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

Robert P. Erickson

Department of Pediatrics

University of Arizona


Arizona; Department of Molecular and Cellular Biology



Name/email consistency: high



  • Department of Pediatrics, University of Arizona, Tucson, Arizona; Department of Molecular and Cellular Biology, Arizona. 2011
  • Department of Pediatrics, University of Arizona College of Medicine, Tucson, Arizona 85724-5073, USA. 2001 - 2010
  • Angel Charity for Children-Wings for Genetic Research, Steele Memorial Children's Research Center, Department of Pediatrics, University of Arizona College of Medicine, USA. 1998 - 2003
  • Department of Pediatrics, Section of Medical and Molecular Genetics, Angel Charity for Children-Wings for Genetic Research, Steele Memorial Children's Research Center, USA. 2002


  1. Insulin receptor-related (Irr) is expressed in pre-implantation embryos: A possible relationship to "growth factor Y" and sex determination. Erickson, R.P., Strnatka, D. Mol. Reprod. Dev. (2011) [Pubmed]
  2. Genes, environment, and orofacial clefting: N-acetyltransferase and folic acid. Erickson, R.P. J. Craniofac. Surg (2010) [Pubmed]
  3. Autosomal recessive diseases among the Athabaskans of the southwestern United States: recent advances and implications for the future. Erickson, R.P. Am. J. Med. Genet. A (2009) [Pubmed]
  4. Variation in NPC1, the gene encoding Niemann-Pick C1, a protein involved in intracellular cholesterol transport, is associated with Alzheimer disease and/or aging in the Polish population. Erickson, R.P., Larson-Thomé, K., Weberg, L., Szybinska, A., Mossakowska, M., Styczynska, M., Barcikowska, M., Kuznicki, J. Neurosci. Lett. (2008) [Pubmed]
  5. Confirmation of the role of N-acetyltransferase 2 in teratogen-induced cleft palate using transgenics and knockouts. Erickson, R.P., Cao, W., Acuña, D.K., Strnatka, D.W., Hunter, R.J., Chau, B.T., Wakefield, L.V., Sim, E., McQueen, C.A. Mol. Reprod. Dev. (2008) [Pubmed]
  6. An N-ethyl-N-nitrosourea-induced mutation in N-acetyltransferase 1 in mice. Erickson, R.P., McQueen, C.A., Chau, B., Gokhale, V., Uchiyama, M., Toyoda, A., Ejima, F., Maho, N., Sakaki, Y., Gondo, Y. Biochem. Biophys. Res. Commun. (2008) [Pubmed]
  7. Navajo microvillous inclusion disease is due to a mutation in MYO5B. Erickson, R.P., Larson-Thomé, K., Valenzuela, R.K., Whitaker, S.E., Shub, M.D. Am. J. Med. Genet. A (2008) [Pubmed]
  8. A new chromosome anomaly in a patient with apparent C (trigonocephaly) syndrome. Erickson, R.P. Am. J. Med. Genet. A (2007) [Pubmed]
  9. Oro-facial-digital syndrome IX with severe microcephaly: a new variant in a genetically isolated population. Erickson, R.P., Bodensteiner, J.B. Am. J. Med. Genet. A (2007) [Pubmed]
  10. A patient with 22q11.2 deletion and Opitz syndrome-like phenotype has the same deletion as velocardiofacial patients. Erickson, R.P., de Ståhl, T.D., Bruder, C.E., Dumanski, J.P. Am. J. Med. Genet. A (2007) [Pubmed]
  11. Agenesis of tibia with bifid femur, congenital heart disease, and cleft lip with cleft palate or tracheoesophageal fistula: possible variants of Gollop-Wolfgang complex. Erickson, R.P. Am. J. Med. Genet. A (2005) [Pubmed]
  12. Liver disease with altered bile acid transport in Niemann-Pick C mice on a high-fat, 1% cholesterol diet. Erickson, R.P., Bhattacharyya, A., Hunter, R.J., Heidenreich, R.A., Cherrington, N.J. Am. J. Physiol. Gastrointest. Liver Physiol. (2005) [Pubmed]
  13. Correlation of susceptibility to 6-aminonicotinamide and hydrocortisone-induced cleft palate. Erickson, R.P., Karolyi, I.J., Diehl, S.R. Life Sci. (2005) [Pubmed]
  14. Somatic gene mutation and human disease other than cancer. Erickson, R.P. Mutat. Res. (2003) [Pubmed]
  15. Does chromosome 22 have anything to do with sex determination: further studies on a 46,XX,22q11.2 del male. Erickson, R.P., Skinner, S., Jacquet, H., Campion, D., Buckley, P.G., Mantripragada, K.K., Dumanski, J.P. Am. J. Med. Genet. A (2003) [Pubmed]
  16. mdr1a deficiency corrects sterility in Niemann-Pick C1 protein deficient female mice. Erickson, R.P., Kiela, M., Devine, P.J., Hoyer, P.B., Heidenreich, R.A. Mol. Reprod. Dev. (2002) [Pubmed]
  17. Genetic variation in beta-adrenergic receptors and their relationship to susceptibility for asthma and therapeutic response. Erickson, R.P., Graves, P.E. Drug Metab. Dispos. (2001) [Pubmed]
  18. Cholesterol signaling at the endoplasmic reticulum occurs in npc1(-/-) but not in npc1(-/-), LDLR(-/-) mice. Erickson, R.P., Kiela, M., Garver, W.S., Krishnan, K., Heidenreich, R.A. Biochem. Biophys. Res. Commun. (2001) [Pubmed]
  19. Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutations. Erickson, R.P., Dagenais, S.L., Caulder, M.S., Downs, C.A., Herman, G., Jones, M.C., Kerstjens-Frederikse, W.S., Lidral, A.C., McDonald, M., Nelson, C.C., Witte, M., Glover, T.W. J. Med. Genet. (2001) [Pubmed]
  20. Forkhead genes and human disease. Erickson, R.P. J. Appl. Genet. (2001) [Pubmed]
  21. Southwestern Athabaskan (Navajo and Apache) genetic diseases. Erickson, R.P. Genet. Med. (1999) [Pubmed]
  22. From "magic bullet" to "specially engineered shotgun loads": the new genetics and the need for individualized pharmacotherapy. Erickson, R.P. Bioessays (1998) [Pubmed]
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