Academic Programs

Academic Resources

Admissions

Student Services

About GPS

Alumni

Corporate Partners

800-618-4681 | Request Info
Mobile Menu

Valerie Greger

Valerie Greger
Email: vgreger@brandeis.edu

Degrees:

University of Essen, Ph.D.
University of Heidelberg, M.S.

Courses:

  • RBIF 102
    Genomics and Genetics

Publications:

  • Greger,Valerie, E. Woolf and M. Lalande. "Cloning of the Breakpoints of a Submicroscopic Deletion in an Angelman Syndrome Patient." Human Molecular Genetics (2030): 921-924.
  • Greger,Valerie. "Methodologies Used for Genetic Linkage Discovery." Asthma and Genetic Symposium, 1999.
  • Greger,Valerie. "The Hunt for Asthma Genes." Scandinavian Genetics of Asthma Study
  • Greger,Valerie, J.Knoll, J.Wagstaff, E. Woolf, P.Lieske, H.Glatt, P.Benn, S.Rosengren, M.Lalande. "Angelman Syndrome Associated with an Inversion of Chromosome 15q11.2q24.3." American Journal of Human Genetics (1997): 574-580.
  • Greger,Valerie, J. Knoll, E. Woolf, K.Glatt, R.Tyndale, T.DeLorey , R.Olson, A.Tobin, J.Sikela, Nakats. "The Gamma-amminobutyric Acid Receptor 3 Subunit Gene (GABRG3) is Tightly Linked to the Alpha5 Subunit Gene (GABRA5) on Human Chromosome 15q11-q13 and is Transcribed in the Same Orientation." Genomics (1995): 258-264.
  • Greger,Valerie, A. Reis and M. Lalande. "The Critical Region for Angelman Syndrome Lies Between D15S122 and D15S113." American Journal of Medical Genetics (1994): 396-398.
  • Greger,Valerie, N. Debus, D. Lohmann, W. Hopping, E. Passarge. "Frequency and Parental Origin of Hypermethylated RB1 Alleles in Retinoblastoma." Human Genetics (1994): 491-196.
  • Greger,Valerie, B. Brownstein, R. Mohr, I. Voiculescu, A. Winterpacht, B. Zabel, K. Buiting, B. Horsthemke. A Putative Gene Family in 15q11-13 and 16p11.2: Possible Implications for Prader-Willi and Angleman Syndromes. Proc. of Proceedings of the National Academy of Sciences. 1992.
  • Greger,Valerie, E.Passarge E and B. Horsthemke. "Somatic Mosaicism in a Patient with Bilateral Retinoblastoma." American Journal Human Genetics (1989): 1187-1193.
  • Greger,Valerie, E.Passarge, W. Höpping, E. Messmer, B.Horsthemke. "Epigenetic Changes May Contribute to the Formation and Spontaneous Regression of Retinoblastoma." Human Genetics (1989): 155-158.
  • Greger,Valerie, S.Kerst, E.Messmer, W.Hopping, E.Passarge, B. Horsthemke. "Applicatino of LInkage Analysis to Genetic Counseling in Families with Hereditary Retinblastoma." American Journal of Medical Genetics (1988): 217-221.

Valerie Greger, PhD, has an extensive background in human genetics, molecular biology, and bioinformatics. She has held positions in both academia and the pharmaceutical industry. Working on the interface between life science and informatics has proven to be a very rewarding experience and motivated her to teach in the Bioinformatics Program at GPS.

Next Virtual Open House

Please join us for our next Virtual Open House.  Check out our Admissions Events to see a listing of upcoming program specific Virtual Open Houses, and get connected with program chairs, current students and administrative staff at GPS.

Get Advice

Brandeis GPS is committed to giving our students the help they need to navigate their degree programs. From the moment you begin the application process to the day you receive your degree, our advising staff is there to support you. Schedule a call with an enrollment advisor now.

Request Info