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

Melanie Ehrlich

Hayward Human Genetics Program and Tulane Cancer Center

Tulane Health Sciences Center

New Orleans LA



Name/email consistency: high



  • Hayward Human Genetics Program and Tulane Cancer Center, Tulane Health Sciences Center, New Orleans LA, USA. 2013
  • Human Genetics Program, Tulane Medical School, New Orleans, USA. 2001 - 2011


  1. DNA methylation and differentiation: HOX genes in muscle cells. Tsumagari, K., Baribault, C., Terragni, J., Chandra, S., Renshaw, C., Sun, Z., Song, L., Crawford, G.E., Pradhan, S., Lacey, M., Ehrlich, M. Epigenetics. Chromatin (2013) [Pubmed]
  2. Gene expression during normal and FSHD myogenesis. Tsumagari, K., Chang, S.C., Lacey, M., Baribault, C., Chittur, S.V., Sowden, J., Tawil, R., Crawford, G.E., Ehrlich, M. BMC. Med. Genomics (2011) [Pubmed]
  3. ICF, an immunodeficiency syndrome: DNA methyltransferase 3B involvement, chromosome anomalies, and gene dysregulation. Ehrlich, M., Sanchez, C., Shao, C., Nishiyama, R., Kehrl, J., Kuick, R., Kubota, T., Hanash, S.M. Autoimmunity (2008) [Pubmed]
  4. Hybridization analysis of D4Z4 repeat arrays linked to FSHD. Ehrlich, M., Jackson, K., Tsumagari, K., Camaño, P., Lemmers, R.J. Chromosoma (2007) [Pubmed]
  5. Quantitative analysis of associations between DNA hypermethylation, hypomethylation, and DNMT RNA levels in ovarian tumors. Ehrlich, M., Woods, C.B., Yu, M.C., Dubeau, L., Yang, F., Campan, M., Weisenberger, D.J., Long, T., Youn, B., Fiala, E.S., Laird, P.W. Oncogene (2006) [Pubmed]
  6. Immunodeficiency, centromeric region instability, facial anomalies syndrome (ICF). Ehrlich, M., Jackson, K., Weemaes, C. Orphanet J. Rare Diseases (2006) [Pubmed]
  7. Cancer-linked DNA hypomethylation and its relationship to hypermethylation. Ehrlich, M. Curr. Top. Microbiol. Immunol. (2006) [Pubmed]
  8. The controversial denouement of vertebrate DNA methylation research. Ehrlich, M. Biochemistry Mosc. (2005) [Pubmed]
  9. Satellite DNA hypomethylation in karyotyped Wilms tumors. Ehrlich, M., Hopkins, N.E., Jiang, G., Dome, J.S., Yu, M.C., Woods, C.B., Tomlinson, G.E., Chintagumpala, M., Champagne, M., Dillerg, L., Parham, D.M., Sawyer, J. Cancer Genet. Cytogenet. (2003) [Pubmed]
  10. Expression of various genes is controlled by DNA methylation during mammalian development. Ehrlich, M. J. Cell. Biochem. (2003) [Pubmed]
  11. The ICF syndrome, a DNA methyltransferase 3B deficiency and immunodeficiency disease. Ehrlich, M. Clin. Immunol. (2003) [Pubmed]
  12. DNA hypomethylation, cancer, the immunodeficiency, centromeric region instability, facial anomalies syndrome and chromosomal rearrangements. Ehrlich, M. J. Nutr. (2002) [Pubmed]
  13. Hypomethylation and hypermethylation of DNA in Wilms tumors. Ehrlich, M., Jiang, G., Fiala, E., Dome, J.S., Yu, M.C., Long, T.I., Youn, B., Sohn, O.S., Widschwendter, M., Tomlinson, G.E., Chintagumpala, M., Champagne, M., Parham, D., Liang, G., Malik, K., Laird, P.W. Oncogene (2002) [Pubmed]
  14. DNA methyltransferase 3B mutations linked to the ICF syndrome cause dysregulation of lymphogenesis genes. Ehrlich, M., Buchanan, K.L., Tsien, F., Jiang, G., Sun, B., Uicker, W., Weemaes, C.M., Smeets, D., Sperling, K., Belohradsky, B.H., Tommerup, N., Misek, D.E., Rouillard, J.M., Kuick, R., Hanash, S.M. Hum. Mol. Genet. (2001) [Pubmed]
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