Connection

BENJAMIN SHNEIDER to Genotype

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

0.140
  1. Recurrent low gamma-glutamyl transpeptidase cholestasis following liver transplantation for bile salt export pump (BSEP) disease (posttransplant recurrent BSEP disease). Liver Transpl. 2010 Jul; 16(7):856-63.
    View in: PubMed
    Score: 0.057
  2. Liver transplantation for progressive familial intrahepatic cholestasis: the evolving role of genotyping. Liver Transpl. 2009 Jun; 15(6):565-6.
    View in: PubMed
    Score: 0.053
  3. Severe bile salt export pump deficiency: 82 different ABCB11 mutations in 109 families. Gastroenterology. 2008 Apr; 134(4):1203-14.
    View in: PubMed
    Score: 0.012
  4. Inhibition of human m-epoxide hydrolase gene expression in a case of hypercholanemia. Biochim Biophys Acta. 2003 Jul 30; 1638(3):208-16.
    View in: PubMed
    Score: 0.009
  5. Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT. Nat Genet. 2003 May; 34(1):91-6.
    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.