Leigha Senter, MS, CGC
Phone: 614-293-6694
Fax: 614-293-2314
leigha.senter@osumc.edu

Select Publications

1.    Clendenning M, Hampel H, LaJeunesse J, Lindblom A, Lockman J, Nilbert M, Senter L, Sotamaa K, and de la Chapelle A.  Long-Range PCR Facilitates the Identification of PMS2-Specific Mutations.  Human Mutation 27(5): 490-495, 2006.

2.    Gururangan S, Frankel W, Broaddus R, Clendenning M, Senter L, McDonald M, Eastwood J, Reardon D, Vredenburgh J, Quinn J, and Friedman H.  Multi-focal anaplastic astrocytoma in a patient with hereditary colorectal cancer, transcobalamin II deficiency, agenesis of the corpus callosum, mental retardation, and inherited PMS-2 mutation.  (Accepted for publication 11/2006 in Neuro-Oncology). 

3.    Kelly, K., Senter, L., Leventhal, H., Ozakinci, G., Porter, K. Subjective and objective risk of ovarian cancer in women at risk to carry mutations in BRCA1 and BRCA2. (2007, in press).  Patient Education and Counseling.

4.    Carl-Christian Jackson, MD, Spring Holter, MSc, Aaron Pollett, MD, Albert de la Chapelle, MD, PhD, Mark Clendenning, PhD, Shirley Chou, MD, MSc Leigha Senter, MS, Raveena Ramphal, MD, Steven Gallinger, MD, MSc, Kym Boycott, MD, PhD.  Café-au-lait macules and pediatric malignancy with recessively inherited mutations in the DNA mismatch repair (MMR) gene PMS2: Case report and review of the literature.  (Accepted to Pediatric Blood and Cancer).