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2001 Polaris Pkwy
Columbus, OH 43240

Phone: (614) 293-5376

Email: sweet.48@osu.edu

 

Current OSU Appointment

Associate Professor-Clinical, Human Genetics

 

Noteworthy Graduate Narrative

As Chair, Jane Engelberg Memorial Fellowship, the primary grant award agency for the National Society of Genetic Counselors, I oversaw development of the "JEMF Graduate Student Award Program" which has since become an annual grant award provided to Genetic Counselor graduate students. Applicants must submit a formal research proposal, which is reviewed and ranked by the JEMF Committee. The award supports ongoing work as part of their graduate thesis project. During my tenure as Chair, we provided awards to 18 graduate students, of which 16 recipients subsequently published their thesis work.

Civic Engagement

Team Leader and 100-Mile Pelotonia Rider (2009-2014), Stefanie's Team of Hope - the largest non-corporate Peloton

Clinical Interest

Genetics, Personalized Medicine

Biographical

My research activity has centered on gene discovery and the study of hereditary cancer and application in the clinical setting to include development of family history risk assessment tools. My work in hereditary cancer syndromes includes establishment in 2002 of ongoing collaboration with investigators at the University of Toronto on hereditary breast-ovarian cancer syndrome (Prospective Carrier Epidemiology study), which, in 2007 extended into a worldwide genetic modifier consortium (CIMBA: Consortium of Investigators of Modifiers of BRCA). Given lack of study on the condition of hyperplastic (serrated) polyposis, upon travel to the University of Brisbane, I was able to establish ongoing collaboration and gene hunting study with local investigators which has become the largest collaborative effort on this rare condition in the world. Through work on family history tools for patient care, our Division has obtained a national reputation and is making inroads into informing public policy. Initially, this work involved development of the JamesLink program, with more than 10,000 patient and general public users. In 2008, I launched Family HealthLink, an automated cancer and coronary heart disease triage tool. Clinical implementation of Family HealthLink® has occurred at the Stefanie Spielman Comprehensive Breast Center. Family HealthLink® has been listed as a general public resource for family history tools on the National Human Genome Research Institute website, and other governmental websites (e.g. U.S. Department of Health and Human Services). In June 2009, it was promoted through a Wall Street Journal article “The Life-Saving Secrets in Your Family Tree”, and has also been advertised on WOSU radio on a number of occasions as well as other local media outlets (i.e. local TV news affiliates). Since appointment to Associate Professor in 2010, and given the need for expansion of personalized genomic medicine initiatives at the Medical Center, I’ve led efforts to establish the OSUWMC-Coriell Personalized Medicine Research Collaborative, a randomized study to evaluate the impact of genomic counseling for common complex disease and pharmacogenomics. This work allowed for genomic data integration into the OSUWMC electronic medical record for patient care purpose, and development of processes for more extensive implementation of genomic data into the physician workflow. Moving forward, these efforts are in part supported through my work as PI on the NIH/NHGRI R21 funded study “Assessing the Utility of Genomic Counseling for Common Complex Disease” and as co-Investigator on the NIH/NIGMS funded Translational Pharmacogenomics Project. In particular, for the R21 work, I approached this as a consortium of investigators from the University of Michigan and the Coriell Medical Institute, which also includes a team of experts in the field of genetic/genomic counseling from Stanford University, University of North Carolina – Chapel Hill, and the University of Pennsylvania. The ongoing collaborative and multi-institutional effort will allow for application for R01 level funding in 2015. More recently, working with colleagues in our Division, we are in process of implementing the “Genomic Medicine Initiative” through our clinical programs. I've also been actively involved with internal and external genomics education. I was a founding member and Chair, National Society of Genetic Counselors (NSGC) Personalized Medicine - Special Interest Group, a core driver for genomics education and development of applications/tools to support the professional genetic counseling community. I served as Chair, Jane Engelberg Memorial Fellowship, the primary grant support mechanism of the NSGC, and currently serve on the Society’s Practice Guidelines Committee. In recent years, I authored two books on precision genomic medicine; one for medical professionals: “The Busy Physician’s Guide to Genetics, Genomics and Personalized Health Care”; the second for the lay public: “Your Genes, Your Health and Personalized Medicine”.

Academic Advising

2014 - present Wernke, Karen The Ohio State University.
2014 - present McFaden, Andrew The Ohio State University.
 

Books

Sweet K, Phelan M, Tarleton J, Crawford E, Christensen B, Schroer R, Taylor H. Counseling Aids for Geneticists. Greenwood: Greenwood Genetic Center, January 1995.

Saul RA, Phelan MC, Geer JS, Seaver LH, Sweet KM. Growth References: Third Trimester to Adulthood. Greenwood: Greenwood Genetic Center, January 1998.

Sweet, Kevin M; Michaelis, Ron C. The Busy Physician's Guide to Genetics, Genomics and Personalized Medicine. Dordrecht; New York: Springer, January 2011.

Michaelis, R. and Sweet, K.. Your Genes, Your Health and Personalised Medicine. Oxford, GB|GBR: Nottingham University Press, August 2012.

 

Certifications

2013 - present Licensed Genetic Counselor: Ohio Board of Medical Examiners
 

Chapters in Books

Teh BT, Sweet K, Morrison CD. "Hyperparathyroidism - Jaw Tumour Syndrome." In Pathology and Genetics of Tumours of Endocrine Organs (WHO Classification of Tumours of Endocrine Organs). Edited by DeLellis RA, Lloyd RV, Heitz PU, Eng C. 228-229. Lyon, FR|FRA: IARC Press, January 2004.

Gimm O, Komminoth P, Morrison CD, Mulligan L, Suster S, Sweet K. "Multiple Endocrine Neoplasia Type 2 (MEN 2)." In Pathology and Genetics of Tumours of Endocrine Organs (WHO Classification of Tumours of Endocrine Organs). Edited by DeLellis RA, Lloyd RV, Heitz PU, Eng C. 211-217. Lyon, FR|FRA: IARC Press, January 2004.

Calender A, Scoazec JY, Morrison CD, Sweet K, Komminoth P, Teh BT. "Multliple Endocrine Neoplasia Type 1 (MEN 1)." In Pathology and Genetics of Tumours of Endocrine Organs (WHO Classification of Tumours of Endocrine Organs). Edited by DeLellis RA, Lloyd RV, Heitz PU, Eng C. 218-227. Lyon, France: IARC Press, January 2004.

 

Clinical Services

08/01/1999 Division of Human Genetics (OSUMC Clinic Locations)
09/01/2007 Director, Family HealthLink Cancer and Coronary Heart Disease Risk Assessment Program (https://familyhealthlink.osumc.edu)
03/01/2011 Division of Human Genetics (Stefanie Spielman Comprehensive Breast Center)
03/01/2011 - 03/01/2013 OSUMC Center for Personalized Health Care (McCampbell Hall)

Degrees

1988 B.S., University of Wisconsin

1994 M.S., Sarah Lawrence College

 

Editorial Activities

2004 - present American Association for Cancer Research
2004 - 2006 Clinical Genetics
2005 - present Journal of Clinical Oncology
2005 - present Journal of Medical Genetics
2005 - present Journal of Genetic Counseling
2011 - present Genetics in Medicine
2011 - present Personalized Medicine
2012 - present PLOS
2012 - present Gynecologic Oncology
2013 - present British Medical Practice
2013 - present British Medical Journal
 

Journal Articles

Zhang Y, Sweet KM, Sognier MA, Belli JA. "Interaction between radiation and drug damage in mammalian cells. VI. Radiation and doxorubicin age-response function of doxorubicin-sensitive and -resistant Chinese hamster cells.." Radiation Research. Vol. 132, no. 1. (January 1992.): 105-111.

