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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. As Chair, Jane Engelberg Memorial Fellowship Advisory Committee (JEMF), the primary funding agency for the National Society of Genetic Counselors, I oversaw development of the "JEMF Graduate Student Award Program" which has since become an annual national award provided to graduate students in training. Applicants submit a formal research proposal, which is reviewed and ranked by the JEMF Advisory Committee. The award supports ongoing work as part of a graduate thesis projects. During my tenure as Chair, we provided awards to 36 graduate students, of which 32 recipients subsequently published thesis work. I was active advisor and mentor on a number of student thesis projects.



I am a faculty adviser for graduate students in the OSU Genetic Counselor Graduate Training Program, and currently a mentor of two graduate students. I provide classroom and clinical instruction for the Training Program.

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

Over the course of 16 years of clinical research at Ohio State University (OSU), my focus of study has been (1) gene discovery and clinical translation for hereditary cancer syndromes, (2) clinical implementation of automated online family history risk assessment tools and, (3) development of genetic/genomic service delivery models. As summarized in the grant and publications sections of my dossier, I have directed and published a number of original investigations (29 since my last promotion) in each of these areas. My work in hereditary cancer syndromes includes 14-year collaboration with investigators at the University of Toronto on hereditary breast-ovarian cancer syndrome. Given lack of study on the condition of hyperplastic (serrated) polyposis, upon professional travel to the University of Brisbane, I was fortunate to make inroads with local investigators which have since become the largest international collaboration on this rare condition. Through work on development of automated family history tools, the OSU Division of Human Genetics has obtained a national reputation and informing public pol icy. In 2008, I launched the online public access version of Family HealthLink® an automated cancer and coronary heart disease family history triage tool. In 2012, I directed the implementation of Family HealthLink® at the OSU Stefanie Spielman Comprehensive Breast Center, and, recently published our findings on clinical utility (i.e. public and patient cohorts) in Genetics in Medicine. Family HealthLink® is listed as a general public resource on the NHGRI website, and the U.S. Department of Health and Human Services. It was promoted through a Wall Street Journal article "The Life-Saving Secrets in Your Family Tree'', and has been advertised on WOSU radio and other local and national media outlets.



As a researcher in the newer field of genomic medicine, I am deeply committed to advancing our understanding of innovative genetic/genomic counseling service delivery models. In 2010, following establishment of an OSU research partnership with the Coriell Personalized Medicine Collaborative, I was asked to lead the design and implementation of a longitudinal study to investigate the impact of in-person genomic counseling in the return of actionable genomic information for complex disease and pharmacogenomics. Specifically, OSU patients with chronic disease managed in an academic medical center receive genomic results through a web-portal, and are randomized to additional in-person post-test genomic counseling versus only the web-based return of results. Through the years, this partnership has evolved into a coordinated effort that takes advantage of the diversity and strengths of each institution. Significant infrastructure was developed that allows confidential sharing of data between institutions, including direct release of study results for uploading to the OSU EHR; extraction of clinical data from the EHR; and transfer of the genomic datasets for research purposes. Study findings led to an NIH/NHGRI R21 award, for which I’m PI on a qualitative research study to assess and develop new genomic counseling service delivery models. In this regard, in the last year we have performed qualitative interviews of OSU-Coriell study participants, and incorporated genomic counseling experts from four academic institutions (University of Michigan; Stanford University; UNC-Chapel Hill; University of Pennsylvania) into the process. I will have a number of first-author publications (2 in process) from this work. This ongoing collaborative and multi-institutional effort will also allow for submission for RO1 level funding in fall of 2015. Lastly, this work also ties into development of the clinical pharmacogenomics program at OSU, and has allowed for my involvement as co-investigator (10% FTE) on the funded Translational Pharmacogenomics Program as part of the NIH/NIGMS Pharmacogenomics Regional Network.



These research accomplishments have resulted in accolades such as invited speaking engagements at international/national/local levels, nominations on four separate committees of the National Society of Genetic Counselors (Jane Engelberg Memorial Fellowship (JEMF); Practice Guidelines Committee; Efficient Delivery of Genetic Services Task Force; and the Personalized Medicine Special Interest Group), and reviewer on numerous outstanding journals. Having now trained and performed research in multiple divergent areas of genetic/genomics, I have gained a unique perspective that is allowing me to forge a novel upward trajectory towards innovative, collaborative and ultimately translational health-related science.



