Jennifer LaJeunesse, BS
Phone: 614-293-6694
Fax: 614-293-2314
Jennifer.LaJeunesse@osumc.edu

Publications

Clendenning M., Hampel H.,LaJeunesse J., et al.:  Long-range PCR facilitates the identification of PMS2-specific mutations. Hum Mutat 27(5): 490-495, May 2006.

Hampel H, Frankel WL, Martin E, LaJeunesse J., et al.:  Screening for the Lynch syndrome (Hereditary nonpolyposis colorectal cancer).  New Eng J Med 352(18): 1851-1860, May 2005.

Frankel W.L., Hampel H.,LaJeunesse J., et al.:  Immunohistochemical staining for MLH1, MSH2 and MSH6 identifies germline mutations in mismatch repair genes in colorectal and endometrial cancers initially found to be microsatellite stable. Lab Invest  85:103A-103A 467 Suppl. 1,  Jan 2005.

Hampel H., Frankel W., Panescu J., LaJeunesse J., et al.:  Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients.  Cancer Res 66(15): 7810-7817, Aug 2006.

Alam S., Hampel H., Bloomston A., LaJeunesse J., et al.:  Tissue microarrays provide a cost-effective method for screening colorectal carcinomas for lynch syndrome.  Modern Pathol 20: 107A-107A, Suppl. 2, 2007.

Hampel H, Panescu J, Lockman J, LaJeunesse J., et al.:  Comment on: Screening for lynch syndrome (Hereditary Nonpolyposis colorectal cancer) among endometrial cancer patients. Cancer Res 67(19): 9603-9603, 2007.

Abstracts

Mahooti S., Hampel H.,LaJeunesse J., et al.:  MLH1 and PMS2 protein expression in 103 colorectal carcinomas with MLH1 promoter methylation and without MLH1 or PMS2 germline mutation.  Modern Pathol 19: 113A-113A 512 Suppl. 1, Jan 2006.

Mahooti S., Hampel H.,LaJeunesse J., et al.:  Amsterdam criteria, Bethesda guidelines and histologic findings in 34 patients with hereditary nonpolyposis colorectal cancer.  Lab Invest 86: 113A-113A 513 Suppl. 1, Jan 2006.