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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Patrick G. Gallagher

Departments of Pediatrics

Yale University School of Medicine

New Haven




Name/email consistency: high



  • Departments of Pediatrics, Yale University School of Medicine, New Haven, Connecticut, USA. 1999 - 2010


  1. Mutation of a barrier insulator in the human ankyrin-1 gene is associated with hereditary spherocytosis. Gallagher, P.G., Steiner, L.A., Liem, R.I., Owen, A.N., Cline, A.P., Seidel, N.E., Garrett, L.J., Bodine, D.M. J. Clin. Invest. (2010) [Pubmed]
  2. Determinants of erythrocyte hydration. Rinehart, J., Gulcicek, E.E., Joiner, C.H., Lifton, R.P., Gallagher, P.G. Curr. Opin. Hematol. (2010) [Pubmed]
  3. An insulator with barrier-element activity promotes alpha-spectrin gene expression in erythroid cells. Gallagher, P.G., Nilson, D.G., Steiner, L.A., Maksimova, Y.D., Lin, J.Y., Bodine, D.M. Blood (2009) [Pubmed]
  4. Erythrocyte disorders in the perinatal period. Steiner, L.A., Gallagher, P.G. Semin. Perinatol. (2007) [Pubmed]
  5. A dinucleotide deletion in the ankyrin promoter alters gene expression, transcription initiation and TFIID complex formation in hereditary spherocytosis. Gallagher, P.G., Nilson, D.G., Wong, C., Weisbein, J.L., Garrett-Beal, L.J., Eber, S.W., Bodine, D.M. Hum. Mol. Genet. (2005) [Pubmed]
  6. GATA-1 and Oct-1 are required for expression of the human alpha-hemoglobin-stabilizing protein gene. Gallagher, P.G., Liem, R.I., Wong, E., Weiss, M.J., Bodine, D.M. J. Biol. Chem. (2005) [Pubmed]
  7. Hematologically important mutations: ankyrin variants in hereditary spherocytosis. Gallagher, P.G. Blood Cells Mol. Dis. (2005) [Pubmed]
  8. Red cell membrane disorders. Gallagher, P.G. Hematology. Am. Soc. Hematol. Educ. Program (2005) [Pubmed]
  9. Mutation of a highly conserved isoleucine disrupts hydrophobic interactions in the alpha beta spectrin self-association binding site. Gallagher, P.G., Zhang, Z., Morrow, J.S., Forget, B.G. Lab. Invest. (2004) [Pubmed]
  10. Update on the clinical spectrum and genetics of red blood cell membrane disorders. Gallagher, P.G. Curr. Hematol. Rep. (2004) [Pubmed]
  11. Altered erythrocyte endothelial adherence and membrane phospholipid asymmetry in hereditary hydrocytosis. Gallagher, P.G., Chang, S.H., Rettig, M.P., Neely, J.E., Hillery, C.A., Smith, B.D., Low, P.S. Blood (2003) [Pubmed]
  12. Regulation of erythrocyte membrane protein gene expression. Gallagher, P.G. Curr. Opin. Hematol. (2003) [Pubmed]
  13. Erythrocyte ankyrin promoter mutations associated with recessive hereditary spherocytosis cause significant abnormalities in ankyrin expression. Gallagher, P.G., Sabatino, D.E., Basseres, D.S., Nilson, D.M., Wong, C., Cline, A.P., Garrett, L.J., Bodine, D.M. J. Biol. Chem. (2001) [Pubmed]
  14. The human ankyrin-1 gene is selectively transcribed in erythroid cell lines despite the presence of a housekeeping-like promoter. Gallagher, P.G., Romana, M., Tse, W.T., Lux, S.E., Forget, B.G. Blood (2000) [Pubmed]
  15. Congenital chylothorax. Dubin, P.J., King, I.N., Gallagher, P.G. Curr. Opin. Pediatr. (2000) [Pubmed]
  16. A recurrent frameshift mutation of the ankyrin gene associated with severe hereditary spherocytosis. Gallagher, P.G., Ferreira, J.D., Costa, F.F., Saad, S.T., Forget, B.G. Br. J. Haematol. (2000) [Pubmed]
  17. A human beta-spectrin gene promoter directs high level expression in erythroid but not muscle or neural cells. Gallagher, P.G., Sabatino, D.E., Romana, M., Cline, A.P., Garrett, L.J., Bodine, D.M., Forget, B.G. J. Biol. Chem. (1999) [Pubmed]
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