Connection

Nima Rezaei to Phenotype

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

0.451
  1. Clinical Manifestations, Immunological Characteristics and Genetic Analysis of Patients with Hyper-Immunoglobulin M Syndrome in Iran. Int Arch Allergy Immunol. 2019; 180(1):52-63.
    View in: PubMed
    Score: 0.087
  2. Congenital neutropenia and primary immunodeficiency diseases. Crit Rev Oncol Hematol. 2019 Jan; 133:149-162.
    View in: PubMed
    Score: 0.083
  3. Association analysis of RAC1 single nucleotide polymorphisms with ulcerative colitis. Clin Res Hepatol Gastroenterol. 2017 09; 41(4):487-489.
    View in: PubMed
    Score: 0.075
  4. Interleukin-4 cytokine single nucleotide polymorphisms in kawasaki disease: a case-control study and a review of knowledge. Int J Rheum Dis. 2018 Jan; 21(1):266-270.
    View in: PubMed
    Score: 0.074
  5. Clinical implications of systematic phenotyping and exome sequencing in patients with primary antibody deficiency. Genet Med. 2019 01; 21(1):243-251.
    View in: PubMed
    Score: 0.020
  6. Ataxia telangiectasia syndrome: moonlighting ATM. Expert Rev Clin Immunol. 2017 12; 13(12):1155-1172.
    View in: PubMed
    Score: 0.019
  7. Clinical, immunologic, and genetic spectrum of 696 patients with combined immunodeficiency. J Allergy Clin Immunol. 2018 04; 141(4):1450-1458.
    View in: PubMed
    Score: 0.019
  8. 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: 0.019
  9. 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: 0.019
  10. The phenotype of human STK4 deficiency. Blood. 2012 Apr 12; 119(15):3450-7.
    View in: PubMed
    Score: 0.013
  11. Cytologic phenotypes of B-cell acute lymphoblastic leukemia-a single center study. Iran J Allergy Asthma Immunol. 2009 Jun; 8(2):99-106.
    View in: PubMed
    Score: 0.011
  12. 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: 0.010
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.