Connection

Nima Rezaei to Genetic Testing

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This is a "connection" page, showing publications Nima Rezaei has written about Genetic Testing.
Nima Rezaei
Connection Strength
0.229
Genetic Testing
  1. 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: 0.140
  2. 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: 0.037
  3. Fourth Update on the Iranian National Registry of Primary Immunodeficiencies: Integration of Molecular Diagnosis. J Clin Immunol. 2018 10; 38(7):816-832.
    View in: PubMed
    Score: 0.036
  4. HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease). Nat Genet. 2007 Jan; 39(1):86-92.
    View in: PubMed
    Score: 0.016
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.