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Division of Human Genetics : Department of Internal Medicine : College of Medicine : The Ohio State University
http://internalmedicine.osu.edu/cardiovascular//genetics/9316.cfm

 
Awards and Publications
:: Directory ::
Faculty
Genetic Counselors
Fellows
Research Coordinators
Ilene Comeras, RN, OCN, CCRC
Elizabeth Solinger, BS
Staff

Ilene R. Comeras, RN, OCN, CCRC
Phone:  614-293-6694
Toll free: 1-888-329-1654
Fax: 614-293-2314
Pager: 614-346-5207
Ilene.Comeras@osumc.edu


Awards and Other Professional Activities

2008 – present

President, Columbus Chapter of Oncology Nursing Society (CCONS)

2007 – present

Clinical Research Practice Council Member

2006 and 2007

CCONS President’s award

2006 – 2007

CCONS President Elect

2005 – present

Chair, Community Outreach CCONS.

2004 – present 

Association of Clinical Research Professionals (ACRP)


Publications 

Christopher D. South , Heather Hampel , Ilene Comeras , Judith A. Westman , Wendy L. Frankel , Albert de la Chapelle. The Frequency of Muir-Torre Syndrome Among Lynch Syndrome Families.  J Natl Cancer Inst 2008;100: 277 – 281

 

Heather Hampel, M.Sc., Wendy L. Frankel, M.D., Scott Ramsey, M.D., Ph.D., Lauren Clarke, M.Sc., Edward Martin, M.D., Mark Arnold, M.D., Karamjit Khanduja, M.D., Philip Kuebler, M.D., Ph.D., Mark Clendenning, Ph.D., Kaisa Sotamaa, M.D., Thomas Prior, Ph.D., Judith Westman, M.D., Jenny Panescu, B.Sc., Dan Fix, B.Sc., Janet Lockman, B.Sc., Jennifer LaJeunesse, B.Sc., Ilene Comeras, R.N., and Albert de la Chapelle, M.D., Ph.D.  Feasibility and economic impact of screening for Lynch syndrome among colorectal cancer patients.

  

Pyatt RE, Nakagawa H, Hampel H, Sedra M, Fuchik MB, Comeras I, de la Chapelle A, Prior TW. Identification of a deletion in the mismatch repeair gene, MSH2, using mouse-human cellhybrids monosomal for chromosome 2.  Clin Genet. 2003 Mar;63(3):215-218.

          

Hampel H, Frankel WL, Martin E, Arnold M, Khanduja K, Kuebler P, Nakagawa H, Sotamaa K, Prior TW, Westman J, Panescu J, Fix D, Lockman J, Comeras I, de la Chapelle A. Screening for the Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer). NEJM. 2005 May 5;352(18):1851-1860.

 

Hampel H, Frankel W, Panescu J, Lockman J, Sotamaa K, Fix D, Comeras I, La Jeunesse J, Nakagawa H, Westman JA, Prior TW, Cendenning M, Penzone P, Lombardi J, Dunn P, Cohn DE, Copeland L, Eaton L, Fowler J, Lewandowski G, Vaccarello L, Bell J, Reid G, de la Chapelle A. Screening for Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) among Endometrial Cancer Patients. Cancer Res. 2006; 66(15):7810-7817.

 

Hampel H, Panescu J, Lockman J, Sotamaa K, Fix D, Comeras I, LaJeunesse J, Nakagawa H, Westman JA, Prior TW, Clendenning M, de la Chapelle A, Frankel W, Penzone P, Cohn DE, Copeland L, Eaton L, Fowler J, Lombardi J, Dunn P, Bell J, Reid G, Lewandowski G, Vaccarello L.  Comment on: Screening for Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer) among Endometrial Cancer Patients.  Cancer Res. 2007 Oct 1;67(19):9603.


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