Zhang Y, Sweet K, Belli J. "An enhanced ability for transforming adriamycin into noncytotoxic form in a multidrug resistant cell line (LZ-8)." Biochem Pharmacol. Vol. 44, no. 9. (January 1992.): 1869-1877.

Sognier MA, Zhang Y, Eberle RL, Sweet KM, Altenberg GA, Belli JA. "Sequestration of doxorubicin in vesicles in a multidrug-resistant cell line (LZ-100).." Biochemical Pharmacology. Vol. 48, no. 2. (January 1994.): 391-401.

Sweet K, Seaver L. "Family with autosomal dominant distal arthrogryposis, ophthalmoplegia and elbow dislocation: extending the spectrum." Proc Greenwood Genet Center. Vol. 17, (January 1998.): 13-19.

Sweet K, Seaver L. "Autosomal dominant transmission of anodontia." Proc Greenwood Genet Center. Vol. 18, (January 1999.): 42-46.

Phelan M, Rogers R, Saul R, Sweet K, Anderson G. "A review of the 22q13.3 deletion syndrome." Proc Greenwood Genet Center. Vol. 19, (January 2000.): 35-43.

Sweet K, Martin E, Eng C, and Shah M. "Familial basal cell carcinoma, melanoma and skin hypersensitivity with GIST: a new hereditary neuroendocrine syndrome involving the SCF/KIT pathway?." J Endocrin Genet. Vol. 2, no. 3. (January 2001.): 161-167.

Phelan MC, Rogers RC, Saul RA, Stapleton GA, Sweet K, McDermid H, Shaw SR, Claytor J, Willis J, Kelly DP. "22q13 deletion syndrome.." Am J Med Genet. Vol. 101, no. 2. (January 2001.): 91-99.

Sweet K, Bradley T, Westman J. "Identification and referral of families at high risk for cancer susceptibility." J Clin Oncol. Vol. 20, no. 2. (January 2002.): 528-537.

Sweet K, Willis S, Asida S, Westman JA. "Use of fear appeal techniques in the design of tailored cancer risk communication messages: implications for health care providers." J Clin Oncol. Vol. 21, no. 18. (October 2003.): 528-537.

Lynch HT, Coronel SM, Okimoto R, Hampel H, Sweet K, Lynch JF, Barrows A, Wijnen J, van der Klift H, Franken P, Wagner A, Fodde R, de la Chapelle A. "A founder mutation of the MSH2 gene and hereditary nonpolyposis colorectal cancer in the United States.." JAMA. Vol. 291, no. 6. (February 2004.): 718-724.

Hampel H, Sweet K, Westman JA, Offit K, Eng C. "Referral for cancer genetics consultation: a review and compilation of risk assessment criteria.." J Med Genet. Vol. 41, no. 2. (February 2004.): 81-91.

Nagy,R; Sweet,K; Eng,C. "Highly penetrant hereditary cancer syndromes." ONCOGENE. Vol. 23, no. 38. (August 2004.): 6445-6470.

Sweet, K. M., Lynch, H. T.. "Genetic aetiology of diffuse gastric cancer: so near, yet so far." J Med Genet. Vol. 41, no. 7. (January 2004.): 481-3.

Sweet K, Willis J, Sawada T, Zhou X-P, Gallione C, Alhopuro P, Khoo SK, Martin C, Bridgeman S, Heinz J, Pilarski R, Lehtonen R, Prior TW, Marchuk DA, Frebourg T, Teh BT, Aaltonen L, Eng C. "Molecular classification of patients with unexplained hamartomatous and hyperplastic polyposis.." JAMA. Vol. 294, no. 19. (November 2005.): 2465-2473.

Weber F, Fukino K, Sawada T, Williams N, Sweet K, Brena RM, Plass C, Caldes T, Mutter GL, Villalona-Calero MA, Eng C. "Variability in organ-specific EGFR mutational spectra in tumour epithelium and stroma may be the biological basis for differential responses to tyrosine kinase inhibitors.." B J Cancer. Vol. 92, no. 10. (May 2005.): 1922-1926.

Narod SA, Lubinski J, Ghadirian P, Lynch HT, Moller P, Foulkes WD, Rosen B, Kim-Sing C, Isaacs C, Domchek S, Domcheck S, Sun P, Hereditary Breast Cancer Clinical Study Group: Wagner, T., Ainsworth, P., Chudley, A., Eisen, A., Golcrist, D., Lemire, E., Provencher, D., Pasini, B., Bellati, C., Couch, F., Daly, M., Eng, C., Fishman, D., Karlan, B., McLennan, J., McKinnon, W., Merajver, S., Neuhasen, S., Pasche, B., Olopade, O., Osborne, M., Sweet, K., Saal, H., Tung, N., Weitzel, J., Wood, M.. "Screening mammography and risk of breast cancer in BRCA1 and BRCA2 mutation carriers: a case-control study.." Lancet oncology. Vol. 7, no. 5. (May 2006.): 402-406.

Gronwald J, Tung N, Foulkes WD, Offit K, Gershoni R, Daly M, Kim-Sing C, Olsson H, Ainsworth P, Eisen A, Saal H, Friedman E, Olopade O, Osborne M, Weitzel J, Lynch H, Ghadirian P, Lubinski J, Sun P, Narod SA, D Gilchrist, D., Weber, B., Rebbeck, T., Isaacs, C., Neuhausen, S., Garber, J., Karlan, B., Fishman, D., Merajver, S., McKinnon, W., Wood, M., Evans, G., Moller, P., B. Pasini, B., Sweet, K., Eng, E., G. Rennert, G., Couch, F., McLennan, J., and Provencher, D.. "Tamoxifen and contralateral breast cancer in BRCA1 and BRCA2 carriers: an update.." Int J Cancer. Vol. 118, no. 9. (May 2006.): 2281-2284.

Metcalfe KA, Birenbaum-Carmeli D, Lubinski J, Gronwald J, Lynch H, Moller P, Ghadirian P, Foulkes WD, Klijn J, Friedman E, Kim-Sing C, Ainsworth P, Rosen B, Domchek S, Wagner T, Tung N, Manoukian S, Couch F, Sun P, Narod SA; Hereditary Breast Cancer Clinical Study Group: : Daly, M., Saal, H.M., Sweet, K., Lyonnet, D., Eisen, A., Rennert, G., McLennan, J., Gershoni-Baruch, R., Garber, J., Cummings, S., Weitzel, J., Karlan, B., Kurz, R., McKinnon, W., Wood, M., Osborne, M., Fishman, D., Meschino, W.S., Lemire, E., Maugard, C., Mills, G., Merajver, S., Rayson, D.. "International variation in rates of uptake of preventive options in BRCA1 and BRCA2 mutation carriers." Int J Cancer. Vol. 122, no. 9. (May 2007.): 2017-2022.

Kelly,K,M; Sweet,K. "In search of a familial cancer risk assessment tool." CLINICAL GENETICS. Vol. 71, no. 1. (January 2007.): 76-83.

Allain, D. C., Sweet, K., Agnese, D. M.. "Management options after prophylactic surgeries in women with BRCA mutations: a review." Cancer Control. Vol. 14, no. 4. (January 2007.): 330-7.

Kelly,Kimberly,M; Sturm,Amy; Ferketich,Amy; Sweet,Kevin; Kemp,Kathleen; Koenig,Clint; Westman,Judith. "DEVELOPING A CANCER FAMILY HISTORY CAMPAIGN: WHAT IS THE NEED IN THE COMMUNITY?." ANNALS OF BEHAVIORAL MEDICINE. Vol. 33, (December 2007.): S16-S16.

