozygous Haplotypes Across the Human Caveolin 1 Upstream Purine Complex in Parkinson’s Disease

    Article • Journal of Molecular Neuroscience, May 2013, Springer Science + Business Media

    Mr Javad Jamshidi, Professor Saman Hosseinkhani