As my teaching has been evaluated by fixed-response surveys with opportunity for open comments, I consistently use this feedback to alter my teaching methodology. I have reflected on and responded to student feedback and have remained motivated to improve the teaching-learning environment through varied instructional approaches. For example, for a new 201 5 graduate level course, Pharmacogenomics 5700, I had opportunity to use online instruction to a larger degree. As effective teaching also involves assessment of student potential for future pursuits in the form of recommendation letters, I’ve had ample opportunity to advise OSU undergraduate/graduate students, with most performing a 1 -2 year internship. These students are evaluated in terms of their academic, clinical, and research capabilities as well as their general character. I have written letters of recommendation for 12 undergraduate/graduate students pursuing advanced degrees, and all have successfully advanced to the next level. As Chair, JEMF, the primary grant funding agency for the National Society of Genetic Counselors (NSGC), I was involved with development of the "JEMF Graduate Student Award" which supports ongoing work for graduate thesis projects of genetic counseling students in training. Applicants submit a formal research proposal, which is reviewed and ranked by the JEMF Advi sory Committee. During my tenure as Chair, we provided awards to 36 graduate students, of which 32 subsequently published thesis work. I was active advisor and mentor for a number of these students. I am also faculty adviser for graduate students in the OSU Genetic Counselor Graduate Training Program and currently a mentor of two graduate students. I provide classroom and clinical instruction for the Training Program. Lastly, in recent years, I authored two peer-reviewed books on genomic medicine; one for medical professionals: "The Busy Physician's Guide to Genetics, Genomics and Personalized Health Care"; the second for the lay public: "You r Genes, Your Health and Personalized Medicine"; each are used in graduate and professional education.



My accomplishments in service include both university and professional/national service. In my capacity as licensed genetic counselor, I provide university service and to the OSU Division of Human Genetics as a licensed and certified genetic counselor. I serve as graduate student adviser, and faculty member for the OSU Genetic Counselor Graduate Training Program. I 'm an active member of the OSU Personalized Genomic Medicine Working group; the OSU Translational Pharmacogenomics Project; and the OSU Bioinformatics Research Group. I served a two-year term on the OSU Cancer Institutional Review Board; and multiple years on the 1) OSU Clinical Implementation Working Group; 2) OSU Personalized Health Assessment Working Group; 3) OSU E-Tablet Initiative; and 4) OSU Personalized Healthcare Virtual Genomics Working Group. At the professional level, through invited presentations locally, nationally and internationally I strive to bring recognition to the tremendous merits of OSU. I was a founding member and Chair, NSGC Personalized Medicine-Special Interest Group, a core driver for genomics education and development of applications/tools to support our profession. I am currently involved (3-year service commitment) as elected Advisor to the NSGC Practice Guidelines Committee, and, more recently asked to join a new NSGC Efficient Delivery of Genetic Services Task Force. I was part of the Planning Comm ittee, invited Abstract Reviewer and Program Moderator for the 2014 American Society of Human Genetics conference. I will continue such service accepting more opportunities as presented as my research continues to attract prominence in multiple disciplines, whilst forging lucrative contacts with colleagues across the world.

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 Journal
2013 - present British Medical Genomics
 

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. Vol. 6, (January 2008.): 288-299.

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. Vol. 36, no. [epub ahead of print]. (February 2009.): 732-741.

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.

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-.

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.

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.

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.

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., 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. "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.

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-.

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-.

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.

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.

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.

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.

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" Vancouver.
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.
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.
September 2014 Sweet, K., Garcia-Espana, F., Sturm, A., Schmidlen, T., Manickam, K., McElroy, J., Toland, M., Roberts, J.S., Christman, M.."Physician Response" San Diego.

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, Atlanta, GA. (June 1996)

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

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

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

"Communicating cancer risk: reaching out to the public and working with families." Presented at National Society of Genetic Counselors Annual Education Conference, Washington, DC. (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, Toronto, CA|CAN. (October 2004)

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

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

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

"Review of the hamartomatous polyposis syndromes." Presented at 9th Annual Meeting of the Collaborative Group of the Americas on Inherited Colorectal Cancer, Salt Lake City, UT. (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, Washington, DC. (April 2006)

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

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

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

"The establishment of the Ohio State University Medical Center-Coriell Personalized Medicine Collaborative Research Study: Genetic Counseling for Patients with Chronic Disease." Presented at American College of Medical Genetics Annual Education Conference, Vancouver, CA|CAN. (May 2011)

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

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

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

"Epigenetics 101." Presented at Nationwide Children's Neonatal/Perinatal Symposium, Columbus, OH, US|USA. (May 2013)

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

 

Unpublished Works

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. March 2015.

Sweet, K., Sturm, A., Schmidlen, T., Manickam, K., McElroy, J., Keller, M., Stack, C.B., Toland, A.E., Roberts, J.S., Christman, M.. Understanding/Satisfaction Outcomes for Genomic Counseling of Patients with Multiplex Results.