Sturm AC, Sweet K, Schwirian PM, Koenig C, Westman J, Kelly KM. "Lessons learned while developing a cancer family history campaign in the Columbus, Ohio metropolitan area." Community Genet. Vol. 11, no. 5. (May 2007.): 304-310.

Spearman,Andrew,D; Sweet,Kevin; Zhou,Xiao-Ping; McLennan,Jane; Couch,Fergus,J; Toland,Amanda,Ewart. "Clinically Applicable Models to Characterize BRCA1 and BRCA2 Variants of Uncertain Significance." JOURNAL OF CLINICAL ONCOLOGY. Vol. 26, no. 33. (November 2008.): 5393-5400.

Eisen A, Lubinski J, Gronwald J, Moller P, Lynch HT, Klijn J, Kim-Sing C, Neuhausen SL, Foulkes WE, Ghadirian P, Manoukian S, Rennert G, Friedman E, Isaacs C, Rosen B, Daly M, Ping Sun P, Narod SA and the Hereditary Breast Cancer Clinical Study Group: Olopade, O., Cummings, S., Nadine Tung, N., Couch, F., Domchek, S., Stoppa-Lyonnet, D., Ruth Gershoni-Baruch, R., Horsman, D., Wagner, T., Saal, H., Warner, E., Meschino, W., Offit, K., Trivedi, A., Robson, M., Osborne, M., Gilchrist, D., Eng, C., Weitzel, J., McKinnon, W., Wood, M., Maugard, C., Barbari Pasini, B., Bellati, C., Ainsworth, P., Osborne, M., Sweet, K., Pasche, B., Karlan, B., Nedelcu, R., Armel, S., Tulman, A., Gilchrist, D., Lemire, E., Mclennan, J., Evans, G., Byrski, T., Huzarski, T.. "Hormone Therapy and the Risk of Breast Cancer in BRCA1 Carriers." JNCI. Vol. 100, no. 19. (October 2008.): 1361-1366.

Ginsburg O, Ghadirian P, Lubinski J, Cybulski C, Lynch H, Neuhausen S, Kim-Sing C, Robson M, Domchek S, Isaacs C, klijn J, Armel S, Foulkes WD, Tung N, Moller P, Sun P, Narod SA; Hereditary Breast Cancer Clinical Study Group: Horsman, D., B. Rosen, B., Isaacs, C., Domchek, S., Gershoni-Baruch, R., Eisen, A., Olopade, O.I., Friedman, E., Saal, H.M., Neuhausen, S., Daly, M., Karlan, B., Kurz,R., Bellati, C., Eng, C., Sweet, K., Wagner, T., D. Provencher, D., Maugard, C., McKinnon, W., Osborne, M., McLennan, J., Pasche, B., Fallen, T., Lemire, E., Chudley, A., Weitzel, J., Meschino, W.S., Rayson, D., G. Evans, G., and Olsson, H.. "Smoking and the risk of breast cancer in BRCA1 and BRCA2 carriers: an update." Breast Cancer Res Treat. no. (Epub). (May 2008.): -.

Metcalfe, K., Lubinski, J., Ghadirian, P., Lynch, H., Kim-Sing, C., Friedman, E., Foulkes, W., Domchek, S., Ainsworth, P., Isaacs, C., Tung, N., Gronwald, J., Wagner, T., Manoukian, S., Sun, P., Narod, S. and the Hereditary Breast Cancer Clinical Study Group: Daly, M., Saal, H.M., Sweet, K., Lyonnet, D., Eisen, A., McLennan, J., Gershoni-Baruch, R., Garber, J., Cummings, S., Weitzel, J., Karlan, B., Kurz, R., McKinnon, W., Wood, M., Chudley, A., Osborne, M., Meschino, W., Maugard, C., Eng, C., Moller, P., Rosen, B., Armel, S., Couch, F., Pasini, B. and Bellati, C. "Predictors of Contralateral Prophylactic Mastectomy in Women with BRCA1 and BRCA2 mutation." J Clin Oncol. (January 2008.): -.

Kotsopoulos J, Librach CL, Lubinski J, Gronwald J, Kim-Sing C, Ghadirian P, Lynch HT, Moller P, Foulkes WD, Randall S, Manoukian S, Pasini B, Tung N, Ainsworth PJ, Cummings S, Sun P, Narod SA; Hereditary Breast Cancer Clinical Study Group: Horsman, D., B. Rosen, B., Isaacs, C., Domchek, S., Gershoni-Baruch, R., Eisen, A., Olopade, O.I., Friedman, E., Saal, H.M., Neuhausen, S., Daly, M., Karlan, B., Kurz,R., Bellati, C., Eng, C., Sweet, K., Wagner, T., D. Provencher, D., Maugard, C., McKinnon, W., Osborne, M., McLennan, J., Pasche, B., Fallen, T., Lemire, E., Chudley, A., Weitzel, J., Meschino, W.S., Rayson, D., G. Evans, G., and Olsson, H.. "Infertility, treatment of infertility, and the risk of breast cancer among women with BRCA1 and BRCA2 mutations: a case-control study." Cancer Causes Control. Vol. 10, no. 19. (January 2008.): 1111-1119.

Spearman A, Sweet K, Zhou XP, McClennan J, Couch FJ, Toland AE. "Clinically applicable models for the characterization of BRCA1 and BRCA2 variants of uncertain significance." J Clin Oncol. no. Sept 2008 (Epub). (October 2008.): -.

Dworkin,Amy,M; Spearman,Andrew,D; Tseng,Stephanie,Y; Sweet,Kevin; Toland,Amanda,Ewart. "Methylation not a frequent "second hit" in tumors with germline BRCA mutations." FAMILIAL CANCER. Vol. 8, no. 4. (December 2009.): 339-346.

Kelly,Kimberly,M; Ferketich,Amy,K; Sturm,Amy,C; Porter,Kyle; Sweet,Kevin; Kemp,Kathleen; Schwirian,Patricia; Westman,Judith,A. "Cancer risk and risk communication in urban, lower-income neighborhoods." PREVENTIVE MEDICINE. Vol. 48, no. 4. (April 2009.): 392-396.

Parry,Susan; Walsh,Michael,D; Pearson,Sally-Ann; Buchanan,Daniel; Walters,Rhiannon; Sweet,Kevin; De la Chapelle,Albert; Walker,Neal,I; Young,Joanne. "Does Expression of the Gastric Mucin MUC6 Help Identify Advanced Serrated Colorectal Polyps?." GASTROENTEROLOGY. Vol. 136, no. 5. (May 2009.): A450-A451.

Pal, T., Keefe, D., Sun, P, Narod, S, and the Hereditary Breast Cancer Clinical Study Group: Kim-Sing, C., Rosen, B., Armel, S., Beth Karlan, B., Sweet, K., Saal, H., Weitzel, J., Eisen, E., Robidoux, A., McKinnon, W., Wood, M. "Fertility in women with BRCA mutations: a case-control study." Fertil Steril. no. [epub ahead of print]. (February 2009.): -.

Vicus, D., Rosen, B., Lubinski, J, Domchek, S, Kauff, N, Lynch, H., Issacs, C. Tung, N. Sun, P., Narod, S, Daly, M. Olopade, O, Neuhausen, S., Foulkes, W., Gilchrist, D., Karlan, B., Lyonnet, S., Sweet, K., Gershoni-Baruch, R., Rayson, D., Ainsworth, P., Weitzel, J., Bordeleau, L., Cybulski, C. and Gronwald, J. "Tamoxifen and the risk of ovarian cancer in BRCA1 mutation carriers." Gynecol Oncol. Vol. 115, no. 1. (October 2009.): 135-137.

