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Connection

Paul Norman to Complement C4

This is a "connection" page, showing publications Paul Norman has written about Complement C4.

 
Connection Strength
 
 
 
0.758
 
  1. Norman PJ, Norberg SJ, Guethlein LA, Nemat-Gorgani N, Royce T, Wroblewski EE, Dunn T, Mann T, Alicata C, Hollenbach JA, Chang W, Shults Won M, Gunderson KL, Abi-Rached L, Ronaghi M, Parham P. Sequences of 95 human MHC haplotypes reveal extreme coding variation in genes other than highly polymorphic HLA class I and II. Genome Res. 2017 05; 27(5):813-823.
    View in: PubMed
    Score: 0.529
  2. Williams J, Marin WM, Wade KJ, Suseno R, Kizer K, Caillier S, Augusto DG, Norman PJ, Hollenbach JA. Copy number variation at the complement C4 locus is associated with risk for multiple sclerosis. Mult Scler. 2025 Sep; 31(10):1243-1246.
    View in: PubMed
    Score: 0.229
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.

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