Connection

Nima Rezaei to Pedigree

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This is a "connection" page, showing publications Nima Rezaei has written about Pedigree.
Nima Rezaei
Connection Strength
0.108
Pedigree
  1. A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity. Sci Immunol. 2018 06 15; 3(24).
    View in: PubMed
    Score: 0.041
  2. The phenotype of human STK4 deficiency. Blood. 2012 Apr 12; 119(15):3450-7.
    View in: PubMed
    Score: 0.026
  3. A homozygous CARD9 mutation in a family with susceptibility to fungal infections. N Engl J Med. 2009 Oct 29; 361(18):1727-35.
    View in: PubMed
    Score: 0.023
  4. HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease). Nat Genet. 2007 Jan; 39(1):86-92.
    View in: PubMed
    Score: 0.018
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.