Buchanan,Daniel,D; Sweet,Kevin; Drini,Musa; Jenkins,Mark,A; Win,Aung,Ko; Gattas,Michael; Walsh,Michael,D; Clendenning,Mark; McKeone,Diane; Walters,Rhiannon; Roberts,Aedan; Young,Alasdair; Hampel,Heather; Hopper,John,L; Goldblatt,Jack; George,Jill; Suthers,Graeme,K; Phillips,Kerry; Young,Graeme,P; Chow,Elizabeth; Parry,Susan; Woodall,Sonja; Tucker,Kathy; Muir,Amanda; Field,Michael; Greening,Sian; Gallinger,Steven; Green,Jane; Woods,Michael,O; Spaetgens,Renee; De la Chapelle,Albert; Macrae,Finlay; Walker,Neal,I; Jass,Jeremy,R; Young,Joanne,P. "Phenotypic diversity in patients with multiple serrated polyps: a genetics clinic study (vol 25, pg 703, 2010)." INTERNATIONAL JOURNAL OF COLORECTAL DISEASE. Vol. 25, no. 12. (December 2010.): 1513-1515.

Sweet,Kevin; Senter,Leigha; Pilarski,Robert; Wei,Lai; Toland,Amanda,Ewart. "Characterization of BRCA1 ring finger variants of uncertain significance." BREAST CANCER RESEARCH AND TREATMENT. Vol. 119, no. 3. (February 2010.): 737-743.

Dennis,Jessica; Ghadirian,Parviz; Little,Julian; Lubinski,Jan; Gronwald,Jacek; Kim-Sing,Charmaine; Foulkes,William; Moller,Pal; Lynch,Henry,T; Neuhausen,Susan,L; Domchek,Susan; Armel,Susan; Isaacs,Claudine; Tung,Nadine; Sweet,Kevin; Ainsworth,Peter; Sun,Ping; Krewski,Daniel; Narod,Steven. "Alcohol consumption and the risk of breast cancer among BRCA1 and BRCA2 mutation carriers." BREAST. Vol. 19, no. 6. (December 2010.): 479-483.

Buchanan,Daniel,D; Sweet,Kevin; Drini,Musa; Jenkins,Mark,A; Win,Aung,Ko; English,Dallas,R; Walsh,Michael,D; Clendenning,Mark; McKeone,Diane,M; Walters,Rhiannon,J; Roberts,Aedan; Pearson,Sally-Ann; Pavluk,Erika; Hopper,John,L; Gattas,Michael,R; Goldblatt,Jack; George,Jill; Suthers,Graeme,K; Phillips,Kerry,D; Woodall,Sonja; Arnold,Julie; Tucker,Kathy; Muir,Amanda; Field,Michael; Greening,Sian; Gallinger,Steven; Perrier,Renee; Baron,John,A; Potter,John,D; Haile,Robert; Frankel,Wendy; De la Chapelle,Albert; Macrae,Finlay; Rosty,Christophe; Walker,Neal,I; Parry,Susan; Young,Joanne,P. "Risk Factors for Colorectal Cancer in Patients with Multiple Serrated Polyps: A Cross-Sectional Case Series from Genetics Clinics." PLOS ONE. Vol. 5, no. 7. (July 2010.): e11636-.

Metcalfe,Kelly; Lubinski,Jan; Lynch,Henry,T; Ghadirian,Parviz; Foulkes,William,D; Kim-Sing,Charmaine; Neuhausen,Susan; Tung,Nadine; Rosen,Barry; Gronwald,Jacek; Ainsworth,Peter; Sweet,Kevin; Eisen,Andrea; Sun,Ping; Narod,Steven,A. "Family History of Cancer and Cancer Risks in Women with BRCA1 or BRCA2 Mutations." JOURNAL OF THE NATIONAL CANCER INSTITUTE. Vol. 102, no. 24. (December 2010.): 1874-1878.

Buchanan,Daniel,D; Sweet,Kevin; Drini,Musa; Jenkins,Mark,A; Win,Aung,Ko; Gattas,Michael; Walsh,Michael,D; Clendenning,Mark; McKeone,Diane; Walters,Rhiannon; Roberts,Aedan; Young,Alasdair; Hampel,Heather; Hopper,John,L; Goldblatt,Jack; George,Jill; Suthers,Graeme,K; Phillips,Kerry; Young,Graeme,P; Chow,Elizabeth; Parry,Susan; Woodall,Sonja; Tucker,Kathy; Muir,Amanda; Field,Michael; Greening,Sian; Gallinger,Steven; Green,Jane; Woods,Michael,O; Spaetgens,Renee; De la Chapelle,Albert; Macrae,Finlay; Walker,Neal,I; Jass,Jeremy,R; Young,Joanne,P. "Phenotypic diversity in patients with multiple serrated polyps: a genetics clinic study." International Journal of Colorectal Disease. Vol. 25, no. 6. (June 2010.): 703-.

Ginsburg OM, Kim-Sing C, Foulkes WD, Ghadirian P, Lynch HT, Sun P, Narod SA; Hereditary Breast Cancer Study Group: Kin-Sing, C., Rosen, B., Armel, S., Sweet, K., Saal, H., Weitzel, J.. "BRCA1 and BRCA2 families and the risk of skin cancer." Fam Cancer. Vol. 4, no. 9. (December 2010.): 489-493.

Steven Narod, Louise Bordeleau, Jan Lubinski, Parviz Ghadirian, William D. Foulkes,Susan Neuhausen, Peter Ainsworth, Ping Sun, Henry T. Lynch, Andrea Eisen, Wendy McKinnon, Marie Wood, Howard Saal, AbChudley, Andre Robidoux, Charmaine Kim-Sing, Nadine Tung, Susan Armel, Tomasz Huzarski, Diane Provencher, Edmond Lemire,Anna Tulman, Marcia Llacuachaqui, Kevin Sweet, Leigha Senter, Dawna Gilchrist, Beth Karlan, Raluca Kurz, Barry Rosen, RochelleDemsky, Seema Panchal, Fergus Couch, Christine Elser, Siranoush Manoukian, Mary Daly, Cezary Cybulski, Jacek Gronwald, TomaszByrski, Olufunmilayo I. Olopade, Dominique Stoppa-Lyonnet, Jeffrey Weitzel, Jane McLennan, Wendy Meschino, Barbara Pasini,Christian Singer, Catharina Dressler, Kelly Metcalfe, Claudine Isaacs.. "Compliance With Tamoxifen inWomen With Breast Cancer anda BRCA1 or BRCA2 Mutation." Journal of Clinical Oncology. (November 2010.): -.

Bordeleau L, Lipscombe L, Lubinski J, Ghadirian P, Foulkes WD, Neuhausen S, Ainsworth P, Pollak M, Sun P, Narod SA, Lynch HT, Eisen A, McKinnon W, Wood M, Saal H, Chudley A, Robidoux A, Kim-Sing C, Tung N, Armel S, Huzarski T, Provencher D, Lemire E, Tulman A, Llacuachaqui M, Sweet K, Gilchrist D, Karlan B, Kurz R, Rosen B, Demsky R, Panchal S, Couch F, Elser C, Manoukian S, Daly M, Cybulski C, Gronwald J, Byrski T, Olapade O, Stoppa-Lyonnet D, Weitzel J, McLennan J, Meschino W, Pasini B, Singer C, Dressler C, Metcalfe K, Domchek S, Isaacs C. "Diabetes and breast cancer among women with BRCA1 and BRCA2 mutations." Cancer. Vol. 9, no. 117. (May 2011.): 1812-1818.

