Connection

Nima Rezaei to Genotype

This is a "connection" page, showing publications Nima Rezaei has written about Genotype.
Connection Strength

1.601
  1. Interleukin-4 and Interleukin-4 Receptor Alpha Gene Polymorphisms in Recurrent Aphthous Stomatitis. Immunol Invest. 2018 Oct; 47(7):680-688.
    View in: PubMed
    Score: 0.309
  2. Single Nucleotide Polymorphisms of PTPN22 Gene in Iranian Patients with Ulcerative Colitis. Fetal Pediatr Pathol. 2019 Feb; 38(1):8-13.
    View in: PubMed
    Score: 0.080
  3. Association of Interleukin-6 and Interleukin-1 Family Gene Polymorphisms in Autoimmune Hepatitis. Ann Hepatol. 2018 10 16; 17(6):1021-1025.
    View in: PubMed
    Score: 0.079
  4. Association of nod-like receptor protein-3 single nucleotide gene polymorphisms and expression with the susceptibility to relapsing-remitting multiple sclerosis. Int J Immunogenet. 2018 Dec; 45(6):329-336.
    View in: PubMed
    Score: 0.078
  5. Autosomal dominant deficiency of the interleukin-17F in recurrent aphthous stomatitis: Possible novel mutation in a new entity. Gene. 2018 May 15; 654:64-68.
    View in: PubMed
    Score: 0.075
  6. Association of interferon regulatory factor 5 (IRF5) gene polymorphisms with juvenile idiopathic arthritis. Clin Rheumatol. 2018 Oct; 37(10):2661-2665.
    View in: PubMed
    Score: 0.075
  7. Single nucleotide polymorphism of Methyl-CpG-binding protein 2 gene associates with juvenile idiopathic arthritis. Clin Rheumatol. 2018 Feb; 37(2):375-381.
    View in: PubMed
    Score: 0.075
  8. Association Study of MECP2 Gene Single Nucleotide Polymorphisms in Juvenile-Onset Systemic Lupus Erythematosus Patients from Iran. Fetal Pediatr Pathol. 2017 Dec; 36(6):423-431.
    View in: PubMed
    Score: 0.074
  9. Association of Transforming Growth Factor-Beta Gene Polymorphisms in Recurrent Aphthous Stomatitis. Acta Med Iran. 2017 Nov; 55(11):672-675.
    View in: PubMed
    Score: 0.074
  10. PDCD1 Single Nucleotide Polymorphisms in Iranian Patients With Juvenile Idiopathic Arthritis. Acta Med Iran. 2017 Nov; 55(11):676-682.
    View in: PubMed
    Score: 0.074
  11. Interleukin-4 and Interleukin-10 Gene Polymorphisms in Patients with Inflammatory Bowel Disease. Immunol Invest. 2017 Oct; 46(7):714-729.
    View in: PubMed
    Score: 0.073
  12. Association of the Single Nucleotide Polymorphisms of the Genes Encoding IL-2 and IFN-? With Febrile Seizure. Acta Med Iran. 2017 Jun; 55(6):354-359.
    View in: PubMed
    Score: 0.072
  13. Association analysis of RAC1 single nucleotide polymorphisms with ulcerative colitis. Clin Res Hepatol Gastroenterol. 2017 09; 41(4):487-489.
    View in: PubMed
    Score: 0.071
  14. PTPN22 Single-Nucleotide Polymorphisms in Iranian Patients with Type 1 Diabetes Mellitus. Immunol Invest. 2017 May; 46(4):409-418.
    View in: PubMed
    Score: 0.071
  15. Lack of Association between STAT4 Single Nucleotide Polymorphisms and Iranian Juvenile Rheumatoid Arthritis Patients. Fetal Pediatr Pathol. 2017 Jun; 36(3):177-183.
    View in: PubMed
    Score: 0.070
  16. Interleukin-2, Interferon-gamma Gene Polymorphisms in Recurrent Aphthous Stomatitis. Prague Med Rep. 2017; 118(2-3):81-86.
    View in: PubMed
    Score: 0.070
  17. Association of STAT4 gene single nucleotide polymorphisms with Iranian juvenile-onset systemic lupus erythematosus patients. Turk J Pediatr. 2017; 59(2):144-149.
    View in: PubMed
    Score: 0.070
  18. STAT4 single nucleotide gene polymorphisms and susceptibility to endometriosis-related infertility. Eur J Obstet Gynecol Reprod Biol. 2016 Aug; 203:20-4.
    View in: PubMed
    Score: 0.067
  19. Expanding the mutational spectrum in Johanson-Blizzard syndrome: identification of whole exon deletions and duplications in the UBR1 gene by multiplex ligation-dependent probe amplification analysis. Mol Genet Genomic Med. 2017 11; 5(6):774-780.
    View in: PubMed
    Score: 0.018
  20. Clinical, immunologic, molecular analyses and outcomes of iranian patients with LRBA deficiency: A longitudinal study. Pediatr Allergy Immunol. 2017 08; 28(5):478-484.
    View in: PubMed
    Score: 0.018
  21. Novel HAX1 mutations in patients with severe congenital neutropenia reveal isoform-dependent genotype-phenotype associations. Blood. 2008 May 15; 111(10):4954-7.
    View in: PubMed
    Score: 0.009
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.