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Investigators and Program Directors

Daniel R. Rosen

Research Scientist, Wadsworth Center, Clinical and Experimental Endocrinology and Immunology

Ph.D. Brandeis University
Postdoctoral training, Dana-Farber Cancer Institute, Massachusetts General Hospital,
Harvard Medical School

<< Research Interests

Select Publications

  • "Linkage of hereditary distal myopathy with desmin accumulation to 2q," C.A. Saavedra-Matiz, N.H. Chapman, E.M. Wijsman, S.H. Horowitz, and D.R. Rosen (2000), Human Heredity 50: 166-170
  • "A missense mutation in the desmin rod domain is associated with autosomal dominant distal myopathy and exerts a dominant negative effect on filament formation," G. Sjoberg, C.A. Saavedra-Matiz, D.R. Rosen, E.M. Wijsman, K. Borg, S.H. Horowitz, and T. Sejersen (1999), Human Molecular Genetics 8: 2191-2198
  • "An atypical intronic deletion widens the spectrum of mutations in hereditary spastic paraplegia," J.J. Higgins, J.M. Loveless, S. Goswami, L.E. Nee, C. Cozzo, A. De Biase, and D.R. Rosen (2001), eurology 56: 1482-1485
  • Rosen, D.R., Bowling, A.C., Patterson, D., Usdin, T.B., Sapp, P., Mezey, E., McKenna-Yasek, D., O'Regan, J., Rahmani, Z., Ferrante, R.J., Brownstein, M.J., Kowall, N.W., Beal, M.F., Horvitz, H.R. and Brown, R.H., Jr. (1994) A Frequent Ala 4 to Val superoxide dismutase-1 mutation is assocaited with rapidly progressive familial amyotrophic lateral Sclerosis. Human Molecular Genetics 3:981-987.
  • Rosen, D.R., Snapp, P., O'Regan, J., McKenna-Yasek, D., Schlumpf, K.S., Haines, J., Gusella, J., Horvitz, H.R. and Brown, R.H., Jr. (1994) Genetic linkage analysis of familial ALS using human chromosome 21 microsatellite DNA markers. American Journal of Medical Genetics 51:61-69.
  • Rosen, D.R., Siddique, T., Patterson, D., Figlewicz, D.A., Sapp, P., Hentati, A., Donaldson, D., Goto, J., O'Regan, J.P., Deng, H-X., Rahmani, Z., Krizus, A., McKenna-Yasek, D., Cayabyab, A., Gaston, S., Tanzi, R., Halperin, J.J., Herzfeldt, B., Van den Berg,R., Hung, W-Y., Bird, T., Deng, G., Mulder, D.W., Smith, C., Laing, N.G., Soriano, E., Pericak-Vance, M.A., Haines,J., Rouleau, G.A., Gusella, J., Horvitz, H.R. and Brown, R.H., Jr. (1993) Familial amyotrophic lateral sclerosis is associated with mutations in Cu/Zn superoxide dismutase. Nature 362:59-62.

Contact Information

E-mail: rosen@wadsworth.org.