Warner, E., Hill, K., Causer, P., Plewes, D., Jong, R., Yaffe, M., Foulkes, W. D., Ghadirian, P., Lynch, H., Couch, F., Wong, J., Wright, F., Sun, P., Narod, S. A., Hereditary Breast Cancer Study Group: Maehle, L., Klijn, J., Friedman, E., Snyder, C., Robidoux, A., Demsky, R., Sweet, K., Kurz, R., Stoppa Lyonnet, D., Olopade, O., Bourdeleau, L., Eng, C., Garber, J., and Metcalfe, K. "Prospective study of breast cancer incidence in women with a BRCA1 or BRCA2 mutation under surveillance with and without magnetic resonance imaging." J Clin Oncol. Vol. 29, no. 13. (May 2011.): 1664-9.

Narod, S., Lubinski, J., Huzarski, P., Lynch, Henry T.; parviz, g., Foulkes, W., Neuhausen, S; Armel, S; Gilchrist, D.; Sweet, K.; Eisen, A; Sun, P.. "The Risk of Breast Cancer in Women with a BRCA1 Mutation from North America and Poland." International Journal of Cancer. (June 2011.): -.

Rosty,Christophe; Buchanan,Daniel,D; Walsh,Michael,D; Pearson,Sally-Ann; Pavluk,Erika; Walters,Rhiannon,J; Clendenning,Mark; Spring,Kevin,J; Jenkins,Mark,A; Win,Aung,K; Hopper,John,L; Sweet,Kevin; Frankel,Wendy,L; Aronson,Melyssa; Gallinger,Steve; Goldblatt,Jack; Woodall,Sonja; Arnold,Julie; Walker,Neal,I; Jass,Jeremy,R; Parry,Susan; Young,Joanne,P. "Phenotype and Polyp Landscape in Serrated Polyposis Syndrome: A Series of 100 Patients From Genetics Clinics." AMERICAN JOURNAL OF SURGICAL PATHOLOGY. Vol. 36, no. 6. (June 2012.): 876-882.

Crowder,Clinton,D; Sweet,Kevin; Lehman,Amy; Frankel,Wendy,L. "Serrated Polyposis Is an Underdiagnosed and Unclear Syndrome The Surgical Pathologist has a Role in Improving Detection." AMERICAN JOURNAL OF SURGICAL PATHOLOGY. Vol. 36, no. 8. (August 2012.): 1178-1185.

Mavaddat,Nasim; Barrowdale,Daniel; Andrulis,Irene,L; Domchek,Susan,M; Eccles,Diana; Nevanlinna,Heli; Ramus,Susan,J; Spurdle,Amanda; Robson,Mark; Sherman,Mark; Mulligan,Anna,Marie; Couch,Fergus,J; Engel,Christoph; McGuffog,Lesley; Healey,Sue; Sinilnikova,Olga,M; Southey,Melissa,C; Terry,Mary,Beth; Goldgar,David; O'Malley,Frances; John,Esther,M; Janavicius,Ramunas; Tihomirova,Laima; Hansen,Thomas,vO; Nielsen,Finn,C; Osorio,Ana; Stavropoulou,Alexandra; Benitez,Javier; Manoukian,Siranoush; Peissel,Bernard; Barile,Monica; Volorio,Sara; Pasini,Barbara; Dolcetti,Riccardo; Putignano,Anna,Laura; Ottini,Laura; Radice,Paolo; Hamann,Ute; Rashid,Muhammad,U; Hogervorst,Frans,B; Kriege,Mieke; van der Luijt,Rob,B; Peock,Susan; Frost,Debra; Evans,D,Gareth; Brewer,Carole; Walker,Lisa; Rogers,Mark,T; Side,Lucy,E; Houghton,Catherine; Weaver,JoEllen; Godwin,Andrew,K; Schmutzler,Rita,K; Wappenschmidt,Barbara; Meindl,Alfons; Kast,Karin; Arnold,Norbert; Niederacher,Dieter; Sutter,Christian; Deissler,Helmut; Gadzicki,Doroteha; Preisler-Adams,Sabine; Varon-Mateeva,Raymonda; Schoenbuchner,Ines; Gevensleben,Heidrun; Stoppa-Lyonnet,Dominique; Belotti,Muriel; Barjhoux,Laure; Isaacs,Claudine; Peshkin,Beth,N; Caldes,Trinidad; de la Hoya,Miguel; Canadas,Carmen; Heikkinen,Tuomas; Heikkila,Paivi; Aittomaki,Kristiina; Blanco,Ignacio; Lazaro,Conxi; Brunet,Joan; Agnarsson,Bjarni,A; Arason,Adalgeir; Barkardottir,Rosa,B; Dumont,Martine; Simard,Jacques; Montagna,Marco; Agata,Simona; D'Andrea,Emma; Yan,Max; Fox,Stephen; Rebbeck,Timothy,R; Rubinstein,Wendy; Tung,Nadine; Garber,Judy,E; Wang,Xianshu; Fredericksen,Zachary; Pankratz,Vernon,S; Lindor,Noralane,M; Szabo,Csilla; Offit,Kenneth; Sakr,Rita; Gaudet,Mia,M; Singer,Christian,F; Tea,Muy-Kheng; Rappaport,Christine; Mai,Phuong,L; Greene,Mark,H; Sokolenko,Anna; Imyanitov,Evgeny; Toland,Amanda,Ewart; Senter,Leigha; Sweet,Kevin; Thomassen,Mads; Gerdes,Anne-Marie; Kruse,Torben; Caligo,Maria; Aretini,Paolo; Rantala,Johanna; von Wachenfeld,Anna; Henriksson,Karin; . "Pathology of Breast and Ovarian Cancers among BRCA1 and BRCA2 Mutation Carriers: Results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)." CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION. Vol. 21, no. 1. (January 2012.): 134-147.

Lubinski,Jan; Huzarski,Tomasz; Byrski,Tomasz; Lynch,Henry,T; Cybulski,Cezary; Ghadirian,Parviz; Stawicka,Malgorzata; Foulkes,William,D; Kilar,Ewa; Kim-Sing,Charmaine; Neuhausen,Susan,L; Armel,Susan; Gilchrist,Dawna; Sweet,Kevin; Gronwald,Jacek; Eisen,Andrea; Gorski,Bohdan; Sun,Ping; Narod,Steven,A. "The risk of breast cancer in women with a BRCA1 mutation from North America and Poland." INTERNATIONAL JOURNAL OF CANCER. Vol. 131, no. 1. (July 2012.): 229-234.

Iqbal, J., Ragone, A., Lubinski, J., Lynch, H. T., Moller, P., Ghadirian, P., Foulkes, W. D., Armel, S., Eisen, A., Neuhausen, S. L., Senter, L., Singer, C. F., Ainsworth, P., Kim-Sing, C., Tung, N., Friedman, E., Llacuachaqui, M., Ping, S., Narod, S. A., Hereditary Breast Cancer Study Group: Maehle, L., Klijn, J., Friedman, E., Snyder, C., Robidoux, A., Demsky, R., Sweet, K., Kurz, R., Stoppa Lyonnet, D., Olopade, O., Bourdeleau, L., Eng, C., Garber, J., and Metcalfe, K. "The incidence of pancreatic cancer in BRCA1 and BRCA2 mutation carriers." Br J Cancer. Vol. 107, no. 12. (December 2012.): 2005-9.

Kotsopoulos, J., Lubinski, J., Salmena, L., Lynch, H. T., Kim-Sing, C., Foulkes, W. D., Ghadirian, P., Neuhausen, S. L., Demsky, R., Tung, N., Ainsworth, P., Senter, L., Eisen, A., Eng, C., Singer, C., Ginsburg, O., Blum, J., Huzarski, T., Poll, A., Sun, P., Narod, S. A., Hereditary Breast Cancer Study Group: Maehle, L., Klijn, J., Friedman, E., Snyder, C., Robidoux, A., Demsky, R., Sweet, K., Kurz, R., Stoppa Lyonnet, D., Olopade, O., Bourdeleau, L., Eng, C., Garber, J., and Metcalfe, K. "Breastfeeding and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers." Breast Cancer Res. Vol. 14, no. 2. (January 2012.): R42-.

