Each student is required to complete a research project on a topic of their choice related to the genetic counseling profession. Students are introduced to the research project in the Fall and Winter semesters of their first year in the Research Project Seminar (MGG 7999, section 001, Fall Y1) and Biostatistics 1 (FPH 7015, Fall Y1). In these courses, students learn about the research process including study design, institutional review boards, data analysis and professional writing. The project is self-directed and generally involves formulating and testing a hypothesis.
Examples of student projects might include the following: a report on a small series of cases which illustrates a novel concept or answers a specific question; the evaluation of an innovative educational tool, screening tool, or counseling strategy; analysis and interpretation of data from an existing research project or database to answer a new question; or generation of new data followed by analysis and interpretation to answer an original question.
Students present their research findings during the genetic counseling seminar series in the final semester of study. It is also expected that students will submit an abstract of their research project to a national meeting (e.g., NSGC, ASHG, ACMG) and for publication when appropriate. The research project falls under the University’s Plan B for Master’s students.
Westrate, L., Brennan, S., Carmany, E.P. (2020) Assessing the availability and quality of Spanish-language genetic resources for patients on the internet. J Genet Couns. 29(3):381-390. doi: 10.1002/jgc4.1267. Epub 2020 Mar 30.
Anbouba, G., Carmany, E.P., Natoli, J. (2020) The characterization of hypodontia, hypohidrosis, and hypotrichosis associated with X-linked hypohidrotic ectodermal dysplasia: A systematic review. Am J Med Genet A. 182(4):831-841. doi: 10.1002/ajmg.a.61493. Epub 2020 Jan 25.
Jackson L, Cichon M, Kleinert H, Trepanier A. (2019) Teaching medical students how to deliver diagnoses of Down syndrome: Utility of an educational tool. Patient Educ Couns. pii: S0738-3991(19)30447-1. doi: 10.1016/j.pec.2019.10.011. Epub ahead of print
VandenBoom E, Trepanier AM, Carmany EP. (2018) Assessment of Current Genetic Counselor Practices in Post-Visit Written Communications to Patients. J Genet Couns. Jun;27(3):681-688. doi: 10.1007/s10897-017-0163-y.
Cunningham M, Morreale M, Trepanier A. (2018) "Referrals to Mental Health Services: Exploring the Referral Process in Genetic Counseling".J Genet Couns. Feb;27(1):289-300. doi: 10.1007/s10897-017-0147-y.
Trepanier A.M, Supplee L., Blakely B., McLosky J., Duquette D. (2016) "Public Health Approaches and Barriers to Educating Providers about Hereditary Breast and Ovarian Cancer Syndrome" Healthcare (Basel), 4(1). pii: E19. doi: 10.3390/healthcare4010019.
Thompson A.B., Cragun D., Sumerau J.E., Cragun R.T., DeGifis V., Trepanier A. (2016) "Be Prepared if I Bring It Up:" Patients' Perceptions of the Utility of Religious and Spiritual Discussion During Genetic Counseling. J Genet Couns. Advance Online Publication doi: 10.1007/s10897-015-9922-9
Zwiesele S., Bannick A., & Trepanier A. (2015) Parental strategies to help children with phenylketonuria (PKU) cope with feeling different. Am J Med Genet A, 167(8), 1787-95. doi: 10.1002/ajmg.a.37088
Reeves A., & Trepanier A. (2015) Comparison of Informed Consent Preferences for Multiplex Genetic Carrier Screening among a Diverse Population. J Genet Couns. Advance Online Publication. doi: 10.1007/s10897-015-9854-4
Burgess K.R., Carmany E.P., & Trepanier A.M. (2015) A Comparison of Telephone Genetic Counseling and In-Person Genetic Counseling from the Genetic Counselor's Perspective. J Genet Couns. Advance Online Publication. doi: 10.1007/s10897-015-9848-2
Cote M.L., Harrison M.J., Wenzlaff A.S., & Schwartz A.G. (2014) Re-contacting participants for inclusion in the database of Genotypes and Phenotypes (dbGaP): Findings from three case-control studies of lung cancer. Genome Med, 6(7), 54. doi: 10.1186/s13073-014-0054-x
Recent Plan B Project Titles
|Student Name||Year||Plan B Project Title|
|Lauren DeMeyer||2020||Exploring hypermobile Ehlers-Danlos syndrome from the parent perspective|
|Taylor Hayes||2020||Investigating factors that influence genetic counselors’ decisions to refer patients to mental health providers|
|Hafsah Jamil||2020||The public's perception of prenatal diagnostic testing: A qualitative analysis of posts on internet forums|
|Nicole Lester||2020||A time-analysis study on genetic counselors and genetic counseling assistants|
|Gabrielle Pormorski||2020||Navigating the competitive landscape of genetic counseling program admission: A qualitative study|
|Siddika Venkatachalam||2020||A time-analysis study on genetic counselors and genetic counseling assistants|
|Natalie Vriesen||2020||Clinical outcomes of preimplantation genetic testing for hereditary cancer predisposition syndromes: A systematic review|
|Kristian Wilks||2020||Predictors of genetic testing disclosures and cascade screening among family members in a cancer setting: A literature review|
|2019||Assessing shared decision making during conversations between patients and oncologists regarding chemotherapy and Oncotype DX score|
|2019||Time to electronic and patient notification of germline genetic test results: One center’s experience|
|2019||Development of a fact sheet about fetal surgery for spina bifida|
|2019||Applying the social ecological model to evaluate the utilization of genetic services by a group of Latina women with a personal history of breast cancer|
|2019||LDS parental decisions to accept or decline prenatal testing for Down syndrome|
|2019||Examining patient factors influencing the interpretation of inconclusive genetic results|
|2019||Michigan health plans and their genetic testing policies on hereditary breast and ovarian cancer syndrome and Lynch syndrome|
|2019||A content analysis of post-visit written summary communication in genetic counseling|
|Grace Anbouba||2018||Characterization of hypodontia, hypohidrosis and hypotrichosis associated with X-linked hypohidrotic ectodermal dysplasia: A systematic review|
|Sarah Austin||2018||Exploring the role of the genetic counselor in cascade screening|
|Lexie Gohlke||2018||Development of a computer-aided genetics education module on screening and testing for fetal chromosome conditions and carrier status|
|Bailey Hulswit||2018||Genetic educational needs of rural Michigan non- genetic health care professionals: Results of a novel survey conducted within the Thumb Rural Health Network|
|Cassidy Measner||2018||Parent perceptions of genetic counseling encounters for prenatal diagnoses of Down syndrome|
|Claire Plack||2018||Patient satisfaction with access to genetic counseling services|
|Chandler Stimach||2018||Genetic counselor interactions with genetic testing industry: Prevalence, influencing factors and perceptions|
Genetic Counseling Graduate Program
Center for Molecular Medicine and Genetics
Wayne State University School of Medicine
3127 Scott Hall
540 E. Canfield Avenue
Detroit, MI 48201
Fax: (313) 577-9137