Kitzmiller, J. P., Embi, P. J., Manickam, K., Sweet, K. M., Phelps, M. A., Jackson, R. D., Marsh, C. B., Sadee, W.. "Program in pharmacogenomics at the Ohio State University Medical Center." Pharmacogenomics. Vol. 13, no. 7. (January 2012.): 751-6.

Senst, N., Llacuachaqui, M., Lubinski, J., Lynch, H., Armel, S., Neuhausen, S., Ghadirian, P., Sun, P., Narod, S.. "Parental origin of mutation and the risk of breast cancer in a prospective study of women with a BRCA1 or BRCA2 mutation." Clin Genet. Vol. 12, (October 2012.): 324-327.

Spurdle, A. B., Whiley, P. J., Thompson, B. et al. "BRCA1 R1699Q variant displaying ambiguous functional abrogation confers intermediate breast and ovarian cancer risk." J Med Genet. Vol. 49, no. 8. (January 2012.): 525-32.

Win,Aung,Ko; Walters,Rhiannon,J; Buchanan,Daniel,D; Jenkins,Mark,A; Sweet,Kevin; Frankel,Wendy,L; De la Chapelle,Albert; McKeone,Diane,M; Walsh,Michael,D; Clendenning,Mark; Pearson,Sally-Ann; Pavluk,Erika; Nagler,Belinda; Hopper,John,L; Gattas,Michael,R; Goldblatt,Jack; George,Jill; Suthers,Graeme,K; Phillips,Kerry,D; Woodall,Sonja; Arnold,Julie; Tucker,Kathy; Field,Michael; Greening,Sian; Gallinger,Steve; Aronson,Melyssa; Perrier,Renee; Woods,Michael,O; Green,Jane,S; Walker,Neal; Rosty,Christophe; Parry,Susan; Young,Joanne,P. "Cancer Risks for Relatives of Patients With Serrated Polyposis." AMERICAN JOURNAL OF GASTROENTEROLOGY. Vol. 107, no. 5. (May 2012.): 770-778.

Buchanan,Daniel,D; Sweet,Kevin; Clendenning,Mark; Walsh,Michael,D; Rosty,Christophe; Young,Joanne,P; Parry,Susan. "A Large Multi -Nation Serrated Polyposis Register: Role in Defining This Syndrome." GASTROENTEROLOGY. Vol. 144, no. 5. (May 2013.): S394-S394.

Rosty,Christophe; Walsh,Michael,D; Walters,Rhiannon,J; Clendenning,Mark; Pearson,Sally-Ann; Jenkins,Mark,A; Win,Aung,Ko; Hopper,John,L; Sweet,Kevin; Frankel,Wendy,L; Aronson,Melyssa; Gallinger,Steve; Goldblatt,Jack; Tucker,Kathy; Greening,Sian; Gattas,Michael,R; Woodall,Sonja; Arnold,Julie; Walker,Neal,I; Parry,Susan; Young,Joanne,P; Buchanan,Daniel,D. "Multiplicity and Molecular Heterogeneity of Colorectal Carcinomas in Individuals With Serrated Polyposis." AMERICAN JOURNAL OF SURGICAL PATHOLOGY. Vol. 37, no. 3. (March 2013.): 434-442.

Sturm, A. C., Sweet, K., Manickam, K.. "Implementation of a clinical research pharmacogenomics program at an academic medical center: role of the genetics healthcare professional." Pharmacogenomics. Vol. 14, no. 7. (January 2013.): 703-6.

Clendenning,Mark; Young,Joanne,P; Walsh,Michael,D; Woodall,Sonja; Arnold,Julie; Jenkins,Mark; Win,Aung,Ko; Hopper,John,L; Sweet,Kevin; Gallinger,Steven; Rosty,Christophe; Parry,Susan; Buchanan,Daniel,D. "Germline Mutations in the Polyposis-Associated Genes BMPR1A, SMAD4, PTEN, MUTYH and GREM1 Are Not Common in Individuals with Serrated Polyposis Syndrome." PLOS ONE. Vol. 8, no. 6. (June 2013.): e66705-.

Senter, L., O'Connor, M., Oriyo, F., Sweet, K. and Toland, AE.. "Linking distant relatives with BRCA gene mutation: potential for cost savings." Clin Genet. Vol. 23, no. 4. (May 2013.): 203-.

Shuldiner,A,R; RELLING,M,V; Peterson,J,F; Hicks,J,K; Freimuth,R,R; Sadee,W; Pereira,N,L; Roden,D,M; Johnson,J,A; Klein,T,E;Pharmacogenomics Research Network Translational Pharmacogenetics Program Group, Shuldiner AR, Vesely M, Robinson SW, Ambulos N Jr, Stass SA, Kelemen MD, Brown LA, Pollin TI, Beitelshees AL, Zhao RY, Pakyz RE, Palmer K, Alestock T, O'Neill C, Maloney K, Branham A, Sewell D, Relling MV, Crews K, Hoffman J, Cross S, Haidar C, Baker D, Hicks JK, Bell G, Greeson F, Gaur A, Reiss U, Huettel A, Cheng C, Gajjar A, Pappo A, Howard S, Hudson M, Pui CH, Jeha S, Evans WE, Broeckel U, Altman RB, Gong L, Whirl-Carrillo M, Klein TE, Sadee W, Manickam K, Sweet KM, Embi PJ, Roden D, Peterson J, Denny J, Schildcrout J, Bowton E, Pulley J, Beller M, Mitchell J, Danciu I, Price L, Pereira NL, Weinshilboum R, Wang L, Johnson JA, Nelson D, Clare-Salzler M, Elsey A, Burkley B, Langaee T, Liu F, Nessl D, Dong HJ, Lesko L, Freimuth RR, Chute CG. "The Pharmacogenomics Research Network Translational Pharmacogenetics Program: Overcoming Challenges of Real-World Implementation." CLINICAL PHARMACOLOGY & THERAPEUTICS. Vol. 94, no. 2. (August 2013.): 207-210.

Valentini A, Lubinski J, Byrski T, Ghadirian P, Moller P, Lynch HT, Ainsworth P, Neuhausen SL, Weitzel J, Singer CF, Olopade OI, Saal H, Lyonnet DS, Foulkes WD, Kim-Sing C, Manoukian S, Zakalik D, Armel S, Senter L, Eng C, Grunfeld E, Chiarelli AM, Poll A, Sun P, Narod SA; Hereditary Breast Cancer Study Group, Ginsburg O, Maehle L, Sweet K, Gilchrist D, Olopade OI, Couch F, Isaacs C, Karlan B, Eng C, Weitzel JN, Daly MB, Garber JE, Zakalik D, Cullinane CA, Stoppa-Lyonnet D, Saal H, Meschino W, McKinnon W, Wood M, Fallen T, Kurz R, Manoukian S, Rosen B, McCuaig J, Demsky R, Lemire E, McLennan J, Panchal S, Chudley AE, Vadaparampil ST, Pal T, Rayson D, Valentini A, Friedman S, Cybulski C, Byrski T, Huzarski T.. "The impact of pregnancy on breast cancer survival in women who carry a BRCA1 or BRCA2 mutation." Breast Cancer Res Treat.. Vol. 142, no. 1. (November 2013.): 177-185.

Sweet K, Gordon E, Sturm AC, Schmidlen T, Manickam K, Toland AE, Keller M, Stack CE, Garcia-Espana F, Bellafante M, Tayal N, Embi P, Binkley P, Hershberger R, Sadee W, Christman M, Marsh C.. "Design and Implementation of a Randomized Controlled Trial of Genomic Counseling for Patients with Chronic Disease." J Pers Med. Vol. 4, (January 2014.): 1-19.

Finch AP1, Lubinski J, Møller P, Singer CF, Karlan B, Senter L, Rosen B, Maehle L, Ghadirian P, Cybulski C, Huzarski T, Eisen A, Foulkes WD, Kim-Sing C,Ainsworth P, Tung N, Lynch HT, Neuhausen S, Metcalfe KA, Thompson I, Murphy J, Sun P, Hereditary Breast Cancer Study Group, Ginsburg O, Robidoux, A, Eng C, Sweet, K, Gilchrist D, Olopade O, Couch C, Weitzel J, Daly M, Garber J, Vadaparampil S, Pal T, Rayson D, Friedman S, Gronwald J, Byrskim T, Narod SA.. "Impact of Oophorectomy on Cancer Incidence and Mortality in Women With a BRCA1 or BRCA2 Mutation." J Clin Oncol.. Vol. 32, (February 2014.): 1-10.

Hooker GW, Ormond KE, Sweet K, Biesecker BB.. "Teaching Genomic Counseling: Preparing the Genetic Counseling Workforce for the Genomic Era." Journal of Genetic Counseling. Vol. Epub, (February 2014.): 10-.

Sweet, K., Sturm, A., Rettig, A. and Agnese, D.. "Clinically Relevant Lessons from Family HealthLink: A Cancer and Coronary Heart Disease Familial Risk Assessment Tool." Genetics in Medicine. Vol. 16, no. 10. (October 2014.): 742-750.

Narod SA, Tung N, Lubinski J, Huzarski T, Robson M, Lynch HT, Neuhausen SL, Ghadirian P, Kim-Sing C, Sun P, Foulkes WD, Hereditary Breast Cancer Clinical Study Group: Euhus D, Garber J, Rennert G, Sweet K, Gershoni-Baruch R, Rappaport C, Lemire E, Maehle L, Stoppa-Lyonnet D, Daly M, Merajver S, Kwong A,Bordeleau L, Cullinane CA, Friedman E, McKinnon W, Wood M, Rayson D, Meschino W, McLennan J, Costalas JW, Reilly RE, Pal T, Vadaparampil S, Offit K, Robson M, Kauff N, Klijn J, Euhus D, Isaacs C, Couch F, Cybulski C, Byrski T, Jakubowska A, Panchal S, Nanda S, Poll A, Metcalfe K,Rosen B, Armel SR, Chudley A, Evans G, Blum J, Karlan B, Zakalik D, Lunn J, Donenberg T, Pasini B, Kurz RN, Fallen T.. "A prior diagnosis of breast cancer is a risk factor for breast cancer in BRCA1 and BRCA2 carriers.." Curr Oncol.. Vol. 21, no. 2. (April 2014.): 64-68.

Gronwald J, Robidoux A, Kim-Sing C, Tung N, Lynch HT, Foulkes WD, Manoukian S, Ainsworth P, Neuhausen SL, Demsky R, Eisen A, Singer CF, Saal H,Senter L, Eng C, Weitzel J, Moller P, Gilchrist DM, Olopade O, Ginsburg O, Sun P, Huzarski T, Lubinski J, Narod SA; Hereditary Breast Cancer Clinical Study Group: Euhus D, Garber J, Rennert G, Sweet K, Gershoni-Baruch R, Rappaport C, Lemire E, Maehle L, Stoppa-Lyonnet D, Daly M, Merajver S, Kwong A,Bordeleau L, Cullinane CA, Friedman E, McKinnon W, Wood M, Rayson D, Meschino W, McLennan J, Costalas JW, Reilly RE, Pal T, Vadaparampil S, Offit K, Robson M, Kauff N, Klijn J, Euhus D, Isaacs C, Couch F, Cybulski C, Byrski T, Jakubowska A, Panchal S, Nanda S, Poll A, Metcalfe K,Rosen B, Armel SR, Chudley A, Evans G, Blum J, Karlan B, Zakalik D, Lunn J, Donenberg T, Pasini B, Kurz RN, Fallen T.. "Duration of tamoxifen use and the risk of contralateral breast cancer in BRCA1 and BRCA2 mutation carriers." Breast Cancer Res Treat. Vol. 146, no. 2. (August 2014.): 421-427.

Hooker,Gillian,W; Ormond,Kelly,E; Sweet,Kevin; Biesecker,Barbara,B. "Teaching Genomic Counseling: Preparing the Genetic Counseling Workforce for the Genomic Era." JOURNAL OF GENETIC COUNSELING. Vol. 23, no. 4. (August 2014.): 445-451.

 

Reference Works

April 1991 Zhang, Y., Sweet, K. and Belli, J."Simultaneous Reversion of Radiation Sensitivity and Adriamycin Resistance Does Not Occur in a Multidrug Resistance Cell Line (LZ) [abstract]." .
April 1992 Sognier, M., Zhang, Y. Sweet, K. and Belli, J."Further Selection of Multidrug Resistant LZ-8 Cells Produces Additional Resistance Mechanisms" .
April 1992 Sognier, M., Zhang, Y. Sweet, K. and Belli, J."Selection for Higher Adriamycin Resistance Does Not Alter Radiation Response" .
January 1998 Sweet, K., Tarleton, J. and Saul, R."Promoting Genetic Education in the Secondary School System" .
January 1998 Sweet, K. and Saul, R."Expanding Community Education in Genetics in South Carolina" .
January 2000 Sweet, K., Bradley, T. and Westman, J."Recognition of High Risk Individuals for Hereditary Cancer Syndromes" .
January 2002 Ashida S, Willis SK, Sweet K, Westman JA."Improving health information provided for those at increased risk of hereditary cancer to increase the use of genetic counseling. Session: Health Communication Messages Used in Infectious and Chronic Disease Prevention Among Youth, and Women" .
January 2003 Goulet, M., Ahonen, L., Hampel, H., Sweet, K., Sickle-Santinello, B., Vassy, L., Eng, C.."Novel Approach to Improved Access to Cancer Genetics Program: the Columbus Ohio Solution" .
January 2003 Hampel, H., Sweet, K., Westman, J.A., Eng, C."Development and use of risk assessment criteria to evaluate cancer family histories" .
June 2004 Lynch, H., Coronel, S., Okimoto, R., Hampel, H., Sweet, K., Lynch, J., Fodde, R., Drouhard, T., Wagner, A., de la Chapelle, A. L."Lynch syndrome founder mutations in families of Navajo and German-American heritage" .
January 2004 Sweet K, Zhou XP, Heinz J, Pilarski R, Willis J, Prior T, Frebourg T, Teh BT, Aaltonen LA, Eng C."Molecular classification of gastrointestinal hamartomatous polyposis as a diagnostic adjunct to genetic counseling?" .
January 2005 Weber, F, Shen, L, Sweet, K, Cooper, K, Morrison, CD, Caldes, T, Eng, C."Genome-wide analysis of allelic imbalance in tumor epithelium and stromal in patients with BRCA1 and BRCA2 mutation positive hereditary breast cancer" .
January 2005 Sweet, K., Petri, K., Westman, J., Kelly, K."The Jameslink: A Tool to Assess Cancer Risk in Your Community." .
January 2005 Kelly, K., Remy, A., Sweet, K."Suitability of the Jameslink cancer risk assessment tool for diverse populations" .
January 2006 Kelly, K.; Sturm, A.; Ferketich, A.; Sweet, K.; Kemp, K., Koenig, C.; Schwirian, P.; Westman, J."Developing a Cancer Family History Public Health Campaign: What is the Need in the Community?" .
January 2006 Kelly, K., Remy, A., Westman, J., Sweet, K."The OSUCAP in the Community: Impact of a Cancer Risk Assessment Program" .
January 2006 Kelly K, Sweet K, Sturm AC, Westman J, Petri K."Partnerships in Developing a Cancer Risk Education e-Tool: the Jameslink-OSUCAP." .
January 2006 Sweet, K., Sturm, A., Westman, J., Kelly, K.."Promotion and Marketing of the Jameslink-OSUCAP - A Web Tool to Assess Cancer Risk" .
January 2006 Sturm AC, Sweet K, Westman J, Kemp K, Philips W, Ferketich A, Kelly K."The Effect of a Cancer Family History Public Health Campaign on Information-Seeking and Genetic Counseling Referrals" .
January 2006 Sturm AC, Sweet K, Koenig C, Schwirian P, Kelly K.."The Development of a Cancer Family History Public Health Campaign in the Columbus, Ohio Metropolitan Area" .
January 2006 Remy, A., Sweet, K., Westman, J., Kemp, K., Philips, W., and Kelly, K."Usability of the Jameslink Cancer Risk Assessment Tool in Minority Populations" .
January 2007 Mendoza-Londono, R., Murphy, J., Balicki, M., Khan, A., Bedford, M., Teshima, I., Sweet, K., XP Zhou, X.P., and Nezarati, M."Skeletal and cardiovascular abnormalities in patients with juvenile polyposis of infance associated with microdeletions involving the BMPR1A and PTEN genes" .
January 2007 Agnese, D., Sweet, K. and Kerner, L."Management of cancer risk in BRCA1/2 mutation carriers in a single institution" .
January 2007 Kelly, K.; Sturm, A.; Ferketich, A.; Sweet, K; Schwirian, P; Kemp, K; Westman, J."How can we reach them? Preferences for a Cancer Family History Day campaign in five lower income communities." .
January 2009 Crowder, C.D., Sweet, K., Bellizzi, A. and Frankel, W.F.."Hyperplastic Polyposis Syndrome is an Underdiagnosed & Unclear Entity: An Opportunity for the Surgical Pathologist?" .
October 2009 Sturm, A., Craven, C., Coss, P., Bennett, B., Nottingham. S., Sweet, K.."Family HealthLink: A Unique, Online, Automated Risk Assessment Tool for Cancer and Coronary Heart Disease" .
March 2011 Sweet, K., Sturm, A., Manickam, M., Gordon, E., Keller, M., Stack, C., Christman, M., Marsh, C.."The establishment of the Ohio State University Medical Center-Coriell Personalized Medicine Collaborative research study: Genetic counseling for patients with chronic disease" .
March 2011 Sturm, A. and Sweet, K.."Lessons Learned in Clinical Implementation of an Automated Cancer and Coronary Heart Disease Family History Risk Assessment Tool at a Comprehensive Cancer Center. Presented at American College of Medical Genetics" .
August 2012 Buchanan, D., Sweet, K., Clendenning, M., Walsh1, M., Rosty, C., Young, J., Parry, S.."Polyposis Mutations" Kingscliff.
May 2013 Buchanan, D., Sweet, K., Clendenning, M., Walsh, M., Rosty, C., Young, J., Parry, S.."Polyposis registry" Washington, DC.
September 2013 Sweet, K., Garcia-Espana, F., Sturm, A., Schmidlen, T., Manickam, K., McElroy, J., Toland, M., Roberts, J.S., Christman, M.."Physician Response" Washington, DC.
May 2014 Clendenning, M., Crawford, W., Woodall, S., Arnold, J., Sweet, K., Gallinger, S., Young, J., Rosty, C., Parry, S., Buchanan, D.."Serrated Polyposis" Washington, DC.

Softwares

January 2005 Westman, J.A., Sweet, K., Hampel, H., Eng, C."Jameslink: Personalized Cancer Risk Assessment." 2MD
January 2008 Sweet, K and Sturm, A."Family HealthLink"

Presentations

"Reaching Out To Science Teachers for Genetic Education." Presented at South Carolina Science Council, . (June 1996)

"Personal and Societal Implications of the Human Genome Project." Presented at Georgia Science Teachers Association, . (August 1998)

"Personal and societal implications of the Human Genome Project." Presented at 18th Annual Meeting of the National Society of Genetic Counselors, . (September 1999)

"Cybercounseling in the 21st century." Presented at 52nd Annual Meeting of the American Society of Human Genetics, . (October 2002)

"Communicating cancer risk: reaching out to the public and working with families." Presented at National Society of Genetic Counselors Region IV Education Conference, . (March 2004)

"Molecular classification of gastrointestinal hamartomatous polyposis as a diagnostic adjunct to genetic counseling." Presented at 54th Annual Meeting of the American Society of Human Genetics, . (October 2004)

"Genetic counseling for non-medullary thyroid cancer." Presented at 24th Annual Meeting of the National Society of Genetic Counselors, . (November 2005)

"Putting risks in writing: from letters to brochures." Presented at 24th Annual Meeting of the National Society of Genetic Counselors, . (November 2005)

"Cancer risk assessment and pattern recognition." Presented at Centers for Disease Control: Family History Tools to Improve the Public's Health, . (November 2005)

"Review of the hamartomatous polyposis syndromes." Presented at 9th Annual Meeting of the Collaborative Group of the Americas on Inherited Colorectal Cancer, . (October 2005)

"The JamesLink: a tool to assess cancer risk in your community." Presented at 10th Biennial Symposium on Minorities, the Medically Underserved and Cancer, . (April 2006)

"Promotion and marketing of the JamesLink: a web tool to assess cancer risk." Presented at 11th International Congress of Human Genetics, Brisbane, AU|AUS. (August 2006)

"Polyposis Syndromes." Presented at Nationwide Children's Hospital - Gastrointestinal Disorders, . (March 2009)

"Genetic Counseling and Personalized Healthcare." Presented at Transforming Health Care Through Personalized Medicine Conference, . (October 2009)

"Pharmacogenomics: Update on the Field and Roles for Genetic Counselors." Presented at National Society of Genetic Counselors Annual Meeting, . (October 2012)

"Jane Engelberg Memorial Fellowship Presentation." Presented at National Society of Genetic Counselors Annual Meeting, . (October 2012)

"Hereditary Cancer and Risk Assessment." Presented at Ohio Society Gastrointestinal Nurses Association, . (March 2013)

"Epigenetics 101." Presented at Nationwide Children's Neonatal/Perinatal Symposium, . (May 2013)

"Platform Session (58) Title: Genetic/Genomic Education and Services Delivery." Presented at 64th Annual Meeting of The American Society of Human Genetics, . (October 2014)

 

Unpublished Works

Sweet, K., Sturm, A., Schmidlen, T., Felipe García-España, F., Gordon, E., Manickam, K., McElroy, J., Keller, M., Stack, C.B., Toland, A.E., Roberts, J.S., Christman, M.. A Randomized Controlled Trial of In-Person Genomic Counseling on Patients with Chronic Disease.

Sweet, K., Garcia-Espana, F., Sturm, A., Schmidlen, T., Manickam, K., McElroy, J., Toland, M., Roberts, J.S., Christman, M.. Physician Response to EMR-Based Results for Complex Disease and Pharmacogenomics in a Randomized Controlled Trial of Genomic Counseling.

Schmidlen T, Scheinfeldt L, Zhaoyang R, Kasper R, Sweet K, Gordon E, Keller M, Stack C, Neda G, Jarvis J, Christman M.. Genetic Knowledge Among Participants in the Coriell Personalized Medicine Collaborative